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脂质体包裹阿片类药物的制备及其体外活性

Preparation and in vitro activity of liposome encapsulated opioids.

作者信息

Reig F, Alsina M A, Busquets M A, Valencia G, Garcia Anton J M

机构信息

Laboratory of Peptides, CID, CSIC, Barcelona, Spain.

出版信息

J Microencapsul. 1989 Jul-Sep;6(3):277-83. doi: 10.3109/02652048909019910.

Abstract

Four opiate molecules: morphine, naloxone, meperidine and codeine have been encapsulated in liposomes. The encapsulation efficiency has been studied as a function of the following parameters: liposome preparation method, lipid composition and opioid molecule hydrophobicity. The most important parameter as far as the entrapment efficiency is concerned is the liposome preparation method. The opioid activity of these molecules in vitro (Guinea Pig Ileum preparation) has been determined. No differences in the IC50 values could be found between encapsulated and free drug molecules.

摘要

四种阿片类分子

吗啡、纳洛酮、哌替啶和可待因已被包裹在脂质体中。研究了包封效率与以下参数的函数关系:脂质体制备方法、脂质组成和阿片类分子疏水性。就包封效率而言,最重要的参数是脂质体制备方法。已测定了这些分子在体外(豚鼠回肠制备)的阿片活性。包封的药物分子和游离药物分子之间的半数抑制浓度(IC50)值未发现差异。

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