Drug delivery systems for fluoroquinolones: New prospects in tuberculosis treatment

被引:19
|
作者
Le-Deygen, I. M. [1 ]
Skuredina, A. A. [1 ]
Kudryashova, E. V. [1 ]
机构
[1] Moscow MV Lomonosov State Univ, Dept Chem, Moscow 119991, Russia
基金
俄罗斯科学基金会;
关键词
drug delivery systems; fluoroquinolones; tuberculosis; CYCLODEXTRIN-CONTAINING POLYMERS; SOLID INCLUSION COMPLEX; BETA-CYCLODEXTRIN; CAPILLARY-ELECTROPHORESIS; CHITOSAN NANOPARTICLES; CIPROFLOXACIN; OFLOXACIN; FORMULATION; LIPOSOMES; MOXIFLOXACIN;
D O I
10.1134/S1068162017050077
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The review focuses on new delivery systems of fluoroquinolones, the highly active antibiotics, the therapeutic application of which is still limited due to low bioavailability and low solubility in biological media. The development of suitable delivery systems seems to be a promising solution to these problems. Here, we consider the delivery systems based on synthetic polymers (polylactic and polyglycolic acids and their copolymers, polycaprolactones, etc.) and natural polymers, in particular, polysaccharides. Oligosaccharide delivery systems, conjugates of fluoroquinolones with natural polymers, as well as lipid delivery systems, including liposomes, solid lipid particles, and hybrid particles, are also discussed. The characteristic features of oral, intravenous, and aerosol delivery methods for fluoroquinolones are revealed, which is especially important in the development of new drugs for the treatment of tuberculosis.
引用
收藏
页码:487 / 501
页数:15
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