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乙酰唑胺片的生物利用度。

Bioavailability of acetazolamide tablets.

作者信息

Yakatan G J, Frome E L, Leonard R G, Shah A C, Doluisio J T

出版信息

J Pharm Sci. 1978 Feb;67(2):252-6. doi: 10.1002/jps.2600670233.

Abstract

Plasma acetazolamide levels were measured by an enzymatic assay following single 250-mg oral tablet doses to 20 healthy volunteers; five different lots of acetazolamide tablets from a single manufacturer were used in a balanced incomplete block design. From the measured plasma levels, estimates of the bioavailability parameters (area under the plasma concentration versus time curve, time to peak plasma concentration, and peak plasm concentration) were obtained by least-squares digital computer fitting. No significant differences among the tablets were observed (alpha = 0.05) for the analysis of variance of the area under the curve or time to peak parameters. Two tablets, however, provided statistically higher peak plasma concentrations than the other three. Thus, lot-to-lot bioinequivalence of acetazolamide tablets was observed. Some in vitro tests employed showed general trends for correlation with the in vivo data. However, considerable refinement of these technique appears necessary for in vitro prediction of the observed lot-to-lot bioinequivalence.

摘要

对20名健康志愿者单次口服250毫克片剂后,采用酶法测定血浆中乙酰唑胺水平;来自同一制造商的五种不同批次的乙酰唑胺片剂用于平衡不完全区组设计。根据测得的血浆水平,通过最小二乘法数字计算机拟合获得生物利用度参数(血浆浓度-时间曲线下面积、血浆浓度达峰时间和血浆峰浓度)的估计值。在曲线下面积或达峰时间参数的方差分析中,未观察到各片剂之间存在显著差异(α=0.05)。然而,有两片药的血浆峰浓度在统计学上高于其他三片。因此,观察到乙酰唑胺片剂存在批次间生物不等效性。所采用的一些体外试验显示出与体内数据相关的总体趋势。然而,为了体外预测观察到的批次间生物不等效性,这些技术似乎需要进行相当大的改进。

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