4.7 Article

Rapid and sensitive determination of nine bisphenol analogues, three amphenicol antibiotics, and six phthalate metabolites in human urine samples using UHPLC-MS/MS

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 410, 期 16, 页码 3871-3883

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-018-1062-2

关键词

Bisphenol analogues; Amphenicol antibiotics; Phthalate metabolites; Mixed-mode solid-phase extraction; Ultra performance liquid chromatography-tandemmass spectrometry; Urine sample

资金

  1. National Natural Science Foundation of China [81373089]
  2. Scientific Research Foundation of Shanghai Municipal Commission of Health and Family Planning [201540053]
  3. National Science Fund for Distinguished Young Scholars of China [81325017]
  4. Key Program of the National Natural Science Foundation of China [81630088]

向作者/读者索取更多资源

Bisphenol analogues, amphenicol antibiotics, and phthalate have widely aroused public concerns due to their adverse effects on human health. In this study, a rapid and sensitive method for determination of nine bisphenol analogues, three amphenicol antibiotics, and six phthalate metabolites in the urine based on ultra-high-performance liquid chromatography coupled with triple quadrupole tandem mass spectrometry was developed and validated. The sample pretreatment condition on the base of mixed-mode anion-exchange (Oasis MAX) SPE was optimized to separate bisphenol analogues and amphenicol antibiotics from phthalate metabolites: the former were detected with a mobile phase of 0.1% ammonium water solution/methanol containing 0.1% ammonium water solution in negative mode, whereas the latter were determined with a mobile phase of 0.1% acetic acid solution/acetonitrile containing 0.1% acetic acid in negative mode. The limits of detection were less than 0.26 ng/mL for bisphenol analogues, 0.12 ng/mL for amphenicol antibiotics, and 0.14 ng/mL for phathalate metabolites. The recoveries of all target analytes in three fortification levels ranged from 72.02 to 117.64% with the relative standard deviations of no larger than 14.51%. The matrix effect was adjusted by isotopically labeled internal standards. This proposed method was successfully applied to analyze 40 actual urines and 13 out of 18 studied compounds were detected.

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