镁离子显色分光光度法测定虎杖中蒽醌类化合物的含量  

Determination of anthraquinones in Rhizome Polygoni Cuspidati by magnesium ion color UV spectrophotometry

作　　者：吴巧生[1] 白小红[2] 田杰[2] 

机构地区：[1]山西医科大学第一临床医院药剂科,太原030001 [2]山西医科大学药学院药物分析教研室

出　　处：《山西医科大学学报》2008年第12期1099-1102,共4页Journal of Shanxi Medical University

基　　金：山西省自然科学基金资助项目(2007011086)

摘　　要：目的镁离子显色分光光度法测定虎杖中蒽醌类化合物的含量。方法镁离子与蒽醌化合物发生配位反应,生成红色的配合物,在505nm处有最大吸收,利用镁离子显色分光光度法可对蒽醌类化合物总量进行测定。结果1,8-二羟基蒽醌与镁离子形成配位化合物在505nm处的表观百分吸收系数为(513.5±8.6)L/(mol·cm),测定总蒽醌化合物的线性范围为0.93-26.00mg/L,检测限为0.31mg/L,日内精密度RSD为0.8%,回收率为(100.2±1.4)%。结论镁离子与蒽醌类化合物反应生成配合物稳定,可用于测定虎杖中蒽醌类化合物的总量。Objective To determine the content of anthraquinones in Rhizome Polygoni Cuspidati by magnesium ion color UV spectrophotometry. Methods The determination was based on the reaction between magnesium ion and , 8-dihydroxyanthraquinone at 505 nm. Magnesium ion color UV spectrophotometry was employed to analyze anthraquinones in Rhizome Polygoni Cuspidati. Results The specific absorptivity coefficient of compound formed by 1,8-dihydroxyanthraquinone and magnesium ion was 513.5 ± 8.6 L/（mol· cm）. The linear range, determination limit, within-day precision RSD and recovery of anthraquinones were 0.93-26,00 mg/L,0.31 mg/L,0.8% and（100.2± 1.4）% ,respectively. Conclusion As a precise, accurate,simple and speedy method, magnesium ion color UV spectrophotometry may be applied for determining the content of anthraquinones in Rhizome Polygoni Cuspidati.

关 键 词：1 8-二羟基蒽醌 蒽醌类化合物 镁离子显色分光光度法 虎杖 

分 类 号：R927.2[医药卫生—药学]