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作 者:刘长安[1] 赵帜平[1] 沈业寿[1] 戴玲[1]
机构地区:[1]安徽大学生命科学学院糖复合物与糖工程实验室,安徽合肥230039
出 处:《中草药》2005年第10期1477-1479,共3页Chinese Traditional and Herbal Drugs
基 金:国家自然科学基金资助项目(30240066);安徽省"十五"重大科技专项基金资助项目(01803011);安徽省自然科学基金资助项目(03043301)
摘 要:目的测定丹皮多糖2b(PSM2b)主要成分的相对分子质量,为建立对照品的标准提供依据。方法PSM2b经Sepharose 4B柱分离,冷冻干燥后得到丹皮多糖的两个成分PSM2b-A和PSM2b-B,采用HPLC法检测均一性和相对分子质量;并分别以0.7%N a2SO4溶液和超纯水作为流动相进行比较。结果PSM2b-A为均一性的糖蛋白,是PSM2b的主要成分。流动相为0.7%N a2SO4溶液时,其相对分子质量为3.596 2×105,分散度指数(D)为4.15。流动相为超纯水时,其相对分子质量为4.758 5×105,分散度指数为1.03。结论采用HPLC法测定丹皮多糖主要成分的相对分子质量时,不同流动相测定的结果有差异,流动相采用超纯水比0.7%N a2SO4溶液更为适合。Objective To determine the relative molecular weight (Mr) of polysaccnaride-2b of moutan (PSM2b) to establish the standard of reference substance. Methods PSM2b, was separated by a Sepharose 4B column and then PSM2b-A and PSM2b-B were obtained after cryodesiccation. Then HPLC was used to determine their Mr. Ultrapure water was used as mobile phase to compare with 0.7% Na2SO4 solution. Results PSM2b-A was pure. The Mr and polydispersity (D) of PSM2b-A obtained by use of dextran as standard were 3. 596 2 × 10^5 and 4.15 in 0.7% Na2SO4 solution phase, respectively, and in ultrapure water phase the Mr and D were 4. 758 5 × 10^5 and 1.03, respectively. Conclusion Different results are detected by different mobile phases in determination of Mr and D of PSM2b-A by HPLC. And the ultrapure water as mobile phase is more suitable than 0.7% Na2SO4 solution.
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