Journal
JOURNAL OF BIOMEDICAL OPTICS
Volume 15, Issue 5, Pages -Publisher
SPIE-SOC PHOTO-OPTICAL INSTRUMENTATION ENGINEERS
DOI: 10.1117/1.3494561
Keywords
photodynamic therapy; dosimetry; tissue optics; optical properties
Funding
- NIH [R29-HL45045, R01-HL084013]
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We describe three lessons learned about how tissue optics affect the dosimetry of red to near-infrared treatment light during PDT, based on working with Dr. Tayyaba Hasan. Lesson 1-The optical fluence rate phi near the tissue surface exceeds the delivered irradiance (E). A broad beam penetrates into tissue to a depth (z) as phi = Eke(-mu z), with an attenuation constant mu and a backscatter term k. In tissues, k is typically in the range 3-5, and 1/mu equals delta, the 1/e optical penetration depth. Lesson 2-Edge losses at the periphery of a uniform treatment beam extend about 3 delta from the beam edge. If the beam diameter exceeds 6 delta, then there is a central zone of uniform fluence rate in the tissue. Lesson 3-The depth of treatment is linearly proportional to delta (and the melanin content of pigmented epidermis in skin) while proportional to the logarithm of all other factors, such as irradiance, exposure time, or the photosensitizer properties (concentration, extinction coefficient, quantum yield for oxidizing species). The lessons illustrate how tissue optics play a dominant role in specifying the treatment zone during PDT. (C) 2010 Society of Photo-Optical Instrumentation Engineers. [DOI: 10.1117/1.3494561]
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