Formulation and Evaluation of Modified release Bilayer Tablet of Paracetamol and Diclofenac sodium

Abstract

The main objective of this research work is to develop a stable formulation of a NASAID drugs an immediate release layer of Paracetamol and sustain release layer of Diclofenac sodium are combine to the bilayer and evaluate their pre-compression and post-compression parameters A bilayer tablet comprises first layer formulated for instant release of the paracetamol from a dissolving tablet and a second layer formulated for sustain release Diclofenac sodium from a bilayer tablet The formulation was initiated with preparing granules of both the drug individually by wet granulation method and then then they were compressed to prepare bilayer tablet. The compressed bilayer tablets were evaluated for weight variation, thickness, hardness, friability, in-vitro drug release using USP dissolution apparatus and interaction study by DSC. The optimized Formulation table of formulations F5 formulation was found to be acceptable because it release drug up to 82.11 % of drug release for bilayer Tablet and this batch passed all the evaluation parameters.