Wei Lu, Shunbo Zhao, Meng Gong, Luning Sun, Li Ding. Simultaneous determination of acetaminophen and oxycodone in human plasma by LC–MS/MS and its application to a pharmacokinetic study[J]. Journal of Pharmaceutical Analysis, 2018, 8(3): 160-167.
Citation:
Wei Lu, Shunbo Zhao, Meng Gong, Luning Sun, Li Ding. Simultaneous determination of acetaminophen and oxycodone in human plasma by LC–MS/MS and its application to a pharmacokinetic study[J]. Journal of Pharmaceutical Analysis, 2018, 8(3): 160-167.
Wei Lu, Shunbo Zhao, Meng Gong, Luning Sun, Li Ding. Simultaneous determination of acetaminophen and oxycodone in human plasma by LC–MS/MS and its application to a pharmacokinetic study[J]. Journal of Pharmaceutical Analysis, 2018, 8(3): 160-167.
Citation:
Wei Lu, Shunbo Zhao, Meng Gong, Luning Sun, Li Ding. Simultaneous determination of acetaminophen and oxycodone in human plasma by LC–MS/MS and its application to a pharmacokinetic study[J]. Journal of Pharmaceutical Analysis, 2018, 8(3): 160-167.
A simple and rapid liquid chromatography–tandem mass spectrometry (LC–MS/MS) method was de-veloped and validated for simultaneous determination of acetaminophen and oxycodone in human plasma. Acetaminophen-d4 and oxycodone-d3 were used as internal standards. The challenge en-countered in the method development that the high plasma concentration level of acetaminophen made the MS response saturated while the desired lower limit of quantification (LLOQ) for oxycodone was hard to reach was well solved. The analytes were extracted by protein precipitation using acetonitrile. The matrix effect of the analytes was avoided by chromatographic separation using a hydrophilic C18 column coupled with gradient elution. Multiple reaction monitoring in positive ion mode was performed on tandem mass spectrometer employing electrospray ion source. The calibration curves were linear over the concentration ranges of 40.0–8000 ng/mL and 0.200–40.0 ng/mL for acetaminophen and oxycodone, respectively. This method, which could contribute to high throughput analysis and better clinical drug monitoring, was successfully applied to a pharmacokinetic study in healthy Chinese volunteers.