Suppr超能文献

壳聚糖/环糊精/TPP 纳米载槲皮素作为新型细菌群体感应抑制剂。

Chitosan/Cyclodextrin/TPP Nanoparticles Loaded with Quercetin as Novel Bacterial Quorum Sensing Inhibitors.

机构信息

Institute for Biology and Biotechnology of Plants, University of Münster, Schlossgarten 3, 48149 Münster, Germany.

Department of Biology, Faculty of Biotechnology, Vietnam National University of Agriculture, Ngo Xuan Quang Street, Hanoi 100000, Vietnam.

出版信息

Molecules. 2017 Nov 15;22(11):1975. doi: 10.3390/molecules22111975.

Abstract

The widespread emergence of antibiotic-resistant bacteria has highlighted the urgent need of alternative therapeutic approaches for human and animal health. Targeting virulence factors that are controlled by bacterial quorum sensing (QS), seems a promising approach. The aims of this study were to generate novel nanoparticles (NPs) composed of chitosan (CS), sulfo-butyl-ether-β-cyclodextrin (Captisol) and/or pentasodium tripolyphosphate using ionotropic gelation technique, and to evaluate their potential capacity to arrest QS in bacteria. The resulting NPs were in the size range of 250-400 nm with CS and 330-600 nm with CS, had low polydispersity index (<0.25) and highly positive zeta potential ranging from ζ ~+31 to +40 mV. Quercetin, a hydrophobic model flavonoid, could be incorporated proportionally with increasing amounts of Captisol in the NPs formualtion, without altering significantly its physicochemical properties. Elemental analysis and FTIR studies revealed that Captisol and quercetin were effectively integrated into the NPs. These NPs were stable in M9 bacterial medium for 7 h at 37 °C. Further, NPs containing Captisol seem to prolong the release of associated drug. Bioassays against an Top 10 QS biosensor revealed that CS NPs could inhibit QS up to 61.12%, while CS NPs exhibited high antibacterial effects up to 88.32%. These results suggested that the interaction between NPs and the bacterial membrane could enhance either anti-QS or anti-bacterial activities.

摘要

抗生素耐药菌的广泛出现凸显了人类和动物健康替代治疗方法的迫切需求。针对受细菌群体感应(QS)控制的毒力因子,似乎是一种很有前途的方法。本研究的目的是使用离子凝胶技术生成由壳聚糖(CS)、磺丁基醚-β-环糊精(Captisol)和/或五钠三聚磷酸酯组成的新型纳米颗粒(NPs),并评估其在抑制细菌 QS 方面的潜在能力。所得 NPs 的大小范围为 250-400nm(CS)和 330-600nm(CS),具有低的多分散指数(<0.25)和高度正的 Zeta 电位,范围从 ζ ~+31 到+40 mV。槲皮素是一种疏水模型类黄酮,可以按比例与 Captisol 的增加量一起掺入 NPs 配方中,而不会显著改变其物理化学性质。元素分析和 FTIR 研究表明,Captisol 和槲皮素有效地整合到 NPs 中。这些 NPs 在 37°C 的 M9 细菌培养基中 7 小时内稳定。此外,含有 Captisol 的 NPs 似乎可以延长相关药物的释放时间。对前 10 个 QS 生物传感器的生物测定表明,CS NPs 可以抑制 QS 高达 61.12%,而 CS NPs 表现出高达 88.32%的高抗菌作用。这些结果表明,NPs 与细菌膜之间的相互作用可以增强抗 QS 或抗菌活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7134/6150374/f8f61ae044f8/molecules-22-01975-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验