Interaction of chlorpromazine and trifluoperazine with ionic micelles: electronic absorption spectroscopy studies

The characteristics of binding of two phenothiazine antipsychotic drugs, na mely, chlorpromazine (CPZ) and trifluoperazine (TFP), to cationic cetyltrim ethylammonium chloride (CTAC), zwitterionic N-hexadecyl-N,N-dimethyl-3-ammo nio-1-propanesulfonate (HPS), neutral t-octylphenoxypolyethoxyethanol (TRIT ON X-100) and polyoxyethylene dodecyl ether (Brij-35) micelles were investi gated using electronic absorption spectroscopy. Binding constants K-b and p K(a) values of drugs in micelles were estimated using the red shifts of the maximum absorption upon alkalization or in the presence of detergents. The pK(a) of TFP seems to be shifted by 2.5-4.1 units to lower values in the p resence of different surfactants as compared to the experimental value of p K(a) obtained in buffer which is around 7.0. Consideration of the second pK (a) around 4.0 reported in the literature for TFP leads to a better rationa lization of pK(a) changes for this compound. The changes in pK(a) contribut ed by electrostatic effects are all positive, small for CTAC (+ 0.2), and g reater for HPS (+ 0.9). For CPZ the pK(a) shift due to its interaction with micelles is in the 0.7-2.3 range, the direction of the shift depending on the charge of the polar head. The electrostatic contribution for the shift is great for CTAC (- 0.8) and smaller for HPS (+ 0.2). This result suggests a more polar localization in the micelle of CPZ as compared to TFP. The va lues of binding constants K-b for TFP and CPZ in different protonation stat es show that electrostatic interactions are essential in the affinity of th e drugs to micelles bearing different charges on their headgroups (CTAC, HP S). Data for Brij-35 demonstrate that the additional charge on the TFP ring at pH 2.0 leads to a decrease of binding constant probably due to the repu lsion of the phenothiazine ring from the protons accumulated at the polar h ead of the micelle at acidic pH values. For this micelle at pH 5.0 TFP has a K-b 3-fold greater than that for CPZ while at pH 2.0 K-b for TFP is 3-fol d less than that for CPZ. So, for more hydrophobic TFP electrostatic intera ctions due to protonation of the ring are quite important even considering its penetration into the micelle interior as compared to CPZ. (C) 1999 Else vier Science B.V. All rights reserved.