Volume 6, Issue 6 , Pages 777-785, December 2010
Study of the stabilization of zinc phthalocyanine in sol-gel TiO2 for photodynamic therapy applications
Abstract
Photodynamic therapy (PDT) has emerged as an alternative and promising noninvasive treatment for cancer. It is a two-step procedure that uses a combination of molecular oxygen, visible light, and photosensitizer (PS) agents; phthalocyanine (Pc) was supported over titanium oxide but has not yet been used for cell inactivation. Zinc phthalocyanine (ZnPc) molecules were incorporated into the porous network of titanium dioxide (TiO2) using the sol-gel method. It was prepared from stock solutions of ZnPc and TiO2. ZnPc-TiO2 was tested with four cancer cell lines. The characterization of supported ZnPc showed that phthalocyanine is linked by the N-pyrrole to the support and is stable up to 250°C, leading to testing for PDT. The preferential localization in target organelles such as mitochondria or lysosomes could determine the cell death mechanism after PDT. The results suggest that nanoparticulated TiO2 sensitized with ZnPc is an excellent candidate as sensitizer in PDT against cancer and infectious diseases.
From the Clinical Editor
Photodynamic therapy is a two-step procedure that uses a combination of molecular oxygen, visible light and photosensitizer agents as an alternative and promising non-invasive treatment for cancer. The results of this study suggest that nanoparticulated TiO2 sensitized with ZnPc is an excellent photosensitizer candidate against cancer and infectious diseases.
Key words: Titania, Phthalocyanine, Cancer, Photodynamic therapies
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This work was supported by the Instituto Colombiano para el Desarrollo de la Ciencia y la Tecnologia “Francisco Jose de Caldas” COLCIENCIAS (Grant 1102-04-14130; RC No 480-2003), the Universidad Industrial de Santander, Bucaramanga, Colombia, and the program “Apoyo a los doctorados nacionales”, from COLCIENCIAS. Thanks to CONACYT-FONCICYT (Grant 96095).
PII: S1549-9634(10)00156-5
doi:10.1016/j.nano.2010.04.007
© 2010 Elsevier Inc. All rights reserved.
Volume 6, Issue 6 , Pages 777-785, December 2010
