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作 者:栾爽[1] 王冬梅[1] 赵怀清[1] 高靥[1] 申涛[1] 石健[1]
出 处:《中国药学杂志》2008年第19期1510-1512,共3页Chinese Pharmaceutical Journal
摘 要:目的利用梯度洗脱,建立高效液相色谱法测定心脑联通胶囊中葛根素、虎杖苷和野黄芩苷含量的方法。方法采用高效液相色谱法。Diamonsil ODS柱(4.6mm×200mm,5μm),流动相为乙腈(A)和0.05%磷酸水溶液(B)梯度洗脱,流速1.0m L.min-1,检测波长336nm。结果葛根素的线性范围为0.0232~0.1856g.L-1(r=0.9995),平均回收率为100.0%,RSD=1.3%,虎杖苷的线性范围为0.0152~0.1216g.L-1(r=0.9996),平均回收率为98.7%,RSD=0.9%,野黄芩苷的线性范围为0.0046~0.0369g.L-1(r=0.9998),平均回收率为100.4%,RSD=0.9%。结论本方法操作简便,测定结果准确可靠,可用于心脑联通胶囊的质量控制。OBJECTIVE To develop a quantitative method simultanous for determination of puerarin, polygonin and scutellarin in Xinnaoliantong capsules by HPLC, METHODS The seperation was performed on a column Diamonsil ODS (4. 6 mm× 200 mm, 5 um) was used. The mobile phase was composed of acetonitrile(A) and 0. 05% H3PO4 (B) with gradient eluation. The flow rate was 1.0 mL · min^-1 with the wavelength at 336 nm. RESULTS For puerarin, the calibration curve was linear ( r = 0. 999 5 ) in the range of 0. 023 2 -0. 185 6 g· L^-1, the average recovery was 100. 0% (RSD = 1.3% ). For polygonin, the calibration curve was linear (r=0.9996) in the range of 0.015 2-0.121 6g· L^-1, the average recovery was 98.7% (RSD=0.9%). For seutellarin, the calibration curve was linear (r =0. 999 8) in the range of 0. 004 6 -0. 036 9g· L^-1, the average recovery was 100. 4% (RSD = 0. 9% ). CONCLUSION The method was sensitive, accurate and can be used in the quality control of Xinnaoliantong capsules.
关 键 词:心脑联通胶囊 高效液相色谱法 葛根素 虎杖苷 野黄芩苷
分 类 号:R917[医药卫生—药物分析学]
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