Higher Fluorescence Intensity Research Articles

Copper-Based Electrochemical Sensor Derived from Thiosemicarbazide for Selective Detection of Neurotransmitter Dopamine.

This paper presents the synthesis of the ligand 1-picolinoyl-4-cyclohexyl-3-thiosemicarbazide (H2pctc) and new metal complexes [Ni(Hpctc)2] (1), [Cu(Hpctc)Cl] (2), and [Cd(Hpctc)2] (3). The synthesized metal complexes were precisely characterized using single crystal X-ray diffraction (SC-XRD). In addition, complexes 1-3 were also characterized by UV-vis, fluorescence, and infrared spectroscopy. SC-XRD data confirmed the distorted octahedral geometry around the Ni(II) and Cd(II) centers and the distorted square planar geometry around the Cu(II) center. Data derived from the emission spectra depict that higher fluorescence intensity was exhibited by complexes 1, 2, and 3 in comparison to that of the free ligand H2pctc, and complex 3 showed the maximum intensity. Further, these metal complex-modified GCEs (glassy carbon electrodes) were utilized for electrochemical sensing of dopamine (DPM). The electrochemical studies of these complexes were performed using modified glassy carbon electrodes supported by electrical impedance spectroscopy (EIS) and cyclic voltammetry (CV) methods. In contrast to complexes 1 and 3, complex 2 is a superior electrode material with a high effective surface area for the electrochemical oxidation of DPM, according to the electrochemical response results. The derived sensor had a wide linear detection range of 1 to 1400 μM, an acceptable sensitivity of 0.01531 μA cm-2 μM-1, and a low LOD of 0.38 μM. The proposed approach was free of the interfering effects of ascorbic acid, uric acid, aminophenol, and other substances. During the successive scans, no fouling of the electrode surface was observed. The proposed electrochemical sensor had excellent stability, sensitivity, and a low detection limit making it suitable for the analysis of a variety of real samples. Additionally, it was proven to be useful for analyzing biological fluids.

Characterization of Low-Temperature Sensitivity and Chlorophyll Fluorescence in Yellow Leaf Mutants of Tomato

Leaf color mutants serve as valuable models for studying the regulation of plant photosynthesis, alternations in chloroplast structure and function, and the analysis of associated gene functions. A yellow leaf mutant, ylm, was separated from the wild tomato M82, with its yellowing intensity influenced by low temperature. To assess the low-temperature sensitivity of this mutant, the photosynthetic and chlorophyll fluorescence responses of ylm and M82 were examined under different temperature conditions. In this study, the ylm mutant and its wild type, M82, were exposed to three temperature levels, 16, 25, and 30 °C, for 48 h. The impact of these temperature treatments on leaf color change, chlorophyll content, photosynthetic performance, and chlorophyll fluorescence characteristics of mutant ylm was investigated. The results revealed the following: (1) After exposure to 16 °C, the ylm mutant exhibited significant yellowing, a marked reduction in chlorophyll content, and a notable increase in carotenoid content. At 25 °C, the differences were less pronounced, and at 30 °C, the differences between ylm and M82 were minimal. (2) The photosynthetic rate of the ylm mutant was lower than that of M82 at 16 °C, with the gap narrowing as temperature increased, eventually converging at higher temperatures. (3) The fluorescence transient curve (OJIP) of the ylm mutant differed significantly from that of M82 at 16 °C, with higher fluorescence intensity at the O point and lower intensity at the J, I, and P points. This difference was decreased at 25 °C and nearly disappeared at 30 °C. Additionally, the Fv/Fm, Fv/Fo, PIabs, PItotal, ABS/CSm, TRo/CSm, and ETo/CSm values of ylm were lower than those of M82 at 16 °C, while the ABS/RC and DIo/RC values were higher, with no significant differences observed at 30 °C. These findings suggest that the ylm mutant is highly sensitive to low temperature, with pronounced yellowing, reduced light energy absorption and capture efficiency, and impaired electron transport at lower temperature.

Pressure-Induced Structural Phase Transitions and Photoluminescence Properties of Micro/Nanocrystals HoF3.

HoF3 crystals of varying sizes and morphologies were synthesized by controlling the amount of water. As the water content gradually decreased, the size of the crystals reduced, transforming from microcrystals to approximately 100 nm nanocrystals with unique morphologies. At room temperature, the pressure-induced phase transitions, and photoluminescence (PL) properties of HoF3 micro/nanocrystals are studied using in situ high-pressure PL technique. The PL spectra show that the HoF3 micro/nanocrystals exhibit two structural phase transformations at 5 (6 GPa for NCs) and 12 GPa. Nanoparticles have higher fluorescence intensity, which initially increases and then decreases with changes in pressure. Based on first-principles calculations, HoF3 transforms from an orthorhombic structure to a hexagonal structure during the phase transition, with the coordination number of holmium atoms increasing from 9 to 11. The high-pressure Raman spectra on lattice modes also confirmed the existence of the two phase transitions. This work not only provides precise structural changes but also facilitates the understanding of two typical structures of rare-earth trifluoride (REF3), which may play an important role in the application of the RE family.

Broad-spectrum detection of benzimidazoles with lateral flow immunoassay: A computational chemistry-assisted hapten design strategy and explore of molecular recognition mechanism

Benzimidazoles (BMZs) are a class of veterinary drugs with a benzimidazole ring, the abuse of which poses a serious threat to ecological balance and human health. Consequently, the development of broad-spectrum antibodies and rapid assays are crucial for detecting BMZs in food samples. Herein, we scientifically designed three hapten structures, predicted the availability of the hapten with computational chemistry, and subsequently verified the broad-spectrum with immunological experiments. A broad-spectrum monoclonal antibody (6F10) was prepared based on the predicted hapten-2. Molecular recognition studies illustrated intricate interactions between mAb 6F10 binding to BMZs attributed to halogen bonds and π-π/π-alkyl interactions, revealing key amino acid sites and demonstrating the reliability of the hapten prediction strategies. Finally, a broad-spectrum, rapid, and sensitive lateral flow immunoassay based on aggregation-induced emission microspheres with high fluorescence intensity was established. The LOD values of the proposed method for eight kinds of BMZs were 0.027, 0.032, 0.058, 0.091, 0.087, 0.246, 0.369, and 0.311 ng mL−1, respectively. In this work, a hapten prediction strategy based on a computational chemistry method effectively guided the preparation of antibodies for broad-spectrum recognition of BMZs, and the molecular recognition studies verified the interaction of mAb 6F10 with BMZs, enabling broad-spectrum and sensitive detection of BMZs in milk.

A Comparative Study of the Linear/Nonlinear Optical, and Dielectric Properties of PVA/CMC/(1−x)ZnWO4−xPbS Blended Polymers for Optoelectronic Applications

An analysis was conducted on the optical, structural, and dielectric characteristics of PVA/CMC/(1−x)ZnWO4/xPbS blends. The structures of the filler samples, undoped, and doped blends were examined using X-ray diffraction. The crystallite sizes of the various phases in the filler samples are affected by the amount of PbS in the nanocomposite. The morphologies of different blends were explored using scanning electron microscopy. The doped blend exhibited superior absorption of Ultraviolet A (UVA) and Ultraviolet B (UVB) types in addition to the visible spectrum. The optical band gaps were minimized to (5.37, 5.56, 4.11) and (4.76, 3.14, 2.92) eV for direct and indirect optical transitions, respectively, when the PVP/CMC doped with nanocomposite had 10% PbS. The highest refractive index, optical dielectric constant,and nonlinear optical parameter values were achieved when the blend was loaded with ZnWO4 only while the highest optical conductivity was obtained as the blend contained 15% PbS. The highest fluorescence intensity was observed when the fillers did not contain PbS, and it decreased as the concentration of PbS in the filler increased.

“Green mathematical approaches in fluorescence spectroscopy for quality control and clinical studies”

In the past decade, significant advancements have been made in mathematical spectral approaches for estimating binary and ternary drug combinations in raw materials and dosage forms. These approaches established on mathematical spectral manipulations of mixture analytes, without the need for separation techniques.The idea of using mathematical spectral approaches in fluorescence spectroscopy was resolving analytical issues and reach to biological concentrations thus, Ratio subtraction (RD) and ratio subtraction coupled with constant multiplication (RS-CM) have been proposed in fluorescence spectroscopy to evaluate the content uniformity of Flunarizine dihydrochloride (FLZ) and Propranolol hydrochloride (PRO) combination in raw materials, tablets, and spiked biological fluids (blood-urine). These approaches have demonstrated the ability to overcome the quantitative analytical challenges posed by the high native fluorescence intensity of the major component (PRO) at λex = 286/λem = 341 nm and the low native fluorescence intensity of the minor component (FLZ) at λex = 254/λem = 311 nm. The linearity range for (PRO) was found to be 25–500 ng/mL, and for (FLZ), it was 50–500 ng/mL. However, the spectrum addition technique was required to estimate (FLZ) in mixtures with concentrations less than 300 ng/mL.The overall validity of the proposed approaches was confirmed through adherence to ICH guidelines, and no statistical variation was observed in comparison to official studies. Additionally, the greenness and whiteness of the proposed approaches were evaluated using the Analytical greenness metric (AGREE), Green Solvents Selecting Tool (GSST), and Red-Green-Blue (RGB) algorithm.

Enhanced mitochondrial fluorescence imaging through confinement fluorescence effect within a rigid silicon suboxide network

Fluorescence imaging technology has emerged as a powerful tool for studying intricate mitochondrial morphology within living cells. However, the need for fluorophores with stable fluorescence intensity and low phototoxicity poses significant challenges, particularly for long-term live-cell mitochondrial monitoring. To address this, we introduce the confinement fluorescence effect (CFE) into the design of fluorophores. This strategy involves confining small-molecule fluorophores within a silicon suboxide network structure of nanoparticles (CEF-NPs), which restricts molecular rotation, resulting in the suppression of non-radiative transition and the isolation of encapsulated fluorophores from surrounding quenching factors. CFE-NPs (SY2@SiOx) exhibit exceptional properties, such as high fluorescence intensity (80-fold) and reduced phototoxicity (0.15-fold). Furthermore, the TPP + -functionalized CFE-NPs (SY2@SiOxTPP) demonstrated efficacy in mitochondrial imaging and mitochondrial dynamics monitoring. Biochemistry assays indicated that SY2@SiOxTPP exhibits significantly lower phototoxicity to mitochondrial functions compared to both small-molecule fluorophore and commercial Mito Tracker. This approach allows for the long-term dynamic monitoring of mitochondrial morphological changes through fluorescence imaging, without impairing mitochondrial functionality.

Lactic acid bacteria fermentation-induced egg white protein structure deformation influencing gelling properties, with membrane concentration as a strategy to improve texture.

Egg white (EW), a rich protein source, holds promise for creating a high-protein, low-fat gel product. However, browning issues during heating and sterilization have hindered its wider application. In this study, lactic acid bacteria fermentation was employed to eliminate reducing sugar in EW, and its impact on the molecular structure and gelling properties was explored. The results revealed that fermentation would trigger protein structural unfolding and aggregation, evident from higher fluorescence intensity and enlarged protein particle diameters, resulting in the decrease in gelling hardness. In comparison, Streptococcus thermophilus-fermented EW (under 6×108CFU/mL incubation rate, fermented for 6h) exhibited the highest gel hardness, ascribed to the relatively weaker structure transformation, with high water holding capacity and stronger intermolecular hydrophobic interaction. To further enhance the gelling properties of fermented EW, membrane concentration treatment was applied, exhibiting superior characteristics in appearance, aroma, and taste. In summary, lactic acid bacteria fermentation and concentration are feasible solutions to improve appearance and texture of EW gels simultaneously. The research findings offer eco-friendly and practical strategies for enhancing the quality of EW gels, providing valuable theoretical insights for the development of innovative, texture-rich, and healthy nutritional foods.

Wafer-level flexible carbon-based film for fluorescent display and optical information storage

Fluorescent materials have garnered significant interest in optical display and information storage fields for their vibrant and distinct color presentation. Extensive research has been conducted on carbon-based fluorescent materials owing to their environmental sustainability, versatility, and adjustable optical properties. However, it is difficult to integrate high-resolution fluorescent structure on various wafer-level substrate for abundant optical display and information storage. This study successfully fabricated wafer-level carbon-based fluorescent flexible film with ∼100 μm thick using a standardized “lithography + annealing” process. The sample demonstrates high fluorescence intensity with a peak at 603 nm and fluorescence lifetime of 0.3517 ns. When excited by light of 365 nm, 485 nm, and 525 nm wavelengths, the film displays yellow, green, and red, showcasing exceptional color tuning capability. This flexible film is portable and can be readily integrated with various substrates, offering significant technical and theoretical support for advancing carbon-based optical display and information storage technologies.

Adapalene as a chemical sensor for sensitive determination of manganese

ABSTRACT The work describes the use of 6-[3-(1-adamantyl)-4-methoxyphenyl]-2- naphthoic acid, or Adapalene (ADP) as a fluorescence tagging reagent, in a straightforward and very specific spectrofluorometric approach for the trace measurement of manganese (VII) in water. The process is based on the redox interaction of ADP with manganese (VII) in an acidic solution, which forms the complex [Mn (II)-ADP] and causes fluorescence at λex max/λem max = 323/400 nm. High-intensity fluorescence at 400 nm was seen in the fluorescence spectra of the formed complex ion association, Mn (II)-ADP, at pH 4. 1.55 µg mL−1 was the quantification limit, and 0.51 µg mL−1 was the detection limit and the correlation coefficient (R2) was 0.9863. 1.2173 L mol−1 was determined to be the Stern-Volmer. Spectrofluorometric technique is used to validate the approach in environmental water samples, yielding reasonable recovery percentages (89–93%). The current approach is advised to be used for reliable and accurate assessment of manganese (VII) in all wastewater and seawater samples, without the need for complex instrumentation and lengthy procedures.

Post-synthetic modification fluorescence UiO-66-Eu immunochromatography for high-performance detection of sodium pentachlorophenoate

Sodium pentachlorophenate (PCP) is widely used as a herbicide, fungicide, or molluscicide. It is highly toxic, easily soluble in water, making it highly prone to diffusion and causing water and soil pollution. Through the food chain, it enters animal bodies and remains in food, causing toxicity to humans and animals. Therefore, establishing a rapid and simple detection method for PCP is crucial for human health and environmental protection. Herein, lanthanide metal Eu3+ was introduced into UiO-66-(COOH)2 by post-synthesis modification, and the nanomaterials prepared based on this method have the advantages of both UiO-66-(COOH)2 and Eu3+. The rigid skeleton structure of UiO-66-(COOH)2 can protect the activity of antibody, the detection environment pH tolerance range of UiO-66-Eu is 3–11. While Eu3+ has long fluorescence lifetime, high fluorescence intensity, high signal-to-noise ratio, and low photobleaching rate. UiO-66-Eu-based immunochromatography assay was successfully applied in PCP detection with the detection limits of 0.84, 0.98, and 0.37 μg/kg for pork, chicken, and shrimp, respectively, which was up to 10-fold more sensitive than the reported ICAs. The recoveries ranged from 79.7 %−113.1 %, with the coefficient of variation from 6.6 %−17.1 %. Parallel detection of 30 samples by LC-MS/MS showed a good correlation with that of our proposed method (R2 >0.98). This work not only provides a creative attempt for UiO-66-Eu based highly sensitive and strongly tolerant ICAs, but also guarantees human health and environmental protection.

Preparation of glutathione-Cu/Ag bimetallic nanoparticles for temperature and metal ion Co2+ sensing

In this work, copper silver bimetallic nanoparticles (Cu/Ag BNPs) with strong fluorescence were prepared using glutathione (GSH) as a reductant and protectant. The range of fluorescence signal of GSH-Cu/Ag BNPs to ambient temperature is 30∼90 °C has a sensitive response and can be used as a temperature sensor. The high fluorescence intensity of GSH-Cu/Ag BNPs at around 30 °C indicates that the detection of Co2+ does not require harsh temperature conditions, which could be very convenient for future practical detection work. In addition, glutathione in Cu/Ag BNPs and the synergistic effect of Cu and Ag nanoparticles in Cu/Ag BNPs can be used as a metal ion sensor for Co2+ fluorescence detection.

Lignocellulose hydrothermal artificial humic acid production: Reaction parameters screening and investigation of model/real feedstock

Utilizing relatively mild hydrothermal conversion technique (under optimized conditions, 200 °C, 4 h, 1:10 solid-liquid ratio, 0.5 M NaOH), lignocellulosic biomass can be efficiently transformed into humic acids, thereby significantly enhancing its utilization. Additionally, this approach provides a means for precise manipulation of the composition and properties of the resulting humic acids. In this comprehensive study, lignocellulosic biomass, comprising various attributes like coniferous, broadleaf, and grassy species, as well as model components like cellulose, hemicellulose, and lignin, underwent hydrothermal reactions to produce humic acids. Firstly, a systematic evaluation was conducted to determine the influence of operational parameters on the formation of humic acids. Subsequently, the characteristics of humic acids derived from diverse lignocellulosic biomass sources were analyzed and benchmarked against commercial humic acids. Based on the empirical findings, a mechanistic pathway for the generation of humic acids was figured out. The results indicate that the primary stages in the hydrothermal conversion of lignocellulosic biomass to humic acids involve initial hydrolysis into smaller molecular components, followed by further reactions leading to the formation of humic acids. Notably, the interplay between cellulose, hemicellulose, lignin, and other minor components, such as tannins and pectins, plays a pivotal role in the synthesis of humic acids. The characterization of the derived humic acids revealed several noteworthy distinctions from commercial products. In the infrared spectroscopy (FTIR) and elemental analysis (EA) characterization, the synthetic humic acid has more oxygen functional groups, alkane groups and aromatic structures. In the X-ray photoelectron spectroscopy (XPS), the synthetic humic acid has more diverse forms and proportions of elements. In thermogravimetric analysis (TGA), the synthesized humic acid has higher thermal stability. The synthetic humic acid has a rougher surface microstructure. The synthetic humic acid has higher fluorescence intensity in three-dimensional fluorescence spectrum (3D EEM). Lignocellulose biomass raw materials with high wood quality content can obtain higher humic acid yield, but the interaction of cellulose, hemicellulose, lignin and other group components (such as tannins, pectin, etc.) in the hydrothermal process plays an important role in the generation of humic acid. This research offers valuable insights into the chemically driven production of humic acids and the strategic control of their properties, based on the structural and compositional nuances of the raw materials.

Simple and eco-friendly fabrication of hempseed protein by one-step low-temperature-induced phase separation and centrifugal removal of oil

Hempseed protein is an emerging plant-derived alternative protein with unmatched nutritional and health benefits. However, the currently available industrial hempseed protein production relies on a defatting step using an organic solvent, hexane with health and environmental risks, which also damages the proteins’ structural and functional properties. In this study, we describe a successful method for the simple and eco-friendly simultaneous extraction of proteins and removal of oil based on the “hydrophilic” properties of hempseed oil. Both hempseed protein isolates (HPIs) extracted from hexane-defatted hempseed flour (HHPI) and non-defatted hempseed flour (NHHPI) exhibited great similarities in protein contents (both >90%), amino acid composition, protein subunits and functional properties (solubility, water retention and foaming). However, NHHPI significantly outperformed HHPI in keeping native structural and some processing properties. NHHPI exhibited a higher percentage of α-helix (44.29%) with lower amount of random coil (15.33%) than HHPI (α-helix 41.71%, random coil 19.07%), higher fluorescence intensity with lower incident wavelength (λmax = 326) than HHPI (incident wavelength λmax = 329). Meanwhile, NHHPI displayed higher surface hydrophobicity (807.01), fat absorption (1.35 g/g) and emulsion activity (2.36 m2/g) as compared to HHPI (743.48, 1.14 g/g, 1.78 m2/g, respectively). These findings highlight the importance of a new defatting method for HPI extraction, which may also be applicable to other oilseed proteins.

Fluorescence and Photophysical Properties of Anthracene and Phenanthrene in Water.

Polyaromatic hydrocarbons (PAHs) are widely spread pollutants in the environment, including soil and water. Anthracene (anth) and phenanthrene (phen) pose severe health impacts on human lives due to their carcinogenic nature by increasing cancer risk to the skin, lungs, and bladder. Fluorescence spectroscopy is a promising , efficient and straightforward tool for characterizing these trace PAHs in water. Therefore, the current work provides a detailed insight into the fluorescence properties of anth and phen in water. The fluorescence EEMs (excitation-emission matrices) of anth showed emissions at 380nm, 400nm, and 425nm with single excitation at 250nm, whereas phen showed two emissions < 380nm, at 350nm and 365 with single excitation at 250nm. Then the theoretical EX/EM wavelengths were calculated by DFT and CIS-B3LYP for these compounds in water. The environmental effect of pH variation on fluorescence EEM shows a significant difference in fluorescence intensity without changing in peak locations, with highest fluorescence intensity at neutral pH than acidic and alkaline. Furthermore, the theoretical pH effect was described for the first time by simulating the protonated (+ 1), deprotonated (-1) and neutral molecules in water at the DFT level of theory. The variation in simulated oscillator strengths was similar in trend with the experimental fluorescence intensity of these compounds. The HOMO-LUMO were calculated to obtain the energy gap, molecular softness, molecular hardness, electronic potential and electrophilicity of anth and phen. To find the fluorophore contribution, the fluorescence of homogeneous mixture of both isomers was analyzed, which showed an enhanced fluorescence intensity of anth by 12-20%, whereas a decrease of 9-14% was observed in phen. This study describes that the fluorescence technique could be a fast and easy method to distinguish and identify PAHs isomers (anth and phen) in water.

Effect of silver nanochitosan on control of seed-borne pathogens and maintaining seed quality of wheat

Seeds, considered as the foundation of agriculture, are invaded by a broad spectrum of seed-borne pathogens. The current study aimed to control seed-borne fungal pathogens of wheat, Aspergillus flavus and A. niger, by using Ag+ nanochitosan (Ag-NC) for nano-priming of seeds and enhancing seed quality. Nanochitosan (NC) and Ag-NC were synthesized using the gelation method and characterized by UV–vis spectrophotometry, FESEM, EDXS, and HRTEM. NC and Ag-NC showed irregular surface topography with an average particle size of 275 and 325 nm, respectively. Antifungal activity of both the nanoparticles at 0.1, 0.2, 0.3, 0.4, and 0.5 mg/mL revealed that Ag-NC at 0.5 mg/mL has completely terminated the mycelial growth of both pathogens. Malonaldehyde content increased to 77.77% in A. flavus and 82.66% in A. niger when exposed to 0.5 mg/mL Ag-NC. High-intensity fluorescence due to oxidative stress was observed in Ag-NC-treated pathogens. Ultra-structural changes in Ag-NC treated pathogenic spores under SEM displayed pronounced membrane damages. Wheat seeds were nano-primed with NC and Ag-NC at 0.5 mg/mL, and fungal load was examined to evaluate the mitigation of pathogenic stress and its effect on seedling growth promotion activity. Ag-NC priming reduced the fungal load and allowed successful seed germination. Ag-NC priming increased the albumin, gliadin, gluten, and glutenin content along with total phenol, reducing sugar and starch levels. Ag-NC priming increased the overall protein levels traced through SDS-PAGE. Seed priming with Ag-NC promotes seed germination, mean germination time, stress tolerance index, vigour, etc. NC and Ag-NC at 0.5 mg/mL showed no cytotoxic effect on the Human Embryonic Kidney (HEK293) cell line that ensures the nanoparticles are non-toxic. Thus, the synthesized nanoparticles exhibit a dual role in antifungal activity and plant growth promotion.

Enhanced fluorescence properties of polyfluorene–based polymer dots through an ascorbic acid-photoaging treatment for living cell imaging

The polymer dots (Pdots) prepared by the conjugated polymer (PFO, poly (9,9-dihexylfluorene-2,7-diyl)) have high fluorescence intensity and are often used in biological fluorescence imaging. However, due to the chain defects, the PFO Pdots suffer from stability issues such as photoinactivation and photobleaching. To solve this problem, we drew inspiration from the preparation process of organic planar light-emitting devices and added an optimization processing after Pdots was prepared. We used illumination as the driving force to activate defects on its chain, and ascorbic acid as a reducing substance to restore the chain defects of the polymer to a more stable state. Through this method, we increased the fluorescence intensity by nearly 1.9 times, and significantly improving their long and short-term stability. In addition, it ensures other properties remain unchanged. This optimization scheme is also fully compatible with the entire biological imaging process, ensuring that other important properties such as cytotoxicity do not undergo unnecessary changes. Furthermore, we conducted material characterization and theoretical simulation, revealing that the optimization scheme mainly serves to repair C-9 alkyl defects on the polyfluorene unit. This study has improved and enhanced the fluorescence performance of PFO Pdots, and also provides a way to optimize the treatment of other similar conjugated polymer material systems.

Fast-Responsive HClO-Activated Near-Infrared Fluorescent Probe for In Vivo Diagnosis of Inflammatory Bowel Disease and Ex Vivo Optical Fecal Analysis.

Inflammatory bowel disease (IBD) is an idiopathic intestinal inflammatory disease, whose etiology is intimately related to the overproduction of hypochlorous acid (HClO). Optical monitoring of HClO in the living body favors real-time diagnosis of inflammatory diseases. However, HClO-activated near-infrared (NIR) fluorescent probes with rapid response and high inflammatory cell uptake are still lacking. Herein, we report an activatable acceptor-π-acceptor (A-π-A)-type NIR fluorescent probe (Cy-DM) bearing two d-mannosamine groups for the sensitive detection of HClO in early IBD and stool testing. Once reacted with HClO, nonfluorescent Cy-DM could be turned on within 2 s by generating a donor-π-acceptor (D-π-A) structure due to the enhanced intramolecular charge transfer mechanism, showing intense NIR fluorescence emission at 700 nm and a large Stokes shift of 115 nm. Moreover, it was able to sensitively and selectively image exogenous and endogenous HClO in the lysosomes of living cells with a detection limit of 0.84 μM. More importantly, because of the d-mannosamine modification, Cy-DM was efficiently taken up by inflammatory cells in the intestine after intravenous administration, allowing noninvasive visualization of endogenous HClO in a lipopolysaccharide-induced IBD mouse model with a high fluorescence contrast of 6.8/1. In addition, water-soluble Cy-DM has also been successfully applied in ex vivo optical fecal analysis, exhibiting a 3.4-fold higher fluorescence intensity in the feces excreted by IBD mice. We believe that Cy-DM is promising as an invaluable tool for rapid diagnosis of HClO-related diseases as well as stool testing.

Synthesis and Characterizations of MoS2 Nanoflowers and Spectroscopic Study of their Interaction with Bovine Serum Albumin.

Molybdenum disulfide nanoflowers (MoS2 NFs) were prepared by hydrothermal method. The prepared MoS2 NFs was characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), specific surface areas, Raman and X-ray photoelectron spectroscopy (XPS). The characterization results show that the flower-like spherical MoS2 is composed of many ultra-thin nanosheets with an average diameter of about 300-400 nm. MoS2 NFs also exhibits excellent UV-vis absorption and high fluorescence intensity. In order to explore the biological behavior of MoS2 NFs, the interaction between MoS2 NFs and bovine serum albumin (BSA) was studied by UV-Vis absorption, fluorescence, synchronous fluorescence spectra, and cyclic voltammetry. The results of absorption and fluorescence show that MoS2 NFs and BSA interact strongly through the formation of complexes in the ground state, and the static quenching is the main mechanism. The Stern-Volmer constant and the quenching constant was calculated about 3.79×107 L mol-1 and 3.79×1015 L mol-1 s-1, respectively. The synchronous fluorescence implied that MoS2 in the complex may mainly bind to tryptophan residues of BSA. The cyclic voltammograms indicated that the addition of BSA makes electron reduction of MoS2 NFs more difficult than the corresponding free state. The results show that hydrophobic forces play a major role in the binding interaction between BSA and MoS2 NFs.

Skin Care Function of Lactoferrin Was Characterized Using Recombinant Human Epidermal Model

The effect of lactoferrin on skin was simulated using a recombinant human epidermal model. The anti-inflammatory and soothing effect of lactoferrin was verified using IL-1α and TSLP Elisa assay. The effects of lactoferrin on the expression of related genes and proteins were detected using qPCR and immunofluorescence staining. The results showed that lactoferrin can effectively enhance the Transepidermal Electrical Resistance (TEER) and inhibit the secretion of inflammatory cytokine IL-1α and TSLP. In addition, it was confirmed using qPCR that lactoferrin had high expression levels on AQP3, FLG, IVL, CLDN1 and HAS1 genes. Immunofluorescence staining confirmed that lactoferrin had high fluorescence intensity and expression in AQP3, Filaggrin and Involucrin. The results showed that lactoferrin improved the skin barrier at higher than 1.5 mg/mL. At the same time, it can have anti-inflammatory and moisturizing effects. This study provides a strong basis for the application of lactoferrin in cosmetics and daily chemical products.