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具有抗氧化和抗糖尿病潜力的儿茶素接枝壳聚糖的制备与表征

Preparation and characterization of catechin-grafted chitosan with antioxidant and antidiabetic potential.

作者信息

Zhu Weili, Zhang Zhanjun

机构信息

Department of Blood Transfusion, Subei People's Hospital of Jiangsu Province, Yangzhou 225001, Jiangsu, China.

College of Biological and Chemical Engineering, Yangzhou Vocational University, Yangzhou 225009, Jiangsu, China.

出版信息

Int J Biol Macromol. 2014 Sep;70:150-5. doi: 10.1016/j.ijbiomac.2014.06.047. Epub 2014 Jul 1.

Abstract

In the present study, the preparation, characterization, antioxidant and antidiabetic activities of catechin-grafted chitosan (catechin-g-chitosan) were investigated. The graft of catechin onto chitosan was achieved by redox system and confirmed using various instrumental methods. Proton nuclear magnetic resonance spectroscopy indicates that catechin has been successfully grafted onto chitosan. The morphology observation shows that chitosan changes to a softened nature with porous surface after grafting. Catechin-g-chitosan also exhibits reduced thermal stability and enhanced crystallinity compared to chitosan. Moreover, catechin-g-chitosan shows 0.51 of reducing power, 46.81% of hydroxyl radical-scavenging activity and 67.08% of DPPH radical-scavenging activity at 1mg/ml, which are much higher than that of chitosan. The antidiabetic activity in vitro assays shows that the α-glucosidase inhibitory effect decreases in the order of catechin-g-chitosan>catechin>acarbose>chitosan, and the α-amylase inhibitory effect decreases in the order of acarbose>catechin-g-chitosan>catechin>chitosan. The improved antioxidant and antidiabetic activities of catechin-g-chitosan are attributed to the phenolic groups in the catechin residues.

摘要

在本研究中,对儿茶素接枝壳聚糖(儿茶素 - g - 壳聚糖)的制备、表征、抗氧化和抗糖尿病活性进行了研究。儿茶素接枝到壳聚糖上是通过氧化还原体系实现的,并使用各种仪器方法进行了确认。质子核磁共振光谱表明儿茶素已成功接枝到壳聚糖上。形态观察表明,接枝后壳聚糖变为具有多孔表面的软化性质。与壳聚糖相比,儿茶素 - g - 壳聚糖的热稳定性降低,结晶度提高。此外,儿茶素 - g - 壳聚糖在1mg/ml时的还原力为0.51,羟自由基清除活性为46.81%,DPPH自由基清除活性为67.08%,均远高于壳聚糖。体外抗糖尿病活性测定表明,α - 葡萄糖苷酶抑制作用顺序为儿茶素 - g - 壳聚糖>儿茶素>阿卡波糖>壳聚糖,α - 淀粉酶抑制作用顺序为阿卡波糖>儿茶素 - g - 壳聚糖>儿茶素>壳聚糖。儿茶素 - g - 壳聚糖抗氧化和抗糖尿病活性的提高归因于儿茶素残基中的酚羟基。

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