内吞作用
渗透(战争)
肿瘤细胞
药物输送
癌症研究
化学
纳米技术
癌症治疗
生物物理学
药品
靶向给药
肿瘤消融
细胞生物学
循环肿瘤细胞
癌细胞
作者
Yuan Liu,Jie Meng,Wenxiong Cao,Shuang Xie,Qin Wang,Xiaohong Li
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-12-18
卷期号:25 (52): 18059-18067
标识
DOI:10.1021/acs.nanolett.5c04897
摘要
Chemotherapeutics encounter poor efficacy and serious adverse effects due to multiple delivery barriers. Inspired by the multipower-unit design and adjustable length of bullet train, we designed a "bullet train"-like transformable nanomotor (f-JSN-u)n to sequentially overcome multiple tumor delivery barriers. Upon administration, these rod-shaped (f-JSN-u)n assemblies achieved long circulation, and the "bullet train"-like motion enhanced their diffusion across tumor vasculatures and selective tumor accumulation. When reaching tumor sites, local NIR irradiation triggered the disassociation of rod-shaped "bullet train" into individual "carriage" with spherical shape and smaller size, enabling deep tumor penetration and enhanced cellular uptake. In the tumor microenvironment, the self-propelled motion further facilitated deeper tumor penetration, where folate-mediated cellular endocytosis and glutathione-triggered drug release ultimately boosted antitumor efficacy. Our study revealed (f-JSN-u)3 exhibited a 3.4-fold longer plasma half-life and a >3-fold higher distribution in tumor tissues compared to f-JSN-u, accompanied by significantly enhanced tumor penetration and remarkable antitumor efficacy.
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