| Literature DB >> 27085647 |
Göktürk Avşar1, Fatma Aslıhan Sari2, A Celil Yuzer2, Hale Melis Soylu3, Ozge Er4, Mine Ince5, Fatma Yurt Lambrecht6.
Abstract
A near IR absorbing phthalocyanine bearing four binaphtyl group has been synthesized in order to investigate its cytotoxicity and intracellular uptake of sensitizer on MCF-7 (human breast cancer), MDAH (ovarian cancer), HeLa (human epitheloid cervix carcinoma), EMT-6 (mouse breast cancer) and WI-38 (human fibroblast lung) cell lines. ZnPc showed four time higher intracellular uptake in carcinoma cells (MCF-7) than normal (WI-38) cell lines. With the aim of studying in detail the biodistribution feature and tumor nuclear imaging capacity, ZnPc was also labeled with I-131. The efficiency of radiolabeled compound was 95±4.6%. In addition, ZnPc reveals to be very efficient singlet oxygen generators (ΦΔ=0.612 in DMSO) and promising PS for PDT application. In vitro fluorescence imaging study with MCF-7 cells showed that ZnPc localized in cytoplasm of the cells. This results showed that synthesized ZnPc is promising candidate for dual fluorescence/nuclear imaging breast cancer and shows potential PS for PDT application.Entities:
Keywords: (131)I; Breast cancer; Dual imaging; Nuclear imaging; Phthalocyanine; Radiolabeling
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Year: 2016 PMID: 27085647 DOI: 10.1016/j.ijpharm.2016.04.023
Source DB: PubMed Journal: Int J Pharm ISSN: 0378-5173 Impact factor: 5.875