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作 者:石慧慧[1,2] 吴凡[1] 鞠建明[1] 华俊磊[1,3] 李振华[1,3] 霍介格[1]
机构地区:[1]中国中医科学院江苏分院,江苏省中医药研究院,江苏210028 [2]安徽中医药大学药学院,安徽230031 [3]南京中医药大学药学院,南京210046
出 处:《中国现代应用药学》2014年第11期1344-1347,共4页Chinese Journal of Modern Applied Pharmacy
基 金:江苏省中医药研究院医院制剂开发专项(Y1201)
摘 要:目的建立预知子中常春藤皂苷元的HPLC-ELSD含量测定方法,并比较果实、种子和果皮3个不同部位中常春藤皂苷元含量差异。方法色谱条件:色谱柱为Ultimate XB柱(4.6 mm×250 mm,5μm),流动相为乙腈-水-甲酸(70∶30∶0.1),流速为1.0 m L·min^-1,柱温为35℃,ELSD漂移管温度为90℃,载气流速为2.5 L·min^-1。结果常春藤皂苷元在0.36-3.60μg内峰面积积分值常用对数与进样量常用对数有良好的线性关系(r=0.999 4);平均回收率为99.04%,RSD为2.0%。预知子果实、种子、果皮中常春藤皂苷元含量范围分别为24.28-35.18,37.21-58.38,7.83-19.44 mg·g^-1。结论本研究所建立的含量测定方法简便、准确、重复性强,可用于预知子药材的质量控制。预知子不同部位中常春藤皂苷元的含量存在显著差异,在临床应用中应根据使用部位确定药材用量。OBJECTIVE To establish a quantitative determination method for hederagenin in Akebia Fructus after being hydrolyzed by HPLC-ELSD, and to compare the content of hederagen in Akebiae Fructus different parts. METHODS Samples were analyzed with Ultimate XB column(4.6 mm×250 mm, 5 μm). Acetonitrile-water-formic acid(70∶30∶0.1) was used as mobile phases. Flow rate was 1.0 m L·min-1. Column temperature was 35 ℃. Drift tube temperature of ELSD was set at 90 ℃. And flow rate of nitrogen was maintained 2.5 L·min-1. RESULTS There were good linear relationship between natural logarithm of peak areas and injection quality at the range of 0.36-3.60 μg(r=0.999 4). The average recovery of hederagenin was 99.04% and RSD was 2.0%. The content of hederagenin in fruit, seed and peel was 24.28-35.18, 37.21-58.38, 7.83-19.44 mg·g-1, respectively. CONCLUSION The method is simple, accurate and specific. It provides a reliable way for evaluating the quality of Akebiae Fructus. The contents of hederagenin in different medicinal parts of Akebiae Fructus were significantly different. The study provides the scientific evidence for using Akebiae Fructus.
分 类 号:R917.101[医药卫生—药物分析学]
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