Experimental Resin Cements Containing Bioactive Fillers Reduce Matrix Metalloproteinase-mediated Dentin Collagen Degradation

Raquel Osorio, Monica Yamauti, Salvatore Sauro, Tim Watson, Manuel Toledano

Research output: Contribution to journalArticlepeer-review

60 Citations (Scopus)

Abstract

Introduction: Collagen dentin matrix may represent a suitable scaffold to be remineralized in the presence of bioactive materials. The purpose of this study was to determine if experimental resin cements containing bioactive fillers may modulate matrix metalloproteinase-mediated collagen degradation of etched dentin. 

Methods: Human dentin beams demineralized using 10% phosphoric acid or 0.5 mol/L EDTA were infiltrated with the following experimental resins: (1) unfilled resin, (2) resin with Bioglass 4555 particles (Sylc; OSspray Ltd, London, UK), and (3) resin with beta-tricalcium phosphate-modified calcium silicate cement (HCAT-beta) particles. The filler/resin ratio was 40/60 wt%. The specimens were stored in artificial saliva, and the determination of C-terminal telopeptide (ICTP) was performed by radioimmunoassay after 24 hours, 1 week, and 4 weeks. Scanning electron microscopic analysis of dentin surfaces after 4 weeks of storage was also executed. 

Results: Collagen degradation was prominent both in phosphoric acid and EDTA-treated dentin. Resin infiltration strongly reduced the MMP activity in demineralized dentin. Resin-containing Bioglass 45S5 particles exerted higher and more stable protection of collagen at all tested dentin states and time points. HCAT-beta induced collagen protection from MMPs only in EDTA-treated specimens. Dentin remineralization was achieved when dentin was infiltrated with the resin cements containing bioactive fillers. 

Conclusions: MMP degradation of dentin collagen is strongly reduced in resin-infiltrated dentin. The inclusion of Bioglass 4555 particles exerted an additional protection of collagen during dentin remineralization.

Original languageEnglish
Pages (from-to)1227-1232
Number of pages6
JournalJOURNAL OF ENDODONTICS
Volume38
Issue number9
DOIs
Publication statusPublished - Sept 2012

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