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Development and validation of an ultra-performance liquid chromatography quadrupole time of flight mass spectrometry method for rapid quantification of free amino acids in human urine.
Joyce, Richard; Kuziene, Viktorija; Zou, Xin; Wang, Xueting; Pullen, Frank; Loo, Ruey Leng.
Afiliação
  • Joyce R; Medway Metabonomics Research Group, Medway School of Pharmacy, Universities of Kent and Greenwich, Kent, UK.
  • Kuziene V; RJMS Consultancy, Rochester, Kent, UK.
  • Zou X; Medway Metabonomics Research Group, Medway School of Pharmacy, Universities of Kent and Greenwich, Kent, UK.
  • Wang X; Medway Metabonomics Research Group, Medway School of Pharmacy, Universities of Kent and Greenwich, Kent, UK.
  • Pullen F; Medway Metabonomics Research Group, Medway School of Pharmacy, Universities of Kent and Greenwich, Kent, UK.
  • Loo RL; Medway Metabonomics Research Group, School of Science, University of Greenwich, Kent, UK.
Amino Acids ; 48(1): 219-34, 2016 Jan.
Article em En | MEDLINE | ID: mdl-26319643
An ultra-performance liquid chromatography quadrupole time of flight mass spectrometry (UPLC-qTOF-MS) method using hydrophilic interaction liquid chromatography was developed and validated for simultaneous quantification of 18 free amino acids in urine with a total acquisition time including the column re-equilibration of less than 18 min per sample. This method involves simple sample preparation steps which consisted of 15 times dilution with acetonitrile to give a final composition of 25 % aqueous and 75 % acetonitrile without the need of any derivatization. The dynamic range for our calibration curve is approximately two orders of magnitude (120-fold from the lowest calibration curve point) with good linearity (r (2) ≥ 0.995 for all amino acids). Good separation of all amino acids as well as good intra- and inter-day accuracy (<15 %) and precision (<15 %) were observed using three quality control samples at a concentration of low, medium and high range of the calibration curve. The limits of detection (LOD) and lower limit of quantification of our method were ranging from approximately 1-300 nM and 0.01-0.5 µM, respectively. The stability of amino acids in the prepared urine samples was found to be stable for 72 h at 4 °C, after one freeze thaw cycle and for up to 4 weeks at -80 °C. We have applied this method to quantify the content of 18 free amino acids in 646 urine samples from a dietary intervention study. We were able to quantify all 18 free amino acids in these urine samples, if they were present at a level above the LOD. We found our method to be reproducible (accuracy and precision were typically <10 % for QCL, QCM and QCH) and the relatively high sample throughput nature of this method potentially makes it a suitable alternative for the analysis of urine samples in clinical setting.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromatografia Líquida de Alta Pressão / Espectrometria de Massas em Tandem / Aminoácidos Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Cromatografia Líquida de Alta Pressão / Espectrometria de Massas em Tandem / Aminoácidos Idioma: En Ano de publicação: 2016 Tipo de documento: Article