Genotoxicity evaluation of five different dentin bonding agents by chromosomal aberration analysis

summary  Dentin bonding agents became unavoidable in today's aesthetic restorative dentistry. Nevertheless, more and more evidences on their possible cytotoxity and/or genotoxicity emerge. Still, only limited number of studies has been published on that issue. In our work we evaluated possible...

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Published in:Journal of oral rehabilitation Vol. 33; no. 6; pp. 462 - 471
Main Authors: PRICA, D., GALIĆ, N., ŽELJEŽIĆ, D., PRICA, A.
Format: Journal Article
Language:English
Published: Oxford, UK Blackwell Publishing Ltd 01-06-2006
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Summary:summary  Dentin bonding agents became unavoidable in today's aesthetic restorative dentistry. Nevertheless, more and more evidences on their possible cytotoxity and/or genotoxicity emerge. Still, only limited number of studies has been published on that issue. In our work we evaluated possible genotoxicity of five different adhesives: AdperTR Single Bond, AdperTR Single Bond 2 with nanofiller, Excite®, OptiBond® Solo PlusTR and PromptTR L‐pop. Genotoxicity assessment was carried out on human lymphocytes in vitro, using chromosomal aberration analysis. Polymerized adhesives were tested at three different dilutions of the 0·5 g mL−1 eluate stock (2·5 × 1:106, 1:106 and 1:105) after 1 h, 24 h and 5 days of elution. Slight but significant increase in the number of chromatid breaks was observed after 24‐h elution period, for adhesives AdperTR Single Bond 2, Excite®, and OptiBond® Solo PlusTR at dilutions of 1:106 and 1:105, and for other two only at dilution of 1:105. First three adhesives also appeared to be slightly genotoxic after 1 h of elution but only at 1:105. As a bonding agent remains in close contact with living dental tissue over a long period of time, information on their possible genotoxicity and carcinogenicity should be more clearly clarified in the near future.
Bibliography:istex:A10348A7087A6DBD6D485CEB2DBF419FD2910A7B
ArticleID:JOOR1606
ark:/67375/WNG-3ZF314BP-K
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
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ISSN:0305-182X
1365-2842
DOI:10.1111/j.1365-2842.2006.01606.x