FORMULATION AND EVALUATION OF LORNOXICAM TABLET BY PRESS COATING METHOD FOR PULSATILE DRUG DELIVERY SYSTEM

The lag time and time controlled release behavior of Ivabradine from press coated tablets could be modulated by varying the concentration of polymer in outer coating layer

polymers (HPMC E15& E50) and coated using pH sensitive polymer (Eudragit L100) and evaluated for lag time and in vitro drug release.  The lag time and in vitro

The compression coated tablets consisted of a core tablet containing drug with natural ocimum gratissimum mucilage a novel superdisintegrant used, which was further

The formulated pulsatile tablets were evaluated for weight variation, hardness, % friability, % drug content and in- vitro drug

Then the pulsatile tablets were evaluated for various tests and drug release studies were conducted for pH 6.8 buffer and optimized formulation which showed satisfactory

Development of pulsatile release tablets: Pulsatile release tablets were prepared by coating core tablets with an inner swelling layer comprising of HPMC E5 20% w/w of core tablet

The aim of present study is to formulate and evaluate Flurbiprofen Pulsatile Drug Delivery system by press coated method to mimic the circadian rhythm of the

Lag time and In vitro drug release profile of PRTs Based on release characteristics RRT1 core tablet was utilized in the development of press-coated tablets.. The profiles relevant