White light diffuse optical spectroscopy for therapy monitoring

Since its rediscovery in 1973, Photodynamic Therapy (PDT) has emerged to be one of the novel cancer treatment modalities. In its very essence, it exploits light-activated drugs or better known as photosensitisers, and laser light to induce selective cytotoxicity. The effect of photosensitiser concen...

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Bibliographic Details
Main Author: Gunawan, Stephen Nathaniel.
Other Authors: Lee Kijoon
Format: Final Year Project (FYP)
Language:English
Published: 2011
Subjects:
Online Access:http://hdl.handle.net/10356/45666
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author Gunawan, Stephen Nathaniel.
author2 Lee Kijoon
author_facet Lee Kijoon
Gunawan, Stephen Nathaniel.
author_sort Gunawan, Stephen Nathaniel.
collection NTU
description Since its rediscovery in 1973, Photodynamic Therapy (PDT) has emerged to be one of the novel cancer treatment modalities. In its very essence, it exploits light-activated drugs or better known as photosensitisers, and laser light to induce selective cytotoxicity. The effect of photosensitiser concentration, blood oxygenation level, and sufficient light on the site play a major role in PDT’s clinical success.[1] A non-invasive therapy monitoring method is simplified by the development of Diffuse Optical Spectroscopy (DOS), where several important chromophores such as oxygenated haemoglobin (HbO2), deoxygenated haemoglobin (Hb), and photosensitiser concentration can be monitored constantly to provide a preliminary overview on the therapy progress[2] for clinicians to chart the subsequent courses of action.
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spelling ntu-10356/456662023-03-03T15:40:54Z White light diffuse optical spectroscopy for therapy monitoring Gunawan, Stephen Nathaniel. Lee Kijoon School of Chemical and Biomedical Engineering DRNTU::Science::Chemistry::Biochemistry::Spectroscopy DRNTU::Science::Medicine::Optical instruments Since its rediscovery in 1973, Photodynamic Therapy (PDT) has emerged to be one of the novel cancer treatment modalities. In its very essence, it exploits light-activated drugs or better known as photosensitisers, and laser light to induce selective cytotoxicity. The effect of photosensitiser concentration, blood oxygenation level, and sufficient light on the site play a major role in PDT’s clinical success.[1] A non-invasive therapy monitoring method is simplified by the development of Diffuse Optical Spectroscopy (DOS), where several important chromophores such as oxygenated haemoglobin (HbO2), deoxygenated haemoglobin (Hb), and photosensitiser concentration can be monitored constantly to provide a preliminary overview on the therapy progress[2] for clinicians to chart the subsequent courses of action. Bachelor of Engineering (Chemical and Biomolecular Engineering) 2011-06-16T01:48:47Z 2011-06-16T01:48:47Z 2011 2011 Final Year Project (FYP) http://hdl.handle.net/10356/45666 en Nanyang Technological University 63 p. application/pdf
spellingShingle DRNTU::Science::Chemistry::Biochemistry::Spectroscopy
DRNTU::Science::Medicine::Optical instruments
Gunawan, Stephen Nathaniel.
White light diffuse optical spectroscopy for therapy monitoring
title White light diffuse optical spectroscopy for therapy monitoring
title_full White light diffuse optical spectroscopy for therapy monitoring
title_fullStr White light diffuse optical spectroscopy for therapy monitoring
title_full_unstemmed White light diffuse optical spectroscopy for therapy monitoring
title_short White light diffuse optical spectroscopy for therapy monitoring
title_sort white light diffuse optical spectroscopy for therapy monitoring
topic DRNTU::Science::Chemistry::Biochemistry::Spectroscopy
DRNTU::Science::Medicine::Optical instruments
url http://hdl.handle.net/10356/45666
work_keys_str_mv AT gunawanstephennathaniel whitelightdiffuseopticalspectroscopyfortherapymonitoring