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作 者:刘洁琼[1] 俞嘉[1] 熊志立[1] 李发美[1]
出 处:《药物分析杂志》2010年第1期12-16,共5页Chinese Journal of Pharmaceutical Analysis
基 金:国家中医药管理局中医药科学技术研究专项项目(04-05ZP14)
摘 要:目的:建立反相高效液相色谱法同时测定银莲提取物中绿原酸、荭草苷、牡荆苷、蒙花苷和木犀草素的含量。方法:采用Thermo Hypersil BDS C18(250 mm×4.6 mm,5μm)色谱柱,流动相为0.4%醋酸水溶液(A)-乙腈(B),梯度洗脱(0~25min,93%A→70%A;25~35 min,70%A),流速为0.7 mL.min-1,检测波长为330 nm,柱温为室温。结果:银莲提取物中绿原酸、荭草苷、牡荆苷、蒙花苷和木犀草素浓度分别在0.290~11.6μg.mL-1(r=0.9998)、0.350~14.0μg.mL-1(r=0.9997)、0.320~12.8μg.mL-1(r=0.9997)、0.280~11.2μg.mL-1(r=0.9995)、0.110~4.40μg.mL-1(r=0.9999)的范围内与峰面积呈良好线性关系;方法的回收率(n=6)分别为99.4%,106%,102%,106%,92.3%,其RSD分别为2.6%,2.1%,2.8%,1.4%,1.5%。结论:本法快速、简便、准确,重复性好,适用于银莲提取物的质量控制。Objective:To develop an RP-HPLC method for simultaneous determining chlorogenic acid,orientin,vitexin,linarin and luteolin in Yinlian extract.Methods:The separation was carried out on Thermo Hypersil BDS C18(250 mm×4.6 mm,5 μm) column with a mobile phase of 0.4% acetic acid solution(A) and acetonitrile(B) in gradient mode(The initial ratio of 0.4% acetic acid solution was 93% and decreased to 70% within 25 minutes,and the ratio of 0.4% acetic acid solution was maintained 70% within following 10 minutes),at a flow rate of 0.7 mL·min-1.The detection wavelength was set at 330 nm and the analysis was performed at room temperature.Results:The linear ranges of chlorogenic acid,orientin,vitexin,linarin and luteolin were 0.290-11.6 μg·mL-1(r=0.9998),0.350-14.0 μg·mL-1(r=0.9997),0.320-12.8 μg·mL-1(r=0.9997),0280-11.2 μg·mL-1(r=0.9995),0.110-4.40 μg·mL-1(r=0.9999),respectively.The average recoveries(n=6)of chlorogenic acid,orientin,vitexin,linarin and luteolin was 99.4%,106%,102%,106%,92.3% and with RSD of 2.6%,2.1%,2.8%,1.4%,1.5%,respectively.Conclusion:This method is fast,simple,reproducible for the simultaneous determination of chlorogenic acid,orientin,vitexin,linarin and luteolin in Yinlian extract.
关 键 词:反相高效液相色谱 银莲提取物 绿原酸 荭草苷 牡荆苷 蒙花苷 木犀草素
分 类 号:R917[医药卫生—药物分析学]
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