FORMULATION DEVELOPMENT AND EVALUATION OF LIQUISOLID SYSTEMS TO IMPROVE THE DISSOLUTION RATE OF KETOPROFEN

Abstract

Liquisolid compacts were used to formulate water insoluble drugs in non-volatile solvents and converting into acceptably flowing and compressible powders. The main objective of present investigation was to enhance the dissolution rate of water insoluble drug ketoprofen by using liquisolid technique. Several liquisolid tablets were prepared by using different carrier materials such as microcrystalline cellulose (Avicel pH-101), starch, dicalcium phosphate and lactose, and coating material such as silica gel, respectively. Polyethylene glycol 400 was used as non volatile water miscible liquid vehicle. The liquid loading factors for such liquid vehicle was calculated to obtain the optimum amounts of carrier and coating materials necessary to produce acceptable flowing and compactable powder admixtures viable to produce compacts. The ratio of carrier to coating material was kept constant in all formulations at 20 to 1. Before compression, powdered mass were evaluated for various parameters like flow properties, content uniformity etc.