Energetically favorable interactions between diclofenac sodium and cyclodextrin molecules in aqueous media.

作者: S.K. Mehta , K.K. Bhasin , Shilpee Dham

DOI: 10.1016/J.JCIS.2008.06.039

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摘要: Abstract The effect of the addition cyclodextrins (CD) viz., α-, β-, HPβ- and γ-CD to aqueous solutions most widely prescribed anti-inflammatory drug, diclofenac sodium (DS), has been fully investigated by means spectroscopic (UV–vis, steady-sate fluorescence, 1H NMR ROESY) thermodynamic (conductivity) techniques. global picture results indicates that penetrates CD cavity. apparent association constants for all inclusion complexes were estimated from fluorescence data. Conductivity measurements performed both as a function DS concentration concentration, at different temperatures ranging 15 40 °C. Results suggested existence 1:1 complex between CD. thermodynamics system was discussed in terms change Gibbs free energy. Free energy DS/W found decrease on cyclodextrin, which points towards energetically favorable interactions drug cyclodextrin molecules solution phase. chemical shift changes ROESY spectra provide powerful probing CD:DS interactions.

参考文章(38)
Einar Stefánsson, Thorsteinn Loftsson, Cyclodextrins in Eye Drop Formulations Journal of Inclusion Phenomena and Macrocyclic Chemistry. ,vol. 44, pp. 23- 27 ,(2002) , 10.1023/A:1023015201493
Marcus E. Brewster, Roger Vandecruys, Geert Verreck, Marc Noppe, Jef Peeters, A Novel Cyclodextrin-containing Glass Thermoplastic System (GTS) for Formulating Poorly Water Soluble Drug Candidates: Preclinical and Clinical Results Journal of Inclusion Phenomena and Macrocyclic Chemistry. ,vol. 44, pp. 35- 38 ,(2002) , 10.1023/A:1023076631110
Syed Mashhood Ali, Fahmeena Asmat, Spectroscopic Study on Interaction of β‐Cyclodextrin with Triprolidine Hydrochloride Chinese Journal of Chemistry. ,vol. 24, pp. 665- 668 ,(2006) , 10.1002/CJOC.200690127
N. Martínez, E. Junquera, E. Aicart, Ultrasonic, density, and potentiometric characterization of the interaction of gentisic and gallic acids with an apolar cavity in aqueous solution Physical Chemistry Chemical Physics. ,vol. 1, pp. 4811- 4817 ,(1999) , 10.1039/A905591F
Noriaki Funasaki, Seiji Ishikawa, Saburo Neya, Proton NMR Study of α-Cyclodextrin Inclusion of Short-Chain Surfactants Journal of Physical Chemistry B. ,vol. 107, pp. 10094- 10099 ,(2003) , 10.1021/JP034127X
J. R. Moyano, M. J. Arias, J. M. Ginés, J. I. Pérez, A. M. Rabasco, Dissolution Behavior of Oxazepam in Presence of Cyclodextrins: Evaluation of Oxazepam-Dimeb Binary Systemxs Drug Development and Industrial Pharmacy. ,vol. 23, pp. 379- 385 ,(1997) , 10.3109/03639049709146140
A.M.L. Denadai, M.M. Santoro, L.H. Da Silva, A.T. Viana, R.A.S. Santos, R.D. Sinisterra, Self-assembly Characterization of the β-Cyclodextrin and Hydrochlorothiazide System: NMR, Phase Solubility, ITC and QELS Journal of Inclusion Phenomena and Macrocyclic Chemistry. ,vol. 55, pp. 41- 49 ,(2006) , 10.1007/S10847-005-9016-7