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Systematic Study on the Remote Triggering of Thermo-Responsive Hydrogels Using RF Heating of Fe3O4 Nanoparticles

Published online by Cambridge University Press:  12 May 2015

Daniel Denmark ,
Devajyoti Mukherjee ,
Janae Bradley ,
Sarath Witanachchi  and
Pritish Mukherjee
Daniel Denmark
Affiliation:
Center for Integrated Functional Materials and Department of Physics, University of South Florida, Tampa, Florida 33620, USA
Devajyoti Mukherjee
Affiliation:
Center for Integrated Functional Materials and Department of Physics, University of South Florida, Tampa, Florida 33620, USA
Janae Bradley
Affiliation:
Center for Integrated Functional Materials and Department of Physics, University of South Florida, Tampa, Florida 33620, USA
Sarath Witanachchi
Affiliation:
Center for Integrated Functional Materials and Department of Physics, University of South Florida, Tampa, Florida 33620, USA
Pritish Mukherjee
Affiliation:
Center for Integrated Functional Materials and Department of Physics, University of South Florida, Tampa, Florida 33620, USA
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Abstract

In this work, a systematic study on the factors that influence the lower critical solution temperature (LCST) of poly(N-isopropylacrylamide) (PNIPAM) solutions during remote radiofrequency (RF) heating, using Fe3O4 magnetic nanoparticles (MNPs) is reported. A series of PNIPAM solutions with varying concentrations of Fe3O4 MNPs were prepared and characterized using transmission electron microscopy and Raman spectroscopy. Preliminary studies showed the highest specific absorption rate (SAR) for 15 nm sized Fe3O4 MNPs, which monotonically decreased as the MNP sizes increased to 20-30 nm. In-situ transmission measurements were used to determine the LCST of PNIPAM under various aqueous concentrations with dispersed Fe3O4 MNPs. A systematic decrease in the LCST from 34 °C to 31 °C was observed as the concentration of PNIPAM was increased from 0.3 wt. % to 1.0 wt. %, keeping the concentration of Fe3O4 MNPs constant. On the other hand, varying the concentrations of the MNPs did not drastically affect the LCSTs of PNIPAM solutions. However, varying the ion concentration of the PNIPAM solutions by adding adjusted KOH pellets, showed a pronounced lowering of the LCST by 2-3 °C at all PNIPAM concentrations. The remote triggering of phase transitions in PNIPAM solutions by raising the temperature above the LCST using Fe3O4 MNPs as reported here is important in targeted drug-delivery applications using thermo-responsive polymers.

Keywords

biomaterialphase transformationpolymer
Type
Articles
Information
MRS Online Proceedings Library (OPL) , Volume 1718: Symposium B – Multifunctional Polymeric and Hybrid Materials , 2015 , pp. 35 - 40
Copyright
Copyright © Materials Research Society 2015 

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References

REFERENCES

Schmaljohann, D., Adv. Drug Delivery Rev. 58, 1655–1670 (2006).CrossRefGoogle Scholar
Schild, H., Prog. Polym. Sci. 17, 163–249 (1992).CrossRefGoogle Scholar
Xia, Y., Burke, N., and Stöver, H., Macromolecules 39, 2275–2283 (2006).CrossRefGoogle Scholar
Schild, H., Muthukumar, M., and Tirrell, D., Macromolecules 24, 948–952 (1991).CrossRefGoogle Scholar
Freitag, R., and Garret-Flaudy, F., Langmuir 18, 3434–3440 (2002).CrossRefGoogle Scholar
Chen, L., Zhang, F. and Wang, C., Small 5, 621–628 (2009).CrossRefGoogle ScholarPubMed
Pankhurst, Q., Connolly, J., Jones, S. and Dobson, J., J. Phys. D: Appl. Phys. 36, R167–R181 (2003).CrossRefGoogle Scholar
Liu, T., Hu, S., Liu, D., Chen, S., and Chen, I., Nano Today 4, 52–65 (2009).CrossRefGoogle Scholar
Binns, C., in Nanostructured Materials for Magnetoelectronics, edited by Atkas, B. and Mikailzade, F. (Springer, Berlin, 2013) pp. 197–215.CrossRefGoogle Scholar
Atkinson, W. and Brezovich, I., IEEE Trans. Biomed. Eng. 31, 70–75 (1984).CrossRefGoogle Scholar
Vallejo-Fernandez, G., Whear, O., Roca, A., Hussain, S., Timmis, J., Patel, V., and O’Grady, K., J. Phys. D: Appl. Phys. 46, 312001 (2013).CrossRefGoogle Scholar
Zadrazil, A., Tokárová, V, and Stepánek, F., Soft Matter 8, 1811 (2012).CrossRefGoogle Scholar
Ahmed, Z., Gooding, E., Wang, L., and Asher, S., J. Phys. Chem. B 113, 4248–4256 (2009).CrossRefGoogle Scholar