Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/87446
Title: Raman Monte Carlo Simulation for light propagation for tissue with embedded objects
Authors: Periyasamy, Vijitha
Jaafar, Humaira
Pramanik, Manojit
Keywords: Monte Carlo Simulation
Raman Imaging
Issue Date: 2018
Source: Periyasamy, V., Jaafar, H., & Pramanik, M. (2018). Raman Monte Carlo simulation for light propagation for tissue with embedded objects. Proceedings of SPIE - Optical Interactions with Tissue and Cells XXIX, 10492, 104920V-.
Abstract: Monte Carlo (MC) stimulation is one of the prominent simulation technique and is rapidly becoming the model of choice to study light-tissue interaction. Monte Carlo simulation for light transport in multi-layered tissue (MCML) is adapted and modelled with different geometry by integrating embedded objects of various shapes (i.e., sphere, cylinder, cuboid and ellipsoid) into the multi-layered structure. These geometries would be useful in providing a realistic tissue structure such as modelling for lymph nodes, tumors, blood vessels, head and other simulation medium. MC simulations were performed on various geometric medium. Simulation of MCML with embedded object (MCML-EO) was improvised for propagation of the photon in the defined medium with Raman scattering. The location of Raman photon generation is recorded. Simulations were experimented on a modelled breast tissue with tumor (spherical and ellipsoidal) and blood vessels (cylindrical). Results were presented in both A-line and B-line scans for embedded objects to determine spatial location where Raman photons were generated. Studies were done for different Raman probabilities.
URI: https://hdl.handle.net/10356/87446
http://hdl.handle.net/10220/44465
DOI: 10.1117/12.2286669
Rights: © 2018 Society of Photo-optical Instrumentation Engineers (SPIE). This paper was published in Proceedings of SPIE - Optical Interactions with Tissue and Cells XXIX and is made available as an electronic reprint (preprint) with permission of SPIE. The published version is available at: [http://dx.doi.org/10.1117/12.2286669]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SCBE Conference Papers

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