Browse
Submit Data
Databases
API
Help

Dataset Information

24 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Evolution of Highly Biocompatible and Thermally Stable YVO₄:Er³⁺/Yb³⁺ Upconversion Mesoporous Hollow Nanospheriods as Drug Carriers for Therapeutic Applications.

ABSTRACT: In recent times, upconversion nanomaterials with mesoporous hollow structures have gained significant interest as a prospective nano-platform for cancer imaging and therapeutic applications. In this study, we report a highly biocompatible YVO₄:1Er³⁺/10Yb³⁺ upconversion mesoporous hollow nanospheriods (YVO₄:Er³⁺/Yb³⁺ UC-MHNSPs) by a facile and rapid self-sacrificing template method. The Rietveld analysis confirmed their pure phase of tetragonal zircon structure. Nitrogen adsorption-desorption isotherms revealed the mesoporous nature of these UC-MHNSPs and the surface area is found to be ~87.46 m²/g. Under near-infrared excitation (980 nm), YVO₄:Er³⁺/Yb³⁺ UC-MHNSPs showed interesting color tunability from red to green emission. Initially (at 0.4 W), energy back transfer from Er³⁺ to Yb³⁺ ions leads to the strong red emission. Whereas at high pump powers (1 W), a fine green emission is observed due to the dominant three-photon excitation process and traditional energy transfer route from Er³⁺ to Yb³⁺ ions. The bright red light from the membrane of HeLa cells confirmed the effective cellular uptake of YVO₄:Er³⁺/Yb³⁺ UC-MHNSPs. The resonant decrease in cell viability on increasing the concentration of curcumin conjugated YVO₄:Er³⁺/Yb³⁺ UC-MHNSPs established their excellent antitumor activity. Therefore, the acquired results indicate that these YVO₄:Er³⁺/Yb³⁺ UC-MHNSPs are promising drug carriers for bioimaging and various therapeutic applications.

SUBMITTER: Pavitra E

PROVIDER: S-EPMC9332312 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

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

Interaction of LiYF4:Yb3+/Er3+/Ho3+/Tm3+@LiYF4:Yb3+ upconversion nanoparticles, molecularly imprinted polymers, and templates.

Project description:In this work, LiYF4:Yb0.25 3+/Er0.01 3+/Tm0.01 3+/Ho0.01 3+@LiYF4:Yb0.2 3+ upconverting nanoparticles (UCNP) were used as luminescent materials for the preparation of molecular imprinting polymer nanocomposites. Three luminescent molecularly imprinted polymer (MIP) nanocomposites were prepared by in situ polymerization. The relationship between the functional monomers, templates, and upconversion nanoparticles was investigated. Two hydrophilic monomers (acrylic acid (AA) and acrylamide (AAm)) and one hydrophobic monomer (N-tert-butylacrylamide (TBAm)) were employed as functional monomers, while one amino acid (cysteine) and two proteins (albumin and hemoglobin) were employed as the templates to investigate the effect of their interaction with LiYF4:Yb3+/Er3+/Ho3+/Tm3+@LiYF4:Yb3+ core/shell UCNPs on the polymerization process, luminescence properties, and adsorption capacity. The results showed that the UCNPs were embedded in the polymeric matrix to form an irregular quasimicrospherical UCNPs@MIP with diameters ranging from several hundred nanometers to several micrometers depending on the functional monomer. The quenching effect was more pronounced for the adsorption of hemoglobin with UCNPs@MIP compared to cysteine and albumin. In addition, the adsorption capacities of the AA- and AAm-made UCNPs@MIP were greater than those of TBAm-made UCNPs@MIP. The rebinding of the templates onto UCNPs@MIP was very fast and approached equilibrium within 30 min, indicating that the synthesized UCNPs@MIP can be employed as fluorescent probes to offer rapid detection of molecules.

| S-EPMC9056933 | biostudies-literature

Internal OH- induced cascade quenching of upconversion luminescence in NaYF4:Yb/Er nanocrystals.

Project description:Internal hydroxyl impurity is known as one of the main detrimental factors affecting the upconversion (UC) efficiency of upconversion luminescence (UCL) nanomaterials. Different from surface/ligand-related emission quenching which can be effectively diminished by, e.g., core/shell structure, internal hydroxyl is easy to be introduced in synthesis but difficult to be quantified and controlled. Therefore, it becomes an obstacle to fully understand the relevant UC mechanism and improve UC efficiency of nanomaterials. Here we report a progress in quantifying and large-range adjustment of the internal hydroxyl impurity in NaYF4 nanocrystals. By combining the spectroscopy study and model simulation, we have quantitatively unraveled the microscopic interactions underlying UCL quenching between internal hydroxyl and the sensitizers and activators, respectively. Furthermore, the internal hydroxyl-involved UC dynamical process is interpreted with a vivid concept of "Survivor effect," i.e., the shorter the migration path of an excited state, the larger the possibility of its surviving from hydroxyl-induced quenching. Apart from the consistent experimental results, this concept can be further evidenced by Monte Carlo simulation, which monitors the variation of energy migration step distribution before and after the hydroxyl introduction. The new quantitative insights shall promote the construction of highly efficient UC materials.

| S-EPMC8134431 | biostudies-literature

Biocompatible Mesoporous Hollow Carbon Nanocapsules for High Performance Supercapacitors.

Project description:A facile and general method for the controllable synthesis of N-doped hollow mesoporous carbon nanocapsules (NHCNCs) with four different geometries has been developed. The spheres (NHCNC-1), low-concaves (NHCNC-2), semi-concaves (NHCNC-3) and wrinkles (NHCNC-4) shaped samples were prepared and systematically investigated to understand the structural effects of hollow particles on their supercapacitor performances. Compared with the other three different shaped samples (NHCNC-1, NHCNC-2, and NHCNC-4), the as-synthesized semi-concave structured NHCNC-3 demonstrated excellent performance with high gravimetric capacitance of 326?F?g-1 (419?F?cm-3) and ultra-stable cycling stability (96.6% after 5000 cycles). The outstanding performances achieved are attributed to the unique semi-concave structure, high specific surface area (1400 m2 g-1), hierarchical porosity, high packing density (1.41?g?cm-3) and high nitrogen (N) content (up to 3.73%) of the new materials. These carbon nanocapsules with tailorable structures and properties enable them as outstanding carriers and platforms for various emerging applications, such as nanoscale chemical reactors, catalysis, batteries, solar energy harvest, gas storage and so on. In addition, these novel carbons have negligible cytotoxicity and high biocompatibility for human cells, promising a wide range of bio applications, such as biomaterials, drug delivery, biomedicine, biotherapy and bioelectronic devices.

| S-EPMC7062802 | biostudies-literature

An upconversion luminescence and temperature sensor based on Yb3+/Er3+ co-doped GdSr2AlO5.

Project description:GdSr2AlO5:Yb3+/Er3+ micro-particles were synthesized by a simple solid state method. The structure, morphology, size and upconversion luminescence features have been characterized. These results indicated that GdSr2AlO5 has a contracted tetragonal cell and has irregular block shaped particles with sizes of about 5 μm. During upconversion, green (2H11/2, 4S3/2 → 4I15/2) (527 nm, 549 nm) and red (4F9/2 → 4I15/2) (665 nm) emissions had been observed, both of which occurred via a two-photon population process. In addition, green UC emission characteristics were studied, and it was found that its temperature ranged from 293 K to 473 K and the sensitivity was 0.0054 K-1 at 473 K. This indicated that GdSr2AlO5:Yb3+/Er3+ micro-particles may have potential application in high temperature environments for safety signs.

| S-EPMC9078722 | biostudies-literature

Thermally boosted upconversion and downshifting luminescence in Sc2(MoO4)3:Yb/Er with two-dimensional negative thermal expansion.

Project description:Rare earth (RE3+)-doped phosphors generally suffer from thermal quenching, in which their photoluminescence (PL) intensities decrease at high temperatures. Herein, we report a class of unique two-dimensional negative-thermal-expansion phosphor of Sc2(MoO4)3:Yb/Er. By virtue of the reduced distances between sensitizers and emitters as well as confined energy migration with increasing the temperature, a 45-fold enhancement of green upconversion (UC) luminescence and a 450-fold enhancement of near-infrared downshifting (DS) luminescence of Er3+ are achieved upon raising the temperature from 298 to 773 K. The thermally boosted UC and DS luminescence mechanism is systematically investigated through in situ temperature-dependent Raman spectroscopy, synchrotron X-ray diffraction and PL dynamics. Moreover, the luminescence lifetime of 4I13/2 of Er3+ in Sc2(MoO4)3:Yb/Er displays a strong temperature dependence, enabling luminescence thermometry with the highest relative sensitivity of 12.3%/K at 298 K and low temperature uncertainty of 0.11 K at 623 K. These findings may gain a vital insight into the design of negative-thermal-expansion RE3+-doped phosphors for versatile applications.

| S-EPMC9019035 | biostudies-literature

Enhancing Upconversion Luminescence Efficiency via Chiral β-NaYF4:Er3+/Yb3+ Microcrystals Based on Mesoscale Regulation.

Project description:Chirality, universal characteristics of nature, introduces asymmetry in synthetic materials. Revealing the microscopic asymmetry of macroscopically symmetric materials is the key to control the growth of chiral materials and give full play to their application potential. Materials for photon upconversion (UC) are of great interest for many applications owing to their anti-Stoke luminescence process, especially for chiral UC materials. For the preparation of UC materials, a tiny change in reaction parameters will lead to variations in morphology, phase components, and fluorescence intensity, as well as its chirality. Because of the strict reaction conditions for the formation of chiral UC materials, there are no reports of the successful synthesis of chiral UC materials. Therefore, a facile method for the controllable synthesis of chiral UC materials is highly desired. Herein, chiral-assembled hexagonal prisms of β-NaYF4:Er3+/Yb3+ microcrystals were synthesized to realize the smart manipulation of their morphology as well as a great improvement of the fluorescence efficiency. We proposed a three-stage doped β-NaYF4 crystal growth mechanism on mesoscale regulation, where the fluorescence enhancement principle of chirality was revealed. The enhancement of fluorescence efficiency of chiral UC materials endows their promising application in luminescent displays.

| S-EPMC6644319 | biostudies-literature

Brilliant Nonlinear Optical Response of Ho3+ and Yb3+ Activated YVO4 Nanophosphor and Its Conjugation with Fe3O4 for Smart Anticounterfeit and Hyperthermia Applications.

Project description:YVO4:Ho3+/Yb3+ nanophosphors prepared by an effective polyol-mediated route show dual-mode behavior in photoluminescence. Upon 980 nm excitation, the upconversion red emission spectrum exhibits a bright red peak at ∼650 nm, characteristic of the electronic transition of the Ho3+ ion via involvement of two-photon absorption, which has been confirmed by the power-dependent luminescence study. Moreover, at 300 nm excitation, downconversion emission peaks are observed at 550, 650, and ∼755 nm. The nonradiative resonant energy transfer occurs from the V-O charge transfer band to Ho3+ ions, resulting in an improved emission of Ho3+ ions. Moreover, polyethylene glycol-coated nanoparticles make it suitable for water dispersibility; and these particles are conjugated with Fe3O4 nanoparticles to form magnetic-luminescent hybrid nanoparticles. Highly water-dispersible magnetic-luminescent hybrid material attained the hyperthermia temperature (∼42 °C) under an applied AC magnetic field. The specific absorption rate value is found to be high (138 W/g), which is more than that of pure superparamagnetic Fe3O4 nanoparticles. At 300 nm excitation, the high quantum yield value of ∼27% is obtained from YVO4:Ho3+/Yb3+, which suggests that it is a good phosphor material. By employing the neutron activation analysis technique, it is shown that nanophosphor particles can absorb Au3+ up to the ppm level. Interestingly, such nanophosphor also shows the potentiality for anticounterfeiting applications.

| S-EPMC8340094 | biostudies-literature

Enhanced upconversion fluorescent probe of single NaYF4:Yb3+/Er3+/Zn2+ nanoparticles for copper ion detection.

Project description:Surface modified NaYF4:Yb3+/Er3+/Zn2+ upconversion nanoparticles were obtained by using branched polyethylenimine (PEI). Strong fluorescence emission was observed and the influence of copper ions on the fluorescence emission of the PEI-modified NaYF4:Yb3+/Er3+/Zn2+ nanoparticles was investigated. It was found that the fluorescence emission can be quenched through luminescence resonance energy transfer from the particle to the copper ions. The results show that the PEI modified NaYF4:Yb3+/Er3+/Zn2+ nanoparticle can be used as a fluorescent probe for highly sensitive and selective detection of copper ions.

| S-EPMC9089350 | biostudies-literature

The Upconversion Luminescence of Ca3Sc2Si3O12:Yb3+,Er3+ and Its Application in Thermometry.

Project description:To develop novel luminescent materials for optical temperature measurement, a series of Yb3+- and Er3+-doped Ca3Sc2Si3O12 (CSS) upconversion (UC) phosphors were synthesized by the sol-gel combustion method. The crystal structure, phase purity, and element distribution of the samples were characterized by powder X-ray diffraction and a transmission electron microscope (TEM). The detailed study of the photoluminescence emission spectra of the samples shows that the addition of Yb3+ can greatly enhance the emission of Er3+ by effective energy transfer. The prepared Yb3+ and Er3+ co-doped CSS phosphors exhibit green emission bands near 522 and 555 nm and red emission bands near 658 nm, which correspond to the 2H11/2→4I15/2, 4S3/2→4I15/2, and 4F9/2→4I15/2 transitions of Er3+, respectively. The temperature-dependent behavior of the CSS:0.2Yb3+,0.02Er3+ sample was carefully studied by the fluorescence intensity ratio (FIR) technique. The results indicate the excellent sensitivity of the sample, with a maximum absolute sensitivity of 0.67% K-1 at 500 K and a relative sensitivity of 1.34% K-1 at 300 K. We demonstrate here that the temperature measurement performance of FIR technology using the CSS:Yb3+,Er3+ phosphor is not inferior to that of infrared thermal imaging thermometers. Therefore, CSS:Yb3+,Er3+ phosphors have great potential applications in the field of optical thermometry.

| S-EPMC10343700 | biostudies-literature