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Related Experiment Videos

Chlorhexidine release from room temperature polymerising methacrylate systems.

P D Riggs1, M Braden, M Patel

  • 1Department of Biomaterials in Relation to Dentistry, St. Bartholomew's and the Royal London School of Medicine and Dentistry, Queen Mary Westfield College, University of London, UK.

Biomaterials
|February 3, 2000
PubMed
Summary

This study shows that tetrahydrofurfuryl methacrylate-based polymers release more chlorhexidine due to channel formation. Higher dimethyl-p-toluidine (DMPT) content increased residual monomer leaching.

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Area of Science:

  • Polymer Chemistry
  • Materials Science
  • Biomaterials

Background:

  • Methacrylate monomers form room temperature curing systems when gelled with poly(ethyl methacrylate) powder containing benzoyl peroxide.
  • Chlorhexidine diacetate is an antimicrobial agent often incorporated into dental materials.
  • Understanding drug release mechanisms and polymerization effects is crucial for biomaterial development.

Purpose of the Study:

  • To investigate the release of chlorhexidine diacetate from various methacrylate monomers.
  • To explore the impact of chlorhexidine doping on methacrylate polymerization.
  • To analyze the effect of dimethyl-p-toluidine (DMPT) concentration on polymer properties and leaching.

Main Methods:

  • Gelling of different methacrylate monomers with poly(ethyl methacrylate) powder and benzoyl peroxide.

Related Experiment Videos

  • Doping polymer samples with 5.625% chlorhexidine diacetate.
  • Utilizing Nuclear Magnetic Resonance (NMR) spectroscopy to analyze released substances and residual monomers.
  • Main Results:

    • Tetrahydrofurfuryl methacrylate-based polymers exhibited significantly greater chlorhexidine diacetate release, attributed to channel formation.
    • Chlorhexidine doping hindered polymerization, leading to increased leaching of residual monomers and low molecular weight components.
    • Higher concentrations of dimethyl-p-toluidine (2.5% DMPT) resulted in greater leaching of unpolymerized components.

    Conclusions:

    • Tetrahydrofurfuryl methacrylate is a promising base for drug delivery systems requiring substantial chlorhexidine release.
    • Polymerization inhibition by chlorhexidine and DMPT necessitates careful formulation to minimize leaching of unreacted monomers.
    • The study highlights the interplay between monomer structure, dopant concentration, and resulting polymer properties for controlled release applications.