Shen Song, Guo Xiaomeng, Wu Lin, Wang Meng, Wang Xinshi, Kong Fenfen, Shen Haijun, Xie Meng, Ge Yanru, Jin Yi
College of Pharmaceutical Sciences, Jiangsu University, Zhenjiang, Jiangsu 212013, China.
J Mater Chem B. 2014 Sep 21;2(35):5775-5784. doi: 10.1039/c4tb00841c. Epub 2014 Jul 28.
Multifunctional dual-core@shell (FeO-NaYF@TiO) nanocomposite (DCSNC) loaded with doxorubicin (DOX) have been developed for synergetic sonodynamic cancer chemotherapy, where titanium dioxide (TiO) is employed as a sonosensitizer for sonodynamic therapy (SDT) of the tumor in deep tissues, and NaYF is used for upconversion luminescence (UCL) imaging. After being coated with hyaluronic acid (HA), the nanocomposites exhibit a time dependent cellular uptake and an excellent nucleus targeting effect in KB and MCF-7 cells. The ultrasound of HA-DCSNCs obviously enhances the apoptosis rate of MCF-7 cells. A greater tumor inhibition rate is observed when the tumor-bearing mice are treated with combined therapy (88.36%) compared with chemotherapy (28.36%) or sonodynamic therapy (38.91%) alone, indicating the potential of sonodynamic chemotherapy for cancer treatment.
负载阿霉素(DOX)的多功能双核@壳层(FeO-NaYF@TiO)纳米复合材料(DCSNC)已被开发用于协同声动力癌症化疗,其中二氧化钛(TiO)用作深部组织肿瘤声动力治疗(SDT)的声敏剂,而NaYF用于上转换发光(UCL)成像。用透明质酸(HA)包被后,纳米复合材料在KB和MCF-7细胞中表现出时间依赖性的细胞摄取和优异的细胞核靶向作用。HA-DCSNCs的超声明显提高了MCF-7细胞的凋亡率。与单独化疗(28.36%)或声动力治疗(38.91%)相比,荷瘤小鼠接受联合治疗(88.36%)时观察到更高的肿瘤抑制率,表明声动力化疗在癌症治疗中的潜力。