
doi: 10.1248/cpb.40.2810
Self-association of irinotecan hydrochloride (CTP-11) in an aqueous solution was studied using UV, circular dichroism (CD), 1H-NMR and the quasi-elastic light scattering (QLS) method. The UV spectra showed a hypochromic effect in the aqueous solution. In the CD spectra, typically positive Davydov splitting was observed and the Δe value was reduced sigmoidally when the concentraion of CTP-11 was decreased. In the 1H-NMR, the aromatic signals of higher concentration shifted to a diamagnetic direction compared with those of lower concentration. These observations suggested that CPT-11 molecules are present as monomer in the lower concentration, and the self-association with positive helicity occurs by vertical stacking more than 10 μM of concentration. Its molecules form complete aggregates at more than 2 mM of the concentration. Results of QLS which coincided in the prediction of partition coefficient experiments suggested that CPT-11 molecules formed dimer under the condition. By the regression analysis of CD spectral data, the equilibrium constant for the self-association was calculated to be 2.41×10-4 M-1.
CD spectrum, UV spectrum, CPT-11, quasi-elastic light scattering, camptothecin, ^1H-NMR, irinotecan hydrochloride trihydrate, partition coefficient, self-association
CD spectrum, UV spectrum, CPT-11, quasi-elastic light scattering, camptothecin, ^1H-NMR, irinotecan hydrochloride trihydrate, partition coefficient, self-association
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