Characterization of The Human Tear Metabolome by LC-MS/MS

被引:103
作者
Chen, Liyan [1 ,2 ]
Zhou, Lei [1 ,3 ]
Chan, Eric C. Y. [2 ]
Neo, Jason [4 ]
Beuerman, Roger W. [1 ,3 ,5 ]
机构
[1] Singapore Eye Res Inst, Singapore, Singapore
[2] Natl Univ Singapore, Fac Sci, Dept Pharm, Singapore 117548, Singapore
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Ophthalmol, Singapore 117595, Singapore
[4] AB Sciex Singapore, Singapore, Singapore
[5] DUKE NUS Grad Med Sch, SRP Neurosci & Behav Disorder, Singapore, Singapore
基金
英国医学研究理事会;
关键词
metabonomics; metabolic profiling; tear fluid; liquid chromatography mass spectrometry; isotope pattern; tear metabolites; biomarkers; chemometric; information dependent acquisition; metabolomics; TANDEM MASS-SPECTROMETRY; HYDROPHILIC INTERACTION; LIQUID-CHROMATOGRAPHY; TOF-MS; IDENTIFICATION; FLUID; GLUCOSE; PROTEINS; REVEALS;
D O I
10.1021/pr2004874
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The tear film overlying the epithelial cells of the eye's surface is vital to visual function, and its composition is reflective of ocular surface health. The ultrasmall volume of tears poses challenges in its analysis, contributing to the limited number of reports on the tear metabolome. In addition, using a standard clinical method of tear collection posed some confounding factors in metabonomic analysis. We sought to establish an analytical platform for the global characterization of human tear metabolites. Following information dependent acquisition (IDA) directed liquid chromatography tandem mass spectrometry (LC-MS/MS), isotope pattern matched peak mining was performed using Extracted Ion Chromatogram (XIC) manager within the PeakView software. Sixty metabolites representing diverse compound classes were identified in human tears, most of which have not been previously reported. Selected metabolites were verified using pure standards. Unsupervised chemometric analysis showed good separation between tear samples and blanks (PC1 = 87%, R-2 = 0.91, Q(2) = 0.87). The results demonstrated the potential of our platform for untargeted metabonomic studies of eye diseases.
引用
收藏
页码:4876 / 4882
页数:7
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