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美洛西林静脉推注或静脉滴注给药时的药代动力学特性比较。

Comparison between the pharmacokinetic properties of mezlocillin when given intravenously as a bolus injection or as an infusion.

作者信息

Ohlsson H, Bergan T

出版信息

Arzneimittelforschung. 1979;29(12a):1958-9.

PMID:543900
Abstract

6-[(R)-2-[3-methylsulfonyl-2-oxo-imidazolidine-1-carboxamido]-2-phenyl-acetamido]-penicillanic acid sodium salt (mezlocillin, Baypen) in doses of 5.0 g was given i.v. as an infusion or as a bolus injection to 5 healthy volunteers. 5 min after the completion of the infusion, the mean serum concentration was 430 +/- 81 microgram/ml compared to 424 +/- 91 microgram/ml after the bolus injection. The half-lives were 1.31 +/- 0.24 h and 1.72 +/- 0.21 h, respectively. These results indicate that differences in serum concentrations between various investigators probably can be attributed to differences in body size and do not seem to depend on the administration route.

摘要

将剂量为5.0克的6-[(R)-2-[3-甲基磺酰基-2-氧代-咪唑烷-1-甲酰胺基]-2-苯基-乙酰胺基]-青霉烷酸钠盐(美洛西林,拜朋)以静脉输注或大剂量注射的方式给予5名健康志愿者。输注结束后5分钟,平均血清浓度为430±81微克/毫升,而大剂量注射后为424±91微克/毫升。半衰期分别为1.31±0.24小时和1.72±0.21小时。这些结果表明,不同研究者之间血清浓度的差异可能归因于体型差异,似乎并不取决于给药途径。

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