纳米探针
荧光
荧光寿命成像显微镜
化学
纳米颗粒
生物物理学
点击化学
肿瘤微环境
谷胱甘肽
纳米技术
光化学
组合化学
材料科学
癌症研究
生物化学
肿瘤细胞
酶
医学
生物
物理
量子力学
作者
Rui Luo,Chunqing Ou,Xinchao Li,Yanfang Wang,Wei Du,Gaolin Liang,Changyang Gong
出处
期刊:Nano Letters
[American Chemical Society]
日期:2021-12-27
卷期号:22 (1): 151-156
被引量:12
标识
DOI:10.1021/acs.nanolett.1c03534
摘要
The deep penetration, real-time monitoring ability, and high resolution of near-infrared (NIR) fluorescence imaging make it suitable for tumor diagnosis. However, the lack of specificity and selectivity restricts its further application. Here, for the first time, we applied a CBT-Cys click condensation reaction to synthesize an acidity-initiated molecular probe (AIM-Probe, Cys(StBu)-Lys(Cy 5.5)-EDA-PMA-CBT), which could self-assemble into nanoparticles (AIM-NP) with self-quenched fluorescence under glutathione (GSH) reduction. AIM-NP could accumulate in tumors after intravenous injection. Subsequently, the EDA-PMA part of AIM-Probe in AIM-NP is fractured by the unique subacid condition in the tumor microenvironment, and AIM-NP disassembles into a small AIM-cleaved molecule (PMA-CBT-Cys-Lys(Cy5.5)-EDA) along with fluorescence switching on. As a result, AIM-NP could switch on fluorescence at the tumor site, thereby achieving tumor-targeted imaging. To our knowledge, utilizing tumor acidity to initiate the disassembly of self-assembled nanoparticles through a CBT-Cys click condensation reaction has not been reported.
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