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新型群体感应抑制剂纳米颗粒经膀胱靶向给药治疗生物膜相关鼠肾盂肾炎的疗效。

Efficacy of intravesical targeting of novel quorum sensing inhibitor nanoparticles against biofilm-associated murine pyelonephritis.

机构信息

a Department of Microbiology, Panjab University , Chandigarh , India.

出版信息

J Drug Target. 2019 Nov;27(9):995-1003. doi: 10.1080/1061186X.2019.1574802. Epub 2019 Feb 11.

Abstract

biofilm-associated pyelonephritis is a severe infection that can lead to mortality. There are no strategies that can effectively manage this infection since the pathogenesis is controlled by quorum sensing (QS) regulated virulence and recalcitrant biofilms. QS inhibitors (QSIs) are emerging therapeutics against such infections but are associated with cytotoxicity or low bioactivity. Hence, we developed novel quorum sensing inhibitor loaded nanoparticles (QSINPs) using the biopolymers, chitosan (CS) and dextran sulphate (DS) and were intravesically targeted against biofilm-associated murine pyelonephritis. The targeting of QSINPs was confirmed by tracking the fluorescein isothiocyanate (FITC) tagged QSINPs in bladder and kidney of mice. On characterising, the QSINPs showed a size of 685.7 nm with a zeta potential of 37.9 and polydispersity index (PDI) of 0.5. Scanning electron microscopy (SEM) indicated spherical shape and bioactivity assays indicated QSI activity till 8 months. Fourier transform infra-red (FTIR) analysis indicated possibility of isothiocyanate bonding in CS with DS and with QSI. The QSINPs showed excellent antivirulence activity by reducing the virulence factors and biofilm of and therapeutic efficacy with ciprofloxacin (CIP). Hence, we propose a novel next-generation therapeutic and its appropriate targeting route against biofilm-associated pyelonephritis.

摘要

生物膜相关肾盂肾炎是一种严重的感染,可导致死亡。由于发病机制受群体感应(QS)调节的毒力和顽固的生物膜控制,因此没有有效的策略可以对此类感染进行管理。QS 抑制剂(QSIs)是针对此类感染的新兴治疗方法,但与细胞毒性或低生物活性有关。因此,我们使用生物聚合物壳聚糖(CS)和硫酸葡聚糖(DS)开发了新型群体感应抑制剂负载纳米颗粒(QSINPs),并针对生物膜相关的小鼠肾盂肾炎进行了膀胱内靶向治疗。通过跟踪荧光素异硫氰酸酯(FITC)标记的 QSINPs 在小鼠膀胱和肾脏中的定位来确认 QSINPs 的靶向性。在表征时,QSINPs 的粒径为 685.7nm,zeta 电位为 37.9,多分散指数(PDI)为 0.5。扫描电子显微镜(SEM)表明其为球形,生物活性测定表明 QSI 活性可持续 8 个月。傅里叶变换红外(FTIR)分析表明 CS 与 DS 以及与 QSI 可能存在异硫氰酸酯键合。QSINPs 通过降低毒力因子和生物膜表现出优异的抗病毒活性,与环丙沙星(CIP)联合具有治疗功效。因此,我们提出了一种针对生物膜相关肾盂肾炎的新型下一代治疗方法及其适当的靶向途径。

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