Tumour-localizing and tumour-photosensitizing properties of zinc(II)-octapentyl-phthalocyanine

被引:26
作者
Fabris, C
Ometto, C
Milanesi, C
Jori, G
Cook, MJ
Russell, DA
机构
[1] UNIV PADUA,DEPT BIOL,I-35121 PADUA,ITALY
[2] UNIV E ANGLIA,SCH CHEM SCI,NORWICH NR4 7TJ,NORFOLK,ENGLAND
关键词
photodynamic therapy; photosensitization; phthalocyanine; tumours;
D O I
10.1016/S1011-1344(97)00018-3
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
Zn(II)-octapentyl-phthalocyanine (ZnOPPc), incorporated into a Cremophor oil emulsion, was found to be a highly selective tumour-targeting agent (50-fold larger concentration in the tumour than in the peritumoral tissue) when injected at a dose of 1.46 mu mol (kg body weight)(-1) in Balb/c mice bearing an intramuscularly transplanted MS-2 fibrosarcoma. The pharmacokinetic properties of this phthalocyanine were closely similar to those found for the analogous octadecyl derivative, whereas the unsubstituted Zn(II)-phthalocyanine showed a lower efficiency and selectivity of tumour targeting than the octaalkyl-substituted phthalocyanines. Irradiation of the ZnOPPc-loaded tumour with 620-700 nm light 24 h after injection caused a significant delay of tumour growth with a gradual shrinkage of the neoplastic mass; the damage involved important contributions from both random necrosis and apoptosis of malignant cells. (C) 1997 Elsevier Science S.A.
引用
收藏
页码:279 / 284
页数:6
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