Liposome-encapsulated antibiotics

被引:44
作者
Salem, II [1 ]
Flasher, DL
Düzgünes, N
机构
[1] Univ Granada, Fac Pharm, Dept Pharm & Pharmaceut Technol, E-18071 Granada, Spain
[2] Univ Pacific, Dept Microbiol, Arthur A Dugoni Sch Dent, San Francisco, CA 94115 USA
来源
LIPOSOMES, PT E | 2005年 / 391卷
关键词
D O I
10.1016/S0076-6879(05)91015-X
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:261 / 291
页数:31
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