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Functionalization of Tetracycline and Evaluation of Its Antibacterial Activity Including Against Resistant Bacteria

机译:四环素的功能化及其抗菌活性(包括抗药性)的评估

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摘要

Ever growing resistance of pathogenic bacteria against the existing antibiotics has forced researchers to look for new methods and techniques to design effective antimicrobial agents. In the present study a new tetracycline-based antimicrobial polymer (AMP) was synthesized from tetracycline and methacrylic acid (MAAc) using lipase as catalyst. The AMP, thus obtained, was transformed into nanoparticles via an emulsion method. The AMP and its nano-form were characterized by FTIR, NMR, XRD, SEM and EDAX. The antibacterial activity of the AMP was studied against both resistant (-) [P. aeruginosa] and susceptible (+) [S. aureus] bacteria. The synthesized AMP, including its nanoform, was observed to be more potent and efficient antimicrobial agent than the precursor tetracycline.
机译:病原细菌对现有抗生素的抗药性日益增强,迫使研究人员寻找设计有效抗菌剂的新方法和技术。在本研究中,使用脂肪酶作为催化剂,从四环素和甲基丙烯酸(MAAc)合成了一种新的基于四环素的抗菌聚合物(AMP)。如此获得的AMP通过乳液法转化为纳米颗粒。通过FTIR,NMR,XRD,SEM和EDAX对AMP及其纳米形式进行了表征。研究了AMP对两种抗药性(-)的抗菌活性[P.铜绿]和易感性(+)[S. [金黄色]细菌。观察到合成的AMP(包括其纳米形式)比前体四环素更有效,更有效。

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