ENHANCING SOLUBILITY AND DISSOLUTION OF MEFENAMIC ACID BY FREEZE DRYING USING β-CYCLODEXTRIN 

Journal Title: International Research Journal of Pharmacy (IRJP) - Year 2011, Vol 2, Issue 9

Abstract

Mefenamic acid, an anti-inflammatory drug, exhibits poor water solubility, dissolution and flow properties. Thus, the aim of the present study was to improve the solubility and dissolution rate of Mefenamic acid by preparing microparticle by Freeze drying technique. Mefenamic acid microparticle containing different ratio of β-cyclodextrin were produced by Freeze drying using water and Isopropyl alcohol as solvent system to enhance solubility and dissolution rate. The prepared formulations containing different ratio of drug and polymer were evaluated for in vitro dissolution and solubility. The prepared formulations were characterized by scanning electron microscopy, differential scanning calorimeter, X-ray diffraction and Fourier transform infrared spectroscopy. Dissolution profile of the Freeze dried microparticle was compared with its physical mixture and pure sample. Freeze dried microparticle exhibited decreased crystallinity and the solubility and dissolution of the microparticle containing different ratio of drug and β-cyclodextrin were significant improved compared with its physical mixture and pure sample of Mefenamic acid. Dissolution of microparticle containing 1:3 w/w (FD 3) showed higher % release i.e. 98.6 % in 60 min compare to other formulation. Consequently, hence, from the above result it can be conclude that Freeze dried microparticle of Mefenamic acid is a useful technique to improve the solubility and dissolution of poorly water soluble drug like Mefenamic acid.  

Authors and Affiliations

Mudit Dixit , Yoshita Bhardwaj, Parthasarathi Kulkarni , Selvam Panner

Keywords

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  • EP ID EP150698
  • DOI -
  • Views 113
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How To Cite

Mudit Dixit, Yoshita Bhardwaj, Parthasarathi Kulkarni, Selvam Panner (2011). ENHANCING SOLUBILITY AND DISSOLUTION OF MEFENAMIC ACID BY FREEZE DRYING USING β-CYCLODEXTRIN . International Research Journal of Pharmacy (IRJP), 2(9), 146-150. https://europub.co.uk./articles/-A-150698