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A simple liquid chromatography/differential ion mobility spectrometry tandem mass spectrometry method for the determination of trimethylamine‐ N ‐oxide in human serum: An application in dialysis patients
Author(s) -
Yang Ping,
Li Xiaona,
Yang Wenling,
He Lian,
Yang Li,
Zhang Xianhua
Publication year - 2020
Publication title -
rapid communications in mass spectrometry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.528
H-Index - 136
eISSN - 1097-0231
pISSN - 0951-4198
DOI - 10.1002/rcm.8965
Subject(s) - chemistry , chromatography , formic acid , ammonium formate , mass spectrometry , selected reaction monitoring , trimethylamine n oxide , electrospray ionization , tandem mass spectrometry , liquid chromatography–mass spectrometry , high performance liquid chromatography , hydrophilic interaction chromatography , trimethylamine , biochemistry
Rationale Trimethylamine‐ N ‐oxide (TMAO) is a potential indicator of cardiovascular disease and chronic kidney disorders. It is important to monitor the TMAO level in plasma or serum of hemodialysis patients. A simple liquid chromatography/differential ion mobility spectrometry tandem mass spectrometry (HPLC/DMS‐MS/MS) method was established and validated for the determination of TMAO in the serum of hemodialysis patients. Methods Chromatographic separation was performed on a Waters Atlantis HILIC silica column (2.1 × 50 mm, 3 μm). The gradient mobile phase consisted of 10 mM ammonium formate buffer and acetonitrile with 0.1% formic acid in both solvents. The serum sample was precipitated with acidic acetonitrile prior to HPLC/DMS‐MS/MS analysis and TMAO‐ d 9 was used as the internal standard. Data acquisition was performed in positive ion mode with a DMS system before the electrospray ionization source. The selected reaction monitoring transitions were m / z 76.0 → 58.0 and m / z 85.2 → 66.1 for TMAO and the internal standard, respectively. Results Excellent linearity was observed over the calibration range 0.05–20 μg/mL ( r 2 > 0.995). The method was validated for good specificity and sensitivity. The inter‐run and intra‐run precision and accuracy were less than 13.6% and 10.7%, respectively. Conclusions We established a novel and robust HPLC/DMS‐MS/MS method for the quantification of TMAO in human serum samples. The validated assay was simple, rapid, sensitive and reliable. The developed method could be applied to the assay of serum samples from patients with kidney disease who are undergoing hemodialysis.