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地西泮控释制剂的临床生物利用度评估

Clinical bioavailability evaluation of a controlled release formulation of diazepam.

作者信息

Gustafson J H, Weissman L, Weinfeld R E, Holazo A A, Khoo K C, Kaplan S A

出版信息

J Pharmacokinet Biopharm. 1981 Dec;9(6):679-91. doi: 10.1007/BF01070900.

Abstract

A controlled release formulation of diazepam was compared to equal daily dose of the trade tablet under single day and steady-state conditions. Virtually no differences were found in the mean steady-state concentrations of diazepam or its metabolites, N-desmethyldiazepam, when the subjects received the 5 mg trade table three times daily or the 15 mg controlled release formulation once daily. Similarly, there was no difference in mean diazepam or N-desmethyldiazepam plasma concentrations when single doses of the controlled release formulation were give to fed or fasted volunteers. These data indicate that the controlled release formulation produces plasma concentrations of diazepam and N-desmethyldiazepam comparable to those achieved with the same daily dose of the trade product given three times daily, suggesting that these regimens can be used interchangeably.

摘要

在单日和稳态条件下,将地西泮控释制剂与同等日剂量的市售片剂进行了比较。当受试者每日三次服用5毫克市售片剂或每日一次服用15毫克控释制剂时,地西泮及其代谢产物N-去甲基地西泮的平均稳态浓度几乎没有差异。同样,当给饱腹或空腹志愿者单次服用控释制剂时,地西泮或N-去甲基地西泮的平均血浆浓度也没有差异。这些数据表明,控释制剂产生的地西泮和N-去甲基地西泮血浆浓度与每日三次服用相同日剂量市售产品所达到的浓度相当,这表明这些给药方案可以互换使用。

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