TY - JOUR
T1 - Microvascular effects of Photofrin®-induced photodynamic therapy
AU - Chang, Cheng Jen
AU - Cheng, Sally M.H.
AU - Nelson, J. Stuart
N1 - Funding Information:
This research was supported by the Chang Gung Memorial Hospital, grant CMRPG33033.
PY - 2007/6/1
Y1 - 2007/6/1
N2 - 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.
AB - 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.
KW - Chick chorioallantoic membrane
KW - Photodynamic therapy
KW - Photofrin
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U2 - 10.1016/j.pdpdt.2007.03.003
DO - 10.1016/j.pdpdt.2007.03.003
M3 - Article
AN - SCOPUS:34248186556
SN - 1572-1000
VL - 4
SP - 95
EP - 99
JO - Photodiagnosis and Photodynamic Therapy
JF - Photodiagnosis and Photodynamic Therapy
IS - 2
ER -