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一种治疗支气管扩张症的潜在群体感应抑制剂:槲皮素-壳聚糖纳米粒子复合物对 native quercetin 表现出优越的生物膜形成抑制作用和泳动性抑制作用。

A Potential Quorum-Sensing Inhibitor for Bronchiectasis Therapy: Quercetin-Chitosan Nanoparticle Complex Exhibiting Superior Inhibition of Biofilm Formation and Swimming Motility of to the Native Quercetin.

机构信息

School of Chemical and Biomedical Engineering, Nanyang Technological University, 62 Nanyang Drive, Singapore 637459, Singapore.

出版信息

Int J Mol Sci. 2021 Feb 3;22(4):1541. doi: 10.3390/ijms22041541.

DOI:10.3390/ijms22041541
PMID:33546487
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7913711/
Abstract

Quercetin (QUE)-a plant-derived flavonoid, is recently established as an effective quorum sensing (QS) inhibiting agent in -the main bacterial pathogen in bronchiectasis lungs. Successful clinical application of QUE, however, is hindered by its low solubility in physiological fluids. Herein we developed a solubility enhancement strategy of QUE in the form of a stable amorphous nanoparticle complex (nanoplex) of QUE and chitosan (CHI), which was prepared by electrostatically driven complexation between ionized QUE molecules and oppositely charged CHI. At its optimal preparation condition, the QUE-CHI nanoplex exhibited a size of roughly 150 nm with a 25% QUE payload and 60% complexation efficiency. The complexation with CHI had no adverse effect on the antibacterial and anticancer activities of QUE, signifying the preservation of QUE's bioactivities in the nanoplex. Compared to the native QUE, the QUE-CHI nanoplex exhibited superior QS inhibition in suppressing the QS-regulated swimming motility and biofilm formation of , but not in suppressing the virulence factor production. The superior inhibitions of the biofilm formation and swimming motility afforded by the nanoplex were attributed to (1) its higher kinetic solubility (5-times higher) that led to higher QUE exposures, and (2) the synergistic QS inhibition attributed to its CHI fraction.

摘要

槲皮素(QUE)是一种植物来源的类黄酮,最近被确定为支气管扩张肺部主要细菌病原体中有效的群体感应(QS)抑制物。然而,QUE 的成功临床应用受到其在生理液中低溶解度的阻碍。在此,我们开发了一种 QUE 的增溶策略,将 QUE 和壳聚糖(CHI)形成稳定的无定形纳米颗粒复合物(纳米复合物),通过带电荷的 QUE 分子与带相反电荷的 CHI 之间的静电相互作用而制备。在其最佳制备条件下,QUE-CHI 纳米复合物的粒径约为 150nm,QUE 载药量为 25%,复合物效率为 60%。与 CHI 复合对 QUE 的抗菌和抗癌活性没有不利影响,表明 QUE 的生物活性在纳米复合物中得到了保留。与天然 QUE 相比,QUE-CHI 纳米复合物在抑制 QS 调节的泳动和生物膜形成方面表现出优越的 QS 抑制作用,但在抑制毒力因子产生方面没有表现出优越的抑制作用。纳米复合物对生物膜形成和泳动的优越抑制作用归因于(1)其更高的动力学溶解度(高 5 倍)导致 QUE 暴露更高,以及(2)其 CHI 部分的协同 QS 抑制作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8f/7913711/79168ae4c676/ijms-22-01541-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8f/7913711/e44bf7cfef82/ijms-22-01541-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8f/7913711/79168ae4c676/ijms-22-01541-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8f/7913711/e44bf7cfef82/ijms-22-01541-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c8f/7913711/79168ae4c676/ijms-22-01541-g009.jpg

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