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超高效液相色谱-四极杆飞行时间质谱法用于快速定量人尿中游离氨基酸的方法开发与验证

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.

作者信息

Joyce Richard, Kuziene Viktorija, Zou Xin, Wang Xueting, Pullen Frank, Loo Ruey Leng

机构信息

Medway Metabonomics Research Group, Medway School of Pharmacy, Universities of Kent and Greenwich, Kent, UK.

RJMS Consultancy, Rochester, Kent, UK.

出版信息

Amino Acids. 2016 Jan;48(1):219-34. doi: 10.1007/s00726-015-2076-0. Epub 2015 Aug 29.

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 (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.

摘要

建立了一种采用亲水相互作用液相色谱的超高效液相色谱四极杆飞行时间质谱(UPLC-qTOF-MS)方法,并对其进行了验证,用于同时定量尿液中的18种游离氨基酸,每个样品的总采集时间(包括柱重新平衡)少于18分钟。该方法涉及简单的样品制备步骤,即用乙腈稀释15倍,最终组成是25%的水相和75%的乙腈,无需任何衍生化。我们校准曲线的动态范围约为两个数量级(从最低校准曲线点起为120倍),线性良好(所有氨基酸的r(2)≥0.995)。使用校准曲线低、中、高浓度范围的三个质量控制样品,观察到所有氨基酸的良好分离以及良好的日内和日间准确度(<15%)和精密度(<15%)。我们方法的检测限(LOD)和定量下限分别约为1-300 nM和0.01-0.5 µM。发现制备的尿液样品中的氨基酸在4°C下72小时、经过一次冻融循环后以及在-80°C下长达4周内均稳定。我们已将此方法应用于定量来自一项饮食干预研究的646份尿液样品中18种游离氨基酸的含量。如果这些尿液样品中18种游离氨基酸的含量高于检测限,我们就能对其进行定量。我们发现我们的方法具有可重复性(QCL、QCM和QCH的准确度和精密度通常<10%),并且该方法相对较高的样品通量特性可能使其成为临床环境中尿液样品分析的合适替代方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ade2/4710665/a9f7ebf1e5bc/726_2015_2076_Fig1_HTML.jpg

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