ポスター発表
第3日 6月12日(水) P会場(多目的ホール・大会議室101+102)P1会場(多目的ホール)・P2会場(会議室101+102)
- 3P-23
イブプロフェンとその類似体の負イオン質量分析
(横市大)
o永田遥輝・ 関本奏子
Ibuprofen, a component of antipyretic analgesics, is an aromatic compound with a carboxyl group and is known to exist as ions in vivo. Since many pharmaceuticals contain carboxyl groups, it is expected that understanding the ion structures and stability of ibuprofen will contribute to develop pharmaceutical research. In this study, we measured ibuprofen and its analogues (aromatics with a carboxylic group) using an atmospheric pressure corona discharge ionization collision-induced dissociation mass spectrometry (APCDI-CID-MS) in negative-ion mode. We performed CID experiments on deprotonated molecules for individual analytes. As a result, it was found that there are two conditions to form negative ions with only C and H atoms: (1) stabilization by forming a double bond by 2H loss and broadening the resonance structure, so making it possible to eliminate CO2, and (2) stabilization by forming a benzyl anion at the α carbon of a carboxyl group or a methyl group via CO2 loss.