Nanoparticles in the Era of Antimicrobial Resistance

Fridoon Jawad Ahmad
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Abstract

Antimicrobial resistance is currently a global crisis and is becoming a major issue for human health. The pharmaceutical industries' efforts to create novel therapeutic choices are being slowed down by the active bacterial resistance to traditional antibiotics. Consequently, the rise in infectious diseases caused by resistant bacteria is accompanied by two main issues. Firstly, there is a rise in antibiotic resistance. Secondly, there is a growing disparity between the discovery of new drugs and the rise in antimicrobial resistance. Different treatment strategies are now being in practice to treat bacterial infections, including targeting bacterial virulence factors, bacteriophage therapy, and alteration of the microbiome. Alternative therapeutic approaches are consequently receiving more consideration as traditional antibiotics grow less effective [1]. The use of nanoparticles is one of the most promising ways for combating microbial drug resistance. Nitric oxide-releasing nanoparticles (NO NPs), chitosan-containing nanoparticles (chitosan NPs), and metal-containing nanoparticles are a few examples of nanoparticle types that use various ways to simultaneously fight against microorganisms. Nanoparticles can be used to overcome existing drug resistance mechanisms such as decreased drug absorption and increased drug efflux from the microbial cell, biofilm formation, and intrinsic resistance. Finally, antimicrobial drugs can be directed via nanoparticles to the site of infection, enabling greater therapeutic doses to be administered there and overcoming resistance. Antibodies directed against a specific antigen on the surface of the target microorganism can be coupled with nanoparticles. For instance, S. aureus can be killed with great specificity using nanoparticles linked with protein A antibodies [2]. Nanoparticles' chemical structure enables longer binding, active targeting of antibiotics with surface functionalization at the target location, and defense against enzymes. As a result, reaching a larger antibiotic concentration in the cell eliminates the need for a higher dose, which reduces adverse effects. Antibiotic nanoparticle conjugates have been recognized by several scientists as a novel class of antibacterial drugs that can lessen the issue of multidrug resistance. Numerous nanoparticles with antimicrobial properties, such as silver, gold, zinc oxide, and titanium oxide, have been tested against microbial pathogens that are multidrug-resistant in conjunction with commercially available antibiotics or peptides [3]. Widespread of infectious diseases caused by multiple resistant bacteria is increased day by day and pose a major threat to public health. Therefore, novel antimicrobial strategies are needed to combat the antimicrobial resistance. To reduce adverse effects, nanoparticles may be a preferable option for treating bacterial infections at very low concentrations.  
抗微生物药物耐药性时代的纳米颗粒
抗微生物药物耐药性目前是一场全球危机,并正在成为人类健康的一个主要问题。由于细菌对传统抗生素产生了活跃的耐药性,制药行业创造新的治疗选择的努力正在放缓。因此,由耐药细菌引起的传染病的增加伴随着两个主要问题。首先,抗生素耐药性上升。其次,新药的发现与抗菌素耐药性上升之间的差距越来越大。目前有不同的治疗策略用于治疗细菌感染,包括靶向细菌毒力因子、噬菌体治疗和改变微生物组。随着传统抗生素的效果越来越差,替代治疗方法因此得到了更多的考虑[1]。纳米颗粒的使用是对抗微生物耐药性最有希望的方法之一。释放一氧化氮的纳米颗粒(NO NPs)、含壳聚糖的纳米颗粒(壳聚糖NPs)和含金属的纳米颗粒是纳米颗粒类型的几个例子,它们使用各种方法同时对抗微生物。纳米颗粒可用于克服现有的耐药机制,如减少药物吸收和增加药物从微生物细胞外排,生物膜的形成和内在耐药性。最后,抗菌药物可以通过纳米颗粒定向到感染部位,从而在那里施用更大的治疗剂量并克服耐药性。针对目标微生物表面特定抗原的抗体可以与纳米颗粒偶联。例如,使用与蛋白A抗体连接的纳米颗粒可以特异性地杀死金黄色葡萄球菌[2]。纳米颗粒的化学结构可以使其结合时间更长,在目标位置具有表面功能化的抗生素的活性靶向,以及对酶的防御。因此,在细胞中达到更大的抗生素浓度就不需要更高的剂量,从而减少了不良反应。抗生素纳米颗粒缀合物已被一些科学家认为是一类新的抗菌药物,可以减轻多药耐药的问题。许多具有抗菌特性的纳米颗粒,如银、金、氧化锌和氧化钛,已被用于与市售抗生素或多肽一起对抗多重耐药的微生物病原体[3]。多种耐药菌引起的传染病日益广泛传播,对公众健康构成重大威胁。因此,需要新的抗微生物策略来对抗抗生素耐药性。为了减少副作用,纳米颗粒可能是治疗低浓度细菌感染的较好选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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