The exact mechanism by which photodynamic therapy (PDT) causes tumor d
estruction has not been elucidated. Early reports indicated that PDT c
auses direct cellular effects probably mediated by unstable oxygen spe
cies, resulting in cellular oxidation and death. More recently, PDT ef
fects on tumor blood flow have been implicated, and there are question
s as to whether the PDT response is specific to tumor tissue. Rats wer
e implanted with a window chamber containing either a mammary adenocar
cinoma or a piece of inert surgical sponge. After growth of the tumor
was ascertained, all rats were given 5 mg/kg Photofrin intraperitoneal
ly, and then were irradiated with 630 nm light 24 hours post-injection
. Caliper thickness and reflectance measurements were performed before
and after irradiation; all animals were sacrificed 72 hours post-PDT
and the chambers submitted for histologic analysis. Animals implanted
with tumors demonstrated marked edema of the chamber with an associate
d decrease in reflectance. No edema response was noted in the chambers
containing inert sponge, or in any controls. Nonselective PDT effects
(characterized by a marked foreign body response) in chambers contain
ing sponge was not seen. Histologic analysis of treated specimens corr
oborate the above data. (C) 1993 Wiley-Liss, Inc.