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双核@壳结构的FeO-NaYF@TiO纳米复合材料作为用于生物成像和联合化学-声动力疗法的磁性靶向药物载体。

Dual-core@shell-structured FeO-NaYF@TiO nanocomposites as a magnetic targeting drug carrier for bioimaging and combined chemo-sonodynamic therapy.

作者信息

Shen Song, Guo Xiaomeng, Wu Lin, Wang Meng, Wang Xinshi, Kong Fenfen, Shen Haijun, Xie Meng, Ge Yanru, Jin Yi

机构信息

College of Pharmaceutical Sciences, Jiangsu University, Zhenjiang, Jiangsu 212013, China.

出版信息

J Mater Chem B. 2014 Sep 21;2(35):5775-5784. doi: 10.1039/c4tb00841c. Epub 2014 Jul 28.

Abstract

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.

摘要

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。

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