强调生物功能化银纳米粒子对模型变形杆菌的抗菌机理研究

Journal of drug delivery Pub Date : 2018-05-22 eCollection Date: 2018-01-01 DOI:10.1155/2018/3850139
Asra Parveen, Manjunath S Yalagatti, Venkataraman Abbaraju, Raghunandan Deshpande
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引用次数: 0

摘要

对生物功能化银纳米粒子进行了抗菌研究,重点是其对革兰氏阳性和阴性细菌的作用机制。考虑到生物功能化银纳米粒子在绿色化学中的重要性,我们采用了生物功能化银纳米粒子,因为它易于合成、非常有用,而且合成过程经济实惠。这些纳米粒子的稳定性是通过 zeta 电位分析仪测定的。通过场发射扫描电子显微镜(FESEM)和能量色散光谱(EDAX)研究了银纳米粒子对神奇变形杆菌(Proteus mirabilis)抗菌活性的可能机制,结果显示银纳米粒子并不存在。银纳米粒子产生的自由基会破坏细胞表面,导致营养和信号供应失调,从而产生致命的抗菌活性。1,1-二苯基-2-苦基肼(DPPH)法证实了银纳米粒子清除自由基的功效。AgNP 通过破坏细胞壁上的蛋白质,增强了还原糖的膜渗漏。这些纳米粒子对人类病原体具有毒性,对金黄色葡萄球菌非常有效。银纳米粒子的作用与浓度有关,与使用的菌株类型无关。
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Emphasized Mechanistic Antimicrobial Study of Biofunctionalized Silver Nanoparticles on Model Proteus mirabilis.

Antimicrobial study of biofunctionalized silver nanoparticles has been done with the emphasis on its mechanism on both gram positive and negative bacteria. The biofunctionalized silver nanoparticles are employed considering their importance in green chemistry with respect to easy synthesis, usefulness, and economic synthetic procedure involved. The stability of these nanoparticles was determined by zeta potential analyzer. The probable mechanism of antibacterial activity was performed on Proteus mirabilis by field emission scanning electron microscopy (FESEM) and energy dispersive spectroscopy (EDAX) study which does not show the presence of silver. The free radicals generated by silver nanoparticles were responsible for lethal antibacterial activity by rupturing the cell surface which causes improper nutrient and signal supply. Free radical scavenging efficacy of silver nanoparticles was confirmed by 1,1-Diphenyl-2-picrylhydrazyl (DPPH) method. AgNP enhanced the membrane leakage of reducing sugars by destroying the proteins existing on the cell wall. These nanoparticles are found to be toxic against human pathogens and are highly effective on Staphylococcus aureus. The effect of silver nanoparticles is concentration dependent and independent of the type of strains used.

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Journal of drug delivery
Journal of drug delivery PHARMACOLOGY & PHARMACY-
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