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Multifunctional superparamagnetic iron oxide nanoparticles for combined chemotherapy and hyperthermia cancer treatment

机译:多功能超顺磁性氧化铁纳米颗粒联合化疗和高热癌症治疗

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摘要

Superparamagnetic iron oxide (SPIO) nanoparticles have the potential for use as a multimodal cancer therapy agent due to their ability to carry anticancer drugs and generate localized heat when exposed to an alternating magnetic field, resulting in combined chemotherapy and hyperthermia. To explore this potential, we synthesized SPIOs with a phospholipid-polyethylene glycol (PEG) coating, and loaded Doxorubicin (DOX) with a 30.8% w/w loading capacity when the PEG length is optimized. We found that DOX-loaded SPIOs exhibited a sustained DOX release over 72 hours where the release kinetics could be altered by the PEG length. In contrast, the heating efficiency of the SPIOs showed minimal change with the PEG length. With a core size of 14 nm, the SPIOs could generate sufficient heat to raise the local temperature to 43 degrees C, sufficient to trigger apoptosis in cancer cells. Further, we found that DOX-loaded SPIOs resulted in cell death comparable to free DOX, and that the combined effect of DOX and SPIO-induced hyperthermia enhanced cancer cell death in vitro. This study demonstrates the potential of using phospholipid-PEG coated SPIOs for chemotherapy-hyperthermia combinatorial cancer treatment with increased efficacy.
机译:超顺磁性氧化铁(SPIO)纳米颗粒有潜力用作一个多通道癌症吗治疗剂由于其承载的能力抗癌药物,产生局部热时接触到一个交变磁场,导致联合化疗和高热。合成SPIOs与phospholipid-polyethylene乙二醇(挂钩)涂层,和负载阿霉素(阿霉素)30.8% w / w装载能力挂钩的长度时优化。表现出持续强力霉素释放超过72小时释放动力学可以改变在哪里挂钩的长度。SPIOs显示最小变化的效率挂钩的长度。SPIOs可能产生足够的热量来提高当地的温度43摄氏度,足够了触发癌细胞凋亡。发现DOX-loaded SPIOs导致细胞死亡与自由阿霉素,阿霉素和SPIO-induced相结合高热增强体外癌细胞死亡。此研究表明,使用的潜力phospholipid-PEG涂布SPIOs为chemotherapy-hyperthermia组合癌症治疗效果增加。

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