Letters in Drug Design & Discovery

G. Perry
University of Texas
San Antonio, TX
USA
Email: lddd@benthamscience.org

Back

Nimesulide Apparent Solubility Enhancement with Natural Cyclodextrins and their Polymers

Author(s): S. Joudieh, M. Lahiani-Skiba, P. Bon, O. Ba, J. M. Le Breton, M. Skiba.

Abstract:

The object of this work is to investigate physicochemical characteristics and inclusion behavior of binary systems based on cyclodextrin polymer (Poly-CD) or native cyclodextrins (CDs) with a poorly water-soluble, nonsteroidal anti-inflammatory drug, nimesulide (NIM) chemically, N-(4-nitro-2-phenoxyphenyl)methanesulfonamide. Our formulations were studied in solution and solid-state. Drug-cyclodextrin solid binary systems were prepared by the freezedrying method. Phase solubility study was used to evaluate the interaction in solution, between NIM/CDs and NIM/(Poly- CD). The stability constants of NIM/CDs and NIM/(Poly-CD) complexes were calculated using the phase solubility method. The apparent solubility of NIM was enhanced especially with Poly-α-CD (up to78-fold) in neutral aqueous solutions without any organic solvents or surfactants. Copmlexes formation was confirmed, in the solid state, by differential scanning calorimetry, infrared spectroscopy and DRX. Complexation spontaneity of drug with cyclodextrin polymers was highlighted using ΔG°values.

Keywords: Nimesulide (NIM), Polymer of cyclodextrin (Poly-CD), Drug solubilization, Stability constant, Differential scanning calorimetry, Fourier transform infrared spectroscopy, DRX

Order Reprints Order Eprints Rights & PermissionsPrintExport

Article Details

VOLUME: 5
ISSUE: 6
Year: 2008
Page: [406 - 415]
Pages: 10
DOI: 10.2174/157018008785777270
Price: $58