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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8705854 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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