98%
921
2 minutes
20
Afterglow luminescence is an internal luminescence pathway that occurs after photo-excitation, holds great promise for non-background molecular imaging in vivo, but suffer from poor quantitative ability owing to luminescent attenuation over time. Moreover, the inert structure and insufficient reactive sites of current afterglow materials make it hard to design activatable afterglow probes for specific detection. Here, we report a ratiometric afterglow luminescent nanoplatform to customize various activatable afterglow probes for reliable quantification and molecular imaging of specific analytes, such as NO, ONOO or pH. Notably, these afterglow probes can not only address the attenuation of afterglow intensity and eliminate the interference of factors (e.g., laser power, irradiation time, and exposure time), but also significantly improve the imaging reliability in vivo and signal-to-background ratios (~1200-fold), both of which enable more reliable quantitative analysis in biological systems. Moreover, as a proof-of-concept, we successfully design an NO-responsive ratiometric afterglow nanoprobe, RAN1. This nanoprobe can monitor the fluctuations of intratumoral NO, as a biomarker of macrophage polarization, making it possible to real-time dynamically evaluate the degree cancer immunotherapy, which provides a reliable parameter to predict the immunotherapeutic effect.
Download full-text PDF |
Source |
---|---|
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9039063 | PMC |
http://dx.doi.org/10.1038/s41467-022-29894-1 | DOI Listing |
Anal Chem
July 2025
Hebei Technology Innovation Center for Energy Conversion Materials and Devices, Hebei Key Laboratory of Inorganic Nanomaterials, Engineering Research Center of Thin Film Solar Cell Materials and Devices, College of Chemistry and Material Science, Hebei Normal University, No. 20Rd. East of 2nd Ring S
Simultaneous detection and discrimination of fluoroquinolone (FQ) subtypes are crucial yet challenging due to their high similarity in molecular structure and optical properties. In this work, we propose a ratiometric afterglow sensor array for the visual detection and discrimination of five FQ subtypes via a universal host-guest doping strategy. Boric acid was used as a universal host to boost the afterglow emission intensities of blue emissive FQs, green emissive 1-naphthaleneboronic acid, and red emissive 1-pyrenylboronic acid by creating a rigid matrix and cross-linked networks.
View Article and Find Full Text PDFSci Adv
March 2025
State Key Laboratory of Chemo and Biosensing, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, China.
Cardiovascular diseases, including stroke driven by atherosclerosis, remain a leading global health concern. Current diagnostic imaging modalities such as magnetic resonance imaging fail to characterize oxidative stress within atherosclerotic plaques. Here, we introduce difuranfluoreno-dithiophen-based polymers designed for afterglow imaging, offering ultrabright luminescence, ultralow-power excitation (0.
View Article and Find Full Text PDFRSC Adv
August 2024
Institute for Frontier Medical Technology, College of Chemistry and Chemical Engineering, Shanghai University of Engineering Science Shanghai 201620 China
MgGaO (MGO) with the spinel structure exhibits abundance defects and could achieve the modulation of emission by ion doping as persistent luminescence nanoparticles (PLNPs). Here, we introduced Cr ions into MGO to achieve near-infrared (NIR) emission, and Pr ions to tune the lattice environment for enhanced NIR emission. The optimal composite, MgGaO: 0.
View Article and Find Full Text PDFBiomater Sci
June 2024
State Key Laboratory of Food Science and Technology, Jiangnan University, Wuxi 214122, China.
Precise imaging-guided therapy of a pulmonary metastasis tumor is of great significance for tumor management and prognosis. Persistent luminescence nanoparticles (PLNPs) are promising probes due to their excitation-free and low-background imaging characteristics. However, most of the PLNP-based probes cannot intelligently distinguish between normal and tumor tissues or balance the needs of targeted accumulation and rapid metabolism, resulting in false positive signals and potential side effects.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
June 2024
State Key Laboratory of Analytical Chemistry for Life Science, School of Chemistry and Chemical Engineering, Chemistry and Biomedicine Innovation Center (ChemBIC), Nanjing University, Nanjing, 210023, China.
Ratiometric afterglow luminescent (AGL) probes are attractive for in vivo imaging due to their high sensitivity and signal self-calibration function. However, there are currently few ratiometric AGL probes available for imaging enzymatic activity in living organisms. Here, we present an energy diversion (ED) strategy that enables the design of an enzyme-activated ratiometric AGL probe (RAG-RGD) for in vivo afterglow imaging.
View Article and Find Full Text PDF