H. Nilsson et al., LASER-INDUCED FLUORESCENCE STUDIES OF THE BIODISTRIBUTION OF CAROTENOPORPHYRINS IN MICE, British Journal of Cancer, 76(3), 1997, pp. 355-364
The biodistribution of two recently developed tumour markers, trimethy
lated (CP(Me)(3)) and trimethoxylated (CP(OMe)(3)) carotenoporphyrin,
was investigated by means of laser-induced fluorescence (LIF) after i.
v. injection into 38 tumour-bearing (MS-2 fibrosarcoma) female Balb/c
mice. At 3, 24, 48 or 96 h after administration, the carotenoporphyrin
fluorescence was measured in tumoral and peritumoral tissue, as well
as in the abdominal, thoracic and cranial cavities. The fluorescence w
as induced by a nitrogen laser-pumped dye laser, emitting light at 425
nm, and analysed by a polychromator equipped with an image-intensifie
d CCD camera. The fluorescence was evaluated at 490, 655 and 720 nm: t
he second and third wavelengths represent the carotenoporphyrin (CP)-r
elated peaks, whereas the first one is close to the peak of the tissue
autofluorescence. The tumour and the liver were the two tissue types
showing the strongest carotenoporphyrin-related fluorescence, whereas
the cerebral cortex and muscle consistently exhibited weak substance-r
elated fluorescence. In most tissue types, the fluorescence intensitie
s decreased over time. A few exceptions were observed, notably the liv
er, in which the intensity remained remarkably constant over the time
period investigated.