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Smart Magnetic Nanocarriers for Multi-Stimuli On-Demand Drug Delivery
In this study, we report the realization of drug-loaded smart magnetic nanocarriers constituted by superparamagnetic iron oxide nanoparticles encapsulated in a dual pH- and temperature-responsive poly (N-vinylcaprolactam-co-acrylic acid) copolymer to achieve highly controlled drug release and locali...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8840331/ https://www.ncbi.nlm.nih.gov/pubmed/35159647 http://dx.doi.org/10.3390/nano12030303 |
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author | Eslami, Parisa Albino, Martin Scavone, Francesca Chiellini, Federica Morelli, Andrea Baldi, Giovanni Cappiello, Laura Doumett, Saer Lorenzi, Giada Ravagli, Costanza Caneschi, Andrea Laurenzana, Anna Sangregorio, Claudio |
author_facet | Eslami, Parisa Albino, Martin Scavone, Francesca Chiellini, Federica Morelli, Andrea Baldi, Giovanni Cappiello, Laura Doumett, Saer Lorenzi, Giada Ravagli, Costanza Caneschi, Andrea Laurenzana, Anna Sangregorio, Claudio |
author_sort | Eslami, Parisa |
collection | PubMed |
description | In this study, we report the realization of drug-loaded smart magnetic nanocarriers constituted by superparamagnetic iron oxide nanoparticles encapsulated in a dual pH- and temperature-responsive poly (N-vinylcaprolactam-co-acrylic acid) copolymer to achieve highly controlled drug release and localized magnetic hyperthermia. The magnetic core was constituted by flower-like magnetite nanoparticles with a size of 16.4 nm prepared by the polyol approach, with good saturation magnetization and a high specific absorption rate. The core was encapsulated in poly (N-vinylcaprolactam-co-acrylic acid) obtaining magnetic nanocarriers that revealed reversible hydration/dehydration transition at the acidic condition and/or at temperatures above physiological body temperature, which can be triggered by magnetic hyperthermia. The efficacy of the system was proved by loading doxorubicin with very high encapsulation efficiency (>96.0%) at neutral pH. The double pH- and temperature-responsive nature of the magnetic nanocarriers facilitated a burst, almost complete release of the drug at acidic pH under hyperthermia conditions, while a negligible amount of doxorubicin was released at physiological body temperature at neutral pH, confirming that in addition to pH variation, drug release can be improved by hyperthermia treatment. These results suggest this multi-stimuli-sensitive nanoplatform is a promising candidate for remote-controlled drug release in combination with magnetic hyperthermia for cancer treatment. |
format | Online Article Text |
id | pubmed-8840331 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88403312022-02-13 Smart Magnetic Nanocarriers for Multi-Stimuli On-Demand Drug Delivery Eslami, Parisa Albino, Martin Scavone, Francesca Chiellini, Federica Morelli, Andrea Baldi, Giovanni Cappiello, Laura Doumett, Saer Lorenzi, Giada Ravagli, Costanza Caneschi, Andrea Laurenzana, Anna Sangregorio, Claudio Nanomaterials (Basel) Article In this study, we report the realization of drug-loaded smart magnetic nanocarriers constituted by superparamagnetic iron oxide nanoparticles encapsulated in a dual pH- and temperature-responsive poly (N-vinylcaprolactam-co-acrylic acid) copolymer to achieve highly controlled drug release and localized magnetic hyperthermia. The magnetic core was constituted by flower-like magnetite nanoparticles with a size of 16.4 nm prepared by the polyol approach, with good saturation magnetization and a high specific absorption rate. The core was encapsulated in poly (N-vinylcaprolactam-co-acrylic acid) obtaining magnetic nanocarriers that revealed reversible hydration/dehydration transition at the acidic condition and/or at temperatures above physiological body temperature, which can be triggered by magnetic hyperthermia. The efficacy of the system was proved by loading doxorubicin with very high encapsulation efficiency (>96.0%) at neutral pH. The double pH- and temperature-responsive nature of the magnetic nanocarriers facilitated a burst, almost complete release of the drug at acidic pH under hyperthermia conditions, while a negligible amount of doxorubicin was released at physiological body temperature at neutral pH, confirming that in addition to pH variation, drug release can be improved by hyperthermia treatment. These results suggest this multi-stimuli-sensitive nanoplatform is a promising candidate for remote-controlled drug release in combination with magnetic hyperthermia for cancer treatment. MDPI 2022-01-18 /pmc/articles/PMC8840331/ /pubmed/35159647 http://dx.doi.org/10.3390/nano12030303 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 Eslami, Parisa Albino, Martin Scavone, Francesca Chiellini, Federica Morelli, Andrea Baldi, Giovanni Cappiello, Laura Doumett, Saer Lorenzi, Giada Ravagli, Costanza Caneschi, Andrea Laurenzana, Anna Sangregorio, Claudio Smart Magnetic Nanocarriers for Multi-Stimuli On-Demand Drug Delivery |
title | Smart Magnetic Nanocarriers for Multi-Stimuli On-Demand Drug Delivery |
title_full | Smart Magnetic Nanocarriers for Multi-Stimuli On-Demand Drug Delivery |
title_fullStr | Smart Magnetic Nanocarriers for Multi-Stimuli On-Demand Drug Delivery |
title_full_unstemmed | Smart Magnetic Nanocarriers for Multi-Stimuli On-Demand Drug Delivery |
title_short | Smart Magnetic Nanocarriers for Multi-Stimuli On-Demand Drug Delivery |
title_sort | smart magnetic nanocarriers for multi-stimuli on-demand drug delivery |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8840331/ https://www.ncbi.nlm.nih.gov/pubmed/35159647 http://dx.doi.org/10.3390/nano12030303 |
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