Department of Microbiology, Savitribai Phule Pune University, Pune 411007, India.
Combichem-Bioresource Center, Organic Chemistry Division, National Chemical Laboratory, Pune, India.
Int J Antimicrob Agents. 2015 Aug;46(2):183-8. doi: 10.1016/j.ijantimicag.2015.03.014. Epub 2015 May 7.
Resistance among mycobacteria leading to multidrug-resistant and extensively drug-resistant tuberculosis is a major threat. However, nanotechnology has provided new insights in drug delivery and medicine development. This is the first comparative report to determine the activity of chemically and biologically synthesised silver nanoparticles (AgNPs) and gold nanoparticles (AuNPs) against mycobacteria. Screening data revealed the high mycobactericidal efficiency of AgNPs, with minimum inhibitory concentrations (MICs) of <3μg/mL, whereas no such activity was exhibited by AuNPs at concentrations up to 100μg/mL. Moreover, in vitro and ex vivo THP-1 infection model assays showed greater efficacy of chemical AgNPs compared with biogenic AgNPs to inhibit active and dormant stage mycobacterial growth. Up to 40% cytotoxicity against human cell lines was observed at a AgNP concentration of 10× MIC (30μg/mL) after 48h. AgNPs were shown to have more specificity towards mycobacteria than towards other Gram-negative and Gram-positive pathogenic bacteria. The selectivity index was found to be in the range of 11-23, indicating the potential of these nanoparticles for use in developing new therapeutics for tuberculosis.
分枝杆菌的耐药性导致了耐多药和广泛耐药性结核病,这是一个主要威胁。然而,纳米技术为药物输送和医学发展提供了新的见解。这是第一份比较报告,旨在确定化学和生物合成的银纳米粒子(AgNPs)和金纳米粒子(AuNPs)对分枝杆菌的活性。筛选数据显示 AgNPs 具有很高的杀菌效率,最低抑菌浓度(MICs)<3μg/mL,而 AuNPs 在高达 100μg/mL 的浓度下没有表现出这种活性。此外,体外和体外 THP-1 感染模型检测表明,与生物合成的 AgNPs 相比,化学合成的 AgNPs 更能有效抑制活性和休眠阶段的分枝杆菌生长。在 48 小时后,AgNP 浓度达到 10×MIC(30μg/mL)时,对人类细胞系的细胞毒性高达 40%。AgNPs 对分枝杆菌的特异性比对其他革兰氏阴性和革兰氏阳性致病菌的特异性更高。选择性指数在 11-23 范围内,表明这些纳米粒子有潜力用于开发治疗结核病的新疗法。