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作 者:任小娜[1] 马永钧[1] 周敏[1] 霍淑慧[1] 姚俊丽[1] 陈慧[1]
机构地区:[1]西北师范大学化学化工学院甘肃省高分子材料重点实验室,甘肃兰州730070
出 处:《色谱》2008年第2期223-227,共5页Chinese Journal of Chromatography
基 金:甘肃省自然科学基金资助项目(No.3ZS051-A25-097)
摘 要:以铕离子掺杂类普鲁士蓝(Eu-PB)化学修饰铂电极为工作电极,采用毛细管电泳-电致化学发光检测法对4种托烷类生物碱成分(如山莨菪碱、东莨菪碱、阿托品和樟柳碱)进行了分离检测。考察了氧化电位值、运行缓冲液酸度、盐浓度和甲醇含量等实验条件对电泳分离效果及检测灵敏度的影响。在优化的实验条件下,以20mmol/L的磷酸盐(pH8.0)-7%(体积分数)甲醇为运行液,各组分在6min内可达到基线分离,其峰面积的相对标准偏差小于5.0%,迁移时间的相对标准偏差小于1.1%(n=12)。并将该法成功地应用于测定中药马尿泡根茎中的山莨菪碱和东莨菪碱的含量,其含量平均值分别为27.8g/kg和4.43g/kg。样品的加标回收率为97.8%~102%。Based on an Eu-PB modified platinum electrode as the working electrode,a method for the simultaneous determination of the four tropane alkaloids,anisodamine,scopolamine,atropine and anisodine,by capillary electrophoresis with electrochemiluminescence detection(CE-ECL)has been established.The effects of several factors,such as the detection potential,the acidity and concentration of the running buffer,and the content of the methanol additive were investigated for the improvement of separation ability and detection sensitivity.Under the optimized conditions,these four components could be fully separated from each other in a 20 mmol/L phosphate(pH 8.0)containing 7%(v/v)methanol buffer within 6 min.The relative standard deviations of the peak area and migration time were less than 5.0% and 1.1%(n=12)respectively for all the four compounds.Thus,the method has been successfully applied to the determination of anisodamine,scopolamine in Przewalskia tangutica Maxim.The average amounts of 27.8 g/kg anisodamine and 4.43 g/kg scopolamine were found in the herbal rootstalk sample.The recoveries of the tropane alkaloids were 97.8%-102%.
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