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作为漂浮药物递送系统的微球,用于增加药物在胃内的滞留时间。

Microspheres as floating drug-delivery systems to increase gastric retention of drugs.

作者信息

Soppimath K S, Kulkarni A R, Rudzinski W E, Aminabhavi T M

机构信息

Department of Chemistry, Karnatak University, Dharwad, India.

出版信息

Drug Metab Rev. 2001 May;33(2):149-60. doi: 10.1081/dmr-100104401.

Abstract

Gastric emptying is a complex process, which is highly variable and makes in vivo performance of the drug-delivery systems uncertain. In order to avoid this variability, efforts have been made to increase the retention time of the drug-delivery systems for more than 12 h. The floating or hydrodynamically controlled drug-delivery systems are useful in such applications. The present review addresses briefly the physiology of the gastric emptying process with respect to floating drug-delivery systems. In recent years, the multiparticulate drug-delivery systems are used in the oral delivery of drugs. One of the approaches toward this goal is to develop the floating microspheres so as to increase the gastric retention time. Such systems have more advantages over the single-unit dosage forms. The development of floating microspheres involves different solvent evaporation techniques to create the hollow inner core. The present review addresses the preparation and characterization of the floating microspheres for the peroral route of administration of the drug.

摘要

胃排空是一个复杂的过程,其变化很大,使得药物递送系统的体内性能具有不确定性。为了避免这种变异性,人们已努力将药物递送系统的保留时间延长至12小时以上。漂浮或流体动力学控制的药物递送系统在此类应用中很有用。本综述简要介绍了与漂浮药物递送系统相关的胃排空过程的生理学。近年来,多颗粒药物递送系统被用于药物的口服给药。实现这一目标的方法之一是开发漂浮微球以增加胃内保留时间。此类系统比单剂量剂型具有更多优势。漂浮微球的开发涉及不同的溶剂蒸发技术以形成中空内芯。本综述阐述了用于药物口服给药的漂浮微球的制备和表征。

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