An animal model of cerebral glioma was utilized by implanting C6 gliom
a cells into the brains of adult Wistar rats. Once tumors developed to
7-12 mm in diameter, we conducted continuous fluorimetry monitoring o
f glioma up to 24 hours using a fibre-optic system connected to an int
ensified multichannel photodetector after an intravenous injection of
hematoporphyrin derivative (HPD) into the rats. The intensity of the f
luorescence in normal brain reached a plateau 6 hours after intravenou
s injection of HPD while that in glioma reached a plateau 80 minutes a
fter injection. These fluorescence intensities of glioma, brain adjace
nt to tumor (BAT), and surrounding normal brain were measured in vivo
24 hours after intravenous administration of 5 mg/kg of HPD. The ratio
of fluorescence intensities between glioma and brain was 6.1 while th
e ratio between BAT and brain was 3.9. There were no obvious differenc
es in shapes between the spectra of the natural fluorescence (autofluo
rescence) of rat glioma and brain but the intensity of autofluorescenc
e was much weaker in glioma. There are many problems in spectroscopic
studies of biological tissues in vivo. It cannot be overemphasized tha
t very strict criteria must be applied in order to get accurate data.
Fluorescence from HPD administration may be used to discriminate tumor
tissue from surrounding normal brain tissue during operation if the m
easuring conditions could be kept constant. It is important to underst
and the photospectral properties of glioma and brain tissue in order t
o get the most benefits in clinical application of light-induced fluor
escence or photoradiation therapy.