An N-Alkylpyridinium-Substituted Cyanine Platform for Constructing Renal-Clearable Near-Infrared Fluorogenic Probes

化学 荧光 吡啶 光诱导电子转移 分子内力 光化学 组合化学 分子探针 分子模型 电子转移 费斯特共振能量转移 纳米技术 分子工程 显像剂 氧化还原
作者
Weizhong Ding,Ming Jia,Shankun Yao,Zhipeng Liu,Fengwu Xu,Mingfeng Li,Chenqi Wang,Weijiang He,Yuncong Chen,Zijian Guo
出处
期刊:Journal of the American Chemical Society [American Chemical Society]
卷期号:147 (51): 47835-47847 被引量:4
标识
DOI:10.1021/jacs.5c19142
摘要

Cyanine dyes are highly valued as imaging agents in molecular imaging and disease diagnosis. However, their slow hepatobiliary clearance often raises concerns about their potential chronic toxicity. As such, developing general strategies to construct renal-clearable activatable probes based on cyanine dyes holds great promise. Herein, we developed a novel cyanine imaging platform that exhibited high renal clearance efficiency, enabling real-time disease monitoring based on urine fluorescence readouts. Through molecular engineering of the meso-position substituents of IR780, we discovered that methylation of the meso-pyridine-modified heptamethine cyanine (CyP) dramatically quenched the fluorescence, probably due to the synergism of photoinduced electron transfer (PET) and twisted intramolecular charge transfer (TICT) effects. Intriguingly, cyanine derivatives with a pyridinium group demonstrated preferential and rapid renal clearance, primarily due to the additional positive charge-mediated electrostatic interactions with anionic proteoglycans in the kidneys. Subsequently, by introducing stimuli-responsive self-immolating groups onto the meso-pyridine ring, we developed a universal renal-clearable imaging platform and designed four representative fluorescent probes. All the probes possessed a distinct near-infrared (NIR) fluorescent "turn-on" response and preferential renal clearance. As a proof of concept, two of them were successfully utilized to visualize fluctuations of redox imbalance across various acute kidney injury (AKI) mouse models, showing sensitivity superior to that of traditional serum creatinine (SCr) and blood urea nitrogen (BUN) assays. In summary, our work not only provides a comprehensive understanding of the structure-property relationship between meso-substituents and quantum yields of cyanine derivatives but also establishes a renal-clearable fluorogenic platform for advanced bioimaging and biomedical diagnostics.
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