4
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: not found
      • Article: not found

      Enhanced Magnetic Fluid Hyperthermia by Micellar Magnetic Nanoclusters Composed of MnxZn1–xFe2O4 Nanoparticles for Induced Tumor Cell Apoptosis

      1 , 1 , 2 , 1 , 2 , 1 , 3 , 3 , 4
      ACS Applied Materials & Interfaces
      American Chemical Society (ACS)

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Monodispersed MnxZn1-xFe2O4 magnetic nanoparticles of 8 nm are synthesized and encapsulated in amphiphilic block copolymer for development of the hydrophilic magnetic nanoclusters (MNCs). These MNCs exhibit superparamagnetic characteristics, high specific absorption rate (SAR), large saturation magnetization (Ms), excellent stability, and good biocompatibility. MnFe2O4 and Mn0.6Zn0.4Fe2O4 are selected as optimum compositions for the MNCs (MnFe2O4/MNC and Mn0.6Zn0.4Fe2O4/MNC) and employed for magnetic fluid hyperthermia (MFH) in vitro. To ensure biosafety of MFH, the parameters of alternating magnetic field (AMF) and exposure time are optimized with low frequency, f, and strength of applied magnetic field, Happlied. Under optimized conditions, MFH of MnFe2O4/MNC and Mn0.6Zn0.4Fe2O4/MNC result in cancer cell death rate up to 90% within 15 min. The pathway of cancer cell death is identified as apoptosis, which occurs in mild hyperthermia near 43 °C. Both MnFe2O4/MNC and Mn0.6Zn0.4Fe2O4/MNC show similar efficiencies on drug-sensitive and drug-resistant cancer cells. On the basis of these findings, those MnxZn1-xFe2O4 nanoclusters can serve as a promising candidate for effective targeting, diagnosis, and therapy of cancers. The multimodal cancer treatment is also possible as amphiphilic block copolymer can encapsulate, in a similar fashion, different nanoparticles, hydrophobic drugs, and other functional molecules.

          Related collections

          Author and article information

          Journal
          ACS Applied Materials & Interfaces
          ACS Appl. Mater. Interfaces
          American Chemical Society (ACS)
          1944-8244
          1944-8252
          September 17 2014
          September 24 2014
          October 08 2014
          : 6
          : 19
          : 16867-16879
          Affiliations
          [1 ]Institute of Nano and Biopolymeric Materials, School of Materials Science and Engineering, Tongji University, 4800 Caoan Road, Shanghai 201804, China
          [2 ]Key Laboratory of Advanced Civil Engineering Materials (Tongji University), Ministry of Education, Shanghai 201804, China
          [3 ]Key Laboratory of Basic Research in Cardiology, Ministry of Education, Shanghai East Hospital, Institute for Biomedical Engineering and Nano Science, School of Medicine, Tongji University, Shanghai 200120, China
          [4 ]Materials Science and Engineering Program, Department of Mechanical and Materials Engineering, Colleague of Engineering and Applied Science, University of Cincinnati, Cincinnati, Ohio 45221-0072, United States
          Article
          10.1021/am5042934
          25204363
          180601d8-c22f-48c9-a139-9af983bf24c3
          © 2014
          Product
          Self URI (article page): http://pubs.acs.org/doi/10.1021/am5042934

          Comments

          Comment on this article