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作 者:时海燕[1] 徐男 王玉团[3] 苏乐群[1] 李宏建[1]
机构地区:[1]山东省千佛山医院,济南250014 [2]山东中医药研究院/国家中医药管理局中药分析重点学科,济南250014 [3]山东省食品药品检验所,济南250101
出 处:《中国药房》2016年第6期833-835,共3页China Pharmacy
摘 要:目的:建立同时测定淡竹叶中绿原酸和牡荆素含量的方法。方法:采用高效液相色谱法。色谱柱为Waters Atlantis C18,流动相为乙腈-水(梯度洗脱),流速为1.0 ml/min,检测波长为280 nm,柱温为35℃,进样量为10μl。结果:绿原酸和牡荆素检测进样量线性范围分别为0.041 0~1.228 8(r=0.999 8)、0.264 0~7.920 0μg(r=0.999 9);精密度、稳定性、重复性试验的RSD〈2%;加样回收率分别为97.6%~102.3%(RSD=1.85%,n=9)、97.6%~101.3%(RSD=1.19%,n=9)。结论:该方法操作简便、稳定、重复性好,可用于淡竹叶中绿原酸和牡荆素含量的同时测定。OBJECTIVE:To establish a method for the simultaneous determination of chlorogenic acid and vitexin in Lophatherum gracile. METHODS:HPLC was performed on the column was Waters Atlantis C18 with mobile phases of acetonitrile- water(gradient elution)at a flow rate of 1.0 ml/min,detection wavelength was 280 nm,column temperature was 35 ℃,and the injection volume was 10 μl. RESULTS:The linear range was 0.041 0-1.228 8 μg for chlorogenic acid(r=0.999 8)and 0.264 0-7.920 0μg for vitexin(r=0.999 9);RSDs of precision,stability and reproducibility tests were lower than 2%;recoveries were97.6%-102.3%(RSD=1.85%,n=9)and 97.1%-101.3%(RSD=1.19%,n=9),respectively. CONCLUSIONS:The method is simple,stable and reproducible,and can be used for the simultaneous determination of chlorogenic acid and vitexin in L. gracile.
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