Determination of Residues of Carbadox,Quinocetone,Mequindox and Their Metabolites in Aquatic Products by Ultra High Performance Liquid Chromatography Tandem Mass Spectrometry
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Determination of Residues of Carbadox,Quinocetone,Mequindox and Their Metabolites in Aquatic Products by Ultra High Performance Liquid Chromatography Tandem Mass Spectrometry
Vol. 30, Issue 10, Pages: 1133-1137(2011)
作者机构:
1. 山东省海洋水产研究所
2. 山东省海洋生态修复重点实验室
3. 烟台大学化学生物理工学院
4. 烟台山水海产有限公司
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Determination of Residues of Carbadox,Quinocetone,Mequindox and Their Metabolites in Aquatic Products by Ultra High Performance Liquid Chromatography Tandem Mass Spectrometry. [J]. 30(10):1133-1137(2011)
DOI:
Determination of Residues of Carbadox,Quinocetone,Mequindox and Their Metabolites in Aquatic Products by Ultra High Performance Liquid Chromatography Tandem Mass Spectrometry. [J]. 30(10):1133-1137(2011)DOI:
Determination of Residues of Carbadox,Quinocetone,Mequindox and Their Metabolites in Aquatic Products by Ultra High Performance Liquid Chromatography Tandem Mass Spectrometry
An ultra performance liquid chromatography-electrospray ionization triple-quadruple tandem mass spectrometric(UPLC-ESI MS/MS) method was established for the determination of residues of carbadox(CBX),quinocetone(QCT),mequindox(MEQ),quinoxaline-2-carboxylic acid(QCA) and 3-methylquinoxaline-2-carboxylic acid(MQCA) in aquatic products.The samples were separately extracted with acetonitrile-ethyl acetate(50∶50) mixed solution and phosphate buffer,then purified with n-hexane.The separation of CBX,QCT,MEQ,QCA and MQCA was carried out on an ACQUITYTM BEH C18 column(1.7 μm,2.1 mm i.d.×100 mm) using methanol-acetronitril(11∶3) and 0.1% formic acid as mobile phases.The target compounds were confirmed and quantified by MS-MS under multiple-reaction monitering(MRM) mode with the external standard method.The results showed that there were good linear relationships between peak area and concentrations of five quinoxalines in the range of 5-50 μg/L,with correlation coefficients more than 0.998 and limits of quantitation(LOQs) of 1.0 μg/kg.The recoveries at spiked levels of 1.0-10 μg/kg ranged from 70% to 108% with relative standard deviations of 2.5%-11%.This method shortened the time of pre-treatment process,and the result was credible.It could satisfy the requirement of mass and fast analysis in the laboratory.
Research on the Residual Detection of Quinocetone,Cyadox and Their Main Metabolites in Aquatic Products by HPLC-MS/MS
Determination of Brilliant Green,Methylene Blue and Their Metabolites in Aquatic Products by Liquid Chromatography-Tandem Mass Spectrometry
Simultaneous Determination of 16 Coumarins and Vanillins and Their Derivatives in Rice by QuEChERS-Isotope Internal Standard/Ultra-high Performance Liquid Chromatography-Tandem Mass Spectrometry
Rapid Detection of Tetrodotoxin in Aquatic Products by Colloidal Gold Immunochromatography Assay
Determination of Herbicides in Agricultural Soils by Solvent Induced Extraction Coupled with UPLC-MS/MS
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