A Self-Activating Cyclic Amplification Near-Infrared Sonoafterglow Probe for High-Contrast Imaging In Vivo

Afterglow luminescence offers a promising strategy for ultrasensitive bioimaging by eliminating tissue autofluorescence and providing a high signal-to-background ratio (SBR). However, afterglow probes face several limitations, including limited luminescence brightness, short half-life, imperfect luminescent mechanisms, and reliance on preirradiation with low-penetration light. Herein, we develop a novel self-activating cyclic amplification near-infrared (NIR) sonoafterglow nanoprobe (3SCe-NP) based on a rationally engineered bis(diarylethenyl)terthiophene scaffold, which demonstrates an ∼270-fold enhancement in afterglow intensity and a 7-fold extension in half-life compared to the commonly used 2-methoxy-5-(2'-ethylhexyloxy)-1,4-phenylenevinylene (MEH-PPV). The probe functions as an integrated single-molecule entity unifying the roles of a highly efficient sonosensitizer and an NIR afterglow emitter, which overcomes the drawbacks of weak afterglow brightness, complex fabrication, and poor reproducibility inherent in multicomponent systems. Furthermore, compared to previously reported single-reactive-site afterglow systems, the multireactive-site architecture of 3SCe-NP enables more extensive interactions with self-generated, multitype reactive oxygen species (ROS), creating a high density of chemical defects. This results in dramatically enhanced energy storage capacity and, consequently, a greatly intensified and sustained NIR afterglow upon ultrasound stimulation. Additionally, we uncovered a unique self-amplification mechanism that facilitates sustained ROS generation even after ultrasound cessation, thereby establishing a cyclic oxidation process that overcomes the constraint of conventional consumable afterglow probes relying on a single, depletable ROS. This nanoprobe achieves a high SBR, deep-tissue penetration, and rechargeable capability for longitudinal tumor imaging in vivo. We further demonstrated its utility by constructing an activatable sonoafterglow probe for monitoring immunotherapy responses, offering a useful tool for biomedical imaging.

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Journal
Journal of the American Chemical Society
Published
2026-03-16
DOI
https://doi.org/10.1021/jacs.6c01285
Primary Topic
Ultrasound and Hyperthermia Applications
Type
article
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article

A Self-Activating Cyclic Amplification Near-Infrared Sonoafterglow Probe for High-Contrast Imaging In Vivo

Yusuke Ishigaki, Deju Ye, Takanori Suzuki, J. Liu et al.
Journal of the American Chemical Society
Ultrasound and Hyperthermia Applications
article

A Self-Activating Cyclic Amplification Near-Infrared Sonoafterglow Probe for High-Contrast Imaging In Vivo

Yusuke Ishigaki, Deju Ye, Takanori Suzuki, J. Liu, Jian Sun, Fangqi Yang, Yinghan Chen, Jiaqi Yuan, Yinxing Miao, Xiang Cao, Yefa Liang, Quli Fan, Yuanjing Zhao, Luyan Wu
article en

Abstract

Afterglow luminescence offers a promising strategy for ultrasensitive bioimaging by eliminating tissue autofluorescence and providing a high signal-to-background ratio (SBR). However, afterglow probes face several limitations, including limited luminescence brightness, short half-life, imperfect luminescent mechanisms, and reliance on preirradiation with low-penetration light. Herein, we develop a novel self-activating cyclic amplification near-infrared (NIR) sonoafterglow nanoprobe (3SCe-NP) based on a rationally engineered bis(diarylethenyl)terthiophene scaffold, which demonstrates an ∼270-fold enhancement in afterglow intensity and a 7-fold extension in half-life compared to the commonly used 2-methoxy-5-(2'-ethylhexyloxy)-1,4-phenylenevinylene (MEH-PPV). The probe functions as an integrated single-molecule entity unifying the roles of a highly efficient sonosensitizer and an NIR afterglow emitter, which overcomes the drawbacks of weak afterglow brightness, complex fabrication, and poor reproducibility inherent in multicomponent systems. Furthermore, compared to previously reported single-reactive-site afterglow systems, the multireactive-site architecture of 3SCe-NP enables more extensive interactions with self-generated, multitype reactive oxygen species (ROS), creating a high density of chemical defects. This results in dramatically enhanced energy storage capacity and, consequently, a greatly intensified and sustained NIR afterglow upon ultrasound stimulation. Additionally, we uncovered a unique self-amplification mechanism that facilitates sustained ROS generation even after ultrasound cessation, thereby establishing a cyclic oxidation process that overcomes the constraint of conventional consumable afterglow probes relying on a single, depletable ROS. This nanoprobe achieves a high SBR, deep-tissue penetration, and rechargeable capability for longitudinal tumor imaging in vivo. We further demonstrated its utility by constructing an activatable sonoafterglow probe for monitoring immunotherapy responses, offering a useful tool for biomedical imaging.

Journal of the American Chemical Society
Hokkaido University (JP), Nanjing University of Posts and Telecommunications (CN), The Synergetic Innovation Center for Advanced Materials (CN), Nanjing University (CN)
Affordable and clean energy
Openalex Percentile: Top 20%
Ultrasound and Hyperthermia Applications
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