Microvascular effects of Photofrin®-induced photodynamic therapy
Summary
Background and objective
The object of our study is to evaluate the feasibility of photodynamic therapy (PDT) for complicated hemangiomas. The photosensitizing activities of Photofrin® have been used in vivo models for our goal of evaluation.
Study design/materials and methods
The in vivo biological activities of Photofrin® exposed to the total laser energy density of 100
J/cm2 with the power density of 100 or 120
mW/cm2 at 630
nm wavelength was studied. The amount of vascular damage produced in the chick chorioallantoic membrane (CAM) was evaluated. At 630
nm wavelength, those individual vessels with a diameter of 40
μm or less and those with a diameter between 40 and 100
μm were treated with Photofrin® at a concentration of about 2.5
mg/mL, and injected intraperitoneally at 2.5
mg/kg, illuminated at 100 and 120
mW/cm2, respectively. Both exhibited coagulation.
Results
There were no statistically significant differences between the two groups (100 and 120
mW/cm2) on vessel damage grade 1. With vessel damage grades 2 and 3, the differences were statistically significant between two groups. Vessel damages between arterioles and venules also demonstrated differences in the 100
mW/cm2 treated group but not in the 120
mW/cm2 group. Statistically significant differences were also shown in arteriole and venules damage between 100 and 120
mW/cm2 treated groups. The severity of vessel damage between grades 1 and 2, 1 and 3, and 2 and 3, were compared. The differences were statistically significant in 100
mW/cm2 treated group. There was no statistically significant difference in 120
mW/cm2 treated group.
Conclusion
Photofrin® has the capabilities for destruction of microvascular vessels of CAM. Extension of this study to the second-generation photosensitizers is underway. The most important treatment variables seem to be the power density.
Keywords: Photodynamic therapy, Photofrin®, Chick chorioallantoic membrane
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PII: S1572-1000(07)00036-1
doi:10.1016/j.pdpdt.2007.03.003
© 2007 Published by Elsevier Inc.
