土拉弗朗西斯菌
环丙沙星
鼠疫耶尔森菌
医学
抗生素
微生物学
生物
生物化学
毒力
基因
作者
David Cipolla,Jim Blanchard,Igor Gonda
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2016-03-01
卷期号:8 (1): 6-6
被引量:160
标识
DOI:10.3390/pharmaceutics8010006
摘要
Except for management of Pseudomonas aeruginosa (PA) in cystic fibrosis, there are no approved inhaled antibiotic treatments for any other diseases or for infections from other pathogenic microorganisms such as tuberculosis, non-tuberculous mycobacteria, fungal infections or potential inhaled biowarfare agents including Francisella tularensis, Yersinia pestis and Coxiella burnetii (which cause pneumonic tularemia, plague and Q fever, respectively). Delivery of an antibiotic formulation via the inhalation route has the potential to provide high concentrations at the site of infection with reduced systemic exposure to limit side effects. A liposomal formulation may improve tolerability, increase compliance by reducing the dosing frequency, and enhance penetration of biofilms and treatment of intracellular infections. Two liposomal ciprofloxacin formulations (Lipoquin® and Pulmaquin®) that are in development by Aradigm Corporation are described here.
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