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作 者:邱建国[1] 张泉龙[1] 李茂星[1] 贾正平[1] 张汝学[1] 赵一[1] 王谨涵[1] 陶锐[1]
机构地区:[1]兰州军区兰州总医院,全军高原环境损伤防治重点实验室,国家中医药管理局临床中药学重点学科,兰州730050
出 处:《中国实验方剂学杂志》2015年第8期43-46,共4页Chinese Journal of Experimental Traditional Medical Formulae
基 金:国家科技重大专项(2008ZXJ09004-XXX);甘肃省科技重大专项(1102FKDA012);甘肃省中医药管理局科研课题(GZK-2014-1);全军中医药研发推广项目(2006032001)
摘 要:目的:建立独一味水提物、水洗脱物和70%乙醇溶液洗脱物中总苯乙醇苷含量的测定方法。方法:加独一味药材质量18倍量水,煎煮提取3次,每次1.5 h,滤过,合并滤液,滤液2-4℃冷藏除尘,60℃减压干燥得到水提物,水提物经聚酰胺和大孔树脂富集分离,分别用水和70%乙醇溶液洗脱,分别得到水洗脱物,70%乙醇溶液洗脱物Ⅰ(通过聚酰胺柱洗脱物)和70%乙醇溶液洗脱物Ⅱ(通过大孔树脂柱洗脱物);在224,252,256,354 nm波长处,采用一阶导数紫外分光光度法测定总苯乙醇苷的含量。结果:建立的一阶导数紫外分光光度法测定总苯乙醇苷的含量,在354 nm波长处加样回收率99.71%,RSD 2.5%。结论:该方法专属性强、灵敏度高、精确度与重复性好,适用于独一味中总苯乙醇苷的含量测定。Objective: To determine the total phenylethanol glycosides in water extract, water eluate and 70% ethanol eluate of Lamiophlomis Herba by first derivative ultraviolet spectrophotometry. Method: Lamiophlomis Herba was extracted with water (18 times) 3 times, 1.5 h per time. The water extract was storage at 2- 4 ℃, was dried under reduced pressure at 60 ℃. Water extract were separated and enriched by polyamide and macroporous resin, to obtain the water eluate and 70% ethanol eluate Ⅰ (polyamide column), 70% ethanol eiuate Ⅱ (macroporous resin column). The total phenylethanol glycosides were determined by first derivative ultraviolet spectrophotometry at 224, 252, 256, 354 nm. Result : Recovery of the total phenylethanol glycosides was 99. 71% , RSD was 2.5% at 354 nm. Conclusion: This method is special, sensitive, accurate and repeatable, and can be used for the quality analysis of the total phenylethanol glycosides in Lamiophlomis Herba.
关 键 词:独一味 提取物 一阶导数紫外分光光度法 总苯乙醇苷
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