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用口服棕榈酸氯霉素制剂治疗肉用型犊牛的药代动力学和毒理学方面

Pharmacokinetic and toxicological aspects of the medication of beef-type calves with an oral formulation of chloramphenicol palmitate.

作者信息

Gassner B, Wuethrich A

机构信息

Department of Veterinary Pharmacology, University of Bern, Switzerland.

出版信息

J Vet Pharmacol Ther. 1994 Aug;17(4):279-83. doi: 10.1111/j.1365-2885.1994.tb00246.x.

Abstract

Chloramphenicol (CAP) plasma levels were determined after oral administration of four doses of CAP palmitate (each dose corresponding to CAP 25 mg/kg/12 h) to four ruminating beef-type calves. Steady-state plasma concentrations of CAP were reached after the fourth oral dose and varied between 5 and 6 micrograms/ml. Half-life of elimination of CAP was 4.5 h. In addition to CAP, dehydrochloramphenicol (DH-CAP), a metabolite of chloramphenicol, was detected in plasma at concentrations between 3 and 7 ng/ml. DH-CAP is known to be produced from CAP by intestinal bacteria. This is significant since DH-CAP is suspected of being involved in the development of fatal aplastic anaemia, which occurs in man after exposure to CAP. Thus, it cannot be excluded that DH-CAP residues may occur in edible tissues. A risk arising from DH-CAP can neither be excluded for the animals being treated with CAP nor for consumers.

摘要

对四头反刍的肉用型小牛口服四剂棕榈酸氯霉素(CAP)(每剂相当于25mg/kg/12h的CAP)后,测定了血浆中氯霉素(CAP)的水平。第四次口服给药后达到了CAP的稳态血浆浓度,范围在5至6微克/毫升之间。CAP的消除半衰期为4.5小时。除了CAP之外,还在血浆中检测到了氯霉素的代谢产物脱氯氯霉素(DH-CAP),其浓度在3至7纳克/毫升之间。已知DH-CAP是由肠道细菌从CAP产生的。这一点很重要,因为DH-CAP被怀疑与致命性再生障碍性贫血的发生有关,人类接触CAP后会出现这种疾病。因此,不能排除DH-CAP残留可能出现在可食用组织中。无论是接受CAP治疗的动物还是消费者,都不能排除DH-CAP带来的风险。

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