光毒性抗生素及其脂质体包封:综述

M. Budai, L. Budai, C. Wijesooriya, R. Roy, I. Petrikovics
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引用次数: 0

摘要

抗生素的脂质体包封在生物利用度和治疗效果方面具有优势。由于抗生素中许多具有光毒性,并且在制备(例如灭菌),储存或局部应用时可能存在紫外线照射,因此应考虑脂质体抗生素的光降解。因此,检查在紫外光存在下脂质-光毒性药物的相互作用是非常重要的。在某些情况下,脂质体包封可以改变光降解的方式和速率,导致或多或少(光)毒性化合物的形成。通过选定的光毒性抗生素(钠啶酸和洛美沙星)的例子,我们强调了脂质体组成在改变药物分子光降解过程中的作用,从而导致其光降解方式或速率的可能变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phototoxic Antibiotics and Aspects of their Liposomal Encapsulation: A Mini-Review
The liposomal encapsulation of antibiotics offers advantages from the aspect of bioavailabilty and therapeutical efficacy. As among antibiotics many possess phototoxic properties, and during preparation (e.g. sterilization), storage or in case of topical application ultraviolet light exposure can be present, photodegradation of liposomal antibiotics should be taken into consideration. Thus, the examination of lipid-phototoxic drug interactions in the presence of ultraviolet light is of great importance. In some cases liposomal encapsulation can alter the ways and rates of photodegradation, leading to the formation of more or less (photo)toxic compounds. Through the examples of selected phototoxic antibiotics (nalidixic acid and lomefloxacin) we highlight the role of liposomal composition in altering the photodegradation process of drug molecules,- leading to possible changes either in the ways or in the rates of their photodegradation.
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