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基于无机杂化的光稳定性吲哚菁绿递药系统的近红外光诱导肿瘤光疗

NIR light-induced tumor phototherapy using photo-stable ICG delivery system based on inorganic hybrid.

机构信息

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.

出版信息

Nanomedicine. 2018 Jan;14(1):73-84. doi: 10.1016/j.nano.2017.08.019. Epub 2017 Sep 7.

Abstract

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.

摘要

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。

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