The main aim of this paper is to describe the state of the art and the key problems of the selective synthesis of phthalocyanines and related compounds. This non-exhaustive overview comments on the synthesis of isomerically pure, unsymmetrically substituted and non-centrosymmetric phthalocyanines as
Selective aggregation of zinc phthalocyanines in the skin
β Scribed by Kenji Tabata; Kaoru Fukushima; Kazuo Oda; Ichiro Okura
- Publisher
- John Wiley and Sons
- Year
- 2000
- Tongue
- English
- Weight
- 80 KB
- Volume
- 04
- Category
- Article
- ISSN
- 1088-4246
No coin nor oath required. For personal study only.
β¦ Synopsis
In photodynamic therapy it is important to avoid undesirable side effects caused by photodynamic reactions with accumulated photosensitizers, especially in the skin. Although phthalocyanine monomers can serve as photosensitizers, aggregated phthalocyanines are inactive. In this study the aggregations of five zinc phthalocyanines (MSPc, TSPc, TX-101A, TX-105A and TX-106A) in the skin and in the tumor are compared. Every phthalocyanine was more dissociated in the tumor than in the skin. In particular, TX-101A and TX-106A remained in monomeric form in the tumor but were aggregated in the skin. The aggregation effects of phthalocyanines in organic solvents and biological materials were also investigated. These phthalocyanines were aggregated in water and ethanol and also by the addition of bovine serum albumin and ghosts of red cells. On the other hand, they were dissociated in propanol and also by the addition of low-density lipoprotein. It was found that the dissociation of these phthalocyanines depended strongly on the polarity of the solvents and on the biological microenvironment.
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