Abstract

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 (r2 ≥ 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.

Highlights

  • An optimal level of amino acids in the body is important for normal homeostasis

  • Quantitative analysis of amino acids by traditional reverse-phase high-performance liquid chromatography (HPLC) is hampered by both the lack of a significant chromophore in many of their structures, which negates the use of UV detection, and by their high polarity, which leads to poor retention on reverse-phase columns

  • This study aimed at the development and validation of a UPLC-qTOF-MS method using Hydrophilic interaction liquid chromatography (HILIC) conditions for absolute quantitation of free amino acids in human urine samples

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Summary

Introduction

An optimal level of amino acids in the body is important for normal homeostasis. They are involved in the regulation of gene expression, cell metabolism and signalling and the biosynthesis of hormones (Wu 2009). Quantification of physiological free amino acids in biofluids is often performed by ion-exchange chromatography with post-column derivatization using ninhydrin as chromophore (Moore et al 1958; Spackman and Moore 1958; Waterval et al 2009) This method typically involves time-consuming derivatization processes and often requires long chromatographic run times of about 2–3 h per sample, and is not suitable for high throughput (Kaspar et al 2009b). The method suffers from lack of analyte specificity due to interference by co-eluting compounds and limits accurate quantitation for some amino acids such as methionine and phenylalanine (Dietzen et al 2008) This technique needs to be performed using dedicated equipment to ensure excellence in reproducibility (Waterval et al 2009)

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