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作 者:Qing Xuan XU Li LI Hao YUE Zhi Qiang LIU Ming Quart GUO Shu Ying LIU
出 处:《Chinese Chemical Letters》2006年第1期65-68,共4页中国化学快报(英文版)
基 金:supported by the National Natural Science Foundation of China(No.30472134,20173057);the State Great Basic Research Project of China(No.2003CCA03100);the Great Research Project of Chinese Academy of Sciences(No.KGCX2-SW-213-06).
摘 要:The non-covalent complexes between lappaconitine (LA) and β-cyclodextrin (β-CD) have been detected and characterized by electrospray ionization combined with ion trap tandem mass spectrometry (ESI-MSn). The experimental results showed that only 1:1 non-covalent complex can be formed in different starting molar ratios of LA to β-CD. Furthermore, the diagnostic fragmentation of the β-CD-LA complex, with a significant contribution of covalent fragmentation of LA leaving the N-acetyl anthranoyl (AN) moiety inserted to β-CD, provided the convincing evidence for the formation of non-covalent complex between LA and β-CD and the cite of LA molecule included to cavity of β-CD assigned to AN residue.The non-covalent complexes between lappaconitine (LA) and β-cyclodextrin (β-CD) have been detected and characterized by electrospray ionization combined with ion trap tandem mass spectrometry (ESI-MSn). The experimental results showed that only 1:1 non-covalent complex can be formed in different starting molar ratios of LA to β-CD. Furthermore, the diagnostic fragmentation of the β-CD-LA complex, with a significant contribution of covalent fragmentation of LA leaving the N-acetyl anthranoyl (AN) moiety inserted to β-CD, provided the convincing evidence for the formation of non-covalent complex between LA and β-CD and the cite of LA molecule included to cavity of β-CD assigned to AN residue.
关 键 词:LAPPACONITINE Β-CYCLODEXTRIN non-covalent complex ESI-MS CID.
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