Centrifugated lateral flow assay strips based on dual-emission carbon dots modified with europium ions for ratiometric determination and on-site discrimination of tetracyclines in environment.

Due to the serious detrimental impact on human health, antibiotic pollution particularly tetracyclines residues has become a serious problem. Herein, a multiple response fluorescent probe consisted of dual-emission carbon dots and Eu3+ (D-CDs@Eu3+) is designed for the determination and discrimination of tetracyclines (TCs). Specifically, the carboxyl and amidogen group of dual-emission carbon dots (D-CDs) can coordinate with Eu3+ to form the D-CDs@Eu3+. Upon adding TCs, the fluorescence intensities of D-CDs at 405 nm and 495 nm are quenched due to inner filter effect (IFE) and the localization of fluorescence resonance energy transfer (L-FRET) between the D-CDs@Eu3+ and TC. Simultaneously, the D-CDs@Eu3+ may chelate with TCs to enhance the occurrence of antenna effect, while the characteristic peaks of Eu3+ at 590 nm and 615 nm are enhanced. On these bases, the TCs detection is achieved with low detection limits from 46.7 to 72.0 nM. Additionally, through the distinct efficiencies of L-FRET, the discrimination of TCs is achieved. Moreover, a novel centrifugated lateral flow assay strips (CLFASs) device is developed by integrating the D-CDs@Eu3+, lateral flow assay strips and smartphone using RGB variations for TCs detection, achieving remarkable recoveries (98.6-103.7 %) in real samples. Therefore, this CLFASs device provides a reliable approach for the TCs detection, demonstrating potential applications.

Colour tunable photoluminescence studies of Dy3+/Eu3+ co-doped BaPbAlFB glasses for epoxy-free w-LED applications.

Barium lead alumino fluoroborate (BaPbAlFB) glasses singly and co-doped with Dy3+ and Eu3+ ions were prepared by melt quench method and studied their photoluminescence (PL) properties along with energy migration. Singly doped Dy3+/Eu3+ ions in BaPbAlFB glasses under 365 and 393 nm excitation wavelengths emit the PL bands through Dy: (4F9/2 → 6H15/2 and 4F9/2 → 6H13/2) and Eu: (5D0→7F2) transitions located at (Dy: 483 and 575 nm) and (Eu: 613 nm) respectively. Further, tunability of PL emissions is achieved by exciting the Dy3+/Eu3+ co-doped BaPbAlFB glasses at various wavelengths. The obtained CIE (0.34, 0.33) and CCT value (5080.4 K) of Dy3+/Eu3+ co-doped BaPbAlFB glass produced white light emission under 365 nm excitation wavelength. The corresponding CCT values of Dy3+/Eu3+ co-doped BaPbAlFB glasses varied from 1580 to 5080 K and their corresponding color emission changes from intense red to white light regime quite suitable for fabrication of epoxy-free w-LED devices.

A dual-response ratiometric fluorescent sensor for oxytetracycline determination in milk and mutton samples.

Owing to the adverse effects of oxytetracycline (OTC) residues on human health, it is of great importance to construct a rapid and effective strategy for OTC detection. Herein, we developed a dual-response fluorescence sensing platform based on molybdenum sulfide quantum dots (MoS2 QDs) and europium ions (Eu3+) for ratiometric detection of OTC. The MoS2 QDs, synthesized through an uncomplicated one-step hydrothermal approach, upon OTC integration into the MoS2 QDs/Eu3+ sensing system, exhibit a significant quenching of blue fluorescence due to the inner filter effect (IFE), simultaneously enhancing the distinct red emission of Eu3+ at 624 nm, a phenomenon attributed to the antenna effect (AE). This sensor demonstrates exceptional selectivity and sensitivity towards OTC, characterized by a linear detection range of 0.2-10 µM and a notably low detection limit of 2.21 nM. Furthermore, we achieved a visual semi-quantitative assessment of OTC through the discernible fluorescence color transition from blue to red under a 365 nm ultraviolet lamp. The practical applicability of this sensor was validated through the successful detection of OTC in milk and mutton samples, underscoring its potential as a robust tool for OTC monitoring in foodstuffs to safeguard food safety.

Color Routing of the Emission from Magnetic and Electric Dipole Transitions of Eu3+ by Broken-Symmetry TiO2 Metasurfaces.

Manipulation of magnetic dipole emission with resonant photonic nanostructures is of great interest for both fundamental research and applications. However, obtaining selective control over the emission properties of magnetic dipole transitions is challenging, as they usually occur within a manifold of spectrally close emission lines associated with different spin states of the involved electronic levels. Here we demonstrate spectrally selective directional tailoring of magnetic dipole emission using designed photonic nanostructures featuring a high quality factor. Specifically, we employ a hybrid nanoscale optical system consisting of a Eu3+ compound coupled to a designed broken-symmetry TiO2 metasurface to demonstrate directional color routing of the compound's emission through its distinct electric and magnetic-dominated electronic transition channels. Using low numerical aperture collection optics, we achieve a fluorescence signal enhancement of up to 33.13 for the magnetic-dominated dipole transition at 590 nm when it spectrally overlaps with a spectrally narrow resonance of the metasurface. This makes the, usually weak, magnetic dipole transition the most intense spectral line in our recorded fluorescence spectra. By studying the directional emission properties for the coupled system using Fourier imaging and time-resolved fluorescence measurements, we demonstrate that the high-quality-factor modes in the metasurface enable free-space light routing, where forward-directed emission is established for the magnetic-dominated dipole transition, whereas the light emitted via the electric dipole transition is mainly directed sideways. Our results underpin the importance of magnetic light-matter interactions as an additional degree of freedom in photonic and optoelectronic systems. Moreover, they facilitate the development of spectrometer-free and highly integrated nanophotonic imaging, sensing, and probing devices.

Luminescence characterization of BioGlass undoped and doped with europium and silver ions.

The objective of this study was to investigate the properties of BioGlass, with and without doping with europium and silver, with a specific focus on its potential application in thermoluminescent (TL) and optically stimulated luminescent (OSL) dosimetry. The structural and optical characteristics of the samples were also analyzed using techniques such as X-ray diffraction (XRD), optical absorption (OA), and fluorescence spectroscopy (FL). An XRD analysis confirmed the amorphous phase of the BioGlass. OA and FL spectra were obtained at room temperature, and characteristic bands of dopant ions were observed which confirmed the incorporation of the Eu3+ ions and silver nanoparticles Ag(NP) ion into the BioGlass. The OSL decay curves exhibited a characteristic exponential behavior, with a notable presence of fast and medium decay components; this suggests that the charge traps within the BioGlass samples possess a high photoionization cross section when exposed to blue LEDs, which are commonly used as the light source in OSL readers. Different TL glow peaks with varying shapes of the glow curve were observed when the dopant, the co-dopant, and the concentration of silver were altered in the samples. The TL kinetic parameters were determined, such as the order value, activation energy, and frequency factor, and the OSL parameters for the compound were also analyzed, including an exponential fit to the curves. Based on these initial results, we conclude that BioGlass has the potential for use in radiation dosimetry.

Enhanced Sorption of Europium and Scandium Ions from Nitrate Solutions by Remotely Activated Ion Exchangers.

The escalating demand for rare earth metals (REM) in situations of limited availability has spurred scientists to seek alternative sources of REM, such as industrial waste solutions. This paper investigates the potential for improving the sorption activity of readily available and inexpensive ion exchangers, specifically the interpolymer systems "Lewatit CNP LF and AV-17-8", towards europium and scandium ions, in comparison to the unactivated ion exchangers. The sorption properties of the improved sorbents (interpolymer systems) were evaluated using conductometry, gravimetry, and atomic emission analysis. The results demonstrate that the "Lewatit CNP LF:AV-17-8" (5:1) interpolymer system exhibits a 25% increase in europium ion sorption compared to the raw Lewatit CNP LF (6:0), and a 57% increase in europium ion sorption compared to the raw AV-17-8 (0:6) ion exchanger after 48 h of the sorption process. In contrast, the "Lewatit CNP LF:AV-17-8" (2:4) interpolymer system exhibits a 310% increase in scandium ion sorption compared to the raw Lewatit CNP LF (6:0), and a 240% increase in scandium ion sorption compared to the raw AV-17-8 (0:6) after 48 h of interaction. The improvement in europium and scandium ion sorption levels by the interpolymer systems, compared to the raw ion exchangers, may be attributed to the high ionization degree resulting from the remote interaction effect of the polymer sorbents as the interpolymer system in aqueous media.

Preparation of Eu(III) Complexes Containing Maleopimaric Acid Anhydride with Ultra-narrow and Efficient Fluorescence Emission for High Determination on Gallic Acid in Acetonitrile Solution.

Two novel Eu(III) complexes constructed by maleopimaric acid anhydride (MPA) and 2,2'-bipyridyl (Bpy) / 1, 10-phenanthroline (Phen), named as MPA-Bpy-Eu / MPA-Phen-Eu, have been synthesized by a one-step precipitation method. FTIR, UV, TG, elemental analysis, XPS, and ESI-MS revealed the successful coordination of Eu(III) ions with MPA and Bpy / Phen through Eu-O and Eu-N bonds, respectively. Introducing MPA into coordinate structure increased the electron cloud density in 3d5/2 orbit of Eu(III) ions, enhanced the absolute quantum yields of MPA-Bpy-Eu (89.27%) and MPA-Phen-Eu (94.41%), and decreased the full width at half maxima of 5D0 → 7F2 transitions of MPA-Bpy-Eu (2.23 nm) and MPA-Phen-Eu (2.93 nm), respectively. The fluorescence quenching experiments showed that there was a good linear relationship between the relative fluorescence intensity of MPA-Bpy-Eu and gallic acid (GA) concentration in acetonitrile solution in the range of 0 to 8.41 × 10-2 mM. The results of UV-vis spectra, the fluorescence lifetimes, and the quantum yields demonstrated that the dynamic quenching model played a major role in the quenching process of GA on MPA-Bpy-Eu. The quenching process of GA on MPA-Phen-Eu involved dual fluorescence quenching mechanistic pathways, including static and dynamic models.

Colorimetric assay for tetracyclines based on europium ion-induced aggregation of gold nanoparticles.

Oxytetracycline-capped gold nanoparticles (OTC-Au NPs) were prepared using sodium borohydride as the reductant and OTC as the capping agent, respectively. The prepared OTC-Au NPs with a size of 6 nm have a maximum surface plasma resonance (SPR) absorption located at 514 nm. The OTC on the surface of Au NPs still can coordinate with Eu3+ ions. Due to the property that OTC has multivalent binding sites with Eu3+ ions, Eu3+ ions can induce the aggregation of OTC-Au NPs. Based on the Eu3+ ions-aggregated OTC-Au NPs, a simple aptamer-free colorimetric sensing method for TCs was developed. Briefly, free TCs compete with OTC on the surface of Au NPs resulting in the change of OTC-Au NPs from an aggregation state to a dispersed state. The whole process takes only 5 min, and as low as 20 nM OTC, 14 nM tetracycline (TC), and 20 nM doxycycline (DC) could be sensitively detected, respectively. The proposed method was also featured as good repeatability and specificity, and was applied to the detection of OTC in lake water with satisfactory recovery.

Assessment of modified Salvadora Persica for removal of 134Cs and 152+154Eu radionuclides from aqueous solution.

Biosorption is a simple and economical method utilized to remove hazardous elements from a waste solution. In this study, a low-cost agricultural waste, Salvadora Persica, was modified with iron oxyhydroxide and evaluated as an economic biosorbent to remove cesium and europium radionuclides from their aqueous solutions. The modified biosorbent was characterized by Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), X-ray diffraction (XRD), elemental analysis as well as thermogravmetirc analysis (TGA). The sorption of 134Cs and 152+154Eu radioisotopes was investigated singly in a batch mode as a function of the solution pH, contact time, and the initial concentrations of the studied ions. The kinetic of the removal process was examined and it was found that the reaction obeys a pseudo-first-order model and the intraparticle diffusion is not the sole mechanism dominating the reaction. Temkin and Sips isotherm models provide the best fit for the equilibrium data. In addition, the sorption of cesium and europium ions was a spontaneous and endothermic process as inferred from thermodynamic studies. The reusability for the sorption of cesium and europium ions reveals the feasibility and efficacy of the modified biosorbent.

Effective Sorption of Europium Ions by Interpolymer System Based on Industrial Ion-Exchanger Resins Amberlite IR120 and AB-17-8.

The research is aimed at checking the impact of a remote interaction phenomenon on growth of sorption properties of ion-exchange resins during sorption of europium ions. Industrial ion exchangers Amberlite IR120 and AB-17-8 were selected as objects for the study. Investigation was undertaken using the following physico-chemical methods of analysis: conductometry, pH-metry, colorimetry, Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), and atomic emission spectroscopy. Remote interaction of the initial ion exchangers in the interpolymer system leads to their transition into highly ionized state due to formation of optimal conformation. Found that high ionization areas of Amberlite IR120 and AB-17-8 are the molar ratios Amberlite IR120:AB-17-8 = 4:2 and 1:5. The remote interaction effect provides significant increase of the following sorption properties: sorption degree, polymer chain binding degree, effective dynamic exchange capacity. A strong increase of the sorption properties (average increase for all time of remote interaction is over 50%) in the interpolymer system Amberlite IR120-AB-17-8 was observed with individual polymer structures of Amberlite IR120 and AB-17-8. The remote interaction phenomenon can be successfully used for effective modification of industrial ion exchangers for sorption of rare-earth metals.

Nanohydroxyapatite as a Biomaterial for Peripheral Nerve Regeneration after Mechanical Damage-In Vitro Study.

Hydroxyapatite has been used in medicine for many years as a biomaterial or a cover for other biomaterials in orthopedics and dentistry. This study characterized the physicochemical properties (structure, particle size and morphology, surface properties) of Li+- and Li+/Eu3+-doped nanohydroxyapatite obtained using the wet chemistry method. The potential regenerative properties against neurite damage in cultures of neuron-like cells (SH-SY5Y and PC12 after differentiation) were also studied. The effect of nanohydroxyapatite (nHAp) on the induction of repair processes in cell cultures was assessed in tests of metabolic activity, the level of free oxygen radicals and nitric oxide, and the average length of neurites. The study showed that nanohydroxyapatite influences the increase in mitochondrial activity, which is correlated with the increase in the length of neurites. It has been shown that the doping of nanohydroxyapatite with Eu3+ ions enhances the antioxidant properties of the tested nanohydroxyapatite. These basic studies indicate its potential application in the treatment of neurite damage. These studies should be continued in primary neuronal cultures and then with in vivo models.

Quenching of the Eu3+ Luminescence by Cu2+ Ions in the Nanosized Hydroxyapatite Designed for Future Bio-Detection.

The hydroxyapatite nanopowders of the Eu3+-doped, Cu2+-doped, and Eu3+/Cu2+-co-doped Ca10(PO4)6(OH)2 were prepared by a microwave-assisted hydrothermal method. The structural and morphological properties of the products were investigated by X-ray powder diffraction (XRD), transmission electron microscopy techniques (TEM), and infrared spectroscopy (FT-IR). The average crystal size and the unit cell parameters were calculated by a Rietveld refinement tool. The absorption, emission excitation, emission, and luminescence decay time were recorded and studied in detail. The 5D0 → 7F2 transition is the most intense transition. The Eu3+ ions occupied two independent crystallographic sites in these materials exhibited in emission spectra: one Ca(1) site with C3 symmetry and one Ca(2) sites with Cs symmetry. The Eu3+ emission is strongly quenched by Cu2+ ions, and the luminescence decay time is much shorter in the case of Eu3+/Cu2+ co-doped materials than in Eu3+-doped materials. The luminescence quenching mechanism as well as the schematic energy level diagram showing the Eu3+ emission quenching mechanism using Cu2+ ions are proposed. The electron paramagnetic resonance (EPR) technique revealed the existence of at least two different coordination environments for copper(II) ion.

Fluorescent Metallosupramolecular Elastomers for Fast and Ultrasensitive Humidity Sensing.

Fluorescent supramolecular polymers that can respond to subtle external stimuli to generate luminescence signals are promising in a wide range of applications, including probes, anti-counterfeiting materials, and sensors. However, complicated preparative procedures, limited responsive speed, and relatively low sensitivity still limit their practical sensing applications. Herein, we report europium-containing metallosupramolecular (PU-Eu) elastomers for fast and ultrasensitive humidity sensing by employing hygroscopic polyurethane (PU), whose urethane groups can coordinate with europium ions (Eu3+), emitting a strong luminescent signal by ligand-to-metal energy transfer. The variant of the coordination bond strength triggered by external humidity imparts the PU-Eu elastomer with a fast (∼1.1 s) and ultrasensitive response to the humid condition, where the external humidity increases by ∼1% and the corresponding fluorescence intensity will drop by ∼421.98 a.u. By a dip-coating process, PU-Eu elastomers can be conveniently coated on a hydrophilic and porous cellulose acetate nanofiber membrane, and the resulting composite membrane can achieve real-time and reversible monitoring of environmental humidity and human respiration. Given the versatility of PU-Eu elastomers, this study provides a low-cost and facile route of obtaining fluorescent metallosupramolecular polymers for fast and ultrasensitive humidity sensing.

Ratiometric method based on silicon nanodots and Eu3+ system for highly-sensitive detection of tetracyclines.

A silicon nanodots (SiNDs)-based ratiometric fluorescent sensor was designed to establish highly sensitive and selective method for detection of tetracyclines (TCs). The sensor comprises the blue fluorescence SiNDs were prepared by hydrothermal method synthesis from (3-aminopropyl)triethoxysilane and low-cost diethylenetriaminepentaacetic acid as the precursor, which serve as co-ligands for covalently bond with europium ions (Eu3+), and also the internal reference signal. In the presence of TCs, the luminescence intensity of Eu3+ was significantly increased, while the luminescence intensity of SiNDs was reduced. The fluorescence intensity ratio of I616/I450 of the sensor exhibits a sensitive linear range from 0.2 to 20 µM with a detection limit of 3 nM for the detection of TCs. This method was successfully applied to determine the levels of TCs in nature river samples and milk samples with good recoveries ranges from 92.2% to 107.4% and relative standard deviations (RSD, n = 3) was below 5%, providing a promising application future in real samples.

Anti-fouling and thermosensitive ion-imprinted nanocomposite membranes based on grapheme oxide and silicon dioxide for selectively separating europium ions.

The increasing amount of europium in aqueous environment from rare earth industry has become a serious environmental challenge. Significant efforts have been focused on ion-imprinting membranes (IIMs) for selective separation of ions from analogues. Based on ion-imprinting technique, we have developed Eu3+-imprinted nanocomposite membranes (Eu-IIMs) for selectively separating Eu3+ from La3+, Gd3+ and Sm3+. Polydopamine (pDA) was previously synthesized on basal membranes to augment the interfacial adhesion. Grapheme oxide (GO) and modified silicon dioxide (kSiO2) were synergistically stacked on pDA-modified substrates to form hydrophilic nanocomposite membranes. Ag nanoparticles were modified on the surface to enhance anti-fouling performance. The temperature-controlled selective recognition sites were formed using N-isopropylacrylamide (NIPAm) and acrylamide (Am) as functional monomers as well as europium ions as templates by RAFT (reversible addition-fragmentation chain transfer) method. Large enhanced Eu3+-rebinding capacity (101.14 mg g-1), adsorptive selectivity (1.82, 1.57, 1.45 for Eu3+/La3+, Eu3+/Gd3+, Eu3+/Sm3+) and permselectivity (3.82, 3.47, 3.34 for La3+/Eu3+, Gd3+/Eu3+, Sm3+/Eu3+) were achieved on Eu-IIMs with superior regeneration performance. Additionally, the negligible damage of the membranes after buried for 20 d indicated the superior anti-fouling property of the Eu-IIMs. The ion-imprinted nanocomposite membranes synthesized in this work have shown great potentials for selective separation of rare earth ions.