| Literature DB >> 29944873 |
Alexander Bollenbach1, Erik Hanff1, Bibiana Beckmann2, Ruan Kruger3, Dimitrios Tsikas4.
Abstract
Circulating and excretory NG,N´G-dimethyl-l-arginine (symmetric dimethylarginine, SDMA) and NG,NG-dimethyl-l-arginine (asymmetric dimethylarginine, ADMA) are cardiovascular risk factors. Despite close chemical structures, the gas chromatography-mass spectrometry (GC-MS) measurement of SDMA is remarkably more difficult than that of ADMA for as yet unknown reasons. Here, we describe an improved GC-MS method for the quantitative determination of SDMA in human urine using commercially available NG,N´G-di-[2H3]methyl-l-arginine (d6-SDMA) as internal standard. The method is based on a single derivatization step with pentafluoropropionic anhydride (PFPA) in ethyl acetate (30 min, 65 °C) to N,N,N,O-tetrakis-pentafluoropropionyl derivatives, electron-capture negative-ion chemical ionization and selected-ion monitoring of the mass-to-charge (m/z) ions of m/z 456 for SDMA and m/z 462 for d6-SDMA.Entities:
Keywords: ADMA; Deuterium; Guanidine methylation; Pentafluoropropionic anhydride; SDMA
Mesh:
Substances:
Year: 2018 PMID: 29944873 DOI: 10.1016/j.ab.2018.06.021
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365