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3D numerical simulation of real-time temperature field in a hyperthermia cancer treatment using OcTree meshes

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Abstract

This paper presents a computational strategy for real-time monitoring of hyperthermia treatment of cancer using nanoparticles. In this strategy, a numerical scheme based on the finite volume method is used for the simulation of heat diffusion in a synthetic biological system. This synthetic model is discretized with OcTree meshes, which can perform local refinement, allowing a good representation of complex geometries, besides having advantages on the use of computational resources. For real-time estimation of temperature in the three-dimensional model, the capture of the temperature field on the external surface of the model is simulated. With the data from these simulations, inverse problems are proposed and solved using the L-BFGS method. The damage caused by a temperature increase in healthy and diseased tissues is estimated, thus simulating a criterion for treatment safety. Numerical examples are analyzed with tumors at different depths, illustrating some particularities of this approach.

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Abbreviations

A :

Empirical constant used in damage simulation, \(\hbox {s}^{-1}\)

c :

Specific heat, J/\(\hbox {Kg}^{\circ }\mathrm{C}\)

\(c_b\) :

Specific heat of the blood, J/\(\hbox {Kg}^{\circ }\mathrm{C}\)

E :

Activation energy for the reaction, J/mol

\(F_j\) :

Face of a control volume

h :

Grid spacing, m

\(n_f\) :

Number of faces

\(n_v\) :

Number of volumes

\(Q_m\) :

Metabolic heat generation, W/\(\hbox {m}^3\)

\(Q_r\) :

Internal heat energy emerged from the nanoparticles, W/\(\hbox {m}^3\)

R :

Universal gas constant, J/\(\hbox {mol}^{\circ }\mathrm{C}\)

\({\mathbf {R}}\) :

Real numbers set

\(S_i\) :

Control volume surface

\(V_i\) :

Control volume

\(W_b\) :

Blood perfusion rate, Kg/s/\(\hbox {m}^3\)

\(W_b^*\) :

Weighted average of the nonlinear perfusion, Kg/s/\(\hbox {m}^3\)

\(\kappa \) :

Thermal conductivity, W/\(\hbox {m}^{\circ }\mathrm{C}\)

\(\rho \) :

Density, Kg/\(\hbox {m}^3\)

\(\phi _a\) :

Arterial temperature, \(^{\circ }\mathrm{C}\)

\(\phi \) :

Tissue temperature, \(^{\circ }\mathrm{C}\)

\(\Delta t\) :

Time increment, s

\(\Omega \) :

Tissue damage

\(\chi \) :

Concentration of nanoparticles in a biological environment

\(\mathbf {U_o}\) :

Temperature values observed on the skin surface

\(\mathbf {U_s}\) :

Temperature values obtained with the computational simulation

\({\mathbf {F}}\) :

Residue function

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Acknowledgements

The authors would like to acknowledge the research support from CAPES (Brazilian Federal Agency for Support and Evaluation of Graduate Education), from CNPq (Brazilian Council for Scientific and Technological Development) with the Grant Nos.: 423794/2016-7, 306.933/2014-4, 423114/2018-2, 306191/2018-0 and 151474/2018-4, and from FAPERJ (Research Foundation of the State of Rio de Janeiro) with the Grant Nos.: 203.021/2017, 203.234/2016, and 210.210/2016. We also thank Petrobras for its support. IN MEMORIAM: Franciane \({\mathrm{Peters}}^\dagger \) (May 22, 1985–July 15, 2020). The authors dedicate this paper to the extraordinary colleague and friend Franciane Peters, co-author of this work. In a very precocious way, dear “Fran” left and left us her example of commitment, competence, and especially how human we should be.

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Correspondence to André Valente.

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Valente, A., Peters, F.C., de Souza, R.V.M. et al. 3D numerical simulation of real-time temperature field in a hyperthermia cancer treatment using OcTree meshes. J Braz. Soc. Mech. Sci. Eng. 43, 15 (2021). https://doi.org/10.1007/s40430-020-02760-1

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