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作 者:吴香婷 刘晴 赵诗聪 程祥 韩晓冉 李海燕 WUXiangting;LIUQing;ZHAO Shicong;CHENG Xiang;HANXiaoran;LI Haiyan(School of Pharmacy,Jilin University,Changchun 130021,China;The Affiliated Hospital of Changchun University of Chinese Medicine,Changchun 130021,China)
机构地区:[1]吉林大学药学院,吉林长春130021 [2]长春中医药大学附属医院,吉林长春130021
出 处:《特产研究》2024年第4期110-115,共6页Special Wild Economic Animal and Plant Research
基 金:吉林省科学技术厅项目(20210204172YY)。
摘 要:为建立同时测定杞菊叶黄素酯颗粒中绿原酸、木犀草苷、异绿原酸A含量的测定方法。本研究采用高效液相色谱法,用Amethyst C18-H(4.6 mm×250 mm,5μm)作为色谱柱选择乙腈-0.1%磷酸水溶液为流动相进行梯度洗脱,检测波长348 nm柱温25℃进样量2μL。结果显示,绿原酸、木犀草苷、异绿原酸A分别在0.01~0.07 mg/mL、0.01~0.05 mg/mL、0.03~0.16 mg/mL范围内与峰面积呈良好的线性关系,相关系数分别为0.999 4、0.999 5、0.999 2;平均回收率分别为101.33%、95.31%、109.60%相对标准偏差为1.59%、1.29%、1.42%;精密度试验结果相对标准偏差(RSD)分别为1.01%、0.73%和0.45%;稳定性试验结果相对标准偏差为1.49%、1.26%、0.72%。该方法测得3批产品中绿原酸、木犀草苷、异绿原酸A的含量均值为(98.94±0.56) mg/100 g、(90.45±0.82) mg/100 g、(145.63±2.21)mg/100g(n=9)。本研究方法简便、准确、可靠,可作为杞菊叶黄素酯颗粒的含量测定方法。To establish a method for the simultaneous determination of chlorogenic acid,luteolin glycoside and isochlorogenic acid A in Qiju lutein ester granules.HPLC was performed with Amethyst C18-H(4.6 mm ×250 mm,5μm)as the chromatographic column,acetonitrile-0.1%phosphoric acid aqueous solution was selected as the mobile phase for gradient elution,the detection wavelength was 348nm,and the column temperature was 25℃,injection volume was 2 μL.Chlorogenic acid,luteolin and isochlorogenic acid A showed good linear relationship with peak area in the range of 0.01~0.07 mg/mL,0.01~0.05 mg/mL and 0.03~0.16 mg/mL,respectively,and the correlation coefficients were 0.9994,0.9995 and 0.9992,respectively;the average recoveries were 101.33%,95.31%and 109.60%,and the relative standard deviations were 1.59%,1.29%and 1.42%,respectively;the relative standard deviations(RSDs)of precision test results were 1.01%,0.73%and 0.45%,respectively;the relative standard deviations(RSDs)of stability test results were 1.49%,1.26%and 0.72%.The average contents of chlorogenic acid,luteolin and isochlorogenic acidAin three batches of products were(98.94±0.56)mg/100 g,(90.45±0.82)mg/100 g and(145.63±2.21)mg/100 g(n=9).The method in this study is simple,accurate and reliable,and can be used for the content determination of Qiju lutein ester granules.
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