The use of PHOTOFRIN(TM) for photodynamic therapy of human gliomas has
been studied by i.v. administration and laser photosensitization. Def
ining the uptake of PHOTOFRIN(TM) in the patient's tumor in comparison
with the surrounding normal brain tissue is highly desirable for pati
ent selection and study of in vivo kinetics. We utilized a non-invasiv
e approach to the detection of PHOTOFRIN(TM) uptake in brain tumors wi
th In-111-oxine radiolabeled PHOTOFRIN(TM) and external imaging and qu
antitation using a gamma camera. Biodistribution of In-111-labeled PHO
TOFRIN(TM) in 13 organs was determined in four dogs and 15 mice with g
liomas. Tc-99m-DTPA was used as a control for nonspecific uptake. The
greatest concentration of In-111-PHOTOFRIN(TM) in the brain tumor occu
rred at 24 hours post i.v. administration. The brain tumor PHOTOFRIN(T
M) uptake was seven times greater than that of normal brain. The decre
ased blood background at 72 hours made this the optimum time for imagi
ng. Specific tumor tissue uptake of In-111-PHOTOFRIN(TM) occurred, wel
l beyond that resulting from blood-brain-barrier (BBB) breakdown.