Dai, Tianhong and Pikkula, Brian M. and Wang, Lihong V. and Anvari, Bahman (2004) Comparison of human skin opto-thermal response to near-infrared and visible laser irradiations: a theoretical investigation. Physics in Medicine and Biology, 49 (21). pp. 4861-4877. ISSN 0031-9155. doi:10.1088/0031-9155/49/21/002. https://resolver.caltech.edu/CaltechAUTHORS:20161207-143714667
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Abstract
Near-infrared wavelengths are absorbed less by epidermal melanin, and penetrate deeper into human skin dermis and blood than visible wavelengths. Therefore, laser irradiation using near-infrared wavelengths may improve the therapeutic outcome of cutaneous hyper-vascular malformations in moderately to heavily pigmented skin patients and those with large-sized blood vessels or blood vessels extending deeply into the skin. A mathematical model composed of a Monte Carlo algorithm to estimate the distribution of absorbed light, numerical solution of a bio-heat diffusion equation to calculate the transient temperature distribution, and a damage integral based on an empirical Arrhenius relationship to quantify the tissue damage was utilized to investigate the opto-thermal response of human skin to near-infrared and visible laser irradiations in conjunction with cryogen spray cooling. In addition, the thermal effects of a single continuous laser pulse and micropulse-composed laser pulse profiles were compared. Simulation results indicated that a 940 nm wavelength induces improved therapeutic outcome compared with a 585 and 595 nm wavelengths for the treatment of patients with large-sized blood vessels and moderately to heavily pigmented skin. On the other hand, a 585 nm wavelength shows the best efficacy in treating small-sized blood vessels, as characterized by the largest laser-induced blood vessel damage depth compared with 595 and 940 nm wavelengths. Dermal blood content has a considerable effect on the threshold incident dosage for epidermal damage, while the effect of blood vessel size is minimal. For the same macropulse duration and incident dosage, a micropulse-composed pulse profile results in higher peak temperature at the basal layer of skin epidermis than an ideal single continuous pulse profile.
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Additional Information: | © 2004 IOP Publishing Ltd. Received 4 July 2004; Published 8 October 2004. This study was supported in part by a grant from the Institute of Arthritis and Musculoskeletal and Skin Disease (IR01-AR47996) at the National Institutes of Health to Dr Bahman Anvari. We thank Dr James W Tunnell from G R Harrison Spectroscopy Laboratory at Massachusetts Institute of Technology for fruitful discussions. | |||||||||
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Issue or Number: | 21 | |||||||||
DOI: | 10.1088/0031-9155/49/21/002 | |||||||||
Record Number: | CaltechAUTHORS:20161207-143714667 | |||||||||
Persistent URL: | https://resolver.caltech.edu/CaltechAUTHORS:20161207-143714667 | |||||||||
Official Citation: | Tianhong Dai et al 2004 Phys. Med. Biol. 49 4861 | |||||||||
Usage Policy: | No commercial reproduction, distribution, display or performance rights in this work are provided. | |||||||||
ID Code: | 72636 | |||||||||
Collection: | CaltechAUTHORS | |||||||||
Deposited By: | Tony Diaz | |||||||||
Deposited On: | 07 Dec 2016 22:48 | |||||||||
Last Modified: | 12 Jul 2022 19:45 |
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