Evaluation and study of antimicrobial activity of nanoliposomal meropenem against Pseudomonas aeruginosa isolates

被引:16
|
作者
Zahra, Momeni-Javid [1 ]
Hamed, Hamishekar [2 ]
Mohammad, Rahmati-Yamchi [1 ,2 ]
Nosratollah, Zarghami [1 ]
Akbarzadeh, Abolfazl [2 ]
Morteza, Milani [2 ,3 ]
机构
[1] Tabriz Univ Med Sci, Fac Adv Med Sci, Dept Med Biotechnol, Tabriz, Iran
[2] Tabriz Univ Med Sci, Drug Appl Res Ctr, Tabriz, Iran
[3] Tabriz Univ Med Sci, Liver & Gastrointestinal Dis Res Ctr, Tabriz, Iran
关键词
Antibiotic resistance; liposomal meropenem; P; aeruginosa; DRUG-DELIVERY; BIOFILM FORMATION; GENTAMICIN; LIPOSOMES; ANTIBIOTICS; CIPROFLOXACIN; RESISTANCE; STRAINS;
D O I
10.1080/21691401.2016.1198362
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
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 mu g/ml vs 100 mu g/ml). Furthermore, liposomal meropenem (>= 1.5 g/ml) completely eradicated biofilm in all P. aeruginosa isolates. While the free form of drug could eradicate biofilm formation in most of isolates in >= 6.25g/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.
引用
收藏
页码:975 / 980
页数:6
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