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HPLC、UPLC法同时测定心可舒胶囊中4种成分的含量

赵振霞, 刘永利, 王敏, 冯丽, 耿韫

赵振霞, 刘永利, 王敏, 冯丽, 耿韫. HPLC、UPLC法同时测定心可舒胶囊中4种成分的含量[J]. 中国药科大学学报, 2014, 45(5): 563-566. DOI: 10.11665/j.issn.1000-5048.20140510
引用本文: 赵振霞, 刘永利, 王敏, 冯丽, 耿韫. HPLC、UPLC法同时测定心可舒胶囊中4种成分的含量[J]. 中国药科大学学报, 2014, 45(5): 563-566. DOI: 10.11665/j.issn.1000-5048.20140510
ZHAO Zhenxia, LIU Yongli, WANG Min, FENG Li, GENG Yun. Simultaneous determination of four components in Xinkeshu capsules by HPLC and UPLC[J]. Journal of China Pharmaceutical University, 2014, 45(5): 563-566. DOI: 10.11665/j.issn.1000-5048.20140510
Citation: ZHAO Zhenxia, LIU Yongli, WANG Min, FENG Li, GENG Yun. Simultaneous determination of four components in Xinkeshu capsules by HPLC and UPLC[J]. Journal of China Pharmaceutical University, 2014, 45(5): 563-566. DOI: 10.11665/j.issn.1000-5048.20140510

HPLC、UPLC法同时测定心可舒胶囊中4种成分的含量

基金项目: 国家“重大新药创制”科技重大专项资助项目(No.2012ZX09304005-005);河北省科技支撑计划资助项目(No.13272513)

Simultaneous determination of four components in Xinkeshu capsules by HPLC and UPLC

  • 摘要: 建立高效液相色谱法(HPLC)、超高效液相色谱法(UPLC)同时测定心可舒胶囊中丹参素钠、原儿茶醛、丹酚酸B和葛根素的含量测定方法。HPLC法采用Thermo C18(4.6 mm×250 mm,5 μm)色谱柱,流速为1.0 mL/min;UPLC法采用Acquity T3 C18(2.1 mm×100 mm,1.8 μm)色谱柱,流速为0.5 mL/min,流动相均为乙腈-0.1%三氟乙酸水溶液,梯度洗脱,柱温均为30℃,检测波长均为287 nm。结果显示,丹参素钠、原儿茶醛、丹酚酸B和葛根素与相邻峰完全分离,线性关系良好,平均加样回收率(%,n=9)分别为100.9,99.4,98.9,101.4(HPLC)和100.3,100.6,99.1,100.7(UPLC)。两种方法测定的4种成分的含量一致,但UPLC法梯度洗脱程序较HPLC法简单。
    Abstract: The aim of the current study was to develop the methods for simultaneous determination of sodium danshensu, protocatechuic aldehyde, salvianolic acid B and puerarin in Xinkeshu capsules by HPLC and UPLC. HPLC was performed on a Thermo C18 column(4. 6 mm×250 mm, 5 μm)with a flow rate of 1. 0 mL/min. UPLC was performed on an Acquity UPLC T3 C18 column(2. 1 mm×100 mm, 1. 8 μm)with a flow rate of 0. 5 mL/min. The mobile phases were both acetonitrile(A)-0. 1% trifluoroacetic acid solution(B)with gradient elution. The column temperatures were both 30 °C and the detection wavelengths were both set at 287 nm. Sodium danshensu, protocatechuic aldehyde, salvianolic acid B and puerarin were separated from adjacent peaks completely. The linear relationships of calibration curves were favorable. The recoveries(%, n=9)of danshensu, protocatechuic aldehyde, salvianolic acid B and puerarin were 100. 9, 99. 4, 98. 9, 101. 4(HPLC)and 100. 3, 100. 6, 99. 1, 100. 7(UPLC), respectively. The content of the two methods for 4 components was consistent, but the procedure of gradient elution of UPLC was simpler than that of HPLC.
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    [2] Chinese Pharmacopoeia Commission.Dispensing Information for Clinic of Ch.P:Chinese Crude Drug (中国药典临床用药须知:中药成方制剂卷)[M].Beijing:Chinese Pharmacopoeia Commission,2010:432.
    [3] Chen J,Wang GL,Yao LW,et al.Recent applications of ultra performance liquid chromatography(UPLC)in pharmaceutical analysis[J]. Chin J Pharm Anal(药物分析杂志),2008,28(11):1 976-1 981.
    [4] Xu DR,Wang KC,Wang ZT,et al.Preliminary study on sources of danshensu and protocatechualdehyde[J]. Chin J Nat Med(中国天然药物),2005,3(3):148-150.
    [5] Liu MY, Zhao SH, Gai XH, et al. Study on determination of water-soluble active principles of Salvia of different extraction methods[J]. Lishizhen Med Mater Med Res(时珍国医国药),2007,18(5):1 186-1 187.
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出版历程
  • 刊出日期:  2014-10-24

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