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Formulation development and optimization of Ibuprofen tablets by direct compression method.

Rabia Bushra1, Muhammad Harris Shoaib, Nousheen Aslam

  • 1Department of Pharmaceutics, Faculty of Pharmacy, University of Karachi, Karachi-7520, Pakistan.

Pakistan Journal of Pharmaceutical Sciences
|April 9, 2008
PubMed
Summary

This study optimized ibuprofen (200mg) tablet manufacturing using direct compression. Formulation F-6 demonstrated superior dissolution and assay, confirming direct compression as an effective, cost-efficient pharmaceutical production method.

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Area of Science:

  • Pharmaceutical Technology
  • Drug Manufacturing
  • Formulation Science

Background:

  • Ibuprofen is a widely used analgesic and anti-inflammatory drug.
  • Direct compression offers a cost-effective and simple manufacturing method for pharmaceuticals.
  • This technique is suitable for hygroscopic and thermolabile substances.

Purpose of the Study:

  • To prepare optimized 200mg Ibuprofen tablets using direct compression.
  • To evaluate the impact of diluent, disintegrant, and lubricant variations on tablet quality.
  • To identify the best formulation based on critical quality attributes.

Main Methods:

  • Nine different Ibuprofen tablet formulations were developed using direct compression.
  • Independent variables included diluent (X1), disintegrant (X2), and lubricant (X3).
  • Response variables assessed were weight variation, thickness, dimensions, hardness, friability, disintegration, dissolution, and pharmaceutical assay.

Main Results:

  • All nine formulations met official compendial standards.
  • Formulation F-6 was selected as optimal due to high dissolution (99.05%) and assay (100.04%).
  • F-6 exhibited minimal weight variation, indicating an optimal excipient ratio.

Conclusions:

  • Direct compression is an effective and efficient method for manufacturing Ibuprofen tablets.
  • Formulation optimization is a crucial tool in pharmaceutical product development.
  • The optimized Ibuprofen tablets (F-6) meet quality standards for patient use.