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Manipulating energy migration within single lanthanide activator for switchable upconversion emissions towards bidirectional photoactivation

  • Qingsong Mei
  • , Akshaya Bansal
  • , Muthu Kumara Gnanasammandhan Jayakumar
  • , Zhiming Zhang
  • , Jing Zhang
  • , Hua Huang
  • , Dejie Yu
  • , Chrishan J. A. Ramachandra
  • , Derek J. Hausenloy
  • , Tuck Wah Soong
  • , Yong Zhang*
  • *Corresponding author for this work

Research output: Journal Publications and ReviewsRGC 21 - Publication in refereed journalpeer-review

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Abstract

Reliance on low tissue penetrating UV or visible light limits clinical applicability of phototherapy, necessitating use of deep tissue penetrating near-infrared (NIR) to visible light transducers like upconversion nanoparticles (UCNPs). While typical UCNPs produce multiple simultaneous emissions for unidirectional control of biological processes, programmable control requires orthogonal non-overlapping light emissions. These can be obtained through doping nanocrystals with multiple activator ions. However, this requires tedious synthesis and produces complicated multi-shell nanoparticles with a lack of control over emission profiles due to activator crosstalk. Herein, we explore cross-relaxation (CR), a non-radiative recombination pathway typically perceived as deleterious, to manipulate energy migration within the same lanthanide activator ion (Er3+) towards orthogonal red and green emissions, simply by adjusting excitation wavelength from 980 to 808 nm. These UCNPs allow programmable activation of two synergistic light-gated ion channels VChR1 and Jaws in the same cell to manipulate membrane polarization, demonstrated here for cardiac pacing. © 2019, The Author(s).
Original languageEnglish
Article number4416
JournalNature Communications
Volume10
Online published27 Sept 2019
DOIs
Publication statusPublished - 1 Dec 2019
Externally publishedYes

Funding

This work was mainly supported by grants from Singapore Ministry of Education (MOE2016-T3-1-004), National Medical Research Council (NMRC/OFIRG/17nov066) and the National Natural Science Foundation of China (21675038, 31671011). D.J.H. was supported by the British Heart Foundation (CS/14/3/31002), the National Institute for Health Research University College London Hospitals Biomedical Research Centre, Duke-National University Singapore Medical School, Singapore Ministry of Health’s National Medical Research Council under its Clinician Scientist-Senior Investigator scheme (NMRC/CSA-SI/0011/2017) and Collaborative Centre Grant scheme (NMRC/CGAug16C006), and the Singapore Ministry of Education Academic Research Fund Tier 2 (MOE2016-T2-2-021). C.J.A.R. was supported by the Singapore Ministry of Health’s National Medical Research Council under its Open Fund-Young Individual Research Grant (OF-YIRG) – [NMRC/OFYIRG/0073/2018] and through the National Health Innovation Centre Singapore under its Innovation to Develop Grant (NHIC-I2S-1811007).

Publisher's Copyright Statement

  • This full text is made available under CC-BY 4.0. https://creativecommons.org/licenses/by/4.0/

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