DYNAMIC FLUORESCENCE CHANGES DURING PHOTODYNAMIC THERAPY IN-VIVO AND IN-VITRO OF HYDROPHILIC AL(III) PHTHALOCYANINE TETRASULFONATE AND LIPOPHILIC ZN(II) PHTHALOCYANINE ADMINISTERED IN LIPOSOMES
A. Ruck et al., DYNAMIC FLUORESCENCE CHANGES DURING PHOTODYNAMIC THERAPY IN-VIVO AND IN-VITRO OF HYDROPHILIC AL(III) PHTHALOCYANINE TETRASULFONATE AND LIPOPHILIC ZN(II) PHTHALOCYANINE ADMINISTERED IN LIPOSOMES, Journal of photochemistry and photobiology.B, Biology, 36(2), 1996, pp. 127-133
The fluorescence emission of hydrophilic tetrasulphonated aluminium ph
thalocyanine (AlPcS(4)) and hydrophobic zinc phthalocyanine (ZnPc), bo
und to the membrane of liposomes, was investigated in vivo in an appro
priate tumour model of the rat bladder and in RR 1022 epithelial cells
of the rat. The sensitizers were administered systemically to the rat
s and photodynamic therapy (PDT) was performed 24 h later. During PDT
treatment, the fluorescence was measured every 30 s. The fluorescence
was excited with 633 nm light from an HeNe laser and the fluorescence
spectra were detected with an optical mulichannel analyser system. PDT
was performed for both sensitizers using 672 nm light from an Ar+ dye
laser. The fluorescence changes during PDT were significantly differe
nt for the two phthalocyanines. For AlPcS(4), an initial fluorescence
intensity increase, followed by subsequent photobleaching, was observe
d. In contrast, ZnPc fluorescence showed an exponential decrease and n
o increase at the start of treatment, Tumour necrosis 24 h after PDT w
as significant only for ZnPc. RR 1022 cells incubated for 24 h with Al
PcS(4) revealed a granular fluorescence pattern, whereas ZnPc was loca
lized diffusely in the cytoplasm of the cells. In agreement with the i
n vivo measurements, subcellular relocalization and a fluorescence int
ensity increase were detected exclusively in the case of AlPcS(4). Mor
phological changes at this time were significant only for ZnPc. The su
bcellular localization and fluorescence kinetics were obtained using a
confocal laser scanning microscope.