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口服萘夫西林在正常健康志愿者体内的吸收情况。

Absorption of orally administered nafcillin in normal healthy volunteers.

作者信息

Watanakunakorn C

出版信息

Antimicrob Agents Chemother. 1977 Jun;11(6):1007-9. doi: 10.1128/AAC.11.6.1007.

Abstract

The absorption of orally administered nafcillin sodium monohydrate buffered with calcium carbonate was studied in 10 healthy human volunteers. Dosages of 500 mg and 1 g were studied in fasting and nonfasting states. There was considerable individual variation in the absorption of nafcillin, although measurable serum concentrations were obtained in all subjects. With few exceptions, peak serum concentrations were reached faster and were more predictable in the fasting state than in the nonfasting state. In the majority of subjects, food interfered with nafcillin absorption. Measurable serum concentrations persisted for 4 h in almost all subjects, but there were no or negligible serum concentrations at 6 h. The mean serum concentrations obtained in the present study were higher than those reported in an earlier study.

摘要

在10名健康人类志愿者中研究了用碳酸钙缓冲的口服一水合萘夫西林钠的吸收情况。在禁食和非禁食状态下研究了500毫克和1克的剂量。尽管在所有受试者中都获得了可测量的血清浓度,但萘夫西林的吸收存在相当大的个体差异。除少数例外,禁食状态下血清浓度峰值出现得更快且更可预测,而非禁食状态则不然。在大多数受试者中,食物会干扰萘夫西林的吸收。几乎所有受试者的可测量血清浓度持续4小时,但6小时时血清浓度无或可忽略不计。本研究中获得的平均血清浓度高于早期研究报告的浓度。

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Pharmacokinetics of nafcillin in patients with renal failure.肾衰竭患者中萘夫西林的药代动力学。
Antimicrob Agents Chemother. 1977 Jul;12(1):98-101. doi: 10.1128/AAC.12.1.98.

引用本文的文献

1
Interactions affecting drug absorption.影响药物吸收的相互作用。
Clin Pharmacokinet. 1984 Sep-Oct;9(5):404-34. doi: 10.2165/00003088-198409050-00002.

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