Document 93My9ZrB5yNv0M5d0qmNvav7D
AR226-2906
_______hag sdsJRistaggii orally so youag adolc
Ie raca at repa?(l do iW&la of lCbr 1,000 ag/kg, 100 ag/kg or
10 g/kg for 10 day over 2-WRfc period. Clinical aigna obrvd included: waknew, Calad prlnal rea, lethargy, protrtlon, buap6d-pocur,
cong*eioa chroBodcryorrha ani valghc lo. Conpound-induced macroccoptc and alcroBcople lloac ver preieat tn Cbil thyauB, <pleen, booe aarrow and
kidaey of high-doM aaiiulf, BBC(U of th ortality aaen la the blghdo group, reversibility of thew leiioax conid not be adequately evaluated. No treatBeot-relaced lealona --re obaarved ia the lov or iatenwdiate doe
group*.
Staciatical analyala of clliaigal_laberator? Mliuraaenta data showed
vlt^HHUBlBIHlHHID'0 that raf doed 10 tia
l*vel of 100
g/kg and 1,000 ng/kg had bigtier! thaft noCMiery^lsyteTounta and
haatos^fca_^ich appeared EO beiral-acadxb-'-tlie-'doll^ Racs dosed lth 1,000
^^KW^IBBIBBiBHBlO14 ^S^^ ^^i?6* ^uota, alaoac twice
ttr norialrangeeliaojBRedT^chtcontrola. tliea^.anlBala alao ahowed a
threa-fold increase ia serua blood urna' oitrogeD nd increaaed hemoglobin,
aerua glutaaic pyruvic traaaaaia^ activity, and creatlnlne. The 100 ag/kg
created raca ahowd a light increaae ia arm total protela. An increaat in
Company Sanitized. Does not contain TSCA CB!
che relative number of neuCro^hlls (1,000 ag/kg group) aod a alight co
moderate hypochrooia (100 og/kg sad 1000 ag/kg groups) was seen.
In Cbe recovery groups, ^ slight Increase in serum creaciaine levels la the 100 ag/kg created racs wa observed* In the absence of this parameter
being significantly differeotfprior to cfcp recovery period, the significance
of the finding is questionable. No other differences clinical pathologic para--ter jstudies la the recovery
were racs
detected la (only I rat
the
was
examined in the 1,000 ag/kg g^oup).
Analysis of blood for or :aaofluorlde revealed a doae-related increase lo concentration following the 1 )tb dose (1, 30 79, and 197 ppa, exposures of 0, 10, 100, and j ,000 s-s/kg, : eapeccively) The8e values dropped to 0.5, 12,
25, and 25 ppo (1 rat), 0 to ,000 og/kg, respectively, 14 days after Che last creacaenc, indicating el i;araac froa the blood is relatively slow,
Procedure; The test gmterlalL as an aqueous solution at con<--;n radons of either 102, 1Z or 0.12, was adainistftrad by totragastric intubation Co 3 groups oz young adult Crl:CD* ale rats, 10 r<its per group, 5 tiaes a week for 2 weeks at repeated dose evels of either 1*000 ag/kg, 100 ag/kg or 10 nig/kg; an additional group of 10 racs served as, cpncrola and was intubacad
with distilled water. Two fcci rats at 1,000 we/kg died before the 6th <*ose and 1 before the 9th dose. F;.ve coafcrol aad 14 cJTsc rats were sacrificed approxiaately 4 hours after tii last dose Two ^se raes at 1,000 ag/kg died during the recovery period, "he reaalntng 5 controls and 11 test rats were observed over a 14-day racove: y period and then''acrlfIced. All racs were examined grossly, selected cii sues were weigfulid aiul selected tissue and organs were evaluated histolo) ically. Clinical pathology aeasureoents were
taken on all surviving rats 4 hours after the ZOtb dose and after the 14-day
recovery p-riod. Blood was a^so collected at the saae periods for fluorine analysis*
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Results:
Dose
(ag/kg/day) 1,000
100
No. of
Doaea 10
10
Mor^ ' '^
9/^0
0/^0
Clinical Signs
First Week; Weakness and weight loss*
Second Week; Weakness, stained per^neal area, lethargy, prostration, lumped posture and freight loss* Two rats died before the 6th dose and 1 died before the 9th dose. Becgviry Period; Weakness, congestion huaped posture, chrooodacryorrhea and . weight loss. Two rats died during the
recovry period.
First tffcdk; Slight weight loss. Second Week; Slight weight loss.
Becovery Period; None*
10
10
First Week- Slight weight loss.
Second^JWeek; Slight weight loss. Itecovery period; None,
Pathologic Changes; See AppendixA (Pathology Report Ho.
Clinical pathology; See Appendix B (Clinical Report forhj
Fluorine Analysts; See AppendixC (Analytical Report job No
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Company Sanitized. Does net contain TSCA C8t
5ejpore bys
Reviewed by;
Study Director
Approved by:
JAH:jrg:WP:1.22 Data laaugd: June 3. 1982
spore No.
Section Supervisor ACH6 laveccigatlons
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APPENDIX A
E. L DU FONT OeNEMOURS S. COMPANY
HASKKU. LABOftATOKY FOR TOXiCOLO^y
ANO INDUSTRIAL MEOICINK
[
El-KTON ROAO, NEWARK, DELAWARE 19711
CENTRAL. RESEARCH AND DEVELOPMENT OCPARTMENT
Pathology Repoi I N11 UH| ^
-14008 Polymer Products Depar&nent & Chemical & Pigments Department
Oral Subaeute Study in CPi> Rats I Aoril 21. 1982
Sunnnary
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Compound-Induced inacroflcjopic and microscopic lesions were present in the
thymua (Lynphocytic depleeloq), spleen (Lynphocytic depletion), bone marrow
(Hypocellularlty), and kidney a (Nephritis) of high-dose animals. Because of
excessive mortality in the high-dose group, reversibility of these lesions was
not adequately evaluated. Conpound-induced lesions yers not observed in the
low or intermediate-dose groubs.
Introduction
Every animal (except 1^30p58) in this study was given a complete post-
i
mortem examination. Microscolc examinations were also performed on selected
I I I-::
tissues from each available a limal.* Groups I (0 ing/kg),
(1000 mg/kg),
^
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(100 mg/kg), and IV (10 mi/kg) consisted of ten male rats each. Each
--''
group had a 12 day feeding phase and a 14 day recovery phase except the
* Adrenal Glands, Thyroid Gland, Parathyroid Glands, Esophagus, Stomach, Oueodenum, Ileum, Jejunum. Ce^um, Colon, Liver, Spleen, Bone Marrow; Thyaus, Heart, Sternum, Eyes, Brain, trachea. Lungs* Kidneys, Tesces and Bpididymides.
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high-dose group. Due to marxed clinical toxicity and early mortality in this
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*
group, only one rat survived the 14 day recovery period. Two additional high-
dose rats survived for fchre^ and seven days in the recovery phase.
Histomorphological lesions were tabulated by individual animal in Table
I and were suiomaziz d in Tattle II.
Results
|
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' '
.
Mscrescopically, coapo^ad-inducsd tissue alterations were restricted to
the spleen (splenic atrophy!- 3 rats) and thymus (thymic atrophy - 3 rats)
in the high-dose group. Both lesions were associated microscopically with
mild Co severe lymphocytic depletion. Aniaals from all groups had multifocal
areas of reddish-gray oottl^ag in the pulmonary.parenchyma. These lesions
were associated hiatonorphologically with multifocal areas of granulomatous
interstitial pneumonlcis.
.
.
i
Microscopically, compotlnd-induced lesions were present in the spleen
(lyiBphocytic detletlon - 7o^9). bone marrow (hypocellularlty - 5 of 7),
thynus (lymphocytic depletion - 5 of 8) fisd kidneys (purulent Cubuloister-
i i .
stifcial nephritis - 8 of 9),' of the high-dose group. Compound-induced lesions
were not present in the other test groups.
i.
.
The renal lesion in this study was rather unique in that there was
selective coxiclty for the dllatal and collecting tubules and the medulla
.
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was more abverely affected than the cortex., TSe lesion was characterized by
L
degeneration and regeneration of the Cybular pitheliuni with tubular
^
ectasla. This was associated with a marked interstitial infiltration with
neutrophils and edema fluid.: Occasionally, there were small foci of renal papillary necrosis assoelatejd with the neutrophllic exudate. One rat (if 301555
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- Group II) that survived the 14-day recovery period did not have similar
compound-induced lesions.
\
There were several other!microscopic Inflammatory and/or degenerative
lesions that were considered,;because of their common occurrence and/or
... '
their low frequency, to be" incidental spontaneous lesions In this group of
:
rats.
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WDK:WCK:vfd
Report by; ^ .
WlUlai/D" Kerns. D.V.M.
Senior Research Pathologist
Tf^Xw^ JWM^/ Approved by:;
WUUaa C. Knrfuss, D.V.M.
Manager, Pathology Division
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PAMOLOCT TABLE CODES
* Tissue Accounting Code:
L Lesion observed
N So significaAS lesion observed
0 Tissue missing
I Tissue insufficient for histomorphologic evaluation
N Only one gland is present and it is normal
Q Specimen quality is inadequate for an accurate assessmentiof subtle tissue alteration, other wise the tissue appears to be normal
A Autolysia
P Present
;
** Degree of Change:
1 - Minimal
:
2 - Mild
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3 Moderate
4 " M&rked
I
5 " Severe
!
*** Mode of Death:
S Sacrificed
D Unscheduled (death
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TABLE II
SUMMARY OF HISTOPATHOLOGY DATA
214M1M 1 Group;
Daya on Study;
No. of Animals; TiBaue/Observation________Sex;
EBOptiagus
I
12 5 M
(4)
26
__8___1_0___1U2 ___1_5 ___2_6
5
12 III
5
M
M_____M
M_____M__
(5)
(2) (1) (4) (0) (1)
(5)
PeriesophagitiB, granuloniacous,
foiial
0
0
0
0
1
-^0.-0^_,-_^0--0- Stomach
---------^----^-
^ ^ _ ^ . Glandular, atrophy, diffuse
0
1
^r 00 000 00 :
.
(5) (5)
(2) (1) (4)
"
:^ 1 0 :H6is||Aij^i^(l(jg^ Hep^i9 ./ .
.^o^i^tilc."'
.
pUrulog^a^<^jiCOH3, "
.
. ' ..".- \ '.-T'J''' '.i f1''-.' .'.A 'yff ' '4. rf'" n
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;,-. .'
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:_
0 0 0 :NI<%^,
.:^^^^.2^^ ^/'^ Lymphocytic, depletion, diffuse
'
'
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-
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0 0 Bone Marrow
(4) (4)
(2) (1) (3)
2 1 3 1 0 0 0 Hypocellularlty. diffuse
0 0 00 'rhyroua
(4) (5)
(2) (0) (4)
1 1 3 0 0 Lymphocycic depletion, diffuse
0 0 0 0 Thyrousiti.s, pyogranulomatous,
2 0 2 1 0 Focal
(0) (1)
::. .
.- ' :'
0
'
-
o. ^o'
(0) (1)
(I) (1)
(5)
' '
0
o ^
:^' "(5) ';<
(1)
(5)
0 0 0 0 0 0 1 00 <) " Number of tissues evaluatfcd
^i^l^is6^,:A^.:.,,^. ^JsM,^::^.;,^ ..^-^s<^^L ;^.
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1W1. 1i.1-^'
L H-14008
TABLE II (Cointiiiued)
SIIJMMABY OF HISTOP,&TH()LOGY DAl'A
Group:
I
Days on Study: 12
26
No. of Animals: 5
5
Tissue/Observation
Sex: H
H
II 8
10
12
15
26
2
1
4
1
1
M
M
M
M
M
12 I I I
5 M
Lymph Node (Thymic)
(4) (5)
(2) (1) (4) (0) (1)
(5)
" '*'. "
Lymphocytic hyperplasia, diffuse
---.----- Trachea
Tracheitia, lymphocytic, focal ;
0
0
0
p
0
0
0
0
-
(4) (4)
<1) (.1) C4) CO) (D
(4)
"
'
0
0
^:^0
0
1
0
0
2
-
^'K (ff
Lungs; ':
' i
"'. ''
'"'" '
,
'"''
. ,
..
'
.
Pneumbnttis,,interstitial, ' .;;gr^ilc^t<)ii(fl^rffua;fc:|^Qcal- .'
<5) (5)
V;4 .':
'
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7'2'v:
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- :'. :'
<1)
: ^..?.:'i.: o
,^K- '"f '-''"
..
S.^- "^ ,.W tS (U 3 '< M
' limeys
"^:^y" ':' ..^^l,'^;
'.
,
;;^^^Ri^it^ia;e^,.tubHl^^
s
''.
~
.' ''-'.!i 'U-'.
purulent, bilateral, inulclfocal 0
0
Nephritis, lymphocytic. Inter
stitial, focal ^
1
1
..' ..'^ (t)'- 1 (1)
2
1
0
0
0
si.
Tubular epithelium, basophllia
?'
focal or multifocal
2
2
0
0
<D
p.
Nephrosis, multifocal,
0 0
unilateral
0
0
0
0
(0
03) Capsulitis, fibrinopurlent,
0
hemorrhagic, multlfocal, uni
8
lateral
0
0
0
0
3
5"
5-<" () " Number of tissues evaluated
w
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0
':. -
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( .1 .,. 0)
0 i i 0
0
(5)
;-,^'2. ;.
(5),
0 2 1 0
0
Group:____I
Days on Study; 12
No. of Animals;
5
Ttasue/Obaervation________Sex; M
26 ___8____10___U12___1_5___2_6
5
2
I
A
1
1
12 HI
5
M
M
M
M_____M
M______M
I
;
:
:
;
1 to
':
i
Teatis (es); Semlniferoua tubular epithelium, atrophy,
diffuse, bilateral
Interstitial.cell hyperplasia, diffuse, bilateral
Epidldymis (des):
(5) (5)
(I) (1) (A) (1) (!)
00 00000
0000000
(5) (5
10 10
0
Epidldymltia, interaitlal,
|
lymphocytic, focal,
g
unilateral
^
m
P
10
00000
00
E
N
----------------------------.--------------------------------------------------------------i___,-----.--.----------
ro
a
() Number of tissues evaluated
3
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o
APPENDIX B
E. 1. DU PONT DE NEMOURS 5 COMPANY
HASKBLL LABORATORY POM ToxiCoijticY AND lNDUrnIAL MBDICINC !
ELKTON ROAD, NCWARK, OCLAWAMI lj711
!
CENTRAL RESEARCH AND DEVCLOPMtMT dePARTMBNT
Subacute Oral Tend.
Medical Research Project So Haakell Laboratory No. 14008 June 29, 1981
Blood s 10 times with1 10 nig/leg and
examined.
rats intragaatrically dosed it levels of 0 ing/kg (controls).
rats dosed with 1000 ag/kg were
After the tenth doae, bLood was taken from the tails of these rats for the measurement of erytb'ocytea (BBC), hemoglobin (Hb), mean corpuscular voluae (MCV), platelets, leucocytes (WBC) and relative number of neutrophils (Neut), lyiaphocytes (Lymph), eosinophil (Eosin), monocytes (Mono) and baaophila (Baso) . The hematocrit (fit)* aeon corpuscular hemoglobin (MCB) and mean corpuscular hemoglobin concentration (MGHC) were calculated from these
data. Alkaline phosphatase CAP),, glutainic-pyruvic Cransaminase (GPI), glutami-c-oxaloacetic transaminale (GOT), urea nitrogen (BUN), creatinine (CHEAT), and total protein (TPROT) were also measured in the serum. Five rats from the 0 ag/kg, 10 mg/kg and 100 mg^kg groups and four, rats from the 1000 mg/kg group were then sacrificed for pafcaology. After a 14-day recovery period, the measurements were repeated oji the surviving rats in each group.
j i B U The data were analysed statistically by a one-way analysi^^^vi
Least significant difference a were calculated to compare
preated racs with the controls when the ratio of variances
Lffaraaes asoag tie groups. Significance was judged at the probability level.
0.05
The results of the clinical laboratory
Table I; statistical analyst^ in Table II.
mals are listed in the computer printout attache
eaenta are summarized in ements on individual ani-
to the report.
^Jftj--ta--ti--st--ic--al--a--n--aly--si--s --of--jjd--ieMledLvatetals sohofw1e0d0cihnagt/kgratasndd1o0s0ed0
10 times with nig/kg had higher
TannocBaI^^yl^^cycecoTOS's and hematocrits which appeared to be related
Co th I'l-se. These two .rou}pa also had a slightly lower MCH and MCHC when
20 Company Sanitised. Dees not contain TSCA CB?
,trol animals. Bats dosed with 1000 fflg/kg
-- ^ang--ee^s--tab--Ils-h^e--dT--oy--th
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s
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animal
-
aS s,
siost
also
twice the normal
showed a three-fold
increase in aerun BUN and increased hemoglobin, GpT and creatinine. The 100 mg/kg
treated rats shoved a slight increase in serum ^ocal protein. Examination
of the differential smears 9 lowed an Increase in .the relative nurAer of
neutrophils in the 1000 iag/k{ group and a lighfc to moderate hypochromia in
the 100 og/kg aad 1000 ag/kg grciipa.
";
__ later, oniy one rat remained'in the 1000 mg/kgl
reaeed group. Statistical analysis at this tine included fkg aad 10) og/kg dose levels, Other than a slight increase
_
and|fmmimB in serum creatinine levels t: th<i 100 mg/ke-treatedrats. nodiaically
significant difference betveiin the control rats preafced rats was coun^i for the other measurements Bade on the blooc
aeport by; /lfi-ti,.:^&.^^fj^u^ Catherine C. Hatarese Technician
CCM:JBB:tBjh
Approved by;
>^^(^k^M^' r\
\ I
'T^
( John R. Bames
'^--^ Chief,
Clinical Pathology Section
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TABLE IT
SUMMARY OF STATISTICAL ANALYSIS ON RATS INTUBATEP
RBC
Hb
Hfc
MCV
MCH
MCHC
Platelet
WBC
Neut Lymph
Eosin
Mono AP
GPT
!
GOT
BUN
GREAT TPROT
p*
23.)
13.1 30.4
3.4 5.2 18.1 1.9 9.4 24.1 15.7 1.0 5.3 5.5 3.8 1.6 122.0 34.2 5.2
10 moflta
0 0 0 0 0 0 0 0 0 0 0 0
0 0 0 0 0
F " Ratio of variance
if? F* " Significant
2.89
fH Significant If 3'3.88
10 DAY
"" --' -
+ 0 +
0
-IW"U mg/kg
+ + +
0
0
0
0
+
0
+
+
0
0
0
+
0
0
0
+
0
0
0
+
0
+
+
0
Vf
0.1 0.0 0.4 0.2 0.1 1.4 2.0 2.9 0.9 1.8
2 i.*
1.6 6.4 0.3 0.5 0.7 10.0 2.3
MSCO
10 ing/kg
0 0 0 0 0 0 0 0 0 0 0 0
-
0 0 0 0 0
(0) " Not significantly different than contr (+) " Significantly highi r than controls (-) - Significantly lower than controls
MR: I
COMPHD:!____ PERIOD:10 DAY
TOKICOLOGIST: DASHIEL
T | 14008
HASKELL CODE#:
..
DPRTMMT.-?PD&CP
-
REPORT acTE: l8-Kay-8l
CLINICAL LAB: MATARESE
GROUP: 1CM
DOSE;
SAMPLE DATE: 15-MAT-81
ANIMALS: 301540 301541 301542 301543 301544 301545 301546 301547 301548 301549
AVG.
S. D. S. 5.
RBC
MM/cn
6.91 6.67 6.41 6.64 6.77 6.35 6.47 6.87 6.86 6.46
6.641 0.208 0*066
Hb
ef
15.2 15.2 14.6 15.9 15.1 14.1 15.3 15.8 16.0 15.4
15.26 0.59 0.19
SEX; MALE .
SPECIES: RAT
BIRTS DATE: 13-MAR-81
It HCV % /C!9fS
3^. 55.
39. 50.
37
58.
38. 58.
38. 57.
36. 57.
38. 58.
41. 59.
"O. 59.
37. 57.
38J.2 57.6
1.5 1.2 0.5 0.4
MCH
/sag 22. 23. 23. 24. 22. 22. 2<. 23.
23<-
24.
23.0 0.8 0.3
MCHC
%
40. 39. 40. 41. 39. 39.
l3.
39. 40. 45.
PLAT
H/CBl^l
1071. 105S. 1005. 698. 1180. 1167. 972. 1080. 1061. 1163.
40.0 1065.5
1.1 90.5 0.3 28.6
GROUP: 2M
DOSE: 1000' MG/KG
SAMPLE DATE: 15-MAY-81
SEX: HALS
SPECIES: RAT
BIRTH DATE: 13-MAP-Sl
ANIMALf: 301550 301551 301553 30155't 301555 301557 301558
RBC
MM/Cffl
7.57 7.21 8.53 8.29 7.66 9.29 8.25
Hb
gf
16.5 15.4 18.3 17.8 16.8 20.5 18.1
AVQ.
S. D* S. E.
8.114 0.698 0.264
17.63 1.63 0.61
Hfe
%
45?
43, 501
.49?
45^
55(
47^
47*7
40
^
HCV
/cmc
59, 59. 59. 59. 58-
51.
5T
58.6 0.8 0.3-
MCH
/W
22. 21. 21. 22. 22.
2S.
sz.
21.7 0.5 0*2
MCHC
%
37. 36. 37. 36. 38.
.3^.
PLAT
M/cnun
1351. 797. 822. 1210. 888. 1329. 802.
37.0 1028.4 0.8 256.4 0.3 96.9
24
Company Sanded. Does not contain TSCA CBl
14008
HASKELL CODEtf:
DPaiMIT: PPD&CP
HEPOST DATE: 9-Jun-8l
CLINICAL LAB: MATARESE
GHOUP; 1CH
DOSE! CONTROL
SAMPLE DATE: 15-MAY-81
:
SEX: KALE
SPECIES: RAT
BiBTy'DATE: 13-MAR-81
ANIMALS: 301540 301541
301542 301543 301544 301545 301546 301547 301548 301549
AVG.
5. 0.
S. E.
WBC
M/cffl
17.9 11.6 12.5 9.6 12.0 13.5 11.1 11.3 13.5 15.8
12.88 2.44 0.77
Neut %
18. 19. 15. 19. 17. 17. 19. 19. 12. 12.
L'yp i
% 7(6
75 82 73 78
48. 76 774
80J
80.
Eoain %
0. 0. 0.
1. 0. 1. 1. 1.
1.
0.
16.7 74J5 0.5 2.8 9^7 0.5 0.9 3.1 0.2
Mono
%
6. 6. 3. 7. 5. 4. 4. 3. 7. 8.
5.3 1.8 0.6
Bnao %
0.
0. 0. 0. 0. 0, 0. 0. 0. 0.
0.0 0.0 0*0
GROUP: 2M
DOSE: 1000 MG/KG
SAMPLE DATE: 15-MAY-81
!
SEX: MALE
SPECIES: RAT
BIBTB DATE: 13-MAR-81
ANIHALf: 301550 301551
301553 301554 301555
3^57 38
a
.
S. D. S. E.
WBC
M/CB
40.4 20.8 16.2 18.2 20.6 16.5 28.6
23.04 8.72 3.30
Neut %
36. 34. 24. 29. 32. 63. 45.
37.6 12.9 4.9
Lyap^ % i
56J
57J
71.) 61.;
63,
22.;
41.1
i
.
53.io 16.It)
6.P
Eoain %
0. 0.
1. 0.
0. 3. 2.
0.9
1.2
0.5
Mono
%
8. 9. 4. 10. 5.
12. 12.
8.6 3.2 1.2
Baao
%
0. 0. 0. 0. 0, 0. 0.
0,0 0.0 0.0
25 Company i
^^ZQ'S.QQS--^^,
t t U j MR?::
HASgELI^i 14008
HASKELL CODES'.
CO>MMPNPD:ND^--------^^----------1
DPHTOHT: PPD&CP
PE;RRIIOODD:'fld DAT
*"
TOXICOLOGIST: DASHIELL
REPORT DATE: 9-Jun-fll
CLINICAL LAB: HATARESE
GROUP: 3M
DOSE: 100 fiG/Z5
SAMPLE DATE: 15-MAY-81
|
SEXs HALE
SPECIES: RAT
BIRTH ;DATE:J3-M&B-81
WBC Neufc Lymph Eoain Mono Baso
ANIMALS: M/CB
%
%
<
(
%
301582
9.7
18.
74.
i ;
0.
301583 14.3
14.
1
79.
0.
301584 13.8 13. 83.
1,
301585 9.0 10. 88,
0.
301586 14.6
5. 88.
1.
301587 10.7
11.
87. ;
0.
301588 19.7
12.
84.
0.
301589 15.8 11. 84.
0.
301590 17.5
10.
85.
1,
301591 15.2
6. 91.
0.
8.
0.
7.
0.
3.
0.
2.
0.
6.
0.
2. 0.
4.
0.
5, 0. K..-;- 0.
3.
0.
k-
AVG. 14.03 11.0 84.:
0.3 4.4 0.0
S. D.
3.40
3.7 4.<
0.5 2.1 0.5
S. E.
1.08
1.2
^
0.2 0.7 0.0
GROUP: 4N
DOSE: 10 MB/KG
SAMPLE DATE: 15-MAX-81
m S S E X :
SPECIES; RAT
BIRTH DATE: 13-MAR-81
ANIMALS: 301592
301593 301594 301595 301596 301597 301598 301599 301600 301601
AVG.
S. D. S. E.
WBC
M/ca 14.9 17.6 13.9 10.4 10.5 10.3
9.5 10.6
10.4 14.6
12.27
2.75 0.87
Neut %
12. 10. 22. 16. 22. 14.
9.
14. 15. 25.
Lymph
i
85. i 86.
69. ;
81.; 72. i 82.
85.J 80. 76. 70. ,
Eoain i
0. 0. 0.
,0.
2. 0. 0. 0.
1.
0.
15.9 78,^ 0.3 5.4 6.4J 0.7 1.7 2.0 0.2
Mono
(
3. 4. 9. 3. 4. 4. 6. 6. 8. 5.
5.2 ; 2.6
0.6
Baso
K
0. 9. 0. 0. 0. 0. 0. 0, 0. 0,
0,0
<h0
0.0
26 - Company Sanltiaed. Does net contain TSCA CIS
| | 14008
HASKELL CODE<P:
DPHTMMT; PPD&CP
~
BEPOST DATE: l-Jun-81 CLINICAL LAB: MATARESE
GROUP; 1C;M SAMPLE DAITE.'
DOSE:
29-MAy^i
V.
CC NTROL
.
SEX: M1ALE
SPECIES: RAT
BIBTH DATE: 13-MAR-81
AWIMALtf:
301540 '. 301541
301542 301543 301544 301545 301546 301547 301548 301549
RBC
MM/en
7.53 6.35 7.02 7.11 7.C2
Hb
^
15.9 14.2 16,2 15.6 15.2
Hfe MCT
r /cce
MJM
/nnng
MCHC
5
PLAT M/cinm
!2.
55< 2T.
38. 1220.
i6. 57. 22. 40. 1062,
(3. 61. 23. 38. 944.
H. 57. 22. 38. 1142.
(0. 57. 22. 38. 980.
AVG.
S. D. S. E.
7.006 0.423 0.189
15.42 0.78 0.35
10.4 57.4 22.0 38.4 1069.6 2.7 2.2 .0.7 0.9 113.7 1.2 1.0 0.3 0.4 50.9
[ GROUP; 2M
DOSE: 10([>M0G/TC
SAMPLE DATE: 29-MIAY-81
SEX; MALE
SPECIES; RAT
BIRTH DATE: 13-HAR-81
ANIMAL)?:
301550 301551 301553 301554 301555 301557 301558
RBC MM/em
6.25
Hb
e3t
14.1
Hfc
%
i
MCV
/cnc
MC /Bung
f"CnC
"
E
PLAT M/cmm
;7. 59. 23. 38. 1214.
AVG.
S. 0. S. E.
6.250 14.10
317.0
1
59.0
23.0
38.0 1214.0
^?-
^ ^
_
Compaq sa.^ed. Dees ^ con^ TSCA CBE
fa I MR:]------
COMPNOr PERIOD:*?0 DA?
TOncOLOG1ST: DASHIEL
STOL U :
|
i
1
GROUP: 3M
DOSE: 10C) KSvfVQ
SAMPLE DATE: 15-WAY-81
140 08
HASKELL CODEtf:
DPRTwr: PPD&CP
REPOlBT DATE: l8-May-8l
CLINI[CAL LAB: MATARESE
1 IT^I
fc
'SEC;: (ALE
SPECIES: RAT
BIRTH DATE; 13-MAR-81
AP
GPT
GO'
BBN CHEAT TPSOT
ANIMAU;
IU
IU
IV W8% B8
gK
301582 225. 23. 7). 25.0 0.6 6.2
301583 235. 25. 7>. 24.0 0.3 5.7
301581 180.
14. 4). 20.0 0.6 6.0
301585 285. 19. 5).. 24.0 0.6 5.7
301586 220. 21. 5?. 19.0 0.6 6.2
301587 230. 16. 6). 21.0 0.5 6.1
301588 330.
19.
5. 21.0 0.6
6.4
301589 290. 25. 6>. 20.0 0.6 6.3
301590 240. 19. 5). 18.0 0.5 6.3
301591 225.
19.
45. 20.0 0.6 6.3
AVG.
S. D. S. E.
246.0 43.3 13.7
20.0 3.6 1-1
5*5 11.4
3.6
21.20
2.35 0.74
0.56 0.10 0.03
6.12 0.25 0.08
GROUP; 4M
DOSE: 10 ffi/KG
SAMPLE DATE: 15-H1AT-81
SEX? MALE
SPECIES: RAT
BIRTH DA1E: 13-MAB-81
ANIMALf: 301592 301593 301594 301595 301596 301597 301598 301599 301600 301601
AVG.
S. D. S. E.
AP
6PT
GCT
BOH GREAT TPROT
ID
10
10 OS% ss%
eK
145. 17. 50. 20.0 0.5 6.1
280. 17. 50. 19.0 0.5 5.8
170.
19.
CO. 25.0 0.6
5.8
195.
17.
* 5. 21.0 0.7 -6.1
230. 21. 5, 22.0 0.5 5.8
170. 19. * 5. 20.0 0.6 5.7
205. 21. <5. 18.0 0.6 5.9
185.
19.
SO. 21.0 0.7
5.5
250. 21. '5. 17.0 0.5 S.7 200. 19. '5. 22.0 0.6 5.6
203.0 40.6 12.8
19.0 1.6
^ &-
^;'
'1.0 20.50. 0.59 ^'5.80
;5.2 2.27 0.06 '0.19
0.5 1.6 0.72 0.02 0.06
28 Company Sanitized. Does not contain TSCA CBf
MR: COWS
____ PERIOD?TO DA1
TOXICOL^GIST: DASHIEL
. W 14008
RASKELL CODEd:
DPRTMHT: PPD&CP
REPORT DATE: l8-May-8l CLINICAL UB: MATARESE
GROUP: 104
DOSE: CONTROL
SAMPLE DATE: 15-MAY-81
SEX: MALE
SPECIES: RAT
BIRTH DAm? 13-MAR-81
ANIMALf! 301540
301541 301542 301543 301544 301545 301546 301547 301518 301549
AP
IU
195.
255. 265. 265. 185. 265. 325. 280. 240. 300.
AVG.. S. D. S. E.
257.5 42.8 13.5
GPT 10
16. 19. 19.
23. 19. 17.
19. 17. 19.
21.
18.9
2.0 0.6
GOT
IU 50,
65).
45*
601
50* 60. 501 45^
504
55.
BBH
mgf
22.0 22.0 18.0 21.0 19.0 20.0 21.0 19,0 20.0 21.0
CHEAT TPROT , ttS^ '8%
6.7 ; 5,8
0,5 5.8 0.7 5.7 0.6 5.9 0.6 5.5 0.7 9 0.6' 6^0 0.7 6.2 0.6 5.0 0.5 5.9
53.JO '20.30 647 1.34
2,1 0.42
0.62 0.06 0.02
5.87 0,19 0.06
GROUP: 2M
DOSE: 1000 MG/1CG
SAMPLE DATE; 15-MAY-81
SEX: HALE
SPECIES: RAT
BIRTH DATE? 13-MAR-81
ANIMALS: 301550 301551 301553 301554 301555 301557
301558
AVG.
S. 0. S. E.
AP
in
290. 395. 305. 240. 315. 210. 285.
291.4 58.9 22.2
GPT 10
19.
28.
19.
25. 28. 25. 19.
23.3 4.2 1,6
GOT'
IU: 45J
65. 55. 60. 75. 70. 50.
BUN
a&f 74.0 61.0 66.0 79.0 91.0 106*0
66.0
GREAT
OgK
1.1 1,0
0.9 1.2 1.3 0.9 0.9
TPor
'
<E<
5.8 5.5 5,8 6.2 5-5
-^
5-B
oo.b 77.57 10,18 16.05
4^ 6.07
1*02
0.18 0.07;
5.76 0.24 0-09
23 -
Co^y ^^ ^ ^ ^^ ^ ^
PERIOD:-TO DAY
ToncoLocrsT: DASHIEL
14008
HASKELL CODE)!:
DPRTMMT: PPD&CP
REPORT DATE: l8-Mgy-8l
CLINICAL LAB: MATABESE
l-l
GBOUP: 3MI
DOSE: 100 HB/KG
SAMPLE DATE: 15-MAY-81
SEX: MALE
SPECIES: RAT
BIBTH VATS: 13-MAR-81
ANIMALS: 301582
301583 301584 301585 301586 301587
301588 301589 301590 301591
RBC
W./cm
7^9
7.01 6.72 7.27 7.20 6.65 7.79 7.41 7.49 7.10
Hb
g%
16.2 16.0 15.0 15.5 15.8 14.6
.'.6
17.0 16.9 15.5
!.It MCV
< /cne
. 55.
.
60.
,
55.
,
55.
.
57.
57.
' ;" 55.
'
.
57.
,
.
56.
57.
MCH
/mag
22. 23. 22. 21. 22. 22. 21. 23. 23, 22.
MCHC
%
39. 38. 40. 39. 38. 38.
39. 40. 39. 39.
PLAT
M/cnan
1021. 1322. 1307. 1089. 1101. 1021. 15C3. 1152. 1157. 1217.
AVG.
S. D. S. E.
7.213 0.356 0.113
15.91 0.79 0.25
40.8
^.0 6.6
"6.6 22.1 38.9 1198.0
1.6 0.7 ' 0.7 148.7 0.5 0.2 0.2 47.0
GROUP: 4M
DOSE: 10 MG/KG
SAMPLE DATE; 15-MAY-81
[
SEX; MALE
SPECIES: BAT
BIRTH PAlE: 13-MAR-81
ANZMALf: 301592 301593 301594
301595 301596 301597 301598 301599 301600 301601
AVG.
S. D. S. E.
RBC
MM/cm
6.78 6.84 6.21 6.89 6.64 6.76 7.10 6.12 6.63 6.41
6.638 0.308 0.098
Hb
8K
14.9 14.9 14.2 15.6 15.6 14.5 15.6 15.0 15.4 14.9
.
15.06
u^9 0.15
Ht
\%
3(
3(, 3!.
3<. 3<. 3(
4C 3< 3 31
37 .9 1.5 0.5
MCV
/cnc 56. 55. 56. 57. 59. 56. 56. 59. 58. 58.
57.0 1.4 0.4
MCH
/Bag
mac
:"%
22. 39.
22. 39. 23. <M. 23. HO.
24. 40.
22. 39.
22. 39. 25. 42.
25. 40.
?'. ,40. -; ?*.
22.9 39.9
1.0 1.0
0.3 0.3
PLAT
M/cina 1226. 1268.
983. 972. 992. 913.
941.
898. 1262. 1231.
-
1068.9 156.2 49.4
30 -
Company Sanitized. Does not contain TSCACBI
MR:L
COMPaD.-l
PERIOD:TteC_O_V_ER_Y
TmriCOLCC-^T; DASHIEL
f l 14008i
HASKBLL CODE<1:
DPRTMNT;,PPD&CP
&
SEPOBT DATE: l-Jun-81
CLINICAI.. LAB: MATARESE
GROUP; 3M
DOSE; TOO MG/W
SAMPLE '.-TE: 29-MAY-81
SEX; MALE
SPECIES: RAT
BIRTH DATE: 13-MAR-81
^ HBC
Hb
ANIMALS: MM/cn
S?
301582
MCW
/eac
MCT /Hms
KCHC
-<
,
PLAT M/cnm
301583
301584
i
i
301585
i
301586
301587 301588
6.90
^.^
Ht
58.
?2.
39. 1112.
^
301589
7.18 6.80
15.1 IS.^t
39.. 54.
39
2.1,..- '39. 1292.
'S
301590 6.69 15.3 39
58.
23.
3S>. 1260.
59. 23. 39. 1020.
?c
301591 7.31 16.0 41
' -i.
22.
39. 1238.
AVG.
S. D. S. B.
6.976 0.261 0.117
15.^
0.34
0.15
39.6
Oi.9
0.4
56.S
2.2
1.0
?2.2 .
0.8 0.4
39.0 1190.4
0.0 110.5 0,0 49.4
GROOP: 411
DOSE:
SAMPLE DJITE: 29-MAT-81
AMIMALtf:
301592 301593 301594 301555 301C;96
301597 301598 301599 301600 301601
RBC MM/cm
7.11 -'.85 6.86 7.44 6.40
Hb
^
15.4 15.0 15.2 16.4 14.7
AVG.
S. D. S. E.
6.932 0.382 0.171
15.34 0.65 0.29
10 Mp/KG
i
"i MCV
/cmc
j
i
. '
i
39. 38
39^
43.' 37.1
39.P 2.3 1.0
55. 56. 57. 58. 57.
56.6 1.1 0.5
SEXt ;HALE
SPECIES: RAT
BIRTH DATE: 13-MAR-81
MCH MCHC
/me
'
..
PLAT M/CHBl
" .
22. 3.
22. 39.
22; ^
22. 38.
23.
.
- y
. ^. ? ? ^
22.2
0^ 0,4
.,---;
0.2 0.3
980. 986. 1066. 1204. 1138.
.C'
1074.8
97.0 43.4
31 Company ^SSK&. sd. Dses j;St ssHsaiii TsCA CBl
mCO'M.VP^NSD:^gJJ|
PERIOD:-RECOVERY TOXICJLOGIST: DASHIELL
gASKJELLt1f:4008
HASKELL CODES'.
DPRTONT; PPD&CP
REPORT PATE: 9Jun-8l CLINICAL LAB: MATARESE
GROUP: 1CM
DOSE: COHT 10L
SAMPLE DATE: 29-tWT-81
SEX: MALE
.
SPECIES: BAT
BIRTH DATE: 13-MAR-81
ANIMALS: 301540 301541 301542 301543 301544 301545 301546 301547 301548 301549
AVG.
S. D. S. E.
WBC
M/ca
12.3 15.4 10.3 14.9 13.2
13.22 2.06 0.92
Neut %
Lyaplb %
i
''
EEooaain %
'
\
12.
84.
29. 67.
13.
82.,
(
20.
75.,
6. 90.;
16.0 79.P 00.6 8*9 8.6 00.5 3.9 4.0 00.2
Mono
?
4. 3. 5. 4. 3. 3.8 0.8 0.4
Baao %
0. 0. 0. 0. 0. 0.0 0.0 0.0
GROUP: 2M
DOSE: 10001/KG
SAMPLE DATE: 29-MAY-81
;
SEX: MALE
SPECIES: RAT
BIRTH DATE; 13-HAR-81
ANIMAL*: 301550 301551
301553 301554 301556 301557 301558
WBC
M/cn
Neut Lynpti Eosin
12.6 22. 67.
1.
Mono
%
10.
Baao
%
0.
AVG. 12.60 22.0 67.6 1.0 10.0 0.0 S. D.
S. E.
32 Company Sam-fesd. Does not ca^am TSCA CB1
FI CMORf.i'^l^--^--^J--^--^^--^--^U--S--K--El--ll^:
mo08I DPBBMT;
8ASKELL CODE?: PPD&CP
*
PERIOD:TlECOVERy
REPORT DATE^ 9-Jun-8l
TQXICOLOSIST: DASHIELL
CLINICAL LAB: HATARESE
GROUP; 3M
DOSE: 100 id/KG
SAMPLE DATK; 29-MAY-81
SBX; KALg
SPECIES; RAT
BIRTB OATB; 13-MAR-81
ANIMALS: 301582 301583 301584 301585 301586 301587 301588 301589
301590 301591
AVG.
5. 0.
S. E.
WBC
M/cn
13.1 18.6 15.2 10.8 10.9
13.72 3.27 1.46
Neut Lymph Eoain
S
%
t
'
9. 87. ^ 1.
15. 81.
0.
17. 80.
0,
19. 75.
0.
14. 84,
0,
14.8 81.4 0.2 3.8 4.5 0.4
1,7 2.0 0.2
Mono %
3. 4. 3. 6. 2. 3.6
1.5
0.7
Baso %
0. 0. 0. 0. 0. 0.0 0.6 0.0
GROUP: 4M
DOSE: TO MG/KG
SAMPLE DATE: 29-MAY-81
SEX: MALE
SPECIES: RAT
BIRTH DATE: 13-MAR-81
ANIMAU; 301592 301593 301S9H 301595 301596 301597 301598 301599 301600 301601
AVG.
3. D.
S. E.
WBC
M/CB
Neut Lyapb Eosin
%
%
%
i
1
Mono
%
Baso
%
-
.
10.4 23. 74.
1.
2.
0.
10.4
14.
82. ,! 1.
3.
0.
9.3 15. 76.
1.
8.
0.
12*0 27. 58.
2. ISr
0.
10.2 21. 73.
0.
6.
0.
10.46 20.0 72.6 1.0 6.4 0.0
0.97 5.5 8.9 0.7 4.4 0.0 0.44 2.4 4.0 0,3 2.0 0.0
33
CompaFiy SsnEtfcsd. Soss nss. cc^Eafs JSi
:IjMB4 MMRR;^
HAggSLLff : 14008
HASKELL CODE)?:
CCOOMPMMDPaND^1------------------rt OPBTMMT; PPD&CP
PPERIOODD:"1TCCOvBH?^^^^^*1
REPORT DATE: 29-May-Sl
TTOOXXIICCOLOGISTT DASHIEL
CLINICAL LAB: MATARESE
GROUP: 1C!M
DOSE: coiniic3L
SAMPLE DA TE: 29-?WY-SI
!
ANIMALS:
301540 301541 301542 301543 301544 301545 301546 301547 301548 301549
AP
IU
290. 300. 275. 225. 290.
GPT
IU
17. 19. 17. 21.
25.
GOT
pJ
'
BUN
Blg$
!
i
y15-,
22.0 18.0
3$. 19.0
iO. 18.0
ro. 22.0
SEX: MALE
SPECIES: PA1
BIRTH 3AiE: 13-MAR-81
GREAT ^ROT
sgf ' 8^
0.6 fi.3
0.6
16.1
0.6 ?6.5
0.6 '6.3
0.7 6.3
AVG.
S. D. S. E.
276.0
29.9
13.4
19.8
3.3 1.5
7.0 19.80 16.8 2.05
7.5 0.92
0.62 0.02 0.01
J8.30
0.14 0.06
GROUP; 2M
DOSE: 101)0 MG/KG
SAMPLE DATE: 29-MAY-Bl
ANIMALS: 301550 301551 301553
30'554 301555 301557 301558
AP
IU
245.
GPT
io
14.
GJ)I BON
iro "S?
25. 29.0
i
SE5K^ HAfeE
SPECIES: RAT
BBCTH SA-TE: 13-MAR-87
CSEAT ;TOSOT
ass$
gl
/,.
. -.;---,
0.6 6.4
'
AVG.
5-. D. S. E.
245.0
14.0
5,0 29.00 0.64 6.40
,..
34 Company Sanitized. Does no} coniain TSCA CBI
^'^Mll^H^HIl M:RT:^ljBtfIHJLl
CQMPND:HH----
HASgELL
PERRIOIOD D.'.T-OTCEWCEOfl VER^^^^^
TOXJCOLOGIST: DASHIEL
14008
HASKELL CODE<(:
DPRTMNT/; PPD&CP
REPOJBT DATE: 29-May-8l CLINKAl. LAB; MATARESE
GRODP: 3M
DOSE: It 0' MGyfKQ
SAMPLE DA'1rE; 29-t!ASr-8l
SEX:: 'MAi LE
SPECIES: RAT
BIRTH ,D1 ATE: 13-MAR-81
ANIMALS:
301582 301583 301584 301585 301586 301587 301588 301589
301590 301591
AP
GPT
( OT
10
IU
Iff
i
240.
14.
S0<
275. , ...24. . 315.
245. 25.
?0.
240.
16.
0.
215.
17.
35-
BON
BgSC
CREA' 'TpROT BKS^ 6<
15.0
20,0,. 19.0 18.0
21.0
0.8 6.1
0.7 ^6.5
0.'8 '^6.6
0.6 : ...6^
0^ '"6.5
AVG.
S. D. S. E.
243.0 21.4
9.6
18.6 4.4 2.0
'Mt.0
10.8
4.8
18.60 2.30 1.03
0.7? ;: 6.U2
0.05 .0.19
0.0^ 0.09
.:.?
'
^' -*.'
i -,
GROUP: 4M
DOSE:
.* .
10 MG/SG
SSX,-, 'W^i
SPECIES; RAT
SAMPLE DATE; 29-MAY-81
BIBTH DATE; 13-MAR-81
ANIMALS: 301592 301593 30159't 301595 301596 301597 301598 301599 301600 301601
AVG.
S. D. S. E.
AP
GPT QV W
CHEAT. TPROT
IU
10
W n^ "g?
g?
'
180. 240. 210. 245. 210.
217.0 26.4 11.8
17. 19. 7. 21. 17.
18.2 1.8 0.8
('0. ''0. *;0.
(0.
* 0.
2.0 8.4 3.7
IS.O 19.0
1^0
18.0 21.6
v^ao'
2.17 0.97
0.6 6.1
0.6 6.0 0.6 '- ^8.1 05 6.5 0.7 6.2
0.59'' 0.0& 0.03
' "
'6.18 0.19 0.09
.
35 Company Sanitized. Does not contain TSCA CBf
2^1 DCV 12-7*
.APPENDIX C
E. 1. DU PONT DE NEMOURS & COMPANY
IHCaOKMUTW
WiLMINGTON, DELAWARE 19898
fOLYMEW PRODUCTS DEPARTMENT EXPKKI MENTAL TATIOM
ANALYTICAL REPORT
September 16, 1981
CENTRAL RESEARC HASKELL LAB
AND DEVELOPMENT
DETERMINATION OFjFLUORININE RAT BLOOD
(Job No. 812-668; PRAL Nps. 8i4-2101-2119.81-2419-?434.81-2611-2612;
__________i|ithe o^studiesf------HIBHHu^6^08111'8 0^ ras tc
37 fBt blobd aanples'?Ubn>ltted 5/20/01 - 6T1.1/81 have been analyzed ToTrBiorine by the WickboXd Tor^ft procedure. The analyses were done by Erik Kissa at Jackson Lab (After prelinina.ry frieze-drying here), and results are given in the attached copy of his report,
< ^ ^ S. S. Stafford
Attachments jah
Key Words:
Analysis Wickbold Torch
- 36 -
Company SaifHSisscL Doss n&i coiRiasii TSGA C!
"niere's a w- Ic of things w'm doing aomattiing about
CH-l-l my. -W
E. 1. OU FONT DENEMOURS 5 COMPANY
WILMINGTON. DELAWARE 19398i
CHCMICAL* AND PIGMENTS OCrAKTMCNT ;
JACKSON LABOKATOKY
:
\ i^ Sally S. Stafford
-"Polymers * & Plastics ' DespatQaesat Experiinental Station 2B9/212
September 1, 1981
FLUORINE IN RAT BLOOD CONTAINING
The fluorine content of dried rat blood was determined by the oxyhydrogen torch method calibrated with p-fluorobenzoic acid (corrected for a blank and adjusted tp 100) fluorinj The results (see attacied pages}' surest thathej
recovery rate is similar to that o^HI|
'
'
^f^^^^^^--^^--H--Bj^|
HBHIHBr60'
''
~
Average F ppm ^Rate Saropled
*0nly one rat survived
25*
25 12
0.5
Two fluorine values, seemingly out of line, were confirmed by
duplicate analyses.
standard deviation of the fluorine
content ^f blood is larger' than that of the analytical method,
indicating a large vana^ o' n of lu0i4,ne in blood from rat to
rat. We need only about ^ 8-1 aa^iaiooit^for analyses. If a
rat can donate this aaiiunt and reeover^jit may be better to
sample the same rat p9;'i,odicicaalllly to follow the decrease of
fluorine in blood with tine,
^^ ^v^^ E. Kissa Physical & Analytical
EK:mml
Attach.
- 37 Company Sanitized. Doss noi contain TSCA CBI
FLUORINE IN RAT BLOOD CCOTAINING
PRAL Ho. 81-2101
81-2102 81-2103 81-2104 81-2105
81-2106 81-2107 81-2108 81-2109
81-2110 81-2111 81-2112 81-2113 81-2114
81-2115 81-2116
81-2117 81-2118 81-2119
Date Received 5/20/81
5/20/81 5/20/81 5/20/81 5/20/81
RAC if. 3(1540 3(1541
3(1542 3(1543
3C1545
Group. Tube ?
I Tr'ie:
I
Tune ,2
I
Tube 3
I
Tube,^
I ;Tube.i:5
5/20/81 5/20/81 5/20/81 5/20/81
5/20/81 5/20/81 5/20/81 5/20/81 5/20/81
5/20/81 5/20/81
3C1550 3( 1551 3C1553 .-3C 1554 3C1582 3(1583 - 3C1584. 301585 301586
3D 1592 301593
II Tube .6 II Tube 7 II Tube 8 II Tube 9
HI Tube"10
III Tube11
til Tube 12
III, Tube 13
III Tube jl4
17 "': Ti*^l5
IV Tube 16
5/20/81 5/20/81 5/20/81
30]l594 IV 3o|l595 IV
3o!l596 IV
Tube p Tube^8
Tube 19
81-2419 81-2420 81-2421 81-2422 81-2423
81-2424
6/1/81 6/1/81 6/1/81 6/1/81 6/1/81
6/1/81
303545 3013546 303S47 303548 30S549
I
Tube: 1
I
Tube 2
I
Tube 3
I
Tube 4
I
Tube-5
301555
II Tube 6
i
rxuurine 1.3
(b)
Lioncenc, ag/icg r
'
'
Grouo Averaae
1.2
X - 0.94
1.4
a " 0.52
0.6
0.2
212
190
K - 197
172
3 " 19.6
213
81
79
X- 79.4
78
0 2.7
S3
76
25.6
31.3, 29.8
---.
AJ
f
16.7 22.8
21.7
X - 23.5 CT - 5.1
0.1
1.0
? 0,48
w
0.5
0 - 0.34
0.5
"
0.3
^
'
23.1, 26.9 Avg. 25.
(
- 38 QsmpQny Semijsgd. Doss RCS ^smaisi TSCA CBi
FLUORINE IN RAT BLOOD COHTAIM
Sample Designation (a)
PRAL No.
Date Received
81-2425 Jl-2426 81-2427 81-2428 81-2429
6/1/81 6/1/81 6/1/81 6/1/81 6/1/81
81-2430 81-2431 81-2432 81-2433 81-2434
6/1/81 6/1/81 6/1/81 6/1/81 6/1/81
81-2611 81-2612
6/11/81 6/11/81
Rat ffL Group. Tube 7
30158 1 30158 1 30158 30159 > 30159 L
30159 r 301598 30159 1
301601
30160
30427^ 30427^
III Tube 7 III Tube 8 III Tube 9 III Tube m III Tuba 11'
iv Tube 12,
IV Tube 13 ,
IV Tube 14 IV Tuba 15^
IV Tuba 16,
Blank
Blank
Fluorine Content, ing/kg F (b)
Group Average
20.4 31.0 22.8 27,7 25.6
X - 25.1
a -4.2
5.4 9.2 11.8 18.6 14.0
X - 11.8 0 - 5.0
0.0 0.2
(a) Sample Designation for|
0
Group Group
II Group
III Group
I - control
i
- high. 1000 o^/kg
Interaedlate.lpO IV a low, 10 og/kg [
i
fflg/fcg
For samples 81-2101 through -2119, recovery fclae w&s 4 hours, after dose 5/15/81. For samples 81-^419 through -2434, recovery cine was
cbe final
14 days.
Samples 51-2611 and 81-2612 we^e "blanks", blood from stock rats not pare of the study but dried and analyzed along with the others.
(b) Total fluorine content, not corrected for inorganic' fluorine values which
are probably Insignificant, i
.^
- 39 Company Sanitised. Doss not contain TSCA CB1