期刊名称:药物分析杂志 主管单位:中国科学技术协会 主办单位:中国药学会承办:中国食品药品检定研究院 主编:金少鸿 地址:北京天坛西里2号 邮政编码:100050 电话:010-67012819,67058427 电子邮箱:ywfx@nifdc.org.cn 国际标准刊号:ISSN 0254-1793 国内统一刊号:CN 11-2224/R 邮发代号:2-237
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硫磺熏蒸前后白芍HPLC-UV特征图谱的比较研究
Comparative study on HPLC-UV specific chromatograms of Paeoniae Radix Alba before and after sulfur-fumigation
作者:
蔡皓1,2,3, 张科卫1, 刘晓1,2,3, 刘静静1,2,3, 马晓青1,2,3, 蔡宝昌1,2,3,4, 李松林5
作者(英文):CAI Hao1,2,3, ZHANG Ke-wei1, LIU Xiao1,2,3, LIU Jing-jing1,2,3, MA Xiao-qing1,2,3, CAI Bao-chang1,2,3,4, LI Song-lin5
单位(英文):1. College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210046, China; 2. Engineering Center of State Ministry of Education for Standardization of Chinese Medicine Processing, Nanjing University of Chinese Medicine, Nanjing 210029, China; 3. Key Laboratory of State Administration of TCM for Standardization of Chinese Medicine Processing, Nanjing University of Chinese Medicine, Nanjing 210029, China; 4. Nanjing Haichang Chinese Medicine Corporation, Nanjing 210061, China; 5. Department of Pharmaceutical Analysis and Metabolomics, Jiangsu Province Academy of Chinese Medicine, Nanjing 210028, China
分类号:
出版年·卷·期(页码):2013,33 (1):0-0
DOI:
10.16155/j.0254-1793.2017.01.01
-----摘要:-------------------------------------------------------------------------------------------
目的: 对白芍硫磺熏蒸前后的HPLC-UV特征图谱进行比较研究,为科学评价及有效控制其质量提供可靠方法。方法: 采用RP-HPLC方法,使用Hypersil ODS C18(250 mm×4.6 mm,5 μm)色谱柱,流动相为乙腈-0.5%醋酸水溶液,流速为1.0 mL·min-1,二元梯度洗脱,二极管阵列检测器,测定未经硫磺熏蒸和经硫磺熏蒸的白芍各10批,以芍药苷为参照物,检测波长为270 nm。结果: 未经硫磺熏蒸的白芍中共有23个共有峰,经硫磺熏蒸的白芍中共有18个共有峰,通过与对照品的保留时间及紫外光谱比较,5、13、16、17号峰的归属分别为没食子酸、儿茶素、白芍苷、芍药苷。结论: 白芍经硫磺熏蒸后,其成分发生了比较明显的变化,同时白芍在硫磺熏蒸前后,某些共有成分的含量也有不同程度的改变,硫磺熏蒸确实对白芍的质量有非常大的影响。
-----英文摘要:---------------------------------------------------------------------------------------
Objective: To comparatively analyze HPLC-UV specific chromatograms of Paeoniae Radix Alba before and after sulfur-fumigation, so as to provide reliable methods for scientifically evaluating and effectively controlling the quality of Paeoniae Radix Alba. Methods: RP-HPLC method was employed, and the chromatographic conditions were as follows:Hypersil ODS C18 column (250 mm×4.6 mm, 5 μm), binary solvent delivery gradient elution of acetonitrile-water(containing 0.5% acetic acid) as mobile phase with a flow rate of 1.0 mL·min-1, photodiode array detector.The detective wavelength was set at 270 nm, and ten batches of sun-dried and sulfur-fumigated Paeoniae Radix Alba were respectively analyzed using paeoniflorin as the reference compound. Results: A satisfactory method for HPLC-UV specific chromatograms of Paeoniae Radix Alba before and after sulfur-fumigation was established.Totally 23 common peaks were observed in the specific chromatogram of sun-dried Paeoniae Radix Alba , while only 18 common peaks were found in the specific chromatogram of sulfur-fumigated Paeoniae Radix Alba.The 5th, 13th, 16th and 17th peaks were identified as gallic acid, catechin, albiflorin and paeoniflorin, respectively, by comparisons with the retention times and UV spectra of the reference substances. Conclusion: The constituents in Paeoniae Radix Alba changed remarkably after sulfur-fumigation;moreover, the contents in some common peaks of Paeoniae Radix Alba also changed in different degree before and after sulfur-fumigation.Taken together, sulfur-fumigation makes great impact on the quality of Paeoniae Radix Alba.
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