4.8 Article

A LRET Nanoplatform Consisting of Lanthanide and Amorphous Manganese Oxide for NIR-II Luminescence Lifetime Imaging of Tumor Redox Status

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 61, Issue 47, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202209592

Keywords

Amorphous Manganese Oxide; Lanthanide; Luminescence Lifetime Imaging; NIR-II LRET; Quantitative Redox Visualization

Funding

  1. National Natural Science Foundation of China [51922111]
  2. Science and Technology Development Fund, Macau SAR [0124/2019/A3]
  3. Guangdong-Hong Kong-Macao Joint Laboratory of Optoelectronic and Magnetic Functional Materials [2019B121205002]
  4. National University of Singapore Startup Fund [NUHSRO/2020/133/Startup/08]
  5. NUS School of Medicine Nanomedicine Translational Research Programme [NUHSRO/2021/034/TRP/09/Nanomedicine]
  6. National Medical Research Council (NMRC) Centre Grant Programme [CG21APR1005]
  7. Singapore Ministry of Education, Academic Research Fund Tier 2 [T2EP30122-0002]

Ask authors/readers for more resources

In this study, we designed and synthesized a tumor-responsive and easily synthesized material for luminescence lifetime sensor, which allowed accurate identification and quantification of cells and tumors with high redox state. The material exhibited the capability of controlling luminescence lifetimes in the second near-infrared window.
Designing luminescence lifetime sensors in the second near-infrared (NIR-II) window is a great challenge due to the difficult structural construction. Here, we report a tumor redox responsive and easily synthesized material, amorphous manganese oxide (MnOx) with indirect band gap of 1.02 eV, as an energy acceptor to build a luminescence resonance energy transfer (LRET) toolbox for universally regulating NIR-I to NIR-II luminescence lifetimes of lanthanide nanoparticles, in which energy transfer is based on matched energy gap instead of conventional overlapped spectra. We further utilize ytterbium (Yb3+)-doped YbNP@MnOx as an NIR-II luminescence lifetime sensor to realize in vitro quantitative redox visualization with relative errors under 5 % in samples covered with mouse skin. Furthermore, HepG2 cells and tumors with high redox state have been accurately distinguished by NIR-II luminescence lifetime imaging. The quantified intracellular and intratumor glutathione (GSH) levels are highly consistent with the commercial kit results, illustrating the reliable redox visualization ability in biological tissue.

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