A critical analysis of research methods and experimental models to study biocompatibility of endodontic materials. (28th February 2022)

• Record Type: Journal Article
• Authors: Hosseinpour, Sepanta; Gaudin, Alexis; Peters, Ove A.
• Other Names: Dummer Paul guestEditor.
• Is Part Of: International endontic journal. Volume 55(2022)Supplement 2
• Page Start: 346
• Page End: 369
• Publication Date: 2022-02-28
• Subjects: animal testing -- biocompatibility -- cytotoxicity -- endodontic materials -- genotoxicity -- mutagenicity; Endodontics -- Periodicals; 617.6342
• DOI: 10.1111/iej.13701
• Languages: English
• ISSNs: 0143-2885

Abstract

Abstract: Materials used for endodontics and with direct contact to tissues have a wide range of indications, from vital pulpal treatments to root filling materials and those used in endodontic surgery. In principle, interaction with dental materials may result in damage to tissues locally or systemically. Thus, a great variety of test methods are applied to evaluate a materials' potential risk of adverse biological effects to ensure their biocompatibility before commercialization. However, the results of biocompatibility evaluations are dependent on not only the tested materials but also the test methods due to the diversity of these effects and numerous variables involved. In addition, diverse biological effects require equally diverse assessments on a structured and planned approach. Such a structured assessment of the materials consists of four phases: general toxicity, local tissue irritation, pre‐clinical tests and clinical evaluations. Various types of screening assays are available; it is imperative to understand their advantages and limitations to recognize their appropriateness and for an accurate interpretation of their results. Recent scientific advances are rapidly introducing new materials to endodontics including nanomaterials, gene therapy and tissue engineering biomaterials. These new modalities open a new era to restore and regenerate dental tissues; however, all these new technologies can also present new hazards to patients. Before any clinical usage, new materials must be proven to be safe and not hazardous to health. Certain international standards exist for safety evaluation of dental materials (ISO 10993 series, ISO 7405 and ISO 14155‐1), but researchers often fail to follow these standards due to lack of access to standards, limitation of the guidelines and complexity of new experimental methods, which may cause technical errors. Moreover, many laboratories have developed their testing strategy for biocompatibility, which makes any comparison between findings more difficult. The purpose of this review was to discuss the concept of biocompatibility, structured test programmes and international standards for testing the biocompatibility of endodontic material biocompatibility. The text will further detail current test methods for evaluating the biocompatibility of endodontic materials, and their advantages and limitations.