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Magnetoliposomes Containing Multicore Nanoparticles and a New Antitumor Thienopyridine Compound with Potential Application in Chemo/Thermotherapy

Multicore magnetic nanoparticles of manganese ferrite were prepared using carboxymethyl dextran as an agglutinating compound or by an innovative method using melamine as a cross-coupling agent. The nanoparticles prepared using melamine exhibited a flower-shape structure, a saturation magnetization o...

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Autores principales: Lopes, Fábio A. C., Fernandes, André V. F., Rodrigues, Juliana M., Queiroz, Maria-João R. P., Almeida, Bernardo G., Pires, Ana, Pereira, André M., Araújo, João P., Castanheira, Elisabete M. S., Rodrigues, Ana Rita O., Coutinho, Paulo J. G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313298/
https://www.ncbi.nlm.nih.gov/pubmed/35884856
http://dx.doi.org/10.3390/biomedicines10071547
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author Lopes, Fábio A. C.
Fernandes, André V. F.
Rodrigues, Juliana M.
Queiroz, Maria-João R. P.
Almeida, Bernardo G.
Pires, Ana
Pereira, André M.
Araújo, João P.
Castanheira, Elisabete M. S.
Rodrigues, Ana Rita O.
Coutinho, Paulo J. G.
author_facet Lopes, Fábio A. C.
Fernandes, André V. F.
Rodrigues, Juliana M.
Queiroz, Maria-João R. P.
Almeida, Bernardo G.
Pires, Ana
Pereira, André M.
Araújo, João P.
Castanheira, Elisabete M. S.
Rodrigues, Ana Rita O.
Coutinho, Paulo J. G.
author_sort Lopes, Fábio A. C.
collection PubMed
description Multicore magnetic nanoparticles of manganese ferrite were prepared using carboxymethyl dextran as an agglutinating compound or by an innovative method using melamine as a cross-coupling agent. The nanoparticles prepared using melamine exhibited a flower-shape structure, a saturation magnetization of 6.16 emu/g and good capabilities for magnetic hyperthermia, with a specific absorption rate (SAR) of 0.14 W/g. Magnetoliposome-like structures containing the multicore nanoparticles were prepared, and their bilayer structure was confirmed by FRET (Förster Resonance Energy Transfer) assays. The nanosystems exhibited sizes in the range of 250–400 nm and a low polydispersity index. A new antitumor thienopyridine derivative, 7-[4-(pyridin-2-yl)-1H-1,2,3-triazol-1-yl]thieno[3,2-b]pyridine, active against HeLa (cervical carcinoma), MCF-7 (breast adenocarcinoma), NCI-H460 (non-small-cell lung carcinoma) and HepG2 (hepatocellular carcinoma) cell lines, was loaded in these nanocarriers, obtaining a high encapsulation efficiency of 98 ± 2.6%. The results indicate that the new magnetoliposomes can be suitable for dual cancer therapy (combined magnetic hyperthermia and chemotherapy).
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spelling pubmed-93132982022-07-26 Magnetoliposomes Containing Multicore Nanoparticles and a New Antitumor Thienopyridine Compound with Potential Application in Chemo/Thermotherapy Lopes, Fábio A. C. Fernandes, André V. F. Rodrigues, Juliana M. Queiroz, Maria-João R. P. Almeida, Bernardo G. Pires, Ana Pereira, André M. Araújo, João P. Castanheira, Elisabete M. S. Rodrigues, Ana Rita O. Coutinho, Paulo J. G. Biomedicines Article Multicore magnetic nanoparticles of manganese ferrite were prepared using carboxymethyl dextran as an agglutinating compound or by an innovative method using melamine as a cross-coupling agent. The nanoparticles prepared using melamine exhibited a flower-shape structure, a saturation magnetization of 6.16 emu/g and good capabilities for magnetic hyperthermia, with a specific absorption rate (SAR) of 0.14 W/g. Magnetoliposome-like structures containing the multicore nanoparticles were prepared, and their bilayer structure was confirmed by FRET (Förster Resonance Energy Transfer) assays. The nanosystems exhibited sizes in the range of 250–400 nm and a low polydispersity index. A new antitumor thienopyridine derivative, 7-[4-(pyridin-2-yl)-1H-1,2,3-triazol-1-yl]thieno[3,2-b]pyridine, active against HeLa (cervical carcinoma), MCF-7 (breast adenocarcinoma), NCI-H460 (non-small-cell lung carcinoma) and HepG2 (hepatocellular carcinoma) cell lines, was loaded in these nanocarriers, obtaining a high encapsulation efficiency of 98 ± 2.6%. The results indicate that the new magnetoliposomes can be suitable for dual cancer therapy (combined magnetic hyperthermia and chemotherapy). MDPI 2022-06-29 /pmc/articles/PMC9313298/ /pubmed/35884856 http://dx.doi.org/10.3390/biomedicines10071547 Text en © 2022 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
Lopes, Fábio A. C.
Fernandes, André V. F.
Rodrigues, Juliana M.
Queiroz, Maria-João R. P.
Almeida, Bernardo G.
Pires, Ana
Pereira, André M.
Araújo, João P.
Castanheira, Elisabete M. S.
Rodrigues, Ana Rita O.
Coutinho, Paulo J. G.
Magnetoliposomes Containing Multicore Nanoparticles and a New Antitumor Thienopyridine Compound with Potential Application in Chemo/Thermotherapy
title Magnetoliposomes Containing Multicore Nanoparticles and a New Antitumor Thienopyridine Compound with Potential Application in Chemo/Thermotherapy
title_full Magnetoliposomes Containing Multicore Nanoparticles and a New Antitumor Thienopyridine Compound with Potential Application in Chemo/Thermotherapy
title_fullStr Magnetoliposomes Containing Multicore Nanoparticles and a New Antitumor Thienopyridine Compound with Potential Application in Chemo/Thermotherapy
title_full_unstemmed Magnetoliposomes Containing Multicore Nanoparticles and a New Antitumor Thienopyridine Compound with Potential Application in Chemo/Thermotherapy
title_short Magnetoliposomes Containing Multicore Nanoparticles and a New Antitumor Thienopyridine Compound with Potential Application in Chemo/Thermotherapy
title_sort magnetoliposomes containing multicore nanoparticles and a new antitumor thienopyridine compound with potential application in chemo/thermotherapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9313298/
https://www.ncbi.nlm.nih.gov/pubmed/35884856
http://dx.doi.org/10.3390/biomedicines10071547
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