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[Simultaneous determination of six estrogens in dairy products by high performance liquid chromatography-triple quadrupole-ion trap mass spectrometry coupled with matrix solid-phase dispersion and solid phase extraction].
Han, Shuying; Yu, Huimin; Song, Yilin; Deng, Haishan; Chai, Chuan; Chi, Yumei.
Afiliación
  • Han S; College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Yu H; College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Song Y; College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Deng H; College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Chai C; College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
  • Chi Y; College of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.ymchii@njutcm.edu.cn.
Se Pu ; 36(3): 285-291, 2018 Mar 08.
Article en Zh | MEDLINE | ID: mdl-30136507
Matrix solid-phase dispersion (MSPD) and solid-phase extraction (SPE) were respectively developed for the pretreatment six estrogens in milk powder and liquid milk. It was implied that MSPD was suitable for the treatment of milk powder, while SPE was suitable for liquid milk treatment. Based on the optimized pretreatment procedures, the method for the simultaneous determination of the six estrogens in different dairy products was established by high performance liquid chromatography-triple quadrupole-ion trap mass spectrometry (HPLC-Q-TRAP-MS). The proposed method provided low limits of detection (LODs, 0.01-0.05 mg/L) and limits of quantification (LOQs, 0.05-0.10 mg/L), wide linearity range of 0.1-200 mg/L (except for estriol of 0.1-20 mg/L) with excellent correlation coefficients (R2)> 0.99. The average recoveries of the six estrogens in milk powder pretreated by MSPD ranged from 71.8% to 106.0% with RSD of 1.6%-9.2% (n=3), while the corresponding average recoveries in liquid milk pretreated by SPE ranged from 70.3% to 108.4% with RSD of 2.0% and 11.0% (n=3) with spiking levels of 1.0, 5.0, and 10 mg/kg, respectively. This sensitive and reliable method meets the demand for the analysis of trace estrogen residues in complex matrices.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromatografía Líquida de Alta Presión / Productos Lácteos / Leche / Estrógenos Límite: Animals Idioma: Zh Revista: Se Pu Año: 2018 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Cromatografía Líquida de Alta Presión / Productos Lácteos / Leche / Estrógenos Límite: Animals Idioma: Zh Revista: Se Pu Año: 2018 Tipo del documento: Article País de afiliación: China
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