美罗培南
铜绿假单胞菌
微生物学
脂质体
抗菌剂
生物膜
抗生素
最小抑制浓度
化学
药理学
生物
细菌
抗生素耐药性
生物化学
遗传学
作者
Momeni-Javid Zahra,Hamed Hamishekar,Mohammad Rahmati,Zarghami Nosratollah,Abolfazl Akbarzadeh,Milani Morteza
标识
DOI:10.1080/21691401.2016.1198362
摘要
Background: The aim of this study was to evaluate the antimicrobial efficacy of liposomal meropenem formulation against clinical and laboratory isolates of Pseudomonas aeruginosa. P. aeruginosa isolates were used to determine the MIC and MBC of free and liposomal meropenem. As well as the effect of free and liposomes meropenem compare the minimum biofilm eradication concentration and inhibition of P. aeruginosa motility was assessed.Results: In this study, the MICs and MBC of liposomal meropenem was more effective against all clinical and laboratory strains were significantly lower than those of free meropenem (6.25 μg/ml vs 100 μg/ml). Furthermore, liposomal meropenem (≥1.5 μg/ml) completely eradicated biofilm in all P. aeruginosa isolates. While the free form of drug could eradicate biofilm formation in most of isolates in ≥6.25 μg/ml concentration. In addition, lower concentrations of liposomal meropenem could inhibit the bacterial motility.Conclusion: The results clearly indicate that the liposomal formulation of drug is more effective than meropenem alone against antibiotic resistant P. aeruginosa isolates.
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