A.D. Passos

Designing and testing regenerative pulp treatment strategies: Modeling the transdentinal transport mechanisms

The need for simulation models to thoroughly test the inflammatory effects of dental materials and dentinogenic effects of specific signaling molecules has been well recognized in current dental research. The development of a model that simulates the transdentinal flow and the mass transfer mechanisms is of prime importance in terms of achieving the objectives of developing more effective treatment modalities in restorative dentistry. The present protocol study is part of an ongoing investigation on the development of a methodology that can calculate the transport rate of selected molecules inside a typical dentinal tubule. The transport rate of biological molecules has been investigated using a validated CFD code. In that framework we propose a simple algorithm that, given the type of molecules of the therapeutic agent and the maximum acceptable time for the drug concentration to attain a required value at the pulpal side of the tubules, can estimate the initial concentration to be imposed.

Computational Modelling for Efficient Transdentinal Drug Delivery

This work deals with the numerical investigation of the delivery of potential therapeutic agents through dentinal discs (i.e., a cylindrical segment of the dentinal tissue) towards the dentin–pulp junction. The aim is to assess the main key features (i.e., molecular size, initial concentration, consumption rate, disc porosity and thickness) that affect the delivery of therapeutic substances to the dental pulp and consequently to define the necessary quantitative and qualitative issues related to a specific agent before its potential application in clinical practice. The computational fluid dynamics (CFD) code used for the numerical study is validated with relevant experimental data obtained using micro Laser Induced Fluorescence (μ-LIF) a non-intrusive optical measuring technique. As the phenomenon is diffusion dominated and strongly dependent on the molecular size, the time needed for the concentration of released molecules to attain a required value can be controlled by their initial concentration. Finally, a model is proposed which, given the maximum acceptable time for the drug concentration to attain a required value at the pulpal side of the tissue along with the aforementioned key design parameters, is able to estimate the initial concentration to be imposed and vice versa.

Study of the transdentinal diffusion of bioactive molecules.

In this work the mass transfer characteristics in a µ-tube that simulates a simplified dentinal tubule geometry are numerically investigated. The aim is to assess the key features that affect transdentinal diffusion of substances and consequently to define the necessary quantitative and qualitative issues related to a specific bioactive agent before its potential application in clinical practice. CFD simulations were performed in an S-shaped tapered micro-tube, while the code was validated using the non-intrusive optical measuring technique Laser Induced Fluorescence (LIF). As the phenomenon is one-dimensional, diffusion dominated and strongly dependent on the molecular size, the time needed for the concentration of released molecules to attain a required value can be controlled by their initial concentration. Thus, we propose a model, which is successfully verified by experimental data using a dentinal disc and which given the type of applied molecules and their critical pulpal concentration is able to estimate the initial concentration to be imposed.