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奈替米星的多房室药代动力学

Multicompartment pharmacokinetics of netilmicin.

作者信息

Wenk M, Spring P, Vozeh S, Follath F

出版信息

Eur J Clin Pharmacol. 1979 Nov;16(5):331-4. doi: 10.1007/BF00605631.

Abstract

The pharmacokinetics of a single dose of netilmicin (NM) was studied in 6 healthy volunteers. Elimination of the drug was followed in serum and urine for 24 h and 72 h, respectively. NM concentrations were measured with a modified radioenzymatic assay. A three compartment open model was employed to calculate the pharmacokinetic parameters. Following the rapid initial distribution, biphasic elimination with half lives of 1.99 (t 1/2 beta) and 36.89 h (t 1/2 gamma) was demonstrated. Measurable amounts of NM were excreted in the urine for up to 72 h. The volume of distribution at steady-state (Vdss) of 0.68 l/kg was 3 to 4 times larger than previously reported for this antibiotic. NM plasma clearance was 91 ml/min and the renal clearance was 67 ml/min. The data indicate that on repetitive dosing the amount of drug in the body would be considerably underestimated if the prolonged terminal elimination phase were not taken into account. During prolonged treatment, accumulation of NM in renal and other tissues is likely to occur, as has been described for other aminoglycosides. The possible consequences of this pharmacokinetic behaviour are discussed.

摘要

在6名健康志愿者中研究了单剂量奈替米星(NM)的药代动力学。分别在血清和尿液中追踪药物消除情况24小时和72小时。采用改良的放射酶法测定NM浓度。采用三室开放模型计算药代动力学参数。在快速初始分布之后,显示出双相消除,半衰期分别为1.99小时(t1/2β)和36.89小时(t1/2γ)。在长达72小时的尿液中可检测到一定量的NM。稳态分布容积(Vdss)为0.68升/千克,比该抗生素先前报道的值大3至4倍。NM的血浆清除率为91毫升/分钟,肾清除率为67毫升/分钟。数据表明,如果不考虑延长的终末消除相,重复给药时体内药物量将被大大低估。正如其他氨基糖苷类药物所描述的那样,在长期治疗期间,NM可能会在肾脏和其他组织中蓄积。讨论了这种药代动力学行为可能产生的后果。

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