Abstract

Results of in vitro and in vivo studies clearly indicate that some endodontic sealers may cause local and systemic adverse effects. Though occasionally contradictory data has been reported from various authors, it may be concluded that zinc-oxide-eugenol sealers possess a marked cytotoxic and tissue-irritating potency. Most Ca(OH)2-based materials, however, were biocompatible. Genotoxic effects have been observed with sealers releasing paraformaldehyde or containing mutagenic substances, such as bisphenol-A-diglycidyl-ether or its derivatives. It cannot be excluded that these materials may pose a systemic risk because formaldehyde is rapidly distributed systemically following its application into the pulp cavity. Furthermore an increasing number of cases with an aspergillosis of the maxillary sinus have been observed which were mainly caused by zinc-releasing endodontic sealers. Overall, it is recommended that for endodontic practice, sealers that have been found to be biocompatible in a "mixed bag" of various in vitro and in vivo tests, be selected. From this point of view, ZnOE-sealers should no longer be used for root canal fillings. This recommendation applies also to sealers containing paraformaldehyde or generating this substance during their setting reaction. More experimental and clinical studies are necessary to elucidate whether new materials, such as mineral trioxide aggregate (MTA) or calcium phosphate cement, will be biocompatible alternatives in the future.

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