We measured the response of normal brain and the human U87 glioma impl
anted in the brain of rats (n = 65) to photodynamic therapy (PDT) usin
g Photofrin as the sensitizer. Normal brain and U87 tumor implanted wi
thin brain of athymic (nude) rats were subjected to PDT (12.5 mg/kg of
Photofrin) at increasing optical energy doses (35 J/cm(2), 140 J/cm(2
), 280 J/cm(2)) of 632 nm light, Photofrin concentration in tumor, bra
in adjacent to tumor and normal brain were measured in a separate popu
lation of rats. Twenty-four hours after PDT, the brains were removed,
sectioned, stained with hematoxylin and eosin (H&E), and the volumes o
f the PDT-induced lesion measured, Photofrin concentration in tumor gr
eatly exceeded that of normal brain and brain adjacent to tumor (>20 x
), Both normal brain and U87 tumor exhibited superficial tissue damage
with PDT at 35 J/cm(2). However, both normal and tumor-implanted brai
n exhibited tissue damage with increasing optical dose, A heterogeneou
s pattern of pannecrosis along with a uniform volume of pannecrosis wa
s detected in the tumor, In contrast, normal brain exhibited a uniform
sharply demarcated volume of necrosis, Our data indicate that the U87
human brain tumor model and the normal brain in the athymic rat are s
ensitive to PDT and Photofrin with an optical dose-dependent response
to treatment.