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出 处:《广东药学院学报》2012年第2期163-166,共4页Academic Journal of Guangdong College of Pharmacy
摘 要:目的建立痛风胶囊中青藤碱、大黄酸含量的测定方法。方法采用HPLC法,青藤碱含量测定的色谱柱为Agilent Eclipse Plus C18(5μm,4.6 mm×250 mm),流动相为乙腈-0.08%(体积分数)三乙胺(体积比21∶79),流速为1.0 mL.min-1,检测波长为262 nm;大黄酸含量测定的色谱柱为Kromasil C18(4.6mm×250 mm,5μm),流动相为甲醇-0.05%(体积分数)H3PO4(体积比85∶15),流速为1.0 mL.min-1,检测波长为254 nm。结果青藤碱在0.115 6~3.855μg范围内与峰面积呈良好的线性关系(r=0.999 5),平均回收率为99.48%,RSD为1.93%;大黄酸在0.083 2~0.832μg范围内与峰面积呈良好的线性关系(r=0.999 5),平均回收率为98.62%,RSD为1.13%。结论本方法专属性强、准确、重复性好,可用于痛风胶囊的质量控制。Objective To develop a method for the determination of sinomenine and rhein in Tongfeng capsule.Methods The assay of sinomenine was performed on Agilent Eclipse Plus C18 column(5 μm,4.6 mm×250 mm) with a DAD(262 nm).The mobile phase was acetonitrile-0.08% triethylamine(21:79) with a flow rate of 1.0 mL·min-1.The determination of rhein was on a Kromasil C18 column(5 μm,4.6 mm×250 mm) with a UVD(254 nm).The mobile phase was methanol-0.05% phosphoric acid(85:15).Results The linear range of sinomenine was 0.115 6-3.855 μg(r=0.999 5),and the average recovery ratio was 99.48%(RSD=1.93%);The linear range of rhein was 0.083 2-0.832 μg(r=0.999 5),and the average recovery ratio was 98.62%(RSD=1.13%). Conclusion The method is exclusive,accurate and reproducible,which may be applied in the quality control of Tongfeng capsule.
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