Document O1NojYeXe1XGeOQdRRxkLnVRL
3M Medical Department Study: T6316-S
Analytical Report: FACT TOX-013 LRN-U2095
Study Title
AnalyticSatludy2(N-Ethylperfluoroocstualnfeonamido)-ethainnol Two Generation Rat Reproduction
AnaVical Laboratory Report Title
Determinationofthe Presence and ConcentrationofPFOS, M556, PFOSAA, and PFOSA inthe Liverand PFOS, M556, PFOSAA, PFOSA, and ETFOS&OH inthe Sera ofCri:CCPBR VAF/Plue
Rats Exposed to ETFOSE-OH
Data Requirement Not Applicable
Author 3M Environmental Laboratory
Study Completion Date At signing
Performing
Sera Anatyses 3M EnvironmentalLaboratory
Building2-3E-09, 935 Bush Avenue St.Paul, MN 55106
Laboratories Uver Analyses
BattellMeemodal Institute
505 King Avenue
Columbus, OH 43201-2693
Project ldentirication
3M Medical Department
Study: T-6316.5
Argus In-LifSetudy:418-009
Analytical Report: FACT TOX-01 3
3M Laboratory Request No. U2095
TotalNumber of Pages 135
3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
Thispage has been reservedforspecificountryrequirements.
3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
GLP Compliance Statement
AnalyticalLaboratory Report Title: Determinationof the Presence and Concentration ofPFOS, M556, PFOSAA, and PFOSA inthe Liverand PFOS, M556, PFOSAA, PFOSA, and ETFOSE-OH inthe Sera of Crl:CCPBR VAF/Plus* Rats Exposed to ETFOSE-OH
Study IdentificatioNnumber: T-6316.5, FACT TOX-01 3, LRN-U2095
This study was conducted incompliance withUnited StatesFood and Drug Administration(FDA) Good LaboratoryPractice(GLP) Regulations21 CFR Part58, withthe exceptionsinthe buileted lisbtelow.Allraw data,protocol,analyticarleportand.samples forthisstudy are retainedin archivesat the 3M Environmental Laboratoryand willbe retainedfora periodof at leastten years. The analyticaplhase completed at the 3M Environmental Laboratorywas performed in accordance with3M ET&SS Standard Operating Procedures.
Exceptions to GLP compliance:
There were two study directorsinthisstudy.This study was designed as two separate studies.The in-lifpehase was considered to end atthe generationand shipment of specimens. The analyticasltudy was considered to startat the receiptofthese specimens foranalysis.This resultedin having two separate study directorso,ne foreach phase of the same study.However, since the technicalperformance of each phase was entirely separate,no effectisexpected from thisexception.
Some changes made inthe standard preparationlogs obscured the originaelntry,did not document the reason forthe change and/orwere not initialeadnd dated by the person making the change.
The samples thatwere analyzed on 3/16/00 utilizesdtandards thathad an expirationdate of 2/00.
Livervalues generated at contractlaboratorieswere correctedby 3M Environmental Laboratoryto reflecthe officiaplurityvalues from the COA. Revised finalreportswillbe solicitefdrom the contractlaboratoryand willbe added as a reportamendment at a later date.
* Expirationdates on some reagents and solutionswere missing.
Study Director
@@
@?@ 3
-// ..-
SponsorRepres-entative
Date
OCA 6-et . Date
3M EnvironmentaLlaboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
GLP Study-Quality Assurance Statement
AnalyticalLaboratoryReport Title: Determinationof the Presence and Concentration of PFOS, M556, PFOSAA, and PFOSA inthe Liverand PFOS, M556, PFOSAA, PFOSA, and ETFOSE-OH inthe Sera of Crl:C(DPBRVAF/PlusO Rats Exposed to
ETFOSE-OH
Study IdentificatiNounmber T-6316.5,FACT TOX-01 3, LRN-U2095
This study has been inspectedby the 3M Environmental LaboratoryQualityAssurance Unit (OAU) as indicatedinthefollowingtable.The findingswere reportedto the study directorand
laboratorymanagement.
Inspection Dates
Phase
Date Reported to Management Study Director
10/12199
Extraction
10/26/99
10/26/99
6/5/00- 6/14/00
Data
6/16/00
6/16/00
9/11/00- 9/13/()0
Draftreport
9/14/00
9/14/00
t: QAURep@rne@stative@
3M Environmental Laboratory
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3M Medical Department Study: T6316.S
Analytical Report: FACT TOX-013 LRN-U2095
Tableof Contents
GLP ComplianceStatement.....................................................3.......................... GLP Study--QualityAssurance Statement ........................................4..........................
Study Personneland Contjibutm ................................................7.......................... Introductioannd Purpose ........................................................a..........................
Test System ...............................................................8.......................... Specimen CoUecfionand Analysis..............................................9.......................... Specimen Receiptand Maintenance ..............................................9.......................... Chemical Characterizatio.n......................................................1.0........................ Dose ConfirmationAna@y@ ..................................................1.0........................ Method Summaries ............................................................I..I........................ 3M EnvironmentalLaboratory..................................................1.1........................
PreparatoryMethod .......................................................1.1........................ AnalyticaMlethod .........................................................1.1........................ AreVical Equipment......................................................1.1........................ Devietk)m..................................................................12......................... Data QualityObjectivesand Data Integrit.y........................................1.2........................ Data Summary, Analyses,and Results...........................................1.3........................ Summary ofQuafityControlAnalyses Results...................................1.3........................ Summary ofSample Results..................................................1.4........................ StatisticMaelthods and Calculations..............................................1.4........................ Statement ofConclusion................................................................................1.4.....................
Appendix A: Chemical CharacterizationC,ontrolMatricesand Dose ConfirmationAnalyses.............................................................1.5........................ Appendix B: Protocol............................................................18........................ AppeMix C: Extracbm and AnalyticaMlethods .....................................3.7........................
ETS43-4.1,ExtractioonfPotassium Perfluorooctanesulfonatoer other Fluorochemical Compounds from Serum forAnalysisUsing HPLC-Electrospray/Mass Spectrometry. (14pages)....................................................................3.8.......................
ETS-8-5.1,AnalysisofPotassium Perfluorooctanesulfonatoer Other FluorochemicaLs inSerum ExtractsUsing HPLC-Electrospray/MassSpectrometry,(9 pages)............5.2........ Appendix D: Data Summary Tables ..............................................6.1........................ Appendix E: Data Spreadsheets ..................................................6.4....................... Appendix F: Example Calculadons................................................7.0....................... Appendix G: ContractLab Report.................................................7.1....................... Appendix H: lntedm CertificatoefAnalysis.........................................1.3.1......................
3M Environmental Lahoratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
Appendix 1:Report Skjnature Page ..................................................1.3.5..........................
Listof Tables
Table 1. Test System Popula6on Demographics and Dosage Levels for S" (418-009.)..........................................................8...........................
Table 2. Characterizationofthe Test Ar6c]einStudy FACT TOX-01 3 ...................1.0............. Table 3. Negafive Ions Monitored in3M LaboratoryAnalyses ..........................1.2................... Table 4. DeviationSummary forFACT TOX-013 .....................................1.2........................... Table 5. Determinationsof the LOO inthe Analyses of Serum Extracts..................13............ Table 6. Characterizatioonf the ControlMatricesUsed forSera Analyses In
S" FACT TOX-01 3 .....................................................1.5.......................... Table 7. Characterizatioonf the ControlMatrices Used forLiverAnalyses in
S" FACT TOX-0 13 .....................................................1.5.......................... Table 8. Characterizatioonf the AnalyticalReference MaterialsUsed forSera Analy@
inStudy FACT TOX-0 13 ...................................................1.6..........................
Table 9. CharactednOon of the AnalyticalReference MaWals Used forLiverAnaty@ InS" FACT TOX-01 3 ...................................................1.6..........................
Table 10. Tween Dosing ConfirmationforStudy In-ffe#418-009 ........................1.7................ Table 11.Tween Dosing Confirmaton--Matrix Spikes forStudy ln4ife#418-009 ..........1.7..... Table 12. Reported Fiuorochemical Levels In Sera Analyses inStudy FACT TOX-0 13 ....6.1.
Table 12. Reported FluorochemicalLevels in Sera Analyses inStudy FACT TOX-013 (continued.)..............................................................6.2..........................
Table 13. Reported FluorochemicalLevels in LiverAnalyses inStudy FACT TOX-013 ....6.2. Table 13. Reported FluorochemicalLevels inLiverAnalyses inStudy FACT TOX-01 3
(continued.)..............................................................6.3..........................
3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
Study Personnel and Contributors
Study Director
Marvin T. Case, D.V.M.,Ph.D, Study Director 3M Corporate Toxicology- MedicalDepartment 3M Center, Building220-2E-02 St.Paul,MN, 55144-1000 651-733-5180
Sponsor
John L. Butenhoff,Ph.D.,Sponsor Representative 3M CorporateToxicology- Medical Department 3M Center, Building220-2E-02 St. Paul,MN 55144-1000
Ana"cal Chemistry Laboratories
Sera Analyses 3M EnvironmentalLaboratory(3M Lab) KristenJ.Hansen Ph.D..AnalyticaIlnvestigator
LiverAnalyses BattellMeemorial Institute ion C. Andre, Ph.D.,AnalyticaIlnvestigator
3M Lab ContributingPersonnel
David R. Bamidge. Ph.D. LisaA. Clemen Lisa Dick,Ph.D. KellyJ. Dorweiler Mark E. Ellefson Sara E. Estes Barb A. Gramenz Sarah A. Heimdal Cari S. Hewitt Marlene M. Heying
Harold 0. Johnson KellyJ. Kuehlwein SallyA. Linda Joseph C. Pilon Scott R. Post 12n A. Smith Kathy M. Stock
Anh-Dao Vo Bob W. Wynne
Location of Archives
Alloriginalraw data,protocol,and analyticarleporthave been archivedat the 3M Environmental Laboratory.The testsubstance and analyticarleferencestandard reservesamples, as wellas the specimens pertainintgo the analyticaplhase ofthisstudy,are archived atthe 3M Environmental Laboratory.Controlsera and liverwillbe maintained at the contractlabalong withthe test substance.
3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
Introductioannd Purpose
The purpose of the study is to determine the presence and concentration of PFOS, PFOSA
PFOSAA, and M556 in liversamples and PFOS, PFOSA, sera samples collectedfrom rats exposed to ETFOSE-OH.
PFOSAA, ETFOSE-OH, and M559 in This study was initiatedon 1 October
1998.
Test Systwn
Five groups of FO generation male and female rats and 3 groups of Fl generation male and female rats were used as the testsystem. Table I outlines the rat population demographics and dosage levels for study 418-009.
On day 4 of lactation,lifterwsere culled to four male and four female pups, where possible. On day 21 of lactation,25 male and 25 female pups in Groups 1,11,and IIIwere selected for continued evaluation. Fl generation male and female rats were given appropriate dosages of the test article via gavage beginning on day 22 of lactationor postpartum through the day before sacrifice.
The testsystem species and strainselected was the Crl:CMR VAF/Plus* (Sprague-Dawley) rat received from Charles River Laboratorias, Inc.,and assigned temporary numbers untilassigned to the study. Rats were permanently identifiedusing Moner self-piercingear tags when assigned to the study. FO generation ratswere identifiedwith ear tags. Pups were not identifiedduring lactation,as parameters were evaluated in terms of the lifterA.t weaning, each Fl generation rat selected for continued observation was identifiedwith a Monei*self-piercing ear tag. FO female rats were approximately 65 days of age and weighed approximately 179-22gg when received. FO male rats were approximately 58-67 days of age and weighed approximately 223-331 g when received. Weight data are included inArgus Research Laboratories, Inc.finalreport (study number 418-009).
Table 1. Test System Population Demographir-s and Dosage Levels for Study (418-009)
Populaflon
Number of FO Generation Rats
per Sex
Number of Fl Generation Rats
per Sex
Dosage (mgfkgiday)
Dosage Group 1 35
(ConbDo
Dosage Group 11
35
Dosage Group 111
35
Dosage Group IV
35
Dosage Gmup V
35
25
0 (vehide)
25
1
25
5
-
10
15
3M Environmental Laboratory
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3m Medical Department Study: T6316.S
Analytical Report: FACT TOX-013 LRN-U2095
Specimen Calkteflonand Analysts
Sample specimenswere collectebdy Argus(study418-009)and senttothe3M Environmental LaboratoryforanalysisL.iverand sera specimens were collectedfrom FO male ratsatthe completionofthe cohabitationperiodand FO female ratson day 21 postpartum.Liverspecimens were collectedfrom FO generationlitterasn,d stomach contentspecimens were collectedfrom the FO and F2 generationlitterTsh.e analysisofthe stomach contentswere not partofthe scope of analysisdetermined by the study directorT.he number and type ofspecimens collectedfor analysesinthe analyticaplhase ofthisstudy are presented below.
Specimens Collectedfrom Study Groups Ithrough V (through 11/30/98): Serum Specimens-45 specimens LiverSpecimen&-65 specimens
Blood specimens were centrifugedaftercollectionS.erum was then harvestedand immediately frozenon dry iceand maintainedfrozenat-70*C untilshipped tothe 3M Environmental Laboratory.Liverspecimens collectedfrom each animalwere frozenand retainedat-70*C until shipped tothe 3M EnvironmentalLaboratory.Stomach contentspecimens were frozenat-20*C untilshipped tothe 3M EnvironmentalLaboratory.Liver,sera,and stomach contentspecimens were shipped tothe 3M EnvironmentalLaboratoryfrozenand on dry ice.
Sera and liversamples were extractedbeginningon October 11, 1999 usingan ionpairing reagentand methyl-tert-buteytlher(MTBE) forthe sera and ethylacetateforthe liversamples. Liversamples were homogenized priortothe extractionprocedure.Sample extractswere analyzed usinghigh-performanceliquidchromatography-electrospray/tandemass spectrometry (HPLC-ESMSMS) inthe multiplreesponse monitoringmode. PFOS, PFOSA, PFOSAA, ETFOSE-OH, and M556 levelswere quantitatedby externalcalibrationP.FOSEA was not analyzed due toinconsistenatnalysisand failedQC. Analyticaldetailsare includedinthisreport.
Specimen Receipt and Maintenance
The 3M EnvironmentalLaboratoryreceivedfrom Argus, serum, liverand stomach content specimens collecteadtpredeterminedtime pointsduringand atthe end ofthein-iffpehase of Argus study 418-009 on 8-4-98,10-1-98 and 1-29-99.Allspecimens were receivedfrozenan dry iceand were immediatelytransferretdostorageat-200C IOOC. Specimens thatwere analyzed at Battellweere shipped frozenon dry ice.
Controlmatricesused inliverand sera analyseswere obtainedfrom commercial sources and are presented inTable 6 and 7.Samples analyzed atthe 3M EnvironmentalLaboratorywillbe maintainedfora periodof10 years and willbe storedatthe laboratoryat-20"C l OOC.
3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
Chemical Characterization
ETFOSE-OH CAS Number: 1691-99-2
Chemical Formula:C,F,7SO,N(CH,CH,)CH2CH,OH MolecularWeight:571.0
Chemical characterizatioinformationon the testarticliespresented intabularform below. Chemical characterizatioinformationon the analyticarleferencematerialsused inthisstudyis presentedintabularform inAppendix A (see Tables 8 and 9)and the interimCertificatoef AnalysisavailableinAppendix 1.
Table 2.Characterizationof the Test Articlein Study FACT TOX-OI 3
Test Article
Chemical Name Soume
ETFOSE-OH
FM-3929 2(N-Ethylperfluorooctanesulfc>namido)-ethanol
3M
ExpirationDate
05/2000
Storage Conditions
Ambient temperature
Chemical Lot
30035,30037,30039
Physical
DescripUon
Waxy Solid
Purity
To be determined*
*Thepuritoyfthetestarticdleeterminerdoominalb@y NMR onslys@S.ubsequentchemical
charactermation isoocumng and th-tsanaV@--al report wil be amended oedfficatoof ana"is isLssued.
to lndkee the puritywhen a
Dose Confinmaton Azmlyses
The dose confirmation data were collected according to a method that was notfullvyalidated. Dose confirmatioannalyseswere performed on testarticlseamples taken atthe startofdosage,
at6 weeks, and atthe end ofdosage duringthe in-lifpehase ofthe study.
Dose confirmationanalyseswere performed on 3 dose levelscollectedduringthe in-lifpehase of the study:the resultsare presentedinAppendix A (see Tables 10 and 11).
Dose confirmatiownas performed by dilutintghe Tween dose samples withMilli-wOater intothe
linearange ofthe instrumentF.or each sample, a matrixspikewas prepared (atapproximately 50-100% ofthe expected dose level). In all cases, samples were analyzed versus an unextracted
curve using HPLC-ES/MS/MS.
The instrumental parameters and analyticalconditions described
inETS-8-5.1 were used fordose solutionanalyses.
3M Environmental
Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
Method Summaries
Following is a brief description of the methods used during this analytical study by the 3M Environmental Laboratory. Detailed descriptions of the methods used are located in Appendix C. The methods and analyticalequipment settingsused by Battelleare presented in the Battellefinal report (see Appendix G).
3M EnArorwnerdal Laboratory
PREPARATORY METHOD ETS-8-4.1, "Extractionof Potassium Perfluorooctanes ulfonate or Other Fluorochemical Compounds from Serum forAnalysis using H PLC-Electrospray/M ass Spectrometry'
Sera samples were extracted using an ion-pairingextraction procedure. An ion pairing reagent was added to the sample and the analyte ion-pairwas partitionedinto MTBE. The MTBE extract was transferred to a centrifuge tube and put onto a nitrogen evaporator untildry. Each extract was reconstituted in 1.0 mL of methanol, then filteredthrough a 3cc plasticsyringe attached to a 0.2@im nylon filteirnto a glass autovial.
At4ALYnCAL METHOD ETS-8-S.i, 'Analysis of Potassium Perfluoroocta nesulfon ate or Other Fluorochemicals in Serum Extracts Using H PLC-Electrospray/M ass Spectrometry'
The analyses were performed by monitoring one or more product ions selected from a slingle
primary ion characteristicof a particular@uorochemical using HPLC-ESMSMS.
For example,
molecular ion 499, selected as the primary-ion for PFOS (QF,7S03-)
analysis, was
fragmented furtherto produce ion 99 (FSO,-). The characteristicproduct-ion 99 was
monitored forquantitative analysis.
ANALY-ncAL EOUIPMENT The followingequipment phase of this study.
and parameters are representative of those used during the analytical
Liquid Chromatograph: Hewlett-Packard* Series 1100 Liquid Chromatograph
Analyticalcolumn: Keystone BetasilTm Cle 2x5O mm (5 pm)
Column temperature: Ambient
Mobile phase components: Component A: 2mM aqueous
ammonium
acetate
Component B: methanol
Flow rate:300 pumin
injectionvolume: 10 pL
Solvent Gradient: 10 minutes
Start at 40%B
Hold at 40%B for I minute
Increase to 95%B over 3.5 minutes
system
3M Environmencal Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
Hold at95%B for2 minutes Return to40%8 over 0.5 minutes Hold at40%B for3 minutes
Mass Spectrometer: Micromass* API/Mass Spectrometer Quattro11-TriplQeuadrupole system
Software:Mass Lynx@ 3.2 Cone Voltage:20-60 V CollisioEnnergy: 25-45 eV Mode: ElectrosprayNegative Source Block Temperature: 1500C l OOC Z-spray source AnalysisType: MultipleReactionMonitoring(MRM)
Table3. NegativeIons Monitored In3M LaboratoryAnalyses
TargetAnalyto
PrimaryIon(AMU)
Product Ion(AMU)
PFOS PFOSA PFOSAA
499.0 498.0 584.0
99.0 78.0 169.0
ETFOSE-OH M556
THPFOS
630.0 556.0 427.0
59.0 78.0,169.0
80.0
oeviatiom Deviationsfrom the originaplrotocoland methods are documented inthe tablebelow:
Table 4. DeviationSummary forFACT TOX-013
Deviatton
Date(s)ofOccurrence
Pk>ettewas used instead Oxford dispenser
IQ/12/99
02-I.OmL ofsample was used forex"ction insteadof l.OmL.
Milkcurd umples were not anawed.
I-
10/12/99 Entirestudy
Impact on Study
Standards and samples were prepared identkmltyN.o adverse knpact on swdy. Cunvnt work IndicatesOW volumes kO.5 mL provideresub equivalentto 1 mL extmctionvolumes. Resub ofsample volumes <0.5 mL have not been valklated and wig be marked inft date taus. No milkcurd data isavailableforft final report
Data QualityObjectives and Data Inte-grity
The followingdata qualitoybjectives(DQOS) were indicatedinthe method performancesectionof ETS-8-5.1,'AnalysisofPotassium Perfluorooctanesulfonatoer Other FluorochemicalsinSerum ExtractsUsing H P LC-Electrospray/Mass Spectrometry*:
3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
0 LinearityT:he coefficieonftdeterminatio(nr2) equaltoorgreaterthan 0.980 0 Limitsof Quantitation(LOQ):The LOQ forPFOS is5.55ppb, PFOSA is4.79 ppb, PFOSAA
is20.5 ppb, ETFOSE-OH is36.2 ppb, and M556 is 19.2ppb.
0 Acceptable Spike Recoveries,70-130%
Data Summary, Analyses, and Results
Withthe exceptionsnotedinthisreportd,ataqualityobjectivefsortheanalyticaplhase ofthis studyoutlinedinthe 3M EnvironmentalLaboratorymethod ETS-8-5.1 (seeAppendix C) and the Battellefinalreport(seeAppendix G) were met. Although extractioannd analysiswere initiateidn September 1998,the study was reprioritizaendd put on hold.Upon restartintghe study,the decisionwas made toreextractand analyze the specimens. No datafrom the originaalnalysisare includedinthisreportT.he datainthisreportreflecotnlythatobtainedfrom specimens extracted on, orafterOctober 11,1999.
Sumrnary of Quality Control Analymm Results
Linearity:The coefficienotfdetermination(r2)ofthe standardcurveswere'->0.980.
CalibrationStandards: Quantitatioonfthe targetanalyteswas based on linearegression analysis(1/xweighted)oftwo extractedmatrixcurves bracketingeach group ofsamples. High or low pointson the curve may have been deactivatedtoprovidea betterlinearfitover the concentrationrange most appropriatetothe data.Allactivecurve pointsare accuratetowithin 70% oftheoreticavlalue.Low curve pointswithpeak areas lessthan two times thatofthe extractionblankswere deactivatedtodisqualifay data range thatmay have been significantly affectedby background levelsofthe analyte.Occasionally,a singleoutliecrurve pointmay have been deactivatedQ.uantitationofeach analytewas based on the response ofone or more specifipcroduction(s)usingthe multipleresponse-monitoringmode ofthe instrument (see Appendix C).
Limitsof Quantitation(LOQ):The LOQ isequaltothe lowestacceptedstandardinthe calibratiocnurve (definedas a standardwitha concentrationthatiswithin30% ofthe theoreticavlalue,and which has atleasttwo times the analytepeak area detectedinthe extractiobnlanks).
Table S.Determinationsof the LOQ inthe Analyses ofSerum Extmcts
Analyto
Method LOQ
PFOS
5.55ppb
PFOSA
4.79 ppb
PFOSAA ETFOSE-OH
20.5 ppb 36.2ppb
M556
24.9 ppb
3M Environmental Laboratory
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3M Medical DeDartment Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
Blanks:Allblankswere below thelowerlimiotfquantitatifoonrthe compounds of interesTto, simplifyanalyses thatwere complicated by endogenous levelsoffluorochemicalsin unexposed ratsera,rabbitsera was selectedas a suitablesurrogatematrixforstandard
curves.
Precision: Precisionwas determined by analysisof MS/MSD 10%.
and was reproducibleto within
a Matrix Spikes: Matrix spikes and matrix spike duplicates were extracted with each set of samples and analyzed duringanalyticarluns.With the exceptionof M556, allsera matrix spikeswere within30% ofthe theoreticacloncentration.Both matrixspikesshowed a recovery of 69% forthe M556. These resultswere verifiedD.ata qualityobjectiveswillbe adjusted to reflecthisrecovery.
Surrogates: The surrogate(THPFOS) was added to allsamples and standards.THPFOS was not used forquantitationb,utwas used to monitorforgross instrumentfailureT.he surrogateresponse of each analyticarlun was verifiedto determine thatitdidnot vary more than:t50% from the mean withineach analyticarlun.
Assuming spikerecovery studiesform a suitableindicatioonf endogenous analyterecovery,sera data are quantitativteo 30% forallanalysisbut M556; M556 data isquantitatedto 31%. The validitoyf thisassumption has not been verifiebdy othertechniques.
Sumnwy of Sample Results Samples from Control Animals: Low levelsof PFOS, PFOSA, PFOSAA, ETFOSE-OH, and
M556 were oftendetected inthe sera and liverof the controlanimals.These levelswere significantloywer than those found inthe low dose testanimals.
Samples from Dosed Animals: In general,PFOS, PFOSA, PFOSAA, ETFOSE-OH, and M556 levelsfound inthe sera and liverofthe testanimals increased withdose group. Detailed sample data tablesare presented inAppendices D and E.
StatisticaMlethods and Calculations
Statisticamlethods were limitedto the calculationof means and standard deviations.See Appendix F forexample calculationsused to generate the liverand serum sample data inFACT TOX-0 13.
Statement of Conclusion
Under the conditionsof the present studies,PFOS, PFOSA, PFOSAA, ETFOSE-OH, and M556 were observed inthe sera and liverof ratsdosed with ETFOSE-OH duringthe in-lifpehase of the study.
3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
Appendix A: Chemical CharacterizationC,ontrolMatricesand Dose ConfirmationAnalyses
Table 6.Characterizationof the Control Matrices Used for Sera Analyses in Study FACT TOX-01 3
Location
3M Lab
ControlMatrix
Rat Serum (TN-A-2001)
Rabbit Serum (TN-A-2573)
Source Expirabon Date
Stor-agCeonditons FChemicalLot #
PhysicalDescription NIR-not recorded
sigma 20io
Ambient 17H93O6 Rat Serum
Sigma
2010
Ambient 11BH8418 RabbitSerum
Table 7.Characterizationof the Control Matrices Used forLiverAnalyses in Study FACT TOX-Oi3
Location
BattelleMemorial Institute
ControlMatrix
Source ExpiratonDate StorageConditions ChemicalLot PhysicalDescription N/R--notrecorded
Rat Liver
Harlan N/R N/R N/R
Rat Liver
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Table 8.Characteftationofthe AnalyticalReference MaterialsUsed forSera Analyses InStudy FACT TOX013
Lor-ation
3M Lab
PFOS
C-pFir%Os.
PFOS@K
C$FgSO@4Hs
PFOSAA
CF,TSOIN((PHXH&) (CHaCO014))
ET.FOSE-OH
CgF,rSON(CHXH2) ..CHICHOH
M556
CFOSCX(H) (CHICHs))
THPF.O$*
CMgF,;NO33
Source
Expira*m Ods storage Coridftkxis
3m Spedwty Ch&rAcais
06131)01
AmbWwA mnv-kire
NR oijoir2olo AmbientWnpwat"
NIR 01101/2010 Affi.4oltempwawra
Chemical Lot
171
Number
L-i5709
NS ll29Wg9
Physical D"crfptlan
Purky
V*Ae ayswpowder
88.4%
Lvt yeb- waxy soM TBD
Tan waxy sold TBD
*Surrogatestandard- 1H,lH,2H,2H-TetrahydropernuorooctanesuKonaiccid KIR-not recorded TBD--to be determred NA--not appkicable
3M CP/PCP DWow ai/01120io
AmbientWyVersture 935
Amber waxy soW TBD
31A alloir4lo Ambwt WMwft" NB 113047-M v@%itsPC-d-
TOD
ICN Bkxnedicals 01/2010
AmbietA*nveratum 53405
Brown waxy sofid NA
Table S.Characterizatioonfthe AnalyticalReference Materials Used forLiverAnalyses inStudy FACT TOX-01 3
LocaUon
BattelleMemorial Institute
Materials
Source
PFOS
3M
MS,@S@6
3M
P FOSAAI,,-.P,.FOSA
3m
THPFCW
r-4
Expiration Date
storage CondlOons
00/31/01
Arnbiard wrvmln
0110112010
AnibWd *nverst"
2010
Oliol/2010
I
Amberit re
AnVYAnt mffversure
MIR
AfftmWnpwah"
Chemical Lot Number
171
NB 113047-80
617
Physical
VJhftcrystawine WvW powder
NIR
Douripdon
pw4der
L-15709
59M
LghtyeM-
NIR
%OOXY
Purity
I 8&4%
TBD
I :@;D
TW
NA
*Sum)gate standard- 1H,IH,2H,2H-Tatrahydroperftuorooctanesulfaocniidc
NIR-not remrded
TBD--to be dateitnited
NA--not appricabic
3M Environmental Laboratory
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Table 10.Tween Dosing ConfiffnationforStudy In-lif#e4ig-009
Group Dose
Sample Number
Expected Conc. Measured Conc. ETFOSE (ng/mL) ETFOSE (ng/mL)
Group 1--Contro0lmg/mL Group 2-0.2 mg/mL Group 3-1.0 mg/mL Group 4-2.0 mg/mL Group 5-3.0 mg/mL
Honwgeneity Sampk@&3.0 mglml
B418-00@A, 06M= -
B418-(X@A, 07/15M8
B41 "09-8, 06=/98 B-41S-Wg-B, 07/15/98 B41 SM9-C, 06A)8/98
B-418M9-C, 07/15198 B-41 8-009-D,06JO8/98 B418-009-D, 07/15/98 B-41B-00@E, 06=/98 B41 8-(X&E. 07/15/98
B418-OMA, 05108/98 1 of6T
B-416-009-A,06/08198 3 of6 M
B-418-009-A,MM&W 5 of6
0.00 NA 200000 200000 1000000 100000 2000000 2000000 3000000 3000000
3000000
3000000
3000000
0.00 NA NA NA 1020000 9.42000 2190000 2750000 3060000 3640000
3250000
3690000
3790000
NA Not applicable
ETFOSE % Recovery Accuracy
NA NA NA NA 102 94 110 138 102 121
108
123
126
Table 11. Tween Dosing Confirmation-Matrix Spikes for Study ln41fe*41"09
Sample Number
Expected Conc. ETFOSE (ng/mL)
Measured Cone. ETFOSE (ng/mL)
ETFOSE % MS Recovery Accuracy
B-418-009-B,06A)8A)8-MS
1200
NA
B-418-009-B,07/15198-MS
1200
NA
B-418-009-C0,6/08A"S
900
818
B-419-009-C,0711&S"S
900
826
B-418-009-D,06108/WMS
900
9io
8-41&409-D,07/1-%"S
900
733
B-418-009-E,06A)8198-Ms
1100
973
B418-009-E, 071ISM8-MS
1100
1089
NA
NA
91
1
92
101
al
as I 99
B-418-009-A,05A)8198
1100
949
86
1 of 6 T-MS
B-418-009-A.W08/98
1100
1053
96
3 of6 M-MS
B41 B-009-A,06/OMB 5 of6 B-MS
T
1100
944
86
NA n Not appkable
3M Environmental Laboratory
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I
3M Medical Department Study: T6316.5
I
Appendix B: Protocol
I
I I I I I I I I I I I
I I
I
I
3M Environmental Laboratory
1
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3M Medical Department Sl@udy: T6316.5
Analytical Rep
3_
To
5
3M ENVIRONTNMNTAL
LABORATORY
PROTOCOL-
ANALYTICAL STUDY
2(N-Ethylperfluorooetanesulfonamidion)-ethanol
Two Generation Rat Reproduction
In-vivostudyreferencneumber: Argus418-009 Studynumber:FACT 060998.1 Testsubstance2:(N-Ethylperflucrooctanesulfonamido()N--eEtthFaOnSoEl-OH)
Name and addressofSponsor:
MarvinCase 3M Toxicology Services
3M Center Building220-2E-02 St.Paul,NlN 55144
Name
and address of testingfacility: 3M EnvironmentalTechnology and Services 935 Bush Avenue, Building2-3E-09 St.Paul,MN 55106
Experimental startdate: Expected terminationdate:December 31, 1998 Method numbers and revisions:
FACT-M-1.0, ExtractionofPotassiumPerfluorooctanesulfonaotreOther Anionic Surfactantfsrom LiverforAnalysisUsing HPLC-Elrctrospray/Mass
Spectrometr@
FACT-M-2.0, Analysisof Fluorochen-iicalisn Liver ExtractsUsing HPLCElectrospray/MassSpectrometry
FACT-M-3.0,
Extractionof Potassium Perfluorooctanesulfonatoer Other Anionic Surfactantsfrom Serum forAnalysisUsing BPLC-Electrospray/Mass Spectrometry
FACT-M-4.0, Analysisof Fluorochernicalisn Serum ExtractsUsing BIPLCElectrospray/MassSpectrometry
Author:LisaClemen
KrisHansen Study Director
1&4e@1.0oc
Date
Marvin Case
Date
Sponsor Representative
3M@Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
1.0 PURPOSE The analyticalportionof thisdosing study isdesigned evaluatethelevelsof perfluorooctane sulfonate(PFOS), or anothermetaboliteof 2(N-ethylperfluorooctanesulfonamido)-etha(nNo-l ]@tFOSE-OH) designatedby the study director,in the liverof theparentand subsequent generationsof the testsystem,or inthe serum as necessary.
The in lifeportionof thisstudywas conducted atArgus Research Laboratories.
2.0 REGULATORY COMPILIANCE This study isconducted in compliance with the Food and Drug AdministrationGood Laboratory Practicesregulationas statedin 21 CFR 58. Any exceptionswillbe noted in the finalreport.
3.0 TFSR MATERIAM 3.1 Test, control,and referencesubstances and matrices
3.1.1 Analyticalreferencesubstance: Potassium perfluorooctanesulfona(tPeFOS), lot # 217
3.1.2 Amalyticalreferencesubstance matrix: Rat liverand serum 3.1.3 Analyticalcontrolsubstance: None 3.1.4 Analyticalcontrolsubstance matrix: Rat liverand serum
3.2 Source of materials 3.2.1 Analyticalreferencesubstance: 3M SpecialtyChemical Division;traceability informationwillbe includedin the finalreport 3.2.2 Analyticalreferencesubstance matrix: Argus ResearchLaboratories; traceabilitiynformationwillbe includedin thefinalreport
3.2.3 Analyticalcontrolmatrix: 3.2.3.1 Rat liver- Argus Research Laboratories;traceabiliitnyformationwillbe includedin thefinalreport;or Rabbitliver- Covance Laboratories;traceabilitiynformationwillbe includedin thefinalreport 3.2.3.2 Rat serum - Sigma Chemical Company; traceabiliitnyformationwillbe includedin thefinalreport
33 Number of testand control samples. Liver samples fortestingwere receivedfrom 40 testanimals and 10 controlanimals. Serum samples willbe testedatthe discretionof the Study Director.
3.4 Identilricatiofn testand control samples: The samples areidentifieudsing theArgus Research Laboratoriesidentifiersw,hich consistof a letterfollowedby the Argus project number, the animal number, the group designation,and the draw date.
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3.5 Purityand strengthofmaterialsC:haracterizatoifotnhepuritayndidentitoyfthe referencematerialistheresponsibilitoyf theSponsor.
3.6 Stabilitoyf testmaterial:Characterizatiofn thestabiliotfy thetestmaterialisthe responsibiliotfy theSponsor.
3.7 Storage conditionsfor testmaterials:Testmaterialasrestoredatroom temperature. Samples arestoredat-20 10 *C.
3.8 Dispositionof testand/or controlsubstances: Biologicaltissuesand fluidsareretained per GLP regulation.
3.9 Safetyprecautions: Refer tothematerialsafetydatasheetsofchemicalsused. Wear appropriatelaboratoryattirea,nd followadequateprecautionsforhandlingbiological materialsand preparingsamples foranalysis.
4.0 ExPERrv[ENTAL
- Overview
Tissuesfrom animalsdosed as describedin Argus Research LaboratoriesProtocol#418-009 are receivedforanalysisof fluorinecompounds. At thediscretioonftheStudy Director,a seriesof analyticatlestswillbe performed on selecttissues.
Initiallayl,lliversamples willbe analyzedforPFOS by electrospray/massspectrometry (ES/MS). On thebasisof findingsfrom theseanalyses,additionaslample matricesmay be evaluatedor othermetabolitesmay be targeted.Ifadditionaalnalysisisperformed,a protocol amendment willbe written.
5.0 EXPERTMFNTAL
-AnalyticalMethods
5.1 FACT-M-1.0, Extractionof PotassiumPerfluorooctanesulfonaotreOther Anionic Surfactantfsrom LiverforAnalysisUsing BPLC-Electrospray/MassSpectrometry
5.2 FACT-M-2.0, AnalysisofFluorochemicalsinLiverExtractsUsing BPLCElectrospray/MassSpectrometry
5.3 FACT-M-3.0, ExtractionofPotassium PerfluorooctanesulfonaotreOther Anionic Surfactantfsrom Serum forAnalysisUsing HPLC-Electrospray/MassSpectrometry
5.4 FACr-M4.0, AnalysisofFluorochcrrlicailnsSerum Extrwts Using HPLCElectrospray/MassSpectrometry
6.0 DATA ANALYSIS
6.1 Data transformationsand analysis:Data willbe reportedastheconcentration (weight/weighto)f fluorideper tissueorsample, orofPFOS per unitoftissueorfluid.
6.2 Statisticaalnalysis:Statistiucsed may includeregressionanalysisoftheserum concentrationosvertime,and standarddeviationscalculatedfortheconcentrationwsithin each dose group. Ifnecessary,simple statistictaelstss,uch as Student'sttest,may be appliedtoevaluatestatisticdailfference.
3M Environmencal Laboratory
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Analytical Report: FACT TOX-013 LRN-U2095
7.0 MAP4TENANCF, oF RAw DATA AND REcoRDs
7.1 The following raw data and recordswill be retainedin the study folderin the archives according toAMDT-S-8: 7.1.1 Approved protocol and amendments 7.1.2 Study correspondence 7.1.3 Shipping records 7.1.4 Raw data 7.1.5 Electroniccopies of data
7.2 Supporting records to be retainedseparatelyfrom the study folder in the archives according toAMDT-S-8 willincludeatleastthe fohowing: 7.2.1 Training records 7.2.2 Calibrationrecords 7.2-3 Instrument maintenance logs 7.2.4 Standard Operating Procedures, Equipment Procedures, and Methods 7.2.5 Appropriate specimens.
8.0 REFERENcFs 8.1 3M Environmental Uboratory QualitySystem Chapters 1,5 and 6 8.2 Other applicable3M Environmental Laboratory Quality System Standard Operating
Procedures
9.0 AYRACHMENTS 9.1 FACT-M-1.0, Extraction of Potassium Perfluorooctanesulfonate or Other Anionic
Surfactantsfrom Liver for Analysis Using EPLC-Electrospray/Mass Spectrometry 9.2 FACT-M-2.0, Analysis of Fluorocheniicalsin Liver ExtractsUsing BPLC-
Electrospray/Mass Spectrometry 9.3 FACT-M-3.0, Extraction of Potassium Perfluorooctanesulfonateor Other Anionic
Surfactantsfrom Serum for Analysis Using BPLC-Electrospray/M ass Spectrometry 9.4 FACT-M4.0, Analysis of Fluorochemicals in Serum ExtractsUsing I-IPLC-
Electrospray/Mass Spectrometry
3M Environmental Laboratory
4 Page 22
3M Medical Department Study: T6316.5
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Study Title Combined Oral(Gavage)FertiliDteyvelopment and-Perinatal/Postnatal
ReproductionToxicityStudy ofN-ETFOSE inRats
PROTOCOL AMENDMENT NO. 1
Amendment Date: July28,1999
Performing Laboratofy 3M EnvironmentalTechnology& SafetyServices
3M EnvironmentalLaboratory 935 Bush Avenue
St Paul,NlN 55106
Laboratory Project ldentfrication ET&SS FACT-TOX-013 LLPN U2095
3M EnvironmentaLlaboratory
3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
ProtocoFlACT-TOX-013 Amendment 1
Thisamendment modifiesthefollowingportion(so)ftheprotocol:
1. PROTOCOL READS: The proposedstudycompletiondateislisteads 12/31/98. AMEND TO READ: The proposedstudycompletiondatais6/30/00. REASON: The proposed completion datewas changed to allow time for analyzingall matricesof interest.
Amendment Approval
Marvin Case Ph.D., Sponsor Representative
!)at
KrisJ.gansen Ph.D.,Study Director
Date
3M Envirt)nmentaLlaboratory
3M Environmental
Laboratory
Page 24
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
ProtocoFlACT Tox-013 Amendment Number 3
3. PROTOCOL READS: DispositioonftestandcontroslubstanceBsi:ologicatlissueasnd fluidasreretainepderGLP regulation.
AMEND TO READ:
Specimens willbe maintainedinthe3M EnvironmentalLaboratoryspecimen archives.All specimens senttosub-contracltaboratoriewsillbe returnedtothe3M Environmental Laboratoryupon completionof analysisand submissionofthe sub-contracltaboratory(s) finalreport.The specimenswillbe returnedwith thefollowingdocumentation:thesigned originalchainof custodyand recordsof storageconditionswhile atthesub-contractfacility.
REASON., To defineindetailtheappropriatedispositioonf specimens analyzedatsubcontract laboratories.
Amendment Approval
Marv Case,D.V.M., Ph.D., Sponsor Representative
Date
@-arK. Lundlbbe@rgg,,-PSPhth.u.D@D.i.,r,Setcuto irector Kristen1.Hansen, Ph.D., PreviousStudy Director
Date
/0/i5115 Date
Dale L.Bacon, Ph-B'@'3M Environmental Laboratory Management
Dite
3M EnvirDnmental Laboratoiy
3M Environmental
Laboratory
Page 30
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
Study Title
Analytical Study of 2(N-Ethylperfluorooctanesulfonamido)-ed=ol
in
Two Generation Rat Reproduction
PROTOCOL AMENDMENT NO. 4
Amendment Date:
20 January 2000
Performing Laboratory
3M Environmental Technology & Safety Services 3M Environmental Laboratory 935 Bush Avenue St.Paul, MN 55106
Laboratory Project Identification ET&SS LRN-U2095 FACT TOX-0 13 Argus Study: 418-009
3M Medical Department Study: T-6316.5
3M EnvironrwntalLaboratofy 3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical
Report: FACT TOX-013 LRN-U2095
Pr,otocoLlRN-U2095 Amendment Number 4
This amendment Modifiesthefollowingportion(so)ftheprotocol:
1. PROTOCOL
READS:
The studydirectofrorthepresentstudywas identifiientdheprotocoals James K.
Lundburg, Ph.D.
AMEND TO READ:
The roleofstudydirectofrorthe presentstudywas reassignedto MarvinT. Case, D.V.M.,Ph.D.,as of20 January 2000. The previousstudydirectorJ,ames K.
Lundburg, has been reassignedtothe roleofPrinciplAenalyticaIlnvestigator.
REASON:
The roleofstudydirectowras reassignedinan efforttoensure compliance with Good LaboratoryPracticeStandards thatoutlinestudypersonnelrequirements (referto21 CFR Part58).
2. PROTOCOL READS: The sponsorforthe presentstudywas identifieads MarvinT. Case, D.V.M.,Ph.D.
AMEND TO READ:
The roleofsponsorforthe presentstudywas reassignedto John L.Butenhoff, Ph.D.,as of20 January 2000.
REASON:
To ensure thatthestudydirectodroes notalsocarrythe dutiesofstudy sponsor,the sponsor rolewas reassigned.Inthismanner, personnelresponsibilitiaensd workload are more evenlybalanced.
3M EnvironmentalLaboratoty
3M Environmental
Laboratory
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3M Medical Department Study: T6316.5
Analytical
Report: FACT TOX-013 LRN-U2095
Protocol LRN-U2095
Amendment Number 4
Amendment Approval
John L ButenhoffPhD.,
Sponsor Representative
/0,,
Date
Jaf
K Lundberg, PhD., 2!@lging Study Director
.0..- JA
q)ate I
Marvin T.Case,b. VM, Ph.D.,IncomingStudyDirector
Date
3M Environmental Laboratory Im 2nvironmental Laboratory
Page 33
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
Study Title AnalyticaSltudyof2(N-Ethylperfluorooctanesulfonamido)i-nethanol
Two GenerationRat Reproduction
PROTOCOL AMENDMENT NO. 5
Amendment Date: August 31,2000
Performing Laboratory
3M Environmental Technology & Safety Services
3M EnvironmentalLaboratory 935 Bush Avenue
St.Paul,NIN 55106
Laboratory Project Identification FACT-TOX-013
ET&SS LRN U2095
Argus Study: 418-009 3M Medical Department Study: T6316.5
3M Environmental Laboratory 3M Environmental Laboratory
Page 34
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
ProtocoFlACT TOX-013 Amendment No. 5
This amendment modifiesthe followingportion(s)of the protocol:
1. PROTOCOL REAos: The PrinciplAenalyticaIlnvestigatfoorrthepresensttudywas identified as James K. Lundberg, Ph.D.
2. AMEND TO READ: The roleof PrincipleAnalyticalInvestigatofrorthepresentstudywas reassignedto KristenJ.Hansen Ph.D.
REASON: The roleof PrincipleAnalyticalInvestigatowras reassigneddue to availabilitoyf resources.
3M Environmental Laboratory
3M Environmental
Laboratory
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Analytical Report: FACT TOX-013 LRN-U2095
ProtocoFlACT TC)X-013 Amendment No. 5
Amendment Approval
-2 .
JohnL.ButenhoffP,h.D.,SponsorRepresentative
ZC@,z@ Date
Ma@vin T. Case, D. V.M., PILD.,Study Director
Date
3M Environmental Laboratory
3M Environmental
Laboratory
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3M Medical Department Study: T6316-S
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Appendix C: Extractionand AnalyticalMethods
This appendix includesthe followingmethods: ETS-8-4.1,Extractionof Potassium Perfluoroactanesulfonatoer Other Fluorochemical Compounds from Serum forAnalysisUsing HPLC-Electrospray/Mass Spectrometry, (14 pages) ETS-8-5.1,Analysisof Potassium Perfluorooctanesuffonatoer Other Fluorochemicalsin Serum ExtractsUsing HPLC-Electrospray/Mass Spectrometry,(9 pages)
3M Environmental Laboratory
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3M ENVIRONMENTAL
LABORATORY
METHOD
EXTRACTIONFLUOROCREMICAL
OF POTASSIUM PERFLUOROOCTANESULFONATE
COMPOUNDS FROM SERUM FOR ANALYSIS
ELEC'fROSPRAY/MASS
SPECTROMETRY
OR OTE[ER
USING HPLC-
Method Number: ETS-8-4.1 Author: Lisa Clemen, Glenn Langenburg
Adoption Date: 03/01/99
Revision Date:
711?1
Approved By:
Laboratory Manager
Date
Group Leader
C,4.,A uilrltll
Technical Reviewer
Date
olzai,/99
Date
1.0 SCOPE AND APPLICATIOrq
1.1 Scope: This method is for the extraction of potassium pertluorooctanesulfonate (PFOS)
or otherfluorochemicalcompounds from serum.
1.2 Applicable compounds: Fluorochemical surfactantsor other fluorinatedcompounds.
1.3 Matrices: Rabbit,rat,bovine,monkey, and human serum or otherfluidsas designatedin the validationreport.
Word 6/95
3M Environmental Laboratory
ETS-9-4.1
Extractionof PFOS from Senirn
Page I of 14
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2.0 SUMMARY OF MFTHOD 2.1 This method describes the procedure for extractingpotassium perfluorooetanesulfonate
(PFOS) or other fluorochemical surfactantsfrom serum, or other fluids,using an ion pairingreagent and methyl-tert-butylether(MtBE). In thismethocl seven fluorochemicals were extracted:PFOS, PFOSA, PFOSAA, ETFOSE-OH, PFOSEA, M556, and surrogatestandard (see 3.0 Definitions).An ion pairingreagent is added to the sample and the analyte ion pair is partitionedintoMTBE. The MTBE extractis removed and put onto a nitrogenevaporator untildry. Each extractisreconstitutedin 1.0 mL of methanol, then filteredthrough a 3 cc plasticsyringe attachedto a 0.2 pm nylon filteirnto glass autovials. 2.2 These sample extractsare analyzed following method ETS-8-5.1 or other appropriate methods.
3.0 DEFINITIONS 3.1 PFOS: perflucrooctanesulfonate(anion of p otassium salt)C,F,IS03-
3.2 PFOSA: perfluorooctanesulfonylamide C,F17So2NH,
3.3 PFOSAA: perfluorooctanesulfonylamido (ethyl)acetatCe@F17SON(CH2CH,)CH,C02-
3.4 ETFOSE-OH: 2(N-ethylperfluorooctanesulfonainido)-ethyallcohol C8Fl7SO2N(CH,CH,)CH2CH20H
3.5 PFOSEA: perfluorooetanesulfonylethylamide C8Fl7SO2N(CH2CH3)H
3.6 M556: C,F,7SON(H)(CH2COOH)
3.7 Surrogate standard:1H-IH-2H-2H perfluorooctanesulfonicacid
4.0 WARNINGS AND CAUTIONS
4.1 Health and safety warnings 4.1.1 Use universal precautions,especially laboratory coats,goggles, and gloves when handling animal tissue,which may contain pathogens.
5.0 INTERFERENCES 5.1 There are no interferencesknown
at thistime.
6.0 EQUIPMENT
6.1 The following equipment isused while performing thismethod. acceptable.
Equivalent equipment is
6.1.1 Vortex mixer, VV;R, Vortex Genie 2
6.1.2 Centrifuge,Mistral1000 or IEC
6.1.3 Shaker, Eberbach or VVvrR
3M Environmental Laboratory
ETS-8-4.1 Extractionof PFOS from Serum
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6.1.4 NitrogenevaporatorO,rganomation
6.1.5 Balance ( 0.100 g)
7.0 SUPPLIES AND MATERIALS
7.1 Gloves 7.2 Eppendorf or disposablepipettes
7.3
Nalgene bottles,capable of holding 250 mL and 1 L
7.4 Volumetricflasksg,lass,typeA
7.5 I-CHEM vials,glass,40 niL glass
7.6 Centrifugetubes,polypropylene,15 mL
7.7
Labels
7.8 Oxford Dispenser- 3.0to 10.0mL
7.9
Syringes, capable of measuring 5 @LLto50 gL
7.10 Graduated pipettes
7.11 Syringes, disposable plastic,3 cc
7.12 Syringe filtersn,ylon, 0.2 gm, 25 rnm
7.13 Timer
7.14 Crimp cap autovials and caps
7.15 Crimpers
Note: Prior to using glassware and bottles,rinse 3 times with methanol and 3 times with
Milli-(@Tmwater. Rinse syringes a minimum separate vials.
of 9 times with methanol, 3 rinses from 3
8.0 REAGENTS AND STANDARDS
8.1
Type I realent grade water, Milli-QTM or equivalent; allwater used in thismethod
be Milli-Q water and may be provided by a Milli-Q TOC PlusT' system
should
8.2
Sodium hydroxide (NaOH), J.T Baker or equivalent
8.3
Tetrabutylanunonium hydrogen sulfate(TBA), Kodak or equivalent
8.4
Sodium carbonate (NaC03), J.T.Baker or equivalent
8.5
Sodium bicarbonate (NaHC03), J.T.Baker or equivalent
8.6
Methyl-T-Butyl Ether, Omnisolv, glass distilledor HPLC grade
8.7
Methanol, Omnisolv, glass distilledor BPLC grade
8.8
Serum or blood, frozen from supplier
8.9
Fluorochemical standards
8.9.1 PFOS (3M Specialty Chemical Division), molecular weight = 538
8.9.2 PFOSA (3M Specialty Chemical Division), molecular weight = 499
ETS-8-4.1 Extractionof PFOS from Senun
Page 3 of 14
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8.10
8.11
8.9.3 PFOSAA (3M SpecialtyChemical Division)m,olecularweight = 585
8.9.4 ETFOSE-OH (3M Specialty Chemical Division),molecular weight = 570
8.9.5 PFOSEA (3M Specialty Chemical Division),molecular weight = 527
8.9.6 M556 (3M SpecialtyChemical Division)m,olecularweight= 557
8.9.7 Surrogatestandard:4-H,perfluorooctanseulfonicacid(1-H,1-H,2-H, 2-H C,F,3So3H) molecularweight= 429
8.9.8 Other fluorochemicalsa,s appropriate
Reagent preparation NOTE: When preparinglargervolumes thanlisteidnreagent,standard,or surrogate
preparationa,djustaccordingly. 8.10.1 10 N sodium hydroxide (NaOH): Weigh approximately 200 g NAOH. Pour into a
1000 niL beakercontaining500 mL Milli-Q' water,mix untilallsolidsare dissolved.Storeina I L Nalgene bottle.
8.10.2
IN sodium hydroxide (NaOH): Dilute ION NAOH 1:10. MeasurelOmLoflO N NAOH solution into a 100 m-L volumetric flask and diluteto volume using Milli-(@" water. Store in a 125 mL Nalgene bottle.
8.10.3
0.5 M tetrabutylammonium hydrogen sulfate(TBA): Weigh approximately 169 g of TBA into a 1 L volumetric containing 500 mL Milli_QTI water. Adjust to pH
1.0using approximately 44 to 54 mL of 10 N NAOH (While adding the lastniL of
NAOH, add slowly because the pH changes abruptly). Dilute to volume with
Milli-Q' water. Store in a 1 L Nalgene bottle.
8.10.3.1 TBA requires a check prior to each use to ensure pH = 10. Adjust as needed using I N NAOH solution.
8.10.4
0.25 M sodium carbonate/sodium bicarbonate buffer (NaCO,/NaHCO,):
Weigh
approximately 26.5 g of sodium carbonate (Na@C03) and 21.0 g of sodium
bicarbonate (NaHCO,) into a 1 L volumetric flask and bring to volume with Milli-
Q TM water. Store in a I L Nalgene bottle.
Standards preparation
8.11.1 Prepare PFOS standards for the standard curve.
8.11.2 Prepare other fluorochemical standards, as appropriate. Multicomponent fluorochemical standards are acceptable (for example, one working standard solution containing 1.00 ppm PFOS, 1.02 ppm PFOSA, 0.987 ppm PFOSAA, and
1.10 ppm EtFOSE-OH.)
8.11.3 Weigh approximately 100 mg of PFOS the actual weight.
into a 100 ML volumetric flask and record
8.11.4 Bring to volume with methanol for a stock standard of approximately 1000 ppm (@Lg/mL).
8.11.5 Dilute the stock solution with methanol for a working standard 1 solution of approximately 50 ppm.
8.11.6 Dilute working standard 1 with methanol for a working standard 2 solution of approx. 5.0 ppm.
ETS-8-4.1 FxtractionofPFOS from Serum
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8.12
8.11.7Diluteworking standard I with methanol for a working standard 3 solution of
approx. 0.50 ppm.
Surrogate stock standard preparation
8.12.1 Weigh approximately 50-60 mg of surrogatestandard 1-H,1-H, 2-H, 2-H, C,F,,SO,H into a 50 mL volumetric flaskand recordthe actualweight.
8.12.2 Bring to volume with methanol for a surrogatestock of approximately 1000- 1200 PPM.
8.12.3 Prepare a surrogateworking standard. Transfer approximately I mL of surrogate stock to a 10 mL volumetric flaskand bring to volume with methanol for a working standard of 100 ppm. Record the actualvolume transferred.
9.0 SAMPLE HANDLING 9.1 All samples are received frozen and must be kept frozen untilthe extractionisperformed. 9.2 Allow samples to thaw to room temperature priorto extraction.
10.0 ()UALITY CONTROL 10.1 Solvent Blanks, Method blanks and matrix blanks
10.1.1 An aliquot of 1.0 ni-Lmethanol is used as a solvent blank.
10.1.2 Extracttwo 1.0mL aliquotsof Milli_QTIIwater following thisprocedure and use as method blanks.
10.1.3 Extracttwo 1.0 mL aliquotsof the serum following thisprocedure and use as matrix blanks. See 11.1.4.
10.2
Matrix spikes
10.2.1 Prepare and analyze matrix spike and matrix spike duplicate samples to determine the accuracy of the extraction.
10.2.2 Prepare each spike using a sample chosen by the analyst,usually the control matrix received with each sample set.
10.2.3 Expected concentrationswill fallin themid-range of the initiaclalibrationcurve. Additional spikesmay be included and may fallin the low-rarigeof the initial calibrationcurve.
10.2.4 Prepare one matrix spike and matrix spike duplicateper 40 swnples, with a minimum of 2 matrix spikes per batch.
10.3
Continuing calibrationchecks
10.3.1 Prepare continuing calibrationcheck samples to ensure the accuracy of the initial calibrationcurve.
10.3.2 Prepare, at a minimum, one continuing check per group of 10 samples. For example, ifa sample set = 34, four checks are prepared and extracted.
10.3.3 Prepare each continuing calibrationcheck from the same matrix used to prepare the initiaclurve.
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10.3.4 The expectedconcentrationwsillfallwithinthemid-rangeof theinitial calibratiocnurve.Additionalspikesmay be includedthatfallinthe low-range of theinitiaclalibratiocnurve.This isnecessaryiftheanalystmust quantitateusing
only the low end of the calibrationcurve (forexample, 5 ppb - 100 ppb, rather
than
5 ppb - 1000 ppb).
11.0 CALIBRATION AND STANDARDTZATION
11.1
Prepare- matrix calibration standards
11.1.1 Transfer 1 mL of serum to a 15 mL centrifuge tube.
11.1.2
Ifmost sample volumes are less than 1.0 mL, extractstandards with matrix volumes equal to the sample volumes. Do not extractless than 0.50 mL of matrix. Record each sample volume on the extraction sheet.
11.1.3 Vaiile preparing a totalof twenty aliquotsin 15 mL centrifuge tubes, mix or shake between aliquots.
11.1.4 Two I mL aliquots,or other appropriate volume, serve as matrix blanks. Typically use the standard concentrzitionsand spiking amounts listedin Table 1, at the end of this section, to spike, in duplicate,two standard curves, for a total of eighteen standards, two matrix blanks, and two method blanks.
11.1.5 Refer to validation report ETS-8-4.0 & ETS-8-5.0-V-1, which liststhe working ranges and the Linear Calibration Range (LCR) for calibrationcurves.
11.2 11.3
11.1.6 Use Attachment D as an aid in calculating the concentrations of the working standards. See Section 13.0 to calculate actual concentrations of PFOS in calibrationstandards.
To each standard, blank, or continuing check, add appropriate amount of surrogate working standard for the concentration to fallwithin the calibrationcurve range 5 ppb 1000 ppb.
Extract spiked matrix standatds following 12.6-12.16 of thismethod. Use these standards to establisheach initialcurve on the mass spectrometer.
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Table I
Approximate spiking amounts for standards and spikes
Using 1.0 mL of matrix
Working standard (approx. conc.)
@iL
Approx. fmal conc. of
analyte in matrix
Blank
0.500 ppm
10
0.005 ppm
0.500 ppm 5.00 ppm
20
O.OIOPPM
5
0.025 ppm
5.00 ppm 5.00 ppm 50.0 ppm 50.0 ppm 50.0 ppm
10
0.050 ppm
20
0. 100 ppm
5
0.250 ppm
10
0.500 ppm
15
0.750 ppm
50.0 ppm
20
1.00 ppm
12.0 PROCEDURE
12.1
Obtain frozen samples and allow to thaw at room temperature or in a lukewarm waterbath.
12.2
Vortex mix for 15 seconds, then transfer1.0 mL or other appropriate volume to a 15 niL polypropylene centrifuge tube.
12.3 Return unused samples to freezer after extraction amounts have been removed.
12.4 Record the initialvolume on the extraction worksheet.
12.5
Label the tube with the study number, sample DD, date and analyst initials.See attached worksheet for documenting the remaining steps.
12.6
Spike allsamples, including blanks and standards, ready for extractionwith surrogate standard as described in 11.2.
12.7
Spike each matrix with the appropriate amount of standard as described in 11.1, or Table 1 in that section,for the calibrationcurve standards. Also prepare matrix spikes and continuing calibrationstandards.
12.8
Vortex mix the standard curve samples, matrix spike samples, and continuing calibration samples for 15 seconds.
12.9 12.10
Check to ensure the 0.5 M TBA reagent is at pH 10. Ifnot, adjust accordingly.
To each sample, add I mL 0.5 M TBA bicarbonate buffer.
and 2 mL of 0.25M sodium carbonate/sodium
12.11 Using an Oxford Dispenser, add 5 mL methyl-tert-butyl ether.
12.12 Cap each swnple and put on the shaker at a settingof 300 rpm, for 20 minutes.
12.13
Centrifuge for20 to 25 minutes at a settingof 3500 rpm, or untillayers are well separated.
ETS-8-4.1 Extractionof PFOS from Senun
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12.14 12.15 12.16
12.17
Label a fresh 15 mL centrifuge tube with the same information as in 12.5. Remove 4.0 mL of the organic layer to this clean 15 mL centrifuge tube. Put each sample on the analyticalnitrogen evaporator untildry, approximately hours.
Add 1.0mL of methanol to each centrifuge tube using a graduated pipette.
I to 2
12.18 Vortex mix for 30 seconds.
12.19 Attach a 0.2 gm nylon mesh filterto a 3 cc syringe and transferthe sample to this syringe. Filterinto a 1.5 mL glass autovial or low-volume autovialwhen necessary.
12.20
Label the autovial with the study number, animal number and gender, sample timepoint, matrix, finalsolvent, extractiondate, and analyst(s)performing the extraction.
12.21 12.22
Cap and store extracts at room temperature or atapproximately 4 *C until analysis.
Complete the extraction worksheet, attached to this document, and tape in the study notebook or include in study binder, as appropriate.
13.0 DATA ANALYSIS AN]) CALCULATIONS
13.1
Calculations
13.1.1 Calculate actual concentrations of PFOS, or other applicable fluorochemical, in calibrationstandards using the following equation:
mL of standard x concentration of standard (4g /mL) mL of standard + mL of surrogate standard + initiamlatrix volume (mL)
Final Concentration (@Lg/mL) of PFOS in matrix
14.0 METHOD PFRFORMANCE
14.1
The method detection limit (MDL) is analyte and matrix specific.Refer to MDL report for specificMDL and limitof quantitation(LOQ) values (see Attachments B and C).
14.2
The following quality control samples are extracted with each batch of samples to evaluate the quality of the extractionand analysis.
14.2.1 Method blanks and matrix blanks.
14.2.2 Matrix spike and matrix spike duplicate samples to determine accuracy and precision of the extraction.
14.2.3 Continuing calibrationcheck samples to determine the continued accuracy of the initialcalibrationcurve.
14.3 Refer to section 14 of ETS-8-5.1 formethod performance criteria.
15.0 POLLUTION PREVENTION AND WASTE MANAGEMENT
15.1
Sample waste is disposed in biohazard containers, fla=able solvent waste is disposed in high BTU containers, and used glass pipette waste is disposed in broken glass containers located in the laboratory.
ETS-8-4.1 Extractionof PFOS from Serum
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16.0 RECORDS
16.1 Complete the extractionworksheet attachedto thismethod, and tape in the study notebook or includein the 3-ringstudybinder,as appropriate.
17.0 ATTACHMENTS 17.1 Attachment A, Extractionworkshect 17.2 Attachment B, NMIJLOQ valuesand summary 17.3 Attachment C, Calibrationstandardconcentrationworksheet
18.0 REFERIENCES 18.1 The validationreportassociated with thismethod isETS-84.0 & 5.0-V-1.
18.2 FACT-M-3.1, "Analysis of Serum or Other Fluid Extracts forFluorochemicals using HPLC-Electrospray Mass Spectrometry"
19.0 AFFECTED DOCUMENTS
19.1 ETS-8-5. 1, "Analysisof Senun or Other FluidExtractsforFluorochemicalsusing HPLC-Electrospray Mass Spectrometry"
20.0 REviS[ONS
Revision Number
I
Reason For Revision Section 12.21 Changed to includesample storageatroom temperature. Section 12.13 Added the shaker speed. Section12.17 Finalvolume is 1.0mL; not adjustedforinitiavlolumes lessthan 1.0mL.
Revision Date
04/02/99
3M Environmental Laboratory
ETS-8-4.1 ExtractionofPFOS from Serum
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ExtractionWorksheet ETS-8-4.1
Study Matrix Box # Wk/Da
DateSpiked/Analyst cc ms MSD
Surrogate Std approx. ppm actual ppm
FC-Mix approx. 0.5 pm actual PPM
FC-Mix approx. 5 ppm actual PPM
FC-Mix approx. 50 ppm actual PPM
Comments
Blank
Std
Serum ExtractionMethod
amount
Vortex 15 sec. PipetteMatn,x
Volume
mL
PipetteI mL of 0.5M TBA, pH 10. pH
Std.#
Pipette2 mL of 0.25NayCO3/0.25M NaHC03 buffer
Std.#
Dispense 5 mL ofmethyl-t-butyelther
TN-A-
Sbake 20 min.
Shaker speed:
Centrifuge20-25 min.
Centrifugespeed:
Remove a 4 mL aliquotoforganiclayer
Put on Nitrogen Evaporatorto dryness
Temperature:
Add methanol
Volume
ML
TN-A-
Vortex 30 sec. Filterusinga 3cc B-D syr-ingweith a 0.2pm filteirntoa 1.5mL autosamplevial Cont. Cal. Verificationsused same matrix as for std curve.
Attachment A 3M Environmental Laboratory
ETS-8-4.1 Extractionof PFOS from Serum
mL Date & Initials
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MDL/LOQ valuesforrabbit serum
Compound
MDL
LOQ Linear Calibration Range (LCR)
(ppb)
(ppb) Approximate concentrations to be used for preparing the
PFOS PFOSA PFOSAA
1.74 1.51 3.46
I 5.5 4.79 20.5
Standard Calibration 5 ppb - 1000 ppb 1 5 ppb -1000 ppb 5 ppb - 1000 ppb
Curve
ETFOSE-OH M556
11.4 6.03
36.2 19.2
5 ppb - 1000 ppb 5 ppb - 1000 ppb
IPFOSEA
1 5.71
18.2 5 ppb - 1000 ppb
NL]DIILOQ values in rat,bovine, monkey, and human serum, and monkey plasma were not statistically
determined. Two curves in each of these matrices were extracted and analyzed with the rabbitserum curves to determine equivalence. Responses in the rat,bovine, monkey, and human were equivalent to the rabbitresponses, therefore,theirMDL and LOQ willbe the same values as determined in rabbit
serum.
Please see LOQ Summary and NML study in ETS-8-4.0 & 5.0-V- I for furtherinformation.
Attachment B: MDL/LOQ Sunmiary 3M Environmental Laboratory
ETS-".l Extractionof PFOS from Ser=
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Compound: PFOS
Prepared range
Rabbit Serum
of standards (ppb) (ng/mL)
Full Range
0.995-978
Low Curve
4.94-248
High curve
97.8-978
1/X
0.995-978
1
Compound:
PFOSA
Rabbit Serum
Prepared range of standards
(ppb) (ng/mL)
Full Range Low Curve High curve I/X
0.993-976 4.93-97.6 24.8-976 0.993-976
LCR from curve (ppb)
(ng/mL) 24.8-978
4.94-248
97.8-978
4.94-978
LCR from curve (ppb)
(ng/mL) 4.93-976
4.93-97.6
24.8-978
4.93- 976
Compound: PFOSAA
Prepared range
Rabbit Serum
of standards
(ppb) (ng/mL)
Full Range Low Curve High curve
ri/X-
0.991-974 4.92-247 49.2-974 0.991-974
LCR from curve (ppb)
(ng/mL) 24.7-974
9.74-247
97.4-974
9.74-974
Recovery Range
83-109 85-104 85-106 94-111
% Recovery Range
88-103 87-105 93-102 94-103
% Recovery Range
81-111 97-107 85-108 95-115
RSD Range
4.67-11.0 5.34-12.0 4.84-9.80 4.60-10.5
RSD Range
5.10-14.7 9.85-14.7 5.08-13.9 5.10-14.5
RSD Range
4.18-10.6 6.38-21.8 4.33-12.5 4.11-23.2
AttaclunentB: MDLRLOQ Sununary 3M Environmental Laboratory
ETS-8-4.1 Extractionof PFOS from Serum
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Compound: ETFOSE-OH
Prepared range
Rabbit Serum
of standards
(ppb) (ng/mL)
Full Range Low Curve High curve I/X
0.993-976 4.93-97.6 49.3-976 0.993-493
LCR from curve (ppb)
(ng/mL) 49.3-976
9.76-97.6
97.6-976
9.76-976
% Recovery Range
77-110 97-107 90-109 86-111
Compound: PFOSEA
Prepared range
Rabbit Senim
of standards
(ppb)(ng/mL)
Full Range Low Curve High curve 1/X
0.993-976 4.93-248 49.3-976 0.993-976
LCR from curve (ppb)
(ng/mL) 24.8-976
9.76-248
49.3-976
9.76-976
% Recovery Range
96-106 91-110 86-106 95-117
Compound: Rabbit Semm
FullRange Low Curve High curve I/X
556 Prepared range of standards (ppb)(ng/mL)
0.993-976
4.93-97.6 97.6-976
0.993-976
LCR from curve (ppb)
(ng/mL) 24.8-976
9.76-97.6
97.6-976
9.76-976
% Recovery Range
88-106 100-105 81-111 97-110
RSD Range
11.2-25.5 14.1-21.3 11.5-19.6 11.1-21.2
RSD Range
10.1-16.2 11.8-19.5 10.2-18.2 10.1-19.1
RSD Range
4.82-17.9 5.95-18.2 5.11-9.74 4.77-19.5
Attachment B-.MDLFLOQ Summary 3M Environmental Laboratory
ETS-8-4.1 Extractionof PFOS from Serum
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Ion PairStandard Curves - Fluids
Prep date(s): Analyte(s): Sample matrix:
Standard number: Equipment number: Final solvent and TN: Blank fluid/identifier:
Method/revision:
Target analyte(s):
FC mix std approx. 0.500 ppm:
FC mix std approx. 5.00 ppm:
FC mix std approx. 50.0 ppm:
Surrogate std approx. 100 ppm:
Actual concentrations of standards in the FC mix
PFOS
PFOSA
PFOSAA
ETFOSE PFOSEA
M556
Std conc Std conc Std conc Std conc Std conc Std conc
ug/mL 0.500
ug/mL 0.507
ug/mL 0.532
ug/mL 1 0.501
ug/mL 0.521
ug/mL 0.501
0.500
0.507
0.532
0.501
0.521
0.501
5.00
5.07
5.32
5.01
5.21
5.01
5.00
5.07
5.32
5.01
5.21
-5.01
5.00
5.07
5.32
5.01
5.21
5.01
50.0
50.1
53.2
50.1
52.1 1 50. 1_
50.0
50.1
53.2
50.1
52.1
50.1
50.0
50.1
53.2
50.1
52.1
50.1
50.0
50.1
531
50.1
52.1
50.1
All Am't spiked mL 0.010 0.020 0.005 0.010 0.020
0-005 0.010 0.015 0.020
All Finalvol
ML 1.015 1.025 1.010 1.015 1.025
L 1-010 1.015 1.020 1.025
Calculated concentrations of standards
PFOS Finalconc
ng/mL
PFOSA Finalconc
ng/mL
PFOSAA Finalconc
ng/rnL
ETFOSE Finalconc
ng/mL
4.93
5.00 1 5.24
4.94
9.76
9.89
10.4
9.78
24.8
25.1
49.3
50.0
26.3 52.4
24.8 49.4
97.6
98.9
104
97.8
248
251
263
248
493
500
524
494
735
746 1 782
737
976
989 1 1038
978
in the sample matrix
PFOSEA
M556
Surrogate
Finalconc Finalconc
ng/mL
ng/mL
Std conc ng/mL
5.01-
5.13
100
9.93 25.2 50.1
10.2 25.8 51.3
Surrogate Final conc
99.3
102
ng/mL
1 252
___258
500
501
513
749
766
993
1017
All Am't spiked
niL
0.005
Validated ranges - approximate concentrations
Serum
-Rabbit Bovine
PFOS
PFOSA
PFOSAA
ETFOSE-OH
5.00-1000 1 5.00-166".. 5.00-1000 1 5.00-1000
Estirmtesonly. Use valuesforrabbit.
Rat
Estiffiatoensly. Use valuesforrabbit.
Monkey & Plasma Estiniateosnly. Use valuesforrabbit.
uman
Estiniateosnly. Use valuesforrabbit.
PFOSEA 5.00-1000
M556 5.00-1000
Attachment C: Ion Pair Standard Curves
ETS-8-4.1
Extractionof PFOS from Serum
3M Environmental Laboratory
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3M ENVIRONMENTAL
LABOF.ATORY
METHOD
ANALYSIS
QF POTASSIUM PERFLUOROOCTANEST-TLFONATE
OR
FLUOROCHEAUCALS
IN SERUM ExTRAcTs USING
HPLC-ELEcTRospRAY/MAss
SPEcrROMETRY
OTHER
Method Number: ETS-8-5.1
Author: Lisa Clemen, Robert Wynne Approved By: LaboratoryManager
Adoption Date: 03/01/99
Revision Date: qlo@i@M
2.c@/ Date
Group Leader
@L A
Technical Reviewer
Date
oyLa4,@l Date
1.0 SCOPE AND APPLICATION
1.1 Scope: This method describesthe analysisof serum extractsforfluorochemicalsurfactants using B?LC-clectrospray/mass spectrometry.
1.2AppUcable Compounds: Fluorochemical surfactantsor other fluorinatecdompounds, or otherionizablecompounds.
1.3Matrices: Rabbit,rat,bovine,monkey, and human serum, or otherfluidsas designateciin the validationreport.
Word 6/95
ETS-8-5.1 Analysis of Seniin ExtractUsing ES/MS
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2.0 SUMMARY
OF METHOD
2.1 This method describesthe analysisof fluorochemicalsurfactantesxtractedfrom serum or other fluids,using BPLC-electrospray/rnassspectrometry,or similarsystem as appropriate.
The analysisisperformed by monitoring a singleion characteristiocf a particular fluorochemical,such as theperfluorooctanesulfonat(ePFOS) anion,M/z= 499. Additionally,swnples may be analyzedusing a tandem mass spectrometerto furtherverify the identityof a compound by detectingdaughter ions of the parention.
3.0 DEFINITIONS
3.1 Atmospheric Pressure Ionization (API): The Micromass QuattroIltriplequadrupole systems allow forvariousmethods of ionizationby utilizinvgarioussources,probes,and interfaces-.These includebut arenot limitedto:ElectrosprayIonization(ESI),Atmospheric Pressure chemical Ionization(APcl),Thermospray, etc.The ionizatiopnrocessin these techniquesoccurs at atmosphericpressure(i.e.n,ot under a vacuum).
3.2 Electrospray Ionization(ES, ESI): a method of ionizatiopnerformed at atmospheric pressure,whereby ions in solutionaretransferredtothe gas phase viatinycharged droplets. These charged dropletsare produced by the applicationof a strongelectricaflield.
3.3Mass Spectrometry, Mass Spectrometer (MS), Tandem Mass Spectrometer (MS/MS): The API Quattro11triplequadrupole systems areequipped with quadrupolemass selective detectors.Ions areselectiveldyiscriminatedby mass to charge ratio(m/z)and subsequently detected.A singleMS may be employed forion detectionor a series(MS/MS) formore specificfragmentationinformation.
3.4 Conventional vs.Z-spray probe interface:The latesmtodels of Micromass QuattroII triplequadrupolesystems (post1998) utilizea "Z-spray"conformation.The spray emitted from a probe isorthogonalto the cone aperture.In the conventionalconformation itisaimed directlyatthe cone aperture,afterpassing through a tortuouspathway inthe counter electrode.Though the configurationisdifferentt,he methods of operation,cleaning,and maintenance are the same. However, Z-spray components and conventionalcomponents are not compatible with one another,but only with similarsystems (i.e.Z,-spraycomponents are compatible with some otherZ-spray systems,etc.)
3.5 Mass Lynx Software: System softwaredesigned forthespecificoperationof theseQuattro IItriplequadrupole systems. CurrentlyMassLynx has Windows 95 and WindowsNT 4.0 versions.All versionsare similar.For more detailssee themanual specificto theinstrument (Micromass QuattroIItriplqeuadrupole MassLynx or MassLynx NT User'sGuide).
4.0 WARNINGS AND CAUTIONS 4.1 Health and SafetyWarnings:
4.1.1 Use cautionwith thevoltagecablesfortheprobe. NVhen engagecltheprobe employs a voltageof approximately 5000 Volts.
4.1.2 When handling samples or solventswear appropriateprotectivegloves,eyewcar, and clothing.
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4.2 Cautions: 4.2.1 DO Dot operatseolvenptumps abovecapacitoyf400 bar(5800psi)backpressure.
If the back pressure exceeds 400 bar, the HP 1100 will initiateautomatic shutdown.
4.2.2 Do not run solventpumps todryness.
5.0 INTFRFERENCES-
5.1 To minimize interferences when analyzing samples, teflon should not be used for sample
storageorany partofinstrumentatiotnhatcomes incontactwiththesample orextract.
6.0 EouipmENT
6.1 Equipment listebdelow may be modified inordertooptimizethesystem. Document any modificationsintheraw dataasmethod deviations.
6.1.1
6.1.2
Micromass QuattroH triplqeuadrupoleMass Spectrometerequippedwith an electrospraiyonizatiosnource
B?l 100 low pulse solvent pumping system, solvent degasser, colurrm compartment, and autosampler
7.0 SUPPLIES AND MATERIALS
7.1 Supplies
7.1.1
High purity grade nitrogen'gas regulated to approximately 100 psi (House air system)
7.1.2
HPLC analyticalcolunin, specifics to be determined by the analyst and documented in the raw data.
7.1.3 Capped autovials or capped 15 mL centrifage tubes
8.0 REAGENTS AND STANDARDS 8.1 Reagents
8.1.1 Methanol, BPLC grade or equivalent
8.1.2 NElli-QTwamter, allwater used in thismethod should be Milli-Q' water or
equivalent, and may be provided by a Milli-Q TOC Plus system or other vendor
8.1.3 Arnmoaium acetate,reagent grade or equivalent
8.2 Standards
8.2.1
Typically two method blanks, two matrix blanks, and eighteen matrix standards are prepared during the extraction procedure. See ETS-84.1.
9.0 SAMPLE HANDLING
9.1 Fresh matrix standards are prepared with each analysis. Extracted standards and samples are stored in capped autovials or capped 15 mL cenhifuge tubes untilanalysis.
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9.2 If analysiswill be delayed, extractedstandards and samples can be refrigeratedat
approximately 4' C, or at room temperature,untilanalysiscan be performed.
10.0 OUALITY CONTROL 10.1 Solvent Blanks, Method
Blanks and Matrix Blanks
10.1.1 Solvent blanks,method blanks and matrix blanks are prepared and analyzed with each baich to determine contamination or cariyover.
10.1.2 Analyze a method blank and a matrix blank priorto each calibrationcurve.
10.2 Matrix Spikes
10.2.1 Matrix spikes are prepared and analyzed to determine the matrix effecton the recovery efficiency.
10.2.2 Matrix spike duplicatesare prepared and analyzed to measure the precision and the recovery for each analyte.
10.2.3 Analyze a matrix spike and matrix spikeduplicateper fortysamples, with a minimum of 2 spikes per batch.
10.2.4 Matrix spike and matrix spike duplicateconcentrationswillfallin then3id-range of the initiaclalibrationcurve. Additional spike concentrationsmay fallin the lowrange of theinitialcalibrationcurve.
10-3 Continuing Calibration Verifications
10.3.1 Continuing calibrationverificationsareanalyzed toverifythe continued accuracy of the calibrationcurve.
10.3.2 Analyze a mid-range calibrationstandard afterevery tenthsample, with a minimum of one per batch.
11.0 CALIBRATION AND STANDARDIZATION
11.1
Analyze the extractedmatrix standardspriorto and following each set of extracts.The average of two standard curves willbe plottedby linearregression(y = my + b),weighted I/x,not forced through zero,using MassLynx or other suitablesoftware.
11.2 If the curve does not meet requirements, perform routinemaintenance or reextractthe standard curve (ifnecessary) and reanalyze.
11.3
For purposes of accuracy when quantitatinglow levelsof analyte,itmay be necessary to use the low end of the calibrationcurve ratherthan the fallrange of the standard curve. Example: when attempting to quantitateapproximately 10 ppb of analyte,generate a
calibrationcurve consistingof the standards from 5 ppb to 100 ppb ratherthan the fan
range of the curve (5 ppb to 1000 ppb). This willreduce inaccuracyattributedto linear regressionweighting of high concentration standards.
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12.0 PROCEDURES
12.1 Acquisition Set up
12.1.1 Click on startbutton in the Acquisition Control Panel.Set up a sample list.Assign a filename using MO-DAY-last digitof year-sample number, assign a method (MS) for acquiring,and type in sample descriptions.
12.1.2 To createa method clickon scan button in the Acquisition controlpanel and select SIR (SingleIon Recording) or MRM. Set IonizationMode as appropriateand mass to 499 or other appropriatemasses. A fullscan is usuallycollectedalong with the SIRS. Save acquisitionmethod. IfMS/MS instrumentsareemployed, additional product ion fragmentation information may be collected.See Micromass MassLynx GUIDE TO DATA ACQUISITION foradditionalinformation and NUZM (MultipleReaction Monitoring).
12.1.3 Typically the analyticalbatch run sequence begins with a setof extractedmatrix standards and ends with a set of extractedmatrix standards.
12.1.4 Samples are analyzed with a continuing calibrationcheck injectedafterevery tenth sample. Solvent blanks should be analyzed periodicallyto monitor possible analyte canyover and are not considered samples but may be included as such.
12.2 Using the Autosampler
12.2.1 Set up sample tray according to the sample listprepared in Section 12.1.1.
12.2.2 S et-up the HP 11 00/autosampler atthe following conditions or atconditions the analystconsiders appropriatefor optimal response.Record actualconditions in the inst-urnentlogbook:
12.2.2.1 Sample size = 10 @iL injection
12.2.2.2 Inject/sample= 1
12.2.2.3 Cycle time = 13.5 minutes
12.2.2.4 Solvent rwnp =
Time
0.00 min. 8.50 min. 11.0 min. 1 .0 min.
MEOH
40% 90% 90% 40%
2.0 mM Ammonium acetate
60% 10% 16% 60%
12.2.2.5Press the "Start"button. 12.3 Instrument Set-up
12.3.1 Refer to ETS-9-24.0 for more details. 12.3.2 Check the solventlevelin reservoirsand refillifnecessary.
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12.3.3 Check thestainlessteelcapillaryattheend of theprobe. Use an eyepiece to check thetip.The tipshouldbe flatwithno jagged edges.Ifthetipisfound to be unsatisfactoryd,isassemblethe probe and replacethestainlesssteelcapillary.
12.3.4 Set EPLC pump to "On". Set theflow to 10 - 500 uumin or as appropriate. Observe dropletscoming out ofthetipof theprobe.Allow to equilibratfeor approximately10 minutes.
12.3.5 Turn orrthenitrogen.A finemistshouldbe expelledwithno nitrogenleaking around thetipof theprobe. Readjustthetipoftheprobe ifno mistisobserved.
12.3.6 The instrumentusestheseparametersatthe followingsettingsT.hese settingsmay change in orderto optimizethe response:
12.3.6.1Drying gas 250-400 liters/hour 12.3.6.2ESI nebulizinggas 10-15 liters/hour 12.3.6.3HPLC constantflow mode, flowrate10 - 500 @iljmin 12.3.6.4Pressure<400 bar (Thisparameterisnotset,itisa guideto ensure the
HPLC isoperatingcorrectl) y.
12.3.7 Carefullyguide theprobe intotheopening.Insertprobe untilitwillnot go any furtherC.onnect thevoltagecablesto theprobe.
12.3.8 Printthetunepage,with itsparameters,and storeitinthestudybinderwith a copy tapedintotheinstrumentlog.
12.3.9 Using thecross-flowcounterelectrodeintheES/MS sourceisrecommended for theanalysisof biologicalmatrices.
12.3.10CIickon startbuttonintheAcquisitionControlPanel(thismay vary among MassLynx versions,see appropriatMeassLynx USER'S GUI]DE). Pressthe start button.Ensure startand end sample number includesallsamples tobe analyzed.
13.0 DATA ANALYSIS AND CALCULATIONS 13.1 Calculations:
13.1.4 Calculatematrix spikepercentrecoveriesusingthefollowingequation:
% Recovery
Observed Result- Backzround Result x 100 Expected Result
13.1.5 Calculatepercentdifferencuesing the followingequation:
% Difference
Expected Conc. - CalculatedConc. x 100 Expected Conc.
13.1.6Calculateactualconcentratioonf PFOS, or otherfluorochemicali,nmatrix
(ng ofPFOS calc.from std.Curve x DilutioFnactor) x I Lig (InitiVaollume ofmatrix(mL) + mL of SurrogateStandard) 1000 ng
FinalVolume (mL)
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14.0 METHOD PERFORMANCE 14.1 Method DetectionLimit(MDL) and Limitof Quantitatio(nLOQ) aremethod, analyte,and
matrix specificP.leaseseeETS-8-4.1,Attachment B, fora listinogfcurrentvalidated MDL and LOQ values.
14.2 SolventBlanks,Method Blanks, and Matrix Blanks -
14.2.1 Solventblanks,method blanks,and matrixblanksvaluesaremust be below the loweststandardinthe calibratiocnurve
14.3 Calibration Curves 14.3.1 The ? value forthe calibratiocnurve must be 0.980 or better.
14.4 Matrix Spikes
14.4.1 Matrix spikepercentrecoveriesare must be within 30% of the spiked concentration.
14.5 Continuing CalibrationVerifications
14.5.1 Continuingcalibratiovnerificatiopnercentrecoveriesmust be 30% ofthe spiked concentration.
14.6 Ifcriterilaistedinthismethod performance sectionisn'tmet,maintenancemay be performed on the system and swnples reanalyzedor otheractionsas determinedby the analyst.Document allactionsinthe appropriatelogbook.
14.7 Ifdata areto be reportedwhen performance criterihaave notbeen met, thedatamust be footnotedon tablesand discussedin thetextof thereport.
15.0 POLLUTION PREVENTION AND WASTE MANAGEMENT 15.1 Sample extractwaste and flammable solventisdisposedinhighBTU containersa,nd glass
pipettewaste isdisposedin broken glasscontainerslocatedinthelaboratory.
16.0 REcoRDs 16.1 Each page generatedfora studymust have thefollowinginformationincludedeitherinthe
header or hand writtenon thepage: study orprojectnumber, acquisitiomnethod, integratiomnethod, sample name, extractiondate,dilutionfactor(ifapplicable)a,nd analyst.
16.2 Printthetunepage,sample lista,nd acquisitiomnethod from MassLynx toincludeinthe appropriatestudyfolder.Copy thesepages and tapeintotheinstrumentrunlog.
16.3 Plotthe calibratiocnurveby linearregression,weighted I/x,thenprintthesegraphs and storein the study folder.
16.4 Printdataintegratiosnummary, integratiomnethod, and chromatograms,from MassLynx, and storeinthestudyfolder.
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16.5 Summarize data using suitablesoftware (Excel 5.0) and storein the study folder,see Attachment A for an example of a sun-Lmary spreadsheet.
16.6 Back up electronicdata to appropriatemedium. Record in studynotebook the filename and locationof backup electronicdata.
17.0 TABLES, DIAGRAms, FLOWCHARTS, AND VALIDATION DATA 17.1 Attachment A: ETS-8-5.1 Data summary spreadsheet.
18.0 REFERFNCES
18.1 FACT-M-4. compounds
1,"Extwtion of Potassium Perfluorooctanesulfonateor Other Fluorochemical from Serum for Analysis Using HPLC-Electrospray/Mass Spectrometry
18.2 ETS-9-24.0, "Operation and Maintenance of the Micromass Atmospheric Pressure Ionization/Mass Spectrometer Quattro U triplequadrupole Systems"
18.3 The validationreportassociatedwith thismethod isETS-8-4.0 & 5.(@-V-1.
19.0 AFFECTED DocuMFNTS
19.1 ETS-8-4. 1, "Extraction of Potassium P erfluorooctanesulfonateor Other Fluorc>chernical Compounds from Serum forAnalysis Using HPLC-Electrospray/Mass Spectrometry"
20.0 P.EVISIONS
Revision Number.
1
Reason For Revision Section6.1.2 ClarificationofBP1100 system components. Section 11.1 Average of two curves, not standard values,are used for plottinglinearregressionand added the I/x weighting of the curve. Section 12.2.2.4Clarificationof solventratnp. Section 17.1 Changed from attachment B to A.
Revision Date
04/02/99
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Laboratory Study
Study: Test Material: Matix/Final Solvent: Method/Revision: AnalyticalEquipment System Number: Instrument Software/Version: Filename: R-Squared Value: Slope: Y InterceptDate of Extraction/Analyst: Date of Amalysis/Analyst:
Group Dose
Sample#
Concentration up,/mL
InitialVol. niL -
Dilution Factor
Final Cone. urtnil
Slope: Taken from linearregressionequatiorl Group/Dose: Taken from thestudy folder. S2mple#: Taken from the study folder. Concentration (ug/niL): Taken from theMassLynx integratiosnummary. InitialVolume (niL): Taken from the studyfolder. DilutionFactor: Taken from thestudy folder. Final Conc. (ug/niL): Calculatedby dividingtheinitiavlolume from theconcentration
Attachment A: Sununary Spreadsheet
ETS-8-5.1
Analysis of Serum Extract Using ES/MS
3M Environmental Laboratory
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Appendix D: Data Summary Tables
Table 12. Reported Fluorochomical Levels in Sera Analyses in Study FACT TOX-013
Dosage Group
Specimen 10
PFOS WWML)
10097F
0.0394
10105F
0.0181
10106F
0.0258
10107F
0.0343
ioioaf
0.0253
9922M*
0.0115
9930M*
0.0134
9931 M
0.00725
rill
9932M 9933M*
0.0162 0.0156
10121F
9.82
10126F
19.8
10136F
5.96
10140F
6.27
10142F
13.1
9961m*
34.8
11
9964M
30.4
11
9965m*
74.9
11
9967M
25.1
11
9970M*
38.9
10155F*
87.8
10 156F
76.1
10164F
49.6
III
10172F
68.4
III
10177F
42.2
III
9997M
108
III
9999m,
178
III
10()OIM
94.9
III
10002M
113
III
10004M
130
IV
10187F
rv
10194F
89.5 73.4
rv
10203F
126
IV
10211 F
99.7
IV
i0214F
98.3
IV
iooigm
302
rv
10024M*
477
rv
10029M*
296
rv
10033M
272
i,r@vIIrvVVvv
10034M
249
Tentativevalues,initivaolluffmw" <0.5 mL
PFOSA 441knL) PFOSAA UotrnL)
<LOQ (4.79ppb)
<LOQ (4.79ppb)
<LOQ (4.79ppb)
<LOO (4.79ppb) <LOQ (4.79ppb)-
<LOQ (4.79ppb)
<LOQ (.4.7p9pb)
<LOQ (4.79ppb)
<LOQ (4.79pp@L
<LOG (4.79ppb)
0.0682
0.112
0.0663
0.0507
0.0665
0.0962
0.188
0.114
0.147
0.165
0.328
0.352
0.265
0.325
0.335
0.574
0.579
0.480
0.393
0.465
0.461
0.576
0.651
0.670
0.569
0,613
0.553
0.610
1
0.804
0.637
<LOQ (20.5ppb) -CLOO (20.5ppb) <LOQ (20.5ppb) <LOO (.20.p5pb) <LOO (20.5ppb) <LOG (20.5ppb) cLOQ (20.5ppb) <LOQ (20.5ppb) -CLOO (20.5ppb) <LOQ (20.5ppb)
1.59 4.55 1.18 0.690 2.09 1.40 5.86 1.96 1.26 5.55 9.9 6.91 4.66 8.17 4.58 11.8 18.7 12.1 10.4 14.9 8.00 10.6 19.0 10.2 12.3 22.5 40.5 28.8 24.5
31.4
ETFOSE-OH (pWmL)
U&N (pWmL)
<LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (38.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb)_ <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <.LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb)
<LOQ (36.2ppb) <LOQ (36.2ppb) 1 <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb)
<LOQ (24.9ppb)
<LOQ (24.9ppb) <LOQ (24.9ppb) <LOQ (24.9ppb) <LOQ (24.9ppb) -CLOQ (24.9ppb) <LOQ (24.9ppb)
<LOQ (24.9ppb) <LOQ (24.9ppb) <LOQ (24.9ppb)
I.W
4.19 0.952 1.15 2.45 4.69
5.18 4.54 3.44 6.11
43.3 22.3 18.0 17.0
17.9
29.1
1
73.6
25.1
38.1
37.8
39.0 25.6 39.6
28.8 33.8
71.3 102
94.9
90.9
1
56.7
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Table 12.Reported Fluorochemical Levels in Sera Analyses in Study FACT TOX-013 (continued)
D---" Group
Spednwn ID
PFOS (pgiml)
v
NR
NR
v
NR
NR
v
NR
NR
v
NR
NR
v
NR
NR
v-
10042M
238
v
10044M
235
v
iOO45M
326
loosim
162
v
10054M
182
NR - Swnpis notrecok-edormported Tent&We vok", lnitkviokww ww <0.5mL
PFOSA (pWmL)
NR NR NR NR NR 0.791 0.972 0.897 0.574 0.669
PFOSAA (pg/mL)
NR NR NR NR NR 25.2 20.7 26.8 14.0 15.8
ETFOSE-OH "ftL)
NR NR NR NR NR <LOQ (36.2ppb) cLOO (36.2ppb) <LOQ (36.2ppb) <LOQ (36.2ppb) <LOQ (36-2ppb)
M556 (pWmL)
NR NR NR NR NR 62.4 55.6 93.8 30 7 55.'5
Table 13.Reported Fluorochemical Levels InLiverAnalyses In Study FACT TOX-013
Do"" Group
I I I I I I I I I I
I
11 11 11
11 it 11 11 It 11 If I) it 11
Spocknon ID
10097F 10105F 10106F 10107F 10108F 9922M 9930M 9931M 9932M 9933M iOO97M 10105M 10106M 10107M iolo8m 10121F 10126F 10136F 10140F 10142F 996im 9964M 9965M 9967M 9970M 10121M 10126M
10,36M iOl4OM 10142M
PFOS (pglg)
0.149 <LOQ 0.121 <LOQ <LOQ 0.585 0,816
o.a36
1.04 1.01 0.281 0.242 0.226 0.221 0.251 25.1 22.9 39.8 23.7 22.1 116 102 89.9 80.7 87.3 54.7 67.8 53.7 28.0 71.5
PFOSA(pWg)
<LOG <LOQ <LOQ <LOQ
<LOQ <LOQ cLOQ <LOQ <LOQ <LOQ <Loa <LO-Q <LOQ <LOG <LOQ 0.514 0.708
1.40 0.601 0.508 4.49 4.10 2.88 3.88 5.42 1.90 2.65 2.35 1.22 2.06
PFOSAA(pWg)
<LOQ <LOQ <LOQ <LOQ <LOQ <LOQ <LOQ <LOQ <LOQ <LOQ <LOQ <LOQ <Loa -CLOO <LOQ
2.68 4.34 5.01 2.67 2.57 11.0 15.6 9.79 8.62 10.4 5.87 14.6 9." 2.82 6.55
mu b")
-CLOO <LOQ <LOQ <LOQ <LOQ <LOQ <LOQ <LOQ <LOQ <LOG <LOQ <LOG <LOG <LOQ <LOQ
1.19 1.75 2.88 1.55 1.41 12.8 10.2 11.6 8.95 11.6 5.39 7.75 4.64 3.27 4.58
3M Environmental Laboratory
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Report: FACT TOX-013 LRN-U2095
Table 13.Reported FluorochemicalLevelsInLiverAnalyses InStudy FACT TOX-01 3 (continued)
Do"" GroW
III III III III III III III III III III III III III rv rv rv r-v rv rv IV IV rv IV IV [V rv rv IV v v v
v -V
Spacimen 10
10155F 10156F 101r>4F 10172F 1017'7F 9997M 9999M ioooim
--10002M 10004M 10155M loi58m 10164M 10172M 10177M iOI87F 10194F 10203F 10211 F 10214F IGOISM ID024M 10029M 10033M 1D034M
-10187M 10194M 10203M 102liM 10214M 10042M 10044M IOG45M 1005im 10054M
PFOS (pg/g)
102 130 179 119 105 415 234 498 257 386 89.0 219 203 188 153 164 240 344 255 264 831 791 556 751 556 226 277 448 457 3" 1218 1356 1132 1063 1054
PFOSA(pWg)
PFOSAA(pog)
2.22 2.24 1.94 2.17 2.88 10.8 9.41 8.67 8.29 8.41 5.11 6.14 6.26 6.20 6.91 2.80 4.06 3.14 3.39 4.56 12.8 11.0 11.2 12.6 11.0 6.36 9.96 9.93
11.4 8.11 16.4 13.0 10.9 9.80 io.8
15.6
20.2
22.7
11.9
20.0
73.5
28.6
85.2
34.2
64.9
12.0
27.3
29.4
--33.7 17.1
31.1
51.5
49.5
46.6
51.4
122
148
86.2 129
135
27.4
45.5
76..
56.2
-60.0 lea
206
150
1
157
165
Us ojwg)
7.17 7.64 8.41 5.87 8.16 53.5 39.3 66.4 38.0 54.6 11.5 33.3 43.1 29.9 31.4 19.8 26.8 26.6 27.5 29.3
84.5 97.5 78.2 117 82.2 39.9 39.5
-@7.8 65.4 64w5 128 152 133 118 161
3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Appendix E: Data Spreadsheets
Analytical Report: FACT TOX-013 LRN-U2095
3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
3M Environmencal Laboratory
Page 65
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
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99 ;21
ZO Odd
d
@dd
@d
dd6d..dd.Zd
d.dilad-
6,d
9
!22
-Lill,
3M Environmental Laboratory
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3M Medical Departmenr- Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
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ggq@g
3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
zz
zz
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3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
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3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
Appendix F:Example Calculations
Formula Used for Sera Analyses in Study FACT TOX-Oi3
AR (ng/mL) x DF x SC x FV (mL) x 1.0 gg EV (ML) TUUO-ng-
x PC = Reported
Concentration
(jig/mL)
Calculation Used for Group 4, Animal ID 10033M
340 ng/mL
x 500 x 0.9275 x I mL 0.5 mL
x 1.0 jig TMU-ng-
x 0.864 = 272 ILg/mL
AR-Analytical resultfrom MassLynx summary
DF-Dilution factor
SC-PFOS
saltcorrection constant (0.9275)
FV-Final extractvolume (1.0 mL unless otherwise noted)
EV-Volume
of sera extracted
PC-PFOS
purity correction factor (86.4%)
3M Environmental Laboratory
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Analytical Report: FACT TOX-013 LRN-U2095
Appendix G: Contract Lab Report
This appendix includesthe followingcontractlaboratoryreport:
BattelleMemorial InstitutSet,udy Number N003604-D, 2 (N-Ethylfiuorooctanesulfonamido)-ethanionlTwo Generation Rat Reproduction, (59 pages)
3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical
Report:
FACT TOX-013 LRN-U2095
BIOLOGICAL SANDIE ANALYSIS BatteUe Study Number: N003604-D 3M EnvironmentalLaboratoryStudy Number: FACT 060998.1
Balffeiie
... Putdng Twhnalogy To Kt,*
FINAL REPORT
2 (N-Ethylfluorooctinesulfonamido)-ethainnol Two GenerationRat Reproduction
SPONS
3M To)dcology Scrvice3 3M Center
Building 220-2E-02 St Paul,UN 55144
StudyInitiatiomSeptember 15, 1999
Testins!Fie'ditv
BatteUt 14emoriallustibge 505 Ying Avenue
Call bilq.Ohio 43201-2693
Prepared PatrickL South,B.S.
3M Environmental Laboratory
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Analytical Report: FACT TOX-013 LRN-U2095
BatteUeSwAy Number N003604-D 3M F-nvkonmenW LaboratoryShidyN=bcr. FACR 060998.1
FINALREPORT
2 (N-'Ethyinuoroactinesulfonamido)@-ethiLnolin Two Genemtion Rat Reproduction
Joa C. Andre, Ph.D. BattellPrmclpalhnwuge=
RichardW. SlautcrP,h.D.,D-kB.T. BatteUeSemor Prog= Dn=tor
Date Date
3M Environmental,.Laboratory
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3M EnNiro@
BattelleSb* I-T=bcr N003 604-D Labamtory Study Numbw. FACT 06o998.i
2 (N-Eth-ylfluorooctanesulfonmnido)-ethanol in Two Generation Rat Reproduction
EXECUTMSUbD4ARY
Rat liversamplw scat to BamUe by 3M Environm--ntal Technology and Senices vmm analyzed by ffie previously validatedmethod "Mzthod forAnalysis of Potassium Perfluorooctanesulfonate(PFOS) inRat Livw by LC/MS/MS". Samples we= cctwted and analyzed by I-ligh-Performanceliquid ChromatogWby Mass Spectroscopy (LC/MS/MS) for PFOS, M-556, PFOSAA, and PFOSA content only. Related fluorocbemic-A-.q mentioned in the analytical=thod were not investigated.
The resultsfor the conc=t-adon determinationsinthe liversamples from thissb* uc attached as appendices to thisreport. Conc=bmfions are reported as rnit-gosf anabytr.(gg) per gram of liver6&sm waractc&
3M Environmental Laboratory
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3M Eav:rO@
BatteUeSb* Number. N003604-D Lab"A)tY StIdY Number. ]FACT 060998.1
QUALrrY
ASSURANCE
STATEMMNT
Ttis study was inspected by the QualiV Assurance Unit and reports were submitted to the task leader, study director,and associated management as follows:
Phase Inspected
Inspection Date
Date Reported to BattelleTask Leader/ Battelle Management
Date Reported to Offsite Study Director/ Management
Sample weights Sample hamogerization Extraction Sample anabrsis
10/12/1999 10/12/1999 10/13/1999 10/13/1999
QuaUVAssurance Unit
Date
]3atteUeMemorial Institute
iv
3M Environmental Laboratory
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Report: FACT TOX-013 LRN-U2095
3M Envio=enW
BatteUtStudyNumber No03604-D
LabaVory Sb* Number. FACT 060998.1
G4DOD IABOIRATORY PRACTICES CONTLIANCE STATENIENT
StudyTitle: 2 (N-EthylfluorooctanesulfoniLmido)-ethiannTowlo GenerationRat Reproduction
Thisstudywas conductedincompliancewiththe Food and Drug Adniir@st-atiotGeosod Laboratory PracticeRegulations(21 CFR 58),with theexceptionthatthemass spectrometrydataforthe liver sarnpleswas collectedand processed.with theMassLynx sofcwaresystem (version3.1),which was not funyvalidated.The studywas fistedon Battelle'Msaster I:isotf regulatedstudies.
Jon C. Andre, Ph-D.
Battelle Principal Inve3tigator
Kris Hamen, PhM. Study Director
v 3M Environmental.Laboratory
Date
Date
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
3M Envi@enW
BattelleSb* Number. N003604-D LabmVOry StudyNumber. FACT 060998.1
Table of Contents
Lage
Executive summary .......................................................................................................m...........................
QualiAtsysura= Statemen.t...................................................................i.v.............. ComplianceStatemenL....:....................................................................v.............
Tableof Contents..........................................................................v.i.............
1.0
lutxkfucdon ........................................................................................I................
2.o Rdcre= Substzwes.................................................................1.............
3.0 ReceiptofSamples.. ................................................................................1...........................
4.0
Analysis of Samples ...........................................................................1...............
4.1
Summary of Medwd .......................................................................1................
4.2
lkjmdts...............................................................................................................2...............
4.2.1 QualityControl....*.......................................................................2...................
4.2.2 Sample Results ...............................................................3...............
5.0
Conclusions ...........................................................................................................3..............
6.0 Aclmowledgements ...........................:.................................................4..............
7.0
Specimen Storage and Record Archives .........................................................4...............
Table I. Example of hmuu=t
List of Tables Parameters UsOd tO Analyze Samples ....................................2...............
Summary
Appendix A (Results) Results forRat liverSiimple Analysis ..................................................A............
DailyAccepm=
Appendix B (DailyAcceptance CriteriaSummaU) CriteriSaummary .....................................................B.-.1.........
Appendix C (Sample Inventory List) Sample InventoryList...............................................................C.-.1.........
Appendix D (Chiomatogram3) RepresentativeChrom,,tgrams ..................................................................
Appendix E (Protocol,Amendments, and Deviations) Prot=L Am=dments, and Deviation.s...................................................E.-.1........
Appendix F (PFOS PurityReport) PFOS PurityReport ..............................................................................
vi 3M Environmental Laboratory
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3M medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
3M Envko=enW
BatteUeStidy Number N0036o4-D Laboratmy Sbidy Number FACT 060998.1
1.0 Introduction
This report presents a dmcription of the method used to analyze PFOS, M-556, PFOSAA, and PFOSA inratliversamples from 3M Study Number FACT 060998.1 (TOX-013) and the resultsfi-omUs analysis.See Appendix E for a copy of the study protoco4 amendnxnts, and protocol deviationreports (sigaed deviationreportswere not availablefor inclusionhem).
2.0 ReferenceSubstances
The analyticalreferencesubstancw for thissti4 were supplied by 3NL The following lot==ber or b=king number designationsapply: PFOS (lot17 1),M-556 (TN-A-2203), PFOSAA (TN-A-1293) and PFOSA (L-15709). Note thatbased on information supplied to'BatteUefrom 3K PFOS has two equivalent names. The nami- appearing on the Matmial Safety Data Sheet and bottlelabelis potassium perfluaroalkyl sulfonate. The name more commonly used by 3M in analyticalmcdwds and correspondence ispotassium perfluorooctanesulfonate.The lattername willbe used in thisreporl See Appendix F for puritydata supplied by 3M to BatteUe. The referencesubstances were stored at room tempo-at=.
The surrogate standard was 11-L1H,2K2H-Perfluorooctane sulfonicacid,lottrumber 59909, supplied by ICN. The surrogate standard was stored at room temperature.
3.0 ReceiptofSamples
Samples were received frozen and intactat Battelle,from 3M Environmental Technology and Services,in one batch on October 6, 1999. Samples were generated by Argm Research under protocol mnnber 418-009. See Appendix C for a copy of the inventory list.The samples were storedat appmximately -20'C.
4.0 Analysis of Samples
4.1 Summary of Method
Samplesw= analy@ by a previousvlaylidatemdethod(BattelslueidynumberN003604-A).The currentversionof themethod isattachedto thisreportin Appendix E. S amples we= analyzedby LC/MS/MS, and an example oftheinstrumentparametersislistediaTable 1.Note thatonlyPFOS, M-556, PFOSAA, and PFOSA (acdthesur-rogatew)ere quantitatedThe otherrelatefdlucrochemicalsa,lthc)tigh presentinthestocksolutionsw,ere not monitored. QuadraticTcg=sions weighted 1/xwere used to constructthecalibratiocnurves.
3M Environmental Laboratory
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4e(i-ca-- :@enar@@,Tenr-Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
BateUt StidyNumber N003604-D 3M Fnviro=mtal Labontory ShidyNumber FACT 060998.1
TiLble 1. Example of Instrument Parameters Used to Analyze Samples
Aut(o-4aiiijiler T[PLC pumis,; IV[iL%S.p%Letriiiiieter Analvticalcciluitiii Nltktlllpelia-ic i.ompt)ncnt-i Gr.idientpr(orile
Make: Gilson Make: Gilson Make: Maromass
)Aodel:234
MO&13:305
and 306
Model: QuattroLC with Z-wroy sour--e
Ycyswnc BetasU C 18, 5 gtn, 2 x 50 mm, Part No. 055-701-2
Component A. Ammonium Component 13:Ammonium
a=ta*2mK:metht=L
60-40.v-.v
aceute(2mK-rnethanol, 5:95,vv
Ttwe. min 0 1 4.5 6 6.1 8.5 9 11
%B 0 0 100 100 100 100 0 0
Flaw. mIJmln 0.3 0.3 0.3 0.3 0.6 0.6 0.3 0.3
[njecti4in Vottillic
Flo,kv column tellel) UPLC prt--,%ure &%IS I(Iurce Dt-%tilvaiiii-i-iit% Neljuliirer-.,it%
S4iurce hlfvcli leiviii
DL-utl%aiiiilneiiii) Cone V4141;t-_-e
Conisitm cncr,-@
CibiliSitift-@A%
10 JIL
LC column flow atswt splito 20 plhnin intotheNO Ambicia Approximately 840 psi atgradientsUd Elech-m@, Negative Ion Nitrogenat-575 llhr Nitmgen at-80 L/hr 1400C 2500C 70 V for S-S.PFOS 20 V forM-556, PFOSAA, PFOSA 40 eV Argor@ Bas ceU,at-2.5xl 0-3 mb
l@luttiplier
Rc%tituti4in Ions m4oniforeti
650 V 12.0for MSI -,10.0 for MS2 427>8 1 MRM tmL,6tionfor SS
499>99 NIRM bvnsitionforPFOS 556>78 NMM transition for M-556 584>1 69 NIRM bwlsitionforPFOSAA 498:>78 URM tansitionforPFOSA
Total run lime
II minutes
Appnk%im;ltc
SS: 4 min
retenti4in time%:
PFOS: 4.2 min
M-556: 4.4
PEOSAA:
4.5
PFOSA: 5
2
--aboratory
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3M Medical Department Study: T6316-S
Analytical Report: FACT TOX-013
LRN-U2095
4.2
Results
BattelleSbi4 Number. N003604-D 3M aviro=cntal LaboratoryStWy Number FACT 060998.1
4.2.1 QualityControl
Sysu= suitabilitaycceptancecriteriwaere establisheduringthemehod vnliintionand arc included inAppendix C, SectionIX Acceptmee Criteria.Relevant statistifcrsom each sample set areprovided inAppendix B. Representativechromatograms aregiven inAppendix D.
4.2.2 Sample Results
The resultsof the sample analysesaswell as a method detectionlimitdeterminationam presentedinAppendix A Allliversamples were initialelxytractedas undilutedhomogenates. After the data were reviewed,dilutionosf the homogenatcs were performed inorderto bring analyu concentrationswithinthe calibratiornange. The firstanalysis-thaptrovided acceptabledata foran analytcwas used inreporting Four extractionsetswere requiredtoprovide data for each analyte.
The limitof qt=titationisdcfmod as theconcentrationof thelowest standardwhich mcets acceptance criterifaor accuracy(25% RE). The notationBLOQ denotes"Below Limit of Quantitatioe forsamples thathad concentrationslower than thetheoreticacloncentrationforthe 0.13 lxgtgcalibratiosntandard.The notationALOQ denotes"Above Limit of Quantitation!f'or samples thathad ccncentrafionshigherthan the theoreticacloncentrationfor the 13 pgtg calibration stnnii.c,L Samples dia were initiallAyLOQ were dilutedwith blank liverhomogenate and reextracted.Samples thatwere expected to be ALOQ were firstdilutedwith blank liverhomogenate bcforccxtraction.T@c"Corrccted PFOS Conc" presentedinthe resultstablesisthcconccnu-ation found forthedilutedsample multipliedby itsdilutionfactor(finalvolume + sample hamogenatp volume).
The method detectionlimit(MDL) of PFOS was calculatedtobe 0.0173 ILglgfrom the analysisof 7 replicatpereparationsof 0.13 liglgcalibratiosntandard.The MDL was calculatedby multiplyingthe standarddeviationof the found concentrationsof the 7 reps by 3.*143;the Signal-toNoisc (S/N) ratiowas caIcuiatedby dividingthe mean found concentrationof the 7 reps by their standard deviation.The 'method of MDL determinationwas provided by theSponsor.
5.0 Conclusions
AR analysesmet acceptancecriteriuanlessotherwisenotccl
3
3M Environmental
Laboratory
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3M Medical Department Study: T6316.S
Analytical Report: FACT TOX-013 LRN-U209S
BaftUe Sb34 Number. N003604-D 3M Envkonmental LaboratmySb3dyNumb=- FACT 060998.1
6.0 Acknowledgements
Acknowledgement of principalcontributorsparticipatinigntheper:forma=c of d3isStt* atBattelle ispresentedin thefollowinglist.
Participant
Title
Jon C. Andre, PILD. RichardW. SlauterP,h.D.,DA.B.T. PatrickL. South,B.S. Gerke IL van derZwaag, US. Bobby C.Braswell,B.A. Cynthia J.Ryan, B.S.
-BattellPerincipalInvestigator SeniorProgram Director Mass spectroscopist Sample preparationchemist Qualityassuranceauditor Lead qualityassuran= auditor
7.0 Specimen Storage and Record Archives
A.Uoriginaplq= data,aswellaselectroniccopiesofdata,willbe forwardedto3M forarchival. Copies of both thefinalreportand alloriginalpaper data generatedinconjunctionwith thisstudywillbe maintainedby BattelleA.U residualiversamples,extractsa,nd unused testarticlweillbe disposedof or returnedtothe Sponsor as directedby theSponsor.
4
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3M Medical Department Study: T6316.5
Analytical
Report:
FACT TOX-013 LRN-U2095
3M Enviro@t8l
BatteUe Study Nwnbw N003604-D LabOntOrY Study Nmnber FACT 060998 1
"FE"IX
A -RESULTS
3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
BatteUeStudy Number-.N003604-D 3M F_aviro=cntalLaboratoryStudyNumber: FACT 06099S.1
"VS. M-MK PPO&AA. PPO" urrsui sluer. SPREADSHM SoFrA"lt
DATA SWrniU
LM PAT UVM% tiougo"
MANUAUY
IKXCEL 97
"Moe
I 2 3 4
7
la 11 12 13 14 Is
Is ,7 Is Is 21) 21 22 23 24 25 29 27
286 30 31 32 33 34
305 37 38 3,04
41 Q 43
IL5 40 47 40 44 so &1 52 83 54
5u,
37
ou an a2 43
kaom Number
Samole Type
om
watwnim
1
om
Waowniw
1
oem
mawnid
om
am
Mobf"Q
2
Oadi
2
ow
Mauwnid
2
ow
matemai
2
ow
Ltmom"
2
90"
MewrnW
3
900
kisurnw
3
om
3
ioooi
wamrmg
3
10002
mabwnw
3
10004
maumm
4
lome
Maurnal
4
10024
matwnw
4
10=
Mabfnw
4
10=
Ab&bN"W
4
10034
10042
wawrmi
10044
WA"ff*A
10043 imi
Matwroi WAlbUnW
1OW4
111
10097
F@W
1
10105
FeW
1
10100
F@tW
1
1("07
F*tW
1
10104
Fmol
2
10135
Few
2
10140
F
2
10142
2
lCi2i
Few
2
10128
FetW
3
10177
Few
3
loi55
F--'
3
IC"58
F*W
3
10154
F4W
3
10172
7
4
10197
F=
A
10194
FWW
4
102M
Few
4
IC211
FeW
1=4
FeW
41
low
Me%' lk@A
1
lolc6
MT*W.W
1
10100
maw(rdw
1
ICHOT
mamcnw
1
1()106
maurnei
2
10130
mah""Nd
2
10140
2
lQi42
k4latmal
2
11)121
ASbfrw
2
10126
mabcnal
3
10177
maumnw
3
10155
14-ftm-'
3
Matpmw
3
i10o1l554 a
matemal
3
10172
mabmnw
4
10167
matmal
4
loi94
mautaw
4
IC203
maowffw
4
IC211
Matunal
4
1=4
MaturW
"03
M-6"
"OS"
Pro"
&77F-01 IL44E-0 9@ma-m I.ME6w 1.17E+(N) 1-349442 1.180"a 14464= 9.349+0
1.019+M 4JWC+= 2.?iR*= ILTSE@= 2A7*4-0 4A7%40 9.829+0 9.159+0 gA3e$42 SA4E+02 aA394a IAIE+= I.ffm-*= 1.319+0 1.239+03 I-TZE+= 1.72E41
5= 1.AOE.01
BLOC BLOQ 4.$iE+(" Z74E+01 2@M" 2-WE-t*l XS$E+01 IME+02 I.ISE+02. i.50E#42 2An+M 1.34E+C I.SGE+02 2.78E4= 3."E+02 2ME+02 3.0s&02 3.26E4" 2.WE-01 ISIE-CM 15ae4n ZOGE-M L21**-M 3.24LLOO
9.209H-0 L33L401 7 *Nt+Oi
77L4= ii.'03t+= 2-%3e',= 2.3aE+02 2-t@E-6-C 2.629+02 3--1E+02 3,t$ 3129e+n 3.$@
BLOQ W-00 BLOO 9= K= 1.2BE401 I=r;2Z I.leE,@M a-sectm
I.laE-401 4-369-+01 &239+*1
L"E+M &WE401 L44EOOI SAZe#Qi L?59+m ?Jd" I.I?E+02 LzLeNn _ue+aa "-ftg+aa
1.33C+02 l.i8E4"
.Siff+02 BLOO SLOO BLOC SLOO SLOO 2-aaE-@m I-M 1.41gtM I.IVE-W 1-75E!Z
&16E+M 7,17E+M T.54E--M &41E--M S.BTE-W IME@01 2ME+41 2.668-001 2.?$E+01
2.93E+01 BLC)O BLOQ BLOO M= BLOQ
4.DAE-M 3.27E-M
4-5GE-M &39eow T.T5&0 3.148"1 1,15E,-Ol L33L40i 4.31 E491 2@"E-01 3.2SC-@01 3@46LL"l a.71E-01 L34L'+Ol
LASE401
P" a. C4
BLOQ BLOQ B= 8= lm 00 1 106-(" I:a4*"l &79E4-(M Lactsm
KDQ
4.4@E*W 4.IOE44M ZUM Lml=
1.04" ?-Im"i 2AU"t L32804M 3A2&N GAS" i.22ei-a IAOE"A &82" I.Ve,42 I.Maqa lien+= xwo+oa
L4z!sR 1.0matal 5,4194M LMIM 12W;M& LAM i.2meo4n i-lopocn 1,12goOt J.UM 1.IOE*(n I.fdE"t 1,3ogo4n
1.34eK2
ij7E4*a
1.$aE*= al 8= BLOQ LOG :Lccl
&01E@.W 207E-W 2JZE=M anctm 4.34E+W
i@ooE-@m
o.ace4m
I.OW-*4n a= MCC 0=
1.4OEtW 0.("941 IOW.&T ILIAE.&T 7,QBE41
2.OOR*M I.SSE+01 M02L4*1 2--rZ+01 I.ISE--(M &11" 3.ISZ+" 4.28e+ot 4.""
IS41+01 BLOO BLO(2 BLOO I 8= M=
&446+W 2&2M 0 5i5E+W &rreow 1.4$ei-Oi 1.71" 1.20E-ol 2.73**4H 2.246+01 &3764@H 2.74" 4-ME+01 7.$Ce**l IL$21-6-01 &009+01
2.8@EOW ZZMIM 224E-tW 1,94C-@W 2inE!I& 2AQE*W 4.DOL4M 3.t4E4(M &ZOE44M IMM!M
SLOO
&= K= am 2-'494M laffm ZDW_+% liggo
L2"
&DIE.W LIIE-#M LL4M 6.20E-.(m SZM OL3aE*00 B.vw;!&m 9-gaE-W 1,1494()t &llr-ow
BLC)Q BELOW LMr OF QUANWATMN
Anoh'dx dab bW.
Nwmw tat - Ocb*w 13.low Undwfbis- Ocb)bw 14,IM N@W - Ccbbw 14,ION
BOM undemhm - Ocmbw m Ing
AM samples AJIsanVW* Allsampw Allsampi"
undiluted unduuted dBuW dRuW
A-1 3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
BattelleStudy N=bcr- N003604-D 3M EnvirarumentalL'a*boratorSytudyNumber. FACT 060998.1
METHOD DETECTION LIMIT (MDL)
STUDY: N003604-D
ANALYSIS DATE AND INSTRUMENT
DATA ENTERED:
SPREADSHEET
SOFTWARE:
RESULTS ID:
130ct99; 9053 Electronir-allyand manually ExceIS7
All concs in pg/g
Calculated Concentration of Replicate 1 Calculated Concenu-ation of Replicate 2 Calculated Conc=b-ation of Replicate3
CalculatedCon-ntrationofReplicate4 CalculatedConcenuafioa of Replicate5 CalculatedConcentrationofReplicate6 CalculatedConcentrationofR@plicate7
Mean Concentration StcLDev.
Sp5ceLevel
SIN ............
LOQ (detf.rom 10 x stddev.Onaise")
LOQ (det.from calm=c low stcl)
Curve Coeff ofDeterrninnfian
Date analyzed
Method
'Kev I - SpikeLeveltoohigh;SpikeLevel must be < lOxMDL 2 - SpflcLeeveltoolovr,SpikeLevelmust be > UDL 3 - SIN toolow-,SIN must be > 5 4 - CoeffofDet ofcahbrationcurveunacceptable
M-556 0.1269 0.1220
0.1433 0.1368 0.1670 0.1225 0.1190
0.1339 0.0170
0.1331
7.88
0.17005 0.1331
0.9979
130ct99
LC/MS/NIS
PFOSAA
0.1484 o.12al
0.14a4 0.1605 0.1681 0.1513 0.1385
0.1488 0.0128
PFOSA
0.1187 0.1325
0.1521 0.1441 0.1490 0.1382 0.1413
0.1391 0.0119
0.1334 11.66
0.1315
3 11.74
im: @4,
0.12763 0.1334
0.11853 0.1315
0.9937
0.9891
130ct99
LGNiS/MS
130ct99
LC/NISINIS
A-2 3M Env4@ronmental Laboratory
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3M medical Department Study: T6316.S
Analytica'l Report: FACT TOX-013 LRN-U2095
BaftUe StudyNumber. N003604-D 3M Envio=CnW L&Ore=Y StudyNumber. FACT 060998.1
AIPIPF,NDIX IEI-DAILY ACCFPTANCIE CRITERIA SUMMARY
3M Environmental Laboratory
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3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
B alleUcSt* Nl=bw. N003 604-D 3M Eaviro=cntal LabOratOrY StudY Number. FACT 060998.1
PFOS ot &I IN RAT STUDY NUMBER:
DATA ENTERED:
SOFTWARE:
LIVER N003604-D
A&ANUALLY
EXCEL97
REGRESS*N PARAMETBU
APAWYWB OM ockaw 13,100 001*bw lk IGN ottobw 1 k Iwo Octi)bw20,ION
PFW b&W PFOSM PFOSA
PFOS M-M PFOSAA p@
PFOO LSMS PFOW PFOSA
PFC)A PFC)SA
)e C"ff
-MOIS4 41DOW
001= .155
4).00389 &m4a OL
-M
CLOD= QLO= a 00= .71.9
ooom5 .153
x CO@ff-
I." CLa27 oam 1.50E-+04
l.A2 0.575 O=i 1.73C-+04
2-17 0.312 O.Om 1--Z3E-"
2.07 1.65E+04
1.11
407n 4IM13 -aco3ag --M
4XOOM ACOW 400321
-M
-MOW5 -mom= 400=
rn
oobcw-waanoalftn
OA"
CLM
Orw omp 4 Cal pt I
DAM
O.M
orw mg d Cal ptI
CL90 txm CA" oow
One rep of oW pt7 ackaded Oro repd cd pt5 ackw*d
O.Sm OAS4 am O.We
Orw at amipt7 ockmiw One rep d pts1, S.5 uckdsd
One repatpto4.7mduded
G.9a7 O.We
3M Environmental Laboratory
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3M Medical Department Study-. T6316.S
Analytical Report: FACT TOX-013 LRN-U2095
BatteUe Study Number N003604-D 3M Enyimxlmcntal Laboratory Study Number FACT060998.1
PFOS st al IN RAT STUDY NUMBER: DATA ENTERED: SOFTWARE:
LIVER N003604-D MANUALLY EXCEL97
QC Resuft AnatysLsDate Ocbober 13,ION
An&Mo PFOS
M-5m
PFOSM
PFOSA
Octobst 16,1989
PFOS
ccb)bw ia,-1989 Octaw 20.1999
PFOSAA PFOSA PFCS M45M PFOSAA PFOSA
PFOS PFOSA
OC Levok no/mL
la
3.3 0.7 0.18
10 33
0.7 0.16 10
&3 CL7 0.16 10
3.3 07
0.16
10
3.3
0.7
0.16
10
3.3
0.7
0.16
10
3.3
0.7
0.18
10
3.3
0.7
1
0.18
10 3.3
0.7 0.15 10
3.3 0.7 0.16
10 3.3 0.7
0.16 10
3.3 0.7 0.18
10 3.3 0.7 0.18 10 3.3 o.7
%RSD
%RE
6.6
-4.0
3.3 .-4.6
7.9
-6.4
3.1
-12.2
4.7
-2.4
11.7
2.5
3.0
-8.8
11.5
-5.1
6.5
-1.7
5.1
-10.4
8.7
43.0
14.5
8.2
16.9
-4.3
2
-2.1
95.a
1.3
1 4.6 1 3.9
5.5 4.5
3.3 9.7 3.4 2.7
8.0 17.7 4.3
2.1 7.4 17.7
11.6 a.i
8.0 8.8
14.5
15.5 8.8 -2-7 -2.a
6.7 -3.7 4.5
-0.8 -2.9 -7.0
15.8 -3.9 5.4
-4.4 1 13.7 1
8.7
11.7 7.0 15.1 14.7
17.0
21.2 25.a 14.7 11.4
15.1 21.3
16.7 11.5 12.6
0.4
-4.5
-1.7 -20.3 -8.1
-2.9 23.4
11.0 15.4 0.8 -1.5
-20.6 -18.5 0.0
13.7 0.0
. 18.0-.
2.4 2.0 3.7 5.3 2.3 4.0 13 3.4
-8.0 -12.0 -21.7 -1&0 -1.6 6.5
1.9 i 11.5
B-2 3M Environmental Laboratory
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Analytical Report: FACT TOX-013 LRN-U2095
BattellSetidyNumber N003604-D 3M aviomnental LabomtoryStidyN=2bw. FACT 060998.1
"IFE"IX C-SE"LE UiW?ffORY LIST
.3M Environmental Laboratory
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Analytical Report: FACT TOX-013 LRN-U2095
BattelleStIdY NuMber. N003604-D 3M Environmentil Laboratory Study Number FACT 06099&.,
ShidyTOX-013.Ar-.LS41&.OCQ.SaffVWlnbm-agonfbrdtnwtb
sample I 2 3 4 5 a 7
10 11 12_ 13 14 15 18 17 18 19 20 21_ 22 23 24 25--28
E=Z: 28 1 29 1 -30 31 32 33 34 35 38 37 38 39 40 41 42 43 44 45 4a 47 48 49 50 51 52 53 54 55 5a 57 58 59 60
a2 e3 84 85
Samote Descripdan 3wnple Type
F@@-o=-grpi-m
MatwnW RatLhw
FC@-Mo-gMt-M FO-OW1.7pi-M
mabomw Ratuvw Mabamal Rat Uyw
FO-O= w
MxtwTwd Rat Lkw
PO,@w FO-N8l-grpi6M
Mabwnal Rat Uvw MntmW RatLKW
FO,@w
-RstLhw
F(@-99&K-opi6m FC-9W-grpiW
Mabu. Rg Lhw MatwnW RatLNw
FC-
li-M Mawnel RatUvw
FO-M7-Mill-M MoftrnidRstUvw
Mawnid RatUvw
FO-10001-CMIII-M Watoo. Rot Uvw
FO-IOOC2-wpllW_ Watwnid Rot Uver
FO-10004grpllw WatwnW RatUver
FO-1001SIPPIV-M FO-IOC24-WpfV-M
Moter@ RutLlvw Ma*mal RetLlvw
FO-10029-gp(V-M MaUwrmi Rat Ltvw FO-10033-=IV-M wtonmi RatLtvw
FO-10034.qprv4A MateffudRatLlvw
FO-100642-MV-M MabwTtalRat Llvw
FO-10044-qpV-M MaWnal RatLlvw
FO-10045-grpV-M M&Wnal Rat Ltvw
FO-10051-grpV-M Matemal RatUver
FO-10054@V-IA
Matwnal RatLhw
FO.10097.qpl.F Fobd Uyw
F-0-10105-ini-F F-staulv*r
FO-10105-gpi-F FetalUvw
PC-10107-7pi-F FetW L?@w
FO-10108-7pi-FetWLNw
FO-10138-grplW FeW LIYW
FC-10140.7plw FetalLhw FO-10142-grpit-F F*tW Lhw
FO-10121-7pit-F FetalLlvw
FO-10125-grpli@- FeW Llvw
FO-10IT7-Wpill.-F FetalL)vw
FO-10155-qplll-F FetalLKw
FO-10158.gTill-F FetalLlvw
FO-10184-mil@-F FetW LIVW
F(@.lOlT2-grpill-F FetalLIVW
FC-10187-MiV-F IFOW
FO-'olG4-j;rp(V-F Fetal
PO-10203-grpN-F IFetalLtvw
FO-10211-gmN-F IFetalLiyw FO-10214-=rV-r- FabiJUvw
FO-10097-qpl-F Matwnel RatUver
F,0.10105-grpw MatwnW Rat Lhw
FO-10106-gvp;-F MatwnidM Llvw
FO-10107-grp@-F FO-10105-MI-F
Mabwrud Rat Uver matemai Ratuyor
F4-10136-=II-F mabon1w Rat uvor
F(@-10140-gipiw MabwW RatUvw
FC-10142-grpl@-F MaWnal RatLKW
FO-10121-grpil-F Matemal RatLNw
F(3-1012"rpll-F Matwrwl RatLhw
FO-10177-gmllw Mawnid RatLlvw
FO-101&5.gplll-F: Lia*n%d RatLKW
F@0-10156-9mill-F Matwrmd Rat UVW FC.-lol64-grpill-FfAstwnW RatLlvw
1 FO-10172-gypill-F MaWnal RatLfvw
F-C@-10187-71)(V-F MatwW Rat
FO-10194-grpN-F mawrnw Rat Llvw
FC@-10203-grpN-F
twruwRat Lhw
1 FO-102li-grpfv.F MFawnW RatUver 1 FC)-.10214-WpN-F Imauwnai Rat Uver
C-1 3M Environmental Laboratory
Page 89
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
BatteUeStudYNumber N003604-D
3M EnviamnenW Labonimy Soj4 Number FACT 060998.1
APPENDIX D-REPRESENTATIW
C]EIROMATOG'RAMS
3M Environmental Laboratory
Page 90
3M. Medical Department Study: T6316.5
Analytical Report:-FACT TOX-013 LRN-U2095
BatteUe Study Number N003604-D 3M Enviro=eatal Laboratory Study Number. FACT 06099 8.1
Baftelle
QLC 9053
ESI-
leOctM Sm (Mn, lx2)
100- 3.44
43*473.47
3_W
3.5a
a 100-
Blank Uver - Surrogate 10 uL; N003604-ri -
4.43
SURRO0G0AT1E.19 SURROGATE
2: MRM
10:58:1381 OPerator. PPLL o@f@2 Chrhaan0tn0ore,rles 1ES-
4C2277..a0708>Ia81. 181
4..3=2
'3 4.64
4.5833@3.00
5 W5.93
5.1955..334 4@5@5@.64 5-IM5
......... 420
r(5honneW ES499.00 > 99.00
1.7ge3
PFOS 1
ol IGC@ctbdtm n, 100-
4.44
5.28
i ..
a5.07
i - - . .-
@:'?AFkM'c;FfChannels ES558.00 > 78.00 317
3.81 01 lei56ti:@S6m'(M.n,. i@2@ ...... loo-
PFOSAA
5.07
5.58
5.8a e.ie
3: M M of 3 Channels Ec-'-
584.00 > 169.
6.3
98
ni ie(@@4 100-
s"m,(Mn, i)d@
4.69 ...............
&07
PFOSA
3.n
4.37
...4.bb'
5.5.@77
nelsES498.00 > 78.00
433
0.211 nme
D-1 3M Environmental Laboratory
Page 91
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
13=eUe Stady Number. N003604-D 3M Environme'ntalLabomtory Shidy Numb= FACT 060998.1
OLC 9063 ESIIeOctO8 Sm
100-
(Mn. l)t2) &94
Calibration Point 7-(0.13.ug/g) 10 uL; N003604-D
SURROGATE
2: MRM
16-OctII:
Operator. PLS
of 2 Channels ES427.00 > 81.00
leoctoo Sm (Mn, ixz) 100-
4.20.
PFOS
0 16C)@@ m n,
10
4.38
@@nel3 E-, 499.00 > 99.
1.08
i: l@AM j-3TChannWs ES556.00 > 78.00 3.gOe3
0-CM8 sm (m le 8 Sm (Mn,-l@@ ......
100-
PFOSAA
..M. -@56
4.54
16(5&b6 SM'(M 100-
PFOSA
5.07
@f @,c@iail@,el3ES584.00 > 189.OC 71@
0.15
5.55
6.01
i-.l@IW c@f@'d
s EtS-
498.00 > 78.m
1.08
Tlme r-r
D-2 3M Envirbnmental.Laboratory
Page 92
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
BattaUeStudY Number. N003604-D
3M ErLYwonimentalLabOrdtOrY StdY Number. FACT 060998.1
lie
"O'LCa"O19053
ESI-
l6Octl6 Sm (Mn, lx2)
ioo-
3.95
QC 4 (0.15U 10 UL; -NO0361
SURROGATE
2:MRM
le-oct-199 12:50:
OPomtor. PL of2 Channels ES-
427.00 > al. O.Ge
nl
1ed@t6it'M'(Mn, ixz)
100-
ol
18
.......
4.22
PFOS
4.42
M-556
100-
4.85
PFOSAA
3.83
-M,C'Mlnx.2) 5.08
PFOSA
3.
-4.b-O'
As.00
MIW W2"C@ha@nnals 'ES-
499.00 > 99.00 1.55o4
i: mAiA of @'dKa@ isESW6.00 > 78.00 4.97e3
i:MIW;i3Ch@annels.E@-I(X 584.00 > IS
31 .31 511..7711 3-: M M of 3 Channels ES498.00 > 78.
1.71
D-3
3M Environmental Laboratory
Page 93
3M Medical Department Study: T6316.5
'Analytical Report: FACT TOX-013 LRN-U2095
BattelleStudy Number N003604-D 3M Environmental Laboratory Study Number. IFACT ()60998.1
Batelle QLC 9063
ESIl3Oct2O Sm
100-
(Mn. Ix2) 3.94
Sample 3 10 uL; N003604-D
SURROGATE
2: MRM
13-Oct-199 16:01-
'Operator. PL of 2 Channels ES-
427.00 > 81.0 3.O8e4
30ct2O Sm (Mn. ixz) 100-
4.22
PFOS
.2: M
of2 Channel3-ES499.00 > 99.OC
a-0204
nI L
136cdd 8 -m'(M'n,i'x'2') 100-
4.44
M-556
i:'NIW -of-37C--h"an@nsisES-r%58.00> 78.OC 347
136c,@id 100-
3.83
..1 'm (wIl'n, Ix2)
PFOSAA
130 100-
'M n.-ik@2
3.88
4.8e3 PFOSA
5.05 5.27 55..5522
5.M94 6.15
@35 3: M
ocff5C3@hCanhna@nenel3 ES564.00 > 189.OC
.36 .583
6.14
3: MFW
c@
ES-
498.00 > 78.00
875
5.41
5.77
71me
D-4 3M Environmental Laboratory
Page 94
3M Medical Department Study: T6316.S
Analytical Report: FACT TOX-013 LEN-U2095
BattellSetudyNurnber-N003604-D 3M EnvironmentalLaboratoryStudyNumber: FACT 060998.1
Battelle
QLC -4063
ESI-
i4SOct56Sm (Mn,lx2)
100-
3.92
Sample 37 10 uL; N0036C4-D
.i
3.39
18oct58.5m.(M,n, 00-
SURROGATE 4.18
PFOS
2:MRM
20:30:
OPOrator. PLS of2 ChanneLs ES.
427.00 > 81.OC
6.94e4
notser,469.00 > 99.OC
6.53ea
7 160ct56 m'imn,'@25 .......
100-
4.40
%
M-556
i:'Mik9of3Channel$ES558.00 > 78.00
i.Beas
160ct58Sm (Mn,1)0-)
4.81
PFOSAA
Idti@@'nalEsS-
584.00 > 169.00
180Oc-t5La-S-m--r(Mn,-I--x'r2-).
100-
5.03
PFOSA
i:'I@Ai;Ai3 ChannelsES498.00 > 78.OC
2.85ea
(""@3. 3M Environmental Laboratory
.......
D-5
TIMO Page 95
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
BaneU SbldyNmbcr. N003604-D 3M Eavhmn=tol LaboratorySbidyNumber. FACT 060998.1
"PE"IX FPROTOCOI.,, AMENDNMNTS, AND DEVIATIONS
3M Environmental-Laboratory
Page 96
3M Medical Department Study: T6316.S
Analytical Report: FACT TOX-013 LRN-U2095
BattelleStudy Niumber.NO03604-D 3M Environmental Labomtmy Study Number. FACT 06099S.1
7 - 7-.Of-
3M ENviRoNmENTAL
LABORATORY
PROTOCOL - ANALrncAL
STUDY
2(N-Ethylperfluorooctanesulfonamido)-ethanol in
Two Generation Rat Reproduction
In-vivostudy reference number. Argus 418-009 Study number. FACR 060998.1 Test substance:2(N-Mylpanuorooc=wffoaamido)-Cd=Ol
(N-ET<)SE-OH)
Name and address of Sponsor:
.
Marvin case 3M ToxicologyServicc3 3M Center
Bilileii2n2g0-2E-02 SL Paul,MN 55144
Nam and address.oftestinsfacmtr. 3M EnvironmrnW Technologyand Senices 935 Bush Avenue, BuUding 2-3E-09 SL Paul,MN 55106
Experimental startdate: Expected ierminationdate:December 31,1998 Method numbers and revisions:
FACr-M-LO, Fxtwdon ofPaUmium PerfluorooctantsulfonoartOetherAnionic Surfactantfsrom liverforAnalysisUsing HPLC-Electrospray/Mass Spectrometry
FACr-M-2.0, AnalysisofFluorochemicalsinIiverExtractUssing HPLCElec=spray/NlassSpectrometry
FACr-MaO,
Extrwdon ofPotassiumPerflucrooctanesulfonoartOetherAnionic
Surfactantfsrom Scn= forAnalysisUsing MILC-ELec@@/Mam Spectrometry
FACr-M-4.0, Analysisof FluorochemicalsinSerum Exbwft Using RPLCElectrosprayJMassSpectrometry
Author.LisaClemea
KzisHan= Study Direcwr r
bam
NiarAn Can
DaW
Sponsor Representadve
3M Environmental Laboratory
Page 97
3M Medical Department Study: T6316.S
Analytical Report: FACT TOX-013 LRN-U2095
BattelleStudy I;Umber N003604-D 3M Environmental Laboratmy Study Number-. FACT 060999.1
I,()PURPM Ilie anilyticalportionof thisdosing study isdesigned evaluatethelevelsof pertluorooc=e mxcnam (PFOS), or another metaboliteof 2(N-ethylperfluorooctanes&onamido)-etiumol(N. PYOSE-OH) desigaatedby the study dirt=r, in theliverof theparentand mbsequw generations of the testsysterm,or in the serum as necessary.
7be in lifeportionof thisstudy was conducted at Argus Research Laboratories
2.0 REGMATORY
COM7LLkNCE
This study isconducted in compliance with ft Food and Drug Admini@on Good IAboratory Practicesregulationas statedin 21 CYR 58. Any exceptionswillbe notedin thefinalrepmt
3.0 TEsTMATmaAts 3.1 Test, contro@ and reference substances and matxices
3.1.1 Analydcal reference substance: Potassium peffluorooctanesulfonat(eP.FOS), lot 217
3.1.2 Anadydcal reference substance matrix: Rat liverand serum
3.1.3 Analydad controlsubstance: Ncrne 3.lA Analytical controlsubstance matrix-. Rat liverand serum
3.2 Source of maw:iah
3.2.1 Analytical reference substance: 3M SpecialtyChemical Division;b2cesbUity informationwillbe included in the finalreport
3= Analydcal reference substance matrix: Argm Re3earch LAboraxnim*. traceabilitiynformationwillbe included in thefinalreport
3.2-3
Analy-deal controlmatru:
3.L3.1 .Rat liver- Argus Research Laboratories;bwubility informadon willbe
included in the finalreport;or
Rabbit liver- Covance Laboratories;U-xzabilityinformationwill be included in thefinalreport
3.M.2
Rat senun - Sigma Chemical Company-, bu=bility informationwM be included in the finalreport
3-3 Number of testand control samples. Liver samples fortestingw= receivedfrom 40 testanimalq and 10 controlanimals. Serum samples willbe testedatthe discretionof the Study Dire=r.
3.4 Identiftcationof testand control samples: ne samples areidentifiedusing theArgas Rrsearcb Laboratoriesidentifiersw,hich consist of a letterfollowed by theArps project number, the anitnnlnumber. the group designation,and thedraw date.
2
3M Environmental Laboratory
Page'98
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
BattellSetudyNumber. N003604-D 3M EnviromentalLabomtory StudyNumber: FACT 060998.1
3.5 Pmrity and strengthof MaOxials: Characterizationfthepurityand identitoyf the referencematmial istheresponsibiliotfytheSponsor.
3.6 Stabilitoyftestmaterw: chmwftrizadon ofthestabiliotfythetestmatmw isthe respon'mbilityoftheSponsor.
3.7 Storage conditionsfor testmaterials:Test materialasm stomd atroom temperatum Samples am stomd at-20 10 *r-.
3.9 Dispedtlon of testand/or controlsubstances'':Biologicatlissueasnd fluids'amretained per G12 mgdation.
33 Safetyprecautions:Refertothematerialsafetydatasheetsofchemicalsusedl Wear appropriatleaboratoraytdm and followadequateprecautionfsorhandlingbiological rnntezialasnd preparingsamplesforanalysis.
4.0 ExpmumENTAL - Overvievy
TLwues from linirnjtldsosed as describedinArgus ResearchLaboratoriePsrotocol#4184M am receivedforanalysiosf fluorinecompounds. At thediscretioonfthe StudyDirectora. seriesof analyticatlestswillbe performed on selectissues.
Initiallayl,lliversampleswillbe analyzedforPFOS by electrospray/masssper-rtometry OLSftAS).On thebasisoffindingsfrom theseanalyses,additionaslample matricesmay be evaluatedor othermetabolitemsay be targetraIfadditionaalnalysisisperforn=cla protocol amendment willbe written.
5.0 Emnumm%rrAL -AnalyticalMethods
5.1 FAC17-M-1.0, Extwdon of PotassiumPcxfluorooctanesulfonaotreOtherAaionic
Surfactantfsrom LiverforAnalysisUsing BPLC-El==SPMYMW3
SPM=MCtry
5.2 FACr-M-2.0, AnalysisofFluorochemicalisnLiverExtractsUsingBIILCElectwpray/Mass Spectrometry
5-3 FACr-M-3.0, Exuwdou ofPotassiumPeffluorooctanesulfonoartOetherAnionic SurfactantfsrothSerum forAnalysisUsing BPLC-Mer-trospray/Mas4Spw=metry
SA FACr-M-4.0, Analysisof FluorochemicalsinSe= Exh-actsUsing EPLCElect,ospray/MassSpectrometry
6.0 DATA &14ALYM
6.1 Data transformntionsand analysis:Data willbe reportedastheconcentration (weight/weighto)f fluoridpeer tissueor sample,or ofPFOS perunitof tissueorfluid.
6.2 Statisticalnalysis:Statistiucsed may hwlude regeseiorainalysisoftheserum concent-ationo3vertime,and standarddeviationscalculatedfortheconcentrationwsithin each dose group. Ifnecessary,simplestatistictaelstss,uch asStudent'sttest@may be appliedtoevaluatestatisticdailff=nce.
3
E-3 3M Environmental Laboratory
Page 99
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 IjRN-U2095
BattelleStudy Number. N003 604-D 3M Enviro=ental LabcratOrY StudY Number. FACT 060998.1
7.0 KkDrrEl4ANCE OF RAW DATA A" RECORDS
7.1 Ile fohowing raw data and records willbe retainedinthe studyfolderin the archives accordingto AM=-S-8:
7AA Appmved protocoland an=dments 7.U Study correspondence
7A3 Shipping records
7.lA Raw data
7.LS Electronicc*es ofdata
7.2 Supporting rwxrds tobe retainedsttaratelyfrom the sti@dyfolderin the =chives accordingto AMM-S-8 willinclude atleastthefohowinir.
7.11 Training records
7= Cahl=don records
7.23 7.2A
bst-m=t msint=ance logs Standard OperatingProcedures, Equip=ut
Pro=&=,
and Methods
71.5 Appropriatespwim=.
ERENCES 8.1 3M Environmental IAboratory Quality System Chapters 1, 5 and 6 8.2 Other applicable3M Envhv=ental Laboratory QualitySystem Standard Operating
Procedures
9.0 ArrACMKE@M
9.1 FACr-M-1.0, Extw-don Of POt333*U= Perfluorooctanesulfonmeor Otber Anionic
Surfactant3from liverforAnalysis Using BPLC-ElectmspmyftAm
SpectromW-y
9.2 FACr-M-2A, Analysisof Fluorochemicals inliver Exuacts Using IR"ICEectroqxmyn.lm spectrometry
93 FACr-M-3.0, Extw:tion of Potassium Perfluorooctancsulfonatoer Other Anionic Surfactant3from Senun forAnalysis Using I-IPLC-EectrosprayftAms Spc=mctry
9A
FACr-M-4.0, Analysisof Fluorochemicals in Sm= Extwu Using BPLC-
Eleamspray/Mass Spectro=try
E-4 3M Environmental Laboratory
4 Page 100
3M Medical Department Study: T6316.5
Analytical
Report: FACT TOX-013 LRN-U2095
BattrllSctudYNumber N003604-D
3M EnviroxumentalLabor=U StudYNumber FACT 060998.1
BWMOD
FOR
pxRlrLuoRoocrANZSULFONATZ
ANALYM
OF POTASSIUM
RPOS) IN RAT IIVZR NY LCMSM
VerAmeLo Shay xw
Vrim=by: PutickL Sac& kpC Andre6Ph-D.
Z,5009r.@
3M Environmental Laboratory
pap I ofLd
C-1
Page 101
3M Medical Department Study: T6316.S
3M Eaviro=cnW
Analytical Report: FACT TOX-013 LRN-U209S
BatteUeStildyN7xmberNO03604-D
Laboratory Study Number. FACT 060998.1
M=MOP
FC)R ANALYSIS OF lOTASSrUM
P=nrOROOCrAXXSULPONATZ
(.FPOS) IN RAT LIV3M BY Lcjbf.%W
Ver3L= LS
SbulYN&:
'L stnaL4xy
S*nm oxadn* ftm "M
=ckL Tasc&Ubradw smodwft on *-dhd
vitbmm*m mndsri.buM=t4 md
Ivft adoiacowl The orgvwcpbom m
wap=md to&7=u md ru=nekwma hLmdhwa itx=Wy* by LCACUIDL
-ra , =dacgb=potmsxi=pmem Sxad tASPMPWZ>XWI" ZU HVM
===Mm=wAnbftdtmomcbmicai=uV=mk
nL SABU.LW
tm r%A. ofC=uAy recank V
IV. G=a3uL IKSTxucnom
CaUbc= aU,
balsom
toft SCF m bsbm= -F
)Ao=
A
T/bw &a VOW= --6A vada ft=adw vah@ soud IntM
method LAbd &U modud uW m
matutb= n spoCI2-1ba*2 appmpdm ". IfyM %*-A In
Tum ILgoludw kc 2AL= %vim be mv to lobd f-4,@ theprqwadm diftmd 9*
tr wbi& ibeso-d- hiddly,
SISMan *0 aml pw cctis=mbod to-1 tWt ym bm &Dowcd &a mdfiadn I
an -,-i-I jwdmgmm &To
andan , *, -benbe= .opafy c&HbtatoLMy=
devim ftm ft mcdkpc do-at tb4-N-ct md obtLbL tke zpymvd of ft a*
andy dtmct-.CC U* U-A- n Swo as V=xMk
Yw.i =d due &a daz -,I- am to pap oaLviblcthheywm nnd& Ifanly@ puma
au dam = a shide don
uloybe me& Ina AnsW W=dm an
Page- If-itip6 mo make ewxiak the-L'Fk4-1 -m@t- muK be bidatedmd daudby the
PC== -king dw -07.
Lbwmxm orNA dabom -t;mAypHcowe.
0 Tba zwlw Isw In c ttoMalys-* It3;; 1
9 suxkzmm toneedtw The-
dganowgkal mtwbot do
atopmmWb4k&%Kod
=am do atftlbrcmft ac&Mw InwocMW
afew soft-- =named cc-I- oabft is
conzkiend=Wed
e I;oconzcdm wal be -- Ix pwiv ar slitcmumt cfmY UK adclobtiPtPOS"
- Use &lawvwumcaic.Eppe-kof vW-t-. - P-hil-41som@ pipcttshrdw=xiag
zcdnno0c swodem
& CANtact whk Tcom b7 dw text -rdd showd be
V.
NIATZRLUA
SeeTjbleI *r In mqwred cbcad=ls.rccgcnm and 2ohectLUn TabltI lbrdacmnc=bm Cho& &a Ilbel=srt6l4 to-,re dw aU --- bt,an om exphedandthotW m tbsFqW
pwdly va&
Pap 2 43fid
c@2 E-6
3M Environmental-Laboratory
Page 102
3M Medical Department Study: T6316.5
Analytical
Report: FACT TOX-013 LRN-IZ2095
BattelleStudyNumber N003604-D 3M Environmental Laboratory Study Number. FACT 060998.1
bf=OD
IPOR ANALYSIS OF POTASSIUM
PEP.7L'UOROOCrANNSULFONATZ
(PYOS) IN RAT L"ZR Vftdm LO
staty
BY IriMSM
TAW L 3[akrbis
t .@t
lip
PodkornactmeI;T,IH
pmdbwcaoctc= Suhgxwf6 Acid
m-sm
PFCSAA PPOSA PFOSF-A Ru Liva
A cot=
Sandad
S=ropm sft.,6.d
Auaydcw Stmdard i AMEIydcd Stmdard AnLbtkaL
SbwAitrd
A-4ikal SundiLrd A-4*:ML I St=d=d M&bi)C
I 16@ Pbase
3m
ict4
3m 3m 3M 3m 3m Ekd=
Spagoo-
ROM Tamp
Rmm T-P
Rom T-M Room To=
Tamp
Tamp
Tmo ---2(rC
RT
Sodtiz- Ey&=odc6
R-gcu Pm
Nam
3-T
TwzbuqW==oni=
E==PRV
RT
CnL*4
SoW= C*bm=M
E.%== P"p
wftcoj
ILT
Iticwbc=-
F@@ Pftp
MaHc%
IT
Etoi Amum
Exta= PrV
KT
mm-q wow
Bvfiw
pEE LO P-tff-
S-+* ws
R-gcm PtcN I Wtobflo'Phan
PH @,
PH uwtw czhbmdcm
A&Mip-
AMU TM I XT
ILT meam Pa= T=pazmm
VL
iquwmcrr
Sm Tsbk 2 ibran requirem-odjarpie= of cquhmccl U@oft iabletodo=meut tteacOW gim (4L&zakoundcl)afcquipmci&CLharkcaM=WcmctalLoquipm@rcquirb2g-wk-g-(44@
bW==) taemsum itIsc=mnl
P&P 3Ciifd
C-3 E-7 3M'Environmental Laboratory
Page 103
3M Medical Department Study: T6316.5
Analytical Report:' FACT TOX-013 LRN-U2095
BatteUe StudY Numbw. N003 604-D 3M Environmental Laboratory Stuty Number. FACT 060998.1
BCMOD FOR PIWLUOROOCRANESULFONATZ
ANALYM OF POTASSIUM
(PMS) IN RAT LXY= VU36M LO
Stad7lqo4
BY LCJBMM
B&bM= we4ft sm
Ptpc= 2ipcm Ptpo=.
T"2. W.IgSb=,d.* w
R-m-a Bahw=
PtpetS-W@ks
ca=-400 PipctR=g=zM WIMS
laX @qgmpl-
Rgpcuw
LIYW &off. 3t=W
en
i hcmc
Sd
E=ad q.ffml
Bim
TnnspcctWb=
mlxnicdc OOAW shakcr
Swm QCs
S& E=aa SL=qim
E=.=
ED=y ZYM-K
isML pdypmvikska.
LS ML
12x7l=* 5 mL
SWIS" 20% 2002
127-Tl6O-W
T."Lv
I
GrindUver
Vabonowe pa@ A
vehudeldcP4m clan A
Tmnsft pipcm plutic
B%"K1m1rhr Ma" V0o.ln,.."i.
Dih -
mm vqmnlc= DUudow
Trmmft Exbun ccnttfi,
4A
MA
MA
3M Environmental Laboratory
Pap 4of16 C-4 E-8
Page 104
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
BaMUe StudY Nu3nber N003604-D 3M E'n"viro=entalLaboratm7 Sbuly Nu3nben FACT 060998.1
M IHOD'FOR p=n-VoRoocrAMSULPONAT3C
ANALYSIS Of PMASSMM (PYM IN RAT LJVKR 13YLCJMIM
Vcr3im Le
vm P.IOC=X= A. rmu-xdon of2 =M Ammahm
Aceftto
twxk.I)t=WvethesdW in-m md dha Novdom wt&
Sotmdm mq be wed
IL
C.
Acmd
of
AcoW And vah=c
Datecepmpumd=
su* NO:
acoft=
prpwti.,
f-2-9% Sdinui H7droxide Shdion
Weigh 2m * 2 g of socgmmhydra@i&bwo abeskw.AM = mL ofUMI-Q W" md mix todinahv. Cod =d U=z&c toa poblxWACM bouk tw IW=p SabldM mq be snumdft 6 -t- atrou-
Acmd n@ of sodtarnb7dr=dde Actmi volum MM-Q -am
No.
preparadon of-"*A Sodlu= U7droxide Soludon
AM la =L of-29% Sod= Fvdraxi& sab*i- to a lwul va=xwc An.- tovclume whh Mn-Q vaul Tn=dw to a potypnvyine b*We Saudon amy be =red tr 6 mondo itxmm U=q=wms.
nuk nd gm mmo@L
Aam, vowm of-29% NaM A@l Jlnd vobm= Dam of pxpm=d=
sohniam
D.
?Mamtion
afTetr2butykm=onhun
solution0..5K (PIEi[(i)
Rligw r.Hy-,Joe
Hydrogenulfxft CLSA)
pg buffer 7 yrbmdcr 10
PH r@rnnr. yR -odbg
AAd 169 a I S afTBA m -5W inL EUM-Q vuw bi a bed= A4= to pE to IILCO
a 0.02uzbms-51-L-MML aflg% so&= By@
saw= om lalow MLVA
Mn-q water,and ulbr-Acquatft pH to 10.00 a O.M usbma -2-9% l@b= md nbL
T=e= to a potyprwykas bocdo Rw
-
hr =6 nmoft
mnd atro= tmcpanlmo, but the nE mak be
to sub m kdjmlo
pH 10.0 2 0.02wft 2.9% Sadin- Hydnod& Saiv#6- n
11
pat@ 5 of id
3M Environmental
Laboratory
C-5
E-9
Page 105
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013' LRN-U2095
BattaUe Study Number. N003604-D 3M Envirorlmenml LabOratory Study Number. FACT 060998.1
B=OD
FOR
PUnIJOROOCTANESULYONA7Z
ANALYSIS OF POTASSRUM
VFOS)J:N RAT UVIR VWAM LO
shmo
IrYLCNVMM
Acmd num of7s&. Acowl BAd voh=C A=md Ami pm Dim ofpvpaad= stav No:
3L Preparation ofO-U M Carbonaft Buffer
welo 26.3* (Ligofmflx= -tmm md 2LO a 0.1goracdhn Wo&=m md
n wdnnmclooo-mLvoh=mctdctLa&Dt=dftdn=dWabkUMK
mium tovolumewithIMII-Qvam. W@ and- toa pobVW@ bmdo fw
swnp Sol,-Icmnay b-cumd fbrI --,h wbes
Mhpmt4
AcuW mm ofso&,- --bons= A=a' @ ofsodum bimrbouatc A--d gn&Lvohmc
atprepamdow Sb* No-.
F. rnpmmt[on of M*bU* Phase
Cauqcm=t A.-Wx uVAbw 600imLct2=M smmmninm
md 400=L at
=06-@al Sdudon=my bewed be Immtb@it --ad atzciownov-3nm
Acmd volume of2 =M
wcuw -mL
A=aivab=aofnieduL=L_,=L Daw ofpzpazdow
Sb* No:
C=paDcot B: lgx wgctbor50 mL of2 mM amnwidum ace= md 950 OL Of
zwtbawl Soludm way beund farI m=th v
atMGM bmupaxbm
Acbmivolumeof2 mM -n=
mL
A=mlwhn=Ofme&anaL -nL
Dan ofprqmxd=
Sb* NO:
G. pmn=tion orstockSurrozab Standard and Warldng Surropft Standard (WSS)
1.
SkickS=optA SumdardCMOOO Pohdl.
Wei& 25 2 2 mg ofIM M 2K 2M-yagcorooctzn
add od
vumfa toa loo-OLvmwmctrk tL*. Dumt" In
vab@
WLth
md niblSton reft!gaamd.;-, t= T.TV
Acmd Velgbt:
AcftW Dffiuka DateM-PTCPUzdm stD4 NO:
pav 6 or16
.3M Environmental Laboratory
C-6 E-10
Page 106
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX@013 LRN-U2095
BatteUe StudY Numimr. N003604-D 3M EnvirotumentalLaboratory Study Number. FACT 060999.1
MM720D FOR PERM'COROOCTANESUWOKATE
ANALYSIS OF POTASSMM
(PFOS) IN RAT LMR Vali= La
SeedyNG.:
BY LCJBMM
IEL
5mck IA smck IB St=k 2A -9@7B $to* 3A Sbxk 3B -Sbxk 4A sbxk 4R Suxk SA, sbxk SB
2. wss (1000avlmlr.
DO= loowl ofawk =mgft soodod m 25mL widlma&@l mdzdx_
A=-' Vab=o at3bxkbnc=l Sumbrct: ACUW Doulka Dam ofpmpandw
Preparition of CaUbradon Sah-entStwJo aid Working Standuds
L
Saltonswckc
I%roub amaym vcio &a spacm ona@m ofoam--d Oodepeadadi@r vicigheadsA gadB rWOcLta) UstodInTable3 andu=sfcrI= opum voh=etdcl4--u-Dinchv Inmcdmol. dlium$avab=c withxmW=i2t.md mixwel Stcmzcbig@y l@p-P,4*=UVHSbL
2. NflxedSolveotSwd=
ptpa theSpedfl-I n%@= ofCU* =LfydoLl@.4@ vqgt- A a lbod b Table3 =d --%- bm a singlevolumcuicZak. Dtnolw inutetad dho tovah=c whh medmal ad mix vmEL Sam reng ' k pectocudtm='UV U&bL Rep= d3apmc= withRgplkaftB nockLVm ; aohwejbdownxx" t*prvwe dw w*Hdmg*wadardl
Dam ofpxcpmztt= su* No:
3. Waddug Smndxtds(WS):
Dilum the
awki avAwarldngsundzrdswith=cdlmal a vp=MW bL
Table 3 and =ix weEL
Dou afpvcps=dc=
cc
M" PMSsm
M-556 M170 Y-M PFOSAA PFCSAA PFOSA FPCISA FFGSF-K
Table:L@CaftradouSaivedSmdamdW=kbegSwzdxrds
f.it @--cl
%4:111.11.%Ili,.tsell %al.11I[ILAI
1.11 L.Cc t:iil.llV..i
I ilt.,tN ..1.
.1111.)
50*imff
1 25 2 0-5 MS
16
1 ME on2m...
10
125 2 0.5m
10
1 -502 1 mff wattwwl
10
1 2.5t 0.5MR
.10
1 93*lvmg
46 * 0.3Mg
So 2 1 MR
-:F5t 0-5 ME
50 1 MR
4
2-4MOM
2,vo.ow 5@004,000 IAMOOO 3@.OOMO. 2,'MOOD
Pap 7 af 16
C-7
3M Environmental Laboratory
Page'107
3M Medical Department Stiidy: T6316.5
Analytical Report: FACT TOX-013 LP-N-U2095
BaMlle StlidyNumber. N003604-D 3M Environmental Laboratory Study Number. FACT 060998.1
FOR PEknUOROOCrANMS=ONATZ
ANALYSIS OF POTASSMM
(PFOS) IN RAT LTYIER BY LCS@ Vftvim Lo
SbbdyNo.:
-Sbxk 6B
Sbzk A 14med SUDCK3 va I
W32
WS 3 -WS 4
W53 W36 -w3 7
PFC97A 1 25 2 0.5MR
stoftI thm iRmA
i wL each
Swxks I dim
3 1INLL
43LWB
aschoo
b&md Sto& A
34med -S&Xk IMLOO
k m@ @
vis 1 WS2
2 ML1 2 ML--
WS3 WS4
WS5
uktim
rm =Ibljtl@@m
10 50=mtu=m=n
21 is
10
0 weighau=Iiy@ -A-.dsioalkakthneeamsta.m0&1 UseVOIUZMCCJC
]@M= 300.000
2000 1000 200
1
pmimtion of CaUbration Standards nd BULnks
1. Lhcr hamov=ato
Prep- hi-t@Umb=cgcnm tabwk by v4tigYmgapproxbmndj4OgaE
blaukUmt=a5WmLNAIB=bOGU=-Ir,'-
2DOmLafMB-Qmm
r,r+mtD&bo=gcnemsmisp=Wm ANquatinmir 3GmLyardmstw
p (IPP-
A-' Mus m'LIvw.A=nd vohl=ofwstcr I)am ofPrep:
Stodr.
r RM.UCM
Det=ninadcmsitoyfcalib@
matcbc
mm RomoaDtATz TEmotiGHLY md --=bu the bm=Mtm= of10mvacaw wci&ngx ofI=L pmtow oftbaTMWUGMYM=
MM ROMOGENATE D&AMLCMY PRIOR TO larm AIZQUOT RMYOVAT-
TableL CAinwationStdi/QC-MMrix D-sky
2. Lt4a C4LU=ti= SaLudards
prep= eachDvermmmatim M&rd b? akitnia.45mL ofmanud Uyw bcuiog== (STIRFAohiC)GENATE W13= ALI(ZUOIM4C;)bw a 13 =L cc=acti4mtibesod addtzl5g0 pL OEVIS 4=MoM P..sL- "4pB=@ clt v=du-ds md 6 bl=kl SeeTabW 3 fm wb=cl Tm An,- Am dank In -nm=cdtobeappm;d=xWTL50-04MT- Mlxv*M
pw a elf16
C4
3M Environmental Laboratory
Page 108
3M Medical Department Study: T6316.5
Analytical
Report': FACT TOX-013 LRN-U2095
BatteUe Study Number N003604-D 3M Enviro=ental LaboratoryStudy Number FACT 060999.1
BWMOD
FOR ANALYSM OF POTAWRUM
pxRyLuoRoocrANESULFONAT:t
(.PFOS)IN RAT LXVXR BY LCIM&M Versim LO
sbaft
C.It
TableS. C$Mradon Sbadards a@d Btmb
!-i.itice 'FArl-'CtVf)l Actig.ItVt@l
rsr.-,Ct
.%ttitit %,Iglliit.lt '%..I.l.l..,l
L)
FiliAlVt.[
I
ws I
so
2
W32
3
WS3
4
W34
50
3
WS5-
50
6
vis6
so
7
W37
50
BLmmk lAcOR
50
0.5
0.5
0.5
0.5
0.5
R
---Oj
0.5
DOIC of ympacadon ofCalnd&tlaz@c
2m
-f3
1000
GA
-400
2A
200
L3
too
OAd
30
om
20
-0.13-
J. PrtpamtiozL of QuaHty ControlIlver SiLmples(QCs)
1. Qmaft C=nml Working Stamiards
Du= do lba0wingxri= Vol,- methanolInvahnnevictwdm md iodk well Prepambt&bwh= used.A=nl Yoh== we bapwmftm
7
rrvii wsi
wts7WS2
WS 3
2.
T Naxed StockA Mbmd StockB
ws vvm aulu
LS,000
QQCC ZSS I2 ICBM,,
?mt=adm atqaallqCzutrolLhwSu*la
P.@pw eachQC Inbulkby I"Itngdinvohunct& Zaakappr=dnsm*baW=
withm)autcd UverbamoAL.IQUOMNGL
CSTIR EXXVSDGENATE VIE= rim QC VM vnhany #ad All-tit,avdum
with=ddutedhwb--gco (TMEEMOCENATRWI=
AL.IQLIOTIN(3@bccx THOROUCMY =4 A
2--mL Akpft boo
yalypv"l=c tibaandam K qTM4=wzly -2M
Tahk 7.QC Prtp=lica
. .........
-QC WS
2
QC WS 2 tmmvr-zs
3 --&CW@wS 3
4
WS4
0.16
1)= ofQC PMV.
Ympamtion ofMS C2ieckStandard forSystrm Saftabi3ity
Ptpct250OALofWS 2 at-10,00n0&lsnalnd2.5=L ciWfSS at-low ashulbt is= thesma5o-mL volumemic'4---uDouto tovolume withMACH nd nLf3L
Page 9 of16
3M Environmental Laboratory
C-9 E-13
Page*io
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
BatteUe Study Nl=bcr. N003604-D 3M F-nvirc)runentLaalboratory study Number. FACT 060998.1
M=OD
YOR
FEMUOROOCTANMULFONATZ
A:NALYM 07 POTASSMX
(PFOS) IN RAT LrM Versim LO
Stutylqo.:
BY LCMSOM
I@ prepa=tlon ofhomagemkw retaywy fter umpks
TOA"-M tbor=mytmm thebo=gcnizmdmpmmx. unkamogeoindunkuvw vM beZ=tUU4 isdcp"- at3 =ncmwdm levelmsd bomoged=W n 20awL Mft
m ba do= av=7 daydm houwgcml=dm ofAU* nzzv- Ispedb=W
L
?um VP odmobely0.5S of sahm
am bm ewh GE6. is =L
t-wyi cmuif= tub= RcmdwdouafUm.
2. Add IW @E.-iWS L.3, d 4(. WS p-
tub=)Ispmpm
trdaclftm atWprwd=L" 4. 0-3.-d 0.4Wg.
3. N02idpotlwmm atUverInS by 2.3and sk tW mxq =L afvjum 4. Ho pni= ewh Ih-e-r=pi- ad hamoV-1-pmbewitk=Ctbw
vot== a( wum usedInxmp 3.addfngA'=-w bonopot=d anpIL
CL= bawatcuimwwithMcCE bct =WW-
Cap andvam= hamoscma tw md In-c=acd=L
bL Prcps=tion of D*auttonCheck Sample
L
Pin= 235 mL of-ffh-A lycrho-ogm MMECMI)aM4A7ZV=Z
AIIQtXnM40) buo a IS mL acuacdm U" zod a& 50 laLofmxod SW* A.
2. Da= 50 PL ofsup I Sol-rt,-(VCR= SoLurmN VIE=
AUQUOTING) -with0.45 mL ofi--4fl-neldim bmwg=- CM
ROMCGEXXTE WFM.E ALIQUOTING) bi3. 15 =L w=acdca -
3. Ti" lashmilbdcp,-; Ifbr--Acdonady m dapwhm zm* nnrffln wM bedllt==dd ==Wtcd.
N. nomotenization ofstudy samples
L
Pb= apprazimLWy 0.5g afwahanotembied mdy sumpleUmbm a 15 =L
hiblR=wdwdou ofltvm
2. )AutdplytbcMR= ofUvw Ing by'7-5=d aM dds n&W mL ofme=
3. Eomagcmi=eachUvcr--pi- wddnml,--g=
pmb*wi&mo&w
valmm ofvm= uscdtmxtop2.addtmgtinu M UMV=bccd M-04
4. Cnes,bomtemimw withMcOH bdv= soomi-
Cap&-Avac=bomge"s tw=sbmexuacdm
0. AnAtyAs StLndards, 13bmk% QCs. and Sa=lples
1. MM LrnM BOMOCENATES THOROUGMY ZMK)IM ALV4UOTM md *a 500;,Lct-ch QC (4r*lc=s p- kwel)-@d oth-s-om b&q c=x=d li=Li-mLpcl)r@@ w=cdm "- The cala& md bh@
am ah-4 allqwtod.
2. To tbABUW= - IS (3fcpsladd100.uLatMeM imd vas
3. To theBlaWn + IS(3 rcps)md tother=Linfnssum- add 100.ULVM =4
vcr=r.
4. Add Q.5mL of0.5M TSA (pFl10) laalltoba md va bddly.
S. Add imL ofo.25U -bom- bi md vw bdeft. 6. Add 2.5=L ofahyl accmm Pi= thetnb= Adcwqs an U -thd *Abw ata
wmbmgof300ft-20,-;-
7. c=m&V mbcxata
af3300rpmtw-20 -t-- tomcpwm BCVCL
L
Transfe2rmL ofdLetop ' S 1 119-m a A.- pab7mi=4 obi6
pw 10of 16
3M Environmental Laboratory
C-10 E- 14
Page 110
3M Medical Department Stud@,,:T6316.5
Analytical Report-.FACT TOX-013 LRN-U2095
BattelleStudy Number: N003604-D 3M Environmental Laboratory Study Number FACT 06099'8.1
METHOD FOR PEItFLUOROOCrAN7SUIXONATIC
ANALYSIS OF POTASSMM
(PFOS) IN RAT LWM Versim Le
StudyNw An&17@ -
BY LCMSM
9. Evaparce to&jwm nmder mkmgm ata xvbg af3C'C lbr-M 10. R==gk= 00 Mdd=$ In 300 JALOf MgftrAg WkhVMVAd2&
ii. srin@ cmam Iwo
vbb ft =WydL Stomvidsnftfauumd
(uptoIm=&) tfLCftASINwM nab@;, m-' Idw@&W.Mom3.der
Teo=wnqwracucmm=
vmsAcmanozomddmb2gvaudffdc&ma.
exuz= ofthecd Ak bunksn.d QC&miWbermmd tw iiipo3 fteobw
th@@@ pmpmadenIfbddatram ucmemmn *ocxpdwvl*Uffnod&06
Dam cocfaludfalmk wmm= prcr. DIP ofQC -ft= pm:
P. LC/MSJM Analysb
&LW *FJP$4%
1. Tise-threyn= condiacmspecifitendT".WMW cmdwam
an
desiva-dmLy be-.dfad byu -RIYU topro&- SC-gah" Pa* AWL
TiLb;IA - LCIBMM Ccmdhtms
ModcL_-
U%
Mai= _
ModcL-
makr.
laodel-
M:
BccLsilCIS,SA 2 x 30 mzc6?=Nix 055-70
C-MMDoncaLA: Ammocii= acetuu=m:du=L 60:40,rv
v-v
Time, min .0
2sa
Flow,UIJ=tn
0
a.3
a
4.5
100
0.3
6
100
0.3
6.1
100
(L6
iu
100
CL6
0
0.3
0
0.3
10 UL LC colu= Bow splhto*30 PLJmin t ;dWn) bm dw NO atranmft
-Ambient
1000yd atip@ mn
on)
E!o@. Necad"Ion *Nlroltactn575ljbr OMImLcn at30 L/hr
L4w)
0140*C
-250-C
-M v ( 020vt
V) Ppcgi.-M-(D 14)PFOSA,PPOSAA, PFOSEA, M-dK W70
040eV L-tv) Ppcs.
PPOSAA. I&S-94U.M
300v(
o4 PFOSEA
An= at@L5 x 10'mb tu ceB
.6m v
V)
inb)
112-0 *r Iwo1
010.0&run(
I
4DSMDL4b Aob
Al fXr/Zr/9?
Pme 11of16
C-1 1
3M Env;-ronmental Laboratory
E-15
Page 111
3M Medical Depart@ment Study: T6316.5
Analytical
Report: FACT TOX-013 LRN-U2095
BatteUe Study Number N003604-D 3M Envirommental Laboratory Study Number. ]FACT 060998.1
NlrMOD FOR ANALYM
OF POTASSRUM
FEP.MUOROOCRANESULFONATZ
(PYOS) IN RAT LRVZR BY LCINMW VersiesLO
ar.-Si
g
499>" I&M manddomft PFM
siom lam -it[.-ftI&M
S?M.16U9RM -W- lbrU=
SW169WUb=ddantrPPOSAA
498>73IfitM"--M- tc PFCDA
loig:-1M6W9 --4Hco fbrPFOSEA
=in)
PFOS.4.3o3Lm - 41 mim
UM. 4.6n%in PFOSAA: 4.1misl
PPOSA: 3.1=bm C YFOSE.4- 5.7mtfn
lam) uda)
Min) mw
Mb) win)
oPammct= tbk=aybe rb=pdby the=sbst A-lyahmala(l
2. The abo"=mdid= *ouldbeambabkftdiom===
QUIMOLCCW
91053)N.loditcadonsrmq be nc=cwy If
Ukr=xm Qmnm Sad"
Is=c& SpllthsIcrwpowcobum viaaraystom =04m w
devim
3. CAL%rjbmthe=Lu
arvm*
thatheaLHbrstiIms=imbtobyvLm3ahlmewan (cm&a ton&pW) to a
xiitrble nobn-pbanIm IsstM
detw-lowRombdoa oW wArAto
behisbc&rm thaund lbrandyzin-anvl-
4. 'ro- the7opcrpwtwmmm ofthe
Wea do bub@ diak
smndard.Tbo resmhzshcuw be ==guxblo loa -b&cdca Ifwnffab?AL
S. Use zLn M-md cbromwngmpby 4nowattomaftwon qia= iocoom da
oatptigtm d@eaulysil
&
--Il-gOrditSrm thelcsd qm ftm dieummaw chmnwoxmpby
batpidansaftwonriu=L
7. Make dn& Weedo- ofmck ed mandardQ.r- a* -mWm orw-k lhks atk= 4 injccd= ofthebmuum= cbeck
L
R= sa slz=showd typ&cLIlmyA cwmd 80 lujacdo=dw to%*"omat
cs IOUCaeouSielpr@i@m T@ n=Uuqbor
A I bmtib@Wpm a
riskafyieldLu=Sac=pudao cum
VILL CALCULANONS
L Sp=dsbee Saftwim
Vend=
2. )M AndysisSmbmm
vec3diamn
3. C-k:ol- the xvcmp d-lily Of ft Uvctbc-ogcuu (10 reps) b2 -mm@MT
4. Udng&ezycmpdcui7aftoba
r-=kulmksdmdmsdq
(-g ofUm pa mL ofduubedhmcv=mlo):
UmdUntedlhw dcm&y (=S'mL) (9ofUm Iwi-p dcns4afl--secaM>U at Hvrx+ & ciwf=)
wh= SofUvcrandgofmam am w&ua =cd top.*- bak U-IfteaNK 6=udryofwi= Is----A tobe Is@ML
Dtlutodbyadwmty(mg(mL)-UndMzmdd-dq*DihFm=
Pap 12of16
C-12
3M Environmental Laboratory
Page 112
.3M Medical IDepartment Study: T6316.S
Analytical Report: FACT TOX-013 LRN-U2095
BatteUeStudyNumber N003604-D 3M F-nvironmentaLlabontmy StudyNumber. FACT 060999.1
BWMOD FOR ANALYSIS OF POTA&MM plp_vLUOROoCTANZSULFONATZ (PPOS)IN 3tATLrM
Verdan Ll
BY LAC/MS/M
Wbem dUs '%- - 21LI- Li 111bDac==tfbr 10% dBa ofUvor
incdxoimd QC -im
ofcaromdmsaodw& md QCsbyufng*A man ofmob md iftdm onlycnohadmsiv cm=d-@
6. Cakzaafttba-1 cmcmwzdan ofPPOS md a&w ancrachamkak biDvw 2c &o --ds md QC& n taowlc
C==WS) - Cc= @m&@ DOoodLhw &=skyOnv@) x10M 6ft x le pgbg
7. Ammm dw thek-vzd- of the peak um cttha Wa -nide=d .1 Fkg@ibnczmtf= wb=pcr&r-A sundanl
=Mud m
L r.,.-6tmmgmui=eqmd=niadngthapmk- g adoCm Wdd6m Ofauk =I%Csd= =Ddud O-Vds)toun -dda coccotnaimInam tx@) ft PPM 1"56. MM, andPFOSA.A---rd toma x@@ cmwca&adm ImLHverbrPPMA imdPFOSZA. PPOS.MSSCN070.&M PFOSAA we g-g-@ by=Lugibem-pa a-d-d Worad amuhrt PFC)SAwm PM.RPA at umndnted@widxmrtehwmm todidmm=m (aftod SMM&rd oilrgdcnCWWI. U3@ & quarxdc.qp wdzhft2d/zo,d& -do" hr
an xujyt=6
9. r.L,.t.adcm=lincadnin@ foreachiniwdcof-1r-,3tiomundud.QC.anduxingdwrqrtuionpmwnm=-dtbsp-kmxpammtimarar=L
10. Cakui. ttmmeativee=w. avcmgoreladvae=. wmdwd dcviodmandmbdn sundwd &@ixd= foraUQCL Cakulawthemiatiw@ce tw OKCIL ofcdDz2d= xmmdm&
IL Cd=hm thexvcmp r---Y f- thvh-Vccb- ==vcryfutULcLdouL 12. r-L-i.tordzdvov2odmddayWicnibrtt*Pl'03taSSP-k-=tiact&orepumft
DL ACCXPTANCZ CRrrx=A
A. ?dS Check.StiLndard(SygtemSufftbAfty)
Atkis 3 hije@ ofthe1-0cl--4Sr--h-1-0 PmvideIL ct10% OcIOU*t dkt ppM toSS peskart&to"
IL C&Ubradon StLndards
Thep== mladw== lbrthe=n==1=4"d zvemgcagftbco3'M-d-M-bzft abowdnwa &a buawing Hwitc
3M gnvikonmental Laboratory
PM 13of16 C-13 E-17
Page 113
3M Medical Department Study: T6316.5
Analytical Report:. FACT TOX-013 LRN-U2095
BattateStudyNumber. N003604-D 3M F-nv;,ronmentLaalboratoryStudyNumber FACT 060998.1
NM-MOD FOR ANALYSN OF POTASSRUM
pIRMUORoocrANFSULPONATZ
(FFOS)Ui PAT IZV3CRBY LCIMM
Versim Lo
Stady Nag
AndrdDoc
TW& 9.C-Hh--4;,S-undwd A=cpumm lwla
PFOS
PPOSA PPOSEA
1 20 CIS% &TLCOM
20r25% stLCCn
20 CIRA - LAM 2f)rli*A mrTIt-h lnmq%L@Tren
194otevIL- T rvlm
UplaSediradonsundtrdWjad
nqboccdndodftmltwcx
pravl&ddwaoe
kjgcdmrw=insywlcvcLR=wvalafLa, I kvdmqbod@IfWpmvalisabu&wA
]rn -.4mjowllm.umv dn - bradamed%ythet-i-in caubratlm=mpvgbe
O-r or
C. Qcs
Ina===auei=Acvd r-rar
orttaiivo-,aatndp,----trebati-msundsrd
dayhdon oftLbe*QC-S#---[UAwa*o &aowlng Hnd=
PF@7CT" 10.QC
0
20
0 556
20
MS,70
20
SSMF PPOSAA
20
PF SA
20
PFOOSS'EJSI
25
R=O,.g ofbxuvidul-lmk= ftm &c QC
bw be dam If&=MvoldA bY a
Leccpl-@tkn(z4,b23trame@E-tMbnelinnorDL=WA Q aK rooft).
Ifthewymp detcrmhkedconcczbad= forou QC levelcmeadz-tm
NMI& 68
tut t-@4- or=w# dim= dwaid'so=)tLaoL Tba r= mri be mpoud or ILPulks Ctdw
T= may be cocsw=cd ==publil For=m3ple, If20 low QC &09 dw stftd maybemceptedtbabx" -"-'a= bmduftd bytheULa@
anda wid4avciW cwc=awiccl
D. 'Homagenjur3tecoveqand DEntionCheck Ss=ples
TM av=p rt=mwyacmm&o 3 kvtbof
I C=Vcj amp," 22iMa M *AtCt
tbsdoud= Cho* nmpl= sbmll bn witbln&a
of70-130%toc@ VA=VD Of
=wbodomtfw=mpniodbyanawmbie
I.;CwwmioAl-OQS)
TmmrxWod U=iuofquan&o@d=ut nominall0y.13;Wg out ibrpFos.)A-M UM md PFO&AA.
PW 14ofli
C-14
3M'Environmental Laboratory
Page 114
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
BatteUc Study Number. N003 604-D 3M Eaviro=ental Laboratc)rSytady Number. FACT 060998.1
ba-MOD FOR A,@@YSIS OF POTASSIUM
PZPJL170ROOcrANISULPONATZ
(PFOS) IN ]tAT LTYM VM-A= Le
BY LcjbtwZ
A-1yodDam
ParPFWA andPYOSB-&%to v&UdMd LOQI - =MBMDY OM PWZ =dL DW ID20
offt
ofdw -Ebatim smodudi6In- cwcu=oi= afPPC" md
ppoWAra=dnuodwcamcdoL
TbeaWymoonowwe=vwnnvMbs
wmbntcdvi*cachrmackoduMbeh-h-windw C ' tfdM=ma=*u=
crbcdlWtoymobchidcd3to#nml vAicbmq==UmdwUmcmomnxd= bd" tMvWWoodWvoi (wabanyOM Wg),wMbe app 4 &am&
ir. srwuscfty
-rbgXgdod MXM= b= -A
biadkeam atsankamood@
20% cfLOQ. Tm 11 1 ofthe='Dead-cum xppcwxit**Mtn= c==:dm lbr=V
m q=udud- A=WtWba px*-
(cam)ofdo Wwca wed mmdard.*waft%
vm be=ida-m -@fRe6-ct/id=m tubmdmed st=V
am qwuuffledkopuly
G, GCU221
Mnabu"acccpu=
tnm-duudlismotbodisca* afr I I =aakmd
O=n mcd& em Dan=, a=opu= cdbwk ofa vatidee-dbM aM oo=mgy).Whom
repucm =ablm kn= ft how- otdmn oc=si=W acdkm
hardwo ofspreadsheeotrme Me annetworkddvl )M COMMir?r3
3M Environmental Laboratory
ftr 15ofils C-15 E-19
Page 115
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
BatteUe StudY-N=ber. 14003604-D 3M Envim=cnt3l LabOratOrY StLIdyNumber. ]FACT 060998.1
?"MOD
FOR ATULYM
OlrPOTA-%SMM
nM@,'UOROOCrANISUIJOZU'n
qM'-'D Df R&T UV=
]BYW,?-MM
XCL CoNcLmareto
Ted-f-I Review QC R&Vicw
Dam
Dam I)atc
3M Environmental Laboratory
pw idof16 C-16 E-20
Page 116
3M Medical Department Study: T6316.5
Analytical Re'p.ort':FACT TOX-013 LRN-U2095
BattelleStudy Number. 14003604-D 3M Eaviromnental Laboratory Study Number. 'FACR 060998.1
combi=d
Stridy Tldo orai (Gavage) FertilitDyevelopment and Pciaaul/PostmaW Reprod=don To@dcity Study ofN-EtFOSE in Rob
PROTOCOL
AMENDMENT
NO. i.
Amendment Date: July28, 1999
Pwfonning Labornfory 3M Environmental Tecbnology & SafetyScm'ces
3M Environmental Laboratory 935 Bush Av=ua
St PmiL UN 55106
Laborstory.Project ldent67cadon ET&SS FACr-TOX-013 LIRN XJ2095
3Ai Eff&wmontiii Labwatory 3M Environmental Laboratory
B-21
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3M Medi.cal Departmen-t Study: T6316.S
3M Envwomment2Ll
Analytical Report: FACT TOX-013 LRN-U2095
BatteUeStudyNumber N003604-D Laborecry Sta4 Number FACT o6o998.1
ProtocolFACT-TOX-013 Amen&rmnt I
This amendment modifies the following portion(s)of the protocol: 1. PROTOCOL pzADs: Tbc proposedstudycompledon dateisUsW as 12/31/99.
AmEmD To READ: The proposedstudy compledon datais6130/00. REAsom.- nic proposedcompletiondatewas changed toallowtime foranalyzing&U matricesof biteresl
Amendmeiit Approval
Mwvin Cue Ph.D.,SponsorRepra=talive Kris J.Hansen PILD.,StudyDirector
DaW.
c 2-/dl
Date
3A4Ewkwvn&-M Lab"fofy
3M Environmental Laboratory
F-,22
Page 118
3M Medical Department Study: T6316.5
Analytical
Report:. FACT TOX-013 -LRN-U2095
BattcUc StLIdyNumber. N003604-D 3M F-nviromnentalLabomu)ry stidy Number FAcro6o998.t
C=bined
Study TWO Oral (Gavage) F=tUity Dmlopment and Pabatd/Pmbidd P,cproductionTo@dcity StLidyofN-EtFOSE in Rib
PROTOCOL
AMENDMENT
NO. 2
Amendment
Dafe:
September 10, 1999
Performing Laboratory 3M Enviromn=tal Tacbnology & SafetySavices
3M ExLvim=ental LaborAtOrY 935 Bush Av-,
St PauL MN 55106
Laboratory project ldentffcadon ET&SS FACT-TOX-013 LIRNU2095
30W Envkww*ntW Lebomfoly 3M Environmental Laboratory
B-23
Page 119
3M Medical Department Study: T6316.5
Analytical
Re@ort@: FACT TOX-013 LRN-U2095
BattaUe Study Number. N003604-D 3M Eavirdmnental Laboratory Study Numb er. FACT 06099g.1
Pn7tOcd FACT-TOX-013 Amendment 2
This amendment modifles the following portion(s) of the p.-aboc 1:
1. PROTOCOL REA= The protocolsl-am thatliverwillbe =twted Enviro=ental Labor=r)r..
and anabrmd atthe 3M
AmEmD To READ: The liverspecimens willbe ccu=tcd and =a47xd blifitute5,05 King Avenue, Columbus, Ohio 43201-2693.
atBaMUe
Memorial
REASON., The liverspecimens will be sent to Battelk Memorial lnsd=e for axtacdon and analysisdue to time constraintsia the 3M Enviro=ental Laboratmy.
2. PROTOCOL READS: The protocol statesthat swm following methods:
specimens willbe cctwted and analy-@AA
FACr-M-3.0, "Extwdon of Potassiu= Perfluarooctanesulfonat@o-r Other Anionic Surfwtanb fiom Sermn forAnalysis Using BPLC-Electrospmy/Mass Spectrometry" FACT-M4.0, "Analysisof Fluorochemicalsin Scn= Ext=U Using I]PLC-
Elec"raymm
Spectrometry"
AMEND TO READ: The serum specunenswillbe odractedand analyzedfollowingmethods:
ETS-84.1,"Extr=tionofPotasai=PcrfluoroocUnesulfanateor0thcrFluorochemical Compounds from Serum forAnalysis Using HPLC-Electrospray Maw Specftmetry" ETS+5.1,."Analysis of P otassium PerfluorooctanesWfonate or Other Fhwrochemical Compounds in Serum Ext -actsI-IPLC-Mectvspray Mass Spect=etry"
REASON.- The extuction and analyticalmethods FACT-M-3.0 and FACT-M-4.0, respectively,were updated on 04/27/99 to ETS-&4.1 and ETS-8-5.1.
3M Envhwmentat Laboratory 3M Environmental*Laboratory
E-24
Pa@e 120
3M Medical Department Study: T6316.S
3M Envimmn=tal
-Analytical Report: FACT TOX-013 LRN-U2095
BancUe Sbl4 Number. N003604-D Laboratory SttidyNumber. FACT 060998.1
PrOtOcci FACT-TOX-013 Amendmo#7t 2
3. PRoTocoL READS: 7'w protocol stnt thatliverspecimens willbe =twaed followingmedu)ds:
and analyzed
FACr-bf-1.0, -Extwdcn of Potassium Perflucrooctm=ulforiateor Other Anionic sur&ctwu from Liver foranabisisUsing EPLC-Electroq)ray/Ma3 SpWftMCtCy"
FACT-M-2.0, -Analysis ofFiiuorocbemicalsinLiverExt=ts Using IIPLC-
Elec"r&YMM
SpectromeW
Amex To RRAD: no liverqxcimens wiU be cd=ted and analyzedfouowing method.-
M@"&@ fbrAnab,3is of Pcriluorwctane Suffonaw (PFOS) in Rat liverby LCftA&?A% Version 1.0
REAsoN.* Since the liver=tracdon and analysiswas mib-m@@
to Bada Mmodal
Insttute,tta3=cndinent was wntten to includethgarlivermethods and titIaL
Amendmen* t Approval
A ma;v@a taw
,Spon=pcprwmtadve
I)ke
Y,d3ten J.Hansgm Ph.D-, Study Director 3M Env*wmr9w Labmfty
3M Environmental Laboratory
E-25
Data Page 121
3M medical Department Study: T6316-S
Analytical Report: FACT TOX-013 LRN-U2095
Baft@e StudY N=2bw. N003 604-D 3M ]EavironmentalLabomtory study Number. FAcr o6o998.1
Shidy Tide
AnalyticalSbidy 2(N-Ethylpcrfimrooctsaegulfo
do)-et@l in
Two C7cneratRiaotRnepmduction
PROTOCOL
AMENDMENT
NO. 3
Amendment
Date.,
October 4. 1999
Pwfbnnlng Laboratory 3M Environmental Tecbnology & SafetySwAca
3M Enviro==IW LaliomtcrY 935 Bush Avenue
SL PRUL IAN 55106
Laboratory Project ldendffcatfan ET&SS FACr-TOX-013 LIRN TnO9S
3M Environmental Laboi@atory
F-,-26
Page 122
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-TJ2095
]3aMcIleStudy N=ber N0036o4.r) 3M F-nvim=cntal Laboratory Study Number. ]FACT 060998.1
PMtOcOl FAC7- TOX-013 Amendment Number 3
Thl3 amendment modiflas the following portion(s) of tho protocol:
1. PRorocoL READS: Kristen 1.H=wn, PhJ). isttacStudy Director.
AMEND To READ: 12m K Lundberg, Pb-D. isthe Study Director.
RE"ON.* Original study design has changed due to irv&ilabt'loiftyresources and 1-mes K. Lun&ag win begin serving as the study directorfor'FACr-TOX-013 as of 4 October 1999.
I PROTbcoLR.E4m: Secti7o.n1st2tthatthefollowrianwgdataandrecorwdislblercudneidnthestudfyolder in the arrbivesaccording to ANM-S-8: Approved protocoland mnendmaras; study correspondence; shipping records;raw data,and electroniccopies of datl Additionally, Section 7.2 sww thatsupporting recordsto be retainedseparatelyftom the xtudy fold= in the arrbivw according to AUDT-S-8 willinclude at leastthe following: Trainingrecords; cah@on records;instrumentm2fiA=ance lop; Standard Opwating Procedures. Equipmcmt PmcedurM and Medw&; and appropriatespecimens.
AMF-ND To READ: Section 7 states:"Me originaldata,or copies th=.wf, wiU be availableatthe 3M Enviro=ental Laboratory to facilitataeuditsof the study during itsProgress and before
acceptance of the finalrcporl Whca the firmlreportiscompleted, alloriging paper dati4
including:appi ved protocol and mnemti-
study correspondence, dappmg rc=ds. raw
data,approved finalreport,and clectmrliccopies of data willbe retainedin the arbives of
the 3M EnvironmenW Laboratory. All COMBPOnding trainingrecords,canr@don records,
instn=cnt maintenance lop, standardoperatingprocedures,"Luipm=t pmeedmm. and methods willbe retainedin the uchivcs of fficfacilitpyerfo=iug each =abrgs-
REASON: To directsubcontractlaboratorieisn the dispositionof the items Usted above.
W Envimnimntal LabaWery 3M Environmental Laboratory
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3M Medical Denartment Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
B=elle Study Number. N003604-D 3M EnvirorumentalL-aboratoryStudy Number. FACT 060998.1
PmtOccl FACT TOX-013 AR*ndment NUmber 3
3. PRorocoL READS.Dispositionof testand controlsubstances:Biological6wues and fluidsam mtgned per GLp
regumom
A mEmD To RuD.-
Specimens wiU be mainbined inthe3M Envuom=LW Laboratoryqmmmm amhrft& An
sentto mib-wntract laboratoriewsillbe ratumed tothe 3M
r-nmpntal
ratoryupon compmon of maalys[sand mibmi&sionofthesub-c@
Wmntory(s)
finalreportThe spec=cns willbe returnedwith thefouowmg d- -cmt-Hon- &egvaed
of4inalchainof custodyand recordsof swnp conditionwsinleatthesub-cauftsa6=Mty.
REASCW.* To defineindetailtheqtr%nixte Evosition of ipwhumd-naly7@
laborztorie&
atmibc@
Amendment Approval
Marv Casa, D.Vl,,L,PILD., Sponsor Rq=scntative J---lY'-L-=A=& Ph-D.Stutf@r Y,ris@ 1.Hamen, Ph.D., Previous Study Director
Date
&ct Date
Date
Dale L Bacon, PbA4, 3M Enviro=crlal LaboratoryManagement
3A4&wtwawnfal Laboratcxy 3M Environmental Laboratory
E-29
Dite Page 124
3M Medical Department Study: T6316.5
Analytical Report: FACT'TOX-013 LRN-U-2095
BattelleStudy Number. N003 604-D 3M F-nviro=ental Laboratory Study Number. FACT 060998.1
DEVIATION REPORT
Batti-TIStudy Number. N003604-D 3M Eaviro=cntal Technology and ScMce3 Study Number.
1 2 (N-Ethylp@oroocftnesulfonamido@@l
Two Gcnemtion Rat P-eprodu@;don
FACR in
060998.1
TYPE OF DEVIA71ON&- PROTOCOL
DA77ES OF DEVIAMONS:
OCUAW is,1999
NARJRE OF DEMAIIONS: Some of theacaydcsl awthod -cc tume critctdwaere wt nut fordo LCJMSMS analysisconductedIgOctW atTt-tteUe7.1am daymem rel&W toprotoool-amenimmt 2. See below for omnmary.
PPOS M-556 M-556 M-556 M-SS6
PFOSAA PFOSAA
QC3 exceeded 20 % error(-20.3% acomal) OC2 exceeded20% error(23.4% wft4 gg exceeded20% R&D 1.2% wbnb QC4 exceeded 20% RSD M.8% =map Diludm recoveryexceeded 130% (131.5% actmd with21.6% RM)
20 % error(-20.6% actad)
QC4 exczoded 20 % RSD (21.3% aebud
CAUSE op DEviAmoNs: Sample proparationand/orLCIMS/MS variabiyitiocveer the cuum of the axople *A may have contzi@ to the devi-ti-
Do(PACr OF DEVIAMONS ON THE M"UDY: Mm arrantQC valueswere bracketedby acceptrble QC conecubadon levelswhich dc=nsb2im thatthecalibratiocnurvesgenerallyprovidedgood aomn%L7 over thekatod range.The dilutiornecoveryforM-556 was not consideredtobe --adin* bi&bl enough, atonlyapproximately1.5% above thenormal acceptancelevel,tohave sipifi-zdy imp-tad.-thedatl.
CORRECTM
ACnON:Mds protocoldeviationmmmm=7 was prepared forlndusionb:L&o flnalreporl
APMOVED BY:
Jon C. Andm Ph.D.
Das
BanoUs PrincipalInvestigator
Kristem1. Hansen. Ph.D. Study Director
Data.
N003604-D ProtocolDeviation 1, Page 1 of 1
3M Environmental Laboratory
F@-29
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3M Medical Department-Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
BaUtUe StudyNumber. No03604-D
3M F-nvirorunentaLlabOmtMy Stidy Number FACT 060998.1
DEM'NON
]REPORT
B2tWl StudyNumber- N003604-D 3M Enviro=cnW Technology and ServicesStudyNumber. FACR 060998.1
2 (N-Ethylperfluorooctanemffonamido)-@iln Two GenerationRat lzcpzoducdm
riPE OP DEVIAMONS: PRCrrOCOL
DATE OF DEVIAMON&-
Odober 20, 1999
NA7UU OF DEVIA71ONS: PFOS QC3 exceeded d3o29% RE madiod totdrammt (sewd -@21.7%). 7u daudon recoverycheck standarddidnot meet the70-lM%. rewverf reqabvmmt (-ti-1,5.0% for PFOS and 4.6% fbrPFOSA). 7bom method &vM=s relatbtoamendment 2 of theibidyptab@wl
CA'USE OF DEVIAMONS: Sample preputdcm =Wor LCJMSMS variabdidmam dw courseofdw sample ad mq haw ccntn'butedfo &a QC deviation.Sample preparationw.c. appearsto have be= the cum fbrthecmuticn. veryreodtl
DdPACr OF DEVIA'NONS ON THE SI'UDY: Mm =ant QC vdm levelwasbmaAMd by a=VW"
QC coacmbzdon laveb which demnerates thatthecahlmdion curv= generallypmvkied good &=nwy
forsuidyn=plcs overthetestedmass.
A comparisonof theresultosbwned fbrthedilutexdu3dynmplas bm 2DOet99andpre%iamresulb thatweresheittyALOQ (130ct9gimd 190et99)demonstrategdoodagrownentbetwom do 2 deu=dnadow. I'hiswould indicattehatthedilutioonfthesbuly==ples was performedwmwdy
200et99 so dmL zw inqmt an the quantitadons occurred.
CORRECMVE ACMON-7bin protocodleviatiomnu=&ry -u preparedforInclusioinndw fmalraporl
APPROVED BY:
Jon C- Andz% Ph.D.
Dam
Ba-li,,PrincipIanlvewptor
Kri*m J.Hmam, Ph.D. StudyDirector
Des
L
N003604-D ProtocolDeviation2,Page I of I
E-30 3M Environmental Laboratory
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3M Medical Department Study: T6316.S
Analytical Report: FACT TOX-013 LRN-U2095
BaMlle Stuty Number. N003604-D 3M Enviro=ental LabcratOrYStutY Number. FACT 060998.1
DEVIATIK)N REPORT
BattelleStudy Number N003604-D 3M Eaviroumeatal Technology and ServicesStudy Number
FACR 060998.1
2 (N-Ethy4=fluoxooctan@onamido)-@01
In
Two Generation Rat Ileproduction
TYPE- OF DEVIATIONS:
PROTOCOL
DATES OF DEVIATIONS: October 12, 1999 through October 20,1999
NATURE OP DEVIATIONS: 7be lotnumber of PFOS used was not 217 as per section3.1.1 of the protocol 7rbe source of mfere= substm= matrix was not Argus Remmh Laboratoriesas specifiedin section3.2.2 of the protocol Tnitiaalwlyse3 of liverdid not exclusivelytargetPFOS as per section4.0 of protocol.
CAUSE OF DEVIATIONS:
Only PFOS lotnumber 171 was availableatBatWI
TTari-qnwas the suppu= of controlratliversused to prepare bLmk3, s=dards, and QCs
for the analyticaplortion of the study. AU 4 analytesof interest(PFOS, M-556,
PFOSAA, and PFOSA) were monitored during each analysis.
IMPACT OF DEVIATIONS ON THE STTJDY- PFOS lotm=ber 171 and HarL-insuppliedliverwere both used forBaUelle's validationof the analyticalmethod (Battac study number N003604-A). These materialsallowed achievement of the reported method accep=w criteriaso thatthem is no impact on the study. Tbz concurrent analysisof PFOS and metaboliteswas an efeciency improvemenl
CORRECTIVE
ACMON:
This protocoldeviationreport was prepared.
APP3LOVED BY.
Son C. Andre, Ph.D. BattellePrincipalInvczdptor
Date
Kristen1.E[==, StLidyDirector
Ph.D.
N003604-D Proto=l Deviation3, Page I of I
3M Environmental Laboratory
E-31
Date Page 127
3M-Medical Department Study: T6316-S
Analytical
Report: FACT TOX-013 LRN-U2095
BaftUt S" Number Noo3604-1) 3M EnvircmmcntalLabmmtmy Sh* Ni=ba: FACT 060998.1
APPENI)IX F - PFOS PUPJAY ]REPORT
3M Environmental Laboratory
Page 128
3M Medical Department Study: T6316.5 ETSS 2 3w
3M Eavim=entd
Analytical Report: FACT TOX-013 LPN-U2095
.'-BattellSetudy Number. N003604-D LaboMory StidyNumber. FACT 060998.1
651 778 42.26
04126/99 09-.5,6f5 :W-103 ?0:341
3NI =C"LW
kDEM.%Vw A CENUCAM
ANiLynCAL L%BORATORY
Lin Ckmm -"Sdl) - ET&SS- 24)3-M
Rnum S 37M
E=
Tom Xastma -(3-5633) -SAAC AzWydcal lAb -236-2B- II
M=h 24,1999: PmUmlnul MpW forFC-95 MCG). kK 171 SAMPLXDTSCRTFMON-.
Tyu sampig vu =bjecmd-to IR-NMR and 4FNNM sp=tralanslyso to determinethspwity of theucmhw prod= and to thar=eri= as nu!nyImpuritycompcncnu as pouibk-
A portionof the=mile wu accmuely wclZhe4 spikedwith a known amount of 1.4-bis(wUbcrourtbyf)benzwe (p-Fg:)Q.wA then totallydissolvedin DWO-4 forsubsequ=t analysisby NNM A 400 MHz mpecmam (0 h5783O.40 1) " a 376 MHz I*F-,NMM spe=m (# f5783(i.410)wao wquired usinga Vuixn tnrrypius 4M FR-NMR spw==ter. trzoof theP-BFX internalst=dard vu intendedtopermit the
datermiwdcm of the absoluteweigbi pem=t concentrationsof theassignedcotrpomats witbout necetluily
needng to Wandf@ or quantityan thec*nvccc= In thAurople mi=m
RESULTS-.
71:ccombined NNM
umple u romiva
spectral d= were used to assign 4 of the wajor and mom of thoiwner componsta in this
7be quxllmtiyc and qm=dtativc =mpositional rcmdts tb2cwere daived ft= the single UW
NMR Internal uxadu@db@on
analyses an u=nia6zed in TABLE-1
an thoofollowing pall I have mparted both
mladve and absolute weight percent conc=tritions. One po3sible mwcn 0= the absoluca wt.% values =W up to
O=n d= 10011 may be due to the f=t h" I ","@
4 of the @omporcns contnl"ed 9 cwlo,,s, 11 lem were
any short= chain homclczs Present Ci.c,7, 6, 5, atr-.=batLs), then ft average emug@c='d molecular weight%
would have be= somcwhu lem dun thou 4sed in the c4leulaiicns. In pderal. the 'F-NUR tochnlq= is w
pwdcul&dy waH suited for Identifying or qmdfying small amunu of various fluorachea@cal homelos hnpuiity
commpm=u
nnlet-athe c!h2i us vtry shon. A mom conviou cha=teriiadott of any otba ftmm=barmc3l
hamolop w=W
require "-ysis by clectospmy MS or a sin-ilartech- qmL
Additional wer!k wa@ld be required in in effortto positiv'elyverify ft =tadvely Luiped compio=t3 Usted In
TABLE- I (dc=ttd by possible). S=U &==a
of other unidentiried 4npuddw in alsode,ect-,'bm tl%iN&M
specm but additiona work would be required in an effortto identifyor quantity dvw other matulall
Copies of the NI@,M sp=tm will be provide@d far yau at 'aIn= dale. If you have any questions about the remalls In this initialreport fcr PC-95, lot 17 1. ple-@l letme know. I apclogiw for the delay In completing this Wtid wc&
Tom K&Stm
c
Rkk Pwftu - SAAC AndrkA Lab - 23&2R-1 I
AW ash==& L=7130J=dl
3M Environmental
Laboratory
Par - tF-I
Page 129
3M Medical Department Study: T6316.5
ETSS 2 3W Much 24. 1"9
3MEnviro=ental
Analytical Report: FACT TOX-013 LRN-U2095-
BancUe Study Number N003604-D LaboratoryStadyN=ben FACTo6oggs.1
651 M 4n6
04126/;9 (*:56 f9 :(3/03 ?0:341
SAA:C Aub-dcd LAb RequM # 37330 Wtw Rwrt forvc.%. lot171
TABLE-1 Sampic PC-95. lot171 OTM
TN-A-CM34
Overall(Zuwdtsdve C=posidang R=WU by.@W'$F-N2vM IM=d Sbmduamdw
Sauc=r2l Aafpments
CF3(cpi)t-SO3(K-()+) LN==d chi= "==a x 07 ft CAICWSAIM papa@")
.
C:FACT2.@c
F3)@(CFUVS03(-)X(+)
owomai saaamokyl brwA;b6-
Z.*Ya S. JL0 (@A y 0 (Lfeecalm'-f4oaparpom)
NMR Almhft Wg&S (lintitsrw mmmmnwt)
70-311
17.7%
=mm x US fbrcak:Watkmpapom)
(:.Pa..rCF(CF3)@-)X(+) (Aipba bruch. mxmme i a 6 fcccalcdadm pwpxm)
PZUMIS F-WrcF@rsc@l(-) K(+)
(&so=* I fcwc4cul&dQupapow)
CFr(CFACCCCFIMCF2)7-SOI(-) K(+) (Intanalpmdlma&@i bmmt6 Luww x+y a 4 and iLo 0 for
3.3% 0.37% (LI6%
Andysm roa iduto va-,&@s (3intiunw
10.2% 3.2% 00.161%
Poodble CFrSF4-C.FU-SO3(-) IL(+) (mgume i I forcakuladcapurpom)
Probabla
IC4+)
(HydrocarboAsWfonwA nlr an=* x- I forc&kwul" purpam)
eibrancIaLs-s.umex 4 forcalc,-Iarp;ucrnpcs&x)
0.11% O.Ml% 0.=%
0.10% OMO% 0=6%
F-2 3M Environmental Laboratory
Page 130
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
Appendix H: InterimCertificatoefAnalysis
3M Environmental Laboratory
Page 131
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
INTE"M CER TIFICA TE OF ANALYSIS
Revision ](917100) Centre Analytical Laboratories COA Reference
023-018B
3M Product: PFOS, Lot 171 Reference #: SD-009
Test Name Purity'
Purity: 86.4% Specifications
Result 86.4%
Appearance Identification
NMR Metals (ICP/MS)
1. Calcium 2. Magnesium 3. Sodium 4. PotassiUM2 5. Nickel 6. Iron 7. Manganese -Total % Impurity (NMR) Total % Impurity (LC/MS) Total % Impurity (GC/MS) Related Compounds POAA Residual Solvents (TGA)
Pur-ity -b-y5--s-C InorganicAnions (IC)
I . Chloride 2. Fluoride 3. Bromide 4. Nitrate 5. Nitrite 6. Phosphate 7. Sulfate' Organic Acids' (IC) 1. TFA 2. PFPA 3. HFBA 4. NFPA Elemental Analysis': I. Carbon 2. Hydrogen 3. Nitrogen
4. Sulfur 5. Fluorine
White CrystallinePowder
I.
Theoretical Value = 17.8%
2.
Theoretical Value = 0%
3.
Tbeoretical Value = 0%
4.
Tbeoretical Value = 5.95%
5.
TheoreticalValue = 60%
Conforms
Positive
1. 0.017 wt./wt.% 2. 0.007 wt.lwt.% 3. 1.355 wt./wt.% 4. 6.552 wtjwt.% 5. 0.003 wt-/wt.% 6. 0.004 wtjwt.% 7. <0.001 wt/wt.%
1.00 wtjwt.% 10.60 wt./wt.%
None Detected
0.30 wt./wt.% None Detected Not Applicable'
I . <0.015 wt./wt.% 2. 0.27 wt./wt.% 3. <0.040 wt./wt.% 4. <0.009 wt./wt.% 5. <0.006 wt./wt.% 6. <0.007 wt./wt.% 7. 8.82 wtjwt.%
1. <0.1 wt./Wt.% 2. <0.1 wtjwt.% 3. <0. I wt./wt.% 4. <0.25 wtjwt.%
1 . 12.08 wt./wt.% 2. 0.794 wtjwt.% 3. 1.61 wtjwt.% 4. 10.1 wtjwt.% 5. 50.4 wtjwt.%
COA023-018B 3M Environmental Laboratory
Pagel of3 Page 132
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
INTEMM CER TIFICA TE OF ANAL YSIS
CentreAnalyticaLlaboratorieCsOA Reference#: 023-018B DateofLastAnalysis0:8/31/00
ExpirationDate: 08/31/01
Storage Conditions:Frozen:S-IO'C
Re-assessment Date: 08/31/01
'Purity= 100% - (sum of metalimpurities1,.39% +LC/MS impurities, 10.60%+InorganicFluoride,0.27%+NMR impurities1,.00%+ POAA, 0.30%)
Totalimpurityfrom alltests= 13.56% Pur-ity= 100% - 13.56% = 86.4%
2potassiumisexpectedinthissaltform and isthereforenot consideredan impurity.
3Purityby DSC isgenerallynot applicabletomaterialsof low purity.No endotherm was observed forthissample.
4S ulfurin thesample appearsto be convertedto S04 and hence detected-usintghe inorganicanionmethod conditions.The anionresultagreeswellwiththe sulfur determinationinthe elementalanalysisl,endingconfidenceto thisinterpretatioBna.sed on theresultst,heS04 isnot consideredan impurity.
'TFA HFBA NFPA PFPA
Trifluoroacetaicid Heptafluorobutyriaccid Nonofluoropentanoicacid Pentafluoropropanoiaccid
6Theoretical value calculations based on the empirical formula, C8Fl7SO3-K@
(MW=538)
This work was conducted under EPA Good LaboratoryPracticeStandards(40 CFR 160).
COA023-01 8B 3M Environmental Laboratory
Page 2 of 3 Page 133
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LP,N-U2095
INTE"M CER TIFICA TE OF ANAL YSIS
Centre Analytical Laboratories COA Reference #: 023-018B
LC/MS Purity Profile:
Impurity C4 C5 C6 C7
Total
WL/wt. % 1.03 1.56 6.38 1.63 10.60
Note: The C4 and C6 values were calculatedusing the C4 and C6 standard calibration curves, respectively.The C5 value was calculatedusing the average response factors from the C4 and C6 standard curves. Likewise, the C7 value was calculatedusing the average response factorsfrom the C6 and C8 standard curves.
Prepared By:
David S. Bell Scientist,Centre AnalyticalLaboratories
Date
Reviewed
By: John Flaherty
Date
Laboratory Manager, Centre Analytical Laboratories
COA023-018B 3M Environmental Laboratory
Page 3 of 3 Page 134
3M Medical Department Study: T6316.5
Analytical Report: FACT TOX-013 LRN-U2095
Appendix 1:Report Signature Page
MarvinT. Case D.V.M..Ph.D.,StudyDirector
Date
John L.ButenhoffP,h.D.,SponsorRepresentative
Date
Dale L.Bacon,Laborator@manager
Date
3M Environmental Laboratory
Page 135