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作 者:刘佳[1] 杨雅欣[1] 刘俊宏[2] 董莉[1] 刘丽娜[1] 李勇军[2]
机构地区:[1]贵阳医学院药学院/贵州省药物制剂重点实验室,贵州贵阳550004 [2]贵阳医学院民族药与中药开发应用教育部工程研究中心,贵州贵阳550004
出 处:《中药材》2014年第11期1980-1983,共4页Journal of Chinese Medicinal Materials
基 金:贵州省中药现代化项目([2011]5028;[2013]4001);贵州省科学技术基金项目(黔科合J字[2012]2035号);贵州省高校2011计划(黔教合协同创新字[2013]04)
摘 要:目的:利用UHPLC-DAD建立黔产苗药百尾参的指纹图谱,为评价其质量提供理论依据。方法:以Agilent Eclipse ZORBAX Plus C18(100 mm×2.1 mm,1.8μm)为色谱柱,0.1%甲酸乙腈(A)-0.1%甲酸水(B)为流动相系统梯度洗脱,流速为0.3 m L/min,检测波长290 nm,柱温40℃,进样量3μL。指纹图谱进行了相似度评价和主成分分析。结果:建立了黔产苗药百尾参的UHPLC-DAD指纹图谱,标定了12个共有峰,确认了其中3个成分。30批药材相似度结果为0.766-0.994,主成分分析提示1号峰和12号峰在指纹图谱中具有代表意义。结论:该方法准确、可靠,可用于百尾参药材的鉴别和质量控制。Objective: To establish an UHPLC-DAD fingerprint of 30 batches of Miao medicine Disporum cantoniense from Guizhou,and to provide a theoretical evidence to evaluate its quality. Methods: The analysis was carried out on an Agilent Eclipse ZORBAX Plus C18( 100 mm × 2. 1 mm,1. 8 μm) column with a mobile phase consisting of acetonitrile-water( containing 0. 1% formic acid)with gradient elution,and the flow rate was 0. 3 m L / min. The column temperature was set at 40 ℃ and UV detection wavelength was set at 290 nm. The sample injection volume was 3 μL. The similarity evaluation and principal component analysis( PCA) of these fingerprints were carried out. Results: The UHPLC-DAD fingerprint was established and compared by 30 batches of samples similarity with 12 common peaks and 3 peaks were identified. The similarities of 30 batches of Disporum cantoniense were between 0. 766 and 0. 994. The principal component analysis showed that compounds 1 and 12 were representative for the fingerprint. Conclusion: The method is accurate and credible,which can be used for identification and quality control of Disporum cantoniense.
关 键 词:百尾参 UHPLC-DAD指纹图谱 相似度评价 主成分分析
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