4.7 Article

Simultaneous determination of methionine cycle metabolites, urea cycle intermediates and polyamines in serum, urine and intestinal tissue by using UHPLC-MS/MS

期刊

TALANTA
卷 224, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.talanta.2020.121868

关键词

Polyamines; Urea cycle intermediates; Methionine cycle metabolites; UIIPLC-MS/MS; Biological matrices; Thyroid disorder

资金

  1. Interdisciplinary Research Matching Scheme (IRMS) of Hong Kong Baptist University [RC-IRMS/13-14/03]
  2. Research Grants Council [RGCGRF 14114615]
  3. Hong Kong PhD Fellowship Scheme (HKPFS)

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The study developed a UHPLC-ESI-MS/MS method to simultaneously determine the levels of 14 metabolites, including methionine metabolism metabolites, urea cycle intermediates, and polyamines. The method showed good selectivity, linearity, recovery, and was successfully applied in urine, serum, and tissue matrices, promising to provide more information in metabolomics research.
Metabolites of methionine cycle, urea cycle and polyamine metabolism play important roles in regulating the metabolic processes and the development of diseases. It is rewarding and interesting to monitor the levels of the above metabolites in biological matrices to investigate pathological mechanisms. However, their quantitation is still unsatisfactory due to the poor retention behavior of the analytes on the traditional reversed-phase column. And never a single analytical method simultaneously quantify these three classes of metabolites. Besides, the concentrations of some metabolites are too low to be detected in the biological samples. In this study, we developed a UHPLC-ESI-MS/MS method to simultaneously determine the levels of 14 metabolites, including 4 methionine metabolism metabolites (methionine, homocysteine, S-adenosylmethionine and S-adenosylhomocysteine), 3 urea cycle intermediates (arginine, citrulline and ornithine) and 7 polyamines (putrescine, spermidine, spermine, N-1-acetylputrescine, N-1-acetylspermidine, N-1-acetylspermine and N-1,N-12-diacetylspermine). The chromatographic separation was performed on the BEH amide column within 14 min using water and acetonitrile (both with 0.1% formic acid) as the mobile phases. The results of method validation showed good selectivity, linearity (r(2) > 0.99), recovery (93.1%-112.1%), inter-day and intra-day precision (RSD < 13.6% and RSD < 11.0%, respectively), stability (RSD < 15.1%) and matrix effect (76.0%-113.2%). The method is simple, quick and sensitive without derivatization processes and the use of ion-pairing reagents. This approach was successfully applied in urine, serum and tissue matrices, as well as in identifying potential biomarkers for hyperthyroidism and hypothyroidism. The method is promising to provide more information on pathophysiological mechanisms in metabolomics study.

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