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[Rapid determination of 25 drug residues in aquatic products by ultra performance liquid chromatography-quadrupole/electrostatic field orbitrap high resolution mass spectrometry].
Zhang, Xianchen; Li, Rong; Zhang, Pengjie; Wu, Xia; Hua, Hongbo; Yang, Luqi; Lu, Junwen; Rong, Yutang.
Afiliação
  • Zhang X; Inspection and Quarantine Technology Center of Zhongshan Entry-Exit Inspection and Quarantine Bureau, Zhongshan 528403, China. zhangxc@zs.gdciq.gov.cn.
  • Li R; Inspection and Quarantine Technology Center of Zhongshan Entry-Exit Inspection and Quarantine Bureau, Zhongshan 528403, China.
  • Zhang P; Inspection and Quarantine Technology Center of Zhongshan Entry-Exit Inspection and Quarantine Bureau, Zhongshan 528403, China.
  • Wu X; Agilent Technologies Co., Ltd. (China), Guangzhou 510000, China.
  • Hua H; Zhongshan ZhuoYa Foreign Language School, Zhongshan 528401, China.
  • Yang L; Inspection and Quarantine Technology Center of Zhongshan Entry-Exit Inspection and Quarantine Bureau, Zhongshan 528403, China.
  • Lu J; Inspection and Quarantine Technology Center of Zhongshan Entry-Exit Inspection and Quarantine Bureau, Zhongshan 528403, China.
  • Rong Y; Inspection and Quarantine Technology Center of Zhongshan Entry-Exit Inspection and Quarantine Bureau, Zhongshan 528403, China.
Se Pu ; 36(2): 114-124, 2018 Feb 08.
Article em Zh | MEDLINE | ID: mdl-29582597
ABSTRACT
An ultra performance liquid chromatography-quadrupole/electrostatic field orbitrap high resolution mass spectrometry (UPLC-Q Orbitrap HRMS) method was developed for the rapid screening of 25 drug residues in aquatic products by the application of a novel enhanced matrix removal of lipids (EMR-Lipid). The samples were extracted with acetonitrile, cleaned-up with EMR-Lipid, and salted out with 3.0 g sodium chloride and 3.0 g sodium sulfate. The separation of the 25 drug residues was performed on an ACQUITY UPLC BEH C18 column (100 mm×2.1 mm, 1.7 µm) with gradient elution. Acetonitrile containing 0.1% (v/v) formic acid and 0.1% (v/v) formic acid aqueous solution were used as mobile phases. The compounds were detected by Full scan/date dependent MS/MS (Full MS/dd-MS2) via heated electrospray ionization (HESI) source. The calibration curves were linear with correlation coefficients (r) greater than 0.997. The limits of detection (LODs) ranged from 0.1 µg/kg to 1.0 µg/kg. The average spiked recoveries of the 25 target compounds were between 70.1% and 108.9% with relative standard derivations (RSDs) from 2.1% to 13.8%. Compared with the previous methods, this method has characteristics of simpler sample preparation and higher sensitivity.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espectrometria de Massas / Resíduos de Drogas / Cromatografia Líquida de Alta Pressão / Alimentos Marinhos Idioma: Zh Revista: Se Pu Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Espectrometria de Massas / Resíduos de Drogas / Cromatografia Líquida de Alta Pressão / Alimentos Marinhos Idioma: Zh Revista: Se Pu Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China