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脂质体包裹的抗生素。

Liposome-encapsulated antibiotics.

作者信息

Salem Isam I, Flasher Diana L, Düzgüneş Nejat

机构信息

Department of Pharmacy and Pharmaceutical Technology, Faculty of Pharmacy, University of Granada, Granada, Spain.

出版信息

Methods Enzymol. 2005;391:261-91. doi: 10.1016/S0076-6879(05)91015-X.

Abstract

Encapsulation of certain antibiotics in liposomes can enhance their effect against microorganisms invading cultured cells and in animal models. We describe the incorporation of amikacin, streptomycin, ciprofloxacin, sparfloxacin, and clarithromycin in a variety of liposomes. We delineate the methods used for the evaluation of their efficacy against Mycobacterium avium-intracellulare complex (MAC) infections in macrophages and in the beige mouse model of MAC disease. We also describe the efficacy of pH-sensitive liposomes incorporating sparfloxacin or azithromycin. We summarize studies with other antibiotics, including rifampicin, rifabutin, ethambutol, isoniazid, clofazimine, and enrofloxacin, and their use against MAC, as well as other infection models, including Mycobacterium tuberculosis.

摘要

将某些抗生素包裹于脂质体中可增强其对侵袭培养细胞的微生物以及在动物模型中的作用效果。我们描述了阿米卡星、链霉素、环丙沙星、司帕沙星和克拉霉素在多种脂质体中的包封情况。我们阐述了用于评估它们对巨噬细胞中鸟分枝杆菌 - 胞内分枝杆菌复合体(MAC)感染以及在MAC疾病的米色小鼠模型中的疗效的方法。我们还描述了包载司帕沙星或阿奇霉素的pH敏感脂质体的疗效。我们总结了使用其他抗生素(包括利福平、利福布汀、乙胺丁醇、异烟肼、氯法齐明和恩诺沙星)及其对MAC的作用,以及对包括结核分枝杆菌在内的其他感染模型的研究。

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