A SIMPLE EFFORT TO ENHANCE SOLUBILITY AND DISSOLUTION RATE OF SIMVASTATIN USING CO-CRYSTALLIZATION

Authors

  • Iyan Sopyan
  • Achmad Fudholi Departement of Pharmaceutical and Technolgy Formulation of University of Gadjah Mada, Yogyakarta, 55281, Indonesia.
  • Muchtaridi Muchtaridi
  • Ika Puspitasari

Keywords:

Simvastatin, Co-crystal, Solubility, Dissolution

Abstract

Objective: The main objective of this study was to explore co-crystallization as an effort to enhance the solubility of simvastatin (SV) using tartaric acid (TA) as co-former.

Methods: The simulation of molecular modeling of TA against SV has been done by in silico using auto dock 4.2. A preparation of co-crystal carried out by using solvent drops grinding (SGD) with an equimolar ratio. A co-crystal formed was confirmed by scanning electron microscopy (SEM), saturated solubility test, in vitro dissolution test, infrared spectrophotometry (FTIR), powder X-ray diffraction (PXRD), and differential scanning calorimetry (DSC).

Results: The in silico studies showed that the interaction of TA and SV has synthon molecular by hydrogen bonding. An increasing of solubility and in vitro dissolution profile of co-crystal resulted as compared to the value of pure SV and its physical mixer. Characterizations of a co-crystal SV: TA (1: 1) including SEM, FTIR, PXRD, and DSC have indicated the formation of new solid crystal phase that different compared to SV, TA, and its physical mixture.

Conclusion: The co-crystallization has been used to enhance the solubility and dissolution of simvastatin. All characterization either in silico and in vitro has shown the formation of co-crystal SV: TA (1:1).

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Published

01-08-2016

How to Cite

Sopyan, I., A. Fudholi, M. Muchtaridi, and I. Puspitasari. “A SIMPLE EFFORT TO ENHANCE SOLUBILITY AND DISSOLUTION RATE OF SIMVASTATIN USING CO-CRYSTALLIZATION”. International Journal of Pharmacy and Pharmaceutical Sciences, vol. 8, no. 8, Aug. 2016, pp. 342-6, https://journals.innovareacademics.in/index.php/ijpps/article/view/13086.

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