Search Results (142)

Aloin, a kind of active phenolic component, is sourced from Aloe vera. Recently, the determination of aloin has received enormous attention, owing to its positive performance (including anti-tumor, antibacterial, detoxification, liver protection, anti-stomach damage, and skin protection activities) and painful side effects (increased carcinogenicity caused by excessive use of aloin) impacting human health. This investigation was inspired by the good fluorescence properties of carbon dots (CDs); CD-based sensors have aroused a great deal of interest due to their excellent sensitivity and selectivity. Thus, it is of great significance to develop novel CD-based sensors for aloin determination. Herein, N,F-CDs were designed and synthesized through a convenient hydrothermal strategy; the synthesized N,F-CDs possessed good fluorescence performance and a small particle size (near 4.3 nm), which demonstrated the successful preparation of N,F-CDs. The resulting N,F-CDs possessed a large Stokes shift and could emit a highly stable green fluorescence. The fluorescence of the N,F-CDs could be effectively quenched by aloin through the inner filter effect. Furthermore, the synthesis procedure was easy to operate. Finally, the N,F-CD-coated test strips were fabricated and combined with a miniaturized fluorimeter for the fluorescence detection of aloin via the inner filter effect for the first time. The N,F-CD-coated test strips were fabricated and used for the fluorescence sensing of aloin, and the results were compared with a typical ultraviolet (UV) method. The N,F-CD-coated test strips exhibited high recovery (96.9~106.1%) and sensitivity (31.8 nM, n = 3), good selectivity, low sample consumption (1 μL), high speed (5 min), good stability, and anti-interference properties. The results indicate that N,F-CD-coated test strips are applicable for the quantitative determination of aloin in bovine serum, orange juice, and urine samples. Full article

Computational limitations of computers have emerged as a critical barrier to the advancement of Computational Fluid Dynamics (CFD). Consequently, exploring novel accelerator architectures tailored for large-scale CFD applications and closely integrated with CFD algorithmic characteristics holds significant value. Through an in-depth analysis of the finite difference method (FDM) for solving Navier–Stokes (N-S) equations, we propose a specialized accelerator architecture for FDM-based CFD (FAcc). Implemented on a 28 nm process, FAcc integrates 16,384 differential computing cores (FCores). Experimental validation demonstrates FAcc’s capability to solve N-S equations of varying complexities by flexibly configuring boundary conditions. Compared to conventional approaches, FAcc achieves significant acceleration performance, with its programmability underscoring adaptability to high-precision, large-scale CFD simulations. As the first CFD-focused accelerator designed from the instruction set architecture (ISA) level, FAcc bridges a critical gap in domain-specific hardware for CFD, offering a paradigm shift in high-performance fluid dynamics computation. Full article

The increasing prevalence of microplastic (MP) pollution and the labor-intensive nature of existing identification methods necessitate improved large-scale detection approaches. Nile Red (NR) fluorescence, which varies with polarity, offers a potential classification method, but standardization of carrier solvents and fluorescence differentiation techniques remains lacking. This study evaluated eight NR-carrier solvents (n-hexane, chloroform, acetone, methanol, ethanol, acetone/hexane, acetone/ethanol, and acetone/water) across ten common MP polymers (HDPE, LDPE, PP, EPS, PS, PC, ABS, PVC, PET, and PA). Fluorescence intensity, Stokes shift, and solvent-induced polymer degradation were analyzed. The study also assessed HSV (Hue/Saturation/Value) color spaces for Stokes shift representation and MP differentiation. Fenton oxidation effectively quenched fluorescence in natural organic matter (e.g., eggshells, fingernails, wood, cotton) while preserving NR-stained MPs. Acetone/water [25% (v/v)] emerged as the optimal solvent, balancing fluorescence performance and minimal degradation. Full article

Lysosomes are important acidic subcellular organelles whose dysfunction can lead to some related diseases. The development of new lysosome-imaging-guided AIEgens for the photodynamic therapy of cancer cells is important. In this work, two novel organic compounds with AIE characteristics, namely, TPAB-CF₃ and TPAB-diCF₃, were designed and synthesized by introducing the weakly basic morpholinyl moiety with lysosome-targeting ability into a triphenylamine-based luminogen. The distorted spatial feature of TPA and the D₁-D₂-π-A structure of these AIEgens prevented the aggregation-caused quenching of traditional fluorescent molecules and efficiently promoted the separation of the HOMO and LUMO. The outcomes were AIE features and a narrow single-triplet energy gap. Furthermore, TPAB-CF₃ and TPAB-diCF₃ showed bright yellow fluorescence emission peaks at 577 and 601 nm; large Stokes shifts of 234 and 256 nm, respectively; and excellent lysosome-targeted imaging of HeLa cells (Pearson’s coefficient = 0.90). In addition to the good ¹O₂-generation ability under light irradiation, these AIEgens achieved the high-efficiency bright lysosome imaging-guided photodynamic killing of cancer cells under white-light irradiation. Full article

Fluorescent proteins (FPs) are widely used as optical probes in molecular and cell biology. tKeima is a tetrameric, large Stokes shift red fluorescent protein and the ancestral protein of mt-Keima, which is widely applied as a pH-sensitive fluorescent probe. While the pH sensitivity of mt-Keima is well characterized, the pH-dependent properties of the ancestral tKeima have not been comprehensively elucidated. To obtain a better understanding of the effects of pH on tKeima, its fluorescent emission intensity at various pH levels was measured, and its crystal structure at pH 4.0 was determined at a resolution of 2.2 Å. The fluorescence emission intensity of tKeima at pH 4.0 decreased by approximately 65% compared with its peak emission at pH 10.0. The crystal structure of tKeima at pH 4.0 revealed both cis and trans conformations of the chromophore, in contrast to previously determined structures at pH 8.0, which showed only the cis conformation. This indicates that pH induces a conformational change of the chromophore in tKeima. Both the cis and trans conformations in tKeima were stabilized by hydrogen bonds with neighboring residues. A comparison of tKeima at pH 4.0 with tKeima at basic pH, as well as with mKeima, highlights its unique structural properties. These results provide a deeper understanding of the structural basis for the pH-induced fluorescence emission changes in the Keima family. Full article

As two significant indicators in the microenvironment, hypochlorous acid and viscosity play important roles in multitudinous physiological metabolic processes. However, it is challenging to determine the dynamic levels of hypochlorous acid and viscosity in living cells and organisms because of the absence of effective molecular tools that can simultaneously detect hypochlorous acid and viscosity in organisms. Herein, a molecular design strategy was presented to fabricate a single fluorescence probe that can simultaneously detect hypochlorous acid and viscosity by using two different emission channels. In JXR, TICT-based 4-(2-(5-(dimethylamino)thiophen-2-yl)vinyl)-1-methylpyridin-1-ium-iodide chromophore serves as energy acceptor in the FRET process and sensors for hypochlorous acid and viscosity. JXR showed a large Stokes shift, wide emission peak distance, high photostability, and low toxicity. JXR could detect hypochlorous acid and viscosity rapidly, sensitively, and selectively by emitting different fluorescence signals. Importantly, JXR was successfully applied to track the intracellular hypochlorous acid and viscosity in living cells. Meanwhile, the generation of endogenous hypochlorite in living cells can be observed by using JXR. Full article

Stroke, primarily ischemic (85%), results from inadequate blood supply and is worsened by ferroptosis, characterized by free radical generation and lipid peroxidation. Monitoring ferroptosis is essential for understanding its mechanisms and developing treatments. Glutathione (GSH) is a key ferroptosis biomarker, but current probes are limited by short excitation/emission wavelengths, small Stokes shifts, and inability to monitor dynamic GSH changes at the cellular membrane, where ferroptosis plays a crucial role. To address these issues, we developed the PM-Red-GSH, a novel near-infrared (NIR) probe based on the Excited-state intramolecular proton transfer (ESIPT) mechanism. It shows strong NIR emission (715 nm), large Stokes shift (290 nm), and enhanced membrane binding (PCC = 0.95) due to its alkyl group. PM-Red-GSH enables dynamic GSH monitoring in an MCAO mouse model. These findings offer new insights into ferroptosis and stroke treatment. Full article

Developing a new type of circularly polarized luminescent active small organic molecule that combines high fluorescence quantum yield and luminescence dissymmetric factor in both solution and solid state is highly challenging but promising. In this context, we designed and synthesized a unique triarylborane-based [2.2]paracyclophane derivative, m-BPhANPh₂-Cp, in which an electron-accepting [(2-dimesitylboryl)phenyl]ethynyl group and an electron-donating N,N-diphenylamino group are introduced into two different benzene rings of [2.2]paracyclophane. Owing to the electronic effect of these two substituents, this compound can display charge-transfer emission with large Stokes shifts (∆υ = 4.23 − 8.20 × 10³ cm⁻¹) and fair quantum yields (Φ_F = 0.15 − 0.37) in solutions. In addition, this compound can emit strong blue fluorescence in the solid state with quantum yields that are even much higher than in solution (Φ_F up to 0.64 in powder and spin-coated film). Moreover, the enantiomeric forms of m-BPhANPh₂-Cp can show strong CPL signals in both dilute solution and solid state with |g_lum|s up to 9.6 × 10⁻³ and 5.4 × 10⁻³, respectively. Thus, it is possible to achieve tunable CPL from blue to yellow in solution with high B_CPLs ranging from 56.7 to 26.6 M⁻¹ cm⁻¹ and intense blue CPL combing high Φ_F and |g_lum| in the solid state. Full article

In a search for dyes photoactivatable with visible light, fluorenes with substituents at positions 2 and 7 were prepared, and their absorption and emission spectra were studied. In particular, the synthesis route to 9-diazofluorenes with 2-(N,N-dialkylamino) and N-modified 7-(4-pyridyl) substituents was established. These compounds are initially non-fluorescent, undergo photolysis with UV or blue light, and—in non-polar media—provide orange- to red-emitting products with a large separation between absorption and emission bands. Irradiation of non-fluorescent 9-diazoderivative 20 in dioxane with the light of 365 nm or 470 nm was accompanied by strong fluorescence gain (10 to 20 times), orange–red emission, and a large Stokes shift of photoproducts, which structurally relate to fluorescent betaine 13 (model compound without diazo group). Photolysis of 20 in protic solvents (ROH = MeOH, H₂O) provided clean transformation to C⁹-OR derivatives, though the emission gain in protic solvents was low. Full article

A novel fluorescent probe, Bibc-DNBS, based on the combination of the PET (photoinduced electron transfer) and ESIPT (excited-state intramolecular proton transfer) mechanisms, was designed and synthesized. Bibc-DNBS exhibited a Stokes shift of 172 nm in the fluorescence detection field. In addition, the probe exhibited good performance in key parameters in bioassays such as sensitivity, specificity, and response time. Based on these properties, Bibc-DNBS successfully monitored the biothiol levels in live cells and zebrafish models, providing an effective analytical tool for real-time monitoring of biothiols. More importantly, Bibc-DNBS could be useful for indirectly detecting β-lactamases. Bibc-DNBS(3-(1H-benzo[d]imidazol-2-yl)-4′-cyano-[1,1′-biphenyl]-4-yl2,4-dinitrobenzenesulfonate) facilitated the screening of β-lactamase inhibitors, using tazobactam and clavulanic acid as model compounds, with respective semi-inhibitory concentration values of 31.32 μM and 2.26 μM, respectively. It might also be applied to distinguish sensitive strain Staphylococcus aureus ATCC 29213 and drug-resistant strain Enterobacter cloacae ATCC 13047, which could provide strong support for the clinical application of antibiotics and the development of new drugs. Full article

The inward vortex–swirl-type motion of convective, rectilinear water flow has been studied vis-à-vis its propensity for bubble formation, with a particular focus on the microbubble region. It has been found that a large population of smaller microbubbles, around 1 μm in diameter, is created in the process of these types of motions, and the time-dependent behaviour of this “micro-bubbly” water is analysed as Stokes’ law for microbubble dissipation occurs, such as bubble population, dissolved oxygen, pH, etc. Exponential decay analysis on the DLS-measured microbubble populations gave relaxation times τ of ~2.4 h and 3.6 h in exp(−t/τ) fits for DI and filtered tap water, respectively. The downward shift in pH was about 0.08 ± 0.016 and 0.11 ± 0.018 for DI and filtered tap water, respectively. For DI water, the level of dissolved oxygen (DO) at room temperature of 19 °C was ~102% at “t = 0”, and it declined to ~87% within 3 h (with the unprocessed background sample being about 84 ± 1.1%). The respective DO decay results in the case of the filtered tap water (at 19 °C) were ~105% at “t = 0”, declining to 91% within 3 h (background = 86 ± 1.2%). This allows for the dynamic properties to be understood in the context of how microbubbles determine the observed properties of post-flow water, including rationalising the observations of its time-transient properties. Naturally, this may well be of interest in gas transfer optimisation in the growing field of “fine-bubble engineering”. Full article

A host–guest-based fluorescent composite with a large Stokes shift was synthesized by intercalating 2,2′-(thiophene-2,5-diyl)bis(benzo[d]oxazol-6-amine) (BBTA) into the nanochannels of zeolite L (ZL) and sealing the pores with (3-aminopropyl)triethoxysilane (APTES). To confirm the orientation of the amino groups in BBTA, a single crystal of 2,5-bis(6-nitrobenzo[d]oxazol-2-yl)thiophene (BBTN) was grown and examined by X-ray crystallography. The evidence of successful intercalation of BBTA into the nanochannels of ZL was provided by fluorescence spectrometry, gas sorption and fluorescence microscopy. BBTA showed a Stokes shift of 6641 cm⁻¹ (157 nm) in ethanol and 4611 cm⁻¹ (93 nm) in toluene. The BBTA-ZL composite (BBTA-ZL-s) showed a Stokes shift of 5677 cm⁻¹ (123 nm) in toluene, and 5450 cm⁻¹ (124 nm) in ethanol. In addition, the degree of loading was determined and stability against leaching was confirmed. We report the synthesis of this novel composite dye material with potential applications where free dyes are not applicable and which retains a large Stokes shift, independent of its chemical environment. Full article

A multifunctional fluorescent probe P based on a naphthalimide derivative for the detection of Ag⁺ and Hg²⁺ through a dual-signal was designed and characterized. P exhibited a large Stokes shift (107 nm), high selectivity, good sensitivity, and fast response time. By adjusting the testing medium and the order of reagent addition, multifunctional detection with P was achieved. The addition of Ag⁺ or Hg²⁺ to P solution in either ethanol or an ethanol–water mixture resulted in a significant quenching of fluorescence emission at 537 nm and caused a decrease in the absorbance at 440 nm accompanied by the appearance of a new absorption peak at around 340 nm, and there was an obvious color change from yellow to colorless. In contrast, the addition of other common metal ions and anions did not produce substantial spectral or color changes. The detection limit of probe P for Ag⁺ and Hg²⁺ was calculated to be 0.33 μM. The sensing mechanism was proposed and validated through MS and ¹H NMR spectrometry methods. Additionally, P demonstrated the capability to recognize Ag⁺ and Hg²⁺ in living cells with satisfactory results. Full article

In this paper, LD-TCF, a targeting probe for lipid droplets (LDs) with a near-infrared emission wavelength and large Stokes shift, was fabricated for polarity detection by assembling a donor–π–acceptor (D–π–A) molecule with typical twisted intramolecular charge transfer (TICT) characteristics. Surprisingly, the fluorescence emission wavelength of the newly constructed probe LD-TCF was stretched to 703 nm, and the Stokes shift was amplified to 126 nm. Furthermore, LD-TCF could specifically answer the change in polarity efficiently and did not experience interference from other biologically active materials. Importantly, LD-TCF exhibited the ability to target lipid droplets, providing valuable insights for the early diagnosis and tracking of pathophysiological processes underlying LD polarity. Full article

In recent years, significant advances in enhancing the quantum yield (QY) of trivalent lanthanide (Ln³⁺) ion-based nanoparticles have been achieved through photosensitization, using host matrices or capping organic ligands as photosensitizers to absorb incoming photons and transfer energy to the Ln³⁺ ions. The Ln³⁺ ion-based nanoparticles possess several excellent fluorescent properties, such as nearly constant transition energies, atomic-like sharp transitions, long emission lifetimes, large Stokes shifts, high photostability, and resistance to photobleaching; these properties make them more promising candidates as next-generation fluorescence probes in the visible region, compared with other traditional materials such as organic dyes and quantum dots. However, their QYs are generally low and thus need to be improved to facilitate and extend their applications. Considerable efforts have been made to improve the QYs of Ln³⁺ ion-based nanoparticles through photosensitization. These efforts include the doping of Ln³⁺ ions into host matrices or capping the nanoparticles with organic ligands. Among the Ln³⁺ ion-based nanoparticles investigated in previous studies, this review focuses on those containing Eu³⁺, Tb³⁺, and Dy³⁺ ions with red, green, and yellow emission colors, respectively. The emission intensities of Eu³⁺ and Tb³⁺ ions are stronger than those of other Ln³⁺ ions; therefore, the majority of the reported studies focused on Eu³⁺ and Tb³⁺ ion-based nanoparticles. This review discusses the principles of photosensitization, several examples of photosensitized Ln³⁺ ion-based nanoparticles, and in vitro and in vivo biomedical fluorescent imaging (FI) applications. This information provides valuable insight into the development of Ln³⁺ ion-based nanoparticles with high QYs through photosensitization, with future potential applications in biomedical FI. Full article