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一种新的头孢菌素衍生物(ST - 21)经口服给予实验动物。

A new cephalosporin derivative (ST-21) orally administered in laboratory animals.

作者信息

Foresta P, Ramacci M T, De Witt P, Capitani N, Fanelli O

出版信息

Arzneimittelforschung. 1977;27(4):819-23.

PMID:577459
Abstract

The pivaloxymethyl ester of 7-(D-2-amino-2-phenylacetamido)-desacetoxicephalosporanic acid hydrochloride (ST-21) and cephalexin possess the same bacteridal activity. In fact, in the animal body ST-21 releases cephalexin. The acute toxicity study shows the good tolerance of both substances, whereas the tissue distribution is different, both after oral and i.v. administration. Cephalexin concentrations in some tissues of rats and rabbits, particularly in the lungs and kidneys, are higher and longer-lasting in the animals treated with ST-21 than in those receiving cephalexin, thus showing a different pattern of distribution in the body. For this reason ST-21 might be more suited for the treatment of lung and kidney infections.

摘要

7-(D-2-氨基-2-苯乙酰胺基)-去乙酰氧头孢烷酸盐酸盐(ST-21)的特戊酰氧甲酯与头孢氨苄具有相同的杀菌活性。事实上,在动物体内ST-21会释放出头孢氨苄。急性毒性研究表明这两种物质的耐受性良好,然而,口服和静脉注射给药后,它们的组织分布有所不同。在用ST-21治疗的大鼠和兔子的某些组织中,尤其是肺和肾脏,头孢氨苄的浓度比接受头孢氨苄治疗的动物更高且持续时间更长,因此显示出在体内不同的分布模式。出于这个原因,ST-21可能更适合用于治疗肺部和肾脏感染。

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