1990
DOI: 10.1007/bf01972985
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A simple method for screening assessment of acute toxicity of chemicals

Abstract: We proposed a simple method for screening assessment of acute oral and dermal toxicity using only three rats and mice of each sex at each dose level. Animals were first treated with chemicals at a dose of 2000 mg/kg and were carefully observed for compound-related morbidity and mortality. If none of the animals died, the following toxicity tests were suspended. If some of the animals died, toxicity tests at doses of 200 and 20 mg/kg were performed. The approximate LD50 values calculated by this method showed l… Show more

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Cited by 26 publications
(13 citation statements)
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“…Six animals were used per sample. To assess peptide toxicity, the maximum non-toxic dose was determined [50] as an amount (mg) of the tested peptide per kg of the mouse weight, at which there was no observed toxic or adverse effect within 24 hours.…”
Section: Toxicitymentioning
confidence: 99%
“…Six animals were used per sample. To assess peptide toxicity, the maximum non-toxic dose was determined [50] as an amount (mg) of the tested peptide per kg of the mouse weight, at which there was no observed toxic or adverse effect within 24 hours.…”
Section: Toxicitymentioning
confidence: 99%
“…Standard diet (SD; 11% energy by fat) and high-fat diet (HFD, 60% energy by fat) were purchased from Safe (Augy, France After one week acclimatization mice were randomly assigned to three experimental protocols described in the following. A first protocol examined the acute oral toxicity of AQL and butanol extract at 2000 mg/kg on 16-weeks SD animals (n = 4/group) according to the procedure of Yamanaka et al (1990). Extracts, dissolved in a suspension of 0.5% aqueous carboxymethyl cellulose (as vehicle), were given orally in the limit of 0.1 mL/10 g body weight.…”
Section: Animals and Study Designmentioning
confidence: 99%
“…This study describes gestational, maternal and fetal effects from oral parental exposure to organophosphorous pesticides formulations. -phenyl-1H-1,2,4-trazol-3-yl phosphorothioate) and Nogos: dichlorvos (2,2-dichlorovinyl dimethyl phosphate)] was prepared by mixing individual pesticide formulations in proportion to their individual LD 50 dose values and LD 50 of the mixture was determined as previously described by Gomes et al (1999b) using a modified protocol from Yamanaka et al (1990) and Bruce (1985). The LD 50 for each of the pesticide formulations for this study were: Salut 160 mg/kg body weight; Selecron 1330 mg/kg body weight; Dursban 670 mg/kg body weight; Actellic 6670 mg/kg body weight; Hostathion 160 mg/kg body weight and Nogos 330 mg/kg body weight; and the LD 50 for the mixture was 67 mg/kg body weight (Gomes et al 1999b).…”
Section: Introductionmentioning
confidence: 99%