纳米探针
荧光
聚集诱导发射
化学
发色团
猝灭(荧光)
一氧化氮
光化学
生物标志物
生物物理学
生物化学
有机化学
生物
量子力学
物理
作者
Junjie Chen,Longqi Chen,Yichang Fang,Fang Zeng,Shuizhu Wu
标识
DOI:10.1016/j.xcrp.2021.100570
摘要
Endogenous nitric oxide is important for living beings; hence, accurate and non-invasive detection of nitric oxide (NO) in situ is of significance. Benzothiadiazole-core chromophores are important near-infrared II (NIR-II) dyes, but such limitations as fluorescence quenching in aqueous media and non-activatable response constitute major barriers for biological applications. To address these issues, here we report an activatable nanoprobe, [email protected]βCD, with aggregation-induced emission for detecting the biomarker NO. The molecular probe BNDA and 2-hydroxypropyl-β-cyclodextrin (HβCD) form the amphiphilic host-guest complex BNDA-HβCD, which readily forms nanoaggregates in aqueous media and thereby affords the nanoprobe [email protected]βCD. NO reacts with the probe and generates the activated probe, which displays strong NIR-II fluorescence emission and optoacoustic signals. [email protected]βCD can detect liver injury and monitor therapeutic outcome in a mouse model by detecting hepatic NO; it can also image NO in soybean sprouts. The results indicate that [email protected]βCD is a robust tool for detecting NO in both animals and plants.
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