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机构地区:[1]赣南医学院附属第一医院药剂科,江西赣州341000 [2]青岛市市立医院,山东青岛266011 [3]赣州市妇幼保健院,江西赣州341000
出 处:《亚太传统医药》2013年第6期42-44,共3页Asia-Pacific Traditional Medicine
摘 要:目的:建立同时测定茵栀黄分散片中绿原酸与栀子苷的含量测定方法。方法:采用HPLC法,Agilent ZorbaxSB-C18(色谱柱(250mm×4.6mm,5μm),流动相:乙腈-0.3%甲酸水,梯度洗脱,柱温30℃,流速:1.0mL.min-1,检测波长:0~9min为327nm(绿原酸),9~30min为238nm(栀子苷)。结果:绿原酸和栀子苷的线性范围分别为1.25~12.50μg.mL-1(r=0.999 6,n=6)、2.23~22.30μg.mL-1(r=0.999 8,n=6),平均回收率分别为99.82%(RSD为1.16%,n=6)与98.49%(RSD为2.27%,n=6)。结论:该方法简便、准确、重现性好,可用于茵栀黄分散片中绿原酸与栀子苷含量的同时测定。Objective : To develop a method for determining chlorogenic acid and jasminoidin in Yinzhihuang dispersible tablets simultaneously by HPLC. Methods: HPLC method was developed for the determinition. Agilent ZorbaxSB-C18 (250mm×4.6mm,5μm) was used. mobile phase was composed acetonitrile-0.3% formic acid water solution with linear gradient elution, The column temperature was 30℃, the flow rate was 1.0 mL·min^-1 , the wavelength was acquired at 327 nm from 0 to 9 min for chlorogenic acid, 238 nm from 9 to 30 min for jasminoidin. Results:The linear range of chlorogenie acid and jasminoidin were 1.25- 12.50 μg · mL^-1(r=0.999 6, n=6), 2.23 - 22.30 μg · mL^-1(r=0.999 8, n=6). The avergerecoverywere99.82%(RSD=1.16%,n=6) and 98.49 % (RSD= 2.27 %, n= 6). Conclusion:The method is simple, reliable, accurate and can be applied to the determination of chlorogenic acid and jasminoidin in Yinzhihuang dispersible tablets simultaneously.
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