Liao Shih-Hsiang, Liu Chia-Hung, Bastakoti Bishnu Prasad, Suzuki Norihiro, Chang Yung, Yamauchi Yusuke, Lin Feng-Huei, Wu Kevin C-W
Department of Chemical Engineering, National Taiwan University No 1, Taipei, Taiwan.
Department of Urology, Taipei Medical University-Shuang Ho Hospital, New Taipei City, Taiwan.
Int J Nanomedicine. 2015 May 4;10:3315-27. doi: 10.2147/IJN.S68719. eCollection 2015.
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 (Fe3O4) nanoparticles as the core, organic alginate as the shell, and cell-targeting ligands (ie, D-galactosamine) decorated on the outer surface (denoted as Fe3O4@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 Fe3O4@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.
热疗是癌症治疗中一种很有前景的治疗方法。然而,开发一种能够选择性靶向肿瘤、有效升高温度同时具有优异生物相容性的磁性流体剂仍然具有挑战性。在此,通过预凝胶法和水溶液中共沉淀相结合的方法,制备了一种新的核壳纳米结构,其以无机氧化铁(Fe3O4)纳米颗粒为核,有机藻酸盐为壳,并在外表面修饰了细胞靶向配体(即D-半乳糖胺)(表示为Fe3O4@Alg-GA纳米颗粒)。经交变磁场处理后,结果表明,Fe3O4@Alg-GA纳米颗粒由于细胞摄取增强,在人肝癌细胞系(HepG2)中具有优异的热疗效果,并显示出作为未来体内药物递送系统治疗剂的巨大潜力。