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NIR-II probes show great potential for fluorescence imaging (FLI) and therapeutics, where the molar extinction coefficient (MEC), a pivotal optical parameter, governs their imaging quality and therapeutic efficacy. Nevertheless, engineering NIR-II probes with ultrahigh MEC remains a formidable challenge, limiting their biomedical applications. In this work, we designed a superior NIR-II D-π-A-π-D probe, SCU-SX-T, which features an S-xanthene core as the conjugate acceptor, a diphenylamine (DPA) rotor, and π-bridge that induces bathochromic shifts in absorption/emission spectra while enhancing molecular rigidity and planarity. This rational molecular design enables the probe to achieve exceptionally ultrahigh MEC of 2.0 × 10 M cm, outstanding photothermal conversion efficiency (PCE) of 91.5%, and fluorescence quantum yield of 0.04%. Notably, the SCU-SX-T NPs facilitated high-resolution vascular imaging of the abdominal region and precise surgery in living mice, demonstrating their robust NIR-II fluorescence capability. Furthermore, NIR-II FLI/photothermal imaging (PTI)-guided tumor visualization and photothermal therapy (PTT) was successfully achieved. The integration of α-PD-L1 checkpoint blockade therapy led to significant inhibition of proximal tumor growth, highlighting the potential of this synergistic therapeutic strategy. Overall, this work provides a comprehensive NIR-II probe with excellent performance and ideas for the future design of NIR-II probes with high MEC.
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http://dx.doi.org/10.1039/d5mh01254f | DOI Listing |
J Mater Chem B
September 2025
State Key Laboratory of Luminescent Materials and Devices, Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates, College of Materials Science and Engineering, South China University of Technology, Guangzhou 510640, China.
Adenosine triphosphate (ATP) is a critical biomolecule in cellular energy metabolism, with abnormal levels in the bloodstream linked to pathological conditions such as ischemia, cancer, and inflammatory disorders. Accurate and real-time detection of ATP is essential for early diagnosis and disease monitoring. However, conventional biochemical assays and other techniques suffer from limitations, including invasive sample collection, time-consuming procedures, and the inability to provide dynamic, monitoring.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
National Engineering Research Centre for Nanomedicine, College of Life Science and Technology, Huazhong University of Science and Technology, Wuhan 430074, P. R. China.
Image-guided surgery plays a critical role in improving the cancer patient prognosis. However, current clinical probes are often single-modal with "always-on" signals, failing to provide complementary and precise guidance across all perioperative phases. To tackle this hurdle, we develop a biomarker-activatable, multimodal nanoprobe - - based on redox-mediated manganese valence switching for tumor-specific, perioperative image-guided surgery.
View Article and Find Full Text PDFMater Horiz
September 2025
Key Laboratory of Green Chemistry and Technology, Ministry of Education, College of Chemistry, Sichuan University, Chengdu, 610064, P. R. China.
NIR-II probes show great potential for fluorescence imaging (FLI) and therapeutics, where the molar extinction coefficient (MEC), a pivotal optical parameter, governs their imaging quality and therapeutic efficacy. Nevertheless, engineering NIR-II probes with ultrahigh MEC remains a formidable challenge, limiting their biomedical applications. In this work, we designed a superior NIR-II D-π-A-π-D probe, SCU-SX-T, which features an S-xanthene core as the conjugate acceptor, a diphenylamine (DPA) rotor, and π-bridge that induces bathochromic shifts in absorption/emission spectra while enhancing molecular rigidity and planarity.
View Article and Find Full Text PDFACS Appl Mater Interfaces
September 2025
Molecular Imaging Center, State Key Laboratory of Chemical Biology, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China.
Nitric oxide (NO) and methylglyoxal (MGO) play a vital part in maintaining redox homeostasis, modulating substances, and signal transduction. Fluctuations in these signaling molecules are closely associated with various pathological processes. However, due to the absence of appropriate multifunctional fluorescent sensors, concurrent identification of NO and MGO has not been achieved in inflammatory diseases.
View Article and Find Full Text PDFActa Pharm Sin B
August 2025
School of Pharmacy, Nanjing University of Chinese Medicine, Nanjing 210023, China.
The precise and rapid monitoring of multiple organ dysfunction is crucial in drug discovery. Traditional methods, such as pathological analysis, are often time-consuming and inefficient. Here, we developed a multiplexed near-infrared window two (NIR-II) fluorescent bioimaging method that allows for real-time, rapid, and quantitative assessment of multiple organ dysfunctions.
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