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|Title: ||Development and Validation of Analytical Models for Diffuse Fluorescence Spectroscopy/Imaging in Regular Geometries|
|Authors: ||Ayyalasomayajula, Kalyan Ram|
|Advisors: ||Yalavarthy, Phaneendra K|
|Keywords: ||Medical Optics|
Diffuse Fluorescence Spectroscopy
Fluorescence Diffuse Optical Imaging
Fluorescence Diffuse Optical Spectroscopy
Diffuse Fluorescence Spectroscopy/Imaging
Fluorescence Spectroscopy/Imaging - Mathematical Models
Fluorescence Optical Breast Imaging
Flrorescence Optical Brain Imaging
Fluorescence Diffuse Optical Imaging
|Submitted Date: ||2013|
|Series/Report no.: ||G25572|
|Abstract: ||New advances in computational modeling and instrumentation in the past decade has enabled the use of electromagnetic radiation for non-invasive monitoring of the physio-logical state of biological tissues. The near infrared (NIR) light having the wavelength range of 600 nm -1000 nm has been the main contender in these emerging molecular imaging modalities. Assessment of accurate pathological condition of the tissue under investigation relies on the contrast in the molecular images, where the endogenous contrast may not be suﬃcient in these scenarios. The ﬂuorescence (exogenous) contrast agents have been deployed to overcome these diﬃculties, where the preferential uptake by the tumor vasculature leads to high contrast,making this modality one of the biggest contenders in small-animal and soft-tissue molecular imaging modalities.
In Fluorescence diﬀuse optical spectroscopy/imaging, this exogenous drug is excited by NIR laser light causing the emission of the ﬂuorescence light. The emitted ﬂuorescence light is typically dependent on the life time and concentration of the exogenous drug coupled with physiology associated with the tissue under investigation. As there is an excitation and emission of the light,the underlying physics of the problem is described by a coupled diﬀusion equations. These coupled diﬀusion equations are typically solved by advanced numerical methods, which tend to be computationally demanding.
In this work, analytical solutions for these coupled partial diﬀerential equations (PDEs) for the regular geometries for both time-domain and frequency-domain cases were developed. Till now, the existing literature has not dealt with all regular geometries and derived analytical solutions were only for couple of geometries. Here a universally acceptable generic solution was developed based on Green’s function approach that is applicable to any regular geometry. Using this, the analytical solutions for the regular geometries that is encountered in diﬀuse ﬂuorescence spectroscopy/imaging were obtained. These solutions can play an important role in determining the bulk ﬂuorescence properties of the tissue, which could act as good initial guesses for the advanced image reconstruction techniques and/or can also facilitate the calibration of experimental ﬂuorescence data by removing biases and source-detector variations.
In the second part of this work, the developed analytical models for regular geometries were validated through comparison with the established numerical models that are traditionally used in the diﬀuse ﬂuorescence spectroscopy/imaging. This comparison not only validated the developed analytical models, but also showed that analytical models are capable of providing bulk ﬂuorescence properties with at least one order of magnitude less computational cost compared to the highly optimized traditional numerical models.|
|Abstract file URL: ||http://etd.ncsi.iisc.ernet.in/abstracts/4137/G25572-Abs.pdf|
|Appears in Collections:||Supercomputer Education and Research Centre (serc)|
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