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超高效液相色谱法测定护肝布祖热颗粒中秦皮乙素含量 被引量:2

Content Determination of Aesculetin in Hugan Buzure Granules by UHPLC
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摘要 目的建立测定护肝布祖热颗粒中秦皮乙素含量的超高效液相色谱(UHPLC)法。方法色谱柱为Acquity UPLC BEH C18柱(100 mm×2.1 mm,1.7μm),流动相为乙腈-0.4%磷酸溶液梯度洗脱,流速为0.21 m L/min,柱温为30℃,检测波长为349 nm,进样量为1μL。结果秦皮乙素质量浓度在1.06-21.16μg/m L范围内与峰面积线性关系良好(r=0.999 7);加样回收率为100.65%,RSD为0.97%(n=6)。结论该方法简便、准确,测得结果稳定性、重复性好,可用于该制剂中秦皮乙素含量测定。 Objective To establish an UHPLC method for the content determination method of aesculetin in Hugan Buzure Granules. Methods The column was Acquity UPLC BEH C18 column ( 100 mm × 2. 1 mm, 1. 7 μm );the mobile phase was acetonitrile -0. 4%phosphoric acid solution, gradient elution;the flow rate was 0. 21 mL/min, the column temperature was 30 ℃, the detection wavelength was 349 nm, the sample volume was 1 μL. Results Aesculetin showed good linear relationship in 1. 06-21. 16 μg/mL ( r=0. 999 7 ) , the average recovery rate was 100. 65% and the RSD=0. 97%( n=6 ) . Conclusion The method is simple, accurate and reproducible. It can be used for the content determination of aesculetin in the preparation.
出处 《中国药业》 CAS 2016年第19期56-58,共3页 China Pharmaceuticals
关键词 含量测定 超高效液相色谱法 秦皮乙素 菊苣 护肝布祖热颗粒 content determination UHPLC aesculetin chicory Hugan Buzure Granules
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  • 1WS3-BW-0135-98,中华人民共和国卫生部药品标准?维吾尔药分册[S].
  • 2吕洋.肝炎检测的临床意义和用药指导[J].中国药物经济学,2014,1:23-26.
  • 3闫明,黄毅,刁娟娟,钟丽,冷英丽,康爱荣,严欢.菊苣子的理化鉴别研究[J].时珍国医国药,2006,17(12):2447-2448. 被引量:7
  • 4Wu HK,Su Z, Aisa HA, et al. Components of Cichorium glandulo- sumseeds[J]. Chem Nat Compd,2007,43(4):472-473.
  • 5Wu HK, Su Z, Yili A, et al. Isolation of esculetinfrom Cichorium glandulosum by high - speed counter - current chromatography [J]. Chem Nat Compd, 2007,43(1):109.
  • 6胡君萍,迪丽拜尔.马木提,李渊,柳惠斌,杨建华.UPLC同时测定维药毛菊苣和菊苣中5种化学成分的含量[J].中国实验方剂学杂志,2014,20(17):65-68. 被引量:17

二级参考文献11

  • 1李鹏,赵红,吴远芳,成玉怀.菊苣的生药鉴定[J].农垦医学,2001,23(3):149-151. 被引量:9
  • 2刘勇民.维吾尔药志(上)[M].乌鲁木齐:新疆科技卫牛出版社,1999.405-407.
  • 3国家药典委员会.中国药典,Ⅰ部[S].北京:化学工业出版社,2005.附录31-附录32.
  • 4中华人民共和国卫生部药典委员会.中华人民共和国卫生部药品质量标准(维吾尔药分册)[M].乌鲁木齐:新疆科技卫生出版社,1999.
  • 5Yang W Z, Wang H, Shang J, et al. Chemical constituents from Cichorium glandulosum [ J ]. Chin J Nat Med, 2009, 7(3) :193.
  • 6Wu H, Su Z, Yang Y, et al. Isolation of three sesquiterpene lactones from the roots of Cichorium glandulosum Boiss. et Huet. by high-speed counter- current chromatography [ J ]. J Chromatogr A, 2007, 1176(1/2) :217.
  • 7Atmaca M, Bilgin H M, Obay B D, et al. The hepatoprotective effect of coumarin and coumarin derivates on carbon tetrachloride-induced hepatic injury by antioxidative activities in rats [ J ]. J Physiol Biochem, 2011, 67:569.
  • 8Ahmed B, Khan S, Masood M H, et al. Anti- hepatotoxic activity of cichotyboside, a sesquiterpene glycoside from the seeds of Cichorium intybus [ J ]. J Asian Nat Prod Res, 2008, 10(3/4) :223.
  • 9罗嫄,刘晟,方鲁延,王建芬,李芳.HPLC测定菊苣药材中的有效成分[J].华西药学杂志,2007,22(6):671-672. 被引量:20
  • 10再娜布.吐合达洪,仲婕,信学雷,阿吉艾克拜尔.艾萨.毛菊苣药材不同部位主要活性成分含量[J].中国中药杂志,2010,35(8):1018-1021. 被引量:15

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