Chelation with Metal is not Essential for Antitumor Photodynamic Activity of Sulfonated Phthalocyanines

• Published in: Photochemistry and photobiology Vol. 75; no. 5; pp. 527 - 533
• Main Authors: Feofanov, Alexei, Grichine, Alexei, Karmakova, Tatyana, Kazachkina, Natalia, Pecherskih, Elena, Yakubovskaya, Raisa, Luk´yanets, Eugene, Derkacheva, Valentina, Egret-Charlier, Marguerite, Vigny, Paul
• Format: Journal Article
• Language: English
• Published: United States Blackwell Publishing Ltd 01.05.2002
• Subjects: Animals; Antineoplastic Agents - toxicity; Cell Division - drug effects; Humans; Indoles - toxicity; Lymphoma; Metals - toxicity; Photochemotherapy; PHOTOMEDICINE; Radiation-Sensitizing Agents - toxicity; Reactive Oxygen Species - metabolism; Tumor Cells, Cultured
• ISSN: 0031-8655; 1751-1097
• DOI: 10.1562/0031-8655(2002)075<0527:CWMINE>2.0.CO;2

It is generally assumed that a central metal is essential for the efficiency of phthalocyanines in photodynamic therapy (PDT) of cancer. Contrary to the set opinion, the results of the present study indicate that the metal-free sulfonated phthalocyanines (H2PcSn, where n is the number of sulfonate groups per molecule) possess a considerable photoactivity. The relative phototoxicities of H2PcS1.5, H2PcS2.4, H2PcS3.1 and H2PcS3.8 on HEp2 human epidermoid carcinoma cells were 3.3, 20, 3.3 and 1, respectively, thus demonstrating dependence of the activity on the sulfonation degree, known for metallo-PcSn. A significant delay in tumor growth and a decrease in tumor regrowth rate were observed in mice after PDT with H2PcS2.4. The antitumor effect declined in the order H2PcS2.4 > H2PcS3.1 > H2PcS1.5 and vanished for H2PcS3.8. We demonstrate here that the high photodynamic activity of H2PcS2.4 can be explained by its physicochemical properties in living cells and tissues. Thus, H2PcSn (n is about 2) can be considered as a new alternative in PDT of light-accessible neoplasms and further clinic-oriented studies are warranted.