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作 者:王文月[1,2] 刘志宏[1] 黄爱文[1] 宋洪涛[1]
机构地区:[1]南京军区福州总医院药学科,福州350025 [2]福建医科大学药学院,福州350108
出 处:《中国药房》2015年第9期1241-1243,共3页China Pharmacy
基 金:军队医疗机构制剂标准提高科研专项课题(No.13ZJ01)
摘 要:目的:建立双波长高效液相色谱(HPLC)法同时测定酸性龙胆合剂中龙胆苦苷和橙皮苷的含量。方法:采用HPLC法。色谱柱为Agilent ZORBAX SB-C18,流动相为甲醇-0.1%磷酸水溶液(梯度洗脱),检测波长为270 nm(龙胆苦苷)、283 nm(橙皮苷),柱温为30℃,进样量为10μl。结果:龙胆苦苷和橙皮苷的质量浓度分别在14.4~100.8μg/ml(r=0.999 7)、8.0~104μg/ml(r=0.999 7)范围内与峰面积呈良好线性关系;精密度、稳定性、重复性试验的RSD均〈2%;平均加样回收率分别为99.92%、102.55%,RSD分别为0.41%、1.84%(n均为9)。结论:该方法简便、快速、灵敏,适用于酸性龙胆合剂中龙胆苦苷和橙皮苷的含量测定。OBJECTIVE:To establish the dual-wavelength HPLC method for content determination of gentiopicrin and hesperidin in Acid gentian mixture. METHODS:HPLC was conducted. The analysis was performed on Agilent ZORBAX SB-C18 column with the mobile phase of methanol-0.1% phosphoric acid solution(gradient elution);the detection wavelength was 270 nm(gentiopicroside)and 283 nm(hesperidin);the column temperature was 30 ℃ and the volume was 10 μl. RESULTS:The linear range of gentiopicroside was 14.4-100.8 μg/ml(r=0.999 7)and that of hesperidin was 8.0-104 μg/ml(r=0.999 7);the RSDs of precision,stability,repeatability tests was all less than 2%;average recoveries were 99.92%(RSD=0.41%,n=9) and 102.55%(RSD=1.84%,n=9),respectively. CONCLUSIONS:The method is simple,accurate and sensitive and can be used for content determination of gentiopicroside and hesperidin in Acid gentian mixture.
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