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A Hybrid System for Magnetic Hyperthermia and Drug Delivery: SPION Functionalized by Curcumin Conjugate

Cancer is among the leading causes of death worldwide, thus there is a constant demand for new solutions, which may increase the effectiveness of anti-cancer therapies. We have designed and successfully obtained a novel, bifunctional, hybrid system composed of colloidally stabilized superparamagneti...

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Autores principales: Lachowicz, Dorota, Kaczyńska, Agnieszka, Wirecka, Roma, Kmita, Angelika, Szczerba, Wojciech, Bodzoń-Kułakowska, Anna, Sikora, Marcin, Karewicz, Anna, Zapotoczny, Szczepan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317039/
https://www.ncbi.nlm.nih.gov/pubmed/30486447
http://dx.doi.org/10.3390/ma11122388
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author Lachowicz, Dorota
Kaczyńska, Agnieszka
Wirecka, Roma
Kmita, Angelika
Szczerba, Wojciech
Bodzoń-Kułakowska, Anna
Sikora, Marcin
Karewicz, Anna
Zapotoczny, Szczepan
author_facet Lachowicz, Dorota
Kaczyńska, Agnieszka
Wirecka, Roma
Kmita, Angelika
Szczerba, Wojciech
Bodzoń-Kułakowska, Anna
Sikora, Marcin
Karewicz, Anna
Zapotoczny, Szczepan
author_sort Lachowicz, Dorota
collection PubMed
description Cancer is among the leading causes of death worldwide, thus there is a constant demand for new solutions, which may increase the effectiveness of anti-cancer therapies. We have designed and successfully obtained a novel, bifunctional, hybrid system composed of colloidally stabilized superparamagnetic iron oxide nanoparticles (SPION) and curcumin containing water-soluble conjugate with potential application in anticancer hyperthermia and as nanocarriers of curcumin. The obtained nanoparticulate system was thoroughly studied in respect to the size, morphology, surface charge, magnetic properties as well as some biological functions. The results revealed that the obtained nanoparticles, ca. 50 nm in diameter, were the agglomerates of primary particles with the magnetic, iron oxide cores of ca. 13 nm, separated by a thin layer of the applied cationic derivative of chitosan. These agglomerates were further coated with a thin layer of the sodium alginate conjugate of curcumin and the presence of both polymers was confirmed using thermogravimetry. The system was also proven to be applicable in magnetic hyperthermia induced by the oscillating magnetic field. A high specific absorption rate (SAR) of 280 [W/g] was registered. The nanoparticles were shown to be effectively uptaken by model cells. They were found also to be nontoxic in the therapeutically relevant concentration in in vitro studies. The obtained results indicate the high application potential of the new hybrid system in combination of magnetic hyperthermia with delivery of curcumin active agent.
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spelling pubmed-63170392019-01-08 A Hybrid System for Magnetic Hyperthermia and Drug Delivery: SPION Functionalized by Curcumin Conjugate Lachowicz, Dorota Kaczyńska, Agnieszka Wirecka, Roma Kmita, Angelika Szczerba, Wojciech Bodzoń-Kułakowska, Anna Sikora, Marcin Karewicz, Anna Zapotoczny, Szczepan Materials (Basel) Article Cancer is among the leading causes of death worldwide, thus there is a constant demand for new solutions, which may increase the effectiveness of anti-cancer therapies. We have designed and successfully obtained a novel, bifunctional, hybrid system composed of colloidally stabilized superparamagnetic iron oxide nanoparticles (SPION) and curcumin containing water-soluble conjugate with potential application in anticancer hyperthermia and as nanocarriers of curcumin. The obtained nanoparticulate system was thoroughly studied in respect to the size, morphology, surface charge, magnetic properties as well as some biological functions. The results revealed that the obtained nanoparticles, ca. 50 nm in diameter, were the agglomerates of primary particles with the magnetic, iron oxide cores of ca. 13 nm, separated by a thin layer of the applied cationic derivative of chitosan. These agglomerates were further coated with a thin layer of the sodium alginate conjugate of curcumin and the presence of both polymers was confirmed using thermogravimetry. The system was also proven to be applicable in magnetic hyperthermia induced by the oscillating magnetic field. A high specific absorption rate (SAR) of 280 [W/g] was registered. The nanoparticles were shown to be effectively uptaken by model cells. They were found also to be nontoxic in the therapeutically relevant concentration in in vitro studies. The obtained results indicate the high application potential of the new hybrid system in combination of magnetic hyperthermia with delivery of curcumin active agent. MDPI 2018-11-27 /pmc/articles/PMC6317039/ /pubmed/30486447 http://dx.doi.org/10.3390/ma11122388 Text en © 2018 by the authors. 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 (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lachowicz, Dorota
Kaczyńska, Agnieszka
Wirecka, Roma
Kmita, Angelika
Szczerba, Wojciech
Bodzoń-Kułakowska, Anna
Sikora, Marcin
Karewicz, Anna
Zapotoczny, Szczepan
A Hybrid System for Magnetic Hyperthermia and Drug Delivery: SPION Functionalized by Curcumin Conjugate
title A Hybrid System for Magnetic Hyperthermia and Drug Delivery: SPION Functionalized by Curcumin Conjugate
title_full A Hybrid System for Magnetic Hyperthermia and Drug Delivery: SPION Functionalized by Curcumin Conjugate
title_fullStr A Hybrid System for Magnetic Hyperthermia and Drug Delivery: SPION Functionalized by Curcumin Conjugate
title_full_unstemmed A Hybrid System for Magnetic Hyperthermia and Drug Delivery: SPION Functionalized by Curcumin Conjugate
title_short A Hybrid System for Magnetic Hyperthermia and Drug Delivery: SPION Functionalized by Curcumin Conjugate
title_sort hybrid system for magnetic hyperthermia and drug delivery: spion functionalized by curcumin conjugate
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6317039/
https://www.ncbi.nlm.nih.gov/pubmed/30486447
http://dx.doi.org/10.3390/ma11122388
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