Abstract
European Journal of Mass Spectrometry
Volume 12 Issue 5, Pages 291–299 (2006)
doi: 10.1255/ejms.818
Determination of dissociation constants of cyclodextrin-ligand inclusion complexes by electrospray ionization mass spectrometry
Huarong Zhang, Hanqi Zhang, Weiqun Jin and Lan Ding
College of Chemistry, Jilin
University, 2699 Qianjin Street, Changchun 130012, PR China
The inclusion complexes of four ligands binding to cyclodextrins (CDs) were studied by electrospray ionization mass spectrometry (ESI-MS) and the dissociation constants of the complexes were obtained. The 1 : 1 stoichiometric inclusion complex was found in the system of CD and fenbufen or aspirin. The obtained KD values of the inclusion complexes of fenbufen binding to α-CD and to β-CD are 4.38 × 104 mol L1 and 2.12 × 104 mol L1, respectively. The KD values of the inclusion complexes of α-CD-aspirin and β-CD-aspirin are 3.33 × 104 mol L1 and 1.83 × 104 mol L1, respectively. A non-linear least squares regression method was applied to validate the results which were consistent with each other. For the system of tetracycline hydrochloride and CD, the 1 : 1 and 1 : 2 stoichiometric inclusion complexes were found in the mass spectra. The KD,1 and KD,2 values of the 1 : 1 and 1 : 2 stoichiometric inclusion complexes of α- CD and tetracycline hydrochloride are 4.47 × 104 mol L1 and 6.51× 104 mol L1, respectively, and those of β-CD and tetracycline hydrochloride are 2.26 × 104 mol L1 and 8.57 × 104 mol L1, respectively. For the system of norfloxacin and CD, besides the 1 : 1 and 1 : 2 inclusion complexes, the 1 : 3 stoichiometric inclusion complex was also found. The KD,1, KD,2 and KD,3 of α- CD and norfloxacin inclusion complexes are 4.61 × 104 mol L1, 6.05 × 104 mol L1 and 1.45 × 103 mol L1, respectively. The three KD values of β-CD and norfloxacin are 1.96 × 104 mol L1, 4.93 × 104 mol L1 and 1.15 × 103 mol L1, respectively.
Keywords: dissociation constant; cyclodextrin; inclusion complex; electrospray ionization; mass spectrometry
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Permalink: http://dx.doi.org/10.1255/ejms.818
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