两亲性
纳米技术
超短脉冲
材料科学
碳纤维
纳米生物技术
线粒体
生物物理学
化学
纳米颗粒
生物化学
生物
物理
光学
聚合物
激光器
复合材料
复合数
共聚物
作者
Feishi Shan,Jing Zhang,Chengshuang Liao,Yanman Liu,Xiangli Li,Haodong Mi,Wei Wang,Shanshan Jiang,Minyong Li,Yanhong Liu,Zhouyu Wang,Leyong Wang,Jun‐Jie Zhu
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-05-18
卷期号:19 (21): 20205-20214
被引量:14
标识
DOI:10.1021/acsnano.5c05934
摘要
Carbon dots (CDs) exhibit exceptional biocompatibility and programmable amphiphilicity, establishing them as transformative nanomaterials for subcellular visualization with exceptional resolution. However, existing CD-based probes lack the spatiotemporal precision required for real-time organelle tracking, particularly in mitochondrial-targeted imaging via ultrafast, wash-free protocols. To overcome these limitations, this study describes the solvent-free, high-temperature (280 °C) and short-time (2 h) preparation of green-emitting CDs (GCDs) with distinctive amphiphilic architectures utilizing benzoylurea and citric acid in a sealed high-pressure reactor. GCDs may form micelle-like structures driven to hydrophobic interactions, producing long-wavelength emission in contrast to blue emission in low-polar solvents. They also simultaneously activate the synergy of numerous endocytotic modes, achieving ultrafast (<5 s) and wash-free imaging. GCDs can also effectively target the mitochondria, more significantly, in both normal and cancer cells (Person's value ≈ 0.90/0.91), which is explained by the minor adjustment of mitochondrial membrane potential. This work describes assembly mechanisms of amphiphilic CDs while establishing potential design principles for mitochondria-targeted nanostructures with wash-free, ultrafast tracking.
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