| Literature DB >> 26186615 |
Sachise Karakawa1, Kazutaka Shimbo2, Naoyuki Yamada2, Toshimi Mizukoshi2, Hiroshi Miyano2, Masashi Mita3, Wolfgang Lindner4, Kenji Hamase5.
Abstract
A highly sensitive and selective chiral LC-MS/MS method for D-alanine, D-aspartic acid and D-serine has been developed using the precolumn derivatization reagents, 6-aminoquinolyl-N-hydroxysuccinimidyl carbamate (AccQ-Tag) or p-N,N,N-trimethylammonioanilyl N'-hydroxysuccinimidyl carbamate iodide (TAHS). The thus N-tagged enantiomers of the derivatized amino acids were nicely separated within 20min using the cinchona alkaloid-based zwittterionic ion-exchange type enantioselective column, Chiralpak ZWIX(+). The selected reaction monitoring was applied for detecting the target d-amino acids in biological matrices. By using the present chiral LC-MS/MS method, the three d-amino acids and their l-forms could be simultaneously determined in the range of 0.1-500nmol/mL. Finally, the technique was successfully applied to rat plasma and tissue samples.Entities:
Keywords: Chiral separation; LC-MS/MS; d-Amino acids
Mesh:
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Year: 2015 PMID: 26186615 DOI: 10.1016/j.jpba.2015.05.024
Source DB: PubMed Journal: J Pharm Biomed Anal ISSN: 0731-7085 Impact factor: 3.935