Fluence rate effects in photodynamic therapy of multicell tumor spheroids

• Published in: Cancer research (Chicago, Ill.) Vol. 53; no. 6; pp. 1249 - 1254
• Main Authors: FOSTER, T. H, HARTLEY, D. F, NICHOLS, M. G, HILF, R
• Format: Journal Article
• Language: English
• Published: Philadelphia, PA American Association for Cancer Research 15.03.1993
• Subjects: Animals; Biological and medical sciences; Cell Hypoxia; Cell Survival - drug effects; Mammary Neoplasms, Experimental - drug therapy; Mammary Neoplasms, Experimental - metabolism; Mammary Neoplasms, Experimental - pathology; Mathematics; Medical sciences; Mice; Oxygen Consumption; Photochemotherapy; Photoradiation therapy and photosensitizing agent; Treatment with physical agents; Treatment. General aspects; Tumor Cells, Cultured; Tumors; Treatment; Fluence; Animal; Cytotoxicity; Spheroid; In vitro; Photosensitizer; Tumor cell; Phototherapy; Dose activity relation
• ISSN: 0008-5472; 1538-7445

EMT6/Ro spheroids approximately 500 microns in diameter were subjected to photodynamic therapy administered at various incident radiation fluence rates. Following 24 h incubation with 10 micrograms/ml Photofrin, groups of spheroids were irradiated at 630 nm with an identical fluence of 60 J/cm2, delivered at fluence rates ranging from 25 to 200 mW/cm2. After treatment, spheroids were dissociated, cell yields were determined, and surviving cells were assayed for their colony-forming ability. A surviving fraction was calculated for each treatment group by computing the product of the fractional cell yield and the plating efficiency. The results exhibit a strong dependence on the fluence rate, with surviving fractions decreasing from approximately 0.5 to 0.07 as the incident fluence rate was lowered from 200 to 25 mW/cm2. These data were analyzed using a mathematical model of photochemical oxygen consumption in spheroids undergoing photodynamic therapy. Calculations showed that therapy-induced oxygen consumption creates hypoxic volumes within which cells would be protected from singlet oxygen-mediated damage and that the magnitude of these hypoxic volumes depends on the radiation fluence rate. The fluence rate dependence of the spheroid cell survival was consistent with such an interpretation.