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伪品血竭中染色剂苏丹红IV的检测

Identification and determination of Sudan Ⅳ in Counterfeit Drug of Sanguis Draconiis

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【作者】 苏晶程显隆张聿梅鲁静林瑞超

【Author】 Su Jing, Cheng Xianlong1, Zhang Yumei1, Lu Jing1, Lin Ruichao1(Chongqing Institute for Drug Control,Chongqing 401121 China; 1National Institute for Control of Pharmacetical and Biological Products,Beijing 100050 China)

【机构】 重庆市药品检验所中国药品生物制品检定所中国药品生物制品检定所 重庆401121

【摘要】 采用高效液相色谱建立了伪品血竭中苏丹红Ⅳ的鉴别和含量测定方法。含量测定采用Agilent Eclipse Plus C18色谱柱,柱温30℃,流动相为乙腈-水(95∶5),流速为1.0mL·min-1,检测波长为520nm;液-质联用验证采用Merck Chromolith Performance RP-18e色谱柱,流动相为乙腈-0.1%的甲酸溶液(95∶5),ESI+扫描模式。供试样品中相关分子离子峰及碎片特征与苏丹红Ⅳ对照品一致,含量测定苏丹红Ⅳ在0.0849~3.3975μg的范围内线性关系良好(r=0.9999),回收率为99.82%。该方法快速、简便,易行,具有良好的专属性、稳定性和重复性。

【Abstract】 To develop a specific method for identification and determination of SudanⅣ in counterfeit drug of Sanguis Draconiis. HPLC-DAD and LC-MS methods were established for the separation and detection. The HPLC system consisted of Agilent Eclipse Plus C18 column,by using acetonitrile and water (95∶5) in HPLC-DAD method, and acetonitrile and 0.1% fomic acid (95∶5) in LC-MS/MS method as the mobile phase separately. SudanⅣ had good linearity in the range of 0.0849~3.3975 μg (r=0.9999). The average recovery was 99.82%. This method is rapid, simple and accurate for quantitative analysis of Sanguis draconiis, and has good specificity, stability and repeatability.

【关键词】 血竭苏丹红Ⅳ高效液相色谱法液相-质谱联用
【Key words】 Sanguis draconiisSudanⅣHPLCLC-MS
  • 【文献出处】 中国药事 ,Chinese Pharmaceutical Affairs , 编辑部邮箱 ,2008年04期
  • 【分类号】R284.1
  • 【被引频次】21
  • 【下载频次】187
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