Browse
Submit Data
Databases
API
Help

Dataset Information

32 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

PEG-Neridronate-Modified NaYF₄:Gd³⁺,Yb³⁺,Tm³⁺/NaGdF₄ Core-Shell Upconverting Nanoparticles for Bimodal Magnetic Resonance/Optical Luminescence Imaging.

ABSTRACT: Upconverting nanoparticles are attracting extensive interest as a multimodal imaging tool. In this work, we report on the synthesis and characterization of gadolinium-enriched upconverting nanoparticles for bimodal magnetic resonance and optical luminescence imaging. NaYF₄:Gd³⁺,Yb³⁺,Tm³⁺ core upconverting nanoparticles were obtained by a thermal coprecipitation of lanthanide oleate precursors in the presence of oleic acid as a stabilizer. With the aim of improving the upconversion emission and increasing the amount of Gd³⁺ ions on the nanoparticle surface, a 2.5 nm NaGdF₄ shell was grown by the epitaxial layer-by-layer strategy, resulting in the 26 nm core-shell nanoparticles. Both core and core-shell nanoparticles were coated with poly(ethylene glycol) (PEG)-neridronate (PEG-Ner) to have stable and well-dispersed upconverting nanoparticles in a biological medium. FTIR spectroscopy and thermogravimetric analysis indicated the presence of ∼20 wt % of PEG-Ner on the nanoparticle surface. The addition of inert NaGdF₄ shell resulted in a total 26-fold enhancement of the emission under 980 nm excitation and also affected the T ₁ and T ₂ relaxation times. Both r ₁ and r ₂ relaxivities of PEG-Ner-modified nanoparticles were much higher compared to those of non-PEGylated particles, thus manifesting their potential as a diagnostic tool for magnetic resonance imaging. Together with the enhanced luminescence efficiency, upconverting nanoparticles might represent an efficient probe for bimodal in vitro and in vivo imaging of cells in regenerative medicine, drug delivery, and/or photodynamic therapy.

SUBMITTER: Kostiv U

PROVIDER: S-EPMC8190901 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Optical Properties Investigation of Upconverting K2Gd(PO4)(WO4):20%Yb3+,Tm3+ Phosphors.

Project description:Nowadays, scientists are interested in inorganic luminescence materials that can be excited with UV or NIR radiation and emit in the visible range. Such inorganic materials can be successfully used as luminescent or anti-counterfeiting pigments. In this work, we report the synthesis and optical properties investigation of solely Tm3+ doped and Yb3+/Tm3+ co-doped K2Gd(PO4)(WO4) phosphors. The single-phase samples were prepared using a solid-state reaction method. The Tm3+ concentration was changed from 0.5% to 5%. Downshifting and upconversion emission studies were performed under 360 nm and 980 nm excitation, respectively. Yb3+ ions were used as sensitizers in the K2Gd(PO4)(WO4) phosphors to transfer the captured energy to Tm3+ ions. It turned out that under UV excitation, phosphors emitted in the blue spectral area regardless of the presence or absence of Yb3+. However, a very strong deep-red (~800 nm) emission was observed when Yb3+ and Tm3+-containing samples were excited with a 980 nm wavelength laser. It is interesting that the highest upconversion emission in the UV/Visible range was achieved for 20% Yb3+, 0.5% Tm3+ doped sample, whereas the sample co-doped with 20% Yb3+, 2% Tm3+ showed the most intensive UC emission band in the NIR range. The materials were characterized using powder X-ray diffraction and scanning electron microscopy. Optical properties were studied using steady-state and kinetic downshifting and upconversion photoluminescence spectroscopy.

| S-EPMC9920437 | biostudies-literature

NaYF4:Er3+,Yb3+/SiO2 Core/Shell Upconverting Nanocrystals for Luminescence Thermometry up to 900 K.

Project description:The rapid development of nanomaterials with unique size-tunable properties forms the basis for a variety of new applications, including temperature sensing. Luminescent nanoparticles (NPs) have demonstrated potential as sensitive nanothermometers, especially in biological systems. Their small size offers the possibility of mapping temperature profiles with high spatial resolution. The temperature range is however limited, which prevents use in high-temperature applications such as, for example, nanoelectronics, thermal barrier coatings, and chemical reactors. In this work, we extend the temperature range for nanothermometry beyond 900 K using silica-coated NaYF4 nanoparticles doped with the lanthanide ions Yb3+ and Er3+. Monodisperse ∼20 nm NaYF4:Yb,Er nanocrystals were coated with a ∼10 nm silica shell. Upon excitation with infrared radiation, bright green upconversion (UC) emission is observed. From the intensity ratio between 2H11/2 and 4S3/2 UC emission lines at 520 and 550 nm, respectively, the temperature can be determined up to at least 900 K with an accuracy of 1-5 K for silica-coated NPs. For bare NaYF4:Yb,Er NPs, the particles degrade above 600 K. Repeated thermal cycling experiments demonstrate the high durability and reproducibility of the silica-coated nanocrystals as temperature probes without any loss of performance. The present results open avenues for the development of a new class of highly stable nanoprobes by applying a silica coating around a wide variety of lanthanide-doped NPs.

| S-EPMC5348100 | biostudies-literature

Luminescence dynamics and enhancement of the UV and visible emissions of Tm3+ in LiYF4:Yb3+,Tm3+ upconverting nanoparticles.

Project description:To maximize the intrinsic luminescence efficiency of the higher energy emissions of Tm3+ in LiYF4:Yb3+,Tm3+ upconverting nanoparticles, we investigated a specific range of Tm3+ dopant concentrations. Reported to be optimized at 25% Yb3+, 0.5% Tm3+, due to the multitude of Tm3+-to-Tm3+ interactions, the Tm3+ concentration commonly used may not be suitable for strong UV and visible emissions. Thus, we varied the concentration of Tm3+ in LiYF4 nanoparticles between 0.08 and 0.55% to elucidate the effect of moderate changes of the dopant concentration on the UV, visible and NIR emissions. We determined a new optimized concentration of 0.24% Tm3+ for maximal UV and visible emissions (nominally 0.2%). An extensive analysis of the luminescence spectra in the UV, visible and NIR regions and decay time measurements provides evidence for new luminescence mechanisms involving cross-relaxation pathways from the UV-emitting states of Tm3+. Furthermore, we performed studies on an azobenzene derivative to demonstrate the substantial enhancement of the UV emissions by the newly optimized composition as evidenced by an increase in the degree of trans-cis photoisomerization.

| S-EPMC9417519 | biostudies-literature

Assessing the protective effects of different surface coatings on NaYF4:Yb3+, Er3+ upconverting nanoparticles in buffer and DMEM.

Project description:We studied the dissolution behavior of β NaYF4:Yb(20%), Er(2%) UCNP of two different sizes in biologically relevant media i.e., water (neutral pH), phosphate buffered saline (PBS), and Dulbecco's modified Eagle medium (DMEM) at different temperatures and particle concentrations. Special emphasis was dedicated to assess the influence of different surface functionalizations, particularly the potential of mesoporous and microporous silica shells of different thicknesses for UCNP stabilization and protection. Dissolution was quantified electrochemically using a fluoride ion selective electrode (ISE) and by inductively coupled plasma optical emission spectrometry (ICP OES). In addition, dissolution was monitored fluorometrically. These experiments revealed that a thick microporous silica shell drastically decreased dissolution. Our results also underline the critical influence of the chemical composition of the aqueous environment on UCNP dissolution. In DMEM, we observed the formation of a layer of adsorbed molecules on the UCNP surface that protected the UCNP from dissolution and enhanced their fluorescence. Examination of this layer by X-ray photoelectron spectroscopy (XPS) and mass spectrometry (MS) suggested that mainly phenylalanine, lysine, and glucose are adsorbed from DMEM. These findings should be considered in the future for cellular toxicity studies with UCNP and other nanoparticles and the design of new biocompatible surface coatings.

| S-EPMC7652843 | biostudies-literature

Upconverting SrF2 nanoparticles doped with Yb3+/Ho3+, Yb3+/Er3+ and Yb3+/Tm3+ ions - optimisation of synthesis method, structural, spectroscopic and cytotoxicity studies.

Project description:For a number of years nanomaterials have been continuously devised and comprehensively investigated because of the growing demand for them and their multifarious applications, especially in medicine. This paper reports on the properties of SrF2 nanoparticles (NPs) for applications in biomedicine, showing effective ways of their synthesis and luminescence under near infrared radiation - upconversion. NPs doped with lanthanide, Ln3+ ions (where Ln = Yb, Ho, Er, Tm) were prepared by the hydrothermal method and subjected to comprehensive studies, from determination of their structure and morphology, revealing small, 15 nm structures, through spectroscopic properties, to cytotoxicity in vitro. The effects of such factors as the reaction time, type and amount of precipitating compounds and complexing agents on the properties of products were characterized. The cytotoxicity of the synthesized and functionalized NPs was investigated, using human fibroblast cell line (MSU-1.1). The synthesized structures may decrease cells' proliferation in a dose-dependent manner in the measured concentration range (up to 100 µg/mL). However, the cells remain alive according to the fluorescent assay. Moreover, the treated cells were imaged using confocal laser scanning microscopy. Cellular uptake was confirmed by the presence of upconversion luminescence in the cells.

| S-EPMC6572793 | biostudies-literature

Poly(N,N-dimethylacrylamide)-coated upconverting NaYF4:Yb,Er@NaYF4:Nd core-shell nanoparticles for fluorescent labeling of carcinoma cells.

Project description:Upconverting luminescent lanthanide-doped nanoparticles (UCNP) belong to promising new materials that absorb infrared light able to penetrate in the deep tissue level, while emitting photons in the visible or ultraviolet region, which makes them favorable for bioimaging and cell labeling. Here, we have prepared upconverting NaYF4:Yb,Er@NaYF4:Nd core-shell nanoparticles, which were coated with copolymers of N,N-dimethylacrylamide (DMA) and 2-(acryloylamino)-2-methylpropane-1-sulfonic acid (AMPS) or tert-butyl [2-(acryloylamino)ethyl]carbamate (AEC-Boc) with negative or positive charges, respectively. The copolymers were synthesized by a reversible addition-fragmentation chain transfer (RAFT) polymerization, reaching Mn ~ 11 kDa and containing ~ 5 mol% of reactive groups. All copolymers contained bisphosphonate end-groups to be firmly anchored on the surface of NaYF4:Yb,Er@NaYF4:Nd core-shell nanoparticles. To compare properties of polymer coatings, poly(ethylene glycol)-coated and neat UCNP were used as a control. UCNP with various charges were then studied as labels of carcinoma cells, including human hepatocellular carcinoma HepG2, human cervical cancer HeLa, and rat insulinoma INS-1E cells. All the particles proved to be biocompatible (nontoxic); depending on their ξ-potential, the ability to penetrate the cells differed. This ability together with the upconversion luminescence are basic prerequisites for application of particles in photodynamic therapy (PDT) of various tumors, where emission of nanoparticles in visible light range at ~ 650 nm excites photosensitizer.

| S-EPMC8560758 | biostudies-literature

Investigation on optical temperature sensing behaviour via Ag island-enhanced luminescence doped β-NaGdF4:Yb3+/Tm3+ films/microfibers.

Project description:In this study, silver (Ag) island modified up-conversion nano-particle (NaGdF4:Yb3+/Tm3+) thin films were prepared via electrostatic layer by layer (LBL) and spin coating techniques. The spectroscopic results indicated that adding Ag nanoparticles could significantly enhance the up-conversion emission of NaGdF4:Yb3+/Tm3+ thin films at 452 nm and 476 nm. The maximum enhancement factor of ∼15.6 was reached at 476 nm. Furthermore, we prepared microfibers from upconverting nanoparticles solution, the application of microfibers as active and passive waveguides was analyzed by observing the performance of microfibers with and without Ag under 980 nm excitation of the laser source. The fluorescence intensity ratio (FIR) method was adopted to evaluate microfiber sensitivity. The intensity-based temperature sensitivity of blue emission from a single microfiber containing up-conversion nanomaterials (NaGdF4:Yb3+/Tm3+) and Ag nanoparticles reached up to 0.018 K-1 at 310 K compared to 0.0029 K-1 in Ag-free microfiber. Our results suggest that the novel material can be used to construct new nano-thermometers, useful both in biological experiments as well as industrial research.

| S-EPMC9043463 | biostudies-literature

Quenching Pathways in NaYF4:Er3+,Yb3+ Upconversion Nanocrystals.

Project description:Lanthanide-doped upconversion (UC) phosphors absorb low-energy infrared light and convert it into higher-energy visible light. Despite over 10 years of development, it has not been possible to synthesize nanocrystals (NCs) with UC efficiencies on a par with what can be achieved in bulk materials. To guide the design and realization of more efficient UC NCs, a better understanding is necessary of the loss pathways competing with UC. Here we study the excited-state dynamics of the workhorse UC material β-NaYF4 co-doped with Yb3+ and Er3+. For each of the energy levels involved in infrared-to-visible UC, we measure and model the competition between spontaneous emission, energy transfer between lanthanide ions, and other decay processes. An important quenching pathway is energy transfer to high-energy vibrations of solvent and/or ligand molecules surrounding the NCs, as evidenced by the effect of energy resonances between electronic transitions of the lanthanide ions and vibrations of the solvent molecules. We present a microscopic quantitative model for the quenching dynamics in UC NCs. It takes into account cross-relaxation at high lanthanide-doping concentration as well as Förster resonance energy transfer from lanthanide excited states to vibrational modes of molecules surrounding the UC NCs. Our model thereby provides insight in the inert-shell thickness required to prevent solvent quenching in NCs. Overall, the strongest contribution to reduced UC efficiencies in core-shell NCs comes from quenching of the near-infrared energy levels (Er3+: 4I11/2 and Yb3+: 2F5/2), which is likely due to vibrational coupling to OH- defects incorporated in the NCs during synthesis.

| S-EPMC5968434 | biostudies-literature

Plasmonic enhanced emissions from cubic NaYF(4):Yb: Er/Tm nanophosphors.

Project description:A metal shell was used in this study to provide significant enhancement of the up-converted emission from cubic NaYF(4) nanoparticles, creating a valuable composite material for labeling in biology and other applications - use of the cubic form of the material obviates the need to undertake a high temperature transformation to the naturally more efficient hexagonal phase. The NaYF(4) matrix contained ytterbium sensitizer and an Erbium (Er) or Thulium (Tm) activator. The particle sizes of the as-synthesized nanoparticles were in the range of 20-40 nm with a gold shell thickness of 4-8 nm. The gold shell was macroscopically amorphous. The synthesis method was based on a citrate chelation. In this approach, we exploited the ability of the citrate ion to act as a reductant and stabilizer. Confining the citrate ion reductant on the nanophosphor surface rather than in the solution was critical to the gold shell formation. The plasmonic shell enhanced the up-conversion emission of Tm from visible and near-infrared regions by up to a factor of 8, in addition to imparting a visible color arising from the plasmon absorption of the gold shell. The up-conversion enhancement observed with Tm and Er were different for similar gold coverages, with local crystal field changes as a possible route to enhance up-conversion emission from high symmetry structural hosts. These novel up-converting nanophosphor particles combine the phosphor and features of a gold shell, providing a unique platform for many biological imaging and labeling applications.

| S-EPMC3119558 | biostudies-literature

Luminescent Nanothermometer Operating at Very High Temperature-Sensing up to 1000 K with Upconverting Nanoparticles (Yb3+/Tm3+).

Project description:Lanthanide-based luminescent nanothermometers play a crucial role in optical temperature determination. However, because of the strong thermal quenching of the luminescence, as well as the deterioration of their sensitivity and resolution with temperature elevation, they can operate in a relatively low-temperature range, usually from cryogenic to ≈800 K. In this work, we show how to overcome these limitations and monitor very high-temperature values, with high sensitivity (≈2.1% K-1) and good thermal resolution (≈1.4 K) at around 1000 K. As an optical probe of temperature, we chose upconverting Yb3+-Tm3+ codoped YVO4 nanoparticles. For ratiometric sensing in the low-temperature range, we used the relative intensities of the Tm3+ emissions associated with the 3F2,3 and 3H4 thermally coupled levels, that is, 3F2,3 → 3H6/3H4 → 3H6 (700/800 nm) band intensity ratio. In order to improve sensitivity and resolution in the high-temperature range, we used the 940/800 nm band intensity ratio of the nonthermally coupled levels of Yb3+ (2F5/2 → 2F7/2) and Tm3+ (3H4 → 3H6). These NIR bands are very intense, even at extreme temperature values, and their intensity ratio changes significantly, allowing accurate temperature sensing with high thermal and spatial resolutions. The results presented in this work may be particularly important for industrial applications, such as metallurgy, catalysis, high-temperature synthesis, materials processing and engineering, and so forth, which require rapid, contactless temperature monitoring at extreme conditions.

| S-EPMC7660569 | biostudies-literature