Microparticulated Mefenamic Acid with High Dispersion Stability for Pediatric Dosage Form

Moe Yamazaki1, Emi Shimamura1, Takehisa Hanawa1

  • 1Faculty of Pharmaceutical Sciences, Tokyo University of Science, Tokyo 162-8601, Japan.

Insights

This study optimized mefenamic acid (MFA) suspension by investigating hydroxypropyl cellulose (HPC) molecular weight and concentration. The best dispersion stability was achieved using a specific HPC-SL and SDS mixture, improving MFA particle size and suspension quality.

Area of Science:

  • Pharmaceutical Sciences
  • Materials Science

Background:

  • Mefenamic acid (MFA) is a water-insoluble drug commonly formulated as a suspension.
  • Current MFA suspensions require vigorous shaking due to poor dispersion stability.
  • Previous attempts to improve stability used wet-milling with hydroxypropyl cellulose (HPC), but optimal HPC parameters were unknown.

Purpose of the Study:

  • To determine the optimal molecular weight and concentration of HPC for micronizing MFA.
  • To evaluate the effect of SDS addition on MFA particle size and suspension properties.
  • To identify the ideal combination of HPC-SL and SDS for maximizing MFA suspension dispersion stability.

Main Methods:

  • Investigated various molecular weights and concentrations of HPC for MFA micronization.
  • Utilized wet-milling techniques for particle size reduction.
  • Assessed the impact of sodium dodecyl sulfate (SDS) as a co-surfactant.
  • Analyzed particle size and dispersion stability of the prepared MFA suspensions.

Main Results:

  • MFA particles were successfully micronized, resulting in finer particles.
  • The addition of SDS further reduced particle size compared to HPC alone.
  • Optimal dispersion stability was achieved with a mixed aqueous solution of 1.0% HPC-SL and 0.12% SDS.

Conclusions:

  • The combination of SDS and 1.0% HPC-SL aqueous solution is optimal for enhancing MFA suspension dispersion stability.
  • This formulation significantly improves the physical properties of mefenamic acid suspensions.
  • The findings provide a basis for developing more stable and effective MFA drug delivery systems.

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