• PAYAL D. BORAWAKE Department of Pharmaceutics, Pune District Education Association's Seth Govind Raghunath Sable College of Pharmacy, Saswad, Pune, Maharashtra.
  • KAUSLYA ARUMUGAM Department of Pharmaceutics, Pune District Education Association’s, Seth Govind Raghunath Sable College of Pharmacy, Saswad, Pune, Maharashtra, India
  • JITENDRA V. SHINDE Department of Pharmaceutics, Pune District Education Association’s, Seth Govind Raghunath Sable College of Pharmacy, Saswad, Pune, Maharashtra, India


Objective: The objective of the present research work was the formulation of solid dispersions of simvastatin for enhancement of its aqueous solubility and dissolution rate.

Methods: Simvastatin is Biopharmaceutical Classification System (BCS) Class II (low soluble, and high permeable) drug employed in the treatment of hypercholesterolemia and dyslipidemia. In the present study, solid dispersions were prepared by Kneading and Solvent evaporation methods. The polymeric carriers like Polyethylene glycol (PEG) 6000 and Polyvinyl Pyrrolidone (PVP) K30 were used in different ratios (ratio of drug: carrier was 1:1, 1:2) to formulate solid dispersions. The prepared solid dispersions were characterized by differential scanning calorimetry (DSC), fourier transform infrared spectroscopy (FTIR) and evaluated for drug content, percentage yield, saturation solubility, in vitro dissolution studies. The best formula of the  solid dispersion was selected according to the solubility and dissolution data.

Results: The F7 formulation was found to be optimized formulation containing PVP K30 in the ratio 1:1. It showed the highest amount of drug release at the end of 60 min than other prepared formulations. The FT-IR spectra revealed that there was no interaction between drug and carriers. DSC thermogram indicated entrapment of simvastatin in PVP K30 and amorphous nature of F7 formulation.

Conclusion: The solubility of simvastatin was successfully enhanced through solid dispersion technique. Solid dispersions prepared with solvent evaporation method was more soluble than solid dispersions prepared with kneading method with carrier PVP K30.  

Keywords: Simvastatin, Polymeric carriers, Solid dispersion, Polyvinyl Pyrrolidone K30, Solvent evaporation method, solubility enhancement.


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How to Cite
BORAWAKE, P. D., K. ARUMUGAM, and J. V. SHINDE. “FORMULATION OF SOLID DISPERSIONS FOR ENHANCEMENT OF SOLUBILITY AND DISSOLUTION RATE OF SIMVASTATIN.”. International Journal of Pharmacy and Pharmaceutical Sciences, Vol. 13, no. 7, June 2021, doi:10.22159/ijpps.2021v13i7.41205.
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