BIOLOGICAL-ACTIVITIES OF PHTHALOCYANINES .12. SYNTHESIS TUMOR UPTAKE AND BIODISTRIBUTION OF C-14-LABELED DISULFONATED AND TRISULFONATED GALLIUM PHTHALOCYANINE IN C3H MICE

被引:26
作者
ROUSSEAU, J [1 ]
LANGLOIS, R [1 ]
ALI, H [1 ]
VANLIER, JE [1 ]
机构
[1] UNIV SHERBROOKE, FAC MED, MRC, RADIAT SCI GRP, SHERBROOKE J1H 5N4, QUEBEC, CANADA
基金
英国医学研究理事会;
关键词
cancer; carbon-14; gallium; pharmacokinetics; photodynamic therapy; Photosensitizers; phthalocyanines;
D O I
10.1016/1011-1344(90)85081-7
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The biodistribution and metabolism of 14C-labeled disulfonated and trisulfonated gallium phthalocyanine (Ga-PcS) was studied in radiation-induced fibrosarcoma tumor-bearing C3H mice. The [14C]Ga-PcS compounds were prepared via the condensation of [14C]phthalic acid and sulfophthalic acid in the presence of gallium chloride and characterized by their spectroscopic and chromatographic properties. The tissue concentrations of the dyes was measured by scintillation counting of the 14C and by extraction and fluorescence measurements. Elevated dye levels were found in the liver, lungs, kidneys and spleen as well as in the tumor. Lower sulfonation of Ga-PcS favored liver and spleen uptake whereas higher dye sulfonation resulted in greater kidney uptake. Both dyes showed high tumor uptake with peak concentrations exceeding those of most tissues except for the liver in the case of Ga-PcS2. The highest tumor uptake was observed with Ga-PcS3. Both dyes were slowly excreted from the body. The liver-feces pathway was favored in the case of Ga-PcS2 with high activities persisting in the liver, even after 21 days. The Ga-PcS3 was preferentially excreted via the kidney-urine pathway. High performance liquid chromatography analysis of the liver and tumor extracts of [14C]Ga-PcS3-treated animals did not reveal desulfonation of the dye. © 1990.
引用
收藏
页码:121 / 132
页数:12
相关论文
共 17 条
[1]   BIOLOGICAL-ACTIVITIES OF PHTHALOCYANINES .10. SYNTHESES AND ANALYSES OF SULFONATED PHTHALOCYANINES [J].
ALI, H ;
LANGLOIS, R ;
WAGNER, JR ;
BRASSEUR, N ;
PAQUETTE, B ;
VANLIER, JE .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1988, 47 (05) :713-717
[2]   DISTRIBUTION AND ELIMINATION OF PHOTOFRIN-II IN MICE [J].
BELLNIER, DA ;
HO, YK ;
PANDEY, RK ;
MISSERT, JR ;
DOUGHERTY, TJ .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1989, 50 (02) :221-228
[3]   BIOLOGICAL-ACTIVITIES OF PHTHALOCYANINES .7. PHOTOINACTIVATION OF V-79 CHINESE-HAMSTER CELLS BY SELECTIVELY SULFONATED GALLIUM PHTHALOCYANINES [J].
BRASSEUR, N ;
ALI, H ;
LANGLOIS, R ;
VANLIER, JE .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1987, 46 (05) :739-744
[4]   BIOLOGICAL-ACTIVITIES OF PHTHALOCYANINES .5. PHOTODYNAMIC THERAPY OF EMT-6 MAMMARY-TUMORS IN MICE WITH SULFONATED PHTHALOCYANINES [J].
BRASSEUR, N ;
ALI, H ;
LANGLOIS, R ;
WAGNER, JR ;
ROUSSEAU, J ;
VANLIER, JE .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1987, 45 (05) :581-586
[5]   BIOLOGICAL-ACTIVITIES OF PHTHALOCYANINES .9. PHOTOSENSITIZATION OF V-79 CHINESE-HAMSTER CELLS AND EMT-6 MOUSE MAMMARY-TUMOR BY SELECTIVELY SULFONATED ZINC PHTHALOCYANINES [J].
BRASSEUR, N ;
ALI, H ;
LANGLOIS, R ;
VANLIER, JE .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1988, 47 (05) :705-711
[6]   C-14 LABELING AND BIOLOGICAL-ACTIVITY OF THE TUMOR-LOCALIZING DERIVATIVE OF HEMATOPORPHYRIN [J].
HO, YK ;
PANDEY, RK ;
MISSERT, JR ;
BELLNIER, DA ;
DOUGHERTY, TJ .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1988, 48 (04) :445-449
[7]   TUMOR-LOCALIZATION AND PHOTOSENSITIZATION BY SULFONATED DERIVATIVES OF TETRAPHENYLPORPHINE [J].
KESSEL, D ;
THOMPSON, P ;
SAATIO, K ;
NANTWI, KD .
PHOTOCHEMISTRY AND PHOTOBIOLOGY, 1987, 45 (06) :787-790
[8]  
MCLEAN JR, 1977, 77EHD16 PUBL, P18
[9]  
Rosenthal I., 1989, PHTHALOCYANINES PROP, V1, P393
[10]   SYNTHESIS, TISSUE DISTRIBUTION AND TUMOR UPTAKE OF TC-99M-TETRASULFOPHTHALOCYANINE AND GA-67 TETRASULFOPHTHALOCYANINE [J].
ROUSSEAU, J ;
ALI, H ;
LAMOUREUX, G ;
LEBEL, E ;
VANLIER, JE .
INTERNATIONAL JOURNAL OF APPLIED RADIATION AND ISOTOPES, 1985, 36 (09) :709-716