Shape and Size Dependent Antimicrobial and Anti-biofilm Properties of Functionalized MoS2.

IF 4 2区 医学 Q2 CHEMISTRY, MEDICINAL
ACS Infectious Diseases Pub Date : 2025-01-10 Epub Date: 2024-12-20 DOI:10.1021/acsinfecdis.4c00860
Navjot Kaur, Mrinmoy De
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引用次数: 0

Abstract

Bacterial resistance, accelerated by the misuse of antibiotics, remains a critical concern for public health, promoting an ongoing exploration for cost-effective and safe antibacterial agents. Recently, there has been significant focus on various nanomaterials for the development of alternative antibiotics. Among these, molybdenum disulfide (MoS2) has gained attention due to its unique chemical, physical, and electronic properties, as well as its semiconducting nature, biocompatibility, and colloidal stability, positioning it as a promising candidate for biomedical research. The impact of the shape and size of MoS2 nanomaterials on the antibacterial activity remains largely unexplored. In this study, we investigated the effect of the shape and size of MoS2 nanomaterials, such as quantum dots, nanoflowers, and nanosheets, on antimicrobial and anti-biofilm activity. As we had established earlier, functionalization with positively charged thiol ligands can enhance colloidal stability, biocompatibility, and antibacterial efficacy; we functionalized all targeted nanomaterials. Our results revealed that functionalized MoS2 quantum dots (F-MQDs) exhibited superior activity compared to functionalized MoS2 nanoflowers (F-MNFs) and functionalized MoS2 nanosheets (F-MNSs) against Staphylococcus aureus (SA), both drug-resistant (methicillin) and nonresistant strains. We observed very low minimum inhibitory concentration (MIC, 30 ng/mL) for F-MQDs. The observed trend in antibacterial efficacy was as follows: F-MQDs > F-MNFs ≥ F-MNSs. We explored the relevant mechanism related to the antibacterial activity where the balance between membrane depolarization and internalization plays the determining role. Furthermore, F-MQDs show enhanced anti-biofilm activity compared to F-MNFs and F-MNSs against mature MRSA biofilms. Due to the superior antibacterial and anti-biofilm activity of F-MQDs, we extended their application to wound healing. This study will help us to develop other appropriate surface modified nanomaterials for antibacterial and anti-biofilm activity for further applications such as antibacterial coatings, water disinfection, and wound healing.

功能化二硫化钼抗微生物和抗生物膜性能的形状和尺寸依赖性。
滥用抗生素加速了细菌耐药性的产生,这仍然是公共卫生的一个重要问题,促使人们不断探索具有成本效益且安全的抗菌剂。最近,人们开始重点关注用于开发替代抗生素的各种纳米材料。其中,二硫化钼(MoS2)因其独特的化学、物理和电子特性,以及半导体性质、生物相容性和胶体稳定性而备受关注,成为生物医学研究的理想候选材料。MoS2 纳米材料的形状和尺寸对其抗菌活性的影响在很大程度上仍未得到研究。在本研究中,我们研究了量子点、纳米花和纳米片等 MoS2 纳米材料的形状和尺寸对抗菌和抗生物膜活性的影响。正如我们之前所证实的,用带正电荷的硫醇配体进行功能化可以增强胶体稳定性、生物相容性和抗菌功效;我们对所有目标纳米材料进行了功能化。我们的研究结果表明,与功能化 MoS2 纳米花(F-MNFs)和功能化 MoS2 纳米片(F-MNSs)相比,功能化 MoS2 量子点(F-MQDs)对金黄色葡萄球菌(SA)(包括耐药菌株(甲氧西林)和非耐药菌株)的活性更强。我们观察到 F-MQDs 的最低抑菌浓度(MIC,30 纳克/毫升)非常低。观察到的抗菌效果趋势如下:F-MQDs > F-MQDs > F-MQDs:F-MQDs > F-MNFs ≥ F-MNSs。我们探索了抗菌活性的相关机制,其中膜去极化和内化之间的平衡起着决定性作用。此外,与 F-MNFs 和 F-MNSs 相比,F-MQDs 对成熟的 MRSA 生物膜具有更强的抗生物膜活性。由于 F-MQDs 具有卓越的抗菌和抗生物膜活性,我们将其应用扩展到了伤口愈合领域。这项研究将有助于我们开发其他具有抗菌和抗生物膜活性的适当表面修饰纳米材料,以进一步应用于抗菌涂层、水消毒和伤口愈合等领域。
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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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