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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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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
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author 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
author_facet 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
author_sort Nistorescu, Simona
collection PubMed
description 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.
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spelling pubmed-87058542021-12-25 Low Blue Dose Photodynamic Therapy with Porphyrin-Iron Oxide Nanoparticles Complexes: In Vitro Study on Human Melanoma Cells 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 Pharmaceutics Article 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. MDPI 2021-12-10 /pmc/articles/PMC8705854/ /pubmed/34959411 http://dx.doi.org/10.3390/pharmaceutics13122130 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
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
Low Blue Dose Photodynamic Therapy with Porphyrin-Iron Oxide Nanoparticles Complexes: In Vitro Study on Human Melanoma Cells
title Low Blue Dose Photodynamic Therapy with Porphyrin-Iron Oxide Nanoparticles Complexes: In Vitro Study on Human Melanoma Cells
title_full Low Blue Dose Photodynamic Therapy with Porphyrin-Iron Oxide Nanoparticles Complexes: In Vitro Study on Human Melanoma Cells
title_fullStr Low Blue Dose Photodynamic Therapy with Porphyrin-Iron Oxide Nanoparticles Complexes: In Vitro Study on Human Melanoma Cells
title_full_unstemmed Low Blue Dose Photodynamic Therapy with Porphyrin-Iron Oxide Nanoparticles Complexes: In Vitro Study on Human Melanoma Cells
title_short Low Blue Dose Photodynamic Therapy with Porphyrin-Iron Oxide Nanoparticles Complexes: In Vitro Study on Human Melanoma Cells
title_sort low blue dose photodynamic therapy with porphyrin-iron oxide nanoparticles complexes: in vitro study on human melanoma cells
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8705854/
https://www.ncbi.nlm.nih.gov/pubmed/34959411
http://dx.doi.org/10.3390/pharmaceutics13122130
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