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降糖类中成药中违禁化学成分的定性分析新方法研究 被引量:2

New method for qualitative screening illegal-added hypoglycemic agents in the traditional Chinese medicine patent prescription
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摘要 以50%乙腈超声提取样品后,再以乙腈-0.02 mol/L乙酸铵溶液(含0.1%甲酸)为流动相,经C18柱分离后,ESI源离子化,然后采用正离子模式定性判别苯乙双胍、格列吡嗪、格列本脲,据此建立了降糖类中成药中非法添加降糖化学成分的快速液质定性方法。此方法检测快速灵敏、选择性强,适用于大批量样品的定性鉴别。 To establish a HPLC/MS/MS method for simultaneous qualitative screening hypoglycemic agents, which were illegally added to proprietary Chinese medicine and health food. Samples were ultrasonic extraction by 50% ACN and then separated by a C18 column with the mobile phase of 0.02 mol/L ammonium acetate (0.1% formic acid) and ACN. Hypoglycemic agents in sample were as certained as compared with the mass spectrogram of samples and reference substance, which gained by electrospray ionization tandem mass in positive ionization model. It is approved the method is rapidly detection with high selectivity and sensitivity.
出处 《应用化工》 CAS CSCD 2009年第5期740-743,共4页 Applied Chemical Industry
基金 国家自然科学基金(20877038) 湖南省卫生厅科研项目(B2006-103)
关键词 降糖类中成药 化学成分 定性分析 液质联用 hypoglycemic Chinese patent drugs chemical constituents qualitative analysis tandem mass
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参考文献5

  • 1方媚媚,王琳,朱德增.糖尿病教育的现状及展望[J].现代预防医学,2008,35(8):1503-1505. 被引量:17
  • 2中国药品生物制品检定所.液质联用(HPLC/MS/MS)分析鉴定苯乙双胍、格列吡嗪及格列本脲的补充检验方法(2006005)[S].北京:国家食品药品监督管理局,2006.
  • 3中国药品生物制品检定所.药品中非法添加的降糖类药物检验方法(2007003)[S].北京:国家食品药品监督管理局,2007.
  • 4The Commission of the European Communites.Commission decision of 12 August 2002 implementing council Directive 96/23/EC concerning the performance of analytical methods and the interpretation of results[C].Official Journal of the European Communities,2002,L221:8-36.
  • 5张喆,高青,余倩,车宝泉,郭洪祝.中药制剂及保健品中违禁添加9种化学降糖药的HPLC-MS/MS定性检测[J].中国医药工业杂志,2007,38(1):39-43. 被引量:45

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