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Updated: Mar 16, 2026

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Synthesis of Core-shell Lanthanide-doped Upconversion Nanocrystals for Cellular Applications
Published on: November 10, 2017
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Enhanced up/down-conversion luminescence and heat: Simultaneously achieving in one single core-shell structure for
Fei He1, Lili Feng1, Piaoping Yang1
1Key Laboratory of Superlight Materials and Surface Technology, Ministry of Education, College of Materials Science and Chemical Engineering, Harbin Engineering University, Harbin 150001, PR China.
Biomaterials
|August 12, 2016
Summary
This study designed a novel core-shell nanoparticle that simultaneously achieves enhanced near-infrared down-conversion luminescence and photothermal therapy. This platform enables effective cancer treatment and multimodal imaging for guided therapy.
Area of Science:
- Materials Science
- Nanotechnology
- Biomedical Engineering
Background:
- Near-infrared (NIR) light offers advantages for bio-imaging and photothermal therapy (PTT).
- Concentration quenching in Nd(3+)-doped materials hinders simultaneous optimization of down-conversion luminescence (DCL) and thermal effects.
- Developing single-particle systems with dual NIR-responsive properties is challenging.
Purpose of the Study:
- To design and synthesize a core-shell nanoparticle capable of simultaneous NIR-to-NIR DCL, NIR-to-Vis up-conversion luminescence (UCL), and photothermal effect.
- To overcome concentration quenching issues for enhanced DCL and thermal properties.
- To develop an imaging-guided cancer therapy platform combining photothermal therapy (PTT) and photodynamic therapy (PDT).
Main Methods:
- Fabrication of a unique NaGdF4:0.3%Nd@NaGdF4@NaGdF4:10%Yb/1%Er@NaGdF4:10%Yb @NaNdF4:10%Yb multiple core-shell structure.
- Utilizing inert layers to mitigate quenching effects and enhance luminescence and thermal properties.
- Integrating Au25 nanoclusters for PDT activation via UCL, and employing NIR DCL for deep-tissue imaging.
Main Results:
- Achieved significantly enhanced NIR-to-NIR DCL, NIR-to-Vis UCL, and photothermal effect under a single 808 nm light excitation.
- Demonstrated effective synergistic cancer inhibition in vitro and in vivo through combined PTT and PDT.
- Successfully performed multimodal imaging (fluorescence imaging, photothermal imaging, photoacoustic imaging) for monitoring therapy and drug delivery.
Conclusions:
- The designed core-shell nanoparticle effectively overcomes concentration quenching, enabling simultaneous DCL, UCL, and PTT.
- The platform shows great potential for imaging-guided synergistic cancer therapy.
- This approach offers a promising strategy for advanced theranostic applications in oncology.

