Document 4a2aJvjJyjpNMyN8VXv7RERDG
TRADE SECRET
Study Title H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
Laboratory Project ID: DuPont-2927
AR226-3157
DuPont-2927
AUTHOR: Carol Finlay, B.A. STUDY COMPLETED ON: August 3, 2000
PERFORMING LABORATORY:
E.I. du Font de Nemours and Company Haskell Laboratory for Toxicology and Industrial Medicine
EUcton Road, P.O. Box 50 Newark, Delaware 19714-0050
WORK REQUEST NUMBER:'p^--ss--ss--^^
SERVICE CODE NUMBER: ^^1 ^------
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H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
CERTIFICATION
We, the undersigned, declare that this report provides an accurate evaluation of data obtained
from this study.
Reviewed by:
^ rGary W. Jepson, Ph.D.
Senior Research Scientist
Reviewed by;
CJ^g^C^f. U:
^{LcL^, Judith C. Stadler, Ph.D., D.A.B.T.
J Director, General Toxicology
Issued by Study Director:
/^fr-t J^L^ Carol Fin&y, B.A. Q
Staff Scientist
<7,A--& 2-000
Date
S-AU&-200Q
Date
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H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
TABLE OF CONTENTS
Page
CERTIFICATION ........................................................................................................................2 LIST OF TABLES........................................................................................................................4 LIST OF FIGURES........ LIST OF APPENDICES.
STUDYINFORMATION.............................................................................................................5
STUDYPERSONNEL..................................................................................................................7 SUMMARY.................................................................................................................................... 8
INTRODUCTION.........................................................................................................................9
MATERIALS AND METHODS ................................................................................................. 9
A. Test Substance and Positive Controls................................................................................. 9 B. Test Species......................................................................................................................... 9 C. Animal Husbandry............................................................................................................ 10
1. Housing Environment.............................................................................................................................10 2. Feed and Water.......................................................................................................................................10 3. Identification.......................................................................................................................................... 10 4. Animal Health Monitoring Program.......................................................................................................10
D. Quarantine and Pretest...................................................................................................... 11 E. Study Design .....................................................................................................................11 F. Assignment to Groups and Study Start............................................................................. 11 G. Dosing Material Preparation and Administration............................................................. 11
1. Test Substance........................................................................................................................................11 2. Positive Controls...................................................................................................................................12 3. Negative Controls...................................................................................................................................12
H. Body Weights.................................................................................................................... 12 I. Mortality and Clinical Observations................................................................................. 12 J. Collection and Analysis of Blood and Livers.................................................................... 12 K. Treatment of Fluorine Data............................................................................................... 13 RESULTS AND DISCUSSION................................................................................................. 14 A. In-Life Toxicology............................................................................................................ 14 B. Fluorine Data..................................................................................................................... 14
1. Factors Influencing Interpretation of Analysis....................................................................................... 14 2. Positive Controls................................................................................................................................... 14 3. Test Substance........................................................................................................................................15
CONCLUSIONS......................................................................................................................... 15
RECORDS AND SAMPLE STORAGE................................................................................... 15
TABLES....................................................................................................................................... 16
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H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
FIGURES ............................................................................................................................ 21
APPENDICES.............................................................................................................................26
LIST OF TABLES
Page
1. MEAN BODY WEIGHTS................................................................................................................................. 17 2. MEAN BODY WEIGHT GAINS........................................................................................................................ 18 3. MEAN BLOOD FLUORINE LEVELS................................................................................................................ 19 4. MEAN BLOOD FLUORINE CONCENTRATION NORMALIZED TO DOSE................................................20
LIST OF FIGURES
Page
1. MEAN BODY WEIGHTS................................................................................................................................... 22 2. MICROMOLAR EQUIVALENTS W RAT BLOOD..........................................................................................23 3. MICROMOLAR EQUIVALENTS IN TEST COMPOUND AND POSITIVE CONTROLS .............................25
LIST OF APPENDICES
Page
A. INDIVIDUAL BODY WEIGHTS.......................................................................................................................27 B. INDIVIDUAL CLINICAL OBSERVATIONS...................................................................................................^ C. ANALYSIS OF BLOOD FLUORINE DATA .....................................................................................................73
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H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
STUDY INFORMATION TEST SUBSTANCE:
Substance Tested:
Synonyms/Codes: H-24018
Haskell Number: 24018
DuPont-2927
POSITIVE CONTROL:
Substance Tested^ Potassium perfluoroalkyi sulfonate Synonyms/Codes. H-24019
Haskell Number: 24019
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study m Rats
DuPont-2927
Known Impurities
POSITIVE CONTROL:
Substance Tested: Octanoic acid, pentadecafluoro-, ammonium salt Synonyms/Codes: H-24020
Perfluorooctanoate, ammonium salt PPOA Ammonium perfluorooctanoate
Haskell Number: 24020
Sponsor:
E. I. du Pont de Nemours and Company Wilmington, Delaware 19898
U.S.A.
Study Initiated/Completed: April 30, 1999 / (see report cover page)
m-Life Initiated/Completed: June 13, 1999 / September 14,1999
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H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
STUDY PERSONNEL
Study Director: Management:
Primary Technician:
Carol Finlay, B.A. Judith C. Stadler, Ph.D., D.A.B.T. Richard P. Mathena
Blood Fluorine Data Analysis: Gary W. Jepson, Ph.D. Management: Matthew S. Bogdanffy, Ph.D., D.A.B.T.
Toxicology Report Preparation: Wanda F. Dinbokowitz
Laboratory Veterinarian: Wanda L. West, D.V.M., A.C.L.A.M.
DuPont-2927
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H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
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SUMMARY
The objective of this study was to evaluate the potential for H-24018, when administered by gavage, to be absorbed and to accumulate in a mammalian system. Six groups of 5 male Crl:CD(SD)IGS BR rats each were exposed to 1000 mg/kg/day of H-24018. The test substance was administered to one group of five rats for 5 consecutive days and to 5 groups for 10 days. Approximately two hours after me first dose, blood was collected from the orbital sinus of each rat from the 5-dose group. On selected days (5,10,13,24, 52,94) 5 rats per group were
euthanized and the blood and livers were collected. Body weights and clinical signs were
recorded on each day of dosing and then approximately every other week during the recovery
period. Additionally, 2 negative controls, corn oil and corn oil/acetone (80:20), and 2 positive controls, H-24019 (10 mg/kg/day) and H-24020 (20 mg/kg/day), were tested as described for H-24018.
One rat dosed with H-24018 was found dead on test day 9. The death of this rat is considered not to be due to the test substance, since no clinical signs oftoxicity were observed and no body weight loss occurred in any of the rats during the study. The death of this rat was probably
caused by a dosing injury.
No compound-related clinical signs oftoxicity were observed in the rats dosed with H-24018. Rats dosed with a positive control material, H-24019, exhibited diarrhea, salivation, alopecia, black ocular discharge, and staining of various parts of the body during the dosing period. Rats dosed with H-24020, the other positive control substance, exhibited wet perineum and diarrhea during the dosing period. Alopecia was observed during the recovery period for rats dosed with H-24018, H-24019, and H-24020. The negative control rats exhibited no clinical signs during
the study.
Comparison of body weights was complicated by a difference in age on test day 1 between the rats dosed with the test substance and those dosed with the positive or negative controls. Accounting for the age difference at study start and the expected rate of body weight gain, the mean body weights and mean body weight gains of the rats dosed with H-24018 were comparable to the negative controls and equal to or greater than the positive controls.
A steady-state for fluorine levels in whole blood may not have been achieved during 10 consecutive days of dosing with 1000 mg/kg H-24018. An area under the curve (estimated to infinity) was calculated and normalized for fluorine content for the test substance and each positive control. The AUCINF/D for the fluorine component of H-24018 was 1402.6, compared
to AUCINF/D values of 566,479.1 and 70,789.6 for H-24019 and H-24020, respectively.
Under the conditions of this study, administration of H-24018 to male rats for 10 consecutive days resulted in limited absorption and retention of fluorine in the blood. Dose-adjusted areas under the curve (AUCINF/D) for positive controls, H-24019 and H-24020, were approximately 400x and 50x the AUCINF/D for the test material.
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INTRODUCTION
The objective of this study was to define the potential of H-24018 to be absorbed and to bioaccumulate in a mammalian system, as indicated by analytical determination of total fluorine
in blood and liver. The test substance was compared to two positive controls that were materials previously shown to bioaccumulate in mammals.
The daily dosage for the test substance was selected based on available toxicity data and the
results of a rangefinding study, m the rangefinding study, a group of 5 male rats was dosed by oral gavage with H-24018 at a dosage of 1000 mg/kg for 5 consecutive days. A group of 5 male
rats was dosed with deionized water for 5 consecutive days and served as controls. The rats
dosed with H-24018 experienced an overall mean body weight gain of 40 grams. The control group had an overall mean body weight gain of 27 grams.
A dosage of 1000 mg/kg was selected for the limit dosage for this project. The limit dosage of
1000 mg/kg was chosen for the main study and was expected to produce less than a 10% difference in mean body weight over 10 days when compared to controls.
All blood samples were analyzed for total fluorine content. This report contains the results of those analyses. Results from analyses of selected liver samples will be presented in a
supplemental report.
MATERIALS AND METHODS
A.
Test Substance and Positive Controls
The test substance, H-24018, was supplied by the sponsor as an amber brown liquid. The positive controls, H-24019 and H-24020, were supplied by the sponsor as white solids. The test substance and positive controls appeared to be stable under the conditions of the study. No evidence of instability, such as a change in color or physical state, was observed.
B.
Test Species
Male Crl:CD(SD)IGS BR rats were received from Charles River Laboratories, Inc., Raleigh, North Carolina. The Crl:CD(SD)IGS BR rat was selected on the basis of extensive experience with this strain and its suitability with respect to longevity, hardiness, sensitivity, and low
incidence of spontaneous diseases.
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C. Animal Husbandry
1.
Housing Environment
Rats were housed singly in stainless steel, wire-mesh cages suspended above cage boards. Animal rooms were maintained on an approximate 12-hour light/dark cycle (fluorescent light)
and at a temperature of 23 1C and a relative humidity of 50 10%. Occasional excursions
outside the accepted ranges were minor and did not affect the study.
2.
Feed and Water
Tap water was provided ad libitum. All rats were fed PMI Nutrition International, me. Certified
Rodent LabDiet 5002 chow. The feed is guaranteed by the manufacturer to meet specified
nutritional requirements and to be free of specified contaminants.
3.
Identification
Prior to assignment to groups, each rat was temporarily identified by cage identification. After assignment to groups, an individual identification number was marked or tattooed on the tail of each rat. The information on the cage labels included the unique 6-digit Haskell animal number
assigned to each rat.
4.
Animal Health Monitoring Program
As specified in the Haskell Laboratory animal health and environmental monitoring program, the following procedures are performed periodically to assure that contaminant levels are below
those that would be expected to impact the scientific integrity of the study:
Water samples are analyzed for total bacterial counts, and the presence ofcoliforms, lead, and other contaminants.
Feed samples are analyzed for total bacterial, spore and fungal counts.
Samples from freshly washed cages and cage racks are analyzed to ensure adequate sanitation by the cagewashers.
Certified animal feed is used, guaranteed by the manufacturer to meet specified nutritional
requirements and not to exceed stated maximum concentrations of key contaminants, including
specified heavy metals, aflatoxin, chlorinated hydrocarbons, and organophosphates. The
presence of these contaminants below the maximum concentration stated by the manufacturer would not be expected to impact the integrity of the study.
The animal health and environmental monitoring program is administered by the attending laboratory animal veterinarian.
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H-24018: Biopersistence Screening 10-Dose Oral Gavage Study m Rats
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D.
Quarantine and Pretest
Upon arrival at Haskell Laboratory, the rats were removed from shipping cartons and quarantined for 6 days. The rats were weighed 3 times during the pretest period and examined daily for any clinically apparent signs of disease or injury. The rats were observed daily for mortality and signs of illness, injury, or abnormal behavior.
On the bases of acceptable body weight gains and freedom from clinically apparent signs of disease or injury, male and female rats were released from quarantine by the laboratory animal
veterinarian or designee.
E.
Study Design
Substance
Vehicle
Negative Controls Corn oil Corn oil: acetone
Positive Controls H-24019
H-24020
Test Substance
H-24018
Not applicable
Corn oil: acetone Corn oil None
Dosage (mg/kg/day)
0 0
10 20
1000
Number of Animals
30 30 30 30 30
F.
Assignment to Groups and Study Start
After the quarantine period, the rats were selected on the bases of adequate body weight gain,
freedom from any clinical signs of disease or injury, and a body weight within 20% of the mean. The selected rats were divided by computerized, stratified randomization into 6 groups of
5 rats, so that there were no statistically significant differences among group body weight means.
After assignment to groups, each rat was housed individually. The last 3 digits of the animal number was marked or tattooed on the tail of each rat. The rats were between 7 and 9 weeks of age at the initiation of dosing. Dosing began on test day 1.
Rats that were not assigned to the study were released for other laboratory purposes, or were sacrificed by carbon dioxide asphyxiation and discarded without pathological evaluation.
G. Dosing Material Preparation and Administration
1.
Test Substance
H-24018 was dosed as received. The amount of test substance each rat received was based on the body weight collected on each day of dosing and the test substance density of 1100 mg/mL.
The test substance was stirred on a magnetic stir plate throughout the dosing procedure.
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2.
Positive Controls
The solid positive control materials were suspended as emulsions in their respective vehicles. Corn oil was used as the vehicle for H-24020. It was necessary to dissolve H-24019 in acetone
before suspending it in corn oil. The ratio of acetone to corn oil was 20:80. The amount each rat received was based on the body weight collected on each day of dosing and the suspension concentration. The dose volumes did not exceed 1 mL/100 g of body weight. The dosing
suspensions were stirred on a magnetic stir plate throughout the dosing procedure to maintain
homogeneity.
3.
Negative Controls
Corn oil and corn oil:acetone (80:20) were chosen as the negative controls because they were the
vehicles for the positive controls. Each negative control rat received 1 mL of corn oil or
corn oil:acetone. These rats were dosed in a separate room from the rats dosed with the test substance or positive controls.
H. Body Weights
The rats were weighed on each day of dosing and then weekly or every other week during the
recovery period.
I.
Mortality and Clinical Observations
Cage-site examinations to detect moribund or dead rats and abnormal behavior and appearance among rats were conducted at least once daily throughout the study. At every weighing, each rat was individually handled and examined for abnormal behavior and appearance.
J.
Collection and Analysis of Blood and Livers
Approximately 2 hours after the first dose, 1-2 mL of blood was collected into EDTA tubes from the orbital sinus of each rat from Group I. At all other selected time points, 5 rats/group were
euthanized by carbon dioxide anesthesia and exsanguination, and the blood and livers were collected according to the following schedules:
Group Dosing Days Tissue Collected
I
1-5
I
1-5
n
1-10
m
1-10
IV
1-10
V
1-10
VI
1-10
Blood Blood and Liver Blood and Liver Blood and Liver Blood and Liver Blood and Liver Blood and Liver
Sampling
Time________________
Test day 1 (2 hours post dosing) Test day 5 at sacrifice (2 hours post dosing) Test day 10 (2 hours post dosing) Test day 13 Test day 24 Test day 52 Test day 94
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H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
Five to 10 mL of blood was collected into EDTA tubes at sacrifice. The livers were weighed.
The blood from all rats was refrigerated, and the livers were frozen. The blood was appropriately packaged and shipped refrigerated to Jackson Laboratory, Deepwater, New Jersey where it was analyzed for total fluorine.
The total fluorine content of the blood samples was determined by using a Wickbold torch combustion method, followed by analysis with a fluoride ion selective electrode. The liquid blood was decomposed or volatilized in the presence of wet oxygen and swept through an oxyhydrogen flame in a closed quartz apparatus. The combustion products were collected in an aqueous absorbing solution and analyzed using a fluoride ion selective electrode. The analytical data (ppm F in each sample) was supplied to Haskell Laboratory for evaluation of fluorine
biopersistence.
K. Treatment of Fluorine Data
Noncompartmental analysis was conducted on blood fluorine data derived from rats dosed with H-24018 by using WinNonlin Version 3.0 software (Pharsight Corp, Mountain View, CA). WinNonlin software provided a means of computing derived pharmacokinetic parameters from data files including area under the curve (AUCINF), Cmax and terminal half-life (Ti/z). The AUCINF (concentration x time) represents the area under the blood concentration curve from the
time of dosing extrapolated to infinity. The maximum observed concentration was Cmax (concentration). The points included in determination of the terminal half-life were selected manually and given in units of time. Since the dosages and fluorine content for each positive
control and the test material varied, all doses were normalized to 0.1 mmole/kg for comparative purposes. The accumulation index (AI, l/O-e'^)) and bioaccumulation index (BI, Cmax x AI) were calculated and reported but not further used.
H-24019 and H-24020 were used as positive controls. Dosing diluents were used as negative
controls, but because of variability and limited sensitivity of the analytical method, the background was set at 0.2 ppm fluorine. Since 0.2 ppm was the fluoride concentration limit of
detection, any values listed as <0.2 ppm were excluded from further treatment.
The percent of fluorine and molecular weight of the test substance and positive controls were used as provided by the sponsor. The measurements resulting from analysis of total blood fluorine were used as received (ppm F) from Jackson Laboratory. Fluoride ion was converted to micromolar (/xM) equivalents of active component for further comparisons. The data and descriptions of data manipulation and presentation are provided in Appendix C.
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H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
RESULTS AND DISCUSSION
DuPont-2927
A.
In-Life Toxicology
(Tables 1 and 2; Figure 1, Appendices A and B)
One rat dosed with H-24018 was found dead on test day 9. The death of this rat is considered not to be due to the test substance, since no clinical signs oftoxicity were observed and no body weight loss occurred in any of the rats during the study. The death of this rat was probably
caused by a dosing injury.
No compound-related clinical signs oftoxicity were observed in the rats dosed with H-24018. Rats dosed with H-24019 exhibited diarrhea, salivation, alopecia, black ocular discharge, and staining of various parts of the body during the dosing period. Rats dosed with H-24020 exhibited wet perineum and diarrhea during the dosing period. Alopecia was observed during the recovery period for rats dosed with H-24019 and H-24020. The negative control rats exhibited no clinical signs during the study.
The mean body weights and mean body weight gains of the rats dosed with H-24018 were comparable to the corn oil controls throughout the study. The mean body weights and mean body weight gains of the rats with H-24018 were greater than the H-24020 positive control rats. Comparison of body weights between the H-24018 rats and the H-24019 positive control and corn oiVacetone negative control rats was complicated by the fact that there was a difference in age on test day 1. This difference resulted in differences in mean body weights on test day 1. The rats dosed with the test substance, H-24018, were younger and lighter in weight than the corn oil/acetone negative control and H-24019 positive control rats. Accounting for the age difference at study start and the expected rate of body weight gain, it appears that the mean body weights and mean body weight gains of the rats dosed with H-24018 was comparable to the corn oiVacetone negative controls and equal to or greater than the H-24019 positive controls.
B.
Fluorine Data
(Tables 3 and 4; Figures 2 and 3; Appendix C)
1.
Factors Influencing Interpretation of Analysis
The data used in the kinetic analysis were derived from a limited screen, and therefore several
caveats and considerations are important. A couple of considerations of particular importance are (1) a single dose was used and kinetics may or may not be linear, (2) the kinetics apply only to blood, (3) steady-state may not have been achieved, and (4) the sample size is low and may impact calculation of the terminal half-life. A more complete list of considerations is shown in
Appendix C.
2.
Positive Controls
The positive controls were H-24019 and H-24020. The H-24019 normalized IJI.M equivalents in rat blood continued to rise throughout the dosing period and may not have reached steady-state
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H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
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(Figure 2A). The Cmax for H-24019 was 989.85 116.90 ppm (Mean SD) with a terminal
half-life of 40.5 days. The H-24019 AI was 59.0 and the BI was 58382.2. The H-24020 normalized jjiM equivalents in rat blood peaked after 5 days of dosing and then decreased
throughout the dosing period (Figure 2B). The Cmax for H-24020 was 518.12 44.89 ppm
(Mean SD) with a terminal half-life of 8.3 days. The H-24020 AI was 12.5 and the BI was 6497.5. For each of the positive controls, blood was sampled at seven time points throughout the study, with only four of them occurring post-dose. The small sample size and analytical
variability should be taken into account when using the derived terminal half-life for comparative purposes. The total internal exposure resulting from a normalized dose was described by AUCINF/D and was the basis for comparison between positive controls and the test material.
The AUCINF/D for the fluorine component was 566,479.1 for H-24019 and 70,789.6 for
H-24020.
3.
Test Substance
The H-24018 normalized /zM equivalents for fluorine in rat blood continued to rise throughout
the dosing period and may not have reached steady-state (Figure 2C). The Cmax for H-24018 was 6.140 1.389 ppm (Mean SD) with a terminal half-life of 29.1 days. Blood was sampled at seven time points throughout the study, with only four of those occurring post-dose. The small sample size and analytical variability should be taken into account when using the derived terminal half-life for comparative purposes. The H-24018 accumulation index (AI) was 42.5 and the bioaccumulation index (BI) was 261.1 ppm. The total internal exposure resulting from a normalized dose was described by AUCINF/D and was the basis for comparison between H-24018 and positive controls. The AUCINF/D for the fluorine component of H-24018 was 1402.6 as compared to AUCINF/D values of 566,479.1 and 70,789.6 for H-24019 and H-24020, respectively. The data, calculations and equations are shown in Appendix C.
CONCLUSIONS
Rats dosed for 10 consecutive days with 1000 mg/kg H-24018 exhibited no test substance-related mortality or clinical signs oftoxicity and had mean body weight gains that were comparable to the negative control rats. A steady state for fluorine in the blood may not have been achieved for H-24018 during the 10-day dosing period.
Under the conditions of this study, administration of H-24018 to male rats for 10 consecutive days resulted in limited absorption and retention of fluorine in the blood. Dose-adjusted areas under the curve (AUCINF/D) for positive controls, H-24019 and H-24020, were approximately 400x and 50x the AUCINF/D for the test material.RECORDS AND SAMPLE STORAGE
Specimens (if applicable), raw data, and the final report will be retained at Haskell Laboratory,
Newark, Delaware, or at Iron Mountain Records Management, Wilmington, Delaware.
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H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
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TABLES
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H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
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TABLE 1 MEAN BODY WEIGHTS (g)
Test Days 1
2 3 4 5 6 7 8 9 10 13
20 24 27 34 38 41 47 48 52
55 61 62 68 69 76 80 81 82 88 90 94
Negiitive Controls
Corn Oil 229.8 234.1
Corn OihAcetone 297.6 299.6
241.4 250.4 259.3 266.8 271.2 281.9 285.2 295.9 321.1
309.4 314.3 321.5 326.0 334.9 339.2 345.2 351.7 350.7
350.5 378.3
369.8 401.0
-
-
407.8
411.4
-
-
434.5
-
454.9
-
-
-
464.7 487.0 505.1
527.6
-
-
-
515.4
-
-
-
-
539.0
-
-
-
-
-
-
-
556.2 566.9
-
562.2 567.8
Indicates that the animal was not weighed.
Positive Controls
H-24019 291.5 291.5 298.3 304.1 308.6 312.7 317.5 317.3 318.4 318.9 329.1 359.7 387.9 393.9 416.9
H-24020 227.5 232.4 242.0 248.9 252.4 259.8 263.3 269.8 278.5 283.9 289.1 311.3 340.9
-
402.9
-
-
-
425.0
-
438.2
-
-
438.1
-
-
523.4
-
465.6 452.3 465.8
-
470.9
-
-
563.4 570.7
-
-
499.2
-
-
-
585.3 597.9
-
527.8 538.7
Test Substance H-24018 234.6 240.8 250.5 258.1 267.2 275.9 283.1 285.3 298.6 306.0 333.8 362.2 406.6
-
432.5 453.9
-
-
483.5 488.9 511.6 530.4
-
-
545.5
-
-
-
570.6 583.1
-
596.5
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TABLE 2 MEAN BODY WEIGHT GAINS (g)
Test Days 1-5 1-10
10-13 10-24 10-52 10-94
Negative Controls
Corn Oil 29.5 66.1
Corn Oil:Acetone 23.9 54.1
25.2 82.4 168.8 271.0
-1.0 49.3 175.9 216.1
Positive Controls
H-24019 H-24020
17.1 27.4 10.2 69.0 119.2
279.0
24.9 56.4
5.2 57.0 181.7 254.8
Test Substance
H-24018 32.6 71.4 27.8
100.6 182.9 290.5
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TABLES MEAN BLOOD FLUORINE LEVELS
Test Days
1 5 10 13
24 52 94
Negative Controls
Corn Oil ppm
<0.2 <0.2 <0.2
0.2s (0.1)
<0.2
0.3^0.1) 0.3a(0.l)
(^om Oil:Acetone
ppm <0.2
00..23s (0.1)''
0.6s (0.6)
O^
0.2 0.2
Positive Controls
H-24019
ppm 2.1 (0.9) 48.8 (17.6) 61.7 (2.8) 64.5 (7.6) 42.2 (2.8) 26.9 (2.6) 13.2 (2.1)
H-24020
ppm 62.6 (3.2) 71.7 (6.2) 54.2 (7.8)
26.6(11.4) 10.5 (3.0) 0.9 (0.2) 0.20 (0.1)
a Mean of 4 of the 5 values. One of the values was below the LOD.
b Standard deviation is in parentheses.
c Mean of 3 of the 5 values. Two of the values were below the LOD. d One value. Four of the values were below the LOD.
Test Substance
H-24018 ppm
2.9(1.1) 9.0 (0.6) 10.6 (2.4) 5.7 (0.9) 2.5 (0.2) 6.6 (0.3) 0.6 (0.3)
-19-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
TABLE 4
MEAN BLOOD FLUORINE CONCENTRATION NORMALIZED TO DOSE
Test Days
1 5 10 13 24 52 94
Positive Controls
Test Substance
H-24019 /zM F Equivalents
28.92 (13.3) 747.69 (271.5) 945.85 (43.5) 989.85(116.9) 645.54 (42.9) 411.38 (40.6) 195.38 (32.5)
H-24020 fJiM F Equivalents
89.28 (23.4) 518.12 (44.9) 391.01 (56.8) 191.45(82.7)
74.35 (22.1) 4.64 (1.1) 0.24 (0.4)
H-24018 /AM F Equivalents
1.6 (0.62)" 5.2 (0.33) 6.1 (1.39) 3.2 (0.52)
1.^(0.12)
0.7 (0.15) 0.3 (0.15)
a Standard deviation is in parentheses.
b Mean of 4 of the 5 values. One of the rats was found dead on test day 9.
-20-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
FIGURES
-21-
QyMpsssy Saartteed. Vwss BoaewtehB weA 81
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study m Rats
400
350 -i
300
@ 250
*-*
to
S
?. 200 S 150
100
FIGURE 1 MEAN BODY WEIGHTS (g)
--^--Negative Control (Corn O --B--Negative Control (Corn O --A--Positive Control H-24019 --^--Positive Control H-24020 --9K-Test Substance H-24018
Test Days
10
12
-22.
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
FIGURE 2 MICROMOLAR EQUIVALENTS IN RAT BLOOD
A. Normalized Rat Blood H-24019 fiM Equivalents Resulting from a 10-Day 0 ral Gavage
Micromolar (^M) equivalents of H-24019 (positive control) in rat blood resulting from a 10-day
oral gavage exposure. Values are means and error bars are standard deviation. B. Normalized Rat Blood H-24020 f(M Equivalents Resulting from a 10-Day 0 ralG avage
Micromolar (jaM) equivalents of H-24020 (positive control) in rat blood resulting from a 10-day
oral gavage exposure. Values are means and error bars are standard deviation. -23-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
C. Normalized Rat Blood H-24018 itM Equivalents Resulting from a 10-Day Oral Gavage
Micromolar (/AM) equivalents of H-24018 (test substance) in rat blood resulting from a 10-day
oral gavage exposure. Values are means and error bars are standard deviation.
-24-
H-24018: Biopersistence Screening 10-Dose Oral Oavage Study in Rats
FIGURES MICROMOLAR EQUIVALENTS IN TEST COMPOUND AND POSITIVE CONTROLS
-25-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
APPENDICES
-26.
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
APPENDIX A Individual Body Weights
-27-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
INDIVIDUAL BODY WEIGHTS
ABBREVIATIONS:
PD SD -
found dead
sacrificed by design
EXPLANATORY NOTES
DuPont-2927
-28-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
627789 627801 627805 627810 627818
DAY 1
222.6 215.9 249.4 230.5 229.7
DAY 2
220.7 209.1 250.1 231.6 228.6
CORN OIL (NEGATIVE CONTROL) INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP I
DAY 3
DAY 4
DAY 5
223.5
223.5 263.3 241.9 239.1
236.9 233.5 273.6 254.4 252.4
247.7 240.1 283.7 265.0
260.2
SD test day 5 SD test day 5 SD test day 5 SD test day 5 SD test day 5
-29-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
627793 627797 627799 627800 627808
ANIMAL NUMBER
627793 627797 627799 627800 627808
DAY 1
214. 8 239. 9 228. 9 246. 9 235. 6
DAY 2
224 .4 245 .9 231 .4 252 .8 241 .6
DAY 8
270. 6 303. 9 280. 2 312. 0 303. 6
DAY 9
274 .9 305 .1 284 .3 315 .4 305 .7
CORN OIL (NEGATIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OP MALE RATS
GROUP II
TEST r )AYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
232.1 257.3 242.3 265.2 250.1
243.1 267.5 246.2 279.3 262.1
TEST DAYS DAY 10
249. 9
280. 7 258. 9 283. 6
270. 4
257.0 288.0 261.5 295.5 284.1
262.0 290.9 266.4 300.1
287.4
283.5 324.2 294.7 331.3
321.8
SD test day 10 SD test day 10 SD test day 10 SD test day 10 SD test day 10
-30-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
627796 627806 627807 627809 627816
ANIMAL NUMBER
627796 627806 627807 627809 627816
DAY 1
239 .8 227 .3 221 .5 234 .2 235 .0
DAY 2
249 .7 234 .2 225 .9 240 .4 238 .6
DAY 8
285 .9 282 .8 270 .7 297 .9 291 .8
DAY 9
290 .1 285 .8 274 .7 300 .2 296 .4
CORK OIL (NEGATIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OP MALE RATS
GROUP III
TEST I )AYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
253.6 239.4 237.1 252.5 250.0
252 .5 242 .9 244 .1 260 .3 258 .9
267.7
258.5 254.9 272.8 265.1
277. 2 270. 4
257. 7 277. 9 274. 5
289 .8 275 .2 260 .3 282 .6 278 .6
TEST DAYS
DAY 10
DAY 13
300.0 302.8 280.7 311.9
305.7
322 .7 320 .3 305 .2 336 .2 330 .2
SD test day 13 SD test day 13 SD test day 13 SD test day 13 SD test day 13
-31
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
627791 627794 627804 627812 627817
ANIMAL NUMBER
627791 627794 627804 627812 627817
DAY 1
231 .1 224 .4 224 .7 221 .9 233 .5
DAY 2
235.4 233.0 228.8 231.5 231.3
DAY 8
274 .0 286 .1 267 .2 278 .2 m .8
DAY 9
279.1 289.5 270.6 282.7 280.4
CORK OIL (NEGATIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP IV
TEST r )AYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
241.2 238.1 230.6 236.3 229.0
246.8 247.8 243.0 245.7 244.8
TEST DAYS
DAY 10
DAY 13
255.9 260.0 251.7 255.5 255.4
DAY 20
262.6 267.4 252.9 264.9 266.4
DAY 24
268.4
270.1 259.5 269.5 270.0
285.0
a
295.4
^a
278.1
a
294.3
^a
294.6
a
334.4 377.4 345.8 356.5 368.7
365.6 416.7 378.1 388.4 407.3
SD test day 24 SD test day 24 SD test day 24 SD test day 24 SD test day 24
a Rat was not weighed.
-32.
''/-'
H-24018: Biopersistence Screening
10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
627792 627798 627813 627814 627815
ANIMAL NUMBER
627792 627798 627813 627814 627815
ANIMAL NUMBER
627792 627798 627813 627814 627815
DAY 1
235 .8 241 .1 214 .8 217 .5 230 .1
DAY 2
240 .8 253 .4 219 .2 220 .5 242 .2
DAY 8
282 .4 294 .3 258 .7 248 .0 289 .2
DAY 9
286 .4 296 .3 259 .2 250 .7 293 .4
DAY 41 456 .5 470 .7 395 .0 358 .7 462 .6
DAY 47 482 .3 496 .9 407 .2
372 .7 487 .3
CORN OIL (NEGATIVE CONTROL) INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP V
TEST E>AYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
244.3 257.6 220.5 223.7 243.8
247.9 266.1 233.2 225.2 255.7
TEST DAYS
DAY 10
DAY 13
252 .5 272 .9 239 .8 233 .8 265 .0 DAY 20
264 .4 281 .9 243 .2 236 .7 270 .0 DAY 24
268.1 286.2 246.8 240.6 274.1
DAY 34
295.2
a
315.7
^a
267.9
a
257.3
a
303.3
a
TEST DAYS DAY 52
360 .0 380 .2 323 .6 299 .3 368 .3
389 .2 403 .5 342 .3 319 .4 396 .5
426.1 443.1 367.9 343.7 434.9
496.8 517.3 416.8 386.9 505.9
SD test day 52 SD test day 52 SD test day 52 SD test day 52 SD test day 52
a Rat was not weighed.
-33.
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
DAY 1
DAY 2
CORN OIL (NEGATIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP VI
TEST I:)AYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
627795 627811 627819 627820 627821
218.0 228.6 248.8 225.5 227.5
219.5 226.3
255.3 228.9 233.2
225.3 236.7 264.9 239.2 240.7
234.3 246.1 274.4 247.9 246.1
239.4 251.5 280.4 255.6 251.2
246.2 259.6 288.0 261.3 259.8
250.1
263.6 290.3 265.3 263.9
ANIMAL
NUMBER
DAY 8
DAY 9
TEST DAYS
DAY 10
DAY 13
DAY 20
DAY 24
DAY 34
627795 627811 627819 627820 627821
261.4
265.0
270.7
a
273.0
276.7
285.6
a
304.5
308.0
324.3
a
281.3
282.9
292.4
^a
272.6
275.3
281.8
a
308.0 337.8 399.7 367.2 330.1
329.8 360.6 431.2 393.0 352.9
362.0 396.4 472.5
445.5 385.6
ANIMAL NUMBER
DAY 41
DAY 47
TEST DAYS
DAY 52
DAY 55
DAY 61
DAY 68
627795 627811 627819 627820 627821
384.2
398.0
a
411.1
435.7
440.7
422.0
439.3
a
455.4
463.0
473.6
505.9
534.9
a
551.7
574.4
588.6
478.0
504.1
a
529.7
547.1
558.6
411.8
426.1
a
439.1
459.0
463.3
a Rat was not weighed.
-34-
^ -i''^'.' ^.sLy''
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
DAY 90
DAY 94
CORN OIL (NEGATIVE CONTROL) INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP VI
TEST DAYS
627795 627811 627819 627820 627821
474.6 503.6 638.1 608.6 509.0
485.0
511.6 653.1 618.0 521.5
SD test day 94 SD test day 94 SD test day 94 SD test day 94 SD test day 94
-35.
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study m Rats
ANIMAL
NUMBER
625361 625363 625364 625380 625383
DAY 1
322.6 273.7 291.1 289.4 304.7
DAY 2
325.0 271.4 290.9 286.2 299.7
CORN OIL:ACETONE (NEGATIVE CONTROL) INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP I
DAY 3
DAY 4
DAY 5
337.6 278.4 299.9
291.5 302.7
340.3 281.7
306.0 300.1 310.7
349.7 286.7 312.0 305.5 313.1
SD test day 5 SD test day 5 SD test day 5 SD test day 5 SD test day 5
-36-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
625355 625362 625367 625368 625378
ANIMAL NUMBER
625355 625362 625367 625368 625378
DAY 1
280 .0 290 .3 301 .5 312 .3 309 .6
DAY 2
282 .0 294 .1 307 .8 318 .0 306 .4
DAY 8
321 .7 323 .9 349 .1 364 .2 350 .1
DAY 9
320 .9 332 .3 352 .4 380 .8 354 .2
CORN OIL:ACETONE (NEGATIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP II
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
293.0 303.5 315.6 326.0 327.3
297.9 308.9
320.1 336.4 328.4
TEST DAYS DAY 10
306 .1 313 .8 327 .7 343 .7 333 .7
311. 2
315. 8 333. 7 347. 5 336. 6
315.7
323.8 345.6 360.8 346.9
333.6 332.9 363.8 386.7 365.4
SD test day 10 SD test day 10 SD test day 10 SD test day 10 SD test day 10
-37-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
625357 625358 625370 625384 625385
ANIMAL NUMBER
625357 625358 625370 625384 625385
DAY 1
311 .9 285 .7 307 .9 294 .2 297 .6
DAY 2
308 .8 286 .3 316 .7 300 .0 304 .6
DAY 8
364 .2 319 .8 373 .4 325 .6 347 .0
DAY 9
370 .3 321 .6 374 .7 331 .0 349 .5
CORN OIL:ACETONE (NEGATIVE Control)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP III
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
320.3 295.5
329.5 312.0 313.0
328.4
296.4 337.9 309.3 320.4
TEST DAYS
DAY 10
DAY 13
340.5
306.0 346.9 316.3 331-9
343.3
302.7 349.8 314.1 334.0
361 .1 309 .2 364 .1 321 .4 345 .4
376.9 320.3 385.6 340.6
358.9
405.6 340.7 407.0 357.1 377.6
SD test day 13 SD test day 13 SD test day 13 SD test day 13 SD test day 13
-38-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
625354 625365 625371 625376 625381
ANIMAL NUMBER
625354 625365 625371 625376 625381
DAY 1
303.0 327.7 294.5 289.7 297.8
DAY 2
304.1 328.7 299.0 289.9 297.5
DAY 8
336.2 370.5 340.3 331.5 321.6
DAY 9
337.0 379.3 345.9 339.0 329.1
CORN OIL:ACETONE (NEGATIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP IV
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
310.5 337.9 313.4 302.2
301.7
312.2 343.6 318.3 304.9 305.6
TEST DAYS
DAY 10
DAY 13
319.3 357.7 321.8 313.2 314.4
DAY 20
324.7 357.2 329.6 317.0 314.4
DAY 24
331.2 364.3 338.5 322.8 321.0
348.8 381.2 351.2 345.2
331.6
355.8 407.1 372.6 363.2
341.2
377.7 438.2 413.0 399.7 358.2
396.1 459.6 447.3 432.9
381.8
SD test day 24 SD test day 24 SD test day 24 SD test day 24 SD test day 24
-39-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
DAY 1
DAY 2
CORN OIL:ACETONE (NEGATIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP V
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
625356 625359 625360 625372 625374
ANIMAL
NUMBER
291.7 297.9 296.8 294.8 295.9
DAY 8
291.2 303.3 300.7 298.8 302.2
DAY 9
304.5 314.0
308.5 310.6 312.1
307.0 315.0 312.7 317.4 321.7
TEST DAYS
DAY 10
DAY 13
316 .9 323 .5 319 .1 324 .0 323 .4
DAY 20
319 .8 323 .5 332 .2 329 .0 328 .3 DAY 24
323.9 333.9 339.5 335.6 337.2
DAY 27
625356 625359 625360 625372 625374
ANIMAL NUMBER
625356 625359 625360 625372 625374
328.8
334.7
341.3
361.9
396 .7
a
339.1
346.2
353.6
372.9
410 .0
a
347.9
354.3
363.4
381.7
419 .8
a
344.7
348.8
355.1
373.1
395 .1
a
.338.0
344.6
350.8
371.5
401 .3
^a
DAY 34
466.2 467.7 484.1 454.7 466.8
DAY 52
533.7 530.3 555.4 506.2 512.3
TEST DAYS
SD test day 52 SD test day 52 SD test day 52 SD test day 52 SD test day 52
431.3 440.9 465.9 432.1 447.2
a Rat was not weighed.
-40-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
625353 625369 625373 625375 625377
ANIMAL NUMBER
625353 625369 625373 625375 625377
ANIMAL NUMBER
625353 625369 625373 625375 625377
DAY 1
305 .9 281 .7 294 .6 289 .1 293 .9
DAY 2
307 .3 279 .9 301 .3 291 .0 294 .8
DAY 8
344 .7 307 .3 340 .6 324 .7 325 .0
DAY 9
352 .7 311 .9 348 .2 336 .0 333 .7
DAY 34 453 .3 388 .2 477 .1 455 .6 419 .1
DAY 52
a a a a a
CORN OIL:ACETONE (NEGATIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP VI
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
316.8 289.7 312.7 298.0 302.9
325. 0
286. 9 317. 0 307. 0
312. 0
TEST DAYS
DAY 10
DAY 13
331.7 292.8 325.4 309.6 318.0
DAY 20
330.1 295.3 329.0 314.2 317.4
DAY 24
342. 5 303. 8 334. 6 323. 5 325. 0
DAY 27
358.1
371. 7
399.1
a
317.2
331. 1
347.6
a
352.6
371. 5
402.3
^a
336.9
350. 1
387.9
a
340.7
353. 5
376.3
a
TEST DAYS
DAY 76
DAY 90
DAY 94
427 .7 374 .9 444 .6 432 .3 405 .2
544.9 483.8 628.8 567.3 470.3
562 .8 505 .3 661 .3 589 .8 492 .0
565.3 514.8 673.7 588.8 496.6
SD test day 94 SD test day 94 SD test day 94 SD test day 94 SD test day 94
a Rat was not weighed.
-41
w
H-24018: B iopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
625322 625323 625336 625343 625349
DAY 1
290.3 285.0 316.5 288.2 303.6
DAY 2
283.7 285.5 313.5 281.9 295.9
H-24019 (POSITIVE CONTROL) INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP I
DAY 3
DAY 4
DAY 5
291.5 290.2 320.1 286.8 308.2
298.9 290.9
327.1 291.0 310.1
298.0 294.0 329.0 293.7 318.1
SD test day 5 SD test day 5 SD test day 5 SD test day 5 SD test day 5
-42-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
625320 625330 625332 625341 625350
ANIMAL NUMBER
625320 625330 625332 625341 625350
DAY 1
279 .3 286 .7 300 .0 304 .9 257 .1
DAY 2
283 .0 286 .1 295 .9 309 .0 268 .5
DAY 8
308 .5 314 .0 324 .1 332 .4 279 .8
DAY 9
306 .3 312 .6 321 .8 320 .3 282 .5
H-24019 (POSITIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP II
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
287.7 291.1 304.1 317.5 267.3
288.4 296.5 308.8 320.0 272.2
TEST DAYS DAY 10
295 .9 304 .0 315 .0 325 .1 272 .6
299 .4 302 .3 322 .4 327 .5 276 .3
300.6 306.7 320.7 327.4 283.6
312.1 310.1 318.3 325.6 284.3
SD test day 10 SD test day 10 SD test day 10 SD test day 10 SD test day 10
-43-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
625321 625327 625342 625345 625348
ANIMAL NUMBER
625321 625327 625342 625345 625348
DAY 1
307 .0 311 .4 273 .7 291 .2 265 .5
DAY 2
307 .8 306 .6 275 .5 291 .7 258 .6
DAY 8
337 .8 334 .3 304 .3 317 .3 302 .7
DAY 9
339 .6 337 .0 305 .9 312 .9 306 .5
H-24019 (POSITIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE KATS
GROUP III
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
311.4
312.5 282.3 297.3 268.0
319 .6 317 .8 285 .8 303 .3 275 .2
TEST DAYS
DAY 10
DAY 13
322.3
318.3 290.8 306.4 280.1
328 .4 319 .3 294 .2 310 .4 285 .2
335.2
327.6 326.6 316.1 290.6
346.1 336.3 307.8 315.0
309.7
371 .2 355 .3 324 .4 336 .9 336 .4
SD test day 13 SD test day 13 SD test day 13 SD test day 13 SD test day 13
-44.
' WH-24018: Biopersistence Screening
10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
DAY 1
DAY 2
H-24019 (POSITIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP IV
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
625325 625328 625338 625340 625352
ANIMAL NUMBER
625325 625328 625338 625340 625352
282.8 315.6 264.6 304.0 285.5
DAY 8
318.6 352.0 287.4 347.0 .316.9
285.9 315.2 261.9 309.2 283.9
DAY 9
321.9 351.7 291.3 352.2 322.3
291.7 323.9 268.5 316.9 289.1
295.5
327.7 272.6 326.0 299.6
TEST DAYS
DAY 10
DAY 13
327.4 357.5 290.2 359.2 321.0
331.6 367.4 291.1 368.1 329.6
303.2 335.0 275.7 329.8 307.9
DAY 20
355.8 400.2 320.4 389.3 355.7
309 .2 340 .4 281 .9 334 .1 308 .2
308.3 340.1 284.4 338.4 312.4
DAY 24
381 .3 423 .9 339 .9 419 .0 375 .3
SD test day 24 SD test day 24 SD test day 24 SD test day 24 SD test day 24
-45-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
DAY 1
DAY 2
H-24019 (POSITIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP V
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
625324 625329 625333 625334 625344
ANIMAL NUMBER
303.0 318.9 292.4 274.6 262.9
DAY 8
298.5 316.3 291.2 277.0 262.2
DAY 9
305.8 326.5 297.8 286.4 269.0
312.1 335.4 304.1 290.6 273.5
TEST DAYS
DAY 10
DAY 13
320 .1 338 .3 307 .7 292 .0 274 .5
DAY 20
322.8 346.7 312.0 300.1 284.1
DAY 24
326.8 351.6 313.5 304.2
DAY 27
625324 625329 625333 625334 625344
ANIMAL NUMBER
332.5
337.9
336.1
299.6
336 .0
^a
352.5
360.1
357.0
364.3
396 .4
a
315.8
316.7
319.3
325.8
349 .2
a
292.6
302.2
305.8
312.0
338 .6
^a
280.7
285.2
289.3
295.8
309 .7
a
DAY 34
DAY 52
TEST DAYS
380.3 423.3 375.2 368.8 330.4
625324 625329 625333 625334 625344
397.3 442.7 384.6
384.2 348.3
447.4 498.1 427.4 426.5
391.0
SD test day 52 SD test day 52 SD test day 52 SD test day 52 SD test day 52
a Rat was not weighed.
-46.
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
DAY 1
DAY 2
H-24019 (POSITIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP VI
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
625326 625335 625346 625347 625351
ANIMAL NUMBER
313.2 301.0 290.2 266.0 310.6
DAY 8
317.1 303.6 293.4 275.6 310.9
DAY 9
325.5 302.3 300.2
287.7 321.1
330.9 310.4 309.5 300.0 329.6
TEST DAYS
DAY 10
DAY 13
336.2 315.1 313.5 308.5 338.2
DAY 20
336.0 299.6 318.6 316.6 341.6
DAY 24
293 .6 326 .0 326 .9 340 .7 DAY 27
625326 625335 625346 625347 625351
ANIMAL NUMBER
311.5 294.2 292.9 330.5 351.1
DAY 34
308.9 285.3 290.8 330.1 357.8
DAY 52
297.5 274.0 288.4 333.0 350.5
274.2 266.3 296.9 355.7 380.0
TEST DAYS
DAY 62
DAY 76
335.4 340.1 352.5 402.1 413.7
DAY 80
a
^a
a a a
DAY 90
390 .7 393 .8 388 .2 436 .2 452 .4 DAY 94
625326 625335 625346 625347 625351
427.5
a
427.0
a
407.4
a
466.4
a
483.3
--a
497.5 506.0 485.8
568.6 559.0
540.0 538.6 523.7 617.8
596.8
547.9 547.7 532.8 618.1 607.2
565.2 562.1 542.4
632.6 624.0
577 .5 579 .5 556 .9 638 .9 636 .8
SD test da SD test da SD test da SD test da SD test da
a Rat was not weighed.
-47-
^aar
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
627756 627767 627771 627773 627777
DAY 1
227.2 227.0 219.5 246.8 225.4
DAY 2
226.4 231.8 214.7 244.4 221.4
H-24020 (POSITIVE CONTROL) INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP I
DAY 3
DAY 4
DAY 5
233.4 237.9 226.1 252.7 232.9
238.6
245.8 233.5 263.8 239.4
237.5 248.6 239.6 262.3
236.0
SD test day 5 SD test day 5 SD test day 5 SD test day 5 SD test day 5
-48-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
627768 627774 627776 627782 627785
ANIMAL NUMBER
627768 627774 627776 627782 627785
DAY 1
236 .9 258 .6 212 .0 221 .6 220 .3
DAY 2
244 .1 261 .6 216 .3 228 .3 221 .7
DAY 8
272 .3 319 .8 246 .1 251 .0 260 .7
DAY 9
291 .9 326 .3 252 .3 264 .0 268 .5
H-24020 (POSITIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP II
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
245.2 275.8 223.7 237.3 234.7
256.5
283.4 226.6 239.0 238.4
TEST DAYS DAY 10
256.2 289.3 229.6 238.8 241.8
265 .5 301 .5 233 .7 244 .7 250 .5
271 .4 303 .2 236 .9 246 .7 255 .6
293.5 338.2 254.4 268.2 267.9
SD test day 10 SD test day 10 SD test day 10 SD test day 10 SD test day 10
-49-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
627758 627763 627764 627787 627788
ANIMAL NUMBER
627758 627763 627764 627787 627788
DAY 1
235. 1 212. 1 230. 0 235. 1 219. 4
DAY 2
240 .3 218 .3 235 .0 241 .0 222 .3
DAY 8
280. 6 255. 2 275. 8 221. 7 274. 1
DAY 9
283 .6 261 .2 281 .9 235 .7 276 .9
H-24020 (POSITIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE HATS
GROUP III
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
248.6 226.5 246.1
250.1 232.2
255.8 234.3 251.3 257.2 239.6
TEST DAYS
DAY 10
DAY 13
261.2 230.8
254.8 258.6 247.6
272 .0 235 .5 261 .7 237 .6 256 .7
276 .1 238 .0 264 .7 240 .3 257 .9
295.8 272.5 288.0
234.7 284.8
308.7
285.8 306.7 234.9
309.4
SD test day 13 SD test day 13 SD test day 13 SD test day 13 SD test day 13
50-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
627759 627761 627770 627779 627786
ANIMAL NUMBER
627759 627761 627770 627779 627786
DAY 1
226.6 240.7 235.6 231.5 211.6
DAY 2
232.9 247.4 244.3 237.9 218.2
DAY 8
277.8 240.1 291.4 289.0 251.3
DAY 9
284.9 257.4 301.3 293.4 255.8
H-24020 (POSITIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP IV
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
241.4 257.1 253.6 252.6 222.5
250.9 262.5 260.1 261.4 230.4
TEST DAYS
DAY 10
DAY 13
254.2 266.7 267.7 262.3 230.6
DAY 20
262.1 259.2 277.3 273.8 240.6
DAY 24
265. 4 262. 6
279. 8 277. 5 244. 1
288.0
a
266.9
^a
306.4
^a
301.0
a
257.0
-a
348.0 335.7 355.8 374.4 304.4
380.1 359.4 379.8 406.2 326.1
SD test day 24 SD test day 24 SD test day 24 SD test day 24 SD test day 24
a Rat was not weighed.
-51
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
DAY 1
DAY 2
H-24020 (POSITIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE HATS
GROUP V
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
627757 627760 627765 627772 627781
ANIMAL
NUMBER
221.2 226.2 228.3 245.2 219.0
DAY 8
225.4 232.0 235.3 256.4 226.3
DAY 9
236.3 244.4 247.1 266.2 236.5
241.1 251.7 251.6 277.0 242.9
TEST DAYS
DAY 10
DAY 13
247.9 260.2 256.4 276.9 247.2
DAY 20
252 .2 254 .5 261 .1 285 .0 251 .6 DAY 24
254.4 258.3 264.7 291.0 256.1
DAY 34
627757 627760 627765 627772 627781
ANIMAL
NUMBER
269.1 262.6 271.5 300.9 258.1
DAY 41
276.7 280.3 282.4 307.5 266.8
DAY 47
279.7
a
287.3
^a
288.1
^a
317.0
a
271.2
a
TEST DAYS DAY 52
324.3 348.6 349.8 375.5 315.1
343 .0 379 .9 382 .7 404 .0 338 .8
372.3 419.4 400.9 446.9 372.0
627757 627760 627765 627772 627781
402.8 437.7 422.9 478.4 389.9
419.7 448.9 444.8 494.3
408.2
436.7 456.5 455.6 513.5 421.0
SD test day 52 SD test day 52 SD test day 52 SD test day 52 SD test day 52
a Rat was not weighed.
-52.
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
DAY 1
DAY 2
H-24020 (POSITIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP VI
TEST DAYS
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
627762 627769 627775 627778 627783
ANIMAL NUMBER
227.2 231.1 224.7 213.1 216.4
DAY 8
235.0 241.1 235.7 217.4 218.2
DAY 9
248.7
255.9 246.8 221.3 226.6
257.3 264.2
254.7 225.5 232.0
TEST DAYS
DAY 10
DAY 13
263.0 272.3 265.7 230.1 238.0
DAY 20
275.1 286.3 276.7 236.9 243.9
DAY 24
279.7 289.9 280.2 240.4 247.6
DAY 34
627762 627769 627775 627778 627783
ANIMAL
NUMBER
285.9 302.0 286.6 244.8 256.6
DAY 41
299.1 309.6 296.0 250.8 259.2
DAY 47
301.5
a
312.5
a
304.5
a
255.1
^a
264.3
a
TEST DAYS
DAY 52
DAY 55
356.5 386.6 353.3 294.0 311.3
DAY 61
381.5 414.4 377.4 320.0 340.9
DAY 68
419.6 456.5 413.9 347.1 380.0
627762 627769 627775 627778 627783
438.7
439.9
a
479.7
474.6
a
433.2
451.1
^a
356.8
373.5
^a
409.6
426-9
a
453.5 512.2 460.8 386.0 449.0
473.0 511.4 477.4 393.3
473.8
471.6 531.4 478.6 398.3 474.8
a Rat was not weighed.
-53.
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
627762 627769 627775 627778
DAY 81
DAY 90
500.3 566.2
510.4 410.1
523.3 603.2 537.5 436.5
H-24020 (POSITIVE CONTROL)
INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
TEST DAYS DAY 94
GROUP VI
528.6
609.6 552.8 445.3
SD test day 94 SD test day 94 SD test day 94 SD test day 94
-54-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
627252 627253 627260 627273 627274
DAY 1
222.5 237.4 232.6 261.1 221.4
DAY 2
224.6 241.2 231.0 259.7 224.9
H-24018 (TEST SUBSTANCE) INDIVIDUAL BODY WEIGHTS (g) OP MALE RATS
GROUP I
DAY 3
DAY 4
DAY 5
233.5 251.9 243.4 275.3 234.2
244.2 260.6
254.2 285.1 243.3
247.9 271.4
265.0 293.7 249.3
SD test day 5 SD test day 5 SD test day 5 SD test day 5 SD test day 5
-55-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
AMIMAL NUMBER
627246 627258 627261 627268 627269
ANIMAL NUMBER
627246 627258 627261 627268 627269
DAY 1
223 .7 226 .4 243 .0 260 .7 216 .2
DAY 2
229 .4 231 .9 251 .8 266 .9 223 .6
DAY 8
265 .1 260 .9 298 .7 315 .2 266 .8
DAY 9
274 .1 262 .4 305 .0 327 .9 266 .4
H-24018 (TEST SUBSTANCE) INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP II
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
233 .9 238 .0 262 .6 277 .8 232 .1
245.6
247.4 286.5 238.9 236.5
252 .9 253 .6 275 .8 296 .9 245 .6
260.2 263.0
283.5 305.9 254.2
262.4 257.8 295.3 314.5 264.1
DAY 10
283 .0 272 .7 314 .3 338 .6 273 .7
SD test day 10 SD test day 10 SD test day 10 SD test day 10 SD test day 10
-56.
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
627249 627262 627265 627266 627277
ANIMAL NUMBER
627249 627262 627265 627266 627277
DAY 1
252 .3 229 .8 233 .4 221 .4 250 .8
DAY 2
260 .7 235 .6 234 .8 230 .1 259 .7
DAY 8
317 .4 280 .5 276 .3 269 .7 309 .1
DAY 9
328 .4 289 .2 281 .5 281 .3 329 .2
H-24018 (TEST SUBSTANCE) INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP III
DAY 3
DAY 4
DAY ;5
DAY 6
DAY 7
270 .2 243 .5 242 .4 238 .9 264 .2
281 .2 253 .6 252 .4 248 .3 275 .1
295. 0
261. 4
256. 6 255. 4 287. 0
301 .5 268 .7 261 .9 261 .3 296 .3
312 .3 277 .8 272 .9 268 .8 308 .5
DAY 10 334 .2
299 .9 286 .7 289 .7 337 .8
DAY 13
357 .2 322 .7 312 .7 309 .1 367 .3
SD test day 13 SD test day 13 SD test day '.13 SD test day 13 SD test day ,13
57-
H-24018; Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
DAY 1
DAY 2
H-24018 (TEST SUBSTANCE) INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP IV
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
627247 627250 627255 627257 627259
ANIMAL NUMBER
211.7 240.0 250.5 232.5 231-5
DAY 8
228.1
251.6 260.6 235.8 236.5
233.7 259.5
271.4 272.9 243.4
251.6
269.5 280.2 255.7 247.8
259.5 279.6
285.5 261.4 253.8
266 .9 291 .4 295 .0 267 .6 260 .4
DAY 9
DAY 10
DAY 13
DAY 20
DAY 24
271. 7
296. 5
305. 2 278. 5 269. 4
627247 627250 627255 627257 627259
275.4
296.7
298.8
a
357.3
397 .3 SD test day 24
296.7
318.9
326.3
a
386.5
419 .9 SD test day 24
306.4
317.5
327.1
a
391.5
430 .7 SD test day 24
280.5
287.7
289.2
a
344.4
378 .3 SD test day 24
273.1
FD test day 9
a Rat was not weighed.
-58.
va^
H-24018: Biopersistence Screening
10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
DAY 1
DAY 2
H-24018 (TEST SUBSTANCE) INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP V
DAY 3
DAY 4
DAY 5
DAY 6
DAY 7
627256 627264 627271 627275 627278
ANIMAL NUMBER
222 .7 229 .4 238 .7 238 .3 245 .9
DAY 8
230 .6 239 .2 244 .0 244 .0 249 .8
236.7 247.8
254.0 254.0 261.8
241.6 259.2
259.2 263.3 275.4
252 .6 264 .2 266 .0 272 .7 281 .0
258.1 277.8
274.9 276.5 286.6
260.7 283.3 281.4 282.2
295.8
DAY 9
DAY 10
DAY 13
DAY 20
DAY 24
DAY 34
627256 627264 627271 627275 627278
263 .6
279 .4
278.8
a
318 .9
-"
401.6
285 .4
302 .2
310.5
3.
364 .8
a
430.8
283 .0
296 .7
297.8
a
354 .2
422.1
283 .9
296 .8
302.0
a
341 .1
-a
395.9
. 297 .6 312 .3 318.8 a 369 .7 --a 461.0
ANIMAL NUMBER
DAY 38
DAY 48
DAY 52
627256 627264 627271 627275 627278
419 .3 450 .2 444 .0 420 .4 484 .7
455 .6 481 .7 481 .1 444 .7 521 .5
468.5 489.0 495.9
455.6 535.5
SD test day 52 SD test day 52 SD test day 52 SD test day 52 SD test day 52
a Rat was not weighed.
-59-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
627248 627251 627254 627263 627270
ANIMAL NUMBER
DAY 1
240 .7 239 .7 234 .7 217 .7 230 .3
DAY 2
250 .0 248 .2 242 .6 219 .7 237 .3
DAY 8
DAY 9
H-24018 (TiEST SU.BSTA]NCE)
INDIVIDUAL BODY WE:IGHTS (g) 'OP MALE RA'rs
DAY 3
GRi3UP VI
DAY 4
DAY 5
DAY 6
DAY 7
257.6 257.3 249.7 229.0 243.6
266.0 268.9
262.0 238.3 252.6
276 .8 282 .4 270 .5 243 .3 259 .2
287.5 293.7
283.9 252.4 269.4
295 .3 301 .0 289 .8 255 .6 277 .6
DAY 10
DAY 13
DAY 20
DAY 24
DAY 34
627248 627251 627254 627263 627270
ANIMAL NUMBER
627248 627251 627254 627263 627270
297 .1
314 .4
326.9
a
302 .6
326 .2
342.3
a
290 .7
306 .7
321.0
a
258 .0
274 .5
280.0
^a
279 .2
290 .5
294.3
a
377 .8
a
401 .4
a
381 .9
^a
330 .3
a
351 .6
-a
443. 6 485. 5 470. 6 396. 1
417.9
DAY 38 463 .9 509 .1 496 .3 410 .9 439 .8
DAY 48
489 .0 537 .6 523 .5 433 .9 466 .7
DAY 52
a a a a
^a
DAY 55
510.0 559.7 552.2 451.8 484.4
DAY 61
531 .7 582 .5 565 .7 470 .6 501 .4
DAY 69
543.7 599.9 581.9 478.2 524.0
a Rat was not weighed.
-60-
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
ANIMAL NUMBER
DAY 82
DAY 88
H-24018 (TEST SUBSTANCE) INDIVIDUAL BODY WEIGHTS (g) OF MALE RATS
GROUP VI
DAY 94
627248 627251 627254 627263 627270
565 .1 627 .7 608 .3 503 .4 548 .4
574 .9 643 .4 622 .6 512 .6 562 .0
591 .0 651 .5 628 .7 531 .5 579 .6
SD test day 94 SD test day 94 SD test day 94 SD test day 94 SD test day 94
-61.
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
APPENDIX B Individual Clinical Observations
-62 'Gwsspwy SanNteed. Qow noS ew8M WftA Cffl
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
Animal
Number
627789 627801 627805 627810 627818
CORN OIL (NEGATIVE CONTROL) INDIVIDUAL CLINICAL OBSERVATIONS IN MALE RATS
GROUP I
_________Observation__________________Test Day
No abnormalities detected
1-5
No abnormalities detected
1-5
No abnormalities detected
1-5
No abnormalities detected
1-5
No abnormalities detected
1-5
Animal Number
627793 627797 627799 627800 627808
GROUP II
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Test Day
1-10 1-10 1-10 1-10 1-10
Animal Number
627796 627806 627807 627809 627816
GROUP III
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Test Day
1-13 1-13 1-13 1-13 1-13
-63
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
Animal
Number
627791 627794 627804 627812 627817
CORN OIL (NEGATIVE CONTROL)
INDIVIDUAL CLINICAL OBSERVATIONS IM MALE RATS
GROUP IV
__ Observation
__
____
No abnormalities detected
No abnormalities detected
No abnormalities detected
No abnormalities detected
No abnormalities detected
Test Day
1-24 1-24 1-24 1-24 1-24
Animal Number
627792 627798 627813 627814 627815
GROUP V
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Test Day
1-52 1-52 1-52 1-52 1-52
Animal
Number
627795 627811 627819 627820 627821
GROUP VI
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Test Day
1-94 1-94 1-94 1-94 1-94
-64-
Comapan^ Sanitized. Does 1
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study mRats
DuPont-2927
CORN OIL:ACETONE (NEGATIVE CONTROL)
Animal
Number
625361 625363 625364 625380 625383
INDIVIDUAL CLINICAL OBSERVATIONS IN MALE RATS
GROUP I
__ ___ ___Observation__________________Test Day
No abnormalities detected
1-5
No abnormalities detected
1-5
No abnormalities detected
1-5
No abnormalities detected
1-5
No abnormalities detected
1-5
Animal Number
625355 625362 625367 625368 625378
GROUP II
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Test Day
1-10 1-10 1-10 1-10 1-10
Animal Number
625357 625358 625370 625384 625385
GROUP III
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Test Day
1-13 1-13 1-13
1,-13 1-13
-65-
Company
Sanitized.
Does
not
contain
TSCA
CB1
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
COHN OIL:ACETONE (NEGATIVE CONTROL)
Animal Number
625354 625365 625371 625376 625381
INDIVIDUAL CLINICAL OBSERVATIONS IN MALE RATS
GROUP IV
________Observation___________________Test Day
No abnormalities detected No abnormalities detected No abnormalities detected
No abnormalities detected No abnormalities detected
1-24 1-24
1-24 1-24 1-24
Animal Number
625356 625359 625360 625372 625374
GROUP V
Observation
No abnormalities detected No abnormalities detected Mo abnormalities detected No abnormalities detected No abnormalities detected
Test Day
1-52 1-52 1-52 1-52 1-52
Animal Number
625353 625369 625373 625375 625377
GROUP VI
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Test Day
1-94 1-94 1-94 1-94 1-94
-66- Companif Sanitized. Does not contain TSCA CBl
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
Animal Number
625322 625323 625336 625343 625349
H-24019 (POSITIVE CONTROL) INDIVIDUAL CLINICAL OBSERVATIONS IN MAIjE RATS
GROUP I
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Test Day
1-5 1-5 1-5 1-5 1-5
Animal Number
625320 625330 625332 625341
625350
GROUP II
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Diarrhea No abnormalities detected
Test Day
1-10 1-10 1-10 1-4, 6-10
5
1-10
Animal Number
625321
625327 625342 625345 625348
GROUP III
Observation
No abnormalities detected Diarrhea
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Test Day
1-4, 6-13 5
1-13 1-13 1-13 1-13
-67-Coiapahy Samteed. uoes *n c^.d&n 1 SCA CBi
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
Animal
Number
625325 625328 625338
625340 625352
H-24019 (POSITIVE CONTROL)
INDIVIDUAL CLINICAL OBSERVATIONS IN MALE RATS
GROUP IV
Observation
Test Day
No abnormalities detected No abnormalities detected
No abnormalities detected Salivation
No abnormalities detected No abnormalities detected
1-24 1-24 1-6, 8-24
7
1-24 1-24
Animal
Number
625324 625329
625333
625334 625344
GROUP V
Observation
No abnormalities detected No abnormalities detected
Salivation No abnormalities detected
Salivation No abnormalities detected No abnormalities detected
Test Day
1-52 1-6, 8-52
7
1-6, 8-52 7 1-52 1-52
Animal Number 625326
625335 625346
625347 625351
GROUP VI
Observation
No abnormalities detected Salivation
Alopecia both front legs Alopecia abdomen
No abnormalities detected Salivation
Black ocular discharge Yellow-stained perineum
Red-stained chin Brown-stained chin No abnormalities detected No abnormalities detected
Salivation
Test Day
1-6, 9-76, 77-94 7-8
76
7, 8, 9, 10, 13, 20, 27
1-6, 11-94 7-8
8 8 8
9-10 1-94 1-6, 8-94
7
-68- Company banned. Does nui contain TSCA CW
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
Animal Number
627756 627767 627771 627773 627777
H-24020 (POSITIVE CONTROL) INDIVIDUAL CLINICAL OBSERVATIONS IN MALE RATS
GROUP I
________Observation__________________Test Day
No abnormalities detected
1-5
No abnormalities detected
1-5
No abnormalities detected
1-5
No abnormalities detected
1-5
No abnormalities detected
1-5
Animal Number
627768 627774 627776 627782 627785
GROUP II
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Test Day
1-10 1-10 1-10 1-10 1-10
Animal
Number
627758 627763 627764 627787
627788
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Wet perineum No abnormalities detected
Diarrhea
Test Day
1-13 1-13 1-13 1-5, 7-13
6
1-8, 10-13 9
-69-
Company Samtaeet. uoes <un c^a.n
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rate
DuPont-2927
Animal Number
627759 627761 627770 627779 627786
H-24020 (POSITIVE CONTROL)
INDIVIDUAL CLINICAL OBSERVATIONS IN MALE RATS
GROUP IV
__ ____Observation__________________Test Day
No abnormalities detected
1-24
No abnormalities detected No abnormalities detected
1-24 1-24
No abnormalities detected No abnormalities detected
1-24 1-24
Animal Number
627757 627760 627765
627772
627781
GROUP V
Observation
No abnormalities detected No abnormalities detected No abnormalities detected
Wet perineum No abnormalities detected
Wet perineum No abnormalities detected
Test Day
1-52 1-52 1, 3-52
2
1, 3-52 2 1-52
Animal Number
627762
627769 627775 627778 627783
GROUP VI
Observation
No abnormalities detected Diarrhea
No abnormalities detected No abnormalities detected
Alopecia perineum No abnormalities detected Alopecia both front paws
Alopecia right front leg
Test Day
1-8, 10-94 9
1-94 1-94 81, 90, 94 1-23, 94 24, 34, 41. 47, 55. 61, 74, 81, 90
-70-
Sanifced.DoesnotcontainTSCACBa
Coropany
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study m Rats
DuPont-2927
Animal
Miunbet'
627252 627253 627260 627273 627274
H-24018 (TEST SUBSTANCE) INDIVIDUAL CLINICAL OBSERVATIONS IN MALE RATS
GROUP I
______Observation___ _______
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
______Test Day
1-5 1-5 1-5 1-5 1-5
Animal Number
627246 627258 627261 627268 627269
GROUP II
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Test Day
1-10 1-10 1-10 1-10 1-10
Animal Number
627249 627262 627265 627266 627277
GROUP III
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Test Day
1-13 1-13 1-13 1-13 1-13
-71 Company Sanitized. Does not contain TSCA GBS
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
Animal Number
627247 627250 627255 627257 627259
H-24018 (TEST SUBSTANCE)
INDIVIDUAL CLINICAL OBSERVATIONS IN MALE RATS
GROUP IV
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Found dead
____Test Day
1-24 1-24 1-24 1-24
9
Animal Number
627256 627264 627271 627275 627278
GROUP V
Observation
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected
Test Day
1-52 1-52 1-52 1-52 1-52
Animal Number
627248
627251 627254 627263 627270
GROUP VI
Observation
No abnormalities detected Alopecia perineum
No abnormalities detected No abnormalities detected No abnormalities detected No abnormalities detected Alopecia both front paws
Test Day
1-82 88, 94
1-94 1-94 1-94 1-38, 69-94 48, 55, 61
-72. Company Sanitized, uoes noi contain TSCA CB1
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
APPENDIX C
Analysis of Blood Fluorine Data
"73 ' Company Samteed. Does nw contain TSCA CB1
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study inRats
Terms and Calculations
DuPont-2927
Terms: Active
Fluorine containing compound
% Active
The % of formulation that is made up of fluorine containing
components
Mol Wt Active
The molecular weight of the fluorine containing components
(g/mole)
Formulation Dose % F in Active
The mg of formulation given per kg of animal body weight
The % fluorine in the fluorine containing components of the
formulation (weight basis)
Mol Wt F
The molecular weight of fluorine g/mol
Compound Calculations:
Dose Active (mg/kg)
The mg of fluorine containing compound administered per kg of
animal body weight. = (% active/I 00) * Formulation Dose
Dose Active (mmole/kg) The mmole of fluorine containing compound administered per kg of
animal body weight
= dose [mg/kg] / Mol Wt Active [mg/mmol]
Dose F (mg/kg)
The mg Fluorine administered per kg of animal body weight = (% F in active/I 00) * Dose Active [mg/kg]
Dose F (mmol/kg)
The mmole of fluorine administered per kg of animal body weight = Dose F [mg/kg] / Mol Wt F [mg/mmol]
Molar Ratio (Active/F)
The moles of fluorine containing compound per mole of fluorine
= Dose Active [mmol/kg] / Dose F [mmol/kg]
Formulation Dose Normalization Factor
The formulation dose that would be required to administer the
amount of active needed to achieve the normalized dose = (Normalized dose of Active [mmol/kg] / Dose Active [mmol/kg]) * Formulation Dose
74Gompany Sanitized. Does not contain TSCACB8
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study m Rats
Individual Animal Measurement:
ppm F in blood
The ppm fluoride measured in blood
DuPont-2927
Individual Animal Calculations:
ppm F in Blood minus Bkg 0.2 ppm
The ppm fluoride measured in plasma minus the background fluoride measured in control animal blood, m this case the value was established at 0.2 ppm.
ppm F in Blood normalized to 0.1 Dose
The ppm fluoride minus background that would be expected if the
mmol/kg active dose was 0.1 mmol/kg instead of the actual active dose. This
assumes linearity between administered dose and blood fluorine
levels, but is needed because different doses of active were used in
the study.
=(0.1 [mmol/kg] / Active dose [mmol/kg]) * (ppm F in blood
minus background)
fJimolar equivalents of
active in blood
The ^molar [^mol/L] concentration of fluorine containing
compound in plasma based on the ppm fluorine in plasma normalized to 0.1 mmol/kg active dose. This assumes that all
plasma fluorine is derived from the fluorine-containing component in the formulation. Note: 1 ppm - 1 mg/L
= (Normalized ppm [mg/L] fluorine in blood / Mol Wt F [mg/mmol]) * molar ratio active/F [mmol active/mmol F] *
1000 /imol/mmol
-75-
Company Sanitized.
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
DuPont-2927
Factors Influencing Interpretation of Kinetic Analysis
Considerations:
The data used for kinetic analysis was from a limited screen and extrapolation should be done cautiously.
Sample size is low Analytical data used without validation Steady-state not reached Terminal phase may not be reached Some compounds are mixtures offluorinated compounds Different active and formulation doses were used Different vehicles were used to deliver formulations The kinetics apply only to plasma, not to specific tissues or the whole body Each compound may have very different potency for producing toxicity
Assumptions: (May or may not be justified in all cases)
- Plasma fluorine concentrations are linear with respect to dose - Analytical method is appropriate for all types of compounds - Elimination kinetics can be determined based on total fluorine rather than on concentrations of
individual components - Background plasma Fluorine is 0.2 ppm - % F data is the % Fluorine of the active (Fluorine containing components) in the formulation
- Molecular weight is the molecular weight of the active component in the formulation
-76-
Company Sanitized. Does not certain TSCA CB8
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
Data for H- 2 4019
Given:
Mol^^t. Active (;g/mole):
Fonnulation Dos<i (mg/kg): % Actiive (F Containing) in
Formulation:
497
% Fin Active:
10
MolWt.F(g/mol):
100
Calculate!i Values: Dose^active (mg/kg): Dose./active(mm ole/kg):
Formullation Dose! Normalisation
Factor:
10 0.020
49.7
Dose F (mmol/kg): Molar Ratio (Active/P): Dose F (mg/kg):
DuPont-2927
65 19
0.342 0.059 6.5
Rat#
Test Day Sample
ppmF
in
blood
Group I
625322
1
1.0
625323
1
1.3
625336
1
2.6
625343
1
2.6
625349
1
2.9
Group I
625322
5
625323
5
625336
5
625343
5
625349
5
51.7 38.0 38.7 78.5 37.1
Group II
625320
10
625330
10
625332
10
625341
10
625350
10
65.6 61.1 60.5 63.1 58.1
ppmF in
blood minus Bkg
0.2 ppm
0.8 1.1 2.4 2.4 2.7
51.5 37.8 38.5 78.3 36.9
65.4 60.9 60.3 62.9 57.9
ppm F in blood Normalized to 0.1 mmoles/kg
Dose
3.98 5.47 11.93 11.93 13.42
255.96 187.87 191.35 389.15 183.39
325.04 302.67 299.69 312.61 287.76
pimolar equivalents of active in
blood
12.31 16.92 36.92 36.92 41.54
792.31 581.54 592.31 1204.62 567.69
1006.15 936.92 927.69 967.69 890.77
-77Company Sanifced. Does not contain TSCA CB8
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
Rat#
Test Day Sample
ppmF
in
blood
Group in
625321
13
625327
13
625342
13
625345
13
625348
13
77.2 61.5 64.6 57.0 62.4
Group IV
625325
24
625328
24
625338
24
625340
24
625352
24
40.3 46.3 43.2 39.1 41.9
Group V
625324
52
625329
52
625333
52
625334
52
625344
52
24.7 29.8 27.3 29.1 23.8
Group VI
625326
94
625335
94
625346
94
625347
94
625351
94
12.4 16.4 13.1 11.0 11.6
ppm F in blood
minus Bkg 0.2 ppm
77.0 61.3 64.4 56.8 62.2
40.1 46.1 43.0 38.9 41.7
24.5 29.6 27.1 28.9 23.6
12.2 16.2 12.9 10.8 11.4
ppm F in blood Normalized to 0.1 mmoles/kg
Dose
382.69 304.66 320.07 282.30 309.13
199.30 229.12 213.71 193.33 207.25
121.77 147.11 134.69 143.63 117.29
60.63 80.51 64.11 53.68 56.66
DuPont-2927
^moiar equivalents of active in
blood
1184.62 943.08 990.77 873.85 956.92
616.92 709.23 661.54 598.46 641.54
376.92 455.38 416.92 444.62 363.08
187.69 249.23 198.46 166.15 175.38
-78Company Sanitized. Does not contain T8CA CBI
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
Data for H- 24K)20
Given:
MorWt. Active (jg/mole):
Form.ulation DOS(3 (mg/kg): %Ac;tive (F Coni;aimng)in
Form ulation:
426
% F in Active:
20
Mol Wt. F (g/mol):
100
Calculated Values: Dose Active (mg/leg): Dose Active (mm.ole/kg): Formulation Dose; Normalization
Factor:
20 0.047
42.6
Dose F (mmol/kg): Molar Ratio (Active/F): Dose F (mg/kg):
DuPont-2927
69 19
0.726 0.065 13.8
Rat#
Test Day Sample
ppmF
in
blood
Group I
627773
1
627771
1
627767
1
627756
1
627777
1
13.2 8.1 16.5 14.1 10.7
Group I
627773
5
627771
5
627767
5
627756
5
627777
5
75.3 66.8 64.8 80.0 71.6
Group II
627768
10
627774
10
627776
10
627782
10
627785
10
56.3 51.0 54.8 43.6 65.1
ppm F in blood
iainus Bkg 0.2 ppm
13.0 7.9 16.3 13.9 10.5
75.1 66.6 64.6 79.8 71.4
56.1 50.8 54.6 43.4 64.9
ppm F in blood Normalized to 0.1 mmoles/kg
Dose
27.69 16.83 34.72 29.61 22.37
159.96 141.86 137.60 169.97 152.08
119.49 108.20 116.30 92.44 138.24
/(molar equivalenits of active in
blood
94.20 57.25 118.12 100.72 76.09
544.20 482.61 468.12 578.26 517.39
406.52 368.12 395.65 314.49 470.29
-79CompawSaniteed.Doesi
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
Rat#
Test Day Sample
ppmF
in
blood
Group ffl
627758
13
627764
13
627787
13
627763
13
627788
13
43.5 20.7 13.2 30.8 24.9
Group IV
627759
24
9.2
627779
24
14.9
627770
24
11.6
627761
24
9.9
627786
24
6.7
Group V
627757
52
0.9
627781
52
0.6
627760
52
1.0
627765
52
0.9
627772
52
0.8
Group VI
627778
94
627783
94
627762
94
627775
94
627769
94
0.3
0.2
0.2
0.2
0.2
* = Below LOD (Level of Detection)
ppmF in
blood minus Bkg
0.2 ppm
43.3 20.5 13.0 30.6 24.7
9.0 14.7 11.4 9.7 6.5
0.7 0.4 0.8 0.7 0.6
0.1
*
0.0 0.0
*
ppm F in b lood
Normalize dto
0.1 mmoles/kg Dose
92.23 43.67 27.69 65.18 52.61
19.17 31.31 24.28 20.66 13.85
1.49 0.85 1.70 1.49 1.28
0.21
*
0.00 0.00
*
DuPont-2927
jamolar equivalents of active in
blood
313.77 148.55 94.20 221.74 178.99
65.22 106.52 82.61 70.29 47.10
5.07 2.90 5.80 5.07 4.35
0.72
*
0,00 0.00
*
-80- Conipany Sanitized. Does not contain TSCACBI
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study in Rats
Data for H-2-4018
Given:
MolVft. Active (,g/mole):
Fonnuilation Dos<3 (mg/kg): % Active (F Coni:ammg)m Formuilation:
Calculated Values: DoSGjtVctive (mg/kg): Dose./Vctive (mmole/kg): Formulation Dose! Normalizalion
Factor:
845 1000 34
340 0.402 248.5
% F in Active:
Mol Wt. F (g/mol):
Dose F (mmol/kg) : Molar Ratio (Acthre/F): Dose F (mg/kg):
DuPont-2927
50 19
8.947 0.045 170
Rat#
Group I 627252 627253 627260
627273 627274
Group I 627252 627253 627260 627273 627274
Group n 627246 627258 627261 627268 627269
Test Day Sample
ppmF
in blood
1
4.1
1
3.5
1
3.1
1
2.7
1
1.3
5
9.9
5
9.0
5
9.0
5
8.7
5
8.4
10
8.7
10
12.3
10
7.8
10
11.0
10
13.4
ppm F in blood
minus Bkg 0.2 ppm
3.9 3.3 2.9 2.5 1.1
9.7 8.8 8.8 8.5 8.2
8.5 12.1 7.6 10.8 13.2
ppm F in blood Normalized to 0.1 mmoles/kg
Dose
0.97 0.82 0.72 0.62 0.27
2.41 2.19 2.19 2.11 2.04
2.11 3.01 1.89 2.68 3.28
pimolar equivalents
of active in blood
2.29 1.94 1.71 1.47 0.65
5.71 5.18 5.18 5.00 4.82
5.00 7.12 4.47 6.35 7.76
-81 Company Sanitized. Does not contain TSCA CBI
H-24018: Biopersistence Screening 10-Dose Oral Gavage Study mRate
Rat#
Test Day Sample
ppmF
in
blood
Group in
627249
13
6.8
627262
13
6.4
627265
13
5.1
627266
13
5.2
627277
13
4.8
Group IV
627247
24
2.3
627250
24
2.8
627255
24
2.5
627257
24
2.5
627259
24
NA
Group V
627256
52
1.7
627264
52
1.2
627271
52
1.3
627275
52
1.4
627278
52
1.0
Group VI
627248
94
0.2
627251
94
0.8
627254
94
0.7
627263
94
0.7
627270
94
0.8
NA Animal found dead on test day 9. No samples collected
ppmF in
blood minus Bkg
0.2 ppm
6.6 6.2 4.9 5.0 4.6
2.1 2.6 2.3 2.3
-
1.5 1.0 1.1 1.2 0.8
0.0 0.6 0.5 0.5 0.6
ppm F in blood Normalized to 0.1 mmoles/kg
Dose
1.64 1.54 1.22 1.24 1.14
0.52 0.65 0.57 0.57
-
0.37 0.25 0.27 0.30 0.20
0.00 0.15 0.12 0.12 0.15
DuPont-2927
jtmolai equivaleiits of active in
blood
3.88 3.65 2.88 2.94 2.71
1.24 1.53 1.35 1.35
-
0.88 0.59 0.65 0.71 0.47
0.00 0.35 0.29 0.29 0.35
-82-
Coropany Sanitized. Does not eontain TSCA CBS