Determination of Bisphenol Substances in Drug and Food Homologous Products by Ultra-performance Liquid Chromatography-Tandem Mass Spectrometry Combined with Accelerated Solvent Extraction and QuEChERS
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Determination of Bisphenol Substances in Drug and Food Homologous Products by Ultra-performance Liquid Chromatography-Tandem Mass Spectrometry Combined with Accelerated Solvent Extraction and QuEChERS
Vol. 39, Issue 6, Pages: 736-742(2020)
作者机构:
1. 上海海关动植物与食品检验检疫技术中心
2. 复旦大学公共卫生学院
3. 北京市疾病预防控制中心
4. 南京海关动植物与食品检测中心
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Determination of Bisphenol Substances in Drug and Food Homologous Products by Ultra-performance Liquid Chromatography-Tandem Mass Spectrometry Combined with Accelerated Solvent Extraction and QuEChERS. [J]. 39(6):736-742(2020)
DOI:
Determination of Bisphenol Substances in Drug and Food Homologous Products by Ultra-performance Liquid Chromatography-Tandem Mass Spectrometry Combined with Accelerated Solvent Extraction and QuEChERS. [J]. 39(6):736-742(2020)DOI:
Determination of Bisphenol Substances in Drug and Food Homologous Products by Ultra-performance Liquid Chromatography-Tandem Mass Spectrometry Combined with Accelerated Solvent Extraction and QuEChERS
A method was developed for the simultaneous determination of bisphenol substances in drug and food homologous products by ultra performance liquid chromatography-tandem mass spectrometry(UPLC-MS/MS) combined with accelerated solvent extraction(ASE) and QuEChERS.The samples were extracted at 80 ℃ via two cycles of ASE,with acetonitrile-acetic acid-water(89∶1∶10,by volume) for 6 min,then purified by QuEChERS.11 bisphenol substances were separated on an ACQUITY UPLC HSS T3 column(2.1 mm×100 mm,1.8 μm) by gradient elution using methanol containing 0.1% formic acid and 5 mmol/L ammonium acetate containing 0.1% formic acid as mobile phases,then analyzed by MS/MS with electrospray ionization in positive and negative mode under multiple reaction monitoring(MRM) mode,finally quantified by internal standard method.There were good linear relationships for 11 bisphenol substances in the concentration range of 0.5-50.0 μg/L,with correlation coefficients(r2) not less than 0.996 0.The limits of detection(LOD) and limits of quantitation(LOQ) for 11 bisphenol substances were in the ranges of 0.1-0.5 μg/kg and 0.3-1.5 μg/kg,respectively.The recoveries at three spiked levels ranged from 72.4% to 108% with relative standard deviations(RSD) of 1.7%-15%.The proposed method was simple,rapid,high sensitive and reproducible,and it was suitable for the rapid determination of 11 bisphenol substances in drug and food homologous products.
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