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Synthesis and Bio-evaluation of 2-Imino-4-amino thiazole Capped Silver Nanoparticles

机译:2-氨基-4-氨基噻唑包覆的银纳米粒子的合成及生物评价

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摘要

Silver nanoparticles capped with N-(4-amino-3,5-diphenyl-3H-thiazol-2-ylidine)benzamide is synthesized by simple chemical reduction method, prepared by treatment of aqueous silver ions with hot ethanolic solution of N-(4-amino-3,5-diphenyl-3H-thiazol-2-ylidine)benzamide. The size and shape of obtained silver nanoparticles are spherical and uniform with average size of 34 nm and are characterized by using UV-visible, FTIR, XRD, SEM and TEM studies. The capped silver nanoparticle showed significant inhibitory activity against various human pathogenic bacteria with different doses of 25, 50, 75 and 100 ug. The synthesized silver nanoparticle capped compound was potent inhibitory agent when compared with standard antibiotic ciprofloxacin.
机译:采用简单的化学还原法合成了N-(4-氨基-3,5-二苯基-3H-噻唑-2-基吡啶)苯甲酰胺封端的银纳米颗粒,其通过用N-(4)的热乙醇溶液处理水银离子而制备。 -氨基-3,5-二苯基-3H-噻唑-2-基吡啶)苯甲酰胺。所获得的银纳米颗粒的尺寸和形状为球形且均匀,平均尺寸为34 nm,并通过使用UV-可见,FTIR,XRD,SEM和TEM研究进行表征。封端的银纳米粒子对各种剂量为25、50、75和100 ug的人类致病细菌显示出显着的抑制活性。与标准抗生素环丙沙星相比,合成的银纳米颗粒封端化合物是有效的抑制剂。

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