website: 86th General Session & Exhibition of the IADR

ABSTRACT: 2358  

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.

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