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An Assessment of Residual Monomer in Endodontic Retrofill Material
C. RHIEU, S. CHOGLE, A. MICKEL, S. SHAIKH, R. REESE, and S. POTLURI, Case Western Reserve University, Cleveland, OH, USA | BACKGROUND: Polymer-Clay Nanocomposites(PNC) are a new
class of polymeric materials composed of nano-sized clay particles that have high
aspect ratios(20-1000) and high surface areas. When dispersed in a polymer
matrix, the nanoparticles tremendously improve overall strength, dimensional stability,
and drug elution control of the matrix. A previous in vitro study
reported that an endodontic retrofill using a Polymer/Monomer Matrix(PMM) with nanocomposite
significantly reduced apical bacterial leakage(p<0.01) than the commercially
available Geristore®. In the same study, however, Geristore® showed lower
leakage than PMM without nanocomposite. HYPOTHESIS: This finding is due to
a lower degree of polymerization in the PMM material. OBJECTIVES: The
objective of this study was to identify and evaluate the release of unpolymerized/residual
monomer and to compare two photoinitiator formulae in reducing residual monomer
release. METHODS: Two monomer matrices(MM) were compared—MM1: 2,2-bis[p-(2-hydroxy-3-methacryloxypropoxy)phenyl]propane(Bis-GMA),
triethylene-glycol-dimethacrylate(TEGDMA), and hydroxyl-ethyl-methacrylate(HEMA);
and MM2: HEMA and urethane-dimethacrylate(UDMA). Each monomer matrix was
photopolymerized with each of the two formulae of photoinitiators, I1(Camphorquinone
and ethyl-4-N,N-dimethylaminobenzoate) and I2(Camphorquinone, ethyl-4-N,N-dimethylaminobenzoate,
2-dimethyl-amino-ethylmethacrylate, and Diphenyliodonium-chloride) at 20, 40,
and 60seconds. Kinetic UV absorbance was utilized to identify the release of
residual monomer in sterile water over a 5-day period. Photoinitiator formulae
I1 and I2 were compared using 1H NMR analysis to
determine the presence of unpolymerized monomer. RESULTS: The UV
absorbance results showed a release of unpolymerized HEMA from both monomer
groups coupled with I1. The 1H NMR analysis revealed alkene
proton peaks for monomer groups with the I1 formula confirming
the existence of unpolymerized HEMA. These were not observed in
the polymerization utilizing the I2 formula indicating a great
reduction of unpolymerized HEMA. There was no significant difference among 20,
40, and 60seconds of photopolymerization(p<0.01). CONCLUSION: Based
on this pilot study, future experiments will compare PMMs with I2
formula.
| Seq #222 - Dental Polymers 3:30 PM-4:45 PM, Friday, July 4, 2008 Metro Toronto Convention Centre Exhibit Hall D-E |
Back to the Dental Materials 5: Polymer-based Materials - Chemistry and Composition Program
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