Nanogel-based nitric oxide-driven nanomotor for deep tissue penetration and enhanced tumor therapy

被引:6
|
作者
Wang, Jianhong [1 ]
Liu, Junjie [2 ]
Sumbelli, Yiitcan [1 ]
Shao, Jingxin [1 ]
Shi, Xiangyang [2 ]
van Hest, Jan C. M. [1 ]
机构
[1] Eindhoven Univ Technol, Inst Complex Mol Syst ICMS, Dept Biomed Engn, Bioorgan Chem, NL-5600 MB Eindhoven, Netherlands
[2] Donghua Univ, Coll Biol Sci & Med Engn, Shanghai Engn Res Ctr Nanobiomat & Regenerat, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
基金
中国国家自然科学基金;
关键词
Nitric oxide; Nanomotors; Self-actuation; Deep penetration; Enhanced therapy; NANOPARTICLES; DELIVERY;
D O I
10.1016/j.jconrel.2024.06.021
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Antitumor agents often lack effective penetration and accumulation to achieve high therapeutic efficacy in treating solid tumors. Nanomotor-based nanomaterials offer a potential solution to address this obstacle. Among them, nitric oxide (NO) based nanomotors have garnered attention for their potential applications in nanomedicine. However, there widespread clinical adoption has been hindered by their complex preparation processes. To address this limitation, we have developed a NO -driven nanomotor utilizing a convenient and scalable nanogel preparation procedure. These nanomotors, loaded with the fluorescent probe / sonosensitizer chlorin e6 (Ce6), were specifically engineered for sonodynamic therapy. Through comprehensive in vitro investigations using both 2D and 3D cell models, as well as in vivo analysis of Ce6 fluorescent signal distribution in solid tumor models, we observed that the self -propulsion of these nanomotors significantly enhances cellular uptake and tumor penetration, particularly in solid tumors. This phenomenon enables efficient access to challenging tumor regions and, in some cases, results in complete tumor coverage. Notably, our nanomotors have demonstrated long-term in vivo biosafety. This study presents an effective approach to enhancing drug penetration and improving therapeutic efficacy in tumor treatment, with potential clinical relevance for future applications.
引用
收藏
页码:59 / 68
页数:10
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