Simulation of Reflectance in Oral Tissue Using MCMatlab

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Introduction

Clinical Motivation

Problem Statement

Background

Previous Work

Optical Tissue Properties in the Literature

Tissue Layer μa [cm⁻¹] 420 nm μs [cm⁻¹] 420 nm μa [cm⁻¹] 450 nm μs [cm⁻¹] 450 nm
Superficial epithelium 3.0 170 (keratinized) / 55 (non keratinized) 2.1 140 (keratinized) / 40 (non keratinized)
Intermediate epithelium 3.0 55 2.1 40
Basal epithelium 3.0 55 2.1 40
Superficial stroma 6.22 267 3.11 248.5
Deep stroma 6.22 267 3.11 248.5
Blood 262 37.8 30 31.1

Methods

Monte Carlo Simulation Principle

A simple Monte Carlo simulation can be used to estimate the value of π by comparing areas of a circle and a square. First, the geometric domain is defined, consisting of a square whose side is equal to twice the radius R of the circle, so that the circle is fully inscribed within the square (see Figure 1a). A large number of points are then generated randomly and uniformly within the square. Each point is classified according to whether it lies inside the circle or outside, and the number of points falling within the circle is counted (see Figure 1b). The ratio of the number of points inside the circle Ncircle to the total number of points in the square Ntotal approaches the ratio of the areas of the circle and the square: NcircleNtotalArea of circleArea of square=πR2(2R)2=π4. Multiplying this ratio by four therefore provides an estimate of π. This example illustrates how probabilistic sampling can be used to approximate geometric quantities.

(a) Definition of the geometric domain (b) Random point generation, classification, and counting
Figure 1: Basic Monte Carlo simulation to compute π

Monte Carlo Simulation for Light Propagation

(a) Launching a photon packet (b) Straight-line propagation over a free path (c) Interaction event (d) Updating the Photon Weight
Figure 2: Monte Carlo simulation for light

Monte Carlo Matlab

Five Layer Model and Geometry

Results

Influence of Keratin on the Optical Response

Fluence Results

Fluence Distribution
Figure 3: Fluence comparison between keratinized and non-keratinized tissue

Absorbance Results

Absorbance Distribution
Figure 4: Absorbance comparison between keratinized and non-keratinized tissue

Reflectance Results

Reflectance Distribution
Figure 5: Reflectance comparison between keratinized and non-keratinized tissue

Influence of Blood Depth on the Optical Response

Fluence Results

(a) Fluence at 415 nm
Non-keratinized tissue
(b) Fluence at 415 nm
Keratinized tissue
(c) Fluence at 450 nm
Non-keratinized tissue
(d) Fluence at 450 nm
Keratinized tissue
Figure 6: Fluence distribution as a function of depth for different wavelengths and tissue types

Absorbance Results

Figure 8: Absorbance as a function of blood depth for different wavelengths and tissue types

Reflectance Results

Figure 7: Reflectance as a function of blood depth for different wavelengths and tissue types

Discussion and Conclusions

Appendix

Our code can be found at (Github link).