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合成并评价载哌拉西林/他唑巴坦聚合物胶束以增强抗菌活性。

Synthesis and evaluation of polymeric micelle containing piperacillin/tazobactam for enhanced antibacterial activity.

机构信息

Infectious and Tropical Diseases Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.

Department of Medical Nanotechnology, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran.

出版信息

Drug Deliv. 2019 Dec;26(1):1292-1299. doi: 10.1080/10717544.2019.1693708.

Abstract

Infections caused by multidrug-resistant bacteria such as are important therapeutic complications. Piperacillin/Tazobactam is considered a safe antimicrobial agent. But we should not ignore the prevalence of resistant strains to this drug. In this work, a new polymeric micelle composed of Piperacillin/Tazobactam-loaded Poly (ethylene glycol) methyl ether-block-poly (lactide-co-glycolide) (PLGA-PEG) was developed to improve the antimicrobial performance of P/T. The SEM and TEM studies of PLGA-PEG micelle showed, semi-spherical morphology with a mean diameter of below 30 nm. Zeta potential results indicated that the surface charge of PLGA-PEG micelle was -2.98 mV, while after encapsulation of P/T, the surface charge decreases to -4.13 mV. Clinical strains of were isolated and their resistance pattern against different antibiotics was evaluated. The MIC of free and P/T -Loaded PLGA-PEG micelles was determined. Also, the effect of free or P/T micelle against minimal biofilm eradication concentration and motility inhibition was evaluated. The bacterial isolates were resistant to most common antibiotics. The MIC of the free drug form and micelle form ranged from 4 to 512 µg/ml and 2 to 256 µg/ml, respectively. Generally, micelle showed more effective antibiofilm activities, inhibition of bacterial motility and reducing the MIC than that free drug form.

摘要

由耐多药细菌引起的感染,如 ,是重要的治疗并发症。哌拉西林/他唑巴坦被认为是一种安全的抗菌药物。但我们不应忽视对这种药物产生耐药菌株的流行。在这项工作中,开发了一种新的聚合物胶束,由哌拉西林/他唑巴坦负载的聚乙二醇甲基醚嵌段聚(乳酸-共- )(PLGA-PEG)组成,以提高 P/T 的抗菌性能。PLGA-PEG 胶束的 SEM 和 TEM 研究表明,其具有平均直径低于 30nm 的半球形形态。Zeta 电位结果表明,PLGA-PEG 胶束的表面电荷为-2.98mV,而在封装 P/T 后,表面电荷降低至-4.13mV。分离了临床分离株,并评估了它们对不同抗生素的耐药模式。测定了游离和 P/T 负载的 PLGA-PEG 胶束的 MIC。还评估了游离或 P/T 胶束对最小生物膜清除浓度和运动抑制的作用。细菌分离株对大多数常用抗生素具有耐药性。游离药物形式和胶束形式的 MIC 范围分别为 4 至 512μg/ml 和 2 至 256μg/ml。通常,胶束显示出比游离药物形式更有效的抗生物膜活性、抑制细菌运动和降低 MIC 的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4c62/6896493/b86d5171f4f7/IDRD_A_1693708_F0001_C.jpg

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