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作 者:李荣辉[1]
出 处:《海峡药学》2007年第12期48-49,共2页Strait Pharmaceutical Journal
摘 要:目的建立HPLC法测定利通淋胶囊中总黄酮醇苷含量。方法采用KromasilC18(4.6×250mm,5μm)色谱柱;流动相:甲醇-0.4%磷酸溶液(55:45);流速:1.0mL·min^-1;测定检测波长为360nm。结果槲皮素在浓度4、067μg·mL^-1-40.67μg·mL^-1范围内线性关系良好(r=0.9998);山奈酚在浓度0.871μg·mL^-1~8.71μg·mL。范围内线性关系良好(r=0.9998);异鼠李素在浓度0.616μg·mL^-1-6.161g·mL^-1范围内线性关系良好(r=0.9996)。结论本方法简便、准确、专属性强,可测定利通淋胶囊中总黄酮醇苷的含量。OBJECTIVE To develop a HPLC method for the determination of total flavonol in Litonglin capsules by HPLC. METHODS The chromatographic analysis was performed on Kromasil C18 (4. 6 × 250mm,5 μm)column. The mobile phase consisted of methonal - 0.4% phosphoric acid ( 55:45 ). The flow rate was 1.0mL · min ^-1. The detection wavelength was at 360nm. RESULTS Quercetin : A good linearity was obtained over the range of 4. 067μg · mL^-1 ~40. 67μg · mL^-1( r =0. 9998). Kaempferol: A good linearity was obtained over the range of 0. 871μg · mL^-1 - 8.71μg · mL^-1 ( r = 0. 9998 ). Isorhamnetin: A good linearity was obtained over the range of 0. 616μg · mL^- 1 ~ 6. 16μg · mL^- 1 ( r = 0. 9996 ). CONCLUSION The method was simple, accurate, specific and could be used for the quality control of quercetin, kaempferol and isorhamnetin in crude saponins of Litonglin capsules.
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