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Facile preparation of multifunctional superparamagnetic PHBV microspheres containing SPIONs for biomedical applications

The promising potential of magnetic polymer microspheres in various biomedical applications has been frequently reported. However, the surface hydrophilicity of superparamagnetic iron oxide nanoparticles (SPIONs) usually leads to poor or even failed encapsulation of SPIONs in hydrophobic polymer mic...

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Autores principales: Li, Wei, Jan Zaloga, Ding, Yaping, Liu, Yufang, Janko, Christina, Pischetsrieder, Monika, Alexiou, Christoph, Boccaccini, Aldo R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804305/
https://www.ncbi.nlm.nih.gov/pubmed/27005428
http://dx.doi.org/10.1038/srep23140
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author Li, Wei
Jan Zaloga,
Ding, Yaping
Liu, Yufang
Janko, Christina
Pischetsrieder, Monika
Alexiou, Christoph
Boccaccini, Aldo R.
author_facet Li, Wei
Jan Zaloga,
Ding, Yaping
Liu, Yufang
Janko, Christina
Pischetsrieder, Monika
Alexiou, Christoph
Boccaccini, Aldo R.
author_sort Li, Wei
collection PubMed
description The promising potential of magnetic polymer microspheres in various biomedical applications has been frequently reported. However, the surface hydrophilicity of superparamagnetic iron oxide nanoparticles (SPIONs) usually leads to poor or even failed encapsulation of SPIONs in hydrophobic polymer microspheres using the emulsion method. In this study, the stability of SPIONs in poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) solution was significantly increased after surface modification with lauric acid. As a result, magnetic PHBV microspheres with high encapsulation efficiencies (71.0–87.4%) were prepared using emulsion-solvent extraction/evaporation method. Magnetic resonance imaging (MRI) showed significant contrast for the magnetic PHBV microspheres. The toxicity of these magnetic PHBV microspheres towards human T-lymphoma suspension cells and adherent colon carcinoma HT-29 cells was investigated using flow cytometry, and they were shown to be non-toxic in a broad concentration range. A model drug, tetracycline hydrochloride, was used to demonstrate the drug delivery capability and to investigate the drug release behavior of the magnetic PHBV microspheres. The drug was successfully loaded into the microspheres using lauric acid-coated SPIONs as drug carrier, and was released from the microspheres in a diffusion controlled manner. The developed magnetic PHBV microspheres are promising candidates for biomedical applications such as targeted drug delivery and MRI.
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spelling pubmed-48043052016-03-24 Facile preparation of multifunctional superparamagnetic PHBV microspheres containing SPIONs for biomedical applications Li, Wei Jan Zaloga, Ding, Yaping Liu, Yufang Janko, Christina Pischetsrieder, Monika Alexiou, Christoph Boccaccini, Aldo R. Sci Rep Article The promising potential of magnetic polymer microspheres in various biomedical applications has been frequently reported. However, the surface hydrophilicity of superparamagnetic iron oxide nanoparticles (SPIONs) usually leads to poor or even failed encapsulation of SPIONs in hydrophobic polymer microspheres using the emulsion method. In this study, the stability of SPIONs in poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) solution was significantly increased after surface modification with lauric acid. As a result, magnetic PHBV microspheres with high encapsulation efficiencies (71.0–87.4%) were prepared using emulsion-solvent extraction/evaporation method. Magnetic resonance imaging (MRI) showed significant contrast for the magnetic PHBV microspheres. The toxicity of these magnetic PHBV microspheres towards human T-lymphoma suspension cells and adherent colon carcinoma HT-29 cells was investigated using flow cytometry, and they were shown to be non-toxic in a broad concentration range. A model drug, tetracycline hydrochloride, was used to demonstrate the drug delivery capability and to investigate the drug release behavior of the magnetic PHBV microspheres. The drug was successfully loaded into the microspheres using lauric acid-coated SPIONs as drug carrier, and was released from the microspheres in a diffusion controlled manner. The developed magnetic PHBV microspheres are promising candidates for biomedical applications such as targeted drug delivery and MRI. Nature Publishing Group 2016-03-23 /pmc/articles/PMC4804305/ /pubmed/27005428 http://dx.doi.org/10.1038/srep23140 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Li, Wei
Jan Zaloga,
Ding, Yaping
Liu, Yufang
Janko, Christina
Pischetsrieder, Monika
Alexiou, Christoph
Boccaccini, Aldo R.
Facile preparation of multifunctional superparamagnetic PHBV microspheres containing SPIONs for biomedical applications
title Facile preparation of multifunctional superparamagnetic PHBV microspheres containing SPIONs for biomedical applications
title_full Facile preparation of multifunctional superparamagnetic PHBV microspheres containing SPIONs for biomedical applications
title_fullStr Facile preparation of multifunctional superparamagnetic PHBV microspheres containing SPIONs for biomedical applications
title_full_unstemmed Facile preparation of multifunctional superparamagnetic PHBV microspheres containing SPIONs for biomedical applications
title_short Facile preparation of multifunctional superparamagnetic PHBV microspheres containing SPIONs for biomedical applications
title_sort facile preparation of multifunctional superparamagnetic phbv microspheres containing spions for biomedical applications
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4804305/
https://www.ncbi.nlm.nih.gov/pubmed/27005428
http://dx.doi.org/10.1038/srep23140
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