Multifunctional Rare-Earth Element Nanocrystals for Cell Labeling and Multimodal Imaging

In this work, we describe a simple solvothermal route for the synthesis of Eu3+-doped gadolinium orthovanadate nanocrystals (Eu:GdVO4–PAA) functionalized with poly­(acrylic)­acid (PAA), that are applicable as cell labeling probes for multimodal cellular imaging. The Eu3+ doping of the vanadate matri...

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Veröffentlicht in:ACS biomaterials science & engineering 2018-10, Vol.4 (10), p.3578-3587
Hauptverfasser: Grunert, Bianca, Saatz, Jessica, Hoffmann, Katrin, Appler, Franziska, Lubjuhn, Dominik, Jakubowski, Norbert, Resch-Genger, Ute, Emmerling, Franziska, Briel, Andreas
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container_issue 10
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container_title ACS biomaterials science & engineering
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creator Grunert, Bianca
Saatz, Jessica
Hoffmann, Katrin
Appler, Franziska
Lubjuhn, Dominik
Jakubowski, Norbert
Resch-Genger, Ute
Emmerling, Franziska
Briel, Andreas
description In this work, we describe a simple solvothermal route for the synthesis of Eu3+-doped gadolinium orthovanadate nanocrystals (Eu:GdVO4–PAA) functionalized with poly­(acrylic)­acid (PAA), that are applicable as cell labeling probes for multimodal cellular imaging. The Eu3+ doping of the vanadate matrix provides optical functionality, due to red photoluminescence after illumination with UV light. The Gd3+ ions of the nanocrystals reduce the T1 relaxation time of surrounding water protons, allowing these nanocrystals to act as a positive MRI contrast agent with a r1 relaxivity of 1.97 mM–1 s–1. Low background levels of Eu3+, Gd3+, and V5+ in biological systems make them an excellent label for elemental microscopy by Laser Ablation (LA)-ICP-MS. Synthesis resulted in polycrystalline nanocrystals with a hydrodynamic diameter of 55 nm and a crystal size of 36.7 nm, which were further characterized by X-ray diffraction (XRD), photoluminescence spectroscopy (PL) and transmission electron microscopy (TEM). The multifunctional nanocrystals were subsequently used for intracellular labeling of both human adipose-derived stem cells (MSCs) and A549 (adenocarcinomic human alveolar basal epithelial) cells.
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