Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

A photochemical determination of luminescence efficiency of upconverting nanoparticles.

ABSTRACT: Upconverting nanoparticles are a rising class of non-linear luminescent probes burgeoning since the beginning of the 2000's, especially for their attractiveness in theranostics. However, the precise quantification of the light delivered remains a hot problem in order to estimate their impact on the biological medium. Sophisticated photophysical measurements under near infrared excitation have been developed only by few teams. Here, we present the first attempt towards a simple and cheap photochemical approach consisting of an actinometric characterization of the green emission of NaYF4:Yb,Er nanoparticles. Using the recently calibrated actinometer 1,2-bis(2,4-dimethyl-5-phenyl-3-thienyl)-3,3,4,4,5,5-hexafluoro-1-cyclopentene operating in the green region of the visible spectra, we propose a simple photochemical experiment to get an accurate estimation of the efficiency of these green-emitting "nanolamps". The agreement of the collected data with the previous published results validates this approach.

SUBMITTER: Amouroux B

PROVIDER: S-EPMC6880820 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Intracellular photoswitchable neuropharmacology driven by luminescence from upconverting nanoparticles.

Project description:Photoswitchable drugs are small-molecule optical probes that undergo chromatically selective control of drug efficacy using, most often, UV-visible light. Here we report that luminescence produced by near-infrared stimulation of NaYF4:TmYb nanoparticles can be used for "remote control" of an azobenzene-based photochromic ion channel blocker of neurons in living brain slices.

| S-EPMC7812838 | biostudies-literature

Manipulating energy transfer in lanthanide-doped single nanoparticles for highly enhanced upconverting luminescence.

Project description:Energy transfer (ET) is of fundamental importance in tuning the optical performance of lanthanide-doped upconversion nanoparticles (UCNPs). However, the fine control and manipulation of the ETs particularly for deleterious cross-relaxation type ETs (CR-ETs) in lanthanide-doped UCNPs remains a formidable challenge to date. Herein, we demonstrate a rational design strategy to manipulate the deleterious CR-ETs in lanthanide-doped UCNPs, by fine-tuning the distances at an extremely large length scale (>20 nm) among multiple lanthanide dopants that are simultaneously embedded into one single nanoparticle with specially designed multilayer nanostructures. The successful inhibition of the CR-ETs leads to a significantly enhanced upconversion luminescence signal with an intensity ∼70 times higher than that of co-doped conventional UCNPs. This finding paves a new way for the better control of the ETs in lanthanide-doped nanoparticles, and offers the possibility of constructing a series of promising single-nanocrystal-based anti-counterfeiting barcodes with well-identified UC emission color and lifetime outputs.

| S-EPMC5846170 | biostudies-literature

Photon-upconverting chiral liquid crystal: significantly amplified upconverted circularly polarized luminescence.

Project description:In this work, we demonstrate a room-temperature chiral liquid crystal which shows remarkable photon upconverted circularly polarized luminescence (UC-CPL). Circularly polarized luminescent materials with higher dissymmetry factor (g lum) underpin the basis for future applications. Since most chiral organic molecules have only a small g lum, it is vital to explore a new pathway to amplify the g lum of organic compounds. Here, by dispersing a chiral emitter and a triplet donor into a room-temperature nematic liquid crystal, highly efficient triplet-triplet annihilation-based photon upconversion (TTA-UC) and UC-CPL were observed in the induced chiral nematic liquid crystal (N*LC). Moreover, this system could simultaneously amplify the promoted circularly polarized luminescence (CPL) and the upconverted circularly polarized luminescence. The dissymmetry factors g lum of CPL and UC-CPL have been amplified by three orders of magnitude and one order of magnitude, respectively.

| S-EPMC6330689 | biostudies-literature

Optically Robust and Biocompatible Mechanosensitive Upconverting Nanoparticles.

Project description:Upconverting nanoparticles (UCNPs) are promising tools for background-free imaging and sensing. However, their usefulness for in vivo applications depends on their biocompatibility, which we define by their optical performance in biological environments and their toxicity in living organisms. For UCNPs with a ratiometric color response to mechanical stress, consistent emission intensity and color are desired for the particles under nonmechanical stimuli. Here, we test the biocompatibility and mechanosensitivity of ?-NaYF4:Yb,Er@NaLuF4 nanoparticles. First, we ligand-strip these particles to render them dispersible in aqueous media. Then, we characterize their mechanosensitivity (?30% in the red-to-green spectral ratio per GPa), which is nearly 3-fold greater than those coated in oleic acid. We next design a suite of ex vivo and in vivo tests to investigate their structural and optical properties under several biorelevant conditions: over time in various buffers types, as a function of pH, and in vivo along the digestive tract of Caenorhabditis elegans worms. Finally, to ensure that the particles do not perturb biological function in C. elegans, we assess the chronic toxicity of nanoparticle ingestion using a reproductive brood assay. In these ways, we determine that mechanosensitive UCNPs are biocompatible, i.e., optically robust and nontoxic, for use as in vivo sensors to study animal digestion.

| S-EPMC6661856 | biostudies-literature

Near-Infrared-Detached Adhesion Enabled by Upconverting Nanoparticles.

Project description:Achieving efficient and biocompatible detachment between adhered wet materials (i.e., tissues and hydrogels) is a major challenge. Recently, photodetachable topological adhesion has shown great promise as a strategy for conquering this hurdle. However, this photodetachment was triggered by UV light with poor biocompatibility and penetration capacity. This study describes near-infrared (NIR) light-detached topological adhesion based on polyacrylic acid coated upconverting nanoparticles (UCNP@PAA) and a photodetachable adhesive (termed Cell-Fe). Cell-Fe is a coordinated topological adhesive consisting of carboxymethylcellulose and Fe3+ that can be photodecomposed by UV light. To prepare a substrate for NIR-detached topological adhesion, UCNP@PAA and Cell-Fe were mixed and brushed on the surface of the model adherent. The UCNP@PAA can harvest NIR light and convert it into UV light, triggering the decomposition of the Cell-Fe and inducing the detachment. This NIR-detached topological adhesion is also feasible in deep tissue because of the ability of NIR light to penetrate tissue.

| S-EPMC6994296 | biostudies-literature

Self-Calibrated Double Luminescent Thermometers Through Upconverting Nanoparticles.

Project description:Luminescent nanothermometry uses the light emission from nanostructures for temperature measuring. Non-contact temperature readout opens new possibilities of tracking thermal flows at the sub-micrometer spatial scale, that are altering our understanding of heat-transfer phenomena occurring at living cells, micro electromagnetic machines or integrated electronic circuits, bringing also challenges of calibrating the luminescent nanoparticles for covering diverse temperature ranges. In this work, we report self-calibrated double luminescent thermometers, embedding in a poly(methyl methacrylate) film Er3+- and Tm3+-doped upconverting nanoparticles. The Er3+-based primary thermometer uses the ratio between the integrated intensities of the 2 H11/2→4 I15/2 and 4 S3/2→4 I15/2 transitions (that follows the Boltzmann equation) to determine the temperature. It is used to calibrate the Tm3+/Er3+ secondary thermometer, which is based on the ratio between the integrated intensities of the 1 G4→3 H6 (Tm3+) and the 4 S3/2→4 I15/2 (Er3+) transitions, displaying a maximum relative sensitivity of 2.96% K-1 and a minimum temperature uncertainty of 0.07 K. As the Tm3+/Er3+ ratio is calibrated trough the primary thermometer it avoids recurrent calibration procedures whenever the system operates in new experimental conditions.

| S-EPMC6482206 | biostudies-other

Experimental observation of spatially resolved photo-luminescence intensity distribution in dual mode upconverting nanorod bundles.

Project description:A novel method for demonstration of photoluminescence intensity distribution in upconverting nanorod bundles using confocal microscopy is reported. Herein, a strategy for the synthesis of highly luminescent dual mode upconverting/downshift Y1.94O3:Ho3+0.02/Yb3+0.04 nanorod bundles by a facile hydrothermal route has been introduced. These luminescent nanorod bundles exhibit strong green emission at 549?nm upon excitations at 449?nm and 980?nm with quantum efficiencies of ~6.3% and ~1.1%, respectively. The TEM/HRTEM results confirm that these bundles are composed of several individual nanorods with diameter of ~100?nm and length in the range of 1-3??m. Furthermore, two dimensional spatially resolved photoluminescence intensity distribution study has been carried out using confocal photoluminescence microscope throughout the nanorod bundles. This study provides a new direction for the potential use of such emerging dual mode nanorod bundles as photon sources for next generation flat panel optical display devices, bio-medical applications, luminescent security ink and enhanced energy harvesting in photovoltaic applications.

| S-EPMC5304174 | biostudies-literature

Nanoplasmonic Upconverting Nanoparticles as Orientation Sensors for Single Particle Microscopy.

Project description:We showed that the anisotropic disk shape of nanoplasmonic upconverting nanoparticles (NP-UCNPs) creates changes in fluorescence intensity during rotational motion. We determined the orientation by a three-fold change in fluorescence intensity. We further found that the luminescence intensity was strongly dependent on the particle orientation and on polarization of the excitation light. The luminescence intensity showed a three-fold difference between flat and on-edge orientations. The intensity also varied sinusoidally with the polarization of the incident light, with an Imax/Imin ratio of up to 2.02. Both the orientation dependence and Imax/Imin are dependent on the presence of a gold shell on the UCNP. Because the fluorescence depends on the NP's orientation, the rotational motion of biomolecules coupled to the NP can be detected. Finally, we tracked the real-time rotational motion of a single NP-UCNP in solution between slide and coverslip with diffusivity up to 10-2 μm2s-1.

| S-EPMC5429696 | biostudies-literature

Upconverting Nanoparticles as Optical Sensors of Nano- to Micro-Newton Forces.

Project description:Mechanical forces affect a myriad of processes, from bone growth to material fracture to touch-responsive robotics. While nano- to micro-Newton forces are prevalent at the microscopic scale, few methods have the nanoscopic size and signal stability to measure them in vivo or in situ. Here, we develop an optical force-sensing platform based on sub-25 nm NaYF4 nanoparticles (NPs) doped with Yb3+, Er3+, and Mn2+. The lanthanides Yb3+ and Er3+ enable both photoluminescence and upconversion, while the energetically coupled d-metal Mn2+ adds force tunability through its crystal field sensitivity. Using a diamond anvil cell to exert up to 3.5 GPa pressure or ∼10 μN force per particle, we track stress-induced spectral responses. The red (660 nm) to green (520, 540 nm) emission ratio varies linearly with pressure, yielding an observed color change from orange to red for α-NaYF4 and from yellow-green to green for d-metal optimized β-NaYF4 when illuminated in the near infrared. Consistent readouts are recorded over multiple pressure cycles and hours of illumination. With the nanoscopic size, a dynamic range of 100 nN to 10 μN, and photostability, these nanoparticles lay the foundation for visualizing dynamic mechanical processes, such as stress propagation in materials and force signaling in organisms.

| S-EPMC6589185 | biostudies-literature

Gated Luminescence Imaging of Silicon Nanoparticles.

Project description:The luminescence lifetime of nanocrystalline silicon is typically on the order of microseconds, significantly longer than the nanosecond lifetimes exhibited by fluorescent molecules naturally present in cells and tissues. Time-gated imaging, where the image is acquired at a time after termination of an excitation pulse, allows discrimination of a silicon nanoparticle probe from these endogenous signals. Because of the microsecond time scale for silicon emission, time-gated imaging is relatively simple to implement for this biocompatible and nontoxic probe. Here a time-gated system with ?10 ns resolution is described, using an intensified CCD camera and pulsed LED or laser excitation sources. The method is demonstrated by tracking the fate of mesoporous silicon nanoparticles containing the tumor-targeting peptide iRGD, administered by retro-orbital injection into live mice. Imaging of such systemically administered nanoparticles in vivo is particularly challenging because of the low concentration of probe in the targeted tissues and relatively high background signals from tissue autofluorescence. Contrast improvements of >100-fold (relative to steady-state imaging) is demonstrated in the targeted tissues.

| S-EPMC4931905 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data