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Low Blue Dose Photodynamic Therapy with Porphyrin-Iron Oxide Nanoparticles Complexes: In Vitro Study on Human Melanoma Cells

The purpose of this study was to investigate the effectiveness in photodynamic therapy of iron oxide nanoparticles (γ-Fe(2)O(3) NPs), synthesized by laser pyrolysis technique, functionalized with 5,10,15,20-(Tetra-4-sulfonatophenyl) porphyrin tetraammonium (TPPS) on human cutaneous melanoma cells, a...

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Detalles Bibliográficos
Autores principales: Nistorescu, Simona, Udrea, Ana-Maria, Badea, Madalina Andreea, Lungu, Iulia, Boni, Mihai, Tozar, Tatiana, Dumitrache, Florian, Maraloiu, Valentin-Adrian, Popescu, Roua Gabriela, Fleaca, Claudiu, Andronescu, Ecaterina, Dinischiotu, Anca, Staicu, Angela, Balas, Mihaela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8705854/
https://www.ncbi.nlm.nih.gov/pubmed/34959411
http://dx.doi.org/10.3390/pharmaceutics13122130
Descripción
Sumario:The purpose of this study was to investigate the effectiveness in photodynamic therapy of iron oxide nanoparticles (γ-Fe(2)O(3) NPs), synthesized by laser pyrolysis technique, functionalized with 5,10,15,20-(Tetra-4-sulfonatophenyl) porphyrin tetraammonium (TPPS) on human cutaneous melanoma cells, after only 1 min blue light exposure. The efficiency of porphyrin loading on the iron oxide nanocarriers was estimated by using absorption and FTIR spectroscopy. The singlet oxygen yield was determined via transient characteristics of singlet oxygen phosphorescence at 1270 nm both for porphyrin functionalized nanoparticles and rose bengal used as standard. The irradiation was performed with a LED (405 nm, 1 mW/cm(2)) for 1 min after melanoma cells were treated with TPPS functionalized iron oxide nanoparticles (γ-Fe(2)O(3) NPs_TPPS) and incubated for 24 h. Biological tests revealed a high anticancer effect of γ-Fe(2)O(3) NPs_TPPS complexes indi-cated by the inhibition of tumor cell proliferation, reduction of cell adhesion, and induction of cell death through ROS generated by TPPS under light exposure. The biological assays were combined with the pharmacokinetic prediction of the porphyrin.