普鲁士蓝
材料科学
光热治疗
体内
生物相容性
体外
热休克蛋白70
生物物理学
辐照
遗传增强
纳米技术
纳米颗粒
癌症研究
热休克蛋白
化学
生物化学
生物
基因
生物技术
物理化学
物理
核物理学
冶金
电化学
电极
作者
Yajuan Liu,Guiming Shu,Xue Li,Hongbin Chen,Bo Zhang,Huizhuo Pan,Tao Li,Xiaoqun Gong,Hanjie Wang,Xiaoli Wu,Yan Dou,Jin Chang
标识
DOI:10.1002/adfm.201802026
摘要
Abstract Realizing precise control of the therapeutic process is crucial for maximizing efficacy and minimizing side effects, especially for strategies involving gene therapy (GT). Herein, a multifunctional Prussian blue (PB) nanotheranostic platform is first designed and then loaded with therapeutic plasmid DNA (HSP70‐p53‐GFP) for near‐infrared (NIR) light‐triggered thermo‐controlled synergistic GT/photothermal therapy (PTT). Due to the unique structure of the PB nanocubes, the resulting PB@PEI/HSP70‐p53‐GFP nanoparticles (NPs) exhibit excellent photothermal properties and pronounced tumor‐contrast performance in T 1 / T 2 ‐weighted magnetic resonance imaging. Both in vitro and in vivo studies demonstrate that mild NIR‐laser irradiation (≈41 °C) activates the HSP70 promoter for tumor suppressor p53‐dependent apoptosis, while strong NIR‐laser irradiation (≈50 °C) induces photothermal ablation for cellular dysregulation and necrosis. Significant synergistic efficacy can be achieved by adjusting the NIR‐laser irradiation (from ≈41 to ≈50 °C), compared to using GT or PTT alone. In addition, in vitro and in vivo toxicity studies demonstrate that PB@PEI/HSP70‐p53‐GFP NPs have good biocompatibility. Therefore, this work provides a promising theranostic approach for controlling combined GT and PTT via the heat‐shock response.
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