Pengyang Xu , Ziyi Zhao , Yunze Liu , Xiaoke Zhang , Xixian Luo
{"title":"用于生物成像的双通道可见光和NIR-III上转换光学探针","authors":"Pengyang Xu , Ziyi Zhao , Yunze Liu , Xiaoke Zhang , Xixian Luo","doi":"10.1016/j.jlumin.2025.121586","DOIUrl":null,"url":null,"abstract":"<div><div>Fluorescence bioimaging, owing to its low invasiveness and real-time feedback capabilities, holds significant promise for biomedical applications. However, conventional fluorescent probes suffer from photobleaching and limited tissue penetration. In this study, we developed a dual-channel upconversion optical probe based on lanthanide-doped core-shell NaErF<sub>4</sub>:Tm<sup>3+</sup>@NaYF<sub>4</sub>:Yb<sup>3+</sup> nanoparticles, capable of simultaneously emitting visible light at 654 nm and third near-infrared window (NIR-III) luminescence at 1523 nm under 980 nm excitation. The Tm<sup>3+</sup> ions serve as energy traps, facilitating the Er<sup>3+</sup>→Tm<sup>3+</sup>→Er<sup>3+</sup> energy transfer pathway, significantly enhancing both red and NIR-III emissions from the transitions of <sup>4</sup>F<sub>9/2</sub> → <sup>4</sup>I<sub>15/2</sub> and <sup>4</sup>I<sub>13/2</sub> → <sup>4</sup>I<sub>15/2</sub>. Moreover, coating the core NaErF<sub>4</sub>:Tm<sup>3+</sup> nanoparticles with an active NaYF<sub>4</sub>:Yb<sup>3+</sup> shell led to a remarkable 210-fold enhancement in red emission intensity and the emergence of effective NIR-III emission This significant improvement in luminescence is attributed to the suppression of surface quenching by the core-shell structure and the enhanced absorption of 980 nm photons by Yb<sup>3+</sup> ion in the shell. This dual-channel red and NIR-III luminescent nanoprobe could be a potential ideal probe for deep-tissue bioimaging. The ex vivo penetration experiment using porcine tissue demonstrated a deep tissue penetration of up to 10 mm in the NIR-III window. The Daphnia magna and Zebrafish treated with the nanoprobes display bright red emission without any background, indicating the excellent in vivo luminescent imaging capacity of NaErF<sub>4</sub>:Tm<sup>3+</sup>@NaYF<sub>4</sub>:Yb<sup>3+</sup> nanoparticles. Our findings present a new class of dual-channel optical probes with visible and NIR-III emissions, enabling multiscale high-resolution biomedical imaging applications.</div></div>","PeriodicalId":16159,"journal":{"name":"Journal of Luminescence","volume":"288 ","pages":"Article 121586"},"PeriodicalIF":3.6000,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dual-channel visible and NIR-III upconversion optical probe for bioimaging\",\"authors\":\"Pengyang Xu , Ziyi Zhao , Yunze Liu , Xiaoke Zhang , Xixian Luo\",\"doi\":\"10.1016/j.jlumin.2025.121586\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Fluorescence bioimaging, owing to its low invasiveness and real-time feedback capabilities, holds significant promise for biomedical applications. However, conventional fluorescent probes suffer from photobleaching and limited tissue penetration. In this study, we developed a dual-channel upconversion optical probe based on lanthanide-doped core-shell NaErF<sub>4</sub>:Tm<sup>3+</sup>@NaYF<sub>4</sub>:Yb<sup>3+</sup> nanoparticles, capable of simultaneously emitting visible light at 654 nm and third near-infrared window (NIR-III) luminescence at 1523 nm under 980 nm excitation. The Tm<sup>3+</sup> ions serve as energy traps, facilitating the Er<sup>3+</sup>→Tm<sup>3+</sup>→Er<sup>3+</sup> energy transfer pathway, significantly enhancing both red and NIR-III emissions from the transitions of <sup>4</sup>F<sub>9/2</sub> → <sup>4</sup>I<sub>15/2</sub> and <sup>4</sup>I<sub>13/2</sub> → <sup>4</sup>I<sub>15/2</sub>. Moreover, coating the core NaErF<sub>4</sub>:Tm<sup>3+</sup> nanoparticles with an active NaYF<sub>4</sub>:Yb<sup>3+</sup> shell led to a remarkable 210-fold enhancement in red emission intensity and the emergence of effective NIR-III emission This significant improvement in luminescence is attributed to the suppression of surface quenching by the core-shell structure and the enhanced absorption of 980 nm photons by Yb<sup>3+</sup> ion in the shell. This dual-channel red and NIR-III luminescent nanoprobe could be a potential ideal probe for deep-tissue bioimaging. The ex vivo penetration experiment using porcine tissue demonstrated a deep tissue penetration of up to 10 mm in the NIR-III window. The Daphnia magna and Zebrafish treated with the nanoprobes display bright red emission without any background, indicating the excellent in vivo luminescent imaging capacity of NaErF<sub>4</sub>:Tm<sup>3+</sup>@NaYF<sub>4</sub>:Yb<sup>3+</sup> nanoparticles. Our findings present a new class of dual-channel optical probes with visible and NIR-III emissions, enabling multiscale high-resolution biomedical imaging applications.</div></div>\",\"PeriodicalId\":16159,\"journal\":{\"name\":\"Journal of Luminescence\",\"volume\":\"288 \",\"pages\":\"Article 121586\"},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2025-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Luminescence\",\"FirstCategoryId\":\"101\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0022231325005265\",\"RegionNum\":3,\"RegionCategory\":\"物理与天体物理\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"OPTICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Luminescence","FirstCategoryId":"101","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022231325005265","RegionNum":3,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPTICS","Score":null,"Total":0}
Dual-channel visible and NIR-III upconversion optical probe for bioimaging
Fluorescence bioimaging, owing to its low invasiveness and real-time feedback capabilities, holds significant promise for biomedical applications. However, conventional fluorescent probes suffer from photobleaching and limited tissue penetration. In this study, we developed a dual-channel upconversion optical probe based on lanthanide-doped core-shell NaErF4:Tm3+@NaYF4:Yb3+ nanoparticles, capable of simultaneously emitting visible light at 654 nm and third near-infrared window (NIR-III) luminescence at 1523 nm under 980 nm excitation. The Tm3+ ions serve as energy traps, facilitating the Er3+→Tm3+→Er3+ energy transfer pathway, significantly enhancing both red and NIR-III emissions from the transitions of 4F9/2 → 4I15/2 and 4I13/2 → 4I15/2. Moreover, coating the core NaErF4:Tm3+ nanoparticles with an active NaYF4:Yb3+ shell led to a remarkable 210-fold enhancement in red emission intensity and the emergence of effective NIR-III emission This significant improvement in luminescence is attributed to the suppression of surface quenching by the core-shell structure and the enhanced absorption of 980 nm photons by Yb3+ ion in the shell. This dual-channel red and NIR-III luminescent nanoprobe could be a potential ideal probe for deep-tissue bioimaging. The ex vivo penetration experiment using porcine tissue demonstrated a deep tissue penetration of up to 10 mm in the NIR-III window. The Daphnia magna and Zebrafish treated with the nanoprobes display bright red emission without any background, indicating the excellent in vivo luminescent imaging capacity of NaErF4:Tm3+@NaYF4:Yb3+ nanoparticles. Our findings present a new class of dual-channel optical probes with visible and NIR-III emissions, enabling multiscale high-resolution biomedical imaging applications.
期刊介绍:
The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid.
We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.