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作 者:林晓春[1] 翁立冬[2] 郑锦坤[1] 李旭桂[1] 黄升昌 陈静梅[2] 林晓佳[2]
机构地区:[1]粤北人民医院,广东韶关512026 [2]南方医科大学,广东广州510515
出 处:《中医药导报》2016年第24期54-57,共4页Guiding Journal of Traditional Chinese Medicine and Pharmacy
基 金:广东省建设中医药强省科研课题(20142143);广东医院药学研究基金(2015A32);韶关市科技计划(2014CX/K204);韶关市医药卫生计划(Y14064)
摘 要:目的:建立气血宁口服液的高效液相指纹图谱分析方法。方法:采用HPLC法,色谱柱:Agilent HCC18(4.6 mm×250 mm,5μm);流动相:0.05%磷酸水溶液-乙腈,梯度洗脱;流速:1.0 m L/min;检测波长随时间依时间变化设定,依次为313、258、250、277、230、321、255、350 nm;柱温:25℃;进样量:10μL;检测时间90 min。结果:确定了15个共有峰,12批样品指纹图谱的相似度均在0.93以上,指认了芍药苷、阿魏酸2个特征峰,并对其余各共有峰进行了药材归属鉴定。结论:该方法准确、精密度高、重复性好,为气血宁口服液的质量控制提供了更全面的信息指标。Objective: To establish fingerprint of Qixuening Oral Liquid (气血宁口服液) by High Perfor- mance Liquid Chromatography. Methods: The separation was performed on a Agilent HC-C18(4.6 mm×250 mm,5μm) with gradient elution, with mobile phase consisting 0.05% Phosphoric acid solution and acetonitrile at the flow rate of 1.0 mL/min, column temperature 25 ℃, sample size 10 μL, test time 90 minutes. Detection wave- length, set according to different time, were 313 nm, 258 nm, 250 nm, 277 nm, 230 ran, 321 nm, 255 nm, 350 nm. Results: 15 common peaks existed in 12 samples with similarity over 0.93. Characteristic peaks of paeoniflorin, ferulic acid were recognized and common peaks were identified herb attribution. Conclusion: The method was accurate, precise, and replicable, providing more information indexes for quality control of Qixuening Oral Liquid.
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