Simultaneous assessment of endogenous thiol compounds by LC–MS/MS
•We develop a mass spectrometry-based method for simultaneous assessment of thiol compounds (GSH, CysGly, Hcy, Cys, and NAC).•The approach is sensitive enough to detect thiols contents in vivo.•The technique tremendously increases detection selectivity.•Chemical derivatization dramatically increases...
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Veröffentlicht in: | Journal of chromatography. B, Analytical technologies in the biomedical and life sciences Analytical technologies in the biomedical and life sciences, 2016-09, Vol.1029-1030, p.213-221 |
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Sprache: | eng |
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Zusammenfassung: | •We develop a mass spectrometry-based method for simultaneous assessment of thiol compounds (GSH, CysGly, Hcy, Cys, and NAC).•The approach is sensitive enough to detect thiols contents in vivo.•The technique tremendously increases detection selectivity.•Chemical derivatization dramatically increases the stability of thiol compounds.
Biological thiol compounds are very important molecules that participate in various physiological events. Alteration in levels of endogenous thiols has been suggested as a biomarker of early stage of pathological changes. We reported a chemical derivatization- and LC–MS/MS-based approach to simultaneously determine thiol compounds including glutathione (GSH), cysteine (Cys), N-acetyl cysteine (NAC), homocysteine (Hcy), and cysteinylglycine (CysGly) in biological samples. Thiol-containing samples were derivatized with monobromobimane (mBrB) at room temperature, followed by LC–MS/MS analysis. Assessment of the analytes with baseline separation was completed within 10min, using a gradient elution on a C18 reversed-phase column. Excellent linearity was observed for all analytes over their concentration ranges of 1–400μM. The lowest limits of detection (S/N=3) in a range from 0.31fmol (for NAC) to 4.98fmol (for CysGly) were achieved. The results indicate that this approach was sensitive, selective, and well suited for high-throughput quantitative determination of the biological thiols. |
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ISSN: | 1570-0232 1873-376X |
DOI: | 10.1016/j.jchromb.2016.06.024 |