School of Chemical and Biomedical Engineering , Nanyang Technological University , 70 Nanyang Drive , Singapore 637457 , Singapore.
J Am Chem Soc. 2019 Jul 10;141(27):10581-10584. doi: 10.1021/jacs.9b02580. Epub 2019 Jul 1.
Real-time multiplex imaging is imperative to biology and diagnosis but remains challenging for optical modality. Herein, a unimolecular chemo-fluoro-luminescent reporter (CFR) is synthesized for duplex imaging of drug-induced hepatotoxicity (DIH), a long-term medical concern. CFR simultaneously detects superoxide anion (O) and caspase-3 (casp3) through respective activation of its independent chemiluminescence and near-infrared fluorescence channels. Such a crosstalk-free duplex imaging capability of CFR enables longitudinal measurement of two correlated biomolecular events (oxidative stress and cellular apoptosis) during the progression of DIH, identifying O as an earlier biomarker for detection of DIH both in vitro and in vivo. Moreover, CFR detects DIH 17.5 h earlier than histological changes. Thus, our study not only develops a sensitive optical reporter for early detection of DIH but also provides a general molecular design strategy for duplex imaging.
实时多重成像对于生物学和诊断至关重要,但对于光学模式仍然具有挑战性。本文合成了一种单分子化学荧光发光报告器 (CFR),用于药物诱导肝毒性 (DIH) 的双模式成像,这是一个长期存在的医学关注点。CFR 通过其独立的化学发光和近红外荧光通道的各自激活,同时检测超氧阴离子 (O) 和半胱天冬酶-3 (casp3)。CFR 的这种无串扰双模式成像能力能够在 DIH 进展过程中进行两种相关生物分子事件(氧化应激和细胞凋亡)的纵向测量,表明 O 作为 DIH 的早期生物标志物,在体外和体内均能检测到 DIH。此外,CFR 比组织学变化更早地检测到 DIH。因此,本研究不仅开发了一种用于早期检测 DIH 的灵敏光学报告器,而且还为双模式成像提供了一种通用的分子设计策略。