Mesoporous silica nanoparticles containing silver as novel antimycobacterial agents against Mycobacterium tuberculosis

抗细菌 介孔二氧化硅 银纳米粒子 结核分枝杆菌 纳米载体 纳米颗粒 纳米技术 材料科学 背景(考古学) 化学 介孔材料 肺结核 生物 有机化学 医学 催化作用 古生物学 病理
作者
Sandra Montalvo-Quirós,Sergio Gómez‐Graña,María Vallet‐Regí,Rafael Prados-Rosales,Blanca González,José L. Luque-García
出处
期刊:Colloids and Surfaces B: Biointerfaces [Elsevier BV]
卷期号:197: 111405-111405 被引量:44
标识
DOI:10.1016/j.colsurfb.2020.111405
摘要

Tuberculosis remains today a major public health issue with a total of 9 million new cases and 2 million deaths annually. The lack of an effective vaccine and the increasing emergence of new strains of Mycobacterium tuberculosis (Mtb) highly resistant to antibiotics, anticipate a complicated scenario in the near future. The use of nanoparticles features as an alternative to antibiotics in tackling this problem due to their potential effectiveness in resistant bacterial strains. In this context, silver nanoparticles have demonstrated high bactericidal efficacy, although their use is limited by their relatively high toxicity, which calls for the design of nanocarriers that allow silver based nanoparticles to be safely delivered to the target cells or tissues. In this work mesoporous silica nanoparticles are used as carriers of silver based nanoparticles as antimycobacterial agent against Mtb. Two different synthetic approaches have been used to afford, on the one hand, a 2D hexagonal mesoporous silica nanosystem which contains silver bromide nanoparticles distributed all through the silica network and, on the other hand, a [email protected] nanosystem with metallic silver nanoparticles as core and mesoporous silica shell in a radial mesoporous rearrangement. Both materials have demonstrated good antimycobacterial capacity in in vitro test using Mtb, being lower the minimum inhibitory concentration for the nanosystem which contains silver bromide. Therefore, the interaction of this material with the mycobacterial cell has been studied by cryo-electron microscopy, establishing a direct connection between the antimycobactericidal effect observed and the damage induced in the cell envelope.
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