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美洲大蠊抗肝纤维化活性提取物ML-D中粘多糖的含量测定
引用本文:李夸巧,李春艳,杨永寿,陈丽娜,肖培云.美洲大蠊抗肝纤维化活性提取物ML-D中粘多糖的含量测定[J].大理师专学报,2013(3):9-12.
作者姓名:李夸巧  李春艳  杨永寿  陈丽娜  肖培云
作者单位:大理学院药学与化学学院,云南大理671000
基金项目:国家自然科学基金资助项目(81060329); 云南省教育厅重点基金资助项目(2011Z053)
摘    要:目的:建立美洲大蠊抗肝纤维化活性提取物ML-D中粘多糖的含量测定方法。方法:采用苯酚-硫酸法测定粘多糖的含量,采用正交试验设计考察ML-D中粘多糖的水解工艺和显色条件,采用单因素试验考察加热显色时间、苯酚和硫酸的用量。结果:ML-D中粘多糖的最佳水解工艺为:盐酸浓度6 mol/L,固液比为1∶1,水解时间1 h;最佳显色条件:苯酚2 mL,硫酸20 mL,加热显色时间10 min。结论:该法操作简便,精密度高,重复性好,可作为美洲大蠊抗肝纤维化活性提取物ML-D中粘多糖含量的测定方法。

关 键 词:美洲大蠊  抗肝纤维化  粘多糖  硫酸-苯酚法  含量测定

Determination of Glycosaminoglycan in Active Extracts ML-D with Anti-hepatic-fibrosis from Periplaneta americana
LI Kuaqiao,LI Chunyan,YANG Yongshou,CHEN Lina,XIAO Peiyun.Determination of Glycosaminoglycan in Active Extracts ML-D with Anti-hepatic-fibrosis from Periplaneta americana[J].Journal of Dali Teachers College,2013(3):9-12.
Authors:LI Kuaqiao  LI Chunyan  YANG Yongshou  CHEN Lina  XIAO Peiyun
Institution:* (College of Pharmacy and Chemistry, Dali University, Dali, Yunnan 671000, China)
Abstract:Objective: To establish a method for determining of glycosaminoglycan in active extracts ML-D with anti-hepatic-fibrosis from Periplaneta americana. Methods: Phenol-vitriol colorimetry was used for determining content of glycosaminoglycan; orthogonal design Lg( 34) was adopted to investigate hydrolysis process of glycosaminoglycan in ML-D; single factor experiment was used to investigate time of color, dosage of phenol and vitriolic. Results: For the best hydrolysis process of glycosaminoglycan in ML-D, the density of hydrochloric acid is 6 tool/L, Solid-liquid ratio is 1 : 1, and time of hydrolysis is 1 h. There are the best conditions of color, the dosage of phenol and vitriolic respectively is 2 mL and 20 mL, heating time is 10 min. Conclusion: The method is simple and accurate with reproducibility; it can be used for the determining content of glycosaminoglycan in active extracts ML-D with anti-hepatic-fibrosis from PeriDlaneta americana.
Keywords:Periplaneta americana  anti-hepatic-fibrosis  glycosaminoglycan  phenol-vitriol colorimetry  content determination
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