15 nm聚乙二醇保护的Au纳米颗粒对HepG2细胞的放射增敏作用

Radiosensitivity enhancement of typical 15 nm polyethylene-glycol-coated Au nanoparticles on HepG2 cell

    摘要
  • 摘要:
    目的 研究Au纳米颗粒对HepG2细胞的放射增敏作用。
    方法 首先制备典型的15 nm聚乙二醇（PEG）包裹的Au纳米颗粒，然后使用紫外可见分光光度计实时定量检测纳米颗粒的血浆稳定性，同时使用噻唑蓝法研究给药后24 h和48 h的细胞活性，最后，通过克隆形成实验研究不同浓度的Au纳米颗粒对HepG2细胞的放射增敏作用。
    结果 PEG包裹的Au纳米颗粒具有较好的血浆稳定性，在24 h及以后未见表面等离子共振吸收峰有明显的偏移。细胞活性实验表明，24 h后，细胞的活性有所降低，但是48 h后细胞的活性迅速恢复到90%。进一步研究克隆形成发现，Au纳米颗粒具有明显的放射增敏作用。
    结论 15 nm PEG包裹的Au纳米颗粒具有较高的血浆稳定性、较低的细胞毒性和较好的放射增敏作用。

     

    Abstract:
    Objective To investigate the radiosensitivity enhancement of Au nanoparticles to HepG2 cell.
    Methods 15 nm polyethylene-glycol-coated(PEG) Au nanoparticles were synthesized, and then blood stability were tested by using the UV-vis optical absorption. Meanwhile, 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide methods were used to investigate the cell viability after 24 and 48 hours treatments, and cloning formation were used to investigate the radiosensitivity enhancement.
    Results It was found that PEG-coated Au nanoparticles presented a high blood stability, and surface plasmon response has not shown significant changes after 24 hours. Cell viability was decreased after 24 hours treatment, but it was recovered to 90% after 48 hours. Cloning formation showed Au nanoparticles presented a significant radiosensitivity enhancement.
    Conclusions 15 nm PEG-coated Au nanoparticles presented a good blood stability, low cytotoxicity and high radiosensitivity enhancement.

     

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