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地龙渗漉工艺参数优选
引用本文:徐玉玲,谭清红,伍利华,王晓霞,吴南轩,梁悦,刘涛.地龙渗漉工艺参数优选[J].中国实验方剂学杂志,2014,20(21):41-43.
作者姓名:徐玉玲  谭清红  伍利华  王晓霞  吴南轩  梁悦  刘涛
作者单位:成都大学 实验技术中心, 成都 610106;四川科伦药物研究院有限公司, 成都 610000;广西中医药大学, 南宁 530001;成都大学 生物产业学院, 成都 610106;成都大学 生物产业学院, 成都 610106;成都大学 生物产业学院, 成都 610106;成都大学 生物产业学院, 成都 610106
基金项目:四川省卫生厅科研课题(130406)
摘    要:目的:优选地龙的渗漉工艺参数。方法:采用体外溶血法,以含固量和蛋白酶活性为综合评价指标,通过单因素试验优选地龙的渗漉工艺。结果:尿激酶在25~125 U·mL-1与溶圈面积呈良好线性关系,最佳渗漉工艺参数为地龙粉碎为粗粉,浸泡时间0.5 h,渗漉速度2 mL·min-1,加8倍量60%乙醇渗漉;渗漉液体积220 mL,含固量3.252 g,蛋白酶活性5 624.7 U·g-1。结论:纤维蛋白原平板法可快速、简便、准确地测定地龙中酶的活性,优选的工艺参数稳定可行,为地龙有效成分的充分利用提供新选择。

关 键 词:地龙  酶活性  渗漉工艺  纤维蛋白原平板法
收稿时间:2014/3/25 0:00:00

Optimization of Percolation Process Parameters of Pheretima
XU Yu-ling,TAN Qing-hong,WU Li-hu,WANG Xiao-xi,WU Nan-xuan,LIANG Yue and LIU Tao.Optimization of Percolation Process Parameters of Pheretima[J].China Journal of Experimental Traditional Medical Formulae,2014,20(21):41-43.
Authors:XU Yu-ling  TAN Qing-hong  WU Li-hu  WANG Xiao-xi  WU Nan-xuan  LIANG Yue and LIU Tao
Institution:Experiment Technology Center of Chengdu University, Chengdu 610106, China;Sichuan Kelun Pharmaceutical Research Institute Co. Ltd, Chengdu 610000, China;Guangxi University of Chinese Medicine, Nanning 530001, China;Faculty of Biotechnology Industry, Chengdu University, Chengdu 610106, China;Faculty of Biotechnology Industry, Chengdu University, Chengdu 610106, China;Faculty of Biotechnology Industry, Chengdu University, Chengdu 610106, China;Faculty of Biotechnology Industry, Chengdu University, Chengdu 610106, China
Abstract:Objective: To optimize percolation parameters of Pheretima. Method: By using external hemolysis method,with solid content and protease activity as indicators,single factor tests were adopted to optimize percolation process. Result: The concentration of urokinase in 25-125 U·mL-1 showed a good linear relationship with soluble circle area,the best percolation processing parameters were:crushed Pheretima to a coarse powder,soaked 0.5 h with percolation rate of 2 mL·min-1,added 8 times the amount of 60% ethanol for percolation;percolate volume,solid content and protease activity were 220 mL,3.252 g,5 624.7 U·g-1. Conclusion: Fibrinogen plate method can be fast,easy and accurate to determine enzyme activity in Pheretima,these optimized process parameters was stable and feasible,it provides new choice for full utilization of active ingredients from Pheretima.
Keywords:Pheretima  enzyme activity  percolation process  fibrinogen plate method
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