{"title":"The Dye-Sensitized Strategy Enhances the Performance of Upconversion Nanoprobes by Improving the Quenching Efficiency.","authors":"Dailiang Zhang, Wenhao Zhong, Zhenhua Liu, Shushu Zhou, Minghui Yang, Jing Luo, Ting Li","doi":"10.1007/s10895-026-04958-3","DOIUrl":null,"url":null,"abstract":"<p><p>Luminescence resonance energy transfer (LRET) serves as the fundamental principle for constructing probes based on lanthanide-doped upconversion nanoparticles (UCNPs). The signal contrast of a UCNP-based probe is determined by the LRET efficiency, which directly limits the maximum signal-to-background ratio (SBR) and the limit of detection (LOD). To enhance the SBR, we developed a dye-sensitized upconversion nanoparticle, denoted as UCNPs@IR780, in which the upconversion luminescence (UCL) is efficiently quenched by LRET acceptors. The dye-sensitized upconversion emission originates from the UCNPs but is enhanced through dye-sensitization by the organic dye IR780. In addition to quenching the luminescence of UCNPs, simultaneous quenching of IR780 further suppressed the UCL, thereby improving the SBR. We employed MnO<sub>2</sub> nanosheets as LRET acceptors, achieving a quenching efficiency of up to 90.8% for UCNPs@IR780. Upon interaction with glutathione (GSH), a molecule involved in numerous physiological processes, the MnO<sub>2</sub> nanosheets were degraded, leading to recovery of the UCL signal. The system achieves a maximum SBR of 9.3 and an LOD of 0.1 µM for GSH. The improved SBR and LOD demonstrate that the dye-sensitized strategy effectively overcomes the inherent SBR limitations of conventional UCNP-based probes, thereby broadening their applicability in biosensing applications.</p>","PeriodicalId":15800,"journal":{"name":"Journal of Fluorescence","volume":" ","pages":""},"PeriodicalIF":3.4000,"publicationDate":"2026-09-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Fluorescence","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1007/s10895-026-04958-3","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0
Abstract
Luminescence resonance energy transfer (LRET) serves as the fundamental principle for constructing probes based on lanthanide-doped upconversion nanoparticles (UCNPs). The signal contrast of a UCNP-based probe is determined by the LRET efficiency, which directly limits the maximum signal-to-background ratio (SBR) and the limit of detection (LOD). To enhance the SBR, we developed a dye-sensitized upconversion nanoparticle, denoted as UCNPs@IR780, in which the upconversion luminescence (UCL) is efficiently quenched by LRET acceptors. The dye-sensitized upconversion emission originates from the UCNPs but is enhanced through dye-sensitization by the organic dye IR780. In addition to quenching the luminescence of UCNPs, simultaneous quenching of IR780 further suppressed the UCL, thereby improving the SBR. We employed MnO2 nanosheets as LRET acceptors, achieving a quenching efficiency of up to 90.8% for UCNPs@IR780. Upon interaction with glutathione (GSH), a molecule involved in numerous physiological processes, the MnO2 nanosheets were degraded, leading to recovery of the UCL signal. The system achieves a maximum SBR of 9.3 and an LOD of 0.1 µM for GSH. The improved SBR and LOD demonstrate that the dye-sensitized strategy effectively overcomes the inherent SBR limitations of conventional UCNP-based probes, thereby broadening their applicability in biosensing applications.
期刊介绍:
Journal of Fluorescence is an international forum for the publication of peer-reviewed original articles that advance the practice of this established spectroscopic technique. Topics covered include advances in theory/and or data analysis, studies of the photophysics of aromatic molecules, solvent, and environmental effects, development of stationary or time-resolved measurements, advances in fluorescence microscopy, imaging, photobleaching/recovery measurements, and/or phosphorescence for studies of cell biology, chemical biology and the advanced uses of fluorescence in flow cytometry/analysis, immunology, high throughput screening/drug discovery, DNA sequencing/arrays, genomics and proteomics. Typical applications might include studies of macromolecular dynamics and conformation, intracellular chemistry, and gene expression. The journal also publishes papers that describe the synthesis and characterization of new fluorophores, particularly those displaying unique sensitivities and/or optical properties. In addition to original articles, the Journal also publishes reviews, rapid communications, short communications, letters to the editor, topical news articles, and technical and design notes.