A Review of Mechano-Biochemical Models for Testing Composite Restorations. (September 2021)

• Record Type: Journal Article
• Authors: Zhang, A.; Ye, N.; Aregawi, W.; Zhang, L.; Salah, M.; VanHeel, B.; Chew, H.P.; Fok, A.S.L.
• Other Names: Ferracane J.L. guest-editor.; Bertassoni L.E. guest-editor.
• Is Part Of: Journal of dental research. Volume 100:Number 10(2021)
• Page Start: 1030
• Page End: 1038
• Publication Date: 2021-09
• Subjects: composite resins -- biofilms -- dental restoration failures -- models -- in vitro testing -- calibration; Dentistry -- Periodicals; Dentistry -- Social aspects -- Periodicals; Dentistry -- Periodicals; Research -- Periodicals; 617.6005
• DOI: 10.1177/00220345211026918
• Languages: English
• ISSNs: 0022-0345

Abstract

Due to the severe mechano-biochemical conditions in the oral cavity, many dental restorations will degrade and eventually fail. For teeth restored with resin composite, the major modes of failure are secondary caries and fracture of the tooth or restoration. While clinical studies can answer some of the more practical questions, such as the rate of failure, fundamental understanding on the failure mechanism can be obtained from laboratory studies using simplified models more effectively. Reviewed in this article are the 4 main types of models used to study the degradation of resin–composite restorations, namely, animal, human in vivo or in situ, in vitro biofilm, and in vitro chemical models. The characteristics, advantages, and disadvantages of these models are discussed and compared. The tooth–restoration interface is widely considered the weakest link in a resin composite restoration. To account for the different types of degradation that can occur (i.e., demineralization, resin hydrolysis, and collagen degradation), enzymes such as esterase and collagenase found in the oral environment are used, in addition to acids, to form biochemical models to test resin–composite restorations in conjunction with mechanical loading. Furthermore, laboratory tests are usually performed in an accelerated manner to save time. It is argued that, for an accelerated multicomponent model to be representative and predictive in terms of both the mode and the speed of degradation, the individual components must be synchronized in their rates of action and be calibrated with clinical data. The process of calibrating the in vitro models against clinical data is briefly described. To achieve representative and predictive in vitro models, more comparative studies of in vivo and in vitro models are required to calibrate the laboratory studies.