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In vivo anticancer evaluation of the hyperthermic efficacy of anti-human epidermal growth factor receptor-targeted PEG-based nanocarrier containing magnetic nanoparticles

Polymeric nanoparticles with targeting moieties containing magnetic nanoparticles as theranostic agents have considerable potential for the treatment of cancer. Here we report the chemical synthesis and characterization of a poly(D,L-lactide-co-glycolide)-b-poly(ethylene glycol)-based nanocarrier co...

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Autores principales: Baldi, Giovanni, Ravagli, Costanza, Mazzantini, Filippo, Loudos, George, Adan, Jaume, Masa, Marc, Psimadas, Dimitrios, Fragogeorgi, Eirini A, Locatelli, Erica, Innocenti, Claudia, Sangregorio, Claudio, Comes Franchini, Mauro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077609/
https://www.ncbi.nlm.nih.gov/pubmed/25028545
http://dx.doi.org/10.2147/IJN.S61273
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author Baldi, Giovanni
Ravagli, Costanza
Mazzantini, Filippo
Loudos, George
Adan, Jaume
Masa, Marc
Psimadas, Dimitrios
Fragogeorgi, Eirini A
Locatelli, Erica
Innocenti, Claudia
Sangregorio, Claudio
Comes Franchini, Mauro
author_facet Baldi, Giovanni
Ravagli, Costanza
Mazzantini, Filippo
Loudos, George
Adan, Jaume
Masa, Marc
Psimadas, Dimitrios
Fragogeorgi, Eirini A
Locatelli, Erica
Innocenti, Claudia
Sangregorio, Claudio
Comes Franchini, Mauro
author_sort Baldi, Giovanni
collection PubMed
description Polymeric nanoparticles with targeting moieties containing magnetic nanoparticles as theranostic agents have considerable potential for the treatment of cancer. Here we report the chemical synthesis and characterization of a poly(D,L-lactide-co-glycolide)-b-poly(ethylene glycol)-based nanocarrier containing iron oxide nanoparticles and human epithelial growth factor receptor on the outer shell. The nanocarrier was also radiolabeled with (99m)Tc and tested as a theranostic nanomedicine, ie, it was investigated for both its diagnostic ability in vivo and its therapeutic hyperthermic effects in a standard A431 human tumor cell line. Following radiolabeling with (99m)Tc, the biodistribution and therapeutic hyperthermic effects of the nanosystem were studied noninvasively in vivo in tumor-bearing mice. A substantial decrease in tumor size correlated with an increase in both nanoparticle concentration and local temperature was achieved, confirming the possibility of using this multifunctional nanosystem as a therapeutic tool for epidermoid carcinoma.
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spelling pubmed-40776092014-07-15 In vivo anticancer evaluation of the hyperthermic efficacy of anti-human epidermal growth factor receptor-targeted PEG-based nanocarrier containing magnetic nanoparticles Baldi, Giovanni Ravagli, Costanza Mazzantini, Filippo Loudos, George Adan, Jaume Masa, Marc Psimadas, Dimitrios Fragogeorgi, Eirini A Locatelli, Erica Innocenti, Claudia Sangregorio, Claudio Comes Franchini, Mauro Int J Nanomedicine Original Research Polymeric nanoparticles with targeting moieties containing magnetic nanoparticles as theranostic agents have considerable potential for the treatment of cancer. Here we report the chemical synthesis and characterization of a poly(D,L-lactide-co-glycolide)-b-poly(ethylene glycol)-based nanocarrier containing iron oxide nanoparticles and human epithelial growth factor receptor on the outer shell. The nanocarrier was also radiolabeled with (99m)Tc and tested as a theranostic nanomedicine, ie, it was investigated for both its diagnostic ability in vivo and its therapeutic hyperthermic effects in a standard A431 human tumor cell line. Following radiolabeling with (99m)Tc, the biodistribution and therapeutic hyperthermic effects of the nanosystem were studied noninvasively in vivo in tumor-bearing mice. A substantial decrease in tumor size correlated with an increase in both nanoparticle concentration and local temperature was achieved, confirming the possibility of using this multifunctional nanosystem as a therapeutic tool for epidermoid carcinoma. Dove Medical Press 2014-06-24 /pmc/articles/PMC4077609/ /pubmed/25028545 http://dx.doi.org/10.2147/IJN.S61273 Text en © 2014 Baldi et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Baldi, Giovanni
Ravagli, Costanza
Mazzantini, Filippo
Loudos, George
Adan, Jaume
Masa, Marc
Psimadas, Dimitrios
Fragogeorgi, Eirini A
Locatelli, Erica
Innocenti, Claudia
Sangregorio, Claudio
Comes Franchini, Mauro
In vivo anticancer evaluation of the hyperthermic efficacy of anti-human epidermal growth factor receptor-targeted PEG-based nanocarrier containing magnetic nanoparticles
title In vivo anticancer evaluation of the hyperthermic efficacy of anti-human epidermal growth factor receptor-targeted PEG-based nanocarrier containing magnetic nanoparticles
title_full In vivo anticancer evaluation of the hyperthermic efficacy of anti-human epidermal growth factor receptor-targeted PEG-based nanocarrier containing magnetic nanoparticles
title_fullStr In vivo anticancer evaluation of the hyperthermic efficacy of anti-human epidermal growth factor receptor-targeted PEG-based nanocarrier containing magnetic nanoparticles
title_full_unstemmed In vivo anticancer evaluation of the hyperthermic efficacy of anti-human epidermal growth factor receptor-targeted PEG-based nanocarrier containing magnetic nanoparticles
title_short In vivo anticancer evaluation of the hyperthermic efficacy of anti-human epidermal growth factor receptor-targeted PEG-based nanocarrier containing magnetic nanoparticles
title_sort in vivo anticancer evaluation of the hyperthermic efficacy of anti-human epidermal growth factor receptor-targeted peg-based nanocarrier containing magnetic nanoparticles
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077609/
https://www.ncbi.nlm.nih.gov/pubmed/25028545
http://dx.doi.org/10.2147/IJN.S61273
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