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作 者:陈凡[1] 陈剑锋[1] 郭养浩[1] 张煜荣[1] 翁娜[1] 李国平[1]
机构地区:[1]福州大学药物生物技术与工程研究所,福州350002
出 处:《天然产物研究与开发》2006年第B06期23-25,共3页Natural Product Research and Development
基 金:福州大学科技发展基金项目(2002-XY-10,XJB-0301,2003-QX-15)
摘 要:通过醋酸-H2O2氧化降解法制备三种不同特性粘数(50℃时,η=4.76mL/g,29.39mL/g和54.93mL/g)的壳聚糖。以小鼠为实验对象,采取灌胃给药方式,考察其降低血浆TCH、TG的能力,并以血浆SOD酶活及MDA含量为指标,进行抗氧化药效学评价。结果显示,给药21d后,三种壳聚糖均能显著降低小鼠血浆TCH和TG含量,降幅分别大于28.2%和22.5%;且三种壳聚糖也能显著降低小鼠血浆MDA含量,降幅大于30.0%,但对小鼠血浆SOD酶活则无显著影响。Chitosan with different intrinsic viscosity such as 11=4.76 mL/g,29.39 mL/g and 54.93 mL/g at 50℃ were obtained using acetic acid-H2O2 degradation method. Rats were treated with these chitosan using ig method, the concentration of plasma TCH,TG and MDA were determined.The results showed:after 21 days,all three kinds of chitosan could Significantly reduce the TCH and TG level of rats' plasma mere than 28.2% and 22.5%, respectivdy. All three kinds of chitosan could significantly reduce the MDA level mere than 30.0% .And the rats' plasma SOD activity were not affected by the chitosan.
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