{"title":"808 nm-excited upconversion single-particle imaging for long-term tracking of cargo transport in live neurons","authors":"Tianli Zhai , Yanxin Zhang , Daoming Guan , Wenrui Zhang , Fan Ding , Xiaochen Qiu , Yunxiang Zhang , Qian Liu","doi":"10.1016/j.jlumin.2025.121483","DOIUrl":null,"url":null,"abstract":"<div><div>Upconversion nanoparticles (UCNPs) activated by 808 nm excitation hold promise for bioimaging due to minimized water absorption and tissue heating. However, their luminescence efficiency and single-particle performance in complex biological systems remain limited. Here, we present a rationally designed core-multishell UCNP structure (NaYbF<sub>4</sub>: x%Er@NaYF<sub>4</sub>: y%Yb@NaYF<sub>4</sub>: z%Nd, 10 %Yb@NaYF<sub>4</sub>) optimized for enhanced upconversion luminescence (UCL) at the single-particle level under 808 nm excitation. By systematically tuning Er<sup>3+</sup> concentration in the emissive core, Yb<sup>3+</sup> in the energy migration shell, and Nd<sup>3+</sup> in the energy-harvesting layers, we achieved efficient energy spatial management. Single-particle analysis revealed power-dependent UCL saturation, with 12 % Er<sup>3+</sup> doping in the core, 10 % Yb<sup>3+</sup> doping in the migration shell, and 30 % Nd<sup>3+</sup> doping in the energy-harvesting layer yielding maximal brightness. These UCNPs were further surface-functionalized for live-cell imaging and enabled continuous cargo tracking in hippocampal neurons for over 30 min under 808 nm excitation. Trajectory analysis revealed hitchhiking-like transport dynamics within axons. This work highlights the potential of UCNPs for advanced biological imaging and mechanistic insights into nanoscale cargo dynamics in neurons.</div></div>","PeriodicalId":16159,"journal":{"name":"Journal of Luminescence","volume":"287 ","pages":"Article 121483"},"PeriodicalIF":3.6000,"publicationDate":"2025-08-25","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/S0022231325004235","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}
引用次数: 0
Abstract
Upconversion nanoparticles (UCNPs) activated by 808 nm excitation hold promise for bioimaging due to minimized water absorption and tissue heating. However, their luminescence efficiency and single-particle performance in complex biological systems remain limited. Here, we present a rationally designed core-multishell UCNP structure (NaYbF4: x%Er@NaYF4: y%Yb@NaYF4: z%Nd, 10 %Yb@NaYF4) optimized for enhanced upconversion luminescence (UCL) at the single-particle level under 808 nm excitation. By systematically tuning Er3+ concentration in the emissive core, Yb3+ in the energy migration shell, and Nd3+ in the energy-harvesting layers, we achieved efficient energy spatial management. Single-particle analysis revealed power-dependent UCL saturation, with 12 % Er3+ doping in the core, 10 % Yb3+ doping in the migration shell, and 30 % Nd3+ doping in the energy-harvesting layer yielding maximal brightness. These UCNPs were further surface-functionalized for live-cell imaging and enabled continuous cargo tracking in hippocampal neurons for over 30 min under 808 nm excitation. Trajectory analysis revealed hitchhiking-like transport dynamics within axons. This work highlights the potential of UCNPs for advanced biological imaging and mechanistic insights into nanoscale cargo dynamics in neurons.
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.