Document BRooOrD4r7D963p7RY32mNX6j
AR226-1751
STUDY TITLE Extraction of Potassium Perfluorooctanesulfonate from Quail Serum and Quail Liver for
Analysis Using HPLC-ElectrosprayMass Spectrometry
DATA REQUIREMENTS Analytical Method Requirements
STUDY DIRECTOR Sean Gallagher
STUDY COMPLETED ON September 06,2001
-F'ERFORMING LABORATORY / TESTING FACILITY
Centre Analytical Laboratories, Inc. (Centre) 3048 Research Drive
State College, PA 16801 Phone: 814-231-8032 STUDY SPONSOR
3M Environmental Technology and Safety Services Building 2-3E-09 PO Box 33331
St. Paul, MN 55133-3331 PROJECT
Centre Protocol Number: OOP-023-041 Centre Study Number: 023-041 Total Pages: 102
GoOD LaBQBBTpBy PRACTICE COMPLIANCE STATEMENT
Cenw Study Number 023-041, entitled "Extraction of Potassium
Perfluoro0c~n~:suUonaftme m Quail Senun and Quat1 Liver far Andysi8 UslnB Hac-
Electrospray/M,ass Spectrometry," conducted for 3M Environmental Techno1ogy and Safety Servico:~,was performed in compliance with US EPA TSCA Good Xaboratary Practice Standadds (40CFR Part 792)by Centre AnalyticalLahatones, Inc.
n
principd hveutfiator Centre Analytical Laboratanas, Inc.
Sean Gallaghtv Study Director
Wildlife International.Ltd.
Dsatle oldl
Date
3MknvlronmentalTLhnology and Safety S m i c c s Centre Anatyticd Laboratories, ne.
Page 2 of 102
Centre Study No.: 023-041
OUALITY ASSURANCE STATEMENT
Centre Analytical Laboratories' Quality Assurance Unit reviewed Centre Study Number 023-041, entitled, "Extraction of Potassium Perfluorooctanesulfonatefrom Quail Serum and Quail Liver for Analysis Using HPLC-ElectrosprayMass Spectrometry". All phases were reviewed for conduct according to Centre Analytical Laboratories' Standard Operating Procedures, the Study Protocol, and all applicable Good Laboratory Practice Standards. All findings were reported to the Study Director and to management.
Phase
1. Protocol Review
2. Extraction
3. Raw Data & Summary Table
Review
4. Raw Data and Draft Report
Review
5. Final Report Review
Date Inspected
Date Reported to Date Reported to
Centre
Study Director and
Management Sponsor ManaPement
12/19/00
12121/00
12/28/00
12/19/00
12121/00
12/28/00
2/28,3/1/01
3/19/01
312310 1
3/23-2610 1
41910 1
51710 1
91610 1
91610 1
91610 1
`.LA-1
Naomi Lovallo Sr. Quality Assurance Auditor
Centre Analytical Laboratories, Inc.
Page 3 of 102
Centre Study No.:a 3 4 4 1
CERTIFICATION OF AUTHENTlCITY
' I l i a eport, far Centre Study Numba 023-041, i s a true and complete representation of
the raw data for the study.
Submitted by:
Cenm Analytical Laboratories,Inc, 3048 Research D r i v e State College,PA 16801
(814) 231-8032
Principal Invczitigator,Centre:
Scientist Ccntre Analytical Laboratories, Inc.
Centre Analfllcal Laboratories,Inc.Facility Management:
/ Richard A. y & z z i e v . President Centre AnaIylical Laboratories,Jnc,
Study Directoa, Wildlife Intarnational:
Sean Gallagha Wildlife Inminational,Ltd,
Sponsor Repixsentatlve,3M:
Centre halyrical Laboaatories, Inc.
E'afic4 of 102
Centre Study No.: 023-041
STUDY IDENTIFICATION
Extraction of Potassium Perfluorooctanesulfonate from Quail Serum and Quail Liver for Analysis Using HPLC-ElectrosprayMass Spectrometry
CENTRE PROTOCOL NUMBER: OOP-023-041
CENTRE STUDY NUMBER:
023-041
TYPE OF STUDY:
Analytical
SAMPLE MATRIX:
Quail Serum and Quail Liver
TEST SUBSTANCE:
Perfluorooctanesulfonate (PFOS)
SPONSOR:
3M Environmental Technology and Safety Services Building 2-3E-09 PO Box 33331 St. Paul, MN 55 133-3331
STUDY DIRECTOR:
Sean Gallagher Wildlife International, Ltd. 8598 Commerce Drive Easton, MD 21601
SPONSOR REPRESENTATIVE:
Rochelle Robideau 3M Environmental Technology and Safety Services Building 2-3E-09 PO Box 33331 St. Paul, MN 55133-3331
TESTING FACILITY:
Centre Analytical Laboratories, Inc. 3048 Research Drive State College, PA 16801
ANALYTICAL PHASE TIMETABLE:
Study Initiation Date: Experimental Start Date: Experimental Termination Date: Study Completion Date:
12./08/00 12./18/00 03/08/01 09/06/01
Centre Analytical Laboratories,Inc.
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Centre Study No.: 023-041
PROJECT PERSONNEL
The Study Director for this project was Sean Gallagher at Wildlife International, Ltd. The following personnel from Centre Analytical Laboratories, Inc., were associated with various phases of the study:
Name Emily Stauffer Dave 13ell Melissa Kennedy Whitsel John Filaherty Tiffany Proctor Angela Morgan Michelle Arjmand Lawrence Ord Rickey Keller
Shawn Robb
Karen Risha
Scientist Scientist Supervisor Operations Manager Technician Technician Technician Sample Custodian Sample Custodian
Sample Custodian
Scientist
Centre Analytical Laboratories, Inc.
Page 6 of 102
. Centre StudyNo. 023-041
TABLE OF CONTENTS
Paae
TITLE PAGE ....................................................................................................................... 1 GOOD LAB0:RATORYPRACTICE COMPLIANCE STATEMENT.............................. 2 QUALITY ASSURANCE STATEMENT .......................................................................... 3 CERTIFICAT1:ONOF AUTHENTICITY........................................................................... 4 STUDY IDENTIFICATION................................................................................................. 5 PROJECT PERSONNEL...................................................................................................... 6 TABLE OF CONTENTS...................................................................................................... 7 LIST OF TAB:LES............................................................................................................... 8 LIST OF FIGURES............................................................................................................. 10 LIST OF APPENDICES.................................................................................................... 11 1.0 SUMMAFLY................................................................................................................ 12 2.0 OBJECTWE ............................................................................................................... 12
3.0 INTRODUCTION....................................................................................................... 12
4.0 TEST SYSTEM .......................................................................................................... 13 5.0 REFERENCE MATERIAL, ......................................................................................... 13 6.0 DESCRIPTION OF ANALYTICAL METHOD ......................................................... 14
6.1 Extraction Procedure ................................................................................................ 14 6.2 Preparation of Standardsand Fortification Solutions................................................ 14 6.3 Chromatography ........................................................................................................ 15 6.4 Instrumeint Sensitivity............................................................................................... 15 6.5 Description of Instrument and Operating Conditions............................................... 15 6.6 Quantitation and Example Calculation..................................................................... 16 7.0 EXPERIMIENTAL DESIGN ...................................................................................... 18 8.0 RESULTS ................................................................................................................... 18 9.0 CONCLlJSIONS...................................................................................................... 18 10.0 RETENTION OF DATA AND SAMPLES ............................................................. 19
Centre AnalyticalLaboratories. Inc.
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Centre Study No.: 023-041
LIST OF TABLES
Table I. Summaryof PFOS in Reagent Blanks............................................................ 21
Table 11. Summary of PFOS in Quail Liver Blanks ...................................................... 22 Table 111. Summary of PFOS in Quail Serum Blanks .................................................... 22 Table IV. Summary of PFOS Recoveries in Quail Liver ................................................ 23 Table V. Summary of PFOS Recoveries in Quail Serum.............................................. 24
Table VI. Summary of PFOS in Adult Liver Samples at 0 ppm a.i. (Test
Termination 19 Weeks) ..................................................................................25
Table VII. Summary of PFOS in Adult Liver Samples at 1.8 ppm a.i. (Test
Termination 6 Weeks) ....................................................................................26
Table VI11 Summary of PFOS in Adult Liver Samples at 6.2 ppm a.i. (Test
Termination 6 Weeks) ................................................................* ...................27
Table E. Summary of PFOS in Adult Liver Samples at 17.6 ppm a.i. (Test
Teimination 19 Weeks) ..................................................................................28
Table X. Summary of PFOS in Juvenile Liver Samples at 0 ppm a.i. (Test
Teirmination 12 Weeks) ..................................................................................29
Table XI. Summary of PFOS in Juvenile Liver Samples at 1.8 ppm a.i. (Test
Termination 12 Weeks) ..............................................................,,...................30
Table XII. Smmmary of PFOS in Juvenile Liver Samples at 6.2 ppm a.i. (Test
Teimination 12 Weeks) ..............................................................#. ..................31
Table XIII. Summary of PFOS in Juvenile Liver Samples at 17.6 ppm a.i. (Test
Teimination 12 Weeks) ..............................................................*. .................32
Table XIV. Smmary of PFOS in Adult Serum Samples at 0 ppm a.i. (Test
Teimination 19 Weeks) ..................................................................................33
Table XV. S u l m a r y of PFOS in Adult Serum Samples at 1.8 ppm a.i. (Test
Termination 6 Weeks) ....................................................................................34
Table XVI. S u m a r y of PFOS in Adult Serum Samples at 6.2 ppm a.i. (Test
Termination 6 Weeks) .................................................................................... 35
Table XVII. Summary of PFOS in Adult Serum Samples at 17.6 ppm a.i. (Test
Termination 19 Weeks) ..................................................................................36
Table XVIII. Sh.unmary of PFOS in Juvenile Serum Samples at 0 ppm a.i. (Test
Teimination 12 Weeks) ..................................................................................37
Table XIX. Summary of PFOS in Juvenile Serum Samples at 1.8 ppm a.i. (Test
Teimination 12 Weeks) ..................................................................................38
Table XX. Smmary of PFOS in Juvenile Serum Samples at 6.2 ppm a.i. (Test
Termination 12 Weeks) ..................................................................................39
Centre Analytical Laboratories, Inc.
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Centre Study No.: 023-041
LIST OF TABLES (continued)
PaRe
Table X X I . Summary of PFOS in Juvenile Serum Samples at 17.6 ppm a.i. (Test
Termination 12 Weeks) ................................................................................ ..40
Table XXII. Summary of Percent Moistures for Quail Liver Samples............................. 41
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Centre Study No.: 023-041
Figure 1.
LIST OF FIGURES
PaRe
Typical Calibration Curve for PFOS .............................................................. 43
Figure 2. Chaomatogram Representing a 0.1 ng/mL standard for PFOS ....................... 44
Figure 3. Chromatogram Representing a 1.0 ng/mL standard for PFOS ....................... 45
Figure 4. Chromatogram Representing a Reagent Blank for PFOS (Centre ID
Reagent Blank A, Set: 122000A)............................................... "..................4.6
Figure 5. Chromatogram Representing Control Quail Serum for PFOS (Centre ID:
0011424Blank A, Set: 122000A).............................................. "..................4.7
Figure 6. Chromatogram Representing Control Quail Liver for PFOS, (Centre ID:
0007870 Blank A, Set: 121900A) .................................................................. 48
Figure 7. Chromatogram Representing Control Quail Serum Fortified with 500 ng/'mL of PFOS (Centre ID: 0011424 Spk A, Set: 122000A)........................ 49
Figure 8. Chromatogram Representing Control Quail Liver Fortified at 10 ppb
with PFOS (Centre ID: 0011423 Spk A, Set: 121800A)................................ 50
Figure 9. Chromatogram Representing Juvenile Quail Serum Sample (Centre ID:
0007965, Sponsor ID: 9544, Set: 122000A)................................................... 51
Figure 10. Chromatogram Representing Juvenile Quail Liver Sample (Centre ID:
0007926, Sponsor ID: 9544, Set: 121800B)................................................... 52
Centre Analytical Laboratories, Inc.
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Centre Study No.: 023-041
LIST OF APPENDICES
PaRe
Appendix A Study Protocol OOP-023-041 (Centre Study No. 023-041) and
Amendmentsand Deviations.....................................................................53
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Centre Study No.: 023-04I
1.0 SUMMARY
Centre Analytical Laboratories, Inc. (Centre) extracted quail liver samples and quail serum samples for the determination of perfluorooctanesulfonate (PFOS) according to protocol OOP-023-041 (Appendix A).
The limit of quantation for quail liver was 10 ppb and for quail serum 10 ng/mL. These were determined in the method verification study (Centre study 023-054). PFOS in the quail liver samples ranged from non-quantifiable levels (a peak was detected at the corresponding analyte retention time but was less than the lowest concentration of the calibration standards (0.0001 pg/mL)) to 8.37 pg/g. These results are reported on a wet weight basis. Residues of PFOS in the quail serum samples ranged from 0.00212 pg/mL levels to 263 pg/mL.
The average percent recovery k standard deviation for PFOS in serum samples was 108% f 10%. The average percent recovery k standard deviation for PFOS in liver samples was 95% f 11%.
2.0 OBJECTIVE
The objective of this study was to determine levels of perfluorooctanesulfonate (PFOS) in specimens of quail liver and quail serum using the analytical methods described in protocol OOP-023-041.
3.0 INTRODUCTION
This report details the results of the analysis for the determination of PFOS in quail serum and quail liver, using the analytical methods entitled, "Extraction of Potassium Perfluorooctanesulfonate or Other Fluorochemical Compounds From Serum for Analysis Using HPLC-ElectrosprayMass Spectrometry" and "Extraction of Potassium Perfluorooctanesulfonate or Other Fluorochemical Compounds From Liver for Analysis Using HPLC-EClectrosprayMass Spectrometry" with the modifications listed in Section 6.
The study was initiated on December 8, 2000, when the study director signed Centre protocol number OOP-023-041. The experimental start date was December 18,2000, and the experimental termination date was March 8,2001.
Centre AnalyticidLaboratories,Inc.
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Centre Study No.: 023-041
4.0 TEST SYSTEM
The control quail serum and liver used for the matrix blanks and matrix fortifications was received on November 28,2000 fiom Wildlife International Ltd., Easton, MD.
The control quail liver was assigned the Centre ID of 001 1423 and the control quail serum was assigned the Centre ID of 0011424. Fifty-six quail serum samples and sixty quail liver samples were received at Centre on August 10, 2000. The samples were stored frozen until they were logged in by Centre personnel on .August 16, 2000 and stored frozen. An additional twenty quail serum samples and twenty quail liver samples were received on February 23, 2001 and stored frozen until they were logged in by Centre personnel on February 26,2001.
Sample login and chain of custody information can be found in the raw data package associated with this study. Storage records will be kept at Centre Analytical Laboratories, Inc. and a truie copy of the storage records can be found in the raw data package associated with this study.
5.0 REFERENCE MATERIAL
The analytical standard PFOS was received at Centre on June 3, 2000 from 3M Environmental Technology and Services.
The available information for the reference material is listed below. The reference material was stored frozen. Stability was not assessed in this study but the reference material was stored according to the certificate of analysis and was used prior to expiration. Thle solubility of the reference material was not relevant to this study.
Compound PFOS
Centre Control No. TCR No. Purity (%) Expiration Date
00-023-042
TCR 00017-46
97.9
08/3 1/O1
The molecular structure of PFOS is given below.
PFOS Chemical Name Molecular weight =
Perfluorooctanesulfonate 499 (CsF17S03-)
Note: `fie neutral molecule and standard form fiom which PFOS (anion) is derived, is potassium perfluorooctanesulfonate [C8F17SO&], molecular weight 538.
Centre Analytical Laboratories, Inc.
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Centre Study No.: 023-041
6.0 DESCRIPTION OF ANALYTICAL METHOD
Analytical meithods entitled "Extraction of Potassium Perfluorooctanesulfonate or Other Fluorochemiceil Compounds From Serum for Analysis Using HPLC-Electrosprayhlass Spectrometry" and "Extraction of Potassium Perfluorooctanesulfonate or Other Fluorochemiczil Compounds From Liver for Analysis Using HPLC-Electrosprayhlass Spectrometry" with the modifications listed below were used for this study.
6.1 Extractioni Procedure
- A 100 pL aliquot of the serum and 0.50 g sample of liver was used for the extraction
- procedure. After fortification of appropriate samples, the samples were vortexed for 15
seconds. One mL of 0.5 M TBA was added to the liver samples and 0.5 mL was added to
the serum samples. Two mL of 0.25 M sodium carbonate/sodium bicarbonate was added
to the liver samples and 1 mL was added to the serum samples. Five mL of MTBE was
added shaker
- to both
for 20
- the serum and liver samples.
min. and then centrifuged for
Each sample 15 min. Four
was mL
placed on wrist-action of the organic layer was
taken and dried on an N-Evap and then reconstituted with 1 mL of methanol. Each
sample was analyzed by LC/MS/MS electrospray.
6.2 Preparation of Standards and Fortification Solutions
Standard solutions were prepared on September 18, 2000 as specified in Centre Analytical Laboratories' protocol OOP-023-041. An individual stock standard solution of PFOS was prelmred at a concentration of 100 pg/mL by dissolving 10 mg of the standard (corrected for purity and salt content) in methanol. From this solution, a 1.0 pg/mL fortification standard solution was prepared by taking 1 mL of the stock and bringing the volume up to 100 mL with methanol.
The 0.1 pg/mL fortification standard was prepared by taking 10 mL of the 1 .O &mL
fortification standard and bringing the volume up to 100 mL with methanol. A 0.01 pg/mL standard was prepared by taking 10 mL of the 0.1 pg/mL standard and bringing to
100 mL with methanol.
A set of standards containing PFOS was prepared by dilution of the 0.1 pg/mL and 0.01 pg/mL solutions in the following manner.
Initial Conc. (pg/mL)' 0.1 0.1 0.1 0.01 0.01
' 0.01
ofPFOS
Centre Analytic(a1Laboratories, Inc.
Volume (mL) 5 2 1 5 2 1
Diluted to (mL) 100 100 100 100 100 100
Final Conc. (pg/mL) 0.005 0.002 0.001 0.0005 0.0002 0.0001
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Centre Study No.: 023-041
The stock startdard solution and all fortification and calibration standard solutions were
stored in a refrigerator (4" k 2OC) when not in use. Documentation of standard
preparation can be found in the raw data associated with this report.
6.3 Chromatography
Quantification of PFOS was accomplished by LC/MS/MS. 'The retention time of PFOS was
-LC/MS/MS 4.4 min.
analysis using electrospray Peaks were detected in the
control matricles corresponding to the analyte retention time and some of the amounts
detected were :significantenough to alter the results reported in this study.
6.4 Instrument Sensitivity
The smallest standard amount injected during the chromatographic run was equivalent to 0.0001 pg/mL of PFOS.
6.5 Description of Instrument and Operating Conditions Mass Spec: PE SCIEX API 3000 Biomolecular Mass Analyzer
Interface:
SCIEX TurboIon Spray Liquid Introduction Interface Harvard infusion pump
Computer: Dell Ultrascan P1110
Software:
HPLC:
PE SciexAnalyst 1.1 Windows NT
Hewlett Packard (HP) Series 1100
HP Quat Pump HP Vacuum Degasser HP Autosampler HP Column Oven
HPLC Co1umn:Genesis CS(Jones Chromatography), 2.1 mni x 50 mm, 4p Column Temp.: 35" C Injection Vol.: 10 pL Mobile Phase (A): 2 mM Ammonium Acetate in ASTM type I water Mobile Phase (B): Methanol Flow Rate: 0.3 mL/min.
Centre Analytical Laboratories, Inc.
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Centre Study No.: 023-041
Time %A %B
0
60
40
1.o
0
100
7.0
0
100
7.5
60
40
11.0
60
40
Ions monitored:
Analyte PFOS
Mode negative
+ Transition Monitored 499 99
Approximate Retention Time (min)
4.40
Tune File Parameters
Controls IS -1ospray DP-Declustering Potential FP-Focusing Potential EP-Entrance Potential CE-Collision Energy CXP-Collision Cell Exit Potential DF-Deflector CEM-Channel Electron Multiplier
Set -4200.0
-51.O
-230.0 10.0 -70 -5 300.0 2800.0
Gas Flows
Nebulizer Gas Curtain Gas
Collision Gas
TIS Temperature
- Set
12 13
4
350C
6.6 Quantitation and Example Calculation
Ten microliters of sample or calibration standard was injected into the LC/MS/MS. The peak area was measured and the standard curve was generated (using l h fit weighted linear regression) by Analyst software using six concentrations of standards. The concentration for quail serum and quail liver was determined from the following equations:
Use Equation 1 to calculate the amount of analyte found (in ng/mL, based on peak area) using the standard curve (linear regression parameters) generated by the Analyst software program. Then use Equation 2 to calculate the amount of analyte found in pg/g (pg/mL for serum samples).
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Centre Study No.: 023-041
Eauation 1:
Analyte found (ng/mL) = (Peak area - intercept)
slope
Eauation 2:
Analyte found (pg/g) = (anal. found (ng/mL) x FV (mL) x DF x EV (mL)) x
(AV (mL) x sample wt. (g))
1000 ng
Where:
FV = Final Volume
DF = Dilution Factor
EV = Extraction Volume
AV = Aliquot Volume
For samples fortified with known amounts of PFOS prior to extraction, use Equation 3 to calculate the percent recovery. Equation 3: Recovery (%) :=
(anal. found (ug/g;)- avg;.analvte in ctrl (ugdg;)) x 1000 ng;x 100% amount added (ng/g) x 1 pg
An example of a calculation using an actual sample follows:
Quail liver sample Centre ID 0007870 Spk A (Set: 121900A), fortified at 1000 ng/g with
PFOS.
Where:
peik area intercept slope
dilution factor
- 11483
- 463
-- 2790
- -
100
ng/g added (fort level) = 1000 ng/g
avg. amt in controls = 0 (Not quantifiable)
final volume
- 1 mL
extraction volume
-- 5 mL
aliiquot volume
- 4 mL
sample weight
-- 0.5 g
From equatioin 1: Analyte found (ng/mL)
= 111483- 4631 2790
From equatioin 2: Analyte found (&g)
= 3.9 n g / d
= J3.9 ndmL x 1 mL x 100 x 5 mL) x lllg
(4 mL x 0.5 g)
1000 ng
= 0.975 pg/mL Centre Analytical Laboratories, Inc.
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Centre Study No.: 023-041
From equation 3: %Recovery =
(0.975 udmL - 0 DdrnL) x (1000 nn/lp,a) x 100%
1000 ng/g
= 98%
7.0 EXPERIMENTAL DESIGN
- Each set of samples (liver or serum) consisted of one reagent blank, one matrix blank,
two matrix blanks fortified at known concentrations, and 20 samples. Each sample was extracted using the appropriate method and then analyzed in duplicate.
8.0 RESULTS
The PFOS found in the reagent blanks are listed in Table I. The PFOS in the quail liver blanks and quail serum blanks are given in Tables I1 & 111.
Individual recoveries for PFOS in the liver samples are detailed in Table IV. The average percent recovery f standard deviation for PFOS in liver samples was 95% f 11%. Individual recoveries for PFOS in the serum samples are detailed in Table V. The average percent recovery f standard deviation for PFOS in serum samples was 108% f 10%.
PFOS in the quail liver samples ranged fiom non-quantifiable levels (a peak was detected at the corresponding analyte retention time but was less than the lowest concentration of the calibration standards (0.0001 pg/mL)) to 8.37 pg/g. Individual results are listed in Tables VI-XIII. The results are reported on a wet weight basis.
PFOS in the quail serum samples ranged fiom 0.00212 pg/mL levels to 263 pg/mL. Individual results are listed in Tables XIV-XXI.
The average percent moistures for the quail liver samples are given in Table XXII.
9.0 CONCLUSIONS
The quail liver and serum samples were successfully extracted and analyzed according to protocol OOP-023-041.
Centre Analyticial Laboratories, Inc.
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Centre Study No.: 023-041
10.0 RETENTION OF DATA AND SAMPLES
When the final report is complete, all original paper data generated by Centre Analytical Laboratories, Inc. will be shipped to the sponsor. This does not include facility-specific raw data such as instrument logs, however exact copies of temperature logs will be submitted. Exact copies of all raw data, as well as a signed copy of the final analytical report and all original facility-specific raw data, will be retained in the Centre Analytical
Laboratories, Inc. archives for the period of time specified in 40 CFR Part 792. Retained
samples of reference substances are archived by the sponsor.
Centre Analytical Laboratories, Inc.
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Centre Study No.: 023-041
TABLES
Centre Analytical Laboratories,Inc.
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Centre Study No.: 023-041
Table I. Summary of PFOS in Reagent Blanks
Sponsor ID
na na na na na na na na na na na na na na
na na
Centre ID
Reagent Blank A Reagent Blank A* Reagent Blank A Reagent Blank A* Reagent Blank A :Reagent Blank A* Reagent Blank A ]ReagentBlank A* Reagent Blank A ]ReagentBlank A* Reagent Blank A ]ReagentBlank A* Reagent Blank A ]Reagent Blank A*
Reagent Blank A Reagent Blank A*
* Duplicate injection
Set Number
121800A 121800A 12 1800B 121800B 121900A 121900A 121900B 121900B 122000A 122000A 122000B 122000B 030501A 030501A
030601A 030601A
Extraction Analysis
Date
Date
12/18/00 12/18/00 12118/00 12/18/00 12/19/00 12/19/00 12119/00 12119/00 12/20/00 12/20/00
12119/00 12/19/00 12/20/00 12/20/00 12/21/00 12/21/00 12121-22100 12121-22/00 12/22/00 12/22/00
12/20/00 12/20/00 31510 1 3/5/0 1
12122-23/00 12122-23/00
316-710 1 3/6-7/0 1
31610 1 31610 1
3/7/0 1 31710 1
AVERAGE:
STANDARD DEVIATION:
Analyte Found (pg/mL)
NQ NQ NQ NQ NQ NQ NQ NQ 0.000200 0.000200 NQ NQ ND ND
NQ NQ
NQ NQ
NQ = Not Quantifiable (A peak was detected at the corresponding analyte retention time but was less th,anthe lowest concentration of the calibration standards (0.0001 pg/mL)) ND = Not Detected
For values recorded as ND,zero was used to calculate the average and standard deviation. For values recorded as NQ, 0.00005 pg/mL (half the value of the lowest calibration standard, 0.0001 pg/mL) was used to calculate the average and standard deviation.
LOQ = 0.01 pg/g for liver and 0.01 pg/mL for serum
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~~
Centre Study No.: 023-041
Table 11. Summary of PFOS in Quail Liver Blanks
Sponsor ID
na na na Na 454 454 456 456
Centre ID
001 1423 Blank A 0011423Blank A* 0011423 Blank A 0011423 Blank A* 0007870 Blank A 0007870 Blank A* 0007872 Blank A 0007872 Blank A*
Set Number
121800A 121800A 121800B 1218OOB 121900A 121900A 030601A 030601A
Extraction Date
Analysis
Analyte
Date - Found (pg/g)
12118/00 12118/00 12/18/00 12118/00
12119/00 12119/00 12/20/00 12/20/00
NQ NQ 0.001 13 0.00109
12119/00 12119/00 31610 1 31610 1
12121/00 12121/00 31710 1 31710 1 AVERAGE:
NQ NQ 0.00120 0.00 110 0.000590
STANDARD DEVIATION: 0.000578
Table 111. Summary of PFOS in Quail Serum Blanks
Sponsor
ID
na na na na na na na na
Centre ID
,0011424Blank A 0011424 Blank A* 0011424 Blank A 001 1424 Blank A* 0011424 Blank A 0011424Blank A* 10011424Blank A 0011424Blank A*
* Duplicate injection
Set Number
121900B 121900B 122000A 122000A 122000B 122000B 030501A 030501A
Extraction Analysis
Analyte
Date
Date Found (pg/mL)
12/19/00 12/19/00 12/20/00 12/20/00
12121-22/00 12121-22/00
12/22/00 12/22/00
0.0136 0.0144 0.0138 0.0151
12/20/00 12122-23/00
12/20/00 12122-23/00
31510 1
316-7101
31510 1
316-7/01
AVERAGE:
STANDARD DEVIATION:
0.0127 0.0109 0.00555 0.00559
0.0115
0.00384
NQ = Not Quantifiable (A peak was detected at the corresponding analyte retention time but was less than the lowest concentration of the calibration standards (0.0001 pg/mL))
For values recorded as NQ, 0.00005 pg/g (half the value of the lowest calibration standard, 0.0001 pg/mL) was used to calculate the average and standard deviation.
LOQ = 0.01 prJg for liver and 0.01 pg/mL for serum
Centre Analytic,alLaboratories, Inc.
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Centre Study No.: 023-041
Table IV. Summary of PFOS Recoveries in Quail Liver
Sponsor
ID
na na na na na na na na 454 454 454 454 456 456 456 456
Centre
ID
0011423 Spk A 0011423 SpkA* 0011423 Spk B 0011423 SpkB* 0011423 Spk A 0011423 Spk A* 001 1423 Spk B 001 1423 Spk B* 0007870 Spk A 0007870 Spk A* 0007870 Spk B 0007870 Spk B* 0007872 Spk A 0007872 Spk A* 0007872 Spk B 0007872 Spk B*
Set Number
121800A 121800A 121800A 121800A 121800B 121800B 121900A 121900A 121900A 121900A 121900A 121900A 030601A 030601A 030601A 030601A
Extraction Analysis
Amt
Date
Date
Added (ng/g)
12/18/00 12/18/00 12/18/00 12/18/00 12/18/00
12/19/00 12/19/00 12/19/00 12/19/00 12/20/00
10 10 2000 2000 1000
12/18/00 12/20/00
1000
12/18/00 12120-21/00
20000
12/18/00 12120-21/00
20000
12/19/00 12/21/00
1000
12/19/00 12/21/00
1000
12/19/00 12/19/00 3/6/01
12/21/00 12/21/00 31710 1
20000 20000
20
3/6/01
31710 1
20
3/6/01
31710 1
200
3/6/01
31710 1
200
AVERAGE: STANDARD DEVIATION:
RELATIVE STANDARD DEVIATION:
YO
Recovery
102 104 101 103 113 110 80 80 99 103 85 84 93 86 82 84 94 11 12
* Duplicate injection
LOQ = 0.01 pg/g for liver and 0.01 pg/mL for serum
Centre Analytic,alLaboratories, Inc.
Page 23 of 102
Centre Study No.: 023-041
Table V. Summary of PFOS Recoveries in Quail Serum
Sponsor
Centre
Set Extraction Analysis
Amt
YO
ID
na
001 1424 Spk A 121900BD 12/19/00 12123-24/00
500
103
na
0011424 Spk A* 121900BD 12/19/00 12123-24/00
500
106
na
001 1424 Spk B 121900BD 12/19/00 12123-24/00
100000
90
na
0011424 Spk B* 121900BD 12/19/00 12123-24/00
100000
93
na
0011424 Spk A 122000A 12/20/00 12/22/00
500
106
na
001 1424 Spk A* 122000A 12/20/00 12/22/00
500
103
na
001 1424 Spk B 122000A 12/20/00 12/22/00
100000
97
na
001 1424 Spk B* 122000A 12/20/00 12/22/00
100000
103
na
0011424 Spk A 122000B 12/20/00 12122-23/00
500
108
na
0011424 Spk A* 122000B 12/20/00 12122-23/00
500
110
na
0011424 Spk B 122000B 12/20/00 12122-23/00
100000
113
na
001 1424 Spk B* 122000B 12/20/00 12122-23/00
100000
98
na
0011424 Spk A 030501A 3/5/01
316-7101
100
122
na
001 1424 Spk A* 030501A 3/5/01
316-7101
100
122
na
0011424 Spk B 030501A 3/5/01
316-710 1
1000
107
na
0011424 Spk B* 030501A 3/5/01
316-710 1
1000
115
AVERAGE: 106
STANDARD DEVIATION:
9
RELATIVE STANDARD DEVIATION:
9
* Duplicate injection
LOQ = 0.01 pg/g for liver and 0.01 p g / d for serum
Centre Analytical Laboratories, Inc.
Page 24 of 102
Centre Study No.: 023-041
Table VI. Summary of PFOS in Adult Liver Samples at 0 ppm a i . (Test Termination 19 Weeks)
Sponsor ID
45 1 451* 452 452* 453 453* 454 454* 455 455* 456 456* 457 457* 458 458* 459 459* 460 460*
Centre ID
0007867 0 0 0 7 8 6 7 0007868 0007868 0007869 0007869 0007870 0007870 000787 1 000787 1 0007872 0007872 0007873 0007873 0007874 0007874 0007875 0007875 0007876 0007876
Set Number
121800AD 121800AD 121800A 121800A 121800AD 12 1800AD 121800A 121800A 121800AD 121800AD 121800A 121800A 121800AD 1218OOAD 121800A 121800A 121800AD 121800AD 121800A 121800A
Extraction Analysis
Date
Date
12118/00
12/20/00
12118/00
12/20/00
12118/00 12118/00 12/18/00
12119/00 12/19/00 12/20/00
12/18/00
12/2.0/00
12118/00 12118/00 12118/00
12119/00 12119/00 12/20/00
12118/00
12/20/00
12118/00 12118/00 12118/00
12/19/00 12/20/00 12/20/00
12118/00
12120100
12118/00
12119/00
12118/00
12119/00
12118/00
1212 0100
12118/00
1212 0100
12/18/00
12119/00
12118/00
12/19/00
AVERAGE:
STANDARD DEVIATION:
Analyte
Found (pg/g)
0.2 15 0.2 15 NQ NQ 0.303 0.304 NQ NQ 0.1 14 0.1 11 NQ NQ 0.0762 0.0739 0.0 103 0.0 104 0.236 0.235 0.001 17 0.001 17 0.0953 0.113
* Duplicate injection
NQ = Not Quantifiable (A peak was detected at the corresponding analyte retention time
but was less than the lowest concentration of the calibration standards (0.0001 pg/mL))
For values recorded as NQ, 0.00005 pg/g (half the value of the lowest calibration standard, 0.0001 pg/mL) was used to calculate the average and standard deviation.
LOQ = 0.01 pg/g for liver and 0.01 pg/mL for serum
-- ~~
Centre Analytical Laboratories, Inc.
Page 25 of 102
Centre Study No.: 023-041
Table VII. Summary of PFOS in Adult Liver Samples at 1.8 ppm a.i. (Test Termination 6 Weeks)
Sponsor
ID
EO1-0259-20780 E0 1-0259-20780* E01-0259-2078 1
EO 1-0259-20781*
EO1-0259-20782 EO 1-0259-20782* EO1-0259-20783 E01-0259-20783* EO 1-0259-20784 EO 1-0259-20784* EO1-0259-20790 EO 1-0259-20790* E01-0259-20791
EO 1-0259-20791*
EO 1-0259-207512 E01-0259-20792* EO 1-0259-207513 E01-0259-20793* EO 1-0259-20704 EO 1-0259-20794*
Centre ID
0102997 0102997 0102998 0 102998 0 102999 0 102999 0103000 0103000 0 103001 0103001 0103007 0103007 0 103008 0 103008 0103009 0103009 0 103010 0 1030 10 010301 1 010301 1
* Duplicate injection
Set Number
03060 1AD 03060 1AD 030601AD 030601AD 030601AD 030601AD 03060 1AD 030601AD 030601AD 030601AD 030601AD 030601AD 03060 1AD 03060 1AD 030601A 030601A 030601AD 03060 1AD 03060 1AD 03060 1AD
Extraction Analysis
Date
Date
31610 1
3/8/0 1
31610 1
3/810 1
31610 1
3/8/0 1
31610 1
3/8/0 1
31610 1
3/8/0 1
31610 1
3/8/01
31610 1
3/8/0 1
31610 1
3/8/0 1
31610 1
3/8/0 1
31610 1
3/8/0 1
31610 1
3/810 1
31610 1
3/8/0 1
31610 1
3/8/0 1
31610 1
31aio 1
31610 1
31710 1
31610 1
31710 1
31610 1
3/8/01
31610 1
3/8/0 1
31610 1
3/8/0 1
31610 1
3/8/0 1
AVERAGE:
STANDARD DEVIATION:
Analyte Found (pglg)
0.800 0.722 0.149 0.134 0.341 0.311 0.455 0.422 0.0988 0.0843 0.210 0.210 0.177 0.191 0.0124 0.0121 0.0381 0.0394 0.0629 0.0720 0.227 0.224
LOQ = 0.01 pFJg for liver and 0.01 pglmL for serum
Centre Analytkal Laboratories, Inc.
Page 26 of 102
Centre StudyNo.: 023-041
Table VIII. Summary of PFOS in Adult Liver Samples at 6.2 ppm a.i. (Test Termination 6 Weeks)
Sponsor ID
EO 1-0259-20785 E01-0259-207885* EO 1-0259-20786 EO 1-0259-2078,6* EO1-0259-207137
EO 1-0259-20787*
EO 1-0259-20788 EO 1-0259-20788* EO 1-0259-20789 E01-0259-20789* EO1-0259-20795 E01-0259-20795* EO1-0259-207!)6 EO 1-0259-20796* EO 1-0259-207!)7 EO 1-0259-20797* E01-0259-207!28 E01-0259-20798* E01 -0259-207!29 EO 1-0259-20799*
* Duplicate injection
Centre ID
0 103002 0103002 0103003 0103003 0103004 0 103004 0103005 0103005 0 103006 0 103006 0 1030 12 0103012 01030 13 01030 13 0 103014 0103014 0 103015 0103015 0 103016 0103016
Set Number
03060 1AD 030601AD 030601AD 030601AD 030601AD 030601AD 030601AD 030601AD 030601AD 030601AD 030601AD 03060 1AD 03060 1AD 03060 1AD 030601AD 03060 1AD 030601AD 030601AD 030601AD 030601AD
Extraction Date
Analysis Date
31610 1
3/8/01
31610 1
31810 1
31610 1
3/8/01
3/6/01
3/8/01
3/6/01
3/8/01
31610 1
3/8/01
3/6/01
3/8/01
3/6/01
3/8/01
3/6/01
3/8/01
31610 1
3/8/01
31610 1
3/8/01
3/6/01
3/8/01
3/6/01
31810 1
31610 1
31810 1
3/6/01
3/8/01
31610 1
31810 1
3/6/01
3/8/01
3/6/01
3/8/01
3/6/01
3/8/01
31610 1
3/8/01
AVERAGE:
STANDARD DEVIATION:
Analyte Found (pg/g)
1.15 1.20 1.18 1.19 1.43 1.42 1.60 1.51 1.06 1.17 0.216 0.208 0.115 0.0934 0.0801 0.0797 0.187 0.218 0.0901 0.0954 0.715 0.606
LOQ = 0.01 plJg for liver and 0.01 pg/mL for serum
Centre Analytical Laboratories, Inc.
Page 27 of 102
Centre Study No.: 023-041
Table IX. Summary of PFOS in Adult Liver Samples at 17.6 ppm a i .
(Test Termination 19 Weeks)
Sponsor
ID
48 1 481* 482 482* 483 483* 484 484* 485 485* 486 486* 487 487* 488 488* 489 489* 490 490*
Centre ID
0007877 0007877 0007878 0007878 0007879 0007879 0007880 0007880 0007881 000788 1 0007882 0007882 0007883 0007883 0007884 0007884 0007885 0007885 0007886 0007886
Set Number
121800AD 121800AD 121800AD 121800AD 1218OOAD 1218OOAD 121800AD 121800AD 121800AD 121800AD 121800AD 121800AD 121800AD 121800AD 121800AD 121800AD 121800AD 121800AD 121800AD 121800AD
Extraction Analysis
Date
Date
12118/00
12/20/00
12/18/00
12/20/00
12/18/00
12/20/00
12118/00
12/20/00
12118/00 12118/00
12/20100 12/20/00
12118/00
12/20/00
12118/00 12118/00 12/18/00 12/18/00
12/20/00 12/20/00 12/20/00 12/20/00
12118/00 12118/00
12/20/00 12120/00
12118/00 12118/00
12/20/00 12/20/00
12/18/00 12118/00 12118/00
12/20/00 12/20/00 12/20/00
12118/00
12/20/00
12118/00
12/20/00
AVERAGE:
STANDARD DEVIATION:
Analyte Found (pg/g)
1.05 1.05 4.10 4.17 8.37 8.30 1.41 1.43 1.54 1.51 0.4 15 0.392 1.17 1.15 0.51 1 0.509 2.42 2.48 0.351 0.360 2.13 2.39
* Duplicate injection
LOQ = 0.01 ppJg for liver and 0.01 pg/mL for serum
Centre Analytical Laboratories, Inc.
Page 28 of 102
Centre Study No.: 023-041
Table X. Summary of PFOS in Juvenile Liver Samples at 0 ppm a.i. (Test Termination 12 Weeks)
Sponsor ID
9503 9503* 9506 9506* 9508 9508* 9512 9512* 9515 9515* 9518 9518* 9520 9520* 9522 9522* 9525 9525* 9526 9526*
Centre ID
0007907 0007907 0007908 0007908 0007909 0007909 00079 10 0007910 00079 1 1 0007911 0007912 00079 12 00079 13 00079 13 0007914 0007914 00079 15 00079 15 0007916 0007916
* Duplicate injection
Set Number
121800B 12 1800B 12 1800B 12 1800B 12 1800B 121800B 121800B 121800B 121800B 12 1800B 12 1800B 121800B 121800B 121800B 121800B 121800B 121800B 12 1800B 12 1800B 12 1800B
Extraction Analysis
Date
Date
12118/00
12/20/00
12/18/00
12/20/00
12118/00
12/20/00
12/18/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12/18/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12/18/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
AVERAGE:
STANDARD DEVIATION:
Analyte Found (pg/g)
NQ NQ NQ NQ NQ NQ NQ NQ 0.000785 0.000755 NQ NQ 0.000734 0.000672 0.0007 18 0.000656 NQ NQ NQ NQ 0.000251 0.000316
NQ = Not Quantifiable (A peak was detected at the corresponding analyte retention time
but was less than the lowest concentration of the calibration standards (0.0001 pg/mL))
For values recorded as NQ, 0.00005 pg/g (half the value of the lowest calibration standard, 0.0001 pg/mL) was used to calculate the average and standard deviation.
LOQ = 0.01 pg/g for liver and 0.01 p g / d for serum
Centre Analytical Laboratories, Inc.
Page 29 of 102
Centre Study No.: 023-041
Table XI. Summary of PFOS in Juvenile Liver Samples at 1.8 ppm ah. (Test Termination 12 Weeks)
Sponsor ID
9528 9528* 9529 9529* 9530 9530* 953 1
953 1*
9533 9533* 9535 9535* 9540 9540* 954 1
9541*
9543 9543* 9544 9544*
Centre ID
0007917 0007917 00079 18 00079 18 00079 19 00079 19 0007920 0007920 000792 1 0007921 0007922 0007922 0007923 0007923 0007924 0007924 0007925 0007925 0007926 0007926
Set Number
121800B 12 1800B 121800B 121800B 12 1800B 12 1800B 121800B 121800B 121800B 121800B 12 1800B 121800B 121800B 12 1800B 121800B 121800B 121800B 121800B 121800B 121800B
Extraction Analysis
Date
Date
12/18/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12/18/00
12/20/00
12/18/00
12/20/00
12/18/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20,/00
12118/00
12/2OlOO
12118/00
12/20/00
12/18/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
12118/00
12/20/00
AVERAGE:
STANDARD DEVIATION:
Analyte Found (pg/g)-
0.0130 0.0128 0.00295 0.00295 0.00904 0.00876 0.00417 0.00435 0.01 19 0.01 17 0.01 13 0.01 14 0.00635 0.00623 0.00305 0.00297 0.0126 0.0126 0.005 14 0.00521 0.00792 0.00393
* Duplicate injection
LOQ = 0.01 ppJg for liver and 0.01 &mL for serum
Centre Analytical Laboratories, Inc.
Page 30 of 102
Centre Study No.: 023-041
Table XII. Summary of PFOS in Juvenile Liver Samples at 6.2 ppm a i . (Test Termination 12 Weeks)
Sponsor
ID
9548 9548* 9549 9549* 955 1 9551* 9552 9552* 9555 9555* 9559 9559* 956 1 9561* 9562 9562* 9563 9563* 9564 9564*
Centre
ID
0007927 0007927 0007928 0007928 0007929 0007929 0007930 0007930 000793 1 000793 1 0007932 0007932 0007933 0007933 0007934 0007934 000793 5 000793 5 0007936 0007936
* Duplicate injection
Set Number
12 1900A 12 1900A 121900A 121900A 12 1900A 121900A 121900A 121900A 12 1900AD 121900AD 121900AD 121900AD 121900AD 121900AD 121900A 121900A 121900AD 12 1900AD 121900A 121900A
Extraction Analysis
Date
Da1:e
12119/00
12121IO0
12119/00
1212 1/00
12119/00
1212 1IO0
12119/00
12121IO0
12/19/00 12/19/00 12119/00 12119/00 12119/00 12119/00 12119/00 12119/00 12/19/00
12121/00 12121IO0 1212 1IO0 12121IO0 12/23/00 12/23/00 12/23/00 12/23/00 12/23/00
12/19/00
12/23/00
12119/00
12121IO0
12119/00
12121IO0
12/19/00
12/23/00
12119/00
12/23/00
12119/00
12121IO0
12/19/00
12121IO0
AVERAGE:
STANDARD DEVIATION:
Analyte Found (pg/g)
0.00303 0.00305 0.0100 0.0105 0.0123 0.0125 0.003 16 0.00302 0.0410 0.0408 0.0340 0.0341 0.0446 0.0445 0.01 16 0.0121 0.0193 0.0197 0.00184 0.00201 0.0182 0.0156
LOQ = 0.01 pglg for liver and 0.01 pglmL for serum
Centre Analytical Laboratories, Inc.
Page 31 of 102
Centre Study No.: 023-041
Table XIII. Summary of PFOS in Juvenile Liver Samples at 17.6 ppm a.i. (Test Termination 12 Weeks)
Sponsor ID
9567 9567* 9570 9570* 9575 9575* 9579 9579* 9580 9580* 9581 9581* 9582 9582* 9583 9583* 9584 9584* 9588 9588*
Centre ID
0007937 0007937 0007938 0007938 0007939 0007939 0007940 0007940 0007941 0007941 0007942 0007942 0007943 0007943 0007944 0007944 0007945 0007945 0007946 0007946
* Duplicate injection
Set Number
121900A 121900A 121900AD 121900AD 12 1900A 121900A 12 1900AD 12 1900AD 12 1900AD 12 1900AD 12 1900AD 121900AD 121900AD 12 1900AD 121900AD 121900AD 12 1900AD 121900AD 121900AD 12 1900AD
Extraction Date
Analysis Date
12119/00
12121IO0
12119/00
12121100
12/19/00
12/23/00
12119/00
12/23/00
12119/00
12/21/00
12119/00
12121/00
12119/00
12/23/00
12119/00
12/23/00
12119/00
12/23/00
12/19/00
12/23/00
12/19/00
12/23/00
12/19/00
12/23/00
12119/00
12/23/00
12/19/00
12/23100
12119/00
12/23/00
12119/00
12/23/00
12119/00
12/23/00
12119/00
12/23/00
12/19/00
12/23/00
12119/00
12/23/00
AVERAGE:
STANDARD DEVIATION:
Analyte Found (pg/g)
0.00904 0.009 12 0.0424 0.0429 0.00629 0.00623 0.0880 0.0898 0.0461 0.0441 0.0492 0.045 1 0.0747 0.0733 0.156 0.132 0.0983 0.101 0.0350 0.0370 0.0593 0.0417
LOQ = 0.01 pg/g for liver and 0.01 pg/mL for serum
Centre Analytkal Laboratories, Inc.
Page 32 of 102
Centre Study No.: 023-041
Table XIV. Summary of PFOS in Adult Serum Samples at 0 ppm a.i. (Test Termination 19 Weeks)
Sponsor ID
45 1 451* 452 452* 453 453* 454 454* 455 455* 456 456* 457 457* 458 458* 459 459*
Centre ID
0007887 0007887 0007888 0007888 0007889 0007889 0007890 0007890 0007891 0007891 0007892 0007892 0007893 0007893 0007894 0007894 0007895 0007895
Set Number
121900BD 121900BD 121900B 121900B 121900BD 12 1900BD 12 1900B 121900B 121900B 121900B 12 1900BD 12 1900BD 12 1900BD 12 1900BD 12 1900BD 12 1900BD 12 1900BD 12 1900BD
Extraction Analysis
Date
Date
12/19/00 12119/00 12/19/00
12/23-24/00 12123-24/00 12121-22/00
12/19/00 12/19/00 12/19/00
12/21-22/00 12123-24/00 12/23-24/00
12/19/00 12119/00 12/19/00 12/19/00 12119/00 12/19/00 12119/00
12121-22/00 12121-22100 12121-22/00 12121-22/00 12/23-24fOO 12/23-24/00 12123-24/00
12/19/00 12119/00 12/19/00 12/19/00 12/19/00
12123-24/00 12/23-24100 12123-24/00 12/23-24/00 12/23-24/00
AVERAGE:
STANDARD DEVIATION:
Analyte Found (pg/mL)
11.6 11.8 0.0102 0.00909 9.04 10.4 0.00274 0.00212 0.0125 0.0123 6.32 6.46 6.58 6.35 0.105 0.102 8.75 8.50 4.78 4.64
* Duplicate injection
LOQ = 0.01 pg/g for liver and 0.01 pg/mL for serum
Centre Analytkal Laboratories, Inc.
Page 33 of 102
Centre Study No.: 023-041
Table XV. Summary of PFOS in Adult Serum Samples at 1.8 ppm a.i. (Test Termination 6 Weeks)
Sponsor ID
EO 1-0259-20752 E01-0259-2075;!* EO 1-0259-20753 E01-0259-20753* EO1-0259-2075.4 EO 1-0259-207541* EO 1-0259-20755 EO 1-0259-20755* EO 1-0259-207516 EO 1-0259-20756* EO1-0259-2076:2 EO1-0259-20762!* EO 1-0259-2076.3
EO 1-0259-207638 *
E01-0259-20764 EO 1-0259-20764.* E01-0259-2076.5 E01-0259-20765* EO 1-0259-20766 E01-0259-207661*
Centre ID
0 102969 0102969 0 102970 0 102970 010297 1 010297 1 0 102972 0 102972 0 102973 0102973 0 102979 0 102979 0102980 0 102980 0102981 0102981 0 102982 0102982 0 102983 0 102983
Set Number
03050 1AD 030501AD 030501AD 030501AD 03050 1AD 030501AD 030501AD 030501AD 03050 1AD 030501AD 030501AD 030501AD 030501AD 03050 1AD 030501AD 030501AD 030501AD 03050 1AD 030501AD 030501AD
Extraction Analysis
Date
Date
3/5/01
317-810 1
3/5/01
317-810 1
3/5/01
317-810 1
3/5/01
317-8/01
3/5/01
317-8/01
31510 1
317-810 1
3/510 1
317-810 1
3/5/01
317-8/01
3/5/01
317-810 1
31510 1
317-810 1
3/901
317-8/01
3/5/0 1
317-810 1
3/5/01
317-8101
3/5/01
317-8/01
31510 1
317-810 1
3/5/01
317-810 1
3/5/01
317-8101
3/5/01
317-8/01
31510 1
317-810 1
3/5/01
317-8101
AVERAGE:
STANDARD DEVIATION:
Analyte Found (pg/mL)
10.9 10.9 7.92 8.01 16.4 16.0 35.8 33.1 24.3 23.7 1.50 1.89 5.01 4.98 1.57 1.84 0.134 0.117 10.5 9.79 11.2 10.7
* Duplicate injection
LOQ = 0.01 pgJg for liver and 0.01 pg/mL for serum
Centre Analyticid Laboratories, Inc.
Page 34 of 102
Centre Study No.: 023-041
Table XVI. Summary of PFOS in Adult Serum Samples at 6.2 ppm a i . (Test Termination 6 Weeks)
Sponsor ID
E01 -0259-20757 EO 1-0259-20757* EO 1-0259-20758 EO 1-0259-20758* EO1-0259-2075'9 EO1-0259-20759* EO 1-0259-207610 EO 1-0259-20760* E01-0259-2076 1 E01-0259-20761* E01-0259-2076'7 EO1-0259-20767* EO 1-0259-20768 EO1-0259-207613* EO 1-0259-2076'3 EO 1-0259-2076S'* EO 1-0259-20770 EO 1-0259-20770* E01-0259-2077 1 E01-0259-20771*
Centre ID
0 102974 0 102974 0102975 0102975 0 102976 0 102976 0 102977 0 102977 0 102978 0 102978 0102984 0 102984 0102985 0 102985 0102986 0102986 0102987 0 102987 0102988 0102988
* Duplicate injection
Set Number
030501AD 030501AD 030501AD 030501AD 030501AD 030501AD 030501AD 03050 1AD 030501AD 030501AD 030501AD 030501AD 030501AD 030501AD 030501AD 030501AD 030501AD 030501AD 03050 1AD 030501AD
Extraction Analysis
Date
Date
31510 1 31510 1 31510 1 31510 1
317-810 1 317-810 1 317-810 1 317-810 1
3/5/01 31510 1 31510 1
317-8101 317-8101 317-8101
31510 1 31510 1 31510 1 31510 1 31510 1 36/01 31510 1
317-8101 317-810 1 317-810 1 317-8101 317-8101 317-810 1 317-810 1
31510 1
317-8101
31510 1
317-8101
31510 1
317-8/01
31510 1
317-8101
31510 1
317-8101
31510 1
317-8101
AVERAGE:
STANDARD DEVIATfON:
Analyte Found (pg/mL)
52.2 56.1 102 94.7 80.4 84.6 69.2 62.9 84.6 86.7 4.57 4.07 2.72 2.61 4.02 3.87 3.24 3.3 1 2.10 1.70 40.3 39.7
LOQ = 0.01 pgJg for liver and 0.01 pg/mL for serum
Centre Analytic(a1Laboratories, Inc.
Page 35 of 102
Centre Study No.: 023-041
Table XVII,, Summary of PFOS in Adult Serum Samples at 17.6 ppm a i . (Test Termination 19 Weeks)
Sponsor ID
48 1 481* 482 482* 484 484* 485 485* 487 487* 488 488* 489 489* 490 490*
Centre
ID
0007896 0007896 0007897 0007897 0007898 0007898 0007899 0007899 0007900 0007900 000790 1 000790 1 0007902 0007902 0007903 0007903
Set Number
12 1900BD 121900BD 12 1900BD 121900BD 12 1900BD 12 1900BD 121900BD 121900BD 121900BD 121900BD 121900BD 12 1900BD 030501AD 030501AD 121900BD 121900BD
Extraction Analysis
Date
Date
12/19/00 12123-24100
12/19/00 12119/00
12123-24/00 12/23-24,100
12/19/00 12123-24/00
12/19/00 12/19/00
12123-24/00 12123-24,100
12/19/00 12/23-24,100
12/19/00 12/19/00
12123-24/00 12123-24/00
12119/00 12/19/00 12119/00
12123-24/00 12123-24/00 12/23-24100
31510 1
3/7-8101
31510 1
317-810 1
12119/00 12123-24/00
12/19/00 12123-24/00
AVERAGE: STANDARD DEVIATION:
Analyte Found (pglmL)
260 263 43.1 42.4 118 106 179 172 133 127 15.8 16.8 232 228 6.87 6.80 122 93.0
* Duplicate injecti.on
LOQ = 0.01 pg/g for liver and 0.01 pg/mL for serum
Centre Analytical Laboratories, Inc.
Page 36 of 102
Centre Study No.: 023-041
Table XVIII. Summary of PFOS in Juvenile Serum Samples at 0 ppm a i . (Test Termination 12 Weeks)
Sponsor ID
9503 9503* 9506 9506* 9508 9508* 9512 9512* 9515 9515* 9518 9518* 9520 9520* 9525 9525* 9526 9526*
Centre ID
0007947 0007947 0007948 0007948 0007949 0007949 0007950 0007950 000795 1 000795 1 0007952 0007952 0007953 0007953 0007954 0007954 0007955 0007955
Set Number
122000A 122000A 122000A 122000A 122000A 122000A 22000A 22000A 22000A 22000A 22000A 122000A 122000A 122000A 122000A 122000A 122000A 122000A
Extraction Analysis
Date
Date
12/20/00
12/22/00
12/20/00 12/20/00
12/22/00 12/22/00
12/20/00
12/22/00
12/20/00 12/20/00
12/22/00 12/22/00
12/20/00 12/20/00
12/22/00 12/22/00
12/20/00 12/20/00 12/20/00 12/20/00 12/20/00 12/20/00
12/22/00 12/22/00 12/22/00 12/22/00 12/22/00 12/22/00
12/20/00
12/22/00
12/20/00 12/20/00
12/22/00 12/22/00
12/20/00
12/22/00
AVERAGE: STANDARD DEVIATION:
Analyte Found (pgJmL)
0.00486 0.00385 0.00718 0.00754 0.00365 0.003 19 0.0043 1 0.00457 0.00789 0.00528 0.00378 0.00481 0.00367 0.00395 0.00552 0.00438 0.00354 0.00388 0.00477 0.00142
* Duplicate injection
LOQ = 0.01 pg/g for liver and 0.01 pg/mL for serum
Centre Analytical Laboratories, Inc.
Page 37 of 102
Centre Study No.: 023-041
Table XIX. Summary of PFOS in Juvenile Serum Samples at 1.8 ppm a i . (Test Termination 12 Weeks)
Sponsor ID
9528 9528* 9529 9529* 9530 9530* 953 1
953 1*
9533 9533* 9535 9535* 9540 9540*
954 1
954 1*
9543 9543* 9544 9544*
Centre ID
0007956 0007956 0007957 0007957 0007958 0007958 0007959 0007959 0007960 0007960 0007961 0007961 0007962 0007962 0007963 0007963 0007964 0007964 0007965 0007965
Set Number
122000D 122000D 122000A 122000A 122000A 122000A 122000A 122000A 122000A 122000A 122000A 122000A 122000A 122000A 122000A 122000A 122000A 122000A 122000A 122000A
Extraction Analysis
Date
Date
12/20/00 12/20/00 12/20/00 12/20/00 12/20/00 12/20/00 12/20/00 12/20/00 12/20/00 12/20/00 12/20/00 12/20/00 12/20/00 12/20/00
12/24/00 12/24/00 12/22/00 12/22/00 12/22/00 12/22/00 12/22/00 12/22/00 12/22/00 12/22/00 12/22/00 12/22/00 12/22/00 12/22/00
2/20/00
12/22/00
2/20/00
12/22/00
2/20/00
12/22/00
2/20/00
12/22/00
12/20/00
12/22/00
12/20/00
12/22/00
AVERAGE:
STANDARD DEVIATION:
Analyte Found (pg/mL)
0.0762 0.0670 0.0273 0.0284 0.00785 0.00824 0.0480 0.0476 0.0488 0.0494 0.0416 0.0413 0.0192 0.0189 0.0321 0.0334 0.00969 0.00983 0.0158 0.0166 0.0324 0.0198
* Duplicate injection
LOQ = 0.01 pg/g for liver and 0.01 pg/mL for serum
Centre Analytical Laboratories, Inc.
Page 38 of 102
Centre Study No.: 023-041
Table XX. Summary of PFOS in Juvenile Serum Samples at 6.2 ppm a i . (Test Termination 12 Weeks)
Sponsor ID
9548 9548* 9549 9549* 955 1 9551* 9552 9552* 9555 9555* 9559 9559* 9561 9561* 9562 9562* 9563 9563* 9564 9564*
Centre ID
0007966 0007966 0007967 0007967 0007968 0007968 0007969 0007969 0007970 0007970 000797 1 000797 1 0007972 0 0 0 7 9 7 2 0007973 0007973 0007974 0007974 0007975 0007975
Set Number
122000D 122000D 122000D 122000D 122000D 122000D 122000B 122000B 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D
Extraction Analysis
Date
Date
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00 12/22-23/00
12/20/00 12122-23/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
AVERAGE:
STANDARD DEVIATION:
Analyte Found (pgjmL)
0.137 0.160 0.382 0.390 0.222 0.208 0.0542 0.0535 0.243 0.218 0.161 0.168 0.185 0.171 0.23 1 0.229 0.259 0.254 0.171 0.173 0.203 0.0838
* Duplicate injection
LOQ = 0.01 pg/g for liver and 0.01 pg/mL for serum
Centre Analytical Laboratories, Inc.
Page 39 of 102
Centre Study No.: 023-041
Table XXI. Summary of PFOS in Juvenile Serum Samples at 17.6 ppm a.i. (Test Termination 12 Weeks)
Sponsor ID
9567 9567* 9570 9570* 9575 9575* 9579 9579* 9580 9580* 9581 9581* 9582 9582* 9583 9583* 9584 9584* 9588 9588*
Centre ID
0007976 0007976 0007977 0007977 0007978 0007978 0007979 0007979 0007980 0007980 0007981 0007981 0007982 0007982 0007983 0007983 0007984 0007984 0007985 0007985
Set Number
122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D 122000D
Extraction Analysis
Date
Date
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/20/00
12/24/00
12/2OlOO
12/24/00
AVERAGE:
STANDARD DEVIATION:
Analyte Found (pdmL)
0.329 0.355 0.483 0.512 0.241 0.252 0.406 0.424 0.287 0.254 0.295 0.285 0.459 0.473 0.521 0.524 0.553 0.564 0.532 0.509 0.413 0.114
* Duplicate injectlion
LOQ = 0.01 pgjg for liver and 0.01 pg/mL for serum
Centre Analytical Laboratories, Inc.
Page 40 of 102
Centre Study No.: 023-041
Table XXII. Summary of Percent Moistures for Quail Liver Samples
Sponsor ID
45 1 452 453 454 455 456 457 458 460 482 484 486 488 490 9506 9508 95 12 9518 9520 9522 9526 9530 9540 9543 9544 9548 955 1 9552 9555
Centre ID
0007867 0007868 0007869 0007870 0007871 0007872 0007873 0007874 0007876 0007878 0007880 0007882 0007884 0007886 0007908 0007909 00079 10 0007912 0007913 00079 14 00079 16 0007919 0007923 0007925 0007926 0007927 0007929 0007930 000793 1
YOMoisture
66.7 64.4 68.4 65.6 64.1 71.8 59.5 71.2 69.0 55.0 60.6 72.5 61.5 65.1 70.7 72.1 67.4 73.2 73.5 68.3 67.9 70.0 66.7 57.1 55.8 59.4 81.3 53.5 65.0
Sponsor ID
9559 956 1 9562 9563 9564 9570 9579 9584 9588 IO 1-0259-20780 :01-0259-2078 1 :01-0259-20782 101-0259-20783 ;01-0259-20784 101-0259-20785 101-0259-20786 :01-0259-20787 :O 1-0259-20788 :O 1-0259-20789 .01-0259-20790
,O1-0259-20791
f01-0259-20792 ,01-0259-20793 ,01-0259-20794 01-0259-20795 0 1-0259-20796 01-0259-20797 01-0259-20798 01-0259-20799
Centre ID
0007932 0007933 0007934 0007935 0007936 0007938 0007940 0007945 0007946 0 102997 0102998 0102999 0103000 010300 1 0 103002 0103003 0103004 0 103005 0103006 0103007 0 103008 0103009 0103010 010301 1 0 103012 01030 13 0103014 0103015 0103016
YOMoisture
78.3 80.6 57.8 63.4 34.6 85.2 88.7 59.6 65.2 70.3 57.8 70.6 67.0 67.7 64.5 72.3 67.6 68.0 68.0 69.3 70.9 67.0 65.3 74.5 65.7 71.7 72.8 71.3 72.1
Centre Analytical Laboratories, Inc.
Page 41 of 102
Centre Study No.: 023-041
FIGURES
Centre Analytical Laboratories, Inc.
Page 42 of 102
1.564
1.4e4
I
1.3e4
1.2e4
l.le4
1 .Oe4
9000.0
n
-!l5 8ooo*o 7000.0
i
6000.C
., . .
e
`
5000.C 4000.C 3000.C
e e
8
2000.c
I
,
1ooo.c
0.c
w P
%
c
0
h)
: I
!
!
' ,/ "
e e
cn
E
Y
Z
0..
0 w h)
b
f:
Centre Study No.:023-041
Figure 2. Chromatogram Representing a 0.1 ng/mL standard for PFOS
pc
9
' Conc.nLrazion:
0.100
233,
I Acq. D a t m : Acq. T h :
12/22/00 10:37:10 AH
220 :
I
' Modified:
Y, .
' Bunching Factor:
1
Uoise Thr.shold:
1.91
AI-. Threshold:
9.55
Num. S-ths:
1
RT M i n d a :
30.0 sc.
Exp.cteg RT:
4.51 .in
Sap. WIdth:
0.20
Sep. Heiqhr:
0.01
m. Exp. Peak Ratio: 5.00 Ad). Ratio: 4.00
Exp. v.1. Ratio: 3.00
Uao R.latrv. RT: No
200,
1 180.
I too!
1
i14D.I
l1Z0O0.
Inc. Type:
Uanurl
I
Retention T i m :
4.49 -in
Ax.: Heiqhr:
21.0183e9r10002 COUcpa.tI W I
Start T h :
4.40 min
End Tim:
4.59 .in
40 1
I
20 1
Centre Analytical Laboratories, Inc. ....... . . . -. . . . - ... . , .
...........
Page 44 of 102
Centre Study No.:023-041
Figure 3. Chromatogram Representing a 1.0 ng/mL standard for PFOS
. . - . .. .
Concentrac&m: A m . Dare: ACq. r1m:
1.000 12f22/00 11:15:09 M
I4cdifi.d:
Y, .
Bunching Factor:
1
NOISa ThraShold:
1.91
ASea Thr*ahold:
9.55
N U . S-Chs:
1
?W. ln'dIow:
30.0 m c
&pQct.d 111:
4.51 .in
Sap. Width: Sop. WeIqht:
B h p . Peak b c i o : f EXP. Adj. b t ~ o :
Exp. Val. b r i o :
f US. R*laLIve RT:
0.20 0.01 5.00
4.00 3.00 No
I n t . type: R.tention T h : A:.I
Hoiqhz: st.rt T h :
End Tim:
H.nu.1 4.50
4881.6
i.i3.+om 4.40 4.61
.in
esunt.
cp. rin
rin
1181 1100. 1000: 900. 800 700 600 do0 400 100 200 100
0
1-
0.5
1.0
1.5
2.0 . 2.5
10
1.5
40
Tmo. mn
Centre Analytical Laboratories, Inc.
Page 45 of 102
. . -. .
, ..-. .. - .. . I
..,?.?
.
.
"
, . .__
- ,
.,
. .
-
.
Centre Study No.: 023-041
Figure 4. Chromatogram Representing a Reagent Blank for PFOS
(Centre ID Reagent Blank A, Set: 122000A)
Sa.plc Index:
;1 S l l p l . Type: Concentration: t Acq. Date:
Acq. time:
8 Bl."k
0.000
12122100 12:05:48 R(
4wi 450
nodifiad:
Y.S
Bunching Factor: 1
Noise 1hz.rhold:
1.91
AT.a Threshold:
9.S5
- Nur. SmothS:
RT Window: Expected RT:
1 3 0 . 0 s.e
4.Sl .in
5.p. Width:
0.20
Sep. Height:
0.01
wlp. Peak Flatdo: 5.00
wlp. Mj. Ratio: 4.00
Exp. V a l . Ratio: 3.00
US. R.l.ti". n1: No
400
550
so0
B
-250 - zoo
Int. Type: Retention T i m : :..IA
Height: stazt Tip.: End Time:
wmu.1 4.50
2299.8 4.50.*002
4.39 4.61
.in counts
Epa mi" min
150
100
50
- ..
0'
- 0.5
1.0
9.5
2.0
2.l
3.0
3.5
4.0
I-- "A.
Centre Analytical Laboratories, Inc.
.. . . .. --.
,. . .
Page 46 of 102
.. .. . . ..
Centre Study No.:023-041
Figure 5. Chromatogram Representing Control Quail Serum for
PFOS (Centre ID: 0011424Blank A,Set: 122000A)
Sample Index:
Sample Type: conc.mtration:
Acq. Oat.:
Acq. I&:
10 Bhnk 0.000
12/??/00 12:Jl:OO M
1083 1000
Wifi*d: Bunchinq h c t o r : Nois. Thr.rhold: Area Ihz*ahold: Nun. S-tha: RT Window: Expected RT: Sap. Width: S e i . Height:
Exp. Peak Ratlo: Em. Mt. Ratio:
Yea 1 1.91 9.55 1 30.0 4.51 0.20 0.01 5.00
4.00
SC.
Din
.
8(.
i
900 800 100 600.
so0 .
+ Xnt. Typ.:
1 R.t.ntion Tim: 41:..IAHeight:
I s t * r t 1Ln: i End T h :
I
hnual 4.50
4110.1
1.03.*003 4.39
4.63
mitn
counts
cpr
Din
min
400;
too: 1
I
1 P
0.5
t.0
1,s
2.0
2.5
3.0
3.5
4.0
Tim. m n
Centre Analytical Laboratories, Inc.
Page 47 of 102
Centre Study No.: 023-041
Figure 6. Chromatogram Representing Control Quail Liver for PFOS, (Centre ID: 0007870 Blank A, Set: 121900A)
1 Acq. O w * :
ACq. T I M :
12/21/00 11:29:44 W
Uodified: Bunchinq Faccoc: Nois. 1hr.shold:
Area Thr.sho1d:
Yea
1 1.91 9.55
Nun. 5-tha: RT Window: Exp.ct.d RT: S.p. Width: Sap. Height:
5 Exp. Peak Ratio:
Exp. Mi. Ratio: Exp. Val. Ratio:
f Use Ralative RT:
1 30.0 a=
4.51 .in 0.20
0.01 s.00
4.00 3.00 No
I n t . Typ.:
htmtion Tim:
A:.I
Height:
SCJCC Tim:
End TIM:
.
Manual 4.48
402.8 1.01.+002
4.37 4.61
rin
COUIILS
cpr rin
.in
i
1
4.37
. . ,.4.64 ' .I 6 ~ .,'* ' 3 . 1 7 5.57 .
6.47
Centre Analytical Laboratories, Inc.
..
Page 48 of 102
.. - . . . .
~ .. - -
^ .
*-
Centre Study No.: 023-041
Figure 7.
Chromatogram Representing Control Quail Serum Fortified with 500 ng/mL of PFOS (Centre ID: 0011424 Spk A, Set: 122000A)
: Sampl. Typ.:
! concencration: Acq. Dace:
I Acq. Tim:
a
2.000 12/22/00 12:56:17 R1
1 1600.
Uodified:
Yes
Bunching Factor:
1
Noise Threshold: 1.91
.IA Threshold:
9.55
1600
1400 !
NU.. Smooths:
1
RT window: Expected 112:
3 0 . 0 s.c 4.51 min
1200 4
Sep. Width:
0.20
i Sap. HeLghC:
GYP. Pk.
R.110:
EXP. Mi. Ratto: exp. V a l . ruc10:
Use R.1atlve RT:
0.01 5.00
4.00 3.00
NO
1000
=
I 4
a00 ;
Int. Type: R.cencion Tim: k..:
I(.nUJl
4.49
7570.8
dn
C0""tI
I
600. I
Height: 5t a r t Tim:
End Tim:
1.79e*003
4- .- 4-04.62
cpr
-4.
.
mm
400.
200 3
i
0
I i
1
-.._---_-_ -_-c
--. --_._.__-
0.5
1.0
1.5
2.0
2.5
3.0
1.5
4.0
d
5.0
5.5
6.0
6.5
7.0.
1.5
Centre Analytical Laboratories, Inc.
Page 49 of 102
Centre Study No.: 023-041
Figure 8.
Chromatogram Representing Control Quail Liver Fortified at 10 ppb with PFOS (Centre ID: 0011423 Spk A, Set: 121800A)
I-I. m..
a
Centre Analytical Laboratories, Inc.
Page 50 of 102
Centre Study No.:023-041
Figure 9.
Chromatogram Representing Juvenile Quail Serum Sample (Centre ID: 0007965, Sponsor ID: 9544, Set: 122000A)
1 i
Acq. Acq.
Dace: Tim:
12/22/00 10:29:16 RI
! Modified:
YO8
. Bunching factor: 1
1 Nois. Threshold: 1.91
Area Threshold:
$.55
I Num. Smoochr:
1
I RT Window:
1 fxwcc.d RI:
30.0 aoc 4.51 l i n
' Sob. Widch:
0.20
I S.D. Hoiaht:
0.01
1200
1100
1000
900
800
700
600
500
400
JW
200,
1W; -
0'
0 5
1.0
1.5
2.0
2.5
J.0
3.1
4.0
- _4.67 .-
5.0
__-___ .-,-.---.--L--* .__C__r ._-/.. ~
5.5
6.0
6.5
7.0
7.5
Centre Analytical Laboratories, Inc.
Page 51 of 102
Centre Study No.: 023-041
Figure 10. Chromatogram Representing Juvenile Quail Liver Sample
(Centre ID: 0007926, Sponsor ID:9544,
Set: 121800B)
I S-1.
Index:
59
I con;*ntr;iion: Acq. mc.: 1 Acq. Tim:
I
U/A 12/20/00 .01:33:11
i I4diti.d:
..I
. Dunchins Factor: 1
I WOia. Thr.shold:
1.91
As'.. Thrashold:
1 Nun. S l w t h a : . j RT Nindw:
9.55 1 30.0
Expactad RT:
I Sep. Nidth:
, Sep. Height:
4.51 0.20
0.01
I rXp. Peak Ratio: Exp. Ad). Patio:' U p . V 8 l . Ratio:
5.00 4.00 3.00
1 Us. Relativ. RT: lo
pw
au mi"
1 2101
1I 1dOO.
j,MOO
1400.
I troo! .
I 1000 !
800
600
400
- zoo. 0
05
10
15
20
25
30
35
40
5
5.0
5.5
6.0
6.5
7.0
7.5
Tnna.mu, ~
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Centre StudyNo.:023-041
APPENDIX A
Study Protocol OOP-023-041 (Centre Study No. 023-041)
and Amendments and Deviations
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Centre protocol No.OOPM3-041
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STUDY PROTOCOL
I
STUDYTITLE
EXTRACTIONOFPOTASSNM PERFLUOROOCT&ULFONATE FROM QUAILSERUM AND QUAELIVER FOR ANALYSIS USING HPLC-
. El,ECTROSPRAY/MASS SPECTROMETRY -
SPONSOR 3M En&onmental Technology and Safety Services
Building 2-3E-09 PO Box 33331 St. Paul, MN 25133-3331
- -
DATAREQUIREMENTS
- h-dytical Method Requirements
TESTING LABORATORY
Centre Analytical Laboratories. Inc. (Centrc)
3048 Rescarch Drive
- Stat+Coll~g,PA16801
Phone 814-231-8032
PROTOCOL IDENTIFICATION M E R
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-Centre Analytical Laboratpries, Inc.
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Centre Protocol No. OOPM3-Wl
Title:EXTRACTION OF POTASSIUMP E R F L U O R O O a ~ W O N A T EFROM
QUAIL SERUM AND QUAE LIVERFOR ANALYSIS USING WLC-
. ELECTROSPRAY/MASS SPECTROMETRY
TABLE OF CONTENTS
Page
TABLEOFC 0 " T S ..... .............................................................................................. 2 ~
1.
PURPOSE ............................................................................
I
.
x.
.................
3 .
2. TESTMATERIALS;.............................................................................................. 3
3. SPONSOR............................................................................................................... 4
4. T'ESTINGFACILlTY AND PERFORMINGLABORATQRY .......... :.......4
5. PROPOSED~ E U M & I T A LTIME-FRAhiE................1.................................. 4
6. JUSTIFICATION FOR "J-E SELECTIONOF THE TEST SYSTJ34.................4
7. . SAMPLEPROCESSING, STORAGEAND IDENTIFICATION ................:.......5
8. ANALYTICAL-OD U.................................................................................. 5
9. EXPERIMENTAI. DESIGN........................................... :...................... 10
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10. PROTOCOLAMENDMENTSAND DEWATIONS........... ...................io ;
11. RECORDS ............. :................................................................................. 11
12. QUALXIY ASSURANCE.......................................................... 1............. 12
13. DATA AND REPORT................... ..................................... 12
14. ARCHIVE STATEMENT........................................ ........................................... 13
i5. REFERENcEs.....1...............,...............................
13 .
16. PROTOCOLAPPROVAL....................................................... i.............. 14 .
APPENDIX:A N A L m C L METHODS...................................... ................................ 15 I
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Centre Study No.: 023-041
i ,
CentreProtocol No.OOP-023-041
$tu& Title:
I
EXTRACI'ION OF POTASSIUMPERFLUOROOC'I'ANESUNATE FROM
QUAIL SERUM AND QUALLIVER FOR ANALYSIS USING HPLC-
ELECl'ROSPRAYMSS SPECTROMEI'RY '
1. PURPOSE
The purpose of this study is to analyze quail serum samples and quail liver samples forresidues of peffluomctanesulfonate(PFOS) using methods entitled, "ix&tion Of Pbtassium PertIuorooctanesulfonate Or Other Fluomchemical
Compounds From. Serum For Analysis Using HPLC-Electrosprayhfas
Spectrometry" (3Mmethod number ETS-84.1) and "Extraction Of Potassium
. Peffluorooctanesulfonate Or Other Fluomchemical Compounds From Liver For
Analysis Using HPLC-Electro~pray/%4aS~pectrometry" (3M method number ETS-8-6.0) with the modifcationslisted in Section 8.
The QualityAssurance Unit of Centre Analytical Laboratories,Inc.. will audit the study for compliance with EPA TSCA Good Laboratory Practice standards 40 CFR Part 792 (1).
2 TESTMATERIALS The following analytical standards will be used: . .
Test Material
PFOS
-
TCfj Number TCR0001748
.Purity (%) 97.9
Expiration Date
08/31/01
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PFOS
ChemicalNme: W A C Name:
CAS Number:
Molecular Weight:
0
0
&gg The neutral molecule and staildard form that PFOS (anion) is derived from is perfluorooctanesulfonatepotassiuin salt [C8nSO3Kl, molecularweight 538.
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A record of test and refemce substance receipt, storage conditions, and a record of use will be maintained at Cencre Analytical Laboratories, Inc. Forms
- documenting chain-of-custody and shipping records 'for tmcking of the test
substanceswill be included as part of the raw data package. All standadtest substances and any pnpand solutions must be identifiedwith a unique label or number on the containeror cross-referencedto the container.
A current MSDS for the chemical(s) used in this study will be maintained at the testingfacility. .
3. SPONSOR
3M EnvironmentalTechnologyand SafetyServices
Building 2-3E-09
PO Box 33331
.-
St.Paul, MN 55133-3331
RSTocUhDelYleDRIoRbEidCeaTuOR -
i-
TEIEPHOm 651-778-7065
f '*..-
FAX NUMBER: 651-778-6176 .
4. TESTING FACILITY AND PERFORMINGLABOFTORY
Centre Analytical Laboratories, Inc. (Centre)
3048 Research Drive
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State College, PA 16801
PRINCIqAL INVESTIGATOR:
Emily R. Stauffer, Centre
TELEPHONE: 814-23 1-8032
\-
FAX NUMBER. 814-231-1580
5. PROPOSEDEXPENMENTALTIME-FRAME
Experimental Start Date Experimental Termination Date Report Issued
Dec. 11,2000 Dec. 15,2000 De. 30,2000
6. JUSTIFICATIONFOR THESELECTION OFTHE TEST SYSTEM !
Quail serum samples arid liver samples collected by Wildlife International,Ltd.
will be used as the test systems for this study. ' Quails represent wild bird
i populations and they arc an EPA recommended species because they do well in a
._.
laboratory environment. Quail habitats include bushy pastures, p i x y roadsides,
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Ceria Protocol No.00PM3-041
farmlands;and open woodlands. and they are considered land grazers. The use of these matrices for the study was to determine if PFOS was deposited in the liver and serum of mating adults that were fed PFOS.
A complete description of the test system along with all of the in-life parameters is documaited in the sponsor's protocol no. 454/0106oO/QP/SuB454, Project
No.454-1,Mthat is associatedwith this analyticalprotocol.
7. SAMPLE PROCESSING,STORAGEAND IDENTIFICATION
No pmcmsing will be q u i d for the mum samples. Due to the small mount
of sample available,the liversampleswill not be homogenizedprior to extraction;
.
however, they will be mashingthan by hand
. homogenized by laying the
as best as possible.
samples
on
a
flat
surface
and
Each sample will be assigned a unique Sample identification number at Centre.
with will be used for tracking and identification of the samples. The samples
will be stored in a temperature-monitored freezer. maintained at < -10" C. except
when .removed for extraction and analysis as described in the method. The
sampleswill be kept isolated from the tcst.substanceduringstorage. . .
Sample receipt and storage location and conditions during the _study will be doymented.' All samples and any nSulting Sample extracts will be identified with a unique label or sample number. Such identification will be either on the container or cioss-referenced to the container.
8. . &AL~CALME"HOD
The saum samples will be analyzed according to the analytical method titled
"Exfraction Of Potassium Peffluorooctanesdfonate Or Other l?Iuorochemical
Compounds -From Serum For Analysis Using HXC-Elemspray/Mass
Spectrometry"(3Mmethod'number ETS-8-4.1) and the control liver sampleswill
be
according to the method titled "Extraction ot Potassium '
. Peffluorooctanesulfonate Or.0ther.Flu~hemicaCl ompounds Frpm Liver For
Analysis Using HPLC-ElcctmsprayIMass Spectrometry" (3M method number
ETS-8-6.0). The followingmodifications will be applied to each method:
1. Then will be no surrogate standard used in the extraction prkcdun. The stock,fortification,and calibrationstandardswill be prepared as follows:
I
Stock Solution
Prepan a stock solution of PFOS at 100 @nL by weighing out 10.0 mg of analytick standard (corrected for percent salt and percent purity). Adjust final volume to 100 d,with methanol in a 100-d, volumetric flask. Store this
stock solution (in 125-mL LDPE bottles) in a refrigerator at 2C to 6C for a
. maximum period of 6 months from the date of preparation.
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Fortif3cation Solutions a 1.0 udmLForo'fication
- Solution Pipette
1.0
mL
of
the
100
p@mL
stock
I
solution into a 100 mL volumetric flask. Bring up to volume with
methanol.
. . - b. QJ&@ Fomfimon Solution Pipette 10.0 mL of the 1.0 pg/d
. fortification solution into a 100-mL volum.etric flask arld bring up to
__- _J- Vamm-K-
e-_
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Forhficahon
Sohh'on
I
Pipette 10.0 mL of the 0.1 pg/mL
fortification solution into a 100-mL volumetric flask and bring up to
volume with methanol
Ston all fortification standard solutions (in 125-mL mPE bottles) in a kfrigerator at 24C to 6C for a maximum period of 6 months from the
date of pnparation.
Calibration Standards
Prepare six Lc/MsIMscalibration standards in methailol via dilution of . the 0.1 pg/mL and the 0.01 pglmL fodfication solutions.
~ This is a typical example; additional concentrations may be p n p m d as needed.
. Initial Conc. (&mL) Volume (mE) Diluted to (mL) Final Conc. ( p d m ~ ) -
0.1
5
100
0,005
0.1
-2
100
0.002 .
0.1
1
100
0.001
0.01
5
100
0.0005
0.01
2
100
, 0.0002
0.01
1
100
0.0001
Store all calibration standard S O ~ U ~ ~ (Oin~ S125-mL LDPE bottles) in a . refrigerator at 2C to 6C for a maximum period of 6 months from the
date of preparation. -
2. The liver samples will not be pro~essedto make the homogenate described in
the method Section 12.2 to 12.12. Due to limited sample available, samples will be mashed on a flat surface by hand prior to extraction.
3. The sample weight for-liverwill be 0.50 g (*0.05) and the sample volume for serum will be 100 pL. The amount of 0.5 M TBA added to the m u m k p l e will be 0.5 mL and the amount of 0.25 M sodium carbonatdsodium
- bicarbonate buffer added will be 1.0 mL Samples will be placed on a wrist-
action shaker for -'20 min. at level 10 and then centrifuged for 15 min @ .-3000 rpm. The sampleswill only be filtmd with 0.2 pm nylon mesh filterif
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necessary. Samples will be reconstituted in a final volume of 1 I& of methanol for both matrices.
4. The samples will be analyzed under the following conditions:
LC/MS/MS System and Op&ating Conditions(TurboIonspray)
Mass Spec: PE SCIEX API 3000 BiomolecularMass Analyzer
~ Interface: SCIEX TurboIon SprayLiquid IntroductionInterface -
. _ Harvard infusion pump
. Computer: Power Macintosh 0 3
Software:
PE SciexAnalyst 1.1
Windows NT
HPLC: .-
HewlettP a c w (HP) Series 1100
W Quat Pump
-
s.Ip Vacuum Degasser
HPAutosampler
HPColumnOven .
HPLC Co1umn:Gmesis CS(JonesChromatography),2.1 -mx 50 mm.4p . ColumnTemp.: 35OC . Injection Vol.: 10pL MobilePhase (A):. 2 mMAmmonium Acetate in ASTM type I water Mobile Phase (B): Methanol
Flow Rate: 0.3 mL.!.min.
nnGu!&B
..
0
60. .40
1.0
0 . - 100
7.0
0 ' 100
7.5 40. 60
11.0 40 - 60
It may be necessary to adjust the HPLC gddient in order to optimize instrument performance. Columns with different dimensions (e.g., 2.1
mm x 30 d)and columns from diffmnt manufacturers (Keystone
Betasil Cls etc.) can be used, provided equivalent chromatography is
obtained.
~ o n smonitored
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a n h e protocolNo.OOP423-041
Analvte
PFOS '
w negative
+ ..
I
Tm10onMonitond
499 99 '
Cm Approximate
Retention Time
4.20
On a day-today basis, the ntention times may vary slighhtlydependingon the batch of mobile phase, etc.
Example Tune Fiie Parameters The following vslue~are p p v i a~s an example. AC~&values may vary from instrumentto instlument. Also. these values may be chmiged from time to time in
order to optimize for greatest sensitivity.
The mass specmmctcr is tuned using a 0.5pg/mL PFOS solution, prepared via dilution of the stock solution in methanol. .The solution is infused (using a 'T' connector) at 10 wmni into a 0.2 d i n i n stream of mobile phase consisting of 4096 methanol and 60% 2 mM ammonium acetate. The analytes arc initially tuned for the parent ion and then tuned for the product ion. Once the instrument is tuned, the optimized parameters are saved as a "tune file". This tune file is then
used during routineanalysis. The tuning proceduremay b.repeated as necessary
. to ensure optimal seositivity.
controls - Is-Iospray
OR-Orifice
- RNG-FocusRing
Q O - Q d 0 R d -Offset
IQL inter quad 1 lens
ST-Stubbies
ROl-QllidlRod Offset
1 Q 2 - hq~uad 2 lens
ROZ-Quad2 d offset
ST3-Stubbia'
.
R03-Qd 3 rodOffset
DF-CEMDeflection Plate
CEM-Channel Electron Multiplier .
QasFlowt
Nebulizer Gas
qntainGas CdlisionGas-
-
TIS Temperature
&' 4000.0
41.0 .
. -270.0-
- 10.0
9.3 -15.0
. .93 20.0
-84.0 100.0 86.0
. 300.0
2800.0
sa'
12 13 4 350OC
,
i
I .,
Calibration Prkdures -
a Inject the same VO~W (bet;veen 10 to 20 &)of each calibration standard (prepared in MeOH).into the u=IMsIMs.
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b. Use line& l/x weighted standard Curves for quantification. Enear
standard curves are generated for each set by linear r e m i o n
using the appropriate softwaresystem. Any calibration standards falling outside f 30% based on its calculated concentration,must be excludedfrom the calibration c u m . However, the total number of calibration standards that may be excluded must not exceed 30% of the total number of standards injected.
c. The corklation coefficient (r) for calibration curves generated
must be 20.9925 ((20.985). If calibrationresults fall outside t h a
limits, then appropriate steps should be taken to adjust instrument
'
operation,and the relevant set of samplesmust be reanalyzed
Sample Analysis Inject the same volume used for the calibration standards (between 10 to 20 p ~ ) of each sample, fortification,-control,etc. into the Lc/MS/Ms.Each sample must
be analyzed in duplicate.
a.
standards comsponding to included in an analytical set.
a- t
least six
concentrationi must
be
- b. Inject an entire set of stan- (six) at the beginning of the a n and inject standards interspersed about every 5-10sample-s. All sample injectionsmustbe bracketed byptandard injections.
c. Each set of-samples analyzed (not to exceed 25) must include at least one reagent control (extraction solvents orily), at least om matrix . control, and two matrix control Samples fortified at known
concentrationsand carriedthrough the P K X ~ W Cto v d f y recovery.
d. The concentration of- each SarnpleD fortification, control, etc. is
determined from the standard curve based on the peak area of the
. n d ~ ein all standards injected during a set. The standard nsponsts
must bracket responses of the residue found in the sample set. .If
-
necessary, dilute the samples and r e - a n a l p to give a rcspon& within
the standard curve range.
e. Fortification recovcxies within 80 to 12096 arc acceptable for fortificationsat the LOQ level. Recoveries between 80 to 120% are
acceptable for fortifications at levels greater than the LOQ? Failure to
mreaentaiiyhscissedcthrietearfifaecrteeqdusiaremsplaens. inv-estigation of cause and a full
f. Samples in which no peaks arc detected at the comsponding andyte
retention times will be nportod as ND (not detected). Samples in
which peaks arc detected at the corresponding analyte retention times
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; but arc less than 3:l signal:noise will be reponed as NQ (not
quantifiable).
...
g. Background levels of analyte found in controhlank samples that comspond to values below the LOQ, but are still quantifiable, will be used toc o w fortificationrecoveries.
h. ' If samplesare not loaded on the insrnunentto be analyzzdthe day they
I arc extracted, samples must be stored refrigerated at approximately . 2OC to 6C until analysisand analyzedpreferably within'a week.
.
A
9. E-RIMEWAL DESIGN
Samples obtained by Wildlife International L.td. have k n shipped to Centre
AnalyticalLaboratories;Inc. for analysis.
AU samples will'be analyzed according to methods, 'Zxtraction.of Potassium Peffluorooctanesulfonatcor Other Fluomchemical Compounds From Serum for
Analysis Using HPLC-Eiectrospray/Mass Spectrometry" and "Extraction of Potassium Pduorooctanesidfonate or Other Fluomchemical Compounds From Liver for Analysis Using H P L C - ~ e c t r o s p yS~pectrometry" with the modificationsdetailed in Section 8.
-. Methods to control bias' will include assay- of untread control saniples, foaifcation of untreated control samplw to obtain recovery data, and replicate . .analysisof fortifiedsamplesto providean indication of reproducibility. .
. The aveige recovery and relative standarddeviation of the fortified samples will
be calculated. Also, the average residue found and standard deviation for each -
matrix will be calculated.
Moisture dctmninationwill be p&onnd bn all liver samples accordingto
Centre SOP CAL-lOBll1with the followingmodifications:
- 1. The sampleweight will be 0.5 g. - 2. The drying time will be 12 hours.-
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10. PROTOCOLMNDMlW'I"'I' AND DEVIATIONS I
Any deviations from the protocol or from the analytical method as provided will
be documentedand reported promptly to the Study Director. Planned changes to
this protocol or to the analyticalmethod will be made in writing as an amendment
and approved by the Principal Investigator and the Study Director. Any . amendments or deviations will be appended to.this protocol and included in the
final report.
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Planned changes to the approved protocol shall be
documentedby amendments that clearly describe the change,justification for
the change, and impact on the study. Amendments will be signed and dated by
the Principal Investigator and Study Director. Copies of mendments will be
sent to the quality assuranceunit.
mol deviations: Protocol deviations, which an one time and unplanned ' deviationsfrom the protocol,shall be documentedin the study records,noting the nature of the deviation, potential effect or impact on the study, and corrective action if required Protocol deviations an signed and dated by the
Principal Investigatorand Study Directorand reviewed by QAU.
11. RECORDS
-.
Records to be maintained inclu&..but are not limited the following (as appropxiate):
. 1. Sampletracking shctt(s). 2. S&nple receipt reco.rds,storagehistory,and chains of custody 3. History and preparationof standards (stock,fortification,&libration)
4. 5.
Descriptionof any modifications to Instrumentrun sheets, bench-sheets
tohrelomgesthod-
6.Analyticaldata tables
.-
7. All chromatographic and instrumentalconditions 8. Sample extraction &d analysis dates .
9. A completelisting of studypersonnel, signaturesand initials
10.Chronologicalpresentationof all study correspondence
11. Any other data necessary for the reconstruction of the study
. All chromatograms will contain the following:
a. Sample identification. date, arrow or Other indication of the area of ' intenst, and injection number comsponding to the run.
b. Additionally, fortifications will include the fortification level of the tlllalyte.
c. Analytical standard Chromatograms will additionally: include the concentration(e-g., p#mL n#mJ-, ppb, ppf etc.).
Each data set will contain information on temperatures,, flow rates, column pmameters, gases, instmmait parameters, and instrument type, etc. The Centre study number will also be recorded on the first chromatogram of each daily analytical run.
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Ceria Q A Unit wili review the protocol, audit the study conduct and the study documentation (including raw data and final report) to ascertain that all QNGLP procedures a~ adhered to. Centre QA Unit will inspect the study at intervals adequate to assure compliance to GLP's, and will report the findings of the audits
to the-PrincipalInvestigator, CmtreManagement,and the StudyDirector.
I
13. DATAANDREPORT '
1. All raw data and the original sigind @Dtocol-Willbe maintained in the study file. This data includes the protocol' amendments, protocol deviations, laboratory notebooks, analytical standard Solution preparation, sample chain
of custody sheets. sample work sheets, chromatograms, calibration curves,
and any other appropriate data generated. Raw. data not wed will be stored in the study file. The reason for exclusion will be documented.
-2. A final report will be issued by Centre. approved and signG by the Study
Director and sufficient for submission to WA. The report contents should ~
- indude, but not limited to:
-
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1. Objectives and pmedtgcs stated in the p:&ol
2. Analytical and statistiealmethods used
3. Test materials identified by name, lot, purity. and other charirctcristics
4. Name of testing facility and study initiation and completion dates
. 5. Statementprepared and signed by the qualify assuranceunit
6. Tablescontainingall applicabledata
7. All chromatographicand instrumental conditions
8. A complete listing of Centre study personnel
- Centre will send a copy of the draft report to the Study Erector. who will rehm ,
the 'cpoa with comments. Centxe Analytical will makc revisions and finalize the
. *port with the approval of the StudyDirector. The Centre Q A unit will conduct
an audit of the final draft report and data files to assure accuracy and GLPcompliance. The final report must be approved by the Study Director prior to signature. A statement of QAU inspections and a statement of GLP compliance will be included in the final report.
Any corrections or additions to the final report shall be in the form of an amendment by the Principal Investigator. The amendment shall clea$y identify the p k of the final report that is being comcted and the'justification for correction. The amendment shall be signed and dated by the principal Investigatorand the StudyDimtor.
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. CentreRotocol No.OoP-023-041
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REPORT DISTRIBUTION:
Original: Study -tor Copy: Centre Archives
14. AR-STATEMJ"
Study records to be maintainee Rcc.ords to be maintained for the study include all
raw data, observations worded. during the conduct of the study, documentation,
chromatograms, specimen tracking information, and study related correspondence.
This includes a description of equipment used during the conduct of the study. All characterizationdata and any shippingrecords shaH be retained.
Document archives: Upon completion of the study, the study records, pmtmoi and amendments, and the final report and amendments shall be retained in the 3M document archives. If it is necessary to substitute a COPY for an original record, it will be certified as an exact copy. Centre will retain facility-relatedoriginals and a copy
' of the find report and raw data package.
1 U.S.Environmental Prot&tion Agency. Toxic Substances Control Act (TSCA).
- Good LaboratoryPractice-Standards.Final Rule, 40 CFRPart 792.
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Centre Protocol No. OOP-oU-041
16. PROTOCOL APPROVAL
This protocol was audited by the Quality Assurance Unit of Centre Analytical
Laboratories, Inc. Quality Assurance Reviewer, Centre
Principai Investigator, Centre
-Facility Management, Centre
ohn Flaherty
/
Fgboratory Manager
Study Director, 3M .. ..
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APPENDIX: ANALYTICAL METHODS A. "Extractionof Potassium Pduorooctanesulfonateor OthqFluorochemical Compounds From Senun for Analysis Using HPLC-Electrospray/Mass Spectrometrf`
B. ``Extractionof Potassium PerfluorooctanesuIfonattor Other Fluomchemical
Compoun+ From Liver for Analysis Using l"LC-Elcctmspray/hh,s
`Spectrometry"
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SEP. 6. 2001 11:39AM ENVIBONENTAL LAB 2 31 09
..
Centre Study No.: 023-041
NO. 5647 P. 2
PROTOCOL AMENDMENT
Page 1 of
Amendment Number: 1 EfYcctivcDate: 12/18100
. IICentt= Study Number 923-041
CentreProtocol N u m k pOP-023-041
AMlmEQm 1. Change the but paragraph to read as follows:
Moimun detumination will be performedon all liver samples according to AOAC
- - officialMethod 950,44SectionB.
1. The #ample weight will be 0.5 2 The drying &e will be 12-14
(a).
g.
ho
with un.
the
following
modifications:
RATIONALE
1. At the requestof the rponsor,maishue deierminatiomwill be done for every liver
sample. Dw to Iimited sample she, the sample weight used will be -0.5 g insread of
., -2 g, The drying time nquired for such a s d sample size docs not have to be 16-18
how, EO the sample0 will be dried for 12-14 hours
ACT ON l"ES W Y
1. No negative impact on the study.
&ds;nt&a;(Study Direct&) Signature
Dak' 1 '
E C E I M D T I M SEP. 6. . . ._
1:Pffl
Centre Analytical Laboratories, Inc.
Page 97 of 102
SIP. 6. 2001 11:39M ENVIBONUNTAL LAB 2 31 09
.. Centre Study No.: 023-041
NO. 5647 P. 5
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~ ~ I V E D T I MSEP. 6. 1:-
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.-
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Centre Study No.: 023-041
CEntrts 'Analytical
3048RuarrL Drive, State Cdlege, PA 16801.
Pbone: (814)231-8032. Faaimtie: (814)231-1253
Centre StudyNumber:Q23-041
PROTOCOL AMENDMENT AmendmentNumber: 2
Date of Occurrence: QW24/0J,
Centre Protocol Number: QOP-073-041
DESCRIPTION OF AMENDEDSECTION
1. 53: SPONSOR
@ENDEDTO
1. Change the study director fiom Rochelle Robideau at 3M Environmental Technology
and Safety Servicesto Scan Gallagherat Wildlife International, LTD, 8598 Commerce
Drive, Easton, MD 21601, phone: 410-822-8600, fax: 410-822-0632.
- 2. ChangeRochelleRobideautothe SponsorRepresentative. RATIONALE
1-2. By request of Rochelle Robideau (fax dated OSnlllol included in correspondence section of the raw data associated with this study)
1-2. No negative impact on the study.
L e*' * ( r
IncomingStudy DDiirectoor Signature
&??/
Date
Date
Centre Analytical Laboratories, Inc.
Page 99 of 102
Centre Study No.: 023-041
SIP. 6. 2001 ll:4OW
9
ENVIBOMNTAL LAB 2 3E 09
NO. 5647 P. 8
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PROTOCOL DEVIATION
i
DeVidmNumba: 1
f I
I DIjscRlpnONOFDEVIATION
. 4 Amendment #1: Did not pafonnmoisturedetumination on the followingsamplesh u e
!
me waa no umpla available &a ex[rocfioll:
i
I
-sJialm
-iahlcn2
oo07875
459
o(107920
953 1
0007879
483
ooo7921
9533
0007881
485
m7922
9535
- !
ow7883
487
0041924
9541
OOO7885
489
mgza
9549
* 9503
0041937
9s6l
ooo7911
9515
0007941
9580
1
0007915
9525
m 2+
9581
0007917
9sta
ooo7943
9582
!
oOol918
9529
m944
9583
i
AcnoNs TAKEN
!
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SEP. 6. 2001 11:40AM ENVIBONMENTAL LAB 2 3E 09 _ - ...
Centre Study No.: 023-041
NO. 5647 P. 7
PROTOCOL DEVIATION
DESQUPTION OF DEVIATION
- 1. 0 Amenrimat #I: Weighsdh r than 0.5 gfor the miamredetumination011 the following
ramplea because it WLI rtl of rhc rampiervrilabkafter d o n :
sumawm
6007913 00071167
maao
om927
0041936
OW7938
aaLLQ!l!&i&u
9sm
0.34
451
0.30
484
0.33
9548
0.32
- 9564
0.26
-95m
0.27
i C
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r
SEP. 6. 2001 11:40AM ENVIBONMENTAL LAB 2 3E 09
Centre Study No.: 023-041
NO. 5647 P. 6
- \
Centre Analytical
Laboratoriss, Inc.
PROTOCOL DEVIATION
DavirrionNUmbsr: 3
,
ECEIMD TIM SEP. 6 . 1:m
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