Document e7k7JBOgLRJ0yJ3qmy2gkGz0p
AR A426 - 332] 503
AR226_ 332
Dupont13830 --~
TRADE SECRET
Study Title H-25425:Repeated-DoseDermal Toxicity
28-Day Study in Male Rats
TesT GUIDELINES: U.S. EPA Health Effects Test Guidelines OPPTS 870.3200 (1998)
SOeEctCiDonG4u: idHeelailnteh fEofrfetchtesT,eNsutimnbgeofrC4h1e0mi(c19a8l1s)
AuTHOR: Carol Finlay, BA.
~~
STUDY COMPLETED ON: November 3, 2004
PERFORMING LABORATORY: E.L du Pont de Nemours and Company HElakstkoenlRloTMaLda,bPo.rOa.toBroyxfo5r0Health and Environmental Sciences Newark, Delaware 19714-0050
LABORATORY PROJECTID: DuPont-13830
Wonk Request Novae (BY
SERVICE CODE Nomen 0}
SPONSOR: WEiLlLmdiungPtoonnt,dDeeNleawmaoruers1a9n89d8Company USA
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H2-82D5a42y5:StuRdeypeinatMeadl-eDoRsaetsDermal Toxicity
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DuPont.13830
GOOD LABORATORY PRACTICE COMPLIANCE STATEMENT
This study was conducted in compliance with U.S. EPA TSCA (40 CFR part 792) Good Laboratory Practice Standards, which are consistent with the OECD PrinciplesofGood Laboratory Practice (as revised 1997) published in ENV/MC/CHEM(98)17, except for the item documented below.
Test substance characterization and stability analyses were performed at Regional Analytical Services (RAS), a non-GLP laboratory. The test substance analyses performed were in compliance with regulatory guidelines. Noneofthe aforementioned analyses were performed under Good Laboratory Practice Standards; however, the analyses were conducted in compliance with [S09002 regulations. Allof the analyses are considered valid and sufficient for the purposesofhis study.
Appli/cSpaonnsotr: E.L du Pont de Nemours and Company Wilmington, Delaware 19898 USA.
`StudyDirector:
A aan Acs ae `Carol Filay, B.A. StaffToxicologist
$3, Neu-2s04 Date
Applicant/ Sponsor:
DuPont Representative
Date
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1252.5D4a2y5:SRteypeiatnehdiDoRsaesDermal Toxicity ~
Duran 13830
QUALITY ASSURANCE DOCUMENTATION
`Work Request Number: il
Study Code Number:
`dTahtescoofndiuncstpoecfttihoins asrteuidnydihcaastbeedebnelsouwb.jected to periodic Quality Assurance inspections. The
Phase Audited
Audit Dates
Conduct: Evaluation
1 Dec 2003
Tables and Appendices
16, 18, 23 Feb 2004
`Tables and Appendices
23-26 Feb 2004
`Tablesand Appendices
9-12, 16Mar 2004
---
Report/Records:
6-8 Oct 2004
Dates Reported to Study Directorand Management
1 Dec 2003 23 Feb 2004 26 Feb 2004 16 Mar 2004 8 Oct 2004
Repost: _Aliza) 2 ;Qe Quality Ass`uM.raJnochensAtuodnitor
2p oof Date.
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CERTIFICATION
`We, the undersigned, declare that this report provides an accurate evaluationofdata obtained from this study.
Chiru
atin br
a7 nm DiplomateA.C.V.P.
) 0%~Mr
Anicaln. Lof-tfo
VeterinaryPathologist
0N033- elosser
- =J ce o PEYEBnA YiN VeterinaryPathologist
rer . er Suoam A Tnac Wir Sem Lelie `Senor Research Toxicologist
0022--4N0O0V.-22004
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`Staff Toxicologist
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2285-0D2ay5:StuRdeypienatMeadl-eDRoastesDermal Toxicity --
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`TABLE OF CONTENTS Page
GOOD LABORATORY PRACTICE COMPLIANCE STATEMENT wcrc
2
QUALITY ASSURANCE DOCUMENTATION ccvcvsssssssmssssmsmssssssnnos3
CERTIFICATION cosmos
LIST OF TABLES cvvosrsmssmssssssssssssssssssssssssssssmsssssssssssnon
LIST OF FIGURES vss smn8
LIST OFAPPENDICES ccs
STUDY INFORMATION ccna)
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INTRODUCTION cosmos 11
STUDYDESIGN crm 11
MATERIALS AND METHODS css
11
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B. ATAGITADTIRY emmmmmmenmmmmsmmmonsinsmmmmmmmn 1
E. QuaraanndtPirenteset .
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F. ASSIZ(A0Gmroeupnsantd SAY SHI cvs sssessssssnesrmsnnnon 13
G. TestSubstancePreparation and AAMIIStTAtion ..........mrrnmmmien 13
A m--
I. Food Consumption and Food EfCIENY.......rmnrmnrnrnn 1
1 CRSmmission 16
K. Total Fluorine and Perfluorooctancic Acid Level EVIUAUions..........ovrorrromen 14
L. Clinical PAhOIOgY EVAON...c.vosrsrssssrosesmsssssnesssssmnensmmsmnon 15
M.ANBIOMic PAhOIORY EVAIUAON..crovenrmrersmrrenrmsrsmsonemsensmnnrnssnenemn 17
RSs ARUN mgm
1
RESULTS AND DISCUSSION c.ccvonssmsmmonmsmsmssmssssmssssmssssmsssssssmssmssnen 19
J ----. J A. Mean Body Weights and Body Weight GainS............creeesmmsreveis 19 B. Food Consumption and F00d EfTCIENCY.........wvemrreemnenrrensnonenrins 19 C. Clinical Observations, Dermal Effects, and MOMEIY .......ouevrvenres 19 D. Perfluorooctanoic Acid (PFOA) and Total Fluorine Evaluations......... wr B) Tabi COR)
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B. COMPO puss
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C.. ClniCal CHEMISTY: 21
D. UHDBIYSES corns 21
E. Urine and PLASMA FIORE...
22.
F. Clinical Pathology CONCIISIONS .......svvsnrsissnis 22.
Anatomic Pathology EVAIIAtON wom32
A CIS ADIG crssmimsenmsn32
B. OBA WEIGHS...
22
C.. GIOSS OBSCIVAONS vcore
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E. Anatomic Pathology CONCIUSIONS .......sssrssimmnnsis23
CONCLUSIONS oss
34
RECORDS AND SAMPLE STORAGE worms 24
REFERENCES sss
35
TABLES cms26
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----_
APPENDICES oss 54.
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1.25425: Repeated-Dose Dermal Toxicity 28-Day Study in Male Rats --
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LIST OF TABLES
Page
1. MEAN BODY WEIGHTS OFMALERATS...
mmm------"
2. MEANBODYWEIGGAIHNSTOFMALERATS.........
semmmmgm----y
3. MEANDAILY FOODCONSUMBYPMATLEION RATS.. wnt
4. MEANDAILYFOODEFFICOIFMEALNECRAYTS.
SR
5. SUMMARY OFCLINICALOBSERVATIONSFORMALERATS -PREDOSING. vcr 33
6. SUMMARY OFCLINICALOBSERVATIONSFORMALERATS -POSTDOSING v.35
7. PERCENTSURVIVALOFMALE RATS...
prmmmmnniS7
8. MEAN PFOACONCENTRAINTMAILEORANTSS...
smith
9. MEASUREDCONCENTRATION(PPB)WHOLE BLOODFLUORINE ...c.c.ccrsreessncrns39
10. SUOM FHEM MATOA LOGR YVALY UES FORMALERATS...
11. SUOM FCOM AGULA ATIOR NVALY UES FORMALERATS...
smd
12.SUMMARYOFCLINICALCHEMISTRY VALUES FORMALE RATS...
A
13. SUMOMFURAINARLYSYIS VAFLORU MALE E RASTS...
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14. MEANFINAL BODYAND ORGAN WEIFOGRMHALETS RATS...
--
15. INCIDENCES OF GROSS OBSERVAINTMAILEORNATSS. FAAS
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16. INCIDENCESAND LESION GRADES OF MICROSCOPIC OBSERVAINTMIALOERNATSS. a
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1. MEANBODY WEIOFGMAHLETS RATS..
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Page mmm
LIST OF APPENDICES
Page
A. INDIVBOIDYDWEUIGAHTLS...
wasmmm----_
B. INDIFOVODICONDSUUMPATIOLN...
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C. INDIVIDUALCLINICAL OBSERVATIONSAND MORTALITY
RECORDS...
10
D. INDIVIDUALCLINICAL OBSERVA- TIONS POSTDING.
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E._ INDEDIEMAVANDIERYDTHEU MASA COREL S...
I
F. PFOA ANALYTICALREPORT c.csmssssssmssmsssssnsis
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G. INDIBLOVODIFLUDORIUNELAEVELLS...
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--_
H. INDIVIDUALANIMAL CLINICAL PATHOLOGY DATA vc
--
I. INDIVIDUAL ANIMAL BODYAND ORGAN
WEIGHTS...
209
J. INDIVIDUALANIMAL GROSS AND MICROSCOPICOBSERVATIONS...
23
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STUDY INFORMATION
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Smonms/Coes: -(NE|
HaskellNumber: 25425
CAS Registry Number: [SN
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`Study Initiated/Completed: November 18, 2003/(see report cover page)
In-life Initiated/Completed: November 25, 2003 / December 23, 2003
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12.82-5D4a2y5:StuRdeypeinatMeadl-eDoRsaetsDermal Tosicity PN
SUMMARY
DuPont 13830
`The objectiveofthis study was to determine the potential toxicity ofH-25425 following repeated dermal exposure. The test substance was applied to the shaved, intact skinof male
Crl:CD(SD)IGS BR rats for 6 hours/day for 28 consecutive days. Three groups of 10 male rats
were treated dermally with 10, 100, or 1000 mg/kg/day H-25425. A control group of 10 male rats was similarly treated with deionized water. The rats were observed for mortality, clinical signs, dermal effects, and body weight effects during the study. Food consumption was determined weekly during the study. Blood samples for total fluorine were collected on test days 0,7, 14,21, and 27. Theday 21 samples were analyzed. Bloodand urinesampleswere: collected for clinical pathology prior to sacrifice on day 28. Blood samples were collected at necropsy for analysisofconcentrationofperfluorooctanoic acid (PFOA). All rats underwent necropsy for gross and microscopic pathological evaluation.
No deaths occurred, and no test substance-related effects on body weight or nutritional parameters were observed. No clinical signs attributable to systemic toxicity occurred. No dermal irritation was observed during the study.
PFOA concentrations in plasma from rats in the control group and the 10 mg/kg/day group were.
below the lower limitof quantitati(o10n ppb). The mean concentrations were 13 ppb in the
--~
100 mg/kg/day group and 105 ppb in the 1000 mg/kg/day group.
Fluorine levels in blood from treated and control rats were either not detectable or below the limit of quantification (500 ppb).
No adverse effects were observed on any clinical pathology parameters (hematology, clinical chemistry, coagulation parameters, urinalysis), organ weights, or gross or microscopic pathology parameters.
`The no-observed-effect level (NOEL)' for male rats was 1000 mg/kg/day, the highest dosage tested. The NOEL is based on a lack ofadverse test substance-related effects on any in-life, clinical pathology, or anatomic pathology parameter in male rats treated dermally at dosages up to 1000 mg/kg/day.
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H2-82-5D4a2y5S:tuRdeypeinatMeadl-eDoRsatesDermal Toricity
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INTRODUCTION
The test substance, H-25425, is belongs to the groupofcompounds known
It a previously conducted 90-day
oral gavage study with the test substance, maleand female rats were dosed at 0 (control), 10,
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hwyepreertorbospehryvewdaisnoabnsyermvaeldeionrtfheem1a0le00domsge/kggr/oudpa.y mRaelveerasinbdlef,emmailneimgraoluptso.miTlhdethnyor-ooibdsefrolvleidc-ular
effect level (NOEL) for subchronic toxicity endpoints in male and female rats was
100 mg/kg/day.
Dose study.
levels
for
the
present
study
were
selected
to
duplicate
the
dose
levelsofthe
oral
gavage
STUDY DESIGN
Group Number/Group Dosage (mg/kg)
xX
10
0 (Control)
--_
XI
10
10
xm
10
100
Xv
10
1000
MATERIALS AND METHODS
A. Test Guidelines
The study design complies with the following test guidelines except as noted below:
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tEhxecseeptoiccoans-ioTnhsethweryapmpaiyngnsoot hf7avreatbsebeenceaxmpeodsiesdlotodgtehde dteusrtinsgubtshteaencxepfoosrur6ehpoeurriso.d.FoThuerroefftohree,seon
araftfsecwtetrhee ionbjtehcetciovnetsroorltghreouvpa,liadintdyotfhrteheerasttsuwdyerbeecianudsief,fecroennstitdeesrtignrgouthpast. noThsiisgneixfciecpanttion did not
toxicological effects were observed at any dosage level, i is not likely that an occasional
~
exposure periodof less than 6 hours for some animals would have changed the study results.
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`Emxacleepstwieorne-mOonrleysmeanlseitriavtestwoetrheettroexaitceodlobgeiccaaulseeffiencptrsetvhiaonusfesmtauldeise.s with.
Dupont 13830 1
B. Test Substance `teTshtestuesbtstsaunbcsetaanpcpee,aHr-e2d5t4o2b5e, swtaasblseuupnpdleiretdhbeyctohnedsiptioonnssoorftashe=-- Study. No evidence of instability, suchas a change in color or physical state, was observed.
C. TestSpecies
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`The Crl:CD(SD)IGS BR
extensive experience with
rat
the
wsatrsaisnelaetcHtaesdkbealsleLdaboonractoonrsiys.tently
acceptable
health
status
and
on
D. Animal Husbandry
1. Housing
~~ Rats were housed siinnsgtailnleyss steel, wire-mesh cages suspended above cage boards.
2. Environmental Conditions
Animal Animal
rooms rooms
were were
maintained at a temperature of 18-26C and artificially illuminated (fluorescent light) on
a relative humidityof 30-70%. an approximate 12-hour
light/dark cycle.
3. Feed and Water
`Tap water was provided ad libitum. PMI Nutrition International, LLC Certified Rodent
LabDiet 5002 meal was available ad libitum except when the rats were fasted.
4. Mdentification
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affixed number
to the which
was tattooed on the tal ofeach rat and included on the cage labels.
5. Animal Health and Environmental Monitoring Program
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+ Water samples are analyzed for total bacterial counts, and the presenceofcoliforms, 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 presenceofthese contaminants below the maximum concentration stated by the manufacturer `would not be expected to impact the integrityofthe study.
`The animal health and environmental monitoring program is administered by the attending laboratory animal veterinarian. Evaluationofthese data did not indicate any conditions that affected the validityofthe study.
E. 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 quarantine period and examined daily for -- any clinically apparent signsof disease or injury. The rats were observed daily for mortalityand signs of illness, injury, or abnormal behavior. On the basesofacceptable body weight gains and freedom from clinically apparent signs of disease or injury, the ras were released from quarantine on testday-1 by the laboratory animal veterinarian.
F. Assignmentto Groups and Study Start Forty rats were selected for study use on the basesofadequate body weight gain, freedom from clinical signsofdisease or injury, and a body weight within + 20%ofthe mean. The selected rats were divided by computerized, stratified randomization into 4 groups of 10rats, so that there `were no statistically significant differences among group body weight means. Dose administration with H-25425 began on test day 0 when the rats were approximately 7 weeks ofage.
G. Test Substance Preparation and Administration
Approximately 24 hours prior to the first treatment, the furofeach rat was closely shaved to
expose the skin from the back and trunk. The area to be treated was marked on the backof each
rat with a water-insoluble marker. The rats were treated for 28 consecutive days at
~
`approximately the same time each day. The exposure period was approximately 6 hours per day.
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`The test substance was moistened with deionized water to form a thick paste and applied as
evenly and thinly as possible to the test site. The amountoftest substance needed to treat cach
rat was based on the most recently determined body weight measurement. The control rats were
treated with deionized water. The test site was covered with a 2-ply porous gauze dressing
followed by successive layersofstretch gauze (no more than layers) and self-adhesive bandage.
After the exposure period, the wrappings were removed and excess test substance was washed
offwith warm tap water. Each rat was then gently patted dry and retumed to the cage. The
control animals received the same washing technique as the treated animals.
Tt was not possible to cover an area of 10%ofthe total body surface for any dose group without excessively diluting the test substance. The approximate total body surface area covered with the thick paste for the 10, 100, and 1000 mg/kg/day groups was 1%, 1%, and 3.3%, respectively.
Following an evaluation rats were reshaved as needed during the study. The entire area that was originally shaved (including the untreated control skin) was reshaved.
H. Body Weights The rats were weighed at 3-4 day intervals throughout the study.
IL Food Consumption and Food Efficiency The amount of food consumed by each rat was determined once per week throughout the study. Individual food consumption was determined by weighing the amountofdiet in each feeder at the beginning and endofthe week and subtracting the final weight and the amountofspillage from the feeder during the week from the initial weight. From these measurements, mean daily food consumption was determined. From the food consumption and body weight data, mean daily food efficiency was calculated.
J. Observations `The rats were observed for clinical signs and dermal effects after washing. The rats were also observed for clinical signs at each weighing. The Draize Scale was used to score skin imitation. Adjacentareasofuntreated skin were used for comparison. The rats were checked twice daily for mortality and for signsofillness, injury, or abnormal behavior.
K. Total Fluorine and Perfluorooctanoic Acid Level Evaluations
Blood was collected into EDTA tubes from the orbital sinusofal rats on test days 0, 7, 14, 21,
and 27 approximately one hour after removalofthe test substance. The blood was refrigerated.
`The total fluorine content ofthe day 21 blood samples was determined by using a Wickbold torch
~
combustion method followed by analysis with a fluoride ion selective electrode.?) The limit of
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H2.82-5D4a2y5:StuRdeypeinatMeadl-eDoRsaetsDermal Toxicity
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~ quantification (LOQ) for this method is 500 ppb. Fluorine blood analysis was performed at Stereochem, Newark, Delaware.
`Additional blood was collected from the vena cavaofall rats at necropsy into a tube containing EDTA. Plasma was prepared and stored frozen at 80C to -20C until analyzed for concentrationof perfluorooctanoic acid (PFOA). PFOA was extracted fromtheplasma by protein precipitation in acetonitrile. The compound was quantified by liquid chromatography/tandem mass spectrometry (LC/MS/MS) analysis using selected reaction `monitoring (SRM). Quantification was performed using extracted calibration standards containing an internal standard. The lower limitof quantitation (LLOQ) for this method is 10 ppb. Plasma samples were analyzed for PFOA at Exygen Research, 3058 Research Drive, State College, PA 16801. See Appendix F for additional details ofthis analysis.
L. Clinical Pathology Evaluation A clinical pathology evaluation was conducted on all animals 28 days aftr initiationofthe study. `The day before collection of samples for the clinical pathology evaluation animals were placed in `metabolism cages. Animals were fasted overnight (approximately 16 hours) and urine collected from each animal. Blood samples for hematology and clinical chemistry measurements were collected fromtheorbital sinusofeach animal while the animal was under carbon dioxide `anesthesia. Blood samples for plasma fluoride, PFOA, and coagulation parameters were collected at sacrifice from the abdominal vena cavaofeach animal while the animal was under ~~ carbon dioxide anesthesia. Additional blood collected from the vena cava was placed in a serum tube, processed toserum,and frozen at -80C. Serum was discarded without analysis because further tests were not required (0 support experimental findings. Bone marrow smears were. inadvertently not collected at sacrifice. All blood samples were evaluated for quality by visual `examination prior to analysis. Results were maintained in the study records and reported only if the sample was analyzed.
1. Hematology and Coagulation
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120
Wright-
Giemsa stained blood smears from all animals were examined microscopically for confirmation
of automated results and evaluationof cellular morphology. Blood smears, stained with new
methylene blue, were prepared from each animal undergoing a hematology evaluation, but were
nCootagnueleadteidonfoArnaelxyazmeirn.ation. Coagulation times were determined on a Sysmex CA-1000
`The following parameters were determined:
red blood cell count hemoglobin hematocrit ~~ mean corpuscular volume
platelet count `white blood cell count differential white blood cell count microscopic blood smear examination
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`mean corpuscular hemoglobin concentration red cell distribution width absolute reticulocyte count
DuPont 13830
pacrtoitvhartoemdbpianrttiailmethromboplastin time
2. Clinical Chemistry
`Serum clinical chemistry parameters were determined on an Hitachi 717 clinical chemistry. PanHa/lIyzSeEr.mePtlerasamnad falufolruiodreidceo-nsceelnetcrtaivteioenlsecwtreordee.determined using a Beckman 12 digital The following parameters were determined:
aspartate aminotransferase: alanine aminotransferase sorbitol dehydrogenase alkaline phosphatase: total bilirubin urea nitrogen --_ creatinine cholesterol triglycerides
glucose total protein albumin globulin calcium inorganic phosphorus. sodium potassium chloride Mioride
3. Urinalysis Urine volume and appearance (quality, color, and clarity) were measured and evaluated visually, Areustpoecmtaitveeldy.UrUirnienCehceomnissttitruyeanntaslwyzeerre. seUmrii-nqeuapnrtoitteaitniwvealsymmeeaassuurreedd oonn aanBHaiytearchCili7n1i7tecklinAitcallasTM chemistry analyzer. Urine osmolality was determined using an Advanced Osmometer 3900.
Urine fluoride concentrations were determined using a Beckman 12 digital pH/ISE meter and
a fluoride-selective electrode, and total urine fluorides were calculated (volume x concentration). Sediments from all urine specimens were evaluated microscopically. `The following parameters were determined:
cquoalloirty clarity volume osmolality
bkieltiornuebin blood urobilinogen fluoride
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Dupont 13830
--~ pH glucose
protein `microscopic urine sediment examination
M. Anatomic Pathology Evaluation
After 28 days ofexposure to the test substance (test day 28), groups of 10 male rats from the 0, 10, 100, and 1000 mg/kg/daygroupswere sacrificedandnecropsied.
"The rats were fasted overnight on the afternoon before their scheduled sacrifice. The order of sacrifice for scheduled deaths was random among all treatment groups. Rats were euthanized by carbon dioxide anesthesia and exsanguination. Gross examinations were performed on all rats.
The following tissues were collected from all rats.
Tver kidneys
sskkiinn ((turnetarteeadt)ed)
thyroid gland
gross observation4s
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uid, ruffed for,
`The following tissues were weighed: liver, kidneys,and thyroid gland (afer fixation). Organ --~ `weight/final body weight ratios were calculated.
Gross lesions for which a microscopic diagnosis would not be additive (c.g., osteoarthritis, `pododermatitis, chronic dermatitis ofthe tai, urinary calculi, and deformity ofthe teeth, toe, tail or pinna) were saved but were generally not processed for microscopic evaluation.
All tissues were fixed in 10% neutral buffered formalin. Processed tissues were embedded in `paraffin, cut ata nominal thickness of micrometers, tained with hematoxylin and cosin (H&E), and examined microscopically.
All collected tissues from rats in the control and 1000 mg/kg/day groups were processed to slides and receiveda full histopathological examination.
N. Statistical Analyses
Significance wasjudged at p <0.05.
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--_
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2152.5D4a2y5S:tRdeypeiantMeadlDeoRsaesDel Tosiity
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~
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performed i htbib on d BIfotnhieeirnocniidecnocneecwtaisonnowtassigunsifdi.cant, but a significant lackoffit occurred, then Fisher's Exact test' with a
---
-- --_--
Company Sanizsd. Does notcontain TSCA Ca1
H2-82-5D4a2y5S:tuRdy ien MpaleDeoRsaetaDsertmaelTodric:ity --~
RESULTS AND DISCUSSION
Dupont 13830
Tu-Life Toxicology
A. Mean Body Weights and Body Weight Gains (Tables 1-2, Figure 1, Appendix A)
No test substance-related effects on mean body weights or mean body weight gains were observed in any groupofmale rats. No statistically significant differences in mean body weights were observed. Mean body weight gains in all groups were greater than control over some intervals (not statistically significant). Mean body weight gains in all test groups were statistically decreased compared to control in the interval days 10-14. The differences were not considered test substance-related because they did not exhibit a monotonic dose-response. The nmoetacnonosveirdaelrledbotdoybewetiegsthtsugbasitnasncien-arlellatetsetdgbreocuapussewetrheeylwoewerre tnhoatnstcaotnitsrtoilc.allTyhseigdniifffiecraenntcaensdwedride not exhibit a monotonic dose-response.
--_
B. Food Consumption and Food Efficiency
(Tables 3-4, Appendix B)
No effects on food consumption were observed. Mean overall food consumption (test days 0-27) in the 1000 mg/kg/day group was 101%ofcontrol (not statistically significant).
No test substance-relatedeffectson food efficiency were observed. Mean food efficiency was statistically decreased in the interval days 7-14 at al dosages. These differences were not considered test substance-related because they did not exhibit a monotonic dose response. Mean overall food efficiency was statistically decreased in the 100 and 1000 mg/kg/day groups. These differences were not considered test substance-related because they were 10% or less than control, mean food efficiency in these groups was greater than control over 1 or 2 weekly intervals (not statistically significant), and the decreased food efficiency did not result in any reduction in final body weight or overall body weight gain.
C. Clinical Observations, Dermal Effects, and Mortality (Tables 5-7, Appendices C-E)
wNeoreclninoitcaclonssiigdnesrreedsutletsitnsgufbsrtoamncsey-srteelmaitcedtoaxsitchietyywocecruerroebds.erOvceudlairn dbiostchhatrregaeteadndanndascaolntdrioslcharge
animals. Dark eyes, comeal opacity, or enophthalmus were observed in several rats during the
--_
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-
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H282-5D4a2y5:StuRdeypeinatMeadl-eDoRsaetsDermal Toricity
Dupont13830
~ Hair loss, superficial wounds, swollen face, and stainingofthe fur/skin were present in both treated and control animals and were not considered test substance-related.
No dermal irritation was observed during the study.
No deaths occurred.
D. Perfluorooctanic Acid (PFOA) and Total Fluorine Evaluations (Tables 8-9, Appendices F-G)
PFOA concentrations in plasma from rats in the control group and the 10 mg/kg/day group were below the lower limitofquantitation (LLOQ or 10 ppb). The mean concentrations were 13 ppb in the 100 mg/kg/day group and 105 ppb in the 1000 mg/kg/day group. These levels were cthoensPiFdeOrAabliyn tlhoeweprlatshmaan,twhhoestehoebrsefrrvoemddiinretchteaoprpallicsattuidoynwoirtmhetthaisbotelsitssmuobfstcahnecmei.c"alTihnetsheoutrecste of substance, is unknown. Fluorine levels in blood from treated and control rats were either not detectableorbelow the limitof quantification (LOQ or 500 ppb). This is in contrast with the measurable total fluorine evident in animals dosed at al levels (10 mg/kg/day and above) in the oral study.
--~ E. In-Life Conclusions No adverse effects were observed on mean body weight, nutritional parameters, mortality, or clinical signs in male rats treated up to and including 1000 mg/kg/day. PFOA was present in plasma from rats treated at 100 and 1000 mg/kg/day. Blood fluorine levels were not detectable at levels above the LOQof 500 ppb inanydose group.
Clinical Pathology Evaluation
A. Hematology (Table 10, Appendix H)
`There were no adverse changes in hematologic parameters in male rats. The following statistically significant changes in mean hematologic parameters were not related to treatment: + Mean corpuscular hemoglobin concentration was minimally but statistically increased in
`omcacluersitnreaatdeodsew-irtehla1t0edorpa1tt0e0r0n,magn/dkgwe(rbeotthhe1r0ef2o%roefcocnosnitdreorlemdetaon)b.e uTnhreeslaetecdhatnogterseadtimdennto.t
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2H-82-5D4a2y5;StuRdeypeinstMcadl-eDoRsaetsDermalToricity
DuPont.13830
~ B. Coagulation (Table 11, Appendix H)
`mTahleererawtse.re no treatment-related or statistically significant changes in coagulation parameters in
C. Clinical Chemistry (Table 12, Appendix H)
`There were no adverse changes in clinical chemistry parameters in male rats. The following statistically significant changes in mean clinical chemistry parameters were cither treatmentrelated and not adverse, or not related to exposure to compound:
+ Minimally decreased urea nitrogen and creatinine in males treated with 100 or 1000mg/kg were considered 10 be treatment-related. Mean concentrationsofurea nitrogen were 83% of controls in both groups, while mean creatinine concentrations were 83% and 76%ofcontrols inratstreated with 100 or 1000 mg/kg, respectively. In addition, with the exception of one: rat treated with 10 mg/kg, creatinine concentrationsofthis group were also decreased. Generally, increases in urea nitrogen and creatinine are considered adverse; minimal decreases in these parameters have no toxicologic significance. The causeofminimally decreased urea nitrogen and creatinine was not addressed in this study.
--~
+ C1h0o0l0esmtge/roklga(nstdattirsitgilcyaclelyrisdiegnciofnicceannttroantliyonfsorwecrhoelemsitneirmola;llmyedaencsrewaesreedi8n1m%alaends 7tr2ea%teodfwith
respective controls). These decreases were likely to be treatment.related based on the
distributionofthe individual animal dataincomparison to control rats. However, because
the rangeof individual values was similar between control and 1000 mg/kg groups, these:
changes were considered to be non-adverse.
+ Potassium was minimally decreased (statistically significant) in males treated with 1000 mg/kg (90%of control group mean). This decrease was likely to be treatment-related based on the consistencyofthe individual animal data. However, in comparison to historical Iaboratory data, individual animal potassium concentrations in both the control and 100 mg/kg groupsofrats were within the historical range for individual animal values (5.17.3 mmol/L), with the exception ofone outlier in the control group (#902) with a phiosttaosrisciaulmrcaonngceeonftrmaetaionnsof(57..77-62.5mmmomlo/lL/.L)I.naTdhdeirteifoonr,e,methainsschfaonrgbeo,thalgtrhoouupgshwterreaetmweintth-in the related, was not considered to be adverse.
D. Urinalyses (Table 13, Appendix H)
`There were no adverse changes in urinalysis parameters in male rats. The following statistically significant change was not related to treatment --
t TT ee `Company Sanitzed.Doen snotcontain TSCA CBI
H2-82-5D4a2y5;StuRdeypeinatMeadl-eDoRsaeisDermal Toxicity
Dupont13830
~~ + Urine protein was increased in males treated with 10 mg/kg. This change occurred only in the low dose group, and therefore was considered to be unrelated to compound.
E. Urine and Plasma Fluoride (Tables 12-13, Appendix H)
`There were no statistically significant or treatment-related changes in plasma fluoride or urine fluoride at the endofthe dosing period.
F. Clinical Pathology Conclusions Treating male rats dermally with H-25425 at dosages up to 1000 mg/kg for 28 days resulted in `minimally decreased urea nitrogen and creatinine at 100 and 1000 mg/kg/day and minimally decreased cholesteral, triglycerides, and potassium at 1000 mg/kg/day. Noneofthese changes wereconsidered to be adverse. Therefore, there were no adverse effects on hematology, coagulation, clinical chemistry, or urinalysis parameters in the dermal study which is consistent with the oral study.
Anatomic Pathology Evaluation --~
A. Causeof Death (Appendix J)
`There were no test substance-related deaths. All 40 rats survived until the scheduled 28-day sacrifice.
B. Organ Weights (Table 14, Appendix I)
`There were no dermal exposure-related effects on absolute or relative organ weights. All individual and mean organ weight differences were considered (0 be spurious and unrelated to test substance administration.
C. Gross Observations (Table 15, Appendix J)
`There were no test substance-related gross observations. The three gross observations made at necropsy were interpreted to be incidental lesions unrelated to test substance administration.
--_
-_--
`CompanySanitized.Doesnot conTtSaCAiCBnI
H2:82-5D4a2y5S:tuRdeypeinatMeadl-eDoRsaetsDermal Tosiciy
DuPont13830
~ D. Microscopic Findings (Table 16, Appendix J)
`There were no test substance-related microscopic findings. All microscopic findingsinthis studyareknown tooccurnaturally in ratsofthis stock and age and were not present in a doseresponse fashion in either incidence or severity.
E. Anatomic Pathology Conclusions No adverse effects were observed on mortality, organ weights, gross pathology, or histopathology in male rats treated dermally up to and including 1000 mg/kg/day. This is in contrast with the reversible, minimal to mild thyroid follicular hypertrophy observed at 1000 mg/kg/day in the oral study.
--~
--_ EE `Company Sanitized. DE oesnotcE ontain TSCA CBI
H2-82-5D4a2y5S;tuRdy ien VpaleDeoRsaetaDsertmaelTodxic:ity PN
DuPont 13830
CONCLUSIONS Urantdsewrasthe10c0o0ndmigt/ikongs/odfayt,hitshesthuidgyh,estthedonos-aogbesetersvteedd.-efTfhecetNlOevEelL(iNsObEaLs)e'd ofonraH-la2c5ko42f5adinvemrasleetest `smuablsetarnactes-trreelaatteedddeefrfmeacltslyonatadnoysaing-elsifue,pctloini1c0a0l0pamtgh/oklgo/gdya,y.or anatomic pathology parameter in
RECORDS AND SAMPLE STORAGE
All data and records for analytical characterizations conducted by or for the sponsor will be
retained by the sponsor. equipment records will
Laboratory-specific or site-specific be retained by the facility where the
raw data, work was
such as done.
personnel
files
and
A sampleofthe test substance will be collected for archive purposes and retained at Haskell Laboratory, Newark, Delaware. Specimens (ifapplicable), 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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definedbythe European Union 09
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REFERENCES
1. DRautPsownittHhaOsnkee-llGeLnaebroartaitoonryRe(2p0r0o3d)u.ctHi-o2n5E4v2a5l:uatSiuobncsh.roUnnipcubTloxiischietdy,e9r0-oDa,y Gavage Study in 2. CblaopokdaaVt.t,rBacoewecrosnc,eCn.r,aNtairovnelseevne,lsJ.bNy.,thaendWiRcokssbio,lRd.dFe.coDmeptoesrimtiinoantimoenothfotdotwailtfhludoirreicnte in
potentiometric detection. Talanta 2004 accepted for publication. 3. DWrialpeeyr,,NNeRw.Yaornkd.Smith, H. (1981). Applied Regression Analysis, 2TM edition, pp 266.273.
4. Saneilmwayln,saMfRet.y s(t1u9d9ie5s)..TJhouerunsaelofoftthreenAdmetersitcsatno dCeotlelremgienoefTaonxo-iocbosleorgvyab1l4e(-2c)f,fe15c8t-l1e6v8e.l in
5.
Jonckheere, AR. (1954). Biometrika 41, 133-145.
Adistribution-free
K-sample
test
against
ordered
alternatives.
6. SLteavteisntei,csH.(1.(1O9l6k0i)n., eRdo.b)upspt 2te7s8t-f2o9r2c.quSatlaintfyoorfdvUanriivaenrcseis.tyCPornestsr,ibPuatlioonAslttoo.Probability and
7.
Shapiro, $5. and Wilk., M.B. (1965). samples). Biometrika 52, 591-611.
An
analysisofvariance
test
for normality (complete
~
8.
Snedecor, 349-352.
G.W. and The lowa
Cochran, W.G. State University
(1967). Press,
Statistical Iowa.
Methods,
6"
edition,
pp
246-248
and
9.
Dunnett, CW. (1964). 482-491.
New tables for multiple comparisons with a control.
Biometrics 20,
10.
Dunnett, C.W. (1980). Pairwise Statist. Assoc. 75, 796-800.
multiple
comparisons
in
the
unequal
variance
case.
J.
Amer.
11. Tunaemqhuaanlev,arAi.aCn.ce(s1.97J9.)A.meAr.coSmtpatairsti.soAnsosofc.pr7o4c,e4d7u1r-e4s8f0o.r multiple comparisonof means with
12.
Kruskal, J. Amer.
WH. and Wallis, Statist. Assoc. 47,
W.A. (1952). 583-621.
Useofranks
in
one-criterion
analysisofvariance
13. Dunn, 0.1. (1964). Multiple contrasts using rank sums. Technometrics 6, 241-252.
14. FNieshwerY,oRrk..A. (1985). Statistical Methodsfor Research Workers, 13" edition. Haffner,
15. HfoarzAanradlyEsviasluaantdioEnvaDliuviastiioonn,ofStSaunbdcarhdroEnviacluaantdioCnhrPornoiccedEuxrpe,osTuorxeicSittuydiPeotsenPtaiyanlt:er,GuOi.dEa.nce
e`Wtaaslh,iUnngtiotne,dDS.tCa.,tes2E0n4v0i6r.onEmPeAn-t5a4l0/P9ro-t8e5c-t0i2o0n.Ag(eJnucnye,1O9f8f5i)c.e ofPesticide Programs,
16.
Risk Assessment (XI/283/94-EN),
oChfaNpotteirfiI,edSeNcetiwonSsub2s.t2a4nacnesd.2.T2e5c.hn1i9c9a4l,
Guidance
Document
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H-25425: Repeated-Dose Dermal Toxicity 28-Day Study in Male Rats --~
DuPont13830
--
TABLES
= -_-- `CompanySanitzed.DossnotconTtSaCAiCBnI
216.2:5D4a2y5:StuRdeypeinatMeadl-eDoRsaetDsermal Toricity
Abbreviations
mg=/ mg/k kg/g day
gan=mgra/ms/adnimaaliyday
TABLES EXPLANATORY NOTES
`Summary of Hematology Values
RBC - redblcoellocodunt
HGB - hemoglobin
HCT - hematocrit
MCV - meancorpuscularvolume
MCH - meancorpuscular hemoglobin
MCHC - mean corpuscular hemoglobin concentration
RDW - redcelldistributwiidotnh
ARET - absolutereticulocytecount
PLT - platelet count
WBC - white blcoellocoudnt
~
ANEU - absoluteneutrophil(al forms)
ALYM - absolute lymphocyte
AMON - absolute monocyte
AEOS - absoluteeosinophil
ABAS - absolutebasophil
ALUC~ -- anodbataslarogeulnstuaintedceell
SummaryofCoagulation Values
PT - prothrombintime
APTT~
- activatedpartialthromboplasttiimne - nodita
DuPont13830
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TABLES
EXPLANATORY NOTES
`SummaryofClinical Chemistry Values
AST - aspartateaminotransferase
ALT - alanineaminotransferase
SDH - sorbitoldehydrogenase
ALKP - alkalinephosphatase
BILI - total bilirubin
BUN - ureanitrogen
CREA - creatinine
CHOL - cholesterol
TRIG - triglycerides
GLUC - glucose
TP - totalprotein
ALB - albumin
GLOB - globulin
CALC - calcium
IPHS - inorganic phosphorous
~
NA - sodium
K - potassium
CL - chloride
PFL~U -- plnaodsamtaafluoride
Summary of Urinalysis Values VOL - volume
UOSM - urineosmolality PH - the logarithmofthe reciprocalofthe hydrogen ion concentration
URO - urobilinogen UFLU - urinefluoride UMTP - urineprotein
~ - nodata
Clinical Pathology Note
``wWehreenpearnfionrdmieviddouanhloablsfetrhveatrieocnowrdaesd vraelcuoer.deFdoarsbeexaimnpglele,issfthbialniraubcienrtwaaisn vraelpuoer,tecdalacsul<a0t.i1o,ns0.05 `was used for any calculations performed with that bilirubin data.
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DuPont 13830
TABLE 7
PERCENT SURVIVAL OF MALE RATS
Group: x
Dosage (mg/kg)
0
x1 xm
xv
10
100
1000
Days on Test
07
110000 110000 110000
110000
2114
110000 110000 101000 110000
28
100 100 100
100
`Numberat studystart Aliveon testday28
10
10
10
10
10
10
10
10
Percent Survival = (Numberofrats alive/Numberofrat at risk)*100 Numberofrats at risk = Number at study start.
-- `There were no statistically significant decreases in survival.
-- - `Company Sanitized. Does not contain TSCA CBI
2285.0D2ay5:StRuedpyeiantMeadl:eDoRsaetsDermal Tosiciy --
DuPon-13830
TABLE 8
MEAN PFOA CONCENTRATIONS IN MALE RATS
PLASMA PFOA (ppb)*
Dosage (mg/kg/day) Mean
SD.
n
0
<10
00
10
10
<10
00
10
100
13
2
10
1000
105
2
10
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(<10 pp)
--~ ---
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H-25425: Repeated-Dose Dermal Toxicity 28-Day Study in Male Rats --_
TABLE9
MEASURED CONCENTRATION (ppb) WHOLE BLOOD FLUORINE
Dosage (mg/kg/day)
Mean
n
0
<500 ppb or ND
5
10
ND
5
100
<500 ppb or ND
5
1000
<500 ppb or ND
5
Nn=Dn=unmobtedreotfescatambpllee=svalues < 200 ppb
Values "lessthan S00ppb"are > 200 ppband < 500ppb. 500ppb =Limiotf quantification (LOQ).
--~
DuPont 13830
--~ - `CompanySanitized. DoesnotconTtSaCAiCanl
H282-5D4a2y5:StuRdeypeinatMeadl-eDoRsaetDsermal Toricity
DuPont. 13830
TABLE 10
SUMMARY OF HEMATOLOGY VALUES FOR MALE RATS
Group IX Omgkg
Group XI 10 mg/kg
Group XI 100mghg
Group XV. 1000 mgkg
RBCDA(xY102%8uL)
731
7.16
7.07
7.18
0.157)
0.259)
0.260)
0360)
HGBDA(gY/d2L8)
146
147
143
14s
HCT (%)
047)
049)
059)
049)
DAY 28
413
467
457
457
15(7)
1.409)
170)
140)
MCVDA(fYL)28
6438
653
646
6.7
MCH (pg)
200)
1.50)
110)
1.60)
--_
DAY 28
200
206
203
201
r
MCHC (g/dL)
0.7(7)
0.609)
0.509)
0.609)
DAY 28
309
315%
314
316
0.67)
0.40)
0.49)
039)
RDW (%)
DAY 28
1s
1.6
nr
n2
ARET (x104L) 0.67) 0.4(9) 090) 030)
DAY 28
219 95.3(7)
2644 58.49)
3020 140.79)
251.0 55.30)
PLT (x10%4L)
DAY 28
1264
na
1210
1242
WBC (x104L) 2602) 177) 8168) 1268)
DAY 28
1485
13.80
3.1107)
2.5009)
1431 24109)
1384 22309)
ANEU (x10%4L)
DAY 28
249
215
225
197
ALYM (x10%4L) 0.95(7) 0.46(9) 1.0209) 0.400)
--
DAY 28
1150 2.937)
10.86 2.0609)
132 1640)
105 1990)
-
Company Sanitized. Does not contain TSCA CBI
2285.0D2ay5:StuRdeypeinatMeadl-eDoRsaetsDermal Toriciy --
Dupont 13830
TABLE 10 (Continued)
SUMMARY OF HEMATOLOGY VALUES FOR MALE RATS
Group IX Omgkg
Group XI 10mglkg
Group XII 100mgkg
Group XV. 1000 mgkg
AMON (x104L)
DAY 28
039
032
036
042
AEOS (x10%4L) 0.08(7) 0.1309) 0119) 0.119)
DAY 28
020
0.15
013
ols
0.1007)
0.069)
0.079)
0.0409)
ABAS (x10%4L)
DAY 28
0.08
0.09
007
0.06
ALUC (x10%4L) 0.047) 0.059)
0.0409)
0.029)
DAY 28
020
023
017
019
0.147)
0.1209)
0.1009)
0.05(9)
--
Dumamngedas: Mean
Standard deviation (Numberof values included incaleultion)
+ Statistically significant differencefromcontrol a p< 0,05 byDunnetyTamhane-Dunnett est
-
a Company Sanitzed. Does notcontainTSCA CBI
H2.82D5a4y25S:tuRdeypeinatMeadl-eDoRsaetsDermal Toxicity --~
DuPont.13830
TABLE 11
SUMMARY OF COAGULATION VALUES FOR MALE RATS
Group IX omgkg
Group XI 10 mg/kg
Group XIII 100 mgkg
Group XV. 1000 mg/kg
PT (sec) DAY 28
APTT (sec) DAY28
155 0.5(10) 180 1.6(10)
159 0.6(10) 187 22(10)
156 0.510) 1.5 12(10)
161 0.8(10) : 188 19(10)
Dara amanged as: M`Setaanndarddeviation(Numberofvalues included in calculation) There were no statistically significant differences from conirol at p < 0.5.
~~
PN -_--
`Company Sanitized. Does not contain TSCA CBI
H2265-4D2a5y:StRuedpyeiantMeadleDoRsaetsDermal Toricity --
TABLE 12
DuPont 13830
SUMMARY OF CLINICAL CHEMISTRY VALUES FOR MALE RATS
Group IX 0mgkg
Group XI 10 mg/kg
Group XII 100mgkg
Group XV 1000 mg/kg
ASTD(AUYL)28
12
122
106
108
3000)
22(10)
20010)
23(10)
ALTDUALY)28
52
st
"
a7
SDH (UL)
7010)
9(10)
9(10)
11010)
DAY28
18.6 7.610)
15.0 7.010)
19 2410)
129 4610)
ALKP (UL)
DAY 28
212
20
205
244
45(10)
47010)
4310)
51010)
BILID(AmYg/2d8L)
0.05
0.06
005
0.06
rm
BUN (mg/dL)
0.0010)
0.02(10)
0.00(10)
0.02(10)
DAY 28
18
17
15
15
CREA (mg/dL) 210) 2010) 2(10) 2(10)
DAY 28
029 0.05(10)
026 0.05(10)
024% 0.02(10)
022+ 0.03(10)
CHOL (mg/dL)
DAY 28
[3
4
43
30+
TRIG (mg/dL) 11010) 710) 5(10) 6(10)
DAY 28
a3
4
36
31
18(10)
24(10)
1300)
1300)
GLUC (mg/dL)
DAY 28
13
104
101
107
TP (g/dL)
2810)
12010)
10010)
1810)
DAY 28
61
6.1
60
60
03(10)
0.4(10)
03(10)
03(10)
ALB (g/dL)
DAY 28
41
a1
a1
a1
~
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03(10)
0.110)
02(10)
-_--
`Company Sanitized. Does not contain TSCA CBI
H2-82.5D4a2y5:StuRdeypeinatMeadl-eDoRsaetsDermal Toxicity
DuPont13830
TABLE 12 (Continued)
SUMMARY OF CLINICAL CHEMISTRY VALUES FOR MALE RATS
Group IX omghkg
Group XI 10 mgkg
Group XII GroupXV 100 meg 1000 mg/kg
GLOB (g/dL)
DAY 28
20
21
20
19
CALC (mgdL) 03(10) 02(10) 02(10) 02(10)
DAY28
14 0.710)
12 0.6(10)
11 0310)
n2 02(10)
IPHS (mg/dL)
DAY28
1.9
12
104
107
22010)
15010)
0.7010)
0.6(10)
NA D(mAmYo2l/8L)
1472
1476
141.7
1482
K (mmol/L)
1.7010)
23010)
1.6(10)
18010)
--_
DAY 28
6.41
625
6.05
5.80
0.65(10)
042(10)
0.45(10)
0.3010)
CL (mmol/L)
DAY 28
1023
102.6
1032
1042
PFLU (ug/ml) 2110) 1.7010) 13010) 25010)
DAY 28
ol
ol
01
ol
0.010)
0.010)
0.010)
0.0(10)
Data amanged as: MSteaanndard deviation (Numofbvaelures includedi calculation) + Sutistically significant difference from control at p< 0.05 byDunner Tamiane-Dunnett est
--~ -_--
ae Company Sanitized. Doesnot contain TSCA CBI
H2-82:5D4a2y5S:tuRdeypeinatMeld-eDoRsaetsDermal Toxicity --_
DuPont 13830
TABLE 13
SUMMARY OF URINALYSIS VALUES FOR MALE RATS
Group IX Omgkg
Group XI 10 mgkg
Group XIII 100 mg/kg
Group XV. 1000 mg/kg
VOL (mL)
DAY 28
90
72
12
8s
UOSM (mOsm) 5.0010) 4510) 5.010) 3.410)
DAY 28
1069
1461
78
924
691010)
662(10) 407(10)
346(10)
pH DAY 28
75
74
76
74
URO (EU/L) 0409) 08(10) 0.510) 0.5(10)
DAY 28
02
02
02
02
UMTP (mg/dL)
0.009)
0.0(10)
0.0(10)
0.0(10)
~
DAY 28
0
ne
a8
59
35(10)
599)
3310)
33(10)
UFLU (kg)
DAY 28
80
7.1
8.1
80
2910)
2.010)
1.6(10)
1.610)
Data arranged as: M`Setaanndard deviation (Numofbvaelures included in calculation) * Suisically significant difference from control atp < 0.05 byDunner TarhaneDunnett est.
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DuPont13830
FIGURE
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DuPont13830
APPENDICES --~
-= Company Sanitized. Doesnotcontain TSCA Cal
H-25425: Repeated-Dose Dermal Toxicity 28-Day Study in Male Rats
DuPont13830
APPENDIX A INDIVIDUAL BODY WEIGHTS
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H2-82-5D4a2y5:StRuedpyeiantMeadl-eDoRsaetsDermal Toxicity --~
DuPont13830
--
APPENDIX B
INDIVIDUAL FOOD CONSUMPTION
~~ e EE e ------ `Company Sanitie zed. Does not contain TSCA CBI
H2-62.5D4a2y5;StuRdeypeinatMeadl-eDoRsaetsDermal Toxicity ~~
INDIVIDUAL FOOD CONSUMPTION EXPLANATORY NOTES
Abbreviation ganm/day = grams/animal/day
DuPont 13830
--~ -______e Comp_ inySanit_ ized. Do_ es notcon_ tain TSC_ A CBI
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H-25425: Repeated-Dose Dermal Toxicity 25-Day Study in Male Rats --_
DuPont13830
APPENDIX C INDIVIDUAL CLINICAL OBSERVATIONS AND MORTALITY RECORDS
--_ Et --`Company Sanitized. Does not contain TSCA CBI
H.25425: Repeated-Dose Dermal Tonicity 26.Day Study in Male Rats
DuPont13830
INDIVIDUAL CLINICAL OBSERVATIONS AND MORTALITY RECORDS EXPLANATORY NOTES
Note Clinical observations reported in this appendix were recorded during body weight collection. Clinical observations recorded post-dosing are not included but are reported in Appendix D.
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H2-82-5D4a2y5S:tuRdeypeinatMeadl-eDoRsaetsDermal Toriity
DuPont. 13830
APPENDIX D INDIVIDUAL CLINICAL OBSERVATIONS - POSTDOSING
TT ---- Company Sanitized. Does not contain TSCA CBI
H.25425; Repeated-DoseDermalToxicity 28-Day Study in Male Rats
DuPont13830
INDIVIDUAL CLINICAL OBSERVATIONS- POSTDOSING
EXPLANATORY NOTES Clinical observations reported in this appendix were recorded daily after removal ofthe test substance. Clinical observations recorded during body weight collection are not included but are reported in Appendix C.
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INDIVIDUAL EDEMA AND ERYTHEMA SCORES EXPLANATORY NOTES
DRAIZE* SCALE FOR SCORING SKIN IRRITATION
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Score
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DuPont13830
--~
APPENDIX F
PFOA ANALYTICAL REPORT
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F2-82-5D4a2y5:StuRdeypeinatMeadl-eDoRsaetsDermal Toxicity
DuPont13830
STUDYTITLE F-25425; RepeDoasetDeermdal Tox28DiaycStuidyitnMiyle Rats
DRAETQAUIREMENTS Analytical Method Requiements
`STUDYDIRECTOR Carol Finlay
ANALPHYASTECOIMPCLETAEDLON March 10,2004
PERFORMINGLABORATORY
--~
30E5x8ygReesncaRrecsheaDrrcihve
`SPtahtoenCeo:ll3e1g4e.,2P72A.110638901
`STUDYSPONSOR E.1 duPont deNemPo.0u.rBsoaxnd0Company(DuPont)
Newark, DE 19714-0050USA
PROIECT `SpEoxnysgoernSSttuuddyyNNou:mbeDruP:o0r0t-814308360
"TotalPages:65
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`QUALITYASSURANCESTATEMENT
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CERTIFOIFCAUATHTENITIO CIN TY
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H-25425: Repeated-DoseDermal Toxicity 28-Day Study in Male Rats --
DuPont13830 ExygenStudy Nos 08-406
EIXYDGEENNSTTUIDYFICATION F-25425:Repestd-DoseDermal Tricity28-DayStyinMileRats
SPONSOR STUDY NUMBER: ~~ DuPont-13630
EXYOEN STUDY NUMBER: 008-406
`TYPE OFANALYTICALPHASE: Residue
SAMPLE MATRIX:
Rat Plasma.
TBST SUBSTANCE:
Pentadecaflsorooctanccaid(PFOA)
SPONSOR:
EPL.L0..dBuoPxo5n0tdeNemaonduComrpasny NPheownaer:k,(3D07E) 1396761-45-2050550
~~
STUDY DIRECTOR:
CDaurPoolnFtinlay
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DuPont13830 BoygenStadyNo. 08-406
PROJECTPERSONNEL
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Name Paul Connally EmilyDeckee Karen isha Mark Anmerman
Shan Robb
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Pagers
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F-25425: Repeated-Dose Dermal Toricity 28-DayStudyin MaleRats --_
DuPont-13830 ExygenStayNos 08-406
`TOAFCBONTLENETS ae GQOUOALDITLYAABSOSRUARTOARNYCPERSATCATITCEEMCOEMNPTLI.A.NC.ErScTrATeEsMsENsTeemsrc. nd.
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60 DESCOFRANIALYPTICTALIMETOHOND
----
62PreparationofStandards4nd FOrcationSaIuions revues 11
L 65Descriptionof stunt 4dOperiingY Conions... ovr 12
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TeblelL. SummaryofRecoveriesof PFOA (%)inRatPlasmaSamples... 18.
TableIIL SummaryofResidueFound for PFOA (ppt)inRatPlas
Samples. 19
EugenResearch
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LISTOFFIGURES
Be
Figur1e. Typical Calbaion Curve 0PFOA verses 21
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--~
LAIPSTPOFENDICES
Bae
Appendix A. Study ProtocolDuPont13830(Exygen Study No. 008-406) nd
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10SUMMARY
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H-25425: Repeated-Dose Dermal Tonicity 28-Day Study in Male e Ratse
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50 REFERENCEMATERIAL
M"aThrecshm0al5y,ic2a0l03stfarnodmarCdproitadePcaatlhoSoerrovoiicaenso.lTchceicdo(nPtFoOlAa)rtiwclser(ientecmaleastiEasnvydgaeenroddn) DpuePcoinoto.roactncic acid (1,2 dC) was eceived st Exygen on Febuary 20, 2003 from Tsthaendaavradilwibalsesionrfeordmaitnion& feofxitgheerseofreeanncdethmaetecroinatlriol lrisitecdebewlaows,stoTrheednaalyfiocoaml lepers,
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ChPeFmOicAal Nome = pefiorooctaaaccid Molecular weight = 414
Ch"ecmi_cparlONAame = perfiorooetasniodi,12:-C) Molecule weight = 416
EBxygenResearch -_--
Page 10065
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A0s.o0l5utiyoanwle.sofie"dCFpFrOcA
001
imcaakcihngfl
inion
"aoTFhpcnma.iiTorheboeaxarndaacoesndesgarneipieroscesesdwihitogyudgahhtoewweonwxeeedok Bnaxppnrrnnoitchoensdm,etcehosnnvaclgdaoitoenc
GSonye Ecc soyoedg.o 0fo0el6lo2w7nin7n g.aThh:fonicadonofte andr bore,excion 5
EE
Paes
--~ ---
`Company Santized. Doss not contain TSCA CBI
H2-52-5D4a2y5:SRtepieuantMdeadly-eDoRsaetDsermal Toxicity
DuPont-13830
EsSaydyNgo.e08-4n06
"CoPFmO.A OfVFooruimfiea(llo)n VaCloummmeiof
FoSroilfuitciaotnon
Semple (ml)
-- oor 0
oF
ooot1 2500 oo1r
ooii 12000 oorr
CEoxtmcotefd CaSltiabnrdaatridon
30 1500 4
Tshoheueixotnacntidobnrsionlguitnigonthweavsoplruempeaurped0by10ta0kmiLngwi0.t5hmaLcroofntihse.T1h0egdi/lmuLt.io"nCsPolFutOioAn vwoalsupmreepuaprteodb10y0mtaLkiwnigt0h.S50m5L0moeftthhano1.l0wautge/rml. "C-PFOAsoutonandbringingthe
i"nThaesetockistang da(r4dseol2utCiro)nawnht deanlnofotionrrset.fDiocaciuosmntaon/fedsaatrnadlnsdotilaurtbdaiporrnetspawareaittriiosonoorcnenadn. oefoundinthe awdatsasocitedwithtisreport
63Chromatography
~
"`TQhuearneitecnatiioonntiomfePoFfOPAFwOiAwsassco~mp2i0mshiend,bwyitahnnaolyssiignsiufsiicnagnetliencterfoesrpinrgapyeLaCk-sM(S</2M0S%.
oftheLO standard)inthcontolsamplescorresponding ttheanalyterientontes.
64InstrumentSensittty
`Thesmallest amountofPFOAinfectedduringthechromatographic onwascquivalert0 10. 65DescriptionofInstrumentand OperatingConditions
sAPcEiSocniexnLdCp-rMocSeIsMsiSncgowueprleepdetcoforamHeodwulseitntgPAancaklayr:dH1.P2LsoCftswyasrte.emwaswed. Data Detailedoperatingconditionsar isedbelow:
MIansersaScpee:c: SoCfotmwpaurtee:r: HPLC:
PSCEISECXITEuXrAboPIIo4n0S0p0raByiLiogumidoInltrMoeadusccstiAuonnalIltyaezrefrace TDuerlbOopltoinpSlepxrOyXt1e1mp0erature =350 Cwith N2st 1Limi FPoEwSlceiesxPaAcnkaalrydst(:HVPe)rSseiroines1.12100
ExygenResearch
Page 120165
BO`Company Saitized.Doesnot conTtSaCAiCBnI
425:2D5a4y25S;uRdeypienseMids-lDoRsaetsDermal Toxiity PN
Dupont 13830
Egg SyNo. 008405
BHEp VqouiotouummDo.gster BHPPCAoulnuonmjneCcoomrpatment
HFPiLrCCCaorlimdag:es:G2enKeesyisstConeHoynpeesrCshhe rntsondmem,tex2o1pmipanoxpm5.h0mym,4.. CNoiluenPTheamsep(,A):320mMCAmmo Aces in wale MoPhbase(i3.eleel
Iw m0e wSA a3s7 vo 22550 "a0 f 55 ew" nition Vol: HL ons monitored:
SB Eowaal33sin 11000 aa3s 10o0 aaass3 o 0033
~~
CATPvORAOeA NNMeeogdgievie Top4i41o13n35M0o3n3i9tored
6QuantasdiExtamapletCaliculoatinon
Fievkemaircrowlienmseofnstaemdp a 1chalalimnrstcaandvaerwdwsegeennieibyhneaeLEegMesSsIiMonS.unTrge
bewctongcheinnugutoofnhoefamaolynsabtoenpceknairoenoffit)esradsaapnadkwrinagveArBSt:h 1t2i o(ofr
noievliloewni)nsgeofvtasnsyn. Toricsconceniraion foPFOA wh deeming,fom
Blaoqofi2|avas psedfcal0semthasamaouantdopfsesnbefoidn hpepsinfdncebasiedscsn
egrsionpregneriedby h Analy sowiepagan.
`EAqnautafolund(pp) =(Aas Penk eass=ecs emtx 1se. fl) XDF
[----
Page 30r6s
-- Company Sanitized. Doesnot contain TSCA CBI
2285.4D2ay5:SuRdeypeinatMeadl-eDoRsaetDsermal Toxicity
--
ema --_--------
DuPont 13830
ExygenSoyNo:008406
wFeordstaompc lesforl itfhedpwiee tchKtnroes wconvearmyo.untsofanalyte prio(0extraction,Equation 2was
REeacuosvieorny2(;9)= Analtefou"nAdm(opupnt)A.naal5y.teAanddaetd(foupn)dincone]ob) x 100
F3owrapslasemdatsoacmpalelloihedpwriethtkrneocowvnearym.os of natepir10exracton,Equation
ReEcaouvmeriyo(n9"Ana0lve2 found(oph).-avz.Aneliefound sampleGpb) x 100 "AAmnaloy usddned(0tb)
AIDn0e3x0a2m2p3l8eoSpfk Aa(lStla01nMuOsiAn)g,afnoartcitfuieadlsaam1p0plepfowlilohwsP:RFOaAt.pasossampleExygen
= maycpekars = 21600
1SSpeeoak.a(rges/ml) =Ss41e67ng/L
--~
smorpceape Gontacor
==Soao1mooedsssiss
pbmafdodndeidnfcoonnmel) == N10D
Fromequation 1: Asaifound(pb)
=
[QIGOH0U.S17I39S0I6ON=00004IS4.I1S6H7)1
= ses
Fromequation2: %Reovey
= 65h=1000
1050
- 0%
Naoytb:TehsilsgexamdpilfefcraelnctulfartoimontwhaesvadooevseusshoiwnsfionutnhodeRdAnuWmbDerAsT,Aa.ndthecfore
BopResearch
Puss bot 6s
Tm `Company Sanitized.Doesnot contain TSCA CBI
12.82-5D4a2y5S;tRuedpyeiantMedl-eDoRsaeDsermal Tosicty
DuPont 13830
ExSadyyNoe:008n406
7.0EXPERIMENTALDESIGN coBnakscnihsostweadnclooftncarrtseratagiewotanbssl,oxko,etan5cedmsesoucmnpiclonenfgtorortloi,mweoatosodkrEneXoVowAr0yc0mo8.tn2c7x6ecRreovnoi,sli2so0nfplo2asrnid Scape,sdone fdsampleexracid idoplcte.
80RESULTS
The PFOAfound ith contortplasmasamplesarlistoinTable. inndiTvaibdlaelIr.eTcohveeriaevsefroagPeFpOrAeintthosvoerrryfanodarrdoevilaatisonsfo pPFeOAcisndthte lat plasmasamwaps 97le13.s3% IRndeivsitdusalofePaFtOsAifnrtthhretPFlOaAsissnatmhpelreastepnlgansosmum<pl1e0s0probgi0ve1n3i4n5T.able IL. FAitgyupriees1lc5a.ibeaioncarvefo PFOAsdrprscottivchomsiogamsasegivenia
9.0 CIRCUTHMATSMAYTHAAVEANFFECCTE EDTSHE
rm
QIUALN ITYT OR EGROI FTHT E DAYTA
Threaroknown circumstancstha haveaffectedtequalityofotegiyof hedia.
100CONCLUSIONS
"RTehvisoitopna2.c sampleswerescssfllysledccndingfomethodExM-008.276
110 RETEOFDNATATANIDSAOMPLNES. fWosililnnbaemtsehaefthloaoil.r1eptBprhrpaiskspcceonoosmpodipre:leTotfh,sislcdooocwnndoattsp,ecpalsewdeealftlgl8oy1essoidcginbeydcrBoarpwyydaotfaRtheseuscihcnaahsl Reslepayriceeho'fsrefpcorrhteivnneds asfoulrbottrhieagpcineearlifroedlcofiyvtsiepmdecsbiycphrosvtsdpaotinasn,erw.4i0lClbFeRrPeaitn79n2t.heREexayigneedn
ExygnResear
Page15t6s
Ee CompanySaniized. Does notconTtSaCAiCBnI
H2.52-5D4a2y5:StuRdeypeinatMeadl-eDoRsaetsDermal Toxicity ~
DuPont13830 BygenStody No 08406.
BoysenReseach
Page 160t6S
-`Company Sanitzed. Doss not contain TSCA G81
H2-82-5D4a2y5:StRuedpyeiantMeadl-eDoRsaetDsermal Toxicity
DuPont-13830
ExygenStyNos 008-406 Tablel. SummoafPrFOyA (ppb)inRatPlasmaControlSamples
SpoDnsor
PFOA (gL)
86160Control A OTI3I0A.
ND
869119ControlA 01/14/04
ND
ND =NotDetcted(isthan 10.0pb)
Borges Reseach
Page 170065
he `Company Sanitized. Doesnotcontain TSCA C81
2285D4a2y5:SRyepnestMeadlDeoRsaetsDermal Toxicity
Dupone13830
Buen SyNo:00806
Table IL. Samples Sum ofRem covea riesr ofPFy OA (%) InRatPlasma
oSteTalcraoeNmroTna a vEeononeanse LCS =LiborstcyCone Spike
ewHooSmrr T semun-5rTM entes MPEo&wmWs EiHi- ==-=tm -ba]
Ten wr
Eaten
Fue tots
Pe EE `Company Sanitized. Doss not contain TSCA CB
H2-82.5D4a2y5:StRueypeinatMeadl-eDoRsaetDsermalToxicity --
Dupont 13830
opm Sty No: 08.405
Table
IIL.
Summaryof Residue Samples
FoundforPFOA (ppb) In
RatPlasma
Spoonsor
pGro)o
90w1oDrp
"o10o0
o0o2
<0t000
00s4
1<i0000
s0o6r
0<1000
w0os
1<10000
1008
p1r0e0
1110082
<<110000
1110048
p<10y0
11o0r8
<110000
rr
1i1o0s8
1<10000
1110
100
1301120D0up
tahs
a13208
1108
11230080
111002
11530078
<uis00
1130080
n12
11551001
12s
1155002
412
11850088
1134
11880078
E1n
11560080
715124
ExygenResarh 1510.
115 Page 19065
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2F-82-5D4a2y5:StuRdeypeinatMeadl-eDoRsaetsDermal Toxicity
DuPont 13830 BasenSudyNo: 08406
BaggeReach
Page200665
wm Company Sanitzed. Doss not contain TSCA CBI
H2-82.5D4a2y5S;tuRdeypeinatMeadl-eDoRsaetsDermal Toxicity
DuPont.13830
Eien Study Nos 008406 Figur1e. TypicalCalibCurrvaeftoriPoFOnA 8110 PRO ir agen viel 0.1708 500510 TET)
|
/ TE ERR RRR EEAS SRR RE Aaa
Fagg Research
Pue21 of
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1252.5D4a2y5:SuRdeypmaaildeDoRsaetDsermal Tricity
Dupont13830
Be StyNo:00406 Figur2e. ChroReprmesenatingtaCaloibragtioneStanadardmfor
PFOA at10ppb with ~ 5ng/mLof "C-PFOA
EST
EE E= Eid
BE n=
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H2.82D5a4y25S:udRyeipensMteadl-eDRoasesDena Tosiity
Dupont 13830
Baya Sy No. 008405 Figure3. ChroRepmreseantintg CoontroglRartPlaasmamfor
PFOAwith ~ 5 ng/moLf C-PFOA(ExygenID:0302238
EEE Control A, Sponsor ID:669160,Set: 0114044) gpos m Er
Ct
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12.82-5D4a2y5:StuRdeypeinatMeld-eDoRsaetsDermal Toxicity --~
Dupont 13830 ErynSay Nos 008406
Figured. Chromatogram Represeating Control Rat Plasma Fortified
2ID:100ppb3witS0hpPk2FA,OSA2paonnd3so~rI58nDg:/66m9L1o6f0,"SCe-:PF0O11A4(0E4x4y)gen
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2285.4D2a5y:SRteypeatMeadlDeoRastes.Dermal Toxicity
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EgeSods No: 008406
Figure. Chromatogram RepresentingRatPlasma Sample or PFOA
`with ~ ng/moLf "C-PFOA(ExygenID:L0001573-0021,
rem SponsorID:1301, Set: 0113048)
Ee
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1282.5D4a2y5:StuRdeypeinatMeadl-eDoRsaetsDerm Tosicty
DuPont 13830 Boren dy No: 008406
Study Protocol DuPont-13830 (Exygen Study No. 008-406)
and Amendments and Deviation
--~ --
Engg Reach
Page260165
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0
907
ND
xX
0
908
ND
xX
0
909
ND
x
0
910
ND
x XI
10
1106
ND
10
1107
ND
Xt
10
1108
ND
XI
10
1109
ND
XI
10
1110
ND
Xm
Xin
pat
Xin
~
Xi
100
1306
less than 500
100
1307
ND
100
1308
ND
100
1309
ND
100
1310
ND
xv xv
1000
1506
less than 500
1000
1507
less than 500
Xv
1000
1508
less than 500
xv
1000
1509
ND
xv
1000
1510
less than 500
ND = not detectable = values <200 ppb `Vales "les than 500 ppb" ae 2 200 ppb and < 500 ppb. S00 ppb = limitofquantification (LOQ)
Te`Company Sanitized. Doss not contain TSCA C8I
H2-82D5a42y5:StuRdeypeinatMeadl-eDoRsaetsDermal Toxicity
DuPont13830
APPENDIX H INDIVIDUAL ANIMAL CLINICAL PATHOLOGY DATA
Tier`sCompanySanitized. DossnotconTtSaCAiC8n.
PZaLps me ------ _
Duron 3820
INDIVIDUALANIMALCLINICAL PATHOLDOAGTYA
EXPLANATORY NOTES
I B onDC E Ep mT mm,aegonrreste,,
CottviitwouensormalE setoen vah eians,
w= B SDCTmIpmI Sm o eete Oar ynheieeee, rien
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phGompany Sanited. Does ot contain TSCA GB!
26H--2D5a42y5S;tuRdyeinpMaeleaRattseDedrm-alDTooxisciety --~
DuPont-13830
INDIVIDUAL ANIMAL CLINICAL PATHOLODAGTYA
EXPLANATORYNOTES (Continued)
AmmREvIATIONS: (Continued)
TadiviSdiuknl Sify
C-linsiecraulm sem
Chlhieeprmeoimlsiytaariys
values:
SAISCT AR
saolseeprnauirmnteaitceatmeiarnumsoitnroatnrsafnesrtaesrease
ABSIoPLH C- Satooltrkabaliltiobnlielidprheuohbsyipdnhraotgaesnease
CGRBoENlA C- eCcehrooslsetsintnieitrnroeolgen
TGGe gtiruisgolnyecerides
Te Total protein
G68 slabalin
ThWiAs snoodriouamnie phosphorous
EAoBH CC ELI? -
Spplloaacrsnima ahleimpoolmyisaisfrofnrobnlboloododsamspalmepleforforFlufolruiodreidedetdeertmeirnmaitniaotnion
~
PFICOE C plleassmaa filcutoerriudse from blood sample for fluoride determination
TndiviQduLal Urisqaulaylsiieey V(arluaedsi:os colon) ciVaoxL GVaorliutmy y
Di tho logaritha of the reciprocal of the hydrogen fon concentration
UKmBrbL C oubrloiononedsbilirubin
WUGAFRPoO
-
uurrriionnbeeilpiFrnlooutgoeerniinde
indivBGRiiImdTeu U-rineGepeiiMtnihecerlwoihsaicltoepcibeelllaEscxdamcienlaltsion Values:
eUCRRRCY - rnmiiocnmreoeorrgceadvnaibtslamoisosd cetis
SPER Cope
Ti89-
Company
-- Sanitized.Does not
-- contTaSiCnA CBI
Z2DH8y-2DS5a4u2yd5:SytiuRdeoypMeinaatMleadlo-eDkoResatessDerm~al~Toxicity --~
DDuuPonot m138i30
INDIVIDUAL ANIMAL CLINICAL PATHOLOGY DATA
EXPLANATORY NOTES (Continued)
WOhtehneriFnadaisvoindsu,alalalntroaflwkdiaccha aacreo neoxtplarienpeordteidn, tLhte msauydyberdeuceordtso:one of the follwing reasons of tthhoVoArsLsLaEwmepsFl.eoinwntasssuticCiolcnoiiteatnetndots(ucbr1oepni)eobtfaoirnedt.est(i0ng) (QS) 2tth0hee'sasaharTmoZpeallawwdaaissedavnaopitrliaosbrulie.ttoabflsoerampTfleoesrtitcnoeglsltei(cnNtgSNi)on
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comps, ptm
H2--2D54a2y5:StRuedpyeiantMeadl-eDoRsaetsDermal Toxicity
DuPont13830
APPENDIX I INDIVIDUAL ANIMAL BODY AND ORGAN WEIGHTS
Es `Company Sanitized. Does not containTSCA C8l
H-25425: Repeated-Dose Dermal Toxicity 28-Day Study in Male Rats
INDIVIDUAL ANIMAL BODY AND ORGAN WEIGHTS EXPLANATORY NOTES
Note mg/kg = mg/kg/day
DuPont-13830
210Company Sanitized. Does not contain TSCA CBI
~~ 8 138!
gBl 1E5!
aiF
qiE i
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a [oF E gimEmmEm a E Bo JR aiRi|
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i Uf sanenneena3n) Fis imeneseeraeled
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Company Saizad. Does notcontain TSCA GBI
2F-82-5D4a2y5:StuRdeypeinatMeadl-eDoRsaetDsermal Toxicity --~
DuPont13830
APPENDIX J INDIVIDUAL ANIMAL GROSS AND MICROSCOPIC OBSERVATIONS
--~ ETNCompany Sanitized. Donote contsain TSCA CBI -
BH2-D82Dy54aS2y5u:SbtRueydpyieiaMnteModaelDeRoRseaetssDermal Toxicity
DDuuPoensti13s83n0
INDIVIDUAL ANIMAL GROSS AND MICROSCOPIC OBSERVATIONS
EXPLANATORY NOTES
Note
mg/kg = mg/kg/day
LesionGrading
Hainsdtosepvaetrhiotlyo.giTchael cdihsatnrgiebsutairoen (deexstcernitboefdtiascscourediinnvgotlovethmeeinrtm)oirspihnodliocagtiecd,chwahreacrteera,ppdriosptrriiabuttei,obny ampopdriofpireirastes,ucishaalssofoacsasl,igmnueldtiafsocfaoll,lodwisf:fuse, unilateral, bilateral, etc.; A soverity score, if
Minnoirmmaalll:imitthse.amount ofchange present barely exceeds that which is considered to be within
Mild: in general, the lesion is easily identified but oflimited severity. The lesion probably
does not produce any functional impairment.
Moderate: the Limited tissue
lesion is or organ
prominent but dysfunction is
there is possible.
significant
potential
for
increased
severity.
-- Severe: the degreeof change i either as complete as considered possible or great enough in
intensity or extent to expect significant tissue or organ dysfunction.
`Comment:
grades minimal continuum with
tmhirnoiumgahlsleevseiroensrebperiensgenttheprloegarstessseivveereinavnodlvseemveenretsleevseiroinstybaelionnggthae
mthoesytaslesvoerien,dicWahtieltehetihrergelraatdievse rbeifoelrogtioctahlesmigonripfhioclanocgei.cal characteristics of lesions,
Gross observations 4 etc)
listing
multiple
masses
for
a
tissue
are
distinguished
with
letters
(i.c.,
a,
b,
,
----
me
--
`Company Saniized. Does notcontainTSCA CBI
H2-82D5a42y5S:tuRdyienpMaeleaRtateDsedrm-alDTooxisciety
DuPont-13830
~
Individual Animal Listing
Date:20-228-013
DsorsoeoyGr|oup + I% 0 MG/KG
an`AiPmPaRlOVdEaDtaPROfoTrOCOiLnd+i)vidual animals (Gontrol) Treatment: 0mg/kg IX Sex: Males
Animal Ret
Microscopic & Macroscopic Findings
=
S01
KteirlmliendalonsDaacyrif: ic2e8
Tr
oT
Animal is signed off from necropsy
Gross pathology
No MLaIcVrEoRs,copKiIDcNEAYbSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
Histopathology :
KvIeDNmETYNSF:LNMATION, SUBACUTE/CHRONIC, mild. CHRONIC PROGRESSIVE NEPHROPATHY, mininal.
No MTiHcrYoRsOcIoDpiGLcANADb,norSKmIaNl,ityTREOAbTsEeDr,vedSKI:N, UNTREMTED
s02
TKeirlmliendalonSDaacyrif+ ic28e
~~
Aninal io signed off from necropsy Gross Pathology :
No MLaIcVrEoRs,copKIiDcNEAYbSn,ormTaHlYRiOtIyDOGbLsAeNrDv,edSK:IN, TREATED, SKIN, TREATED
Histopathology
LIvERIN: FLNGGTION, SUBACUTE/CHRONIC, mild. KIoveAYGsGR:EGATES, LYMPHOID, minimal. THYROIBD0RG0PLIACNDTMS TISSUE.
No mTiHcrYoRsOcIoDpiGLcANADb,norSKmIaNl,ityTREONbTsEeDr,vedSKI:N, UNTREATED
--~ ais-Compiiny Sanitized. Does not contain TSCA CBI
ZH2D-82u-5DS4a2ye5S:tduRdyeypiMenaaMtaeeld-eRDRoeastessDerm~al~Toxicity
DDuuPeomnit1s3l83o0
--_
n
a anIinnaailvidduataal AfnoirmailndiLviisdtuianlg animals Date:20-pEa-04
sDorsoeovGr| up
(+ AtProPlR)OVEDTrePaRtOmTeOnCtO:L +)0 ma/kg IX Sex: Males
Animal Ret
Microscopic & Macroscopic Findings
503
TKeirlmliendalonSDaacyrif: ic2e8
Cr
Animal is signed off from necropsy
Gross pathology :
No MLOaINcVTrERoREs,cAoTpEKiIDDcNEAYbSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
Histopathology
xLrovweEmYTSF: LAMATION, SUBACUTE/CHRONIC, minimal.
CHRONIC PROGRESSIVE NEPHROPATHY, minimal.
No M`iTcHrYoRsOcIoDpiGLcANADb,norSmKIaNl,ityTREOAbTsEeDr,vedSKI:N, UNTREATED
90
TKoirlnliendalonsDaacyrif: ic28e
nina is signed off from necropsy
~
Gross pathology +
No MOaLNcIVTrERoREs,cAoTpEKiIDDcNEAYbSn,ormTaHlYiRtOyIDOGbLseArDv,edSK:IN, TREATED, SKIN,
Histopathology
LirovweEnYDSF: LA+ MKATION, SUBACUTE/CHRONIC, minimal
`CHRONIC PROGRESSIVE NEPHROPATHY, minimal.
No MTiHcrYoRsOcIoDpiGLcANADb,noSrKmIaNl,ityTREOAbTsEeDr,vedSKI:N, UNTREATED
~ _
26. CompanySanitized. DoesnotcontTSaCAiCBnI
H2-62-5D4a2y5S:tuRdeypieantMeadl-eDRoastesDermal Tonicity
DuPont-13830
~~
naividual Animal Listing
Date:20-7z8-013
sDotsoer .
+anAiemPaRlOVEdDataBROfTorOCOiLndi+)vidual animals dontzol) Treatment: ma/kg IX Sex: Males
Animal Ret
Microscopic i Macroscopic Findings
505
Txeirlmliendalon SaDcaryif: ic2e8
Animal io signed off from necropsy
Gross pathology :
No MLOaIcNVrTEoRRsE,cAoTpKEiIDDcNEAYbSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSKIN, TREATED, SKIN,
Histopathology :
KIDNEY`SINFLAMMATION, SUBACUTE/CHRONIC, minimal AGGREGATES, LYMPHOID, minimal.
No MiTcHrYoRsOcIoDpiGLcANADo,rmSKaIlNi,tyFREONbTsEeDr,vedSKI:N, UNTREATED
30
TKeirlmliendalonsDaacyri:fic38e
Animal 15 signed off from necropsy
Gross pathology
Yo MaLcIVrEoRs,copKiIDcNEAYmSo,maTHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
istopathology
KIowEYHISENMFALTAOMPMOAITEISOINS,,SUESXATCRUATMEE/DCUHLRLOANRIYC,, ImNiCnRiEmAaSlE.D, minimal. `AGGREGATES, LYMPHOID, mininal.
No M`iTcHrYoRsOcIoDpiGLcANADb,aorSKmIaNl,ityTREOAbTsEeDr,vedSKIN, UNTREATED
_--
air Company Sanitized. Does not contain TSCA CBI
25H--2D5a42y5S;tuRdyienpMaeleaRattseDedrm-alDTooxiscitey
DuPont-13830
~
anIinmdailvidduaatla AfonrimiandLiviisdtuianlg animals Date:20-FEB-04
sDorsueoGylow
o+"ntArBoPlR)OVEDTrePaRtOmTeOnCtO:L +)0 mg/kg It Sex: Males
Animal Ret
Microscopic & Macroscopic Findings
TT
507
T KRielrlmeidnalonsDaacyrif:ic26e
TTT
Animal is signed off from necropsy
Gross ratholosy
No MaLcIVrEoRs,cop"KiIcDNAEbYnS,ormTaHlYRiOtIyDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
TREATED
Histopathology :
LaverI:NPLNGGTION, THYROID GLAND.
SUBACUTE/CHRONIC,
minimal.
HYPERTROPHY, FOLLICULAR CELL, minimal
No wKiIcDrNoEsYcSo,picSKIANb,norTmREaAlTiEtDy,ObSsKIeNr,vedUNTREATED
908
TKeirlmliendalonsaDcaryif: ic2e8
Animal io signed of from necropsy
~
Gross Pathology :
No MUaLNcIVTrERoREs,cAoTpEKiIDDcNEAYbSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
Histopathology :
LivenI:NFLAMMATION, SUBACUTE/CHRONIC, minimal KroeANsGEGC:RREOGSAITSE,S,FOLCYALM,PHOmIiDn,imamli.nimal. THYROHIYDPGELRATNRDO.PHY, FOLLICULAR CELL, minimal.
No miScKIrNo,scoTpREiAcTEADo,rmSaKIlNi,tyUNTORbEsNeTrEveDd :
ETCompany Sanitized.Doesnot contain TSCA C81
28H--2D5a42y5S:tuRdeypienatMeadl-eDRoastesDermal Toxicity
Dupont13830
~~
Individual Animal Listing
Date:20-7Es-08s
DsotsoeorGRP
+an"AiPnPaRlOVdEaDta7ROfTorOCOiLndi+)vidual animals ontrol) Treatment: mg/kg IX Sex: Males
Animal Ret
Microscopic & Macroscopic Findings
505
TKeirlmliendalon SDaacyrif: ic2e6
-
Animal io signed off from necropsy
Gross pathology
KIDNEDYISL:ATATION, RIGHT, PELVIS. No MaLcIVrEoRs,copTiHcYRAObInDorGmLAaNlDi,tySOKIbNs,erTvReEdNTED, SKIN, UNTREATED Histopathology
LivenI:NFLATION, SUBACUTE/CHRONIC, minimal.
HEMATOPOTESIS, EXTRAMEDULLARY, INCREASED, minimal
`HCYHDRROONNIECBHSRROOSGTRSE,SSUINVIELANTEEPRHARLO,PATmHiYn,imamli.nisal
No M`iTcHrYoRsOcIoDpiGcLANADb,norSKmIaNl,ityTREOAbTsEeDr,vedSKIN, UNTREATED
-
910
mKeirlmliendalon SaDcaryif: ic2e8
Aninal io signed off from necropsy
Gross athology :
No MLaIcVrEoRs,coKpIiDcNEAYbSn,ormTaHlYiRtOyIDOGbLsAeWrDv,edSKIN, TREATED, SKIN,
Bistopathology : LIVERIN:FLAMMNTION, SUBACUTE/CHRONIC, mild. KaoNEYACSCHGRRO:ENGIACTEPSR,OGLRYEMSPSHIOVIED,NEmPiHnRiOmPaAlT.HY, minimal
910 Continued on the next aga ....
-a CompanySanitized. DoesnotconTtSaCAiCnBI
ZDH2:8w2-5DS4a2yu5S;dtuRydeynpieMnaMtieadle-eDRRoaestessDermalToxicity
DPDuePmonit-d1t38w30
--
.
io anIinndailvidduaacla AfnoirmailndLiviisdtuianlg animals Dace:20-FzB-01
DsorseoG:roupe
(o+ntAzvoelr)oveDTrepartommeoncto:r, +) mg/kg IX Sex: Males
Animal Ref
Microscopic & Nacroscopic Findings
si
Continued fron previous page
o
TT
Histopathology
Ho MiTcHrYoRsOcIoDpiGLcANADb,norSKmIaNl,ityTREOAbTsEeDr,vedSKI:N, UNTREATED
-_--
m0-
`Company Sanitized. Does not contain TSCA CBI
2B8DF--y2D5Sa4uy25Sd:tuyRdiyiennMpMlaeleeaRRatatsseDedrm-alDToosisciety
DDuePwonlts13t83n0
sDotsoerGRP ninal Ret 1101
Gross
+"aAnIPinBrdRailOvVidEduDaatlaFRAfOnoTirOmCaOilLndiL+)viisdtuianlg animals Treatment: 10 mg/kg XI Sex: Males Microscopic & Macroscopic Findings TKeirlmliendalon SDacaryif: ic26e Animal is signed off from necropsy pathology : No MLUaINcVTrERoREs,cAoTpEKiIDDcNEAYbSn,ormTaHlYRiOtIyDOGbLsAeNrDv,edSK:IN, TREATED,
Date:20-FE8-04
ol oT
SKIN,
1102
TKeirlmliendalonSaDcaryif: ic2e8
Animal is signed off from necropsy
Gross pathology
No MoaLNcIVTrERoREs,cAoTpEKiIDDcNEAYmSo,rmTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
103
TKeirlmliendalonsDaacyrif: ic2e8
Animal is signed off from necropsy
'
Gross zathology :
No MLUaINcVTrERoREs,cAoTpEKiIDDcNEAYbSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TRENTED, SKIN,
108
TKeirlmliendalon SDacaryif: ic2e6
Animal is signed off from necropsy
Gross Pathology :
No MLTaIcRVrEEoRAs,cToEpKDIiDcNEAYmSo,rmTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
-------- ois ------ Compdny Sanitized. Does not contain TSCA CBI
2H8--2D54a2yS5;tuRdeypienatMeadl-eDRoastesDermalT-- oxicity
DDuuPPoontm1i38s30n
--_
.
anIinmdailvidduaatla AfnoirmailndiLviisdtuianlg animals Date:20-rE8-04
sDroosoeyGroup
+rreAaetenreonuce:n s1R0oTmooc/okLg+)XI Sex: Males
Animal Ret
Microscopic & Macroscopic Findings
1105
zKeirlmliendalonSDacaryif: ic2e6
Animal io signed off from necropsy
Gross Pathology
No MUaLNcIVTrERoREs,cAoTpEKiDIDcNEAYbSn,ormTaHlYRiOtIyDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
1208
TKeirlmliendalon SaDcaryif: ic2e8
Animal io signed off from necropsy
Gross pathology :
No MULaNIcVTrERoREs,AcToEpKDiIDcNEAYbSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
07
TKoirlnliendalonsDaacyri:fic28e
nial is signed off from necropsy
~~
Gross pathology
`DISCOLORATION, BROWN, RIGHT DORSAL LOBE.
No MKaIcDrNoEsYcSo,picTHYARbOmoImDmGaLlAiNtDy,ObSsKIeNr,veTdRE:ATED, SKIN, UNTREATED Histopathology :
FIBROSIS, FOCAL, CENTRILOBULAR, mild, with inflammation
_--
Tm
CompanySanilized. DoesnotcontainTSCAC81
BH28-l-2D5oa4y25SS:tuuRdbeyppienMatMbeadle-eDkRoaestessDermal Toricity
DDo uPonmt13s830
--~
Date:20-7En-015
sroor |
anIinmaailvidduaatla AfnoirmailndiLviisdtuianlg animals (+ APEROVED PROTOCOL +)
Dose or
Treatment: 10 mg/kg XI Sex: Males
Antal Ret
Microscopic & Macroscopic Findings
1108
KTielrlmiendalonSaDcaryif: ic28e
TT
Animal is signed off from necropsy
Gross athology
No MLUaINcVTrERoREs,cAoTpEKiDIDcNEAYbSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREMTED, SKIN,
.
1100
TKeirlmliendalonsDacaryif:ic2e8
Animal is signed of from necropsy
Gross Pathology
No MLaIcVrEoRs,coKpIiDcNEAYbSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
mo
TKeirlmliendalonsDaacyrif: ic28e
Animal io signed off from necropsy
~
Gross pathology
No MOaLNcIVTrERoREs,cAoTpEKiDIDcNEAYbSn,ormTaHlYRiOtIyDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
_--
Ts
CompanySanitized.DoesnotconTtSaCAiC8n1
H-25425: Repeated-DoseDermalToxicity 28-Day StudyinMaleRats
DuPont-13830
~~
Individual Animal Listing
Date:20-FE8-0140
stoov
ig+an*AiPnTaRlOVdEaDta$ROfoTrOCOiLndi+)vidual animals
Dose Growp
Treatment: 100 mg/kg XIII Sex: Males
nial Rot
Microscopic & Macroscopic Findings
-
B01
TKeirlmliendalonSDacaryi:fic2e8
Animal is signed off from necropsy
Gross Pathology
oRaL `cUaLvCEeRr/EROSION, BETWEEN UPPER INCISORS <21f DIA.
No MLaIcVrEoRs,cop"KiIcDNAEbYnS,ormTaHlYRiOtIyDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
1302
TKeirlmliendalonsaDcaryi:fic2e8
Animal io signed off from necropsy
Gross pathology :
No MLaIcVrEoRs,copKiIDcNEAYbSn,ormTaHlYRiOtIyDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
UNTREATED
_ 1303
ATKenirilmmliaenldaloinssDasaciyrginfe:idc2e8off from necropsy
Gross Pathology :
No
MLaIcVrEoRs,coKpIiDcNEAYbSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSKIN, ONTREATED
TREATED,
SKIN,
1308
mKeirlmliendalonsaDcaryi:fic2e8
Animal is signed off from necropsy
Gross Pathology
No MLTaIcRVrEEoRAs,cToE"pDKiIcDNAEbYSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
-- CompanySanitized. Doesnotcontain TSCA Cal
ZDH2--u2D5Sa4y2u5dS:tvuRdeiypioenaMMtaeldle-eDRRoasetessDermal Toxicity
DDeuPmonti138n30
--_
n
uty anIinmdailvidduaatla AfnoirmailndLiviisdtuianlg animals Date:20-7E8-04
sDotseoGr| oUPM
+ APTPreRaOtVmEeDnt:PROT1O0C0OLmg+)/kg XIII Sex: Males
Animal Ret
Microscopic & Macroscopic Findings
1308
KTeirlmliendalonsaDcaryif: ic2e8
-
Aninal ic signed off from necropsy
Gross Pathology :
No MLUaINcVTrERoREs,cAoTpE"KiDIcDNAEbYSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
1306
Keirlnliendalon sDaacyrif: i3c8e
Animal is signed off from necropsy
Gross pathology :
No MLTaIcRVrEEoRAs,cToEp"DKiIcDNAEbYSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
107
KTielrlmiendalonSDaacyrif: ic28e
Animal io signed o from necropsy
~~
Gross Bathology
No MaLcIVrEoRs,copKiIDcNEAYoS,maTlHiYRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
1308
TKeirlmliendalonsDacaryif: ic2e8
nial is signed off from neczopsy
Gross Pathology :
No
MaLcIVrEoRs,copKiIDcNEAYbSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSKIN, ONTREATED
TREATED,
SKIN,
_--_--nm
`CompanySanitized. Doesnotcontain TSCAG81
282HD-82o-5Dy4aS2y5wS:dtuyRdiyeninMpMaaelleaoRRtaatessDedrm-alDTooriscitey
DDuuoPmonits1s3l83o0
~~
Individual Animal Listing
Date:20-7E8-0142
sroov |
an"AiPmPaRlOVEdDa.taPROfoTrOCOiLnd+i)vidual animals
Dose orp ?
5 Treatment: 100 ng/kg XIII Sex: Males
Animal Ret
Microscopic i Macroscopic Findings
1305
KTeirlmliendalonSDaacyrif: ic26e
Animal is signed off from necropsy
Gross pathology :
No MLaIcVrEoRs,copKiIDcNEAYbSn,orTmHaYlRiOtIyDOGbLsAeNrDv,edSK:IN, TRENTED, SKIN,
1310
KTielrlmeidnalonSDaacyrif: ic2e8
Animal is signed off from necropsy
Gross ratholoay
No MOLaNIcVTrERoREs,AcToEpKIDiDcNEAYbSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
--_~
_--m
Tee Company Sanitized. Doesnotcontain TSCA Cal
28H-:2D5a4y25S;tuRdeypienaMtaedl-eDRoastesDermal Toricity
DuPont 13830
~~
Individual Animal Listing
Date:20-rER-0113
DsotseuGLE
+"aAnTriPenBaaRtlOmVeEdnDatc:aPROfT1o0Or0C0OiLnmda1i/vkigdusWlV
animals Sex: Males
Aninal Ret
Microscopic i Macroscopic Findings
501
TKeirlmliendalonSDaacyrif: ic28e
Animal is signed off from necropsy
Gross Pathology
No MOLaNIcVTrERoREs,AcToEpKDiIDcNEAYbSn,ormTaHlYRiOtIyDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
Histopathology :
L1veRTNFLNGATION, SUBACUTE/CHRONIC, mild.
No MKiIcDrNoEsYcSo,picTHAYRmOoImDmaGlLiAtNDy,ObSsKIeNr,vedTRE:ATED, SKIN, INTRENTED
1502
TKeirlmliendalonsDaacyrif: ic2e8
Animal io signed off from necropsy
Grose pathology
~
No MLTaIcRVrEEoRAs,cToEpKDiIDcNEAYbSn,orTmHaYlRiOtIyDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
Histopathology
LrvemINFLATION, SUBACUTE/CHRONIC, minimal
No MKiIcDrNoEsYcSo,picTHAYbRnOoIrDmaGlLAiNtDy,ObSsKIeNr,vedTRE:ATED, SKIN, UNTREATED
1503
TKeirlmliendalonsDaacyrif: ic3e
Animal is signed off from necropsy
Gross Pathology :
No OLMNIaVTcERrREo,AsTcEoRpDIDiNcEVASb,norTmHaYlRiOtIyD OGLbAsNeDr,vedSKI:N, TREATED, SKIN,
-_--
mre
Company Sanitized. Doss not contain TSCA CBI
Z28DH--2uD5a4S2y5S:utubRdeypibenaMMtaeedl-eDRkoastsesDermal Toxicity
DDuuPonot-1m383o0
~
Inaividual Animal Listing
Date:20-PEB-0140
sDtooseyGroup + HY.
(-a*nAivmearlovdeantsarofroorcoirndi+)vidusl animals Treatment: 1000 mg/kg XV Sex: Males
Animal Rot
Microscopic i Macroscopic Findings
1503
Continued from previous page
Histopathology :
LaveI:NPLNGATION, owes
SUBACUTE/CHRONIC,
minimal.
THYROICADGHGRRGOELNGAIANCTDEPSR:,OGLRYEMSPSHIOVIED,NEmPiHnRiOmPaAlT.HY, minimal
`HYPERTROPHY, FOLLICULAR CELL, minimal.
No MSiKcIrNo,scoTpREiAcTEADb,norSKmIaNl,ityUNOTbRsEeNrTvEeDd
1502
KTielrlmeidnalon SDaacyrif: ic38e
nial is signed off from necropsy
Gross Pathology :
--~
No MLOaINcVTrERoREs,cAoT"pEKiDIcDNAEbYSn,ormTaHlYiRtOyIDoGbLsAeNrDv,edSK:IN, TREATED, SKIN,
Histopathology :
LiveTN; FLAMATION, SUBACUTE/CHRONIC, mild.
No MiKcIDrNoEsYcSo,picTHAYbRnOoIrDmGaLlAiNtDy,OSbKsIeNr,vedTRE:ATED, SKIN, UNTREATED
1505
KTielrlmeidnaolnSDaacyri:fic28e
Animal is signed off from necropsy
Gross pathology :
No MLUaNIcTVrREoERsA,cToEKpDIi.DcNEAYbSn,ormTaHlYRiOtIyDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
1505 Continued on the next page...
-_--
Tm
`CompanySanitized. Dosnot contain TSCACBI
ZD0 H2-8w2-5SD4a2uy5:bStyuRdiyeMinpiMaeeleRaRetatseDsedrm-alDTooriscitey DDuupoonmt1u38s3n0
anIinmdailviddautael AfnoirmailndLiviisdtuianlg animals Date:20-7E8-04
Dsorsoeoy "
+" ATrPePaRtOmVeEnDt:PROT10O0C0OLng+/)kg XV Sex: Males
Animal Ret
Microscopic i Macroscopic Findings
50s
Continued from previous page
Histopathology :
LivenTNFLNGIATION, SUBACUTE/CHRONIC, minimal.
No MiKcIDrNoEsYcSo,picTHAYbRnOoIrDmaGlLAiNtDy,ObSsKIeNr,vedTREATED, SKIN, UNTREATED
1506
TKeirlmliendalonsDaacyrif: ic2e8
Animal {s signed off from necropsy
Gross Pathology
No MLNaIcTVrREoERsA,cToE"pDKiIcDNAEbYSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
Histopathology
.
--~
venINPLAGTION, SUBACUTE/CHRONIC, minimal.
Ho MiKcIrDNoEsYcSo,picTHYARbOnIoDrmGaLlAiNtDy, OSbKsIeNr,vedTRE:ATED, SKIN, UNTREATED
1507
TKAneiirlmmlaielndaloinsssDaicagrynief:dic2e8off from necropsy
Gross zathology :
No MLUaIcNVrTEoRRsE,cAoTp"EKiDIcDNAEbYSn,orsTaHlYiRtOyIDOGbLsAeNrDv,edSKIN, TREATED, SKIN, Histopathology 1507 ContinuedLoanvetrhI;eNFnLexAtTIpOagNe, -.SUBACUTE/CHRONIC, minimal
-- -_--
-CompanySanitized. Dossnotcontain TSCA C81
28H--2D5a42y5S; tRdienpMaeleaRRatetseDedrm-alDTooriscitey
DDuuPPoontm1n38g30
~
Individual Animal Listing
Date:20-rz8-0146
DsotsoerGibup
i(o+anAipnEaRlovEdDataProfmoorcoiL.ndi+)vidual animals Treatment: 1000 mg/kg XV Sex: Males
Animal Rot
Microscopic & Macroscopic Findings
1507
Continued from previous page
Histopathology +
mxeavnR,OHIYODPNERGRELTAARTNOEDPDH.Y, FOLLICULAR CELL, minimal
INPLAMTION, FOCAL, SUBACUTE/CHRONIC, minimal, dermal.
No MKiIcDrNoEsYcSo,picSKIANb,norTmRaElAiTtEyD Observed
1508
TKAneiirlmmlaielndaloisnssDaaicygrnief:dic28oeff from necropsy
ross pathology :
No MLUaINcVTrERoREs,cAoTpE"KiDIcDNAEbYSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
Histopathology :
~
KLIrDvNeEmYISNF+ LATION, SUBMCUTE/CHRONIC, mild.
`CHRONIC PROGRESSIVE NEPHROPATHY, minimal.
No MTiHcrYoRsOcIoDpGiLcANADb,norSKmIaNl,itTyREOAbTsEeDr,vedSKI:N, UNTREATED
1509
TKeirlmliendalon sDaacyrif: ic2e8
Animal is signed off from necropsy
Gross rathology
No MOaLNcIVTrERoREs,cAoTpEKiDIDcNEAYmSo,rmTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
1509 Continued on the next page ....
-_-- 230`CompanySanitized. Doesnot contTSaCAiCnBI
H2-82-5D4a2y5S:tuRdeypienatMeadl-eDRoastesDermal Toricity
De DuPomnt1s 3830
--~
ww
stovy
"aAnIPinPmdRaiOlvViEddDauatlaPROAfTnoOirCmOaiLl,ndLi+)ivsidtuianlg animals Date:20-783-04
Dose GratET
Treatment: 1000 mg/kg XV Sex: Males
Animal Ret
Microscopic & Macroscopic Findings
"-
1505
Continued from previous page
-
oT
Histopathology :
LivenNI.ENCFRLOMSGIAST,IOFNO,ALS,UBAmiCnUiTmEa/lC.HRONIC, minimal.
SKIN, IUNNPTLRAEGAITTEIDON, FOCAL, SUBACUTE/CHRONIC, minimal, muscular.
No MKiIcDrNoEsYcSo,picTHAYbRnOoTrDmaGlLAiNtDy,ObSsKIeNr,vedTREATED
1510
KTielrlmeidnalonsDaacyrif: ic28e
Aninal is signed off from necropsy
Gross Pathology :
No MUaLNcIVTrERoREs,cAoTpEKiDIcDNAYbSn,ormTaHlYiRtOyIDOGbLsAeNrDv,edSK:IN, TREATED, SKIN,
Hissttopoapthaotlohgoylogy :
LKIiovweErYIsNFLRBATION, SUBACUTE/CHRONIC, mild. SKIN,CHTRROENAITCEDPR+ OGRESSIVE NEPHROPATHY, minimal.
INFLAMIATION, OCAL, ACUTE, minimal, epidermal. Mo M`iTcHrYoRsOcIoDpGiLcANADb,norSKmIaNl,ityUNTORbEsNeTrEvDed :
"++ Listing complete wer
--_ TT -- `Company Sanitized. Does notcontainTSCA CBI