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Simultaneous determination of 9 environmental pollutants including bisphenol A in vegetable oil by solid phase extraction-liquid chromatography-tandem mass spectrometry.
Wang, Hao; Li, Xing; Shao, Mingyuan; Lin, Li; Mu, Tongna; Liu, Yanqin.
Afiliação
  • Wang H; Beijing Food Safety Monitoring and Risk Assessment Center, Beijing 100094, P. R. China. Lixing188117@163.com.
  • Li X; Beijing Food Safety Monitoring and Risk Assessment Center, Beijing 100094, P. R. China. Lixing188117@163.com.
  • Shao M; Beijing Food Safety Monitoring and Risk Assessment Center, Beijing 100094, P. R. China. Lixing188117@163.com.
  • Lin L; Beijing Food Safety Monitoring and Risk Assessment Center, Beijing 100094, P. R. China. Lixing188117@163.com.
  • Mu T; Beijing Food Safety Monitoring and Risk Assessment Center, Beijing 100094, P. R. China. Lixing188117@163.com.
  • Liu Y; Beijing Food Safety Monitoring and Risk Assessment Center, Beijing 100094, P. R. China. Lixing188117@163.com.
Anal Methods ; 13(31): 3527-3534, 2021 08 12.
Article em En | MEDLINE | ID: mdl-34279017
ABSTRACT
In this study, a high performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method with solid phase extraction was established for the simultaneous determination of bisphenol A, bisphenol F, bisphenol S, 4-nonylphenol, n-nonylphenol, octylphenol, n-octylphenol, perfluorooctane sulfonate acid and perfluorooctanoic acid in vegetable oil. The sample was extracted with ammonia acetonitrile solution (1 9, V/V) by ultrasonication. And the obtained extract was purified by using a PRIME HLB solid phase extraction column. The identification and quantification of the compounds was performed by liquid chromatography-tandem mass spectrometry in multiple reaction monitoring (MRM) mode. The internal standard method was used for quantitative analysis. Under optimal experimental conditions, the limits of quantitation of bisphenol A, bisphenol F, bisphenol S, 4-nonylphenol, n-nonylphenol, octylphenol and n-octylphenol in vegetable oil were 1.0 µg kg-1. The limits of quantitation of perfluorooctane sulfonic acid and perfluorooctanoic acid in vegetable oil were 0.1 µg kg-1. The average spiked recoveries of the method were in the range of 89.2-117.1% with the relative standard deviations (RSD) of 2.9-9.8% (n = 6). This method is sensitive, versatile and reproducible, and is suitable for the simultaneous determination of bisphenol A, bisphenol F, bisphenol S, 4-nonylphenol, n-nonylphenol, octylphenol, n-octylphenol, perfluorooctane sulfonate acid and perfluorooctanoic acid in vegetable oil.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Poluentes Ambientais / Espectrometria de Massas em Tandem Idioma: En Revista: Anal Methods Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Poluentes Ambientais / Espectrometria de Massas em Tandem Idioma: En Revista: Anal Methods Ano de publicação: 2021 Tipo de documento: Article