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Keywords = α-NaYF4

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12 pages, 2991 KiB  
Article
The Down-Shifting Luminescence of Rare-Earth Nanoparticles for Multimodal Imaging and Photothermal Therapy of Breast Cancer
by Tingting Gao, Siqi Gao, Yaling Li, Ruijing Zhang and Honglin Dong
Biology 2024, 13(3), 156; https://doi.org/10.3390/biology13030156 - 28 Feb 2024
Cited by 4 | Viewed by 2534
Abstract
Nanotheranostic agents capable of simultaneously enabling real-time tracking and precise treatment at tumor sites play an increasingly pivotal role in the field of medicine. In this article, we report a novel near-infrared-II window (NIR-II) emitting downconversion rare-earth nanoparticles (RENPs) to improve image-guided therapy [...] Read more.
Nanotheranostic agents capable of simultaneously enabling real-time tracking and precise treatment at tumor sites play an increasingly pivotal role in the field of medicine. In this article, we report a novel near-infrared-II window (NIR-II) emitting downconversion rare-earth nanoparticles (RENPs) to improve image-guided therapy for breast cancer. The developed α-NaErF4@NaYF4 nanoparticles (α-Er NPs) have a diameter of approximately 24.1 nm and exhibit superior biocompatibility and negligible toxicity. RENPs exhibit superior imaging quality and photothermal conversion efficiency in the NIR-II range compared to clinically approved indocyanine green (ICG). Under 808 nm laser irradiation, the α-Er NPs achieve significant tumor imaging performance and photothermal effects in vivo in a mouse model of breast cancer. Simultaneously, it combines X-ray computed tomography (CT) and ultrasound (US) tri-modal imaging to guide therapy for cancer. The integration of NIR-II imaging technology and RENPs establishes a promising foundation for future medical applications. Full article
(This article belongs to the Special Issue Molecular Mechanisms and Molecular Imaging of Cancer)
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10 pages, 42376 KiB  
Article
Uniform Spheres of α-NaYF4:RE3+ (RE=Eu, Tb, Ce, Er, and Tm): Template-Free Synthesis, Multi-Color Photoluminescence, and Their Application in Cellular Imaging
by Xiaofeng Fan, Laiqin Gu, Yiling Hu and Qi Zhu
Crystals 2020, 10(2), 119; https://doi.org/10.3390/cryst10020119 - 14 Feb 2020
Cited by 6 | Viewed by 3890
Abstract
Uniformly dispersed luminescent probes with a high brightness and high resolution are desired in bio imaging fields. Here, ~100 nm sized and well-dispersed spheres of RE3+ doped α-NaYF4 (rare earth (RE) = Eu, Tb, Ce, Er, and Tm) have been facile [...] Read more.
Uniformly dispersed luminescent probes with a high brightness and high resolution are desired in bio imaging fields. Here, ~100 nm sized and well-dispersed spheres of RE3+ doped α-NaYF4 (rare earth (RE) = Eu, Tb, Ce, Er, and Tm) have been facile synthesized through hydrothermal processing in the absence of a template, followed by a proper annealing. The processing window of the cubic structured spheres is wide, because the hydrothermal products are independent of the processing conditions, including reaction time and temperature. The original morphology and crystal structure can be well retained with a calcination temperature up to 600 °C. However, calcination gives rise to a reduction of particle sizes, as a result of the crystallite growth and densification. Under ultraviolet radiation, α-NaYF4:RE3+ spheres show characteristic f-f emissions of RE3+ (RE = Eu, Tb, Ce, Er, and Tm), and exhibit orange red, green, ultraviolet (UV), blue green, and blue emissions, respectively. Mainly because of the near-infrared emission at ~697 nm (5D07F4 transitions of Eu3+), the successful imaging of macrophages was achieved by NH2-NaYF4:Eu3+ probes, indicating their excellent imaging capacity for cells in vitro. Full article
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10 pages, 1847 KiB  
Communication
A Polyol-Mediated Fluoride Ions Slow-Releasing Strategy for the Phase-Controlled Synthesis of Photofunctional Mesocrystals
by Xianghong He, Yaheng Zhang, Yu Fu, Ning Lian and Zhongchun Li
Nanomaterials 2019, 9(1), 28; https://doi.org/10.3390/nano9010028 - 26 Dec 2018
Cited by 1 | Viewed by 3186
Abstract
There are only a few inorganic compounds that have evoked as much interest as sodium yttrium fluoride (NaYF4). Its extensive applications in various fields, including transparent displays, luminescence coding, data storage, as well as biological imaging, demand the precise tuning of [...] Read more.
There are only a few inorganic compounds that have evoked as much interest as sodium yttrium fluoride (NaYF4). Its extensive applications in various fields, including transparent displays, luminescence coding, data storage, as well as biological imaging, demand the precise tuning of the crystal phase. Controlling the emergence of the desired α-phase has so far remained a formidable challenge, especially via a simple procedure. Herein, we represented a polyol-assisted fluoride ions slow-release strategy for the rational control of pure cubic phase NaYF4 mesocrystals. The combination of fluorine-containing ionic liquid as a fluoride source and the existence of a polyalcohol as the reactive medium ensure the formation of uniform α-phase mesocrystallines in spite of a higher temperature and/or higher doping level. Full article
(This article belongs to the Special Issue Green Synthesis of Nanomaterials)
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10 pages, 2717 KiB  
Article
Spectral Selectivity of Plasmonic Interactions between Individual Up-Converting Nanocrystals and Spherical Gold Nanoparticles
by Dawid Piątkowski, Mikołaj K. Schmidt, Magdalena Twardowska, Marcin Nyk, Javier Aizpurua and Sebastian Maćkowski
Materials 2017, 10(8), 905; https://doi.org/10.3390/ma10080905 - 4 Aug 2017
Cited by 4 | Viewed by 4509
Abstract
We experimentally demonstrate strong spectral selectivity of plasmonic interaction that occurs between α-NaYF4:Er3+/Yb3+ nanocrystals, which feature two emission bands, and spherical gold nanoparticles, with plasmon frequency resonant with one of the emission bands. Spatially–resolved luminescence intensity maps acquired [...] Read more.
We experimentally demonstrate strong spectral selectivity of plasmonic interaction that occurs between α-NaYF4:Er3+/Yb3+ nanocrystals, which feature two emission bands, and spherical gold nanoparticles, with plasmon frequency resonant with one of the emission bands. Spatially–resolved luminescence intensity maps acquired for individual nanocrystals, together with microsecond luminescence lifetime images, show two qualitatively different effects that result from the coupling between plasmon excitations in metallic nanoparticles and emitting states of the nanocrystals. On the one hand, we observe nanocrystals, whose emission intensity is strongly enhanced for both resonant and non-resonant bands with respect to the plasmon resonance. Importantly, this increase is accompanied with shortening of luminescence decays times. In contrast, a significant number of nanocrystals exhibits almost complete quenching of the emission resonant with the plasmon resonance of gold nanoparticles. Theoretical analysis indicates that such an effect can occur for emitters placed at distances of about 5 nm from gold nanoparticles. While under these conditions, both transitions experience significant increases of the radiative emission rates due to the Purcell effect, the non-radiative energy transfer between resonant bands results in strong quenching, which in that situation nullifies the enhancement. Full article
(This article belongs to the Special Issue Advance in Plasmonics and Metamaterials)
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