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Magnetically responsive polycaprolactone nanocarriers for application in the biomedical field: magnetic hyperthermia, magnetic resonance imaging, and magnetic drug delivery

Authors :
Krzysztof Szczepanowicz
Marta Szczęch
Natalia Łopuszyńska
Davide Orsi
Władysław P. Węglarz
Krzysztof Jasiński
Luigi Cristofolini
Sami Kereïche
Franca Albertini
Source :
RSC Advances. 10:43607-43618
Publication Year :
2020
Publisher :
Royal Society of Chemistry (RSC), 2020.

Abstract

There are huge demands on multifunctional nanocarriers to be used in nanomedicine. Herein, we present a simple and efficient method for the preparation of multifunctional magnetically responsive polymeric-based nanocarriers optimized for biomedical applications. The hybrid delivery system is composed of drug-loaded polymer nanoparticles (poly(caprolactone), PCL) coated with a multilayer shell of polyglutamic acid (PGA) and superparamagnetic iron oxide nanoparticles (SPIONs), which are known as bio-acceptable components. The PCL nanocarriers with a model anticancer drug (Paclitaxel, PTX) were formed by the spontaneous emulsification solvent evaporation (SESE) method, while the magnetically responsive multilayer shell was formed via the layer-by-layer (LbL) method. As a result, we obtained magnetically responsive polycaprolactone nanocarriers (MN-PCL NCs) with an average size of about 120 nm. Using the 9.4 T preclinical magnetic resonance imaging (MRI) scanner we confirmed, that obtained MN-PCL NCs can be successfully used as a MRI-detectable drug delivery system. The magnetic hyperthermia effect of the MN-PCL NCs was demonstrated by applying a 25 mT radio-frequency (f = 429 kHz) alternating magnetic field. We found a Specific Absorption Rate (SAR) of 55 W g−1. The conducted research fulfills the first step of investigation for biomedical application, which is mandatory for the planning of any in vitro and in vivo studies.

Details

ISSN :
20462069
Volume :
10
Database :
OpenAIRE
Journal :
RSC Advances
Accession number :
edsair.doi.dedup.....42a0cc2c2299d83c6e38455aca22c838
Full Text :
https://doi.org/10.1039/d0ra07507h