2006
DOI: 10.1051/rnd:2006007
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Genotoxical, teratological and biochemical effects of anthelmintic drug oxfendazole Maximum Residue Limit (MRL) in male and female mice

Abstract: -Oxfendazole, methyl-5 (6)-phenylsulfinyl-2-benzimidazole carbamate, is a member of the benzimidazole family of anthelmintics. Anthelmintic benzimidazoles are widely used in meat producing animals (cattle, sheep and pigs) for control of endoparasites. The extensive use of veterinary drugs in food-producing animals can cause the presence of small quantities of the drug residues in food. Maximum residue limit or "MRL" means the maximum concentration of residue resulting from the use of a veterinary medicinal pro… Show more

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Cited by 28 publications
(15 citation statements)
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References 33 publications
(33 reference statements)
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“…If genotoxicity were to occur during key reproduction or embryogenesis stages it could cause offspring loss or impact hatchling development (El-Makawy et al, 2006; Keshava and Ong, 1999; Nayak et al, 1989). These outcomes would reduce the ability of an affected individual to survive or reproduce, resulting in detrimental effects to the population which is small in number and endangered.…”
Section: Discussionmentioning
confidence: 99%
“…If genotoxicity were to occur during key reproduction or embryogenesis stages it could cause offspring loss or impact hatchling development (El-Makawy et al, 2006; Keshava and Ong, 1999; Nayak et al, 1989). These outcomes would reduce the ability of an affected individual to survive or reproduce, resulting in detrimental effects to the population which is small in number and endangered.…”
Section: Discussionmentioning
confidence: 99%
“…Trees, unpublished observations), and this trial had to be abandoned for welfare reasons. Data indicating that certain benzimidazoles can also induce genotoxicity ([ 45 ] and WHO internal report) and cytotoxicity [ 46 ] are of related concern, and as a result further development of UMF-078 as a macrofilaricide has been halted.…”
Section: Discussionmentioning
confidence: 99%
“…However, this alleged safety relies on a disproportioned difference of available information among the different benzimidazolic compounds. The developmental adverse effects of most benzimidazole derivatives have been comprehensively studied in vivo [ 10 , 11 , 12 , 13 , 14 , 15 ] and in vitro [ 16 , 17 , 18 , 19 , 20 ] while the adverse effects of developmental exposure to TCBZ have been scarcely described and extrapolation from the data obtained from the other benzimidazolic compounds is not possible since the mechanism of action of TCBZ seems to be different [ 21 , 22 ]. There is a single original article available about developmental exposure to TCBZ which describes that it has no teratogenic or embryocidal effects in rats, but the study only covers a third part of the gestation period, leaving the initial and final developmental stages unstudied [ 23 ].…”
Section: Introductionmentioning
confidence: 99%