DocumentCode
1766175
Title
Magnetic Heating of Iron Oxide Nanoparticles and Magnetic Micelles for Cancer Therapy
Author
Glover, Amanda L. ; Bennett, James B. ; Pritchett, Jeremy S. ; Nikles, Sarah M. ; Nikles, David E. ; Nikles, Jacqueline A. ; Brazel, Christopher S.
Author_Institution
Dept. of Chem., Univ. of Alabama, Tuscaloosa, AL, USA
Volume
49
Issue
1
fYear
2013
fDate
Jan. 2013
Firstpage
231
Lastpage
235
Abstract
The inclusion of magnetic nanoparticles into block copolymer micelles was studied towards the development of a targeted, magnetically triggered drug delivery system for cancer therapy. Herein, we report the synthesis of magnetic nanoparticles and poly(ethylene glycol-b-caprolactone) block copolymers, and experimental verification of magnetic heating of the nanoparticles, self-assembly of the block copolymers to form magnetic micelles, and thermally-enhanced drug release. The semicrystalline core of the micelles melted at temperatures just above physiological conditions, indicating that they could be used to release a chemotherapy agent from a thermoresponsive polymer system. The magnetic nanoparticles were shown to heat effectively in high frequency magnetic fields ranging from 30-70 kA/m. Magnetic micelles also showed heating properties, that when combined with a chemotherapeutic agent and a targeting ligand could be developed for localized, triggered drug delivery. During the magnetic heating experiments, a time lag was observed in the temperature profile for magnetic micelles, likely due to the heat of fusion of melting of polycaprolactone micelle cores before bulk solution temperatures increased. Doxorubicin, incorporated into the micelles, released faster when the micelles were heated above the core melting point.
Keywords
drug delivery systems; iron compounds; magnetic particles; nanobiotechnology; nanoparticles; polymer blends; radiation therapy; FexOy; block copolymer micelle; cancer therapy; chemotherapy agent; core melting point; iron oxide nanoparticle; magnetic heating; magnetic micelle; magnetically triggered drug delivery system; poly(ethylene glycol-b-caprolactone); self assembly thermally enhanced drug release; Drugs; Heating; Magnetic cores; Magnetic recording; Magnetic resonance imaging; Magnetic separation; Nanoparticles; Block copolymer micelles; drug delivery; hyperthermia; iron oxide nanoparticles;
fLanguage
English
Journal_Title
Magnetics, IEEE Transactions on
Publisher
ieee
ISSN
0018-9464
Type
jour
DOI
10.1109/TMAG.2012.2222359
Filename
6392354
Link To Document