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

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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Journal
Journal of the American Chemical Society
Published
2025-12-14
DOI
https://doi.org/10.1021/jacs.5c19142
Primary Topic
Nanoplatforms for cancer theranostics
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article
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article

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

Weijiang He, Weizhong Ding, Yuncong Chen, Mingfeng Li et al.
Journal of the American Chemical Society
Nanoplatforms for cancer theranostics
article

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

Weijiang He, Weizhong Ding, Yuncong Chen, Mingfeng Li, Zijian Guo, Chenqi Wang, Fengwu Xu, Shankun Yao, Zhipeng Liu, Ming Jia
article en

Abstract

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.

Journal of the American Chemical SocietyVol. 147(51)
Nanjing Forestry University (CN), Nanjing Drum Tower Hospital (CN), Division of Materials Science and Engineering (AU), Nanjing University (CN)
Openalex Percentile: Top 61%
Nanoplatforms for cancer theranostics
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