Development And Characterization of Bilayered Tablet of Paracetamol & Diclofenac Sodium

By defining a bilayer tablet with a immediate release layer of paracetamol and a sustain release layer of diclofenac sodium, and by evaluating their pre-compression and post-compression parameters, the primary goal of this research project is to create a steady detailing of a NASAID. A bilayer tablet consists of a moment layer for support discharge of diclofenac sodium and a layer for moment discharge of paracetamol. At that point, the bilayer tablet is planned by weighing all necessary fixings and following the coordinated compression strategy. Using a USP disintegration device, the compressed bilayer tablets were evaluated for weight variety, thickness, hardness, friability, and in-vitro sedate discharge. Since it discharges medication up to 82.11% of sedate discharge for bilayer tablets and this group met all assessment criteria, the optimized Detailing table of definitions F5 definition was deemed worthy.

Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-03-17
DOI
https://doi.org/10.5281/zenodo.15041970
Primary Topic
Drug Solubulity and Delivery Systems
Type
article
Field-Weighted Citation Impact
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article

Development And Characterization of Bilayered Tablet of Paracetamol & Diclofenac Sodium

Zenodo (CERN European Organization for Nuclear Research)
Drug Solubulity and Delivery Systems
article

Development And Characterization of Bilayered Tablet of Paracetamol & Diclofenac Sodium

article en

Abstract

By defining a bilayer tablet with a immediate release layer of paracetamol and a sustain release layer of diclofenac sodium, and by evaluating their pre-compression and post-compression parameters, the primary goal of this research project is to create a steady detailing of a NASAID. A bilayer tablet consists of a moment layer for support discharge of diclofenac sodium and a layer for moment discharge of paracetamol. At that point, the bilayer tablet is planned by weighing all necessary fixings and following the coordinated compression strategy. Using a USP disintegration device, the compressed bilayer tablets were evaluated for weight variety, thickness, hardness, friability, and in-vitro sedate discharge. Since it discharges medication up to 82.11% of sedate discharge for bilayer tablets and this group met all assessment criteria, the optimized Detailing table of definitions F5 definition was deemed worthy.

Zenodo (CERN European Organization for Nuclear Research)
Openalex Percentile: Top 59%
Drug Solubulity and Delivery Systems
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Development And Characterization of Bilayered Tablet of Paracetamol & Diclofenac Sodium · Zenodo (CERN European Organization for Nuclear Research) (2025) | TGRS Research Map | TGRS