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作 者:闵云山[1] 焦正花[1] 张小华[1] 杨晔[1]
机构地区:[1]甘肃省中医院,甘肃兰州730050
出 处:《中国中医药信息杂志》2012年第7期52-53,共2页Chinese Journal of Information on Traditional Chinese Medicine
基 金:甘肃省自然科学基金(1010RJZ206)
摘 要:目的建立测定止痛膏中大黄酸、大黄素和大黄酚含量的方法。方法采用反相高效液相色谱法,十八烷基键合硅胶柱分离大黄酸、大黄素和大黄酚,以甲醇-水(85∶15)为流动相,流速为1.0 mL/min,检测波长254 nm。结果大黄酸在0.208~1.040μg范围内线性关系良好(r=0.9990,n=5),平均加样回收率为98.37%(RSD=0.57%,n=5);大黄素在0.192~0.96μg范围内线性关系良好(r=0.9997,n=5),平均加样回收率为98.45%(RSD=0.99%,n=5);大黄酚在0.596~2.980μg范围内线性关系良好(r=0.999 5,n=5),平均加样回收率为98.18%(RSD=1.50%,n=5)。结论本方法简单、灵敏、准确、重复性好,可用于该制剂的质量控制。Objective To establish the method to determine the contents of rhein,emodin and chrysophanol in Zhitonggao.Methods RP-HPLC method was adopted with Hypersil ODS C18 as column.The mobile phase consisted of methanol-water(85∶15) with a flow rate of 1.0 mL/min.The detection wavelength was 254 nm.Results The linear correlation of rhein was good in the range of 0.208-1.040 μg(r=0.999 0,n=5) and the recovery was 98.37%(RSD=0.57%,n=5).The linear correlation of emodin was good in the range of 0.192-0.96 μg(r=0.999 7,n=5) and the recovery was 98.45%(RSD=0.99%,n=5).The linear correlation of chrysophanol was good in the range of 0.596-2.980 μg(r=0.999 5,n=5) and the recovery was 98.18%(RSD=1.50%,n=5).Conclusion The method is simple,sensitive and accurate,with good reproducibility.It can be applied to control the quality of the preparation.
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