Abstract

The Monte Carlo method is a versatile simulation algorithm to model the propagation of photons inside the biological tissues. It has been applied to the reconstruction of the fluorescence molecular tomography (FMT). However, such method suffers from low computational efficiency, and the time consumption is not desirable. One way to solve this problem is to introduce a priori knowledge which will facilitate iterative convergence. We presented an in vivo simulation environment for fluorescence molecular tomography (ISEFMT) using the Monte Carlo method to simulate the photon distribution of fluorescent objects and their sectional view in any direction quantitatively. A series of simulation experiments were carried out on different phantoms each with two fluorescent volumes to investigate the relationship among fluorescence intensity distribution and the excitation photon number, the locations and sizes of the fluorescence volumes, and the anisotropy coefficient. A significant principle was discovered, that along the direction of the excitation light, the fluorescent volume near the excitation point will provide shelter effect so that the energy of the fluorescent volume farther away from the excitation point is relatively lower. Through quantitative analysis, it was discovered that both the photon energy distribution on every cross section and the fluorescence intensity distributed in the two volumes exhibit exponential relationships. The two maximum positions in this distribution correspond to the centers of fluorescent volumes. Finally, we also explored the effect of the phantom coefficients on the exponential rule, and found out that the exponential rule still exists, only the coefficient of the exponential rule changed. Such results can be utilized in locating the positions of multiple fluorescent volumes in complicated FMT reconstruction involving multiple fluorescent volumes. Thus, a priori knowledge can be generalized, which would accelerate the reconstruction of FMT and even other images.

Highlights

  • Fluorescence imaging technology has been translated into a potent tool in medical diagnostics.1 The development of biotechnologies, especially genetic engineering and molecular °uorescence technologies, enabled the revolutionary technology of °uorescence molecular tomography (FMT)

  • To study the photon distribution pattern, we developed an in vivo simulation environment for °uorescence molecular tomography (ISEFMT) which uses the Monte Carlo method to predict the threedimensional photon distribution of the °uorescent biomarkers and their sectional view in any direction

  • We presented a new Monte Carlo simulation program to explore the propagation of photons in °uorescent imaging

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Summary

Introduction

Fluorescence imaging technology has been translated into a potent tool in medical diagnostics. The development of biotechnologies, especially genetic engineering and molecular °uorescence technologies, enabled the revolutionary technology of °uorescence molecular tomography (FMT). The development of biotechnologies, especially genetic engineering and molecular °uorescence technologies, enabled the revolutionary technology of °uorescence molecular tomography (FMT). Such technology works with near-infrared (NIR) light (600–900 nm) which demonstrates the best tissue penetration property, and provides information about the three-dimensional distribution of molecular (or nano-) °uorescent probes, can reveal molecular processes in vivo.. Such technology works with near-infrared (NIR) light (600–900 nm) which demonstrates the best tissue penetration property, and provides information about the three-dimensional distribution of molecular (or nano-) °uorescent probes, can reveal molecular processes in vivo.2 This marks the evolution of tissue optical imaging technology from the organ-level to the molecular and cellular levels.. Rapid progress has been made in the reconstruction of FMT images, and algorithms, such asnite-element-based methods, ̄nite di®erence methods and Monte Carlo methods are being extensively studied.

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