In vivo to post-mortem change in tissue penetration of red light |
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Authors: | C. Whitehurst M. L. Pantelides J. V. Moore T. A. King N. J. Blacklock |
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Affiliation: | (1) Wolfson Laser and Fibre Optic Unit, Physics Department, Schuster Laboratory, University of Manchester, M13 9PL, UK;(2) University Department of Urology, University Hospital of South Manchester, Nell Lane, West Didsbury, M20 9LE Manchester, UK;(3) Radiobiology Laboratory, Paterson Institute for Cancer Research, Christie Hospital and Holt Radium Institute, Wilmslow Road, M20 9BX Manchester, UK |
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Abstract: | For precise light dosimetry in photodynamic therapy (PDT), the light penetration characteristics of the tissue concerned need to be assessed. Several attenuation coefficients have so far been measured using 633 nm wavelength red light and human tissue obtained from autopsy or surgery. However, the validity of such ex vivo derived values remains uncertain, and hence is evaluated further in this study. Using a rat thigh muscle model, the tissue transmittance of 633 nm red light was compared between in vivo and ex vivo. Transmittance (in vivo) following preliminary injection of 40 mg kg–1 haematoporphyrin derivative (HPD) was also measured in muscle and liver. The effective attenuation coefficient (eff) ex vivo in muscle was 0.98±0.06 mm–1 and in vivo 0.97 ± 0.05 mm–1. Values agreed within experimental error indicating that in this tissue, changes from in vivo to post-mortem produced no alteration in optical penetration at 633 nm. Preliminary injection of HPD did not influence the penetration depth in muscle although significant changes were observed in an organ of high porphyrin avidity, the liver (0.68±0.08 mm vs 0.40±0.08 mm with HPD). Until techniques for in vivo measurements of light attenuation coefficient become available, the use of ex vivo derived values with 633 nm wavelength light would seem appropriate. |
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Keywords: | Photodynamic therapy Lasers Light dosimetry Skeletal muscle |
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