论文标题
多氨基苯二氨基酯纤维中的阿霉素和氧化铁纳米管共同载荷,以结合对癌细胞的磁性热和化学疗法作用
Co-loading of doxorubicin and iron oxide nanocubes in polycaprolactone fibers for combining Magneto-Thermal and chemotherapeutic effects on cancer cells
论文作者
论文摘要
在与癌症作斗争的策略中,多治疗方法被认为是制定多种武器以抑制肿瘤的明智选择。在这项工作中,在使用生物相容性支架时将化学治疗效应结合到磁性高温中,我们建立了一种静电纺丝方法,以产生装有磁性纳米颗粒作为热介质的多碳酸酯的纳米纤维,以在交替的磁场和毒素蛋白质为化学药物下选择性地激活。在临床磁性高温条件下提供基准热性能,研究了纤维的产生(在立方体边缘15和23 nm)进行了研究。将23 nm的纳米管纳入纤维时,获得了链条的布置。磁性纳米颗粒的这种线性构型类似于磁性细菌产生的磁体的线性构型,我们的磁纤维像磁体体一样表现出显着的加热作用。当缺少化学治疗剂时,磁纤维支架在成纤维细胞上表现出极好的生物相容性,并且在不暴露于磁性高热状态时,如生存力分析所示。相反,在暴露于磁性高温后,含有磁性纳米纸和阿霉素的纤维对宫颈癌细胞显示出显着的细胞毒性作用。值得注意的是,这些测试是在临床使用的磁性高温野外条件下进行的。如下所示,在阿霉素敏感的宫颈癌细胞上,磁性高温损伤与阿霉素在治疗温度下的扩散相结合是更有效的癌疗法。
Among the strategies to fight cancer, multi-therapeutic approaches are considered as a wise choice to put in place multiple weapons to suppress tumors. In this work, to combine chemotherapeutic effects to magnetic hyperthermia when using biocompatible scaffolds, we have established an electrospinning method to produce nanofibers of polycaprolactone loaded with magnetic nanoparticles as heat mediators to be selectively activated under alternating magnetic field and doxorubicin as a chemotherapeutic drug. Production of the fibers was investigated with iron oxide nanoparticles of peculiar cubic shape (at 15 and 23 nm in cube edges) as they provide benchmark heat performance under clinical magnetic hyperthermia conditions. With 23 nm nanocubes when included into the fibers, an arrangement in chains was obtained. This linear configuration of magnetic nanoparticles resemble that of the magnetosomes, produced by magnetotactic bacteria, and our magnetic fibers exhibited remarkable heating effects as the magnetosomes. Magnetic fiber scaffolds showed excellent biocompatibility on fibroblast cells when missing the chemotherapeutic agent and when not exposed to magnetic hyperthermia as shown by viability assays. On the contrary, the fibers containing both magnetic nanocubes and doxorubicin showed significant cytotoxic effects on cervical cancer cells following the exposure to magnetic hyperthermia. Notably, these tests were conducted at magnetic hyperthermia field conditions of clinical use. As here shown, on the doxorubicin sensitive cervical cancer cells, the combination of heat damage by magnetic hyperthermia with enhanced diffusion of doxorubicin at therapeutic temperature are responsible for a more effective oncotherapy.