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作 者:池玉梅[1] 崔小兵[1] 陈维[1] 李伟[1] 狄留庆[1]
机构地区:[1]南京中医药大学,南京210029
出 处:《中国药学杂志》2007年第17期1348-1350,共3页Chinese Pharmaceutical Journal
基 金:国家863计划资助项目(2003AA2Z3247);江苏省自然基金资助项目(Bk2005150)
摘 要:目的研究同时测定通塞脉微丸中绿原酸、阿魏酸及甘草苷含量的方法。方法KromasilC18色谱柱,乙腈-2%冰醋酸为流动相,梯度洗脱,检测波长λ1=324nm,λ2=276nm。结果绿原酸、阿魏酸、甘草苷分别在0.2084~3.334、0.05035~0.8056,0.2315~3.704μg内有良好的线性关系,r>0.9999;平均加样回收率分别为99.07%,100.40%,98.13%,相应的RSD分别为0.73%,1.32%,0.97%(n=6)。结论本法操作简便,结果可靠,重现性好,可作为产品质量控制的方法。OBJECTIVE To establish a method tor the determination of chlorogenic acid and ferulic acid and liquiriitin in Tong Sai Mai tinypil. METHODS The separation was performed on a Kromasil C18 column with the mobile phase consisting of acetonitrile-2% acetic acid for gradient elution. Chlorogenic acid, ferulic acid and liquiriitin were determined by dual wavelength of 324 nm( λ1 ) and 276 nm( λ2 ). RESULTS The linearities were in the ranges of 0. 208 4-3. 334 μg for chlorogenic acid, 0. 050 35 - 0. 805 6μg for ferulic acid, and 0.231 5-3. 704 μg for liquiriitin, respeetively. The average recoveries was 99.07% ( HSD =0. 73% n =6), 100.40% (RSD=l.32% n=6), 98.13% (RSD=0.97% n=6), respectively. CONCLUSION This method is convenient, rapid and accurate. It ca, be used for quality control in production of Tong Sai Mai tinypill.
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