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作 者:张新国[1] 王强林[1] 李春雷[1] 张应鹏[1] 李坤[1] 胡淑娟[1] 任菁[1] 周莉[1] 智康康[1] 代兴超[1]
机构地区:[1]兰州理工大学生命科学与工程学院,甘肃兰州730050
出 处:《中医药学报》2012年第3期96-100,共5页Acta Chinese Medicine and Pharmacology
基 金:甘肃省科技支撑计划-社会发展类(1011FKCA147);大学生创新性实验计划项目支持(091073117)
摘 要:目的:研究当归多糖的酶法提取新工艺,并就提取多糖的抗肿瘤活性进行评价。方法:采用生物酶辅助提取技术进行当归多糖提取工艺研究,选用单因素实验探索酶用量、酶解温度、酶解时间及pH值对当归多糖提取率的影响,在单因素实验的基础上,采用正交试验对工艺条件进行优化,并采用MTT法评价当归多糖对hela细胞的抗肿瘤活性。结果:各因素对提取效果影响由大到小依次为:酶浓度>酶解时间>pH值>酶解温度,最佳提取工艺条件为,纤维素酶浓度:0.4mg/mL、提取温度:60℃、提取时间:4h,pH=5.0,当归多糖得率为150.34mg/g,MTT结果证实提取多糖具有一定的抗肿瘤活性。结论:该工艺操作简单,成本较低,本研究为当归多糖的深度开发提供了科学依据。Objective: Enzymatic extraction technology of polysaecharide from Angelica and its antitumor activity were studied. Method: The effects of enzyme dosage, enzymolysis temperature, enzymolysis time, enzymolysis pH value on the extraction rate of polysaeeharide were studied by single - factor test. Then, the orthogonal experiment was performed to screen the optimum extraction technology. Antitumor activity of Angelica polysaecharide was evaluated by MTr meth- od in hela cells. Result: The factors influencing the extraction process were in the order:enzyme dosage 〉 enzymolysis time 〉 enzymolysis pH value 〉 enzymolysis temperature, and the optimum extracting technology was as follows : enzyme dosage 0.4mg/ml, enzymolysis temperature 60℃, enzymolysis time 4h and enzymolysis pH value 5. The polysaccharide extraction rate was 150.34mg/g under these conditions. The results of MTr method confirmed that Angelica polysaccha- ride had some antitumor activity. Conclusion: The enzymatic extraction technology is simple with low cost and provides a scientific basis for the further development of Angelica polysaccharide.
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