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使用载有β-内酰胺类抗生素和β-内酰胺酶抑制剂的壳聚糖纳米粒的新型联合治疗耐药菌的方法。

A novel combination therapy for multidrug resistant pathogens using chitosan nanoparticles loaded with β-lactam antibiotics and β-lactamase inhibitors.

机构信息

Emerging Pathogens Institute, University of Florida, Gainesville, FL 32611, USA; Department of Animal Sciences, University of Florida, Gainesville, FL 32611, USA.

Department of Agricultural and Biological Engineering, University of Florida, Gainesville, FL 32611, USA.

出版信息

Int J Biol Macromol. 2022 Jan 15;195:506-514. doi: 10.1016/j.ijbiomac.2021.12.035. Epub 2021 Dec 14.

Abstract

Antimicrobial resistance is one of the greatest global threats. Particularly, multidrug resistant extended-spectrum β-lactamase (ESBL)-producing pathogens confer resistance to many commonly used medically important antibiotics, especially beta-lactam antibiotics. Here, we developed an innovative combination approach to therapy for multidrug resistant pathogens by encapsulating cephalosporin antibiotics and β-lactamase inhibitors with chitosan nanoparticles (CNAIs). The four combinations of CNAIs including two cephalosporin antibiotics (cefotaxime and ceftiofur) with two β-lactamase inhibitors (tazobactam and clavulanate) were engineered as water-oil-water emulsions. Four combinations of CNAIs showed efficient antimicrobial activity against multidrug resistant ESBL-producing Enterobacteriaceae. The CNAIs showed enhanced antimicrobial activity compared to naïve chitosan nanoparticles and to the combination of cephalosporin antibiotics and β-lactamase inhibitors. Furthermore, CNAIs attached on the bacterial surface changed the permeability to the outer membrane, resulting in cell damage that leads to cell death. Taken together, CNAIs have provided promising potential for treatment of diseases caused by critically important ESBL-producing multidrug resistant pathogens.

摘要

抗菌药物耐药性是全球面临的最大威胁之一。特别是,产多药耐药性扩展谱β-内酰胺酶(ESBL)的病原体对许多常用的重要医学抗生素具有耐药性,尤其是β-内酰胺类抗生素。在这里,我们通过用壳聚糖纳米粒子(CNAIs)包封头孢菌素类抗生素和β-内酰胺酶抑制剂,开发了一种针对多药耐药病原体的治疗创新组合方法。四种包含两种头孢菌素类抗生素(头孢噻肟和头孢曲松)和两种β-内酰胺酶抑制剂(他唑巴坦和克拉维酸)的 CNAIs 组合被设计成水包油包水乳液。四种 CNAIs 组合对产多药耐药性 ESBL 的肠杆菌科具有有效的抗菌活性。与原始壳聚糖纳米粒子和头孢菌素类抗生素与β-内酰胺酶抑制剂的组合相比,CNAIs 显示出增强的抗菌活性。此外,附着在细菌表面的 CNAIs 改变了对外膜的通透性,导致细胞损伤,从而导致细胞死亡。总之,CNAIs 为治疗由具有重要临床意义的产 ESBL 多药耐药病原体引起的疾病提供了有希望的潜力。

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