School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, China; Key Laboratory of Targeting Therapy and Diagnosis for Critical Diseases, Henan Province, Zhengzhou, China; Collaborative Innovation Center of New Drug Research and Safety Evaluation, Henan Province, Zhengzhou, China.
School of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, China.
Nanomedicine. 2018 Jan;14(1):73-84. doi: 10.1016/j.nano.2017.08.019. Epub 2017 Sep 7.
NIR responsive inorganic hybrid (Ti@GO) was synthesized. It could absorb NIR light and convert it into local hyperthermia and ROS synchronously. Ti@GO was firstly developed as a photosensitizer and a photothermal agent to realize tumor PTT and PDT. For anti-tumor application, HA was grafted on Ti@GO simultaneously as water solubility improver and tumor targeting moiety. ICG was chosen as a model drug. Results demonstrated that HA-Ti@GO could remarkably improve ICG stability and drug accumulation in 4T1 cells, enhance tumor phototherapy efficiency and reduce light-associated side effects. HA-Ti@GO/ICG under NIR laser irradiation showed a significant decreased cell viability of 20.7±2.6% and a high DNA damage degree of 82.4±8.3%. Moreover, in vivo results showed that HA-Ti@GO/ICG plus NIR laser achieved almost complete tumor regression on 4T1 tumor-bearing mice, with a tumor volume of 67.0 mm. Taken together, our study provided a promising strategy to realize synergistic PTT/PDT tumor therapy with a single NIR light.
近红外响应无机杂化(Ti@GO)被合成。它可以吸收近红外光,并将其同步转化为局部热疗和 ROS。Ti@GO 首先被开发为光敏剂和光热剂,以实现肿瘤 PTT 和 PDT。为了进行抗肿瘤应用,同时将 HA 接枝到 Ti@GO 上,以提高其水溶性和肿瘤靶向性。ICG 被选为模型药物。结果表明,HA-Ti@GO 可显著提高 ICG 在 4T1 细胞中的稳定性和药物积累,增强肿瘤光疗效率,并降低光相关的副作用。在近红外激光照射下,HA-Ti@GO/ICG 表现出 20.7±2.6%的显著降低细胞活力和 82.4±8.3%的高 DNA 损伤程度。此外,体内结果表明,HA-Ti@GO/ICG 加近红外激光在 4T1 荷瘤小鼠上几乎完全实现了肿瘤消退,肿瘤体积为 67.0mm。综上所述,我们的研究提供了一种有前途的策略,可通过单一近红外光实现协同的 PTT/PDT 肿瘤治疗。