Suppr超能文献

口服吸收的头孢呋辛与阿莫西林/克拉维酸的药代动力学比较。

The pharmacokinetics of orally absorbed cefuroxime compared with amoxycillin/clavulanic acid.

作者信息

Wise R, Bennett S A, Dent J

出版信息

J Antimicrob Chemother. 1984 Jun;13(6):603-10. doi: 10.1093/jac/13.6.603.

Abstract

The pharmacokinetics of a new orally absorbed pro-drug of cefuroxime were compared with those of co-administered amoxycillin and clavulanic acid in six healthy male volunteers. Doses of 600 mg of acetoxyethyl cefuroxime and 500 mg amoxycillin plus 250 mg clavulanic acid were each administered for ten doses 8 hourly. Tissue penetration after the first dose of the antibiotic was estimated by a cantharides blister method. The faecal flora of the volunteers was studied throughout the study. The pharmacokinetics of cefuroxime and amoxycillin were very similar, peak levels of about 6.4 mg/l being found between 2 and 2.5 h after administration. The peak serum level of clavulanic acid was 4.3 mg/l at 1.25 h after administration. The serum half-lives were about 1.1 h for all three agents. No drug accumulation occurred over the four days of the study. The 0-8 h urinary recovery of cefuroxime was 30%. All three agents penetrated the blister fluid rapidly, the main peak levels being 64% of the peak serum level for cefuroxime, 72% for amoxycillin and 55% for clavulanic acid. The incidence of side effects was similar for each regimen. Three volunteers having diarrhoea after cefuroxime showed significant alterations in their bowel flora.

摘要

在六名健康男性志愿者中,对一种新的口服吸收型头孢呋辛前体药物的药代动力学与联合使用的阿莫西林和克拉维酸的药代动力学进行了比较。分别给予600毫克乙酰氧乙酯头孢呋辛和500毫克阿莫西林加250毫克克拉维酸,每8小时给药十次。采用斑蝥水疱法估计首次给予抗生素后的组织穿透情况。在整个研究过程中对志愿者的粪便菌群进行了研究。头孢呋辛和阿莫西林的药代动力学非常相似,给药后2至2.5小时之间的峰值水平约为6.4毫克/升。克拉维酸给药后1.25小时的血清峰值水平为4.3毫克/升。三种药物的血清半衰期约为1.1小时。在研究的四天内未发生药物蓄积。头孢呋辛0至8小时的尿回收率为30%。三种药物均迅速渗透到水疱液中,主要峰值水平分别为头孢呋辛血清峰值水平的64%、阿莫西林的72%和克拉维酸的55%。每种用药方案的副作用发生率相似。三名服用头孢呋辛后出现腹泻的志愿者的肠道菌群有明显改变。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验