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Preparation and antibacterial activity of Schiff bases from O-carboxymethyl chitosan and para-substituted benzaldefaydes

机译:O-羧甲基壳聚糖和对位取代的苯甲醛的席夫碱的制备及其抗菌活性

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摘要

Seven Schiff bases were synthesized from O-carboxymethyl chitosan (CMC) and para-substituted benzaldehydes. The Schiff bases were characterized through Fourier Transform Infrared Spectroscopy, Carbon-13 Nuclear Magnetic Resonance (~(13)C NMR), Distortionless Enhancement of Polarization Transfer (DEPT) 135 NMR, elemental analysis, and acid-base titration. Antibacterial activities of the Schiff bases against Escherichia coli (E. coli, ATCC 35218) and Staphylococcus aureus (S. aureus, ATCC 25923) were measured through the optical density method. Antibacterial activity of the Schiff bases differs from the substituent at the para position of benzaldehyde, and decreases as the sequence OCH3 > CH3 > H > F > CI > Br > N02. The IC_(50) of the Schiff base from 4-mefhoxylbenzylaldehyde against E. coli and S. aureus is 30 and 34 ppm, respectively, much lower than that of chitosan (53,48 ppm) and CMC (58, 60 ppm).
机译:由O-羧甲基壳聚糖(CMC)和对位取代的苯甲醛合成了七个席夫碱。 Schiff碱通过傅里叶变换红外光谱,碳13核磁共振(〜(13)C NMR),极化转移的无畸变增强(DEPT)135 NMR,元素分析和酸碱滴定进行了表征。通过光密度法测量席夫碱对大肠杆菌(E.coli,ATCC 35218)和金黄色葡萄球菌(S. aureus,ATCC 25923)的抗菌活性。 Schiff碱的抗菌活性不同于苯甲醛对位上的取代基,并随着OCH3> CH3> H> F> CI> Br> N02的顺序而降低。 4-甲氧基苄基醛对大肠杆菌和金黄色葡萄球菌的席夫碱的IC_(50)分别为30和34 ppm,远低于壳聚糖(53,48 ppm)和CMC(58,60 ppm)。

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