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Revision of ex vivo endodontic biofilm model using computer aided design. | LitMetric

Revision of ex vivo endodontic biofilm model using computer aided design.

J Dent

Bioengineering Institute of Technology (BIT), Universitat Internacional de Catalunya, 08017, Barcelona, Spain; Basic Sciences Department, Faculty of Medicine and Health Sciences, Universitat Internacional de Catalunya, 08017, Barcelona, Spain. Electronic address:

Published: October 2024

AI Article Synopsis

  • The study aimed to create a refined ex vivo endodontic biofilm model by using human teeth, computer-guided design, and 3D printing to improve the testing of antibacterial treatments for dental infections.
  • Various cutting methods were compared, with computer-aided guided cutting (CGC) showing superior precision and liquid tightness, while allowing for the development of stable and active Enterococcus faecalis biofilms over 21 days.
  • The new model demonstrated a more reliable way to assess the effectiveness of antibacterial treatments, revealing that while standard treatments could completely eradicate bacteria, commercial disinfectants had varying success rates in the new ex vivo setup.

Article Abstract

Objective: Most endodontic diseases are bacterium-mediated inflammatory or necrotic process induced by contaminated dental pulp. Although great advances are being performed to obtain more efficient antibacterial strategies for persistent infections, most studies lack of representative models to test their antibacterial effects and their outcomes cannot be promptly translated to clinical practice. Therefore, this study aimed to refine an ex vivo endodontic biofilm model combining human tooth, computer guided design and 3D printing to obtain a more reproducible and predictable model.

Methods: Monoradicular teeth were cut using three different methods: hand-held (HCC), mechanical precision (MPC) and computer aid guided cutting (CGC). Then, blocks were reassembled. The different model preparations were assessed in terms of dimensional tolerance, surface analysis, liquid tightness and Enterococcus faecalis biofilm development for 21 days, which was studied by metabolic assays and confocal microscopy. Then, the proposed model was validated using different commercial disinfecting treatments.

Results: CGC exhibited significantly lower deviation and surface without defects compared to HHC and MPC, leading to superior liquid tightness. Similarly, mature biofilms with high metabolic activity and vitality were observed in all conditions, CGC showing the lowest variation. Regarding the model validation, all antibacterial treatments resulted in the complete eradication of bacteria in the standard 2D model, whereas commercial treatments exhibited varying levels of efficacy in the proposed ex vivo model, from moderately reduction of metabolic activity to complete elimination of biofilm.

Conclusions: The novel guided approach represents a more reliable, standardized, and reproducible model for the evaluation of endodontic disinfecting therapies.

Clinical Significance: During antibacterial treatment development, challenging 3D models using teeth substrates to test antibacterial treatments novel guided approach represents a more reliable, standardized, and reproducible model for the evaluation of endodontic disinfecting therapies.

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Source
http://dx.doi.org/10.1016/j.jdent.2024.105270DOI Listing

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