A V Yadav1, A P Dabke, A S Shete. 1. KIMS University and College of Pharmacy, Karad, Maharashtra, India. avyadav03@rediffmail.com
Abstract
BACKGROUND: Pharmaceutical cocrystallization is a promising alternative for improving the solubility and dissolution rate or manipulating other physical properties of active pharmaceutical ingredients. The objective of this investigation was to study the effect of cocrystallization with different cocrystal formers on physicochemical properties of mefloquine hydrochloride. METHOD: Cocrystals were prepared by solution crystallization method--mefloquine hydrochloride (414.8 mg, 1 mmol) and different cocrystal formers (1/2 mmol) were dissolved in 20 mL of ethanol with warming. Solution was cooled in ice bath for 6 hours. The crystals were isolated by filtration through a membrane (0.45 microm) and dried in the air. The pure drug and the prepared cocrystals were characterized in terms of saturation solubility, drug content, infrared spectroscopy, differential scanning calorimetry, powder X-ray diffraction, scanning electron microscopy, in vitro dissolution studies, and stability studies. RESULTS: The cocrystals showed enhanced solubility and dissolution rate. The cocrystals were found to be stable over the period of 6 months confirmed from stability studies. CONCLUSION: Cocrystals resist the conversion of anhydrous form of drug into its hydrate which is responsible for the drugs less solubility and dissolution rate.
BACKGROUND: Pharmaceutical cocrystallization is a promising alternative for improving the solubility and dissolution rate or manipulating other physical properties of active pharmaceutical ingredients. The objective of this investigation was to study the effect of cocrystallization with different cocrystal formers on physicochemical properties of mefloquine hydrochloride. METHOD: Cocrystals were prepared by solution crystallization method--mefloquine hydrochloride (414.8 mg, 1 mmol) and different cocrystal formers (1/2 mmol) were dissolved in 20 mL of ethanol with warming. Solution was cooled in ice bath for 6 hours. The crystals were isolated by filtration through a membrane (0.45 microm) and dried in the air. The pure drug and the prepared cocrystals were characterized in terms of saturation solubility, drug content, infrared spectroscopy, differential scanning calorimetry, powder X-ray diffraction, scanning electron microscopy, in vitro dissolution studies, and stability studies. RESULTS: The cocrystals showed enhanced solubility and dissolution rate. The cocrystals were found to be stable over the period of 6 months confirmed from stability studies. CONCLUSION: Cocrystals resist the conversion of anhydrous form of drug into its hydrate which is responsible for the drugs less solubility and dissolution rate.
Authors: Dário Silva; Márcio V C Lopes; Željko Petrovski; Miguel M Santos; Jussevania P Santos; Sueli F Yamada-Ogatta; Marcelle L F Bispo; Marcus V N de Souza; Ana Rita C Duarte; Maria C S Lourenço; Raoni Schroeder B Gonçalves; Luis C Branco Journal: Molecules Date: 2022-08-13 Impact factor: 4.927
Authors: Adam J Smith; Padmini Kavuru; Kapildev K Arora; Sheshanka Kesani; Jun Tan; Michael J Zaworotko; R Douglas Shytle Journal: Mol Pharm Date: 2013-06-26 Impact factor: 4.939