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

Citation
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
Citations number
30
Categorie Soggetti
Biophysics,Biology
ISSN journal
10111344
Volume
36
Issue
2
Year of publication
1996
Pages
127 - 133
Database
ISI
SICI code
1011-1344(1996)36:2<127:DFCDPT>2.0.ZU;2-R
Abstract
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.