SOFT 2004 Meeting Abstracts - Society of Forensic Toxicologists
SOFT 2004 Meeting Abstracts - Society of Forensic Toxicologists
SOFT 2004 Meeting Abstracts - Society of Forensic Toxicologists
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TOXICOKINETICS, RECOVERY, RESIDUES AND CYTOTOXICITY OF ACTP-ESTER IN<br />
THE GOAT<br />
C.R. Sahu*" Biplab Bagchi <br />
Department <strong>of</strong>Zoology, Kalyani University, Kalyani, West Bengal, India <br />
ACTP- Ester (Triclopyr butyl) marketed by Dow Elanco, USA is a selective herbicide used widely in<br />
agricultural field. In order to study the toxicokinetic, total recovery and cytotoxicity study <strong>of</strong> ACTP- Ester<br />
and its two potential metabolites - triclopyr acid (M]) and 3,5,6- trichloro-2 pyridinol (M2), the compound<br />
ACTP- Ester was administered orally 396 mglkg body wt. to Black Bengal Goats (Capra capra). The<br />
control groups were however treated with the same amount <strong>of</strong> carboxymethyl cellulose (CMC).<br />
Blood samples were collected before (0 hr) and after 0.25,0.50,0.75, 1,2,3,4,6,8,12,36,48,60,72,84,96,<br />
120, 144 and 168hr post administration (Pd) and were prepared for HPLC analysis following standard<br />
protocols. Toxicokinetic parameters <strong>of</strong> ACTP Ester were determined from computerized interactive curve<br />
fitting programme <strong>of</strong> respective blood level time pr<strong>of</strong>ile and data were analyzed as per the standard formula<br />
using various disposition kinetic parameters. Gross lesions for different tissues like liver, kidney, lung,<br />
brain etc were recorded for ACTP-Ester induced cytotoxicity in goats sacrificed on 4,5,6 and 7-day pd. An<br />
adequate blood level <strong>of</strong> ACTP-' Ester was detected as 4.94 ± 0.43 at 0.25 hr (pd). The concentration (C B<br />
max 25.15 ± 2.62 j.lg Iml was recorded at 6 hr followed by a slow decline and minimum (C B min 3.52 ±<br />
0.23 j.lg Iml) was detected at 60 hr pd. Kinetic behaviour <strong>of</strong> ACTP- Ester in goats followed a "two<br />
compartmental open model kinetics". The blood level for M] and M2 was 6.52 ± 0.89 and 2.61 ± 0.13<br />
. j.lg/ml respectively. The lower absorption rate constant suggested slow absorption <strong>of</strong> ACTPEster from<br />
GJ.tract. The CI H value, which is equivalent to CI B value suggested that major route <strong>of</strong> elimination <strong>of</strong><br />
ACTP-Ester be directed through liver. Very poor CI g value suggested that urine is the minor route <strong>of</strong><br />
excretion <strong>of</strong> the compound. The concentration <strong>of</strong> both metabolites appears zigzag fashion, which might be<br />
due to variable quantity as well as rate <strong>of</strong> metabolism in every unit <strong>of</strong> time.<br />
The recovery percentage <strong>of</strong> ACTP-Ester from faeces, G.I.tract content, urine and tissues were respectively<br />
65.38, 63.34, 66.10 and 66.24 in goats sacrificed on 4, 5, 6 and 7-day pd. Liver and lung showed gross<br />
malformations than other tissues due to the treatment.<br />
Keywords: Toxicokinetic, residue cytotoxicity ACTP, goat<br />
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