Simultaneous determination of total homocysteine, cysteine, glutathione, and N-acetylcysteine in brain homogenates by HPLC.
Adrianna KamińskaPatrycja OlejarzKamila BorowczykRafał GłowackiGrażyna ChwatkoPublished in: Journal of separation science (2018)
We have developed a simple, fast, accurate, and cheap method for the simultaneous determination of total cysteine, homocysteine, glutathione, and N-acetylcysteine in brain homogenates based on the reduction of disulfide bonds by tris(2-carboxyethyl) phosphine, pre-column derivatization of free thiol groups with 2-chloro-1-methylquinolinium tetrafluoroborate followed by ion-pair reversed-phase high-performance liquid chromatography separation with ultraviolet detection. The separation of thiol derivatives was achieved in 10 min. Linearity was observed in the range of 10-300, 0.7-10, 2-30, and 3-20 μmol/L homogenate with a limit of detection of 3.7, 0.2, 0.8, and 1.2 μmol/L homogenate for cysteine, homocysteine, glutathione, and N-acetylcysteine, respectively. The precision, calculated as relative standard deviation, was in the range of 1.21-4.77, 1.53-14.35, 0.47-1.92, and 1.61-8.95% for cysteine, homocysteine, glutathione, and N-acetylcysteine, respectively. The presented method was successfully applied to the selective determination of total amino thiols in pig brain tissue samples.
Keyphrases
- simultaneous determination
- high performance liquid chromatography
- solid phase extraction
- liquid chromatography
- tandem mass spectrometry
- liquid chromatography tandem mass spectrometry
- ultra high performance liquid chromatography
- mass spectrometry
- high resolution mass spectrometry
- resting state
- molecularly imprinted
- fluorescent probe
- white matter
- living cells
- gas chromatography mass spectrometry
- gas chromatography
- functional connectivity
- cerebral ischemia
- multiple sclerosis
- single molecule
- subarachnoid hemorrhage