Document K67aEobBNg1ER1jdQOmxk2EY0
i
Northwest Bioanalytical
Study No. NWBS99-117 Report No. NWBR99-114
^4Hlt(p-17X1
Quantitative Determination of PFOS, PFOSA, PFOSAA, PFHS, POAA, M556 and M570 in Human
Serum by LC/MS/MS
Sample Analysis Report for Protocol EPI-PEuro
Northwest Bioanalytical (NWB) A Division of NWT Inc. 1121 East 3900 South Salt Lake City, UT 84124
PREPARED FOR: 3M Environmental Technology and Services (3M) 935 Bush Avenue St. Paul, MN 55133
_____AUTHOR: 14-
David Vollmer, Ph.D., NWB Project Manager
APPROVED FOR
BY:
RodgerL. Foltz, Ph.D., NWB Laboratory Director
Page 1
DATE: DATE:
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Northwest Bioanalytical
QUALITY ASSURANCE STATEMENT
Study No. NWBS99-117 Report No. NWBR99-114
LABORATORY:
NAS11aoD2lrt1tiLhvEwaiskaeiseosttnC3BNi9ti0yWo0,aUTnSa,TolIyun8tteih4c.1a2l 4(NWB)
SPONSOR:
39S3Mt.5PEBanuuvls,ihrMoAnNvme5en5nu1tea3l3Technology Services (3M)
COMPOUND(S):
PFOS, PFOSA, PFOSAA, PFHS, POAA, M556 and M570
NWB STUDY NUMBER: NWBS99-117
SPONSOR STUDY NUMBER: EPI-PEuro
NWB STUDY TITLE:
EHxutmraacntioSneraunmd bAynHalPysLisCo/EflPeFctOroSsparnadyoMthaesrsFSlupeocrotrcohmemetricyals in
rPPTo2e1rafhga,rteucthPltce5aiAlc8tUiBeen),d.iSScNthna.taoleoFntnsDOidafcaimAElcirnCadpGtilDicOeooanroalPdndrsNiiatnnLuolaycda.nisyb4pci.os2eler4Hsafs.tot)uooordwrfTNyyeGhovdPeoneerocarsfd,locciNlrtnLliiiocboacewerbadtRloihnrLiwegnagateiutobsnhlrotsaiyrsBptaiPerioteoocrnaptarsicyonotfarniSotclsytreiustwNdianceinoaeordnlsetcctioplhnoineencnrlitdfJuchoauaderpclematSdLsneaaweadfbeslilbeottyhsyrMatiountthoHdfteriDhWeyNesruSWwdGgteusioBftdhoi(inOideQnistrLAidto(haTiUnnbeiaotopglnrefeuacrait2edo1SGeNrOylLCionPP.Fe.Rs
Inspection and Reporting Statement.
I200001n138977s--DpDSS32eeee20ecppcctASi11o11eu9999npg9999D9999119a99t9e99
FARPASSihaaennnmmapaaasolllppeyyrlRlttteeoiieDccfRApaarSlloenatcrPaPfutetlldl/yiaaRypsnntaisDwrDafatta
N002003389220WDDASSSBeeeeeupppccgP111r111o999D999j999999ea999999ctet MInaspneacgteiron Re333333*p100000NorWADDSSSteeeueeIBpppsccgs1Mu11111999e999a999d999n999999Tagoement
^Reports to NWB Management are issued monthly.
Athsiscfainnarlearespoonratbalyccbueraetsetlaybrleisfhleecdt,tthheermawethdoadtas. and procedures described and the results incorporated into
Date
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Northwest Bioanalytical
Study No. NWBS99-117 Report No. NWBR99-114
Compliance Statement TdehfeinciltiinoincaolfsaamGpLlPe raengaulylastiesdstnuodnycldiensiccarilbsetdudwyitsheitnfothritshrienpToirttleis2n1otoifntchleuUde.Sd.wCitohdien othfe Federal Regulations Part 58. However, to the best of our knowledge, this project was conducted in accordance with the guidelines of the U.S. FDA Good Laboratory Practice Regulations for Nonclinical Laboratory Studies (Title 21 CFR Part 58) and according to the mgueitdheoldinseasnodfpthroecOedEuCreDs Pdreisnccriipbleeds wofitGhionotdhiLsarbeoproartto. ryInPardacdtiitcioena,ntdhethsetuJdaypafnoellsoewMedHtWhe Good Laboratory Practice Standard Ordinance for Nonclinical Laboratory Studies on the Safety of Drugs (Ordinance No. 21, PAB Notification No. 424.) There were no known incidents that affected the quality or integrity of the project or data reported. This report represents an accurate record of the raw data.
David Vollmer, Ph.D. NWB Project Manager NWB Laboratory Director
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Northwest Bioanalytical
TABLE OF CONTENTS
Study No. NWBS99-117 Report No. NWBR99-114
SIGNATURE PAGE..... ........................................................................................................................... 1
QUALITY ASSURANCE STATEMENT....................................................................... ....................2
COMPLIANCE STATEMENT...............................................................................................................3
TABLE OF CONTENTS......................................................................................................................... 4
LIST OF TABLES................................................................................
4
1. INTRODUCTION.............................................................................................................................6
2. METHODOLOGY........................................................................................................................... 7
3. SAMPLE ANALYSIS.......................
9
4. RESULTS AND DISCUSSION...................................................................................................10
5. REFERENCES....................................................................................................
10
LIST OF TABLES
Table 1. Calibration Curve Summary for PFOS in Human Serum.................................................12
Table 2. Calibration Curve Summary for PFOSA in Human Serum..............................................12
Table 3. Calibration Curve Summary for PFOSAA in Human Serum............................................12
Table 4. Calibration Curve Summary for PFHS in Human Serum................................................... 13
Table 5. Calibration Curve Summary for POAA in Human Serum................................................. 13
Table 6. Calibration Curve Summary for M556 in Human Serum...................................................13
Table 7. Calibration Curve Summary for M570 in Human Serum.................................................. 14
Table 8. Back-Calculated Concentrations of Calibration Standards for PFOS in Human Serum.....................................................................
15
Table 9. Back-Calculated Concentrations of Calibration Standards for PFOSA in Human Serum.....................................................................................................15
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Table 10. Back-Calculated Concentrations of Calibration Standards for PFOSAA in Human Serum.................................................................................................. 16
Table 11. Back-Calculated Concentrations of Calibration Standards for PFHS in Human Serum........................................................................................................ 16
Table 12. Back-Calculated Concentrations of Calibration Standards for POAA in Human Serum.........................................................................................
17
Table 13. Back-Calculated Concentrations of Calibration Standards for M556 in Human Serum........................................................................................................ 17
Table 14. Back-Calculated Concentrations of Calibration Standards for M570 in Human Serum.........................................................................................................18
Table 15. Analytical QC Summary for PFOS in Human Serum............................................19
Table 16. Analytical QC Summary for PFOSA in Human Serum...................................................19
Table 17. Analytical QC Summary for PFOSAA in Human Serum...............................................20
Table 18. Analytical QC Summary for PFHS in Human Serum.................................................... 20
Table 19. Analytical QC Summary for POAA in Human Serum...................................................21
Table 20. Analytical QC Summary for M556 in Human Serum............................................21
Table 21. Analytical QC Summary for M570 in Human Serum........................................... 22
Table 22. Study Sample Concentrations............................................................................................ 23
/
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Northwest Bioanalytical
Study No. NWBS99-117 Report No. NWBR99-114
Quantitative Determination of PFOS, PFOSA, PFOSAA, PFHS, POAA, M556 and M570 in Human Serum by LC/MS/MS
Sample Analysis for Protocol EPI-PEuro
1. INTRODUCTION
This report summarizes the analytical results from the quantitation of PFOS, PFOSA, PFOSAA, PFHS, POAA, M556 and M570 in human serum samples for 3M Environmental Technology and Services in support of Protocol EPI-PEuro [5.1]. The validated LC/MS/MS method provided a lower limit of quantitation (LLOQ) of 31.4 (PFOS), 1.00 (PFOSA), 1.45 (PFOSAA), 2.61 (PFHS) and 5.27 (POAA) ppb. All analytes exhibited a linear response to approximately 500 ppb with the exception of PFOSAA, which had an upper limit of quantitation (ULOQ) of 270 ppb [5.2]. The nonvalidated method for the quantitation for M556 and M570 in human serum provided a lower limit of quantitation (LLOQ) of 1.00 and 5.00 ppb, respectively, and exhibited a linear response to 500 ppb for both analytes.
The testing facility was 3M Corporate Occupational Medicine (Bldg. 220-3W-05, St. Paul, MN 55144-1000), and Jean Burris at the facility served as the Principal Investigator. The following is a list of NWB supervisory personnel involved in the completion of this work: David Vollmer, Ph.D. (NWB Project Manager); Rodger L. Foltz, Ph.D. (NWB Laboratory Director).
NWB SOPs were used in the conduct of this study and were available to study personnel in electronic and/or hard copy formats.
Date Study Initiated: September 7, 1999 Date Analyses Completed: September 20, 1999 The clinical study described in this report is not included within the definition of a GLP regulated nonclinical study. However, Northwest Bioanalytical conducts all studies within the guidelines of the U.S. FDA Good Laboratory Practice Regulations for
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Study No. NWBS99-117 Report No. NWBR99-114
Nonclinical Laboratory Studies (Title 21 CFR Part 58), the OECD Principles of Good Laboratory Practice and the Japanese MHW Good Laboratory Practice Standard Ordinance for Nonclinical Laboratory Studies on the Safety of Drugs (Ordinance No. 21, PAB Notification No. 424). Any changes to or deviations from the original protocol (Analytical Plan) were documented through approved protocol amendments or deviation
memos and are retained within the raw data.
2. METHODOLOGY
The validated assay used for this study is Meth98082.00 and was reported in Northwest Bioanalytical report NWBR99-005 [5.2].
Samples for this study were received at NWB on the following date:
Receipt Date
August 27,1999
Reference Material
Number ofSamples Received Storage Condition (except during analysis)
18 - 20C
Analyte Lot Number Purity Expiration Date Source Storage Conditions
*PFOS (FC-95) 193
100% 12/31/2010
3M Room Temperature (dry)
PFOSA
214 100% 12/31/2010 3M Room Temperature
*PFOSAA (FC-129)
617 53.8% 12/31/2010 3M Room Temperature
PFHS
S398-182 100% 12/31/2010
3M
- 20C
*POAA (FC 143)
245 100% 12/31/2010 3M Room Temperature (dry)
M556 NB 99.89% 12/31/2010 3M Room Temperature 113047-80
M570
118506-26 99.75% 12/31/2010
3M Room Temperature
SDS (sodium 17H0459 99% dodecylsulfate)
1/16/2001 Sigma Room Temperature
* Analyte names used throughout this report do not include their FC identifier; for example, PFOS is synonymous with PFOS (FC-95)
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Study No. NWBS99-117 Report No. NWBR99-114
Nine calibration standards were prepared fresh daily by adding the appropriate spiking standard solution into 0.200 mL of human serum. The final calibration standard concentrations in human serum for each analyte were as follows:
Analyte
PFOS PFOSA PFOSAA PFHS POAA M556 M570
Calibrdtion Standard Concentrations (ppb)
31.4, 35.4, 40.4, 55.4, 80.4, 130, 280, 430, 530 1.00, 5.00, 10.0, 25.0, 50.0, 100, 250, 400, 500 1.45, 3A 6.29, 14.4, 27.8, 54.7, 135, 216, 270 2.6frj6$L>1.6, 26.6, 51.6, 102, 252, 402, 502 5.277^27, 14.3, 29.3, 54.3, 104, 254, 404, 504 1.00, 5.00, 10.0, 25.0, 50.0, 100, 250, 400, 500 1.00, 5.00,10.0, 25.0, 50.0, 100,250, 400, 500
Analytical QCs were prepared in human serum on September 13,1999 and frozen in a -20C freezer. Analytical QCs at the following levels were assayed in duplicate in each analytical ran:
Analyte
PFOS PFOSA PFOSAA PFHS POAA M556 M570
QC Concentrations (ppb)
Low (50.4) and High (380) Low (20.0) and High (350) Low (11.7) and High (189) Low (21,6) and High (352) Low (24.3) and High (354) Low (20.0) and High (350) Low (20.0) and High (350)
After the addition of HPLC-grade water and sodium dodecyl sulfate (SDS, internal
standard) to 0.200 mL of human serum, the serum mixture is made basic with the addition of 0.5 M tetrabutylammonium hydrogen sulfate (TBA, pH 10) and 0.25 M carbonate buffer. This mixture is then extracted with methyl-tert-butyl ether. After sufficient mixing, the sample is centrifuged. The organic layer is transferred via pipette into a clean test tube. The organic layer is then evaporated to dryness and the sample is
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Study No. NWBS99-117 Report No. NWBR99-114
reconstituted into 2 raM ammonium acetate water:methanol (50:50 v/v). The extracts are then analyzed by liquid chromatography/tandem mass spectrometry using negative-ion electrospray ionization and multiple reaction monitoring.
3. SAMPLE ANALYSIS
The prepared samples, calibration standards and QCs were injected into the PE Sciex API 3000 LC/MS/MS system in a systematic order.
Chromatographic peak integrationwas performed using MacQuan software (version 1.6). Quadratic regression analysis (weighted 1/x) all analytes was performed using the peak
area ratio vs. concentration utilizing Watson DMLIMS software (version 5.4.10.2).
3.1. Acceptance Criteria
For an analytical run to be accepted, it must have met the acceptance criteria listed below which are consistent with regulatory and industry recommendations.
Calibration Curve
Each run will include duplicate calibration standards at 7 or more concentrations covering the lower to upper limit of quantitation. At least two-thirds of the
calibration standard's back-calculated concentrations must be within 15% ( 20% for LLOQ) of their individual target concentrations. If a calibration standard is not within the acceptance criteria, it is deactivated. This process starts from the highest calibration standard down to the lowest until all the active standards are within the acceptance criteria.
Lower Limit of Quantitation
The back-calculated concentrations of at least one of the duplicate lowest points in the
calibration curve must be within 20% of the target concentration to qualify as the LLOQ. If this criterion is not met, the next level is subjected to the same test and the LLOQ raised accordingly.
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Quality Control Samples
Study No. NWBS99-117 Report No. NWBR99-114
Each analytical run will include low and high QC samples in triplicate. The measured concentrations of at least two-thirds of all analytical QCs must be within 20% of their target concentrations. If study samples require dilution, a dilution QC is analyzed in duplicate for each dilution level. At least one dilution QC at each level
must be within 20% in order to accept study sample results at that dilution level. The dilution QC acceptance was independent of the undiluted analytical QC acceptance.
4. RESULTS AND DISCUSSION
Each accepted run met the acceptance criteria set for the calibration curve points, for the lower limit of quantitation (LLOQ) and for the analytical quality control (QC) samples.
Run ID
PFOS Result
PFOSA PFOSAA Result Result
RPFesHuSlt
POAA Result
M556 Result
M570 Comments Result
1 accepted accepted accepted accepted accepted accepted accepted
There were no known circumstances that may have affected the quality or integrity of the data.
In conclusion, based on the quality control and calibration curve data, it is our opinion that the data submitted to 3M Environmental Technology and Services for PFOS, PFOSA, PFOSAA, PFHS, POAA, M556 and M570 are accurate for all of the EPI-PEuro study samples. Please note that the results for analytes M556 and M570 should be considered unvalidated data.
5. REFERENCES
5.1. 3M Protocol EPI-PEuro, "Analysis of Fluorochemicals in Pooled Sera from Europe," August 24, 1999.
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Study No. NWBS99-117 Report No. NWBR99-114
5.2. D. Vollmer, "Quantitative Determination of PFOS, PFOSA, PFOSAA, N-MeFOSEOH, N-EtFOSE-OH, POAA and PFHS in Human Serum by LC/MS/MS," NWB Study Number NWBS98-082, NWB Report Number NWBR99-005, May 13, 1999.
The raw data and final report for this study will be stored in the NWB Archives, 1121
East 3900 South, Salt Lake City, UT 84124 per regulations and contract agreement. After submission of the final report to the Sponsor, remaining study samples will be stored under required conditions until confirmation of Sample Disposition/Retum Authorization is received from the Sponsor. 3M Environmental Technology and Services and 3M Corporate Occupational Medicine will be notified concerning final disposition of records at completion of contract obligations.
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Study No. NWBS99-117 Report No. NWBR99-114
Table 1. Calibration Curve Summary for PFOS in Human Serum
Quadratic weighted 1/x. All concentrations are expressed as ppb.
Run Date Run Numbr
A
B
C R-Squared IXOQ ULOQ
17-Sep-1999 1 -0.000003 0.007758 0.060028 0.9961 31.4 530
Mean -0.000003 0.007758 0.060028 0.9961 n 1 11 1
* A, B and C are coefficients used to define the quadratic curve.
Table 2. Calibration Curve Summary for PFOSA in Human Serum
Quadratic weighted 1/x. All concentrations are expressed as ppb.
Run Date NuRmubner
A
B
C R-Squared LLOQ ULOQ
17-Sep-1999 1 -0.000007 0.016542 0,006140 0.9960 1.00 500
Mean -0.000007 0.016542 0.006140 0.9960 n 1 11 1
* A, B and C are coefficients used to define the quadratic curve.
Table 3. Calibration Curve Summary for PFOSAA in Human Serum
Quadratic weighted 1/x. All concentrations are expressed as ppb.
Run Date Run A B C R-Squared LLOQ ULOQ Number
17-Sep-1999 1 -0.000002 0.001907 0.002064 0.9971 1.45 270
Mean -0.000002 0.001907 0.002064 0.9971 n 1 11 P
* A, B and C are coefficients used to define the quadratic curve.
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Study No. NWBS99-117 Report No. NWBR99-114
Table 4. Calibration Curve Summary for PFHS in Human Serum
Quadratic weighted 1/x. All concentrations are expressed as ppb.
Run Date NuRmunber
A
B
C R-Squared LLOQ ULOQ
17-Sep-1999
1 -0.000006 0.012069 0.031955 0.9980 6.61 502
Mean -0.000006 0.012069 0.031955 0.9980 n 1 11 1
* A, B and C are coefficients used to define the quadratic curve.
Table 5. Calibration Curve Summary for POAA in Human Serum
Quadratic weighted 1/x. All concentrations are expressed as ppb.
Run Date Run Number
A
B
C R-Squared LLOQ ULOQ
17-Sep-1999 1 -0.000006 0.014672 0.018212 0.9977 5.27 504
Mean -0.000006 0.014672 0.018212 0.9977 n 1 11 1
* A, B and C are coefficients used to define the quadratic curve.
Table 6. Calibration Curve Summary for M556 in Human Serum
Quadratic weighted 1/x. All concentrations are expressed as ppb.
Run Date Run Number A B c R-Squared LLOQ ULOQ 17-Sep-1999 1 0.000000 0.000556 0.001320 0.9977 1.00 500
Mean 0.000000 0.000556 0.001320 0.9977
n
111
b
* A, B and C are coefficients used to define the quadratic curve.
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Study No. NWBS99-117 Report No. NWBR99-114
Table 7. Calibration Curve Summary for M570 in Human Serum
Quadratic weighted 1/x. All concentrations are expressed as ppb.
Run Date Run Number
A
B
C R-Squared LLOQ ULOQ
17-Sep-1999 1 -0.000001 0.002742 0.015241 0.9984 5.00 500
Mean -0.000001 0.002742 0.015241 0.9984 n 1 11 1
* A, B and C are coefficients used to define the quadratic curve.
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Table 8. Back-Calculated Concentrations of Calibration Standards for PFOS in Human Serum
Quadratic weighted 1/x. All concentrations are expressed as ppb.
Run Date Run Number 31.4 35.4 40.4 55.4 80.4 130 280 430 530
17-Sep-1999
1 29.7 34.4 41.4 57.2 88.2 126 266 444 490 27.5. 35.9 42.2 56.2 84.3 130 278 417 581
Mean 28.6 35.2 41.8 56.7 86.3 128 272 431 536 S.D. 1.56 1.06 0.566 0.707 2.76 2.83 8.49 19.1 64.3 %CV 5.5 3.0 1.4 1.2 3.2 2.2 3.1 4.4 12.0 %Bias -8.9 -0.6 3.5 2.3 7.3 -1.5 -2.9 0.2 1.1
n 22 2 2 22222
Table 9. Back-Calculated Concentrations of Calibration Standards for PFOSA in Human Serum
Quadratic weighted 1/x. All concentrations are expressed as ppb.
Run Date Run Number 1.00 5.00 10.0 25.0 50.0 100 250 400 500 17-Sep-1999 1 0.958 *7.04 10.3 *28.8 55.5 99.2 241 438 451
0.852 *6.51 11.3 *30.0 51.2 88.5 259 377 542
Mean 0.905 10.8 53.4 93.9 250 408 497 S.D. 0.0750 0.707 3.04 7.57 12.7 43.1 64.3 %CV 8.3 6.5 5.7 8.1 5.1 10.6 12.9 %Bias -9.5 8.0 6.8 -6.1 0.0 2.0 -0.6
n 2 2 2 2- 2 2 2
* Sample deactivated as an outlieT (> 15% theoretical for non-LLOQ; > 20% theoretical for LLOQ)
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Study No. NWBS99-117 Report No. NWBR99-114
Table 10. Back-Calculated Concentrations of Calibration Standards for PFOSAA in Human Serum
Quadratic weighted 1/x. All concentrations are expressed as ppb.
Run Date
Run Number
1.45
3.60
6.29
14.4 27.8 54.7 135 216 270
17-Sep-1999 1 1.16 3.60 6.37 14.7 30.9 53.5 125 217 251
*0.720 3.53 6.41 14.9 30.6 54.9 133 214 300
Mean 1.16 3.57 6.39 14.8 30.8 54.2 129 216 276 S.D. N.C. 0.0495 0.0283 0.141 0.212 0.990 5.66 2.12 34.6
%CV N.C. 1.4 0.4 1.0 0.7 1.8 4.4 1.0 12.5
%Bias -20.0 -0.8 1.6 2.8 10.8 -0.9 -4.4 0.0 2.2
n 1 2 2 2 2 2 222
* Sample deactivated as an outlier (> 15% theoretical foTnon-LLOQ; > 20% theoretical for LLOQ)
N.C. = not calculable
Table 11. Back-Calculated Concentrations of Calibration Standards for PFHS in Human Serum
Quadratic weighted 1/x. All concentrations are expressed as ppb.
Run Date Run Number 2.61 6.61 11.6 26.6 51.6 102 252 402 502
17-Sep-1999
1 *0.735 5.57 10.9 27.3 58.3 101 232 404 491 *0.571 6.57 11.7 27.7 56.4 102 243 412 523
Mean 6.07 11.3 27.5 57.4 102 238 408 507 S.D. 0.707 0.566 0.283 1.34 0.707 7.78 5.66 22.6 %CV 11.6 5.0 1.0 2.3 0.7 3.3 1.4 4.5 %Bias -8.2 -2.6 3.4 11.2 0.0 -5.6 1.5 1.0
n 2 2 2 2 2 222
* Sample deactivated as an oudier (> 15% theoretical for non-LLOQ; > 20% theoretical for LLOQ )
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Study No. NWBS99-117 Report No. NWBR99-114
Table 12. Back-Calculated Concentrations of Calibration Standards for POAA in Human Serum
Quadratic weighted 1/x. All concentrations are expressed as ppb.
Run Date Run Number 5.27 9.27 14.3 29.3 54.3 104 254 404 504
17-Sep-1999 1
4.41 9.29 14.7 30.1 60.2 99.9 235 403 480 4.35 9.85 15.0 31.4 59.3 103 246 421 533
Mean 4.38 9.57 14.9 30.8 59.8 101 241 412 507 S.D. 0.0424 0.396 0.212 0.919 0.636 2.19 7.78 12.7 37.5 %CV 1.0 4.1 1.4 3.0 1.1 2.2 3.2 3.1 7.4
%Bias -16.9 3.2 4.2 5.1 10.1 -2.9 -5.1 2.0 0.6
n 2 2 2 2 2 2222
Table 13. Back-Calculated Concentrations of Calibration Standards for M556 in Human Serum
Quadratic weighted 1/x. All concentrations are expressed as ppb.
Run Date Run Number 1.00 5.00 10.0 25.0 50.0 100 250 400 500
17-Sep-1999
1 1.03 4.49 *7.17 21.3 50.5 103 239 394 467 *<LLOQ *2.56 10.1 27.7 54.9 101 248 401 544
Mean 1.03 4.49 10.1 24.5 52.7 102 244 398 506 S.D. N.C. N.C. N.C. 4.53 3.11 1.41 6.36 4.95 54.4 %CV N.C. N.C. N.C. 18.5 5.9 1.4 2.6 1.2 10.8 %Bias 3.0 -10.2 1.0 -2.0 5.4 2.0 -2.4 -0.5 1.2 n 1 1 1 222222
* Sample deactivated as an outlier (> 15% theoretical for non-LLOQ; > 20% theoretical for LLOQ)
N.C. = not calculable
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Study No. NWBS99-117 Report No. NWBR99-114
Table 14. Back-Calculated Concentrations of Calibration Standards for M570 in Human Serum
Quadratic weighted 1/x. All concentrations are expressed as ppb.
Run Date Run Number 1.00 5.00
17-Sep-1999
1 *<LLOQ 4.82 *<LLOQ 4.17
10.0 25.0 50.0 100 250
10.4 27.9 *61.7 102 240 9.69 26.3 54.1 96.9 242
400 500
425 485 386 517
Mean 4.50 10.0 27.1 54.1 99.5 241 406 501 S.D. - 0.460 0.502 1.13 N.C. 3.61 1.41 27.6 22.6 %CV * 10.2 5.0 4.2 N.C. 3.6 0.6 6.8 4.5 %Bias -10.0 0.0 8.4 8.2 -0.5 -3.6 1.5 0.2
n 2 2 2 1 2222
* Sample deactivated as an outlier (> 15% theoretical for non-LLOQ; > 20% theoretical for LLOQ)
N.C. = not calculable
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Study No. NWBS99-117 Report No. NWBR99-114
Table 15. Analytical QC Summary for PFOS in Human Serum
All concentrations are expressed as ppb.
Run Date Run Number
17-Sep-1999
1
Low QC 50.4 ppb
49.9 49.4
53.5
High QC 380 ppb
393 322 369
Mean S.D. %CV
%Theoretical %Bias n
50.9 361 2.24 36.1 4.4 10.0
101.0 95.0 1.0 -5.0
33
Table 16. Analytical QC Summary for PFOSA in Human Serum
All concentrations are expressed as ppb.
Run Date Run Number
17-Sep-1999
1
Low QC 20.0 ppb
18.0
20.0
18.5
High QC 350 ppb
302
*264
280
Mean S.D. %CV %Theoretical %Bias
n
18.8 1.04 5.5 94.0 -6.0 3
* > 20%theoretical
282 19.1 6.8
80.6 -19.4
3
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Study No. NWBS99-117 Report No. NWBR99-114
Table 17. Analytical QC Summary for PFOSAA in Human Serum
All concentrations are expressed as ppb.
Run Date Run Number
17-Sep-1999
1
Low QC 11.7 ppb
11.0 10.1
11.0
High QC 189 ppb
186 156 184
Mean S.D.
%cv
%Theoretical %Bias n
10.7 175 0.520 16.8 4.9 9.6 91.5 92.6 -8.5 -7.4
33
Table 18. Analytical QC Summary for PFHS in Human Serum
All concentrations are expressed as ppb.
Run Date Run Number
17-Sep-1999
1
Low QC 21.6 ppb
21.7 20.9 22.6
High QC 352 ppb
374 313
356
Mean
S.D. %CV %Theoretical %Bias
n
21.7 348 0.850 31.3 3.9 9.0 100.5 98.9. 0.5 -1.1
33
Page 20
Northwest Bioanalytical
Study No. NWBS99-117 Report No. NWBR99-114
Table 19. Analytical QC Summary for POAA in Human Serum
All concentrations are expressed as ppb.
Run Date Run Number
17-Sep-1999
1
Low QC 24.3 ppb
23.5 22.9
25.6
High QC 354 ppb
362 311
357
Mean
S.D. %CV %Theoretical %Bias
n
24.0 343
1.42 28.1 5.9 8.2 98.8 96.9 -1.2 -3.1 33
Table 20. Analytical QC Summary for M556 in Human Serum
All concentrations are expressed as ppb.
Run Date Run Number
17-Sep-1999
1
2L0o.w0 pQpCb 16.7 *15.6 18.5
H35ig0hpQpbC 290 281 352
Mean
S.D. %CV
%Theoretical %Bias n
16.9 1.46 8.6 84.5 -15.5 3
* > 20%theoretical
308
38.7 12.6 88.0 -12j0 3
Page 21
Northwest Bioanalytical
Study No. NWBS99-117 Report No. NWBR99-114
Table 21. Analytical QC Summary for M570 in Human Serum
All concentrations are expressed as ppb.
Run Date Run Number
17-Sep-1999
1
Low QC 20.0 ppb
19.7 18.2 19.2
High QC 350 ppb
340 280 342
Mean S.D.
%CV %Theoretical
%Bias n
19.0 321 0.764 35.2
4.0 11.0 95.0 91.7 -5.0 -8.3 33
Page 22
Northwest Bioanalytical
Sample ID
-- - 9545 , 9546
9547
.9548
9549
- 9550
9551
* 9552
'*9553
9554
y---- 9555
H-riti
---9-556 955/7
* `9558
9559
9560
9561
9565
PFOS
45.6 39.7 32.7 32.6 32.0 41.7 <LLOQ(31.4) <LLOQ(31.4) <LLOQ(31.4) <LLOQ(31.4) <LLOQ(31.4) 43.7 60.6 42.2 64.5 38.9 V 58=8
*
PFOSA
<LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1,00) <LLOQ(1.00) <LLOQ(l .00) <LLOQ(1.00) <LLOQ(LOO) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00)
*
Table 22. Study Sample Concentrations
All concentrations are expressed as ppb.
PFOSAA
<LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45) <LLOQ(1.45)
*
PFHS ^N n?.tj h\,Y\i <LLOQ(fe.61) <LLOQ(6.61) <LLOQ(6.61) <LLOQ(6:61) <LLOQ(6.61) <LLOQ(6.61) <LLOQ(6.61) <LLOQ(6.61) <LLOQ(6.61) <LLOQ(6.61) <LLOQ(6.61) <LLOQ(6.61) <LLOQ(6.61) <LLOQ(6.61) <LLOQ(6.61) <LLOQ(6.61)
_ _ I Z E _<LLOQ(^l)
POAA
8.56 7.94 7.74 7.49 7.02 8.35 <LLOQ(5.27) <LLOQ(5.27) <LLOQ(5.27) <LLOQ(5.27) 5.46 8.13 10.1 10.0 15.7 9.01 9.61
*
L &Cuuy J J L j f i L i l
P ff)^
() value in parentheses ip the LLOQ
SLMzjj>J**l*.s r1 "' * TI hIieq;^s)daXmIippilCe XreCcCeCiIvVeCdU was not in extractadle form and was not analyzed.
<%?55Ts<3t_
m t s &
su0>-,njr
H .*
?
S&.%-
Page 23
ttf'fJ I
>J- fit ?' \ *
Study No. NWBS99-117 Report No. NWBR99-114
M556
<LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00)
3.89 ' <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00) <LLOQ(1.00)
*<LLOQ(1.00)
<LLOQ(l .00)
M570
<LLOQ(5.00) <LLOQ(5.00) . <LLOQ(5.00) <LLOQ(5.00) <LLOQ(5.00) <LLOQ(5.00) <LLOQ(5.00) <LLOQ(5.00) <LLOQ(5.00) <LLOQ(5.00) <LLOQ(5.00) <LLOQ(5.00) <LLOQ(5.00) <LLOQ(5.00) <LLOQ(5.00)
*<LLOQ(5.00)
<LLOQ(5.00)