ENHANCED INTESTINAL ABSORPTION AND BIOAVAILABILITY VIA PRONIOSOMES FOR BAZEDOXIFENE ACETATE DRUG

  • Smitha Gandra Sri Venkateshwara cllege of pharmacy

Abstract

The main objective of the present study was to develop proniosomal formulations to enhance the oral bioavailability of bazedoxifene acetate by improving solubility, dissolution and/or intestinal permeability. Proniosomal powder formulations were prepared with bazedoxifene acetate drug varying the span 60 and cholesterol ratio in the range of 0.8:0.2 to 0.2:0.8 using maltodextrin as carrier by slurry method. The prepared proniosomal powder was filled into capsules. The bioavailability enhancement of proniosomes loaded with drug was studied focusing on non-ionic surfactants composition and drug:span 60 ratio. Prepared proniosomes were characterized for their particle size distribution, zeta potential, entrapment efficiency, in vitro dissolution study and thermal characteristics to understand the phase transition behavior. Further, the formulated proniosomes were subjected to stability behaviour, ex vivo permeation studies using rat intestine followed by in vivo studies. Physico-chemical studies help in optimization of formulations. Enhancement in dissolution is due to incorporation of bazedoxifene acetate into the non-ionic surfactant and change in the physical state from crystalline to amorphous, thus improving oral bioavailability. Ex vivo studies show significant permeation enhancement across gastrointestinal membrane compared to control. In conclusion, proniosomes provide a powerful and functional way of distribution of inadequately soluble bazedoxefene acetate drug which is proved from in vivo studies based on the enhanced oral delivery.    

Keywords: Nanodrug delivery system

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Gandra, S. “ENHANCED INTESTINAL ABSORPTION AND BIOAVAILABILITY VIA PRONIOSOMES FOR BAZEDOXIFENE ACETATE DRUG”. International Journal of Pharmacy and Pharmaceutical Sciences, Vol. 12, no. 12, Nov. 2020, https://innovareacademics.in/journals/index.php/ijpps/article/view/39576.
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Original Article(s)