
Proceedings Paper
Determination of surface temperature distribution in biological tissues during laser-immunotherapyFormat | Member Price | Non-Member Price |
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Paper Abstract
An ideal cancer treatment method should not only cause primary tumor suppression but also induce an
antitumor immunity, which is essential for control of metastatic tumors. A combination therapy using a
laser, a laser-absorbing dye, and an immunoadjuvant guided by temperature measurement probes such as
magnetic resonance imaging thermometry (MRT) and infrared thermography (IRT) can be an ideal treatment
modality. Temperature distribution inside the target tissue is important in laser treatment. The surface
temperature often serves as an indicator of the treatment effect. However, real-time monitoring of surface
temperature during laser irradiation poses a great challenge. In this study, we investigated the surface
temperature distribution using direct measurement and theoretical simulation. The preliminary results of in
vitro and in vivo studies are presented. Gel phantom and chicken breast tissue were irradiated by an 805 nm
laser and the surface temperature distribution was obtained using an infrared thermal camera. EMT-6 breast
tumors in mice were treated using the 805 nm laser and with different dye and immunoadjuvant
combinations, including intratumor injections of indocyanine green (ICG) and glycated chitosan (GC).
Monte Carlo simulation for selective photothermal-tissue interaction was also performed for the surface
temperature distributions. Our results demonstrated that the tissue temperature can be accurately monitored
in real time and can be controlled by appropriate treatment parameters.
Paper Details
Date Published: 13 February 2007
PDF: 11 pages
Proc. SPIE 6438, Biophotonics and Immune Responses II, 64380D (13 February 2007); doi: 10.1117/12.698017
Published in SPIE Proceedings Vol. 6438:
Biophotonics and Immune Responses II
Wei R. Chen, Editor(s)
PDF: 11 pages
Proc. SPIE 6438, Biophotonics and Immune Responses II, 64380D (13 February 2007); doi: 10.1117/12.698017
Show Author Affiliations
Surya C. Gnyawali, Oklahoma State Univ. (United States)
Yichao Chen, Univ. of Central Oklahoma (United States)
Feng Wu, Chongqing Univ. of Medical Sciences (China)
Kenneth E. Bartels, Oklahoma State Univ. (United States)
Yichao Chen, Univ. of Central Oklahoma (United States)
Feng Wu, Chongqing Univ. of Medical Sciences (China)
Kenneth E. Bartels, Oklahoma State Univ. (United States)
Jerry W. Ritchey, Oklahoma State Univ. (United States)
James P. Wicksted, Oklahoma State Univ. (United States)
Hong Liu, Univ. of Oklahoma (United States)
Wei R. Chen, Univ. of Central Oklahoma (United States)
James P. Wicksted, Oklahoma State Univ. (United States)
Hong Liu, Univ. of Oklahoma (United States)
Wei R. Chen, Univ. of Central Oklahoma (United States)
Published in SPIE Proceedings Vol. 6438:
Biophotonics and Immune Responses II
Wei R. Chen, Editor(s)
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