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Journal of Pharmaceutical Innovation

, Volume 6, Issue 4, pp 232–240 | Cite as

Studies on Flash Evaporation for Preparation of Porous Solid Dispersions Using Piroxicam as a Model Drug

  • Manish Dhall
  • Sanju Nanda
  • A. K. MadanEmail author
Research Article

Abstract

An amalgamation of solid dispersion and capillarity has been attempted in present study for enhancement of dissolution rate of poorly soluble drugs. Flash evaporation technique was utilized for enhancement of the dissolution rate of piroxicam. One of the major problems with this drug is its very low solubility in biological fluids, which results in poor bioavailability after oral administration. An attempt was made to enhance the dissolution rate of piroxicam by converting it into porous solid dispersion by flash evaporation method using polyvinylpyrrolidone (PVP) 40,000 as a water-soluble carrier. The resulting solid dispersions were characterized by DSC, FTIR, and X-ray diffraction. In vitro dissolution study revealed significant improvement of dissolution profile of piroxicam. The release of drug from porous solid dispersions containing PVP was superior to those of marketed product, conventional nonporous solid dispersion prepared by solvent evaporation method and drug alone. The steep increase in dissolution rate of porous form is attributable to combined effect of solid dispersion and capillarity.

Keywords

Piroxicam Solid dispersion Polyvinylpyrrolidone Dissolution rate Flash evaporation Capillarity 

Notes

Acknowledgments

Thanks are due to Bangia Pharmaceuticals, Karnal (Haryana), India, for providing gift sample of piroxicam. Thanks are also due to Jubilant Organosys Ltd., Noida, Uttar Pradesh, India, for providing facilities to carry out DSC, FTIR, and XRD studies.

Declaration of Interest

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of the paper.

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Copyright information

© Springer Science+Business Media, LLC 2011

Authors and Affiliations

  1. 1.Faculty of Pharmaceutical Sciences, Pt. B. D. SharmaUniversity of Health SciencesRohtakIndia
  2. 2.Faculty of Pharmaceutical SciencesM.D. UniversityRohtakIndia

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