4.6 Article

In vitro study on apoptotic cell death by effective magnetic hyperthermia with chitosan-coated MnFe2O4

Journal

NANOTECHNOLOGY
Volume 27, Issue 11, Pages -

Publisher

IOP PUBLISHING LTD
DOI: 10.1088/0957-4484/27/11/115101

Keywords

MnFe2O4 nanoparticles; magnetic hyperthermia; chitosan; cell death; apoptosis; cellular uptake

Funding

  1. Marine Biotechnology Program - Ministry of Oceans and Fisheries, Republic of Korea [20150220]
  2. Korea Institute of Marine Science & Technology Promotion (KIMST) [201502202] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  3. National Research Foundation of Korea [21A20130012185] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Magnetic nanoparticles (MNPs) have been widely investigated as a hyperthermic agent for cancer treatment. In this study, thermally responsive Chitosan-coated MnFe2O4 (Chitosan-MnFe2O4) nanoparticles were developed to conduct localized magnetic hyperthermia for cancer treatment. Hydrophobic MnFe2O4 nanoparticles were synthesized via thermal decomposition and modified with 2,3-dimercaptosuccinic acid (DMSA) for further conjugation of chitosan. Chitosan-MnFe2O4 nanoparticles exhibited high magnetization and excellent biocompatibility along with low cell cytotoxicity. During magnetic hyperthermia treatment (MHT) with Chitosan-MnFe2O4 on MDA-MB 231 cancer cells, the targeted therapeutic temperature was achieved by directly controlling the strength of the external AC magnetic fields. In vitro Chitosan-MnFe2O4-assisted MHT at 42 degrees C led to drastic and irreversible changes in cell morphology and eventual cellular death in association with the induction of apoptosis through heat dissipation from the excited magnetic nanoparticles. Therefore, the Chitosan-MnFe2O4 nanoparticles with high biocompatibility and thermal capability can be an effective nano-mediated agent for MHT on cancer.

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