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Pesticide residues in food — 2007: Toxicological ... - ipcs inchem

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311<br />

Lowest relevant <strong>in</strong>halation NOAEC<br />

Genotoxicity<br />

Long-term studies of toxicity and carc<strong>in</strong>ogenicity<br />

Target/critical effect<br />

Lowest relevant NOAEL<br />

Carc<strong>in</strong>ogenicity<br />

Reproductive toxicity<br />

Reproduction target/critical effect<br />

Lowest relevant reproductive NOAEL<br />

Developmental target/critical effect<br />

Lowest relevant developmental NOAEL<br />

Neurotoxicity/delayed neurotoxicity<br />

Other toxicological studies<br />

Medical data<br />

No data<br />

Unlikely to be genotoxic <strong>in</strong> vivo<br />

Liver histology and body-weight decrease (rats)<br />

36.3 mg/kg bw per day<br />

Not carc<strong>in</strong>ogenic<br />

No reproductive effects<br />

80 mg/kg bw per day, the highest dose tested<br />

Increased <strong>in</strong>cidence of total litter losses (rats and rabbits)<br />

60 mg/kg bw per day (rats)<br />

No evidence <strong>in</strong> conventional studies<br />

In pharmacological studies, evidence for an <strong>in</strong>crease <strong>in</strong><br />

phenobarbital sleep<strong>in</strong>g time<br />

Medical surveillance of workers <strong>in</strong> a plant produc<strong>in</strong>g dimethomorph<br />

did not reveal any adverse health effects.<br />

Summary<br />

Value Study Safety factor<br />

ADI 0–0.2 mg/kg bw Dog, 13-week and 1-year study 100<br />

ARfD 0.6 mg/kg bw Rat, study of developmental toxicity 100<br />

References<br />

Afzal, J. & Wu, D. (1995a) Dimethomorph (CL 336,379): blood pharmacok<strong>in</strong>etics of C-14 CL 336,379 derived<br />

<strong>residues</strong> <strong>in</strong> the rat. Unpublished report No. DK-452-008 from XenoBiotic Laboratories, Inc., North Branch,<br />

USA. Submitted to WHO by BASF, Ecully Cedex, France.<br />

Afzal, J. & Wu, D. (1995b) Dimethomorph (CL 336,379): tissue distribution of C-14 CL 336,379 derived <strong>residues</strong><br />

<strong>in</strong> the rat. Unpublished report No. DK-440-013 from XenoBiotic Laboratories Inc., Pla<strong>in</strong>sboro NJ<br />

08536, USA. Submitted to WHO by BASF, Ecully Cedex, France.<br />

A<strong>in</strong>sworth, G.A. & Wright, A. (1991a) Anticonvulsive activity <strong>in</strong> mice. Unpublished report No. DK-451-004<br />

from Toxicol Laboratories Ltd, Ledbury Herefordshire, England. Submitted to WHO by BASF, Ecully<br />

Cedex, France.<br />

A<strong>in</strong>sworth, G.A. & Wright, A. (1991b) Assessment of potential anti-<strong>in</strong>flammatory activity us<strong>in</strong>g the carrageenan<br />

<strong>in</strong>duced rat paw oedema model. Unpublished report No. DK-452-004 from Toxicol Laboratories<br />

Ltd, Ledbury Herefordshire, England. Submitted to WHO by BASF, Ecully Cedex, France.<br />

A<strong>in</strong>sworth, G.A. & Wright, A. (1991c) Cardiovascular, respiratory and nictitat<strong>in</strong>g membrane alterations produced<br />

by test compound <strong>in</strong> the anaesthetised cat. Unpublished report No. DK-452-006 from Toxicol Laboratories<br />

Ltd, Ledbury Herefordshire, England. Submitted to WHO by BASF, Ecully Cedex, France.<br />

A<strong>in</strong>sworth, G.A. & Wright, A. (1991d) Charcoal meal transit times <strong>in</strong> the rat small <strong>in</strong>test<strong>in</strong>e. Unpublished<br />

report No. DK-452-003 from Toxicol Laboratories Ltd, Ledbury Herefordshire, England. Submitted to<br />

WHO by BASF, Ecully Cedex, France.<br />

DIMETHOMORPH 273–315 JMPR <strong>2007</strong>

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