Author/Authors :
Tapas، A.R. نويسنده Sudhakarrao Naik Institute of Pharmacy, Pusad-445204, Dist: Yavatmal, Maharashtra, India. , , Kawtikwar، P.S. نويسنده Shri Sureshdada Jain Institute of Pharmaceutical Education and Research, Jamner-424206, Dist: Jalgaon, Maharashtra, India. , , Sakarkar، D.M. نويسنده Department of Pharmacology and Physiology, Sudhakarrao Naik Institute of Pharmacy, Nagpur road Pusad 445204 (M.S) India. ,
Abstract :
Felodipine is a second generation calcium channel blocker widely used as antihypertensive and antianginal drug which belongs to BCS class II category. Hence, its low water solubility limits the pharmacological effect. The aim of this study was to improve the dissolution rate of felodipine using spherical agglomeration technique with acetone, water and dichloromethane as good solvent, poor solvent and bridging liquid, respectively. The quasi emulsion solvent diffusion technique was used as a method for spherical agglomeration. Inutec SP1 was used as an emulsion stabilizer and as hydrophilic polymer in agglomeration process. The FTIR and DSC results showed no change in the drug after crystallization process. PXRD studies showed sharp peaks in the diffractograms of spherical agglomerates with minor reduction in height of the peaks. The particle size of spherical agglomerates (FI-2) was about 134.33 ± 13.57 µm, n=3 and the dissolution efficiency of felodipine up to 120 min increased to about 4-fold in phosphate buffer containing 1.8% Tween 80 (pH 6.8). Spherical agglomerates showed enhanced solubility compared to untreated powder possibly due to the partial conversion to amorphous form.