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[羧苄青霉素的急性毒性及蓄积特性]

[Acute toxicity and the cumulative properties of carfecillin].

作者信息

Lidovskiĭ M Z, Zel'tser I Z, Berezina E K

出版信息

Antibiotiki. 1978 May;23(5):450-3.

PMID:655692
Abstract

Acute toxicity of oral and intraperitoneal carfecillin was studied on different species of laboratory animals, such as albino mice, rats and guinea pigs. The average lethal doses equal to 3040 (2393.7-3860.8) and 1325 (1104.2-1590) mg/kg for oral and intraperitoneal administration respectively allowed the authors to consider the antibiotic as a low toxic substance under conditions of a single administration. Higher toxicity of carfecillin as compared to carbenicillin may be due to production of free phenol on carfecillin hydrolysin in the animal organism. The different laboratory animals of both sexes had almost the same sensitivity to the antibiotic. On repeated administration of carfecillin to the albino mouse stomach (in portions of LD50) no cumulative properties of the antibiotic were observed.

摘要

对白化病小鼠、大鼠和豚鼠等不同种类的实验动物研究了口服和腹腔注射羧苄青霉素苯酯的急性毒性。口服和腹腔注射的平均致死剂量分别为3040(2393.7 - 3860.8)mg/kg和1325(1104.2 - 1590)mg/kg,这使作者认为在单次给药条件下该抗生素为低毒物质。与羧苄青霉素相比,羧苄青霉素苯酯的毒性较高可能是由于其在动物体内水解产生游离酚所致。不同性别的不同实验动物对该抗生素的敏感性几乎相同。对白化病小鼠进行胃内重复给药(按半数致死量的剂量分份给药)时,未观察到该抗生素的累积特性。

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The availability of carfecillin and its phenol moiety in rat and dog.
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