Complexation study of diclofenac with β-cyclodextrin and spectrofluorimetric determination

The inclusional complexation between the anti-inflammatory pharmaceutical diclofenac and beta-cyclodextrin (beta-CD) was studied by potentiometry, spectrophotometry and spectrofluorimetry, in both acid and neutral pH. Guest-host 1 : 1 stoichiometries for the complexes in both media were determined, and their equilibrium constants were calculated. The values obtained from the different methods used are in very good agreement and are in the order of 10(3). From the analysis of the pK(a) value for diclofenac in both the absence and presence of beta-CD (4.84 and 4.90 respectively), it was inferred that in the inclusion complex the carboxylic group is located outside the cavity. Further structural characterization of the inclusate was carried out by means of H-1 NMR spectra and AM1 semiempirical calculations. Based on the obtained results, a spectrofluorimetric method for the determination of diclofenac in the presence of beta-CD was developed in the range of 0-5 mu g ml(-1). Better limits of detection (0.03 mu g ml(-1)) and quantification (0.1 mu g ml(-1)) were obtained in this latter case with respect to those obtained in the absence of beta-CD. The method was satisfactorily applied to the quantification of diclofenac in pharmaceutical preparations.