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Polyaniline shell cross-linked Fe3O4 magnetic nanoparticles for heat activated killing of cancer cells.

Abstract
Superparamagnetic Fe3O4 nanoparticles are appealing materials for heat activated killing of cancer cells. Here, we report a novel method to enhance the heat activated killing of cancer cells under an AC magnetic field (AMF) by introducing a polyaniline impregnated shell onto the surface of Fe3O4 nanoparticles. These polyaniline shell cross-linked magnetic nanoparticles (PSMN) were prepared by in situ polymerization of aniline hydrochloride on the surface of carboxyl PEGylated Fe3O4 nanoparticles. XRD and TEM analyses revealed the formation of single phase inverse spinel Fe3O4 nanoparticles of a size of about 10 nm. The successful growth of the polyaniline shell on the surface of carboxyl PEGylated magnetic nanoparticles (CPMN) is evident from FTIR spectra, DLS, TGA, zeta-potential and magnetic measurements. Both CPMN and PSMN show good colloidal stability, superparamagnetic behavior at room temperature and excellent heating efficacy under AMF. It has been observed that the heating efficacy of PSMN under AMF was slightly reduced as compared to that of CPMN. The enhanced toxicity of PSMN to cancer cells under AMF suggests their strong potential for magnetic hyperthermia. Furthermore, PSMN shows high loading affinity for an anticancer drug (doxorubicin), its sustained release and substantial internalization in tumor cells.
AuthorsSuman Rana, Neena V Jadhav, K C Barick, B N Pandey, P A Hassan
JournalDalton transactions (Cambridge, England : 2003) (Dalton Trans) Vol. 43 Issue 32 Pg. 12263-71 (Aug 28 2014) ISSN: 1477-9234 [Electronic] England
PMID24948377 (Publication Type: Journal Article)
Chemical References
  • Aniline Compounds
  • Magnetite Nanoparticles
  • polyaniline
Topics
  • Aniline Compounds (chemistry, pharmacology)
  • Animals
  • Cell Line, Tumor
  • Cell Survival (drug effects)
  • Hot Temperature
  • Hyperthermia, Induced
  • Magnetic Fields
  • Magnetite Nanoparticles (chemistry, ultrastructure)
  • Mice
  • Microscopy, Confocal
  • Microscopy, Electron, Transmission
  • Neoplasms (therapy)
  • X-Ray Diffraction

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