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青霉素和头孢菌素。药物及生物基质中的物理化学性质与分析

Penicillins and cephalosporins. Physicochemical properties and analysis in pharmaceutical and biological matrices.

作者信息

Van Krimpen P C, Van Bennekom W P, Bult A

出版信息

Pharm Weekbl Sci. 1987 Feb 20;9(1):1-23. doi: 10.1007/BF01956487.

Abstract

Penicillins and cephalosporins belong to the most prescribed antibiotics. Despite the relatively extended knowledge of these drugs, the qualitative and quantitative analysis of the compounds still gives rise to many problems. These difficulties are due to the chemical instability of the common beta-lactam nucleus, the minor differences in chemical structures between the analogues, and the complex and relatively fast degradation of the compounds in aqueous solutions. In this review a compilation of the physicochemical properties, the degradation routes and methods for analysis of these substances in biological and other matrices is presented.

摘要

青霉素和头孢菌素属于处方量最大的抗生素。尽管对这些药物的了解相对广泛,但对其化合物进行定性和定量分析仍会产生许多问题。这些困难是由于常见β-内酰胺核的化学不稳定性、类似物之间化学结构的细微差异以及化合物在水溶液中复杂且相对快速的降解。本综述介绍了这些物质在生物和其他基质中的物理化学性质、降解途径及分析方法。

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