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Review
. 2021 Sep;100(10):1030-1038.
doi: 10.1177/00220345211026918. Epub 2021 Aug 7.

A Review of Mechano-Biochemical Models for Testing Composite Restorations

Affiliations
Review

A Review of Mechano-Biochemical Models for Testing Composite Restorations

A Zhang et al. J Dent Res. 2021 Sep.

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.

Keywords: biofilms; calibration; composite resins; dental restoration failures; in vitro testing; models.

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Conflict of interest statement

Declaration of Conflicting Interests: The authors declared no potential conflicts of interest with respect to the research, authorship, and/or publication of this article.

Figures

Figure 1.
Figure 1.
This is a clinical picture of a lower molar with a class II tooth-colored restoration. Secondary caries or caries around restoration (CAR) is observed at the buccal margins of the restoration indicated by the asterisk (*).
Figure 2.
Figure 2.
Material parameter determination and failure prediction for dental restoration. (A) Dentin–composite disc specimen used to derive (B) stress–life curves and (C) failure probability parameters for dentin–composite interface. (D) Finite element model used to predict (E) failure probability of restoration versus time, validated with clinical data.
Figure 3.
Figure 3.
Calibration of laboratory fatigue data using clinical data. (A) Clinical data for class II restorations made of Herculite. (B) Laboratory-accelerated fatigue data of dentin–composite discs made with Herculite and (C) relationship between number of laboratory cycles and clinical times to failure for Herculite. *Kopperud SE, Tveit AB, Gaarden T, Sandvik L, Espelid I. 2012. Longevity of posterior dental restorations and reasons for failure. Eur J Oral Sci. 120:539–548.
Figure 4.
Figure 4.
Relationships between dentin demineralization depth and duration for biofilm (Streptococcus mutans) model at different pH values and the in situ data used for calibration. Reprinted from Zhang et al. 2020. Development and calibration of biochemical models for testing dental restorations. Acta Biomateriala 109:132–141, with permission from Elsevier.
Figure 5.
Figure 5.
Comparison of characteristics, advantages, and disadvantages of models for testing resin composite restorations. AFM, atomic force microscopy; CT, computed tomography; OCT, optical coherence tomography; SEM, scanning electron microscopy; TEM, transmission electron microscopy.

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