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作 者:刘艳红[1] 欧阳辉[2] 黄小方[2] 黎田儿 周茂福[2] LIU Yan-hong;OUYANG Hui;HUANG Xiao-fang;LI Tian-er;ZHOU Mao-fu(The Affiliated Hospital of Jiangxi University of Traditional Chinese Medicine,Nanchang 330006,China;Jiangxi University of Traditional Chinese Medicine,Nanehang 330004,China)
机构地区:[1]江西中医药大学附属医院,南昌330006 [2]江西中医药大学,南昌330004
出 处:《江西中医药大学学报》2018年第6期72-74,共3页Journal of Jiangxi University of Chinese Medicine
基 金:江西民族传统药现代科技与产业发展协同创新中心开放项目(JXXT201402009)
摘 要:目的:建立蓝盆花药材的UHPLC特征图谱并运用LC-MS技术对主要色谱峰进行定性分析。方法:采用Welch Ultimate UHPLC XB-C18(2. 1mm×100 mm,1. 7μm)色谱柱;以0. 3%磷酸水-乙腈为流动相梯度洗脱;流速为0. 25mL·min-1;柱温40℃;检测波长254nm;进样量3μL。结果:首次建立了蓝盆花药材的UHPLC特征图谱共有模式,共检定出22个相对保留时间稳定的共有峰; 10个特征峰初步鉴定为:芹菜素、木犀草苷、大波斯菊苷、野漆树苷、木犀草素、异荭草苷、咖啡酸、绿原酸、芦丁、槲皮素。各样品特征图谱与对照特征图谱的相似度均大于0. 99。结论:该方法准确、可靠,可为蓝盆花药材质量控制提供科学的方法。To study the HPLC specific chromatogranls testing method of the Flos Scabiosae. and to identify the primary chromatogranl peaks by LC - MS. Methods : UHPLC was utilizaed for quality assessment of 10 batches of samples. UHPLC analysis was performed on Welch Ultimate UHPLC C18 column (100mm × 2. 1mm,1.7μm) with the mixture of acetonitrile (A) and 0.3% phosphonic acid solution(B) as mobile phase in gradient mode. The flow rate was 0.25 mL · min ^-1 The detective UV wavelength was 245 nm. Results: Twenty- - two common peaks from the specific ehromatograms of 10 batches of Flos Seabiosae were determined, 10 peaks were identified by LC - MS. The similarities of the specific ehromatograms of 10 batches of samples were all above 0.99. Conclusion: This method is accurate and reliability, which could offer scientific approach for quality control of Flos Scabiosae.
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