许晓辉, 李晨曦, 吴福祥, 张虹艳, 潘秀丽, 李赟, 王小乔. QuEChERS-分散固相萃取-液质联用法快速测定地龙中黄曲霉毒素[J]. 分析测试技术与仪器, 2021, 27(1): 18-23. DOI: 10.16495/j.1006-3757.2021.01.003
引用本文: 许晓辉, 李晨曦, 吴福祥, 张虹艳, 潘秀丽, 李赟, 王小乔. QuEChERS-分散固相萃取-液质联用法快速测定地龙中黄曲霉毒素[J]. 分析测试技术与仪器, 2021, 27(1): 18-23. DOI: 10.16495/j.1006-3757.2021.01.003
XU Xiao-hui, LI Chen-xi, WU Fu-xiang, ZHANG Hong-yan, PAN Xiu-li, LI Yun, WANG Xiao-qiao. QuEChERS-Dispersed Solid Phase Extraction-Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry for Rapid Determination of Aflatoxin in Pheretima[J]. Analysis and Testing Technology and Instruments, 2021, 27(1): 18-23. DOI: 10.16495/j.1006-3757.2021.01.003
Citation: XU Xiao-hui, LI Chen-xi, WU Fu-xiang, ZHANG Hong-yan, PAN Xiu-li, LI Yun, WANG Xiao-qiao. QuEChERS-Dispersed Solid Phase Extraction-Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry for Rapid Determination of Aflatoxin in Pheretima[J]. Analysis and Testing Technology and Instruments, 2021, 27(1): 18-23. DOI: 10.16495/j.1006-3757.2021.01.003

QuEChERS-分散固相萃取-液质联用法快速测定地龙中黄曲霉毒素

QuEChERS-Dispersed Solid Phase Extraction-Ultra Performance Liquid Chromatography-Tandem Mass Spectrometry for Rapid Determination of Aflatoxin in Pheretima

  • 摘要: 黄曲霉毒素是影响动物源性中药材质量安全的主要风险因子之一,建立了QuEChERS-分散固相萃取- 液质联用法(QuEChERS-dSPE-UPLC-MS/MS)快速测定地龙中黄曲霉毒素的方法. 样品采用QuEChERS方法提取,然后采用增强型脂质去除-分散固相萃取(EMR Lipid-dSPE) 进行净化,多反应监测采集模式进行定性和定量检测,外标法定量,4种黄曲霉毒素测定的线性范围在0.00 ~1.60 ng/mL之间,相关系数在0.990 0~0.994 1之间,检出限在0.013~0.365 ng/g之间,定量限在0.044~0.913 ng/g之间,3个添加水平的回收率在72.0% ~113.0%之间,精密度在2.5%~3.3%之间. 测定10批样品,未检出黄曲霉毒素. 方法基质去除效果良好,具有前处理操作简单、结果准确和灵敏度高等优点,适用于中药材地龙中黄曲霉毒素快速筛查.

     

    Abstract: Aflatoxin, affecting the quality and safety of Pheretima, is one of the major risk factors. The QuEChERS-dispersed solid phase extraction-ultra performance liquid chromatography-tandem mass spectrometry (QuEChERS-dSPE-UPLC-MS/MS) has been established for the rapid determination of aflatoxin in Pheretima powder. The sample was extracted with quick, easy, cheap, effective, rugged and safe (QuEChERS), then purified with the enhanced matrix removal lipid-dispersed solid phase extraction (EMR-Lipid-dSPE). The multiple reaction monitor (MRM) acquisition mode was used for qualitative and quantitative detections, and an external standard method was used for the quantitative detection. The analytes showed good linearities in corresponding concentration ranges of 0.00~1.60 ng/mL with their correlation coefficients (R2) between 0.990 0 and 0.994 1. The limit of detection were 0.013~0.365 ng/g, the limit of quantitative were 0.044~0.913 ng/g, the spiked recoveries for analytes at three spiked levels were in the range of 72.0%~113.0%, the precision were 2.5%~3.3%. No aflatoxin was detected in 10 batches of samples. The matrix removal effect of this method is sufficient, the pretreatment method is simple, reproducible and sensitive, and is suitable for the rapid screening of aflatoxin in Pheretima.

     

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