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Functionalized magnetic iron oxide/alginate core-shell nanoparticles for targeting hyperthermia

Hyperthermia is one of the promising treatments for cancer therapy. However, the development of a magnetic fluid agent that can selectively target a tumor and efficiently elevate temperature while exhibiting excellent biocompatibility still remains challenging. Here a new core-shell nanostructure co...

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Detalles Bibliográficos
Autores principales: Liao, Shih-Hsiang, Liu, Chia-Hung, Bastakoti, Bishnu Prasad, Suzuki, Norihiro, Chang, Yung, Yamauchi, Yusuke, Lin, Feng-Huei, Wu, Kevin C-W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4427608/
https://www.ncbi.nlm.nih.gov/pubmed/26005343
http://dx.doi.org/10.2147/IJN.S68719
Descripción
Sumario:Hyperthermia is one of the promising treatments for cancer therapy. However, the development of a magnetic fluid agent that can selectively target a tumor and efficiently elevate temperature while exhibiting excellent biocompatibility still remains challenging. Here a new core-shell nanostructure consisting of inorganic iron oxide (Fe(3)O(4)) nanoparticles as the core, organic alginate as the shell, and cell-targeting ligands (ie, D-galactosamine) decorated on the outer surface (denoted as Fe(3)O(4)@Alg-GA nanoparticles) was prepared using a combination of a pre-gel method and coprecipitation in aqueous solution. After treatment with an AC magnetic field, the results indicate that Fe(3)O(4)@Alg-GA nanoparticles had excellent hyperthermic efficacy in a human hepatocellular carcinoma cell line (HepG2) owing to enhanced cellular uptake, and show great potential as therapeutic agents for future in vivo drug delivery systems.