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三种多柔比星制剂在人体中的生物利用度与模拟吸收数据的相关性。

Correlation of bioavailability in man with simulated absorption data for three doxantrazole preparations.

作者信息

Jones H, Bye A

出版信息

J Pharm Pharmacol. 1979 Nov;31(11):730-3. doi: 10.1111/j.2042-7158.1979.tb13646.x.

Abstract

The in vitro and in vivo availability of doxantrazole, a potential antiallergic compound has been evaluated. A solution was significantly less bioavailable than either tablet or suspension formulations and it is suggested that this is associated with the large volume of the solution vehicle altering the hydrophilicity of the gastrointestinal fluids. In vitro availability was determined from absorption rate constants and absorption profiles obtained using the Sartorius absorption and solubility simulators. A statistically significant correlation was found between the percentage absorbed in vitro at 1 h and both total urinary recovery and area under plasma curve values in vivo. It is considered that in vitro determination of diffusion through artificial lipid membranes may be a useful predictive method of in vivo availability.

摘要

已对一种潜在的抗过敏化合物多沙唑进行了体外和体内可用性评估。一种溶液的生物利用度明显低于片剂或混悬液制剂,据推测这与溶液载体的大量存在改变了胃肠液的亲水性有关。体外可用性是根据使用赛多利斯吸收和溶解度模拟器获得的吸收速率常数和吸收曲线来确定的。在体外1小时时的吸收百分比与体内的总尿回收率和血浆曲线下面积值之间发现了具有统计学意义的相关性。据认为,通过人工脂质膜的体外扩散测定可能是一种有用的体内可用性预测方法。

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