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Ultrathin two-dimensional covalent organic framework nanoprobe for interference-resistant two-photon fluorescence bioimaging

机译:超薄二维共价有机骨架纳米探针用于抗干扰双光子荧光生物成像

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摘要

The complex environment of living organisms significantly challenges the selectivity of classic small-molecule fluorescent probes for bioimaging. Due to their predesigned topological structure and engineered internal pore surface, covalent organic frameworks (COFs) have the ability to filter out coexisting interference components and help to achieve accurate biosensing. Herein, we propose an effective interference-resistant strategy by creating a COF-based hybrid probe that combines the respective advantages of COFs and small-molecule probes. As a proof of concept, a two-photon fluorescent COF nanoprobe, namely >TpASH-NPHS, is developed for targeting hydrogen sulfide (H2S) as a model analyte. >TpASH-NPHS exhibits limited cytotoxicity, excellent photostability and long-term bioimaging capability. More importantly, compared with the small-molecule probe, >TpASH-NPHS achieves accurate detection without the interference from intracellular enzymes. This allows us to monitor the levels of endogenous H2S in a mouse model of cirrhosis.
机译:活生物体的复杂环境极大地挑战了经典的小分子荧光探针对生物成像的选择性。由于其预先设计的拓扑结构和经过设计的内部孔表面,共价有机框架(COF)具有过滤掉共存的干扰成分并有助于实现准确的生物传感的能力。在这里,我们通过创建结合了COF和小分子探针各自优点的基于COF的混合探针,提出了一种有效的抗干扰策略。作为概念的证明,开发了一种以双光子荧光COF纳米探针> TpASH-NPHS 为目标,以硫化氢(H2S)为模型分析物。 > TpASH-NPHS 具有有限的细胞毒性,出色的光稳定性和长期生物成像能力。更重要的是,与小分子探针相比,> TpASH-NPHS 实现了准确的检测,而不受细胞内酶的干扰。这使我们能够监测肝硬化小鼠模型中内源性H2S的水平。

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