Liquisolid ibuprofen tablets
Ibuprofen is an antiinflamatory drugs with poor solubility in water but good permeability in the gastrointestinal tract. Liquisolid tablet is the one method of increasing solubility and dissolution rate of ibuprofen. The aims of this study was to determine the effect of glycerine and propylene glicol as non volatile solvent and PVP K-30 as hydrophilic polymer on the dissolution rate of liquisolid ibuprofen tablets. In this research, there are 7 formulas of liquisolid ibuprofen tablets were made. The ratio of ibuprofenin glycerine is 1 : 3 and of propilene glicol is 5:1 with various concentration of PVP K-30 (5, 10, and 15%). Formula I was made as a control so there was no addition of non volatile solvent and hydrophilic polymer. Based on the results, liquisolid ibuprofen tablets using glycerine or propylene glycol as a non volatile solvent and PVP K-30 as a hydrophilic polymer can increase the dissolution rate constant of liquisolid
ibuprofen tablets comparedthat of ibuprofen conventional tablets (non liquisolid). The addition of PVP K-30 as a hydrophilic polymer can increase the dissolution rate constants liquisolid ibuprofen tablets until a concentration of more than 10% because the polymer will swell and form a viscous layer that inhibits the disintegration so that the percent release decrease.
Key words:Ibuprofen, liquisolid, non volatile solvent, hydrophilic polymer.
Anonim, 1979, Farmakope Indonesia, ed. III, Departemen Kesehatan RI, Jakarta.
Anonim, 1995, Farmakope Indonesia, ed. IV, Departemen Kesehatan RI, Jakarta.
Gubbi S. and R. Jarag, 2009, Liquisolid Technique for Enhancement of Dissolution Properties of Bromhexine Hydrochloride, Res. J. Pharm and Tech.,2(2), 382 – 386.
Javadzadeh, Y., M.R. Siahi-Shadbad, S. Asnaashari, and A. Nokhodchi, 2007a, Liquisolid Technique as a Tool for Enhancement of Poorly Water-Soluble Drugs and Evaluation of Their Physicochemical Properties, Acta Pharm, 57, 99 – 109.
Javadzadeh, Y., B. J. Navimipour, and A. Nokhodchi,2007b, Liquisolid Technique for Dissolution Rate Enhancement of a High Dose Water Insoluble Drug (Carbamazepine), Int. J. of Pharmaceutics, 341, 26 – 34.
Khan, K.A., 1975, The Concept of Dissolution Efficiency. J. of Pharm. and Pharmacology.,, 27(1), 48-49.
Ohwoavworhua, F.O., T.A.Adelakun, and A.O. Okhamafe, 2009, Processing Pharmaceutical Grade Microcrystalline Cellulose from Groundnut Husk: Extraction Methods and Characterization, Int. J. of Green Pharmacy, 3(2), 97-104.
Sweetman, S. C., 2009, Martindale The Complete Drug Reference, 36th ed., The Pharmaceutical Press, London.
Voigt, R., 1995, Buku Pelajaran Teknologi Farmasi, Terjemahan S. Noerono dan M. S. Reksohardiprojo, Gadjah Mada University Press, Yogyakarta.
Yadav, V.B. and Yadav, A.V. 2009, Liquisolid granulation technique for tablet manufacturing: an overview. J. of Pharmacy Research 2009, 2(4),670-674.
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