[氨基糖苷类抗生素(阿米卡星、庆大霉素、西索霉素、妥布霉素)的药理学研究]。

Advances in clinical pharmacology Pub Date : 1978-01-01
H Lode, K Grunert, B Kemmerich, P Koeppe
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引用次数: 0

摘要

在一项12名健康受试者的随机研究中,在输注庆大霉素、西索霉素和妥布霉素(1.0 mg/kg体重)1小时后,测定了每种药物的药代动力学。三种药物在治疗意义上没有药代动力学差异。注射结束时庆大霉素和西索霉素的平均血清浓度分别为3.85微克/ml和4.66微克/ml, 8小时后分别降至0.12微克/ml和0.26微克/ml。生物半衰期在96 ~ 122min之间,分布的表观体积与胞外空间的大小密切相关。——持续输注1小时后测定阿米卡星的药代动力学数据,阿米卡星的平均血清浓度为37.5微克/毫升,8小时后降至平均1.3微克/毫升。生物半衰期平均为114.2 +/- 16.7 min,表观分布体积按18.1 +/- 1.81/100 kg体重计算。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Pharmacologic studies or aminoglycoside antibiotics (amikacin, gentamicin, sisomicin, tobramycin)].

In a randomized study of 12 healthy subjects, the pharmacokinetics of gentamicin, sisomicin and tobramycin were determined after a one-hour infusion of each drug (1.0 mg/kg body-weight). There were no pharmacokinetic differences of therapeutic significance between the three drugs. The mean serum concentrations at the end of infusion were 3.85 microgram/ml for gentamicin and 4.66 microgram/ml for sisomicin, falling to 0.12 and 0.26 microgram/ml, respectively, after eight hours. The biological half-life varied between 96 and 122 min and the apparent volumes of distribution corresponded closely to the size of the extracellular space.--The pharmacokinetic data of amikacin were determined after a one-hour constant infusion, the mean amikacin serum concentration was 37.5 microgram/ml and, 8 hours later, decreased to an average of 1.3 microgram/ml. The biological half-life amounted to a mean of 114.2 +/- 16.7 min, and the apparent volume of distribution could be calculated with 18.1 +/- 1.81/100 kg body weight.

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