Fast Green Research Articles

Organic Solvent Nanofiltration Membrane with In Situ Constructed Covalent Organic Frameworks as Separation Layer

Organic solvent nanofiltration (OSN) technology is advantageous for separating mixtures of organic solutions owing to its low energy consumption and environmental friendliness. Covalent organic frameworks (COFs) are good candidates for enhancing the efficiency of solvent transport and ensuring precise molecular sieving of OSN membranes. In this study, p-phenylenediamine (Pa) and 1,3,5-trimethoxybenzene (Tp) are used to construct, in situ, a TpPa COF skin layer via interfacial polymerization (IP) on a polyimide substrate surface. After subsequent crosslinking and activation steps, a kind of TpPa/polyimide (PI) OSN membrane is obtained. Under optimized fabrications, this OSN membrane exhibits an ethanol permeance of 58.0 LMH/MPa, a fast green FCF (FGF) rejection of 96.2%, as well as a pure n-hexane permeance of 102.0 LMH/MPa. Furthermore, the TpPa/PI OSN membrane exhibits good solvent resistance, which makes it suitable for the separation, purification, and concentration of organic solvents.

Linking antibody against apolipoprotein A-1 to metabolic dysfunction-associated steatohepatitis in mice

Abstract Background Metabolic dysfunction-associated fatty liver disease (MASLD) is a common liver condition associated with increased cardiovascular disease (CVD) risk. Cytokeratin 18 (CK-18) is indicative of liver injury and used as a surrogate biomarker covering MASLD to cirrhosis phenotypes. Autoantibodies against apolipoprotein A-1 (AAA-1) are known CVD risk factors inducing MASLD in vitro, but their role in modulating steatohepatitis and fibrosis in vivo is still elusive. We investigated AAA-1's contribution to systemic low-grade inflammation, liver steatosis, and fibrosis using a MASLD mouse model and a validated passive immunization protocol (PIP). Methods 10 weeks-old male C57BL/6J mice were fed a choline-deficient, L-amino acid-defined, high-fat diet (CDAHFD) and immunized with AAA-1 (200ug) or control antibodies for ten days. At sacrifice, plasma samples were collected, and CK-18 levels, and proinflammatory cytokines were measured using the Mesoscale Discovery platform. Hematoxylin and Eosin and Sirius Red Fast Green staining were used to reveal liver steatosis and fibrosis, respectively. RNA were extracted from mouse liver samples and mRNA were then analyzed using a commercial fibrosis-specific genes panel (nCounter Human Fibrosis V2 Panel) and the nCounter Analysis System. Results Compared to control IgG recipients, CDAHFD mice injected with AAA-1 exhibited significantly elevated plasma levels of CK-18 (5.3 vs 2.1, p=0.031), IL-6 (13 vs 6.9, p=0.035), IL-10 (27.3 vs 9.8, p=0.007) and TNF-α (32.1 vs 24.2, p=0.032), and liver steatosis (93.4% vs 73.8%, p=0.007). Nanostring technology experiments revealed upregulation of several pro-fibrotic m-RNAs in liver tissue from AAA-1 immunized mice compared to the IgG immunized control group. These included Serum Amyloid A (Fold Change (FC) AAA-1 vs IgG : 2.5, p=0.02) , G-protein coupled receptors 65 (FC: 2.7, p=0.01), Periostin (FC: 2.6, p=0.001), Phospholipid transfer protein (FC: 2.2, p=0.0004), Vascular Cell Adhesion Molecule 1 (FC: 2.5, p=0.02) and Angiopoietin-like 4 (FC: 2.8, p=0.01). Histologically, the amount of liver fibrosis remained unaffected, probably due to the short time of the study. Conclusions Short AAA-1 PIP induced enhanced liver steatosis and inflammation accompanied by an elevation of the expression of several pro-fibrotic genes in CDAHFD mice, suggesting that AAA-1 may contribute to the transition from MASLD to MASH. Knowing whether increased exposure time to AAA-1 could lead to end stage disease (including cirrhosis and HCC), and if this could apply to humans as well warrant further investigations.

Fast Green FCF Improves Depiction of Extracellular Matrix in Ex Vivo Fluorescence Confocal Microscopy.

Rapid microscopic analysis of tissue is an essential diagnostic tool in oncological surgery. The gold standard for intraoperative histological tissue evaluation is frozen sections. However, frozen sections are prone to a variety of artefacts and require skilled staff and specialized lab equipment. A potential method for rapid intraoperative tissue evaluation that does not require fixation, freezing, or sectioning of the tissue is ex vivo fluorescence confocal microscopy (FCM). The visualization of the structurally important extracellular matrix (ECM) in conventional ex vivo FCM lags behind the standards of conventional histology. The objective of this study was to find a stain that would improve the depiction of the ECM to resemble FFPE H&E sections as closely as possible. Eleven different tissue stains were tested on 122 tissue samples submitted to the Department of Pathology at the Medical University of Vienna. This study was conducted on the RS-G4 Upright (Caliber I.D. Rochester, NY, USA, distributed in Europe by MAVIG GmbH, Munich, Germany). Fast Green FCF (FGFCF) in combination with acridine orange as a nuclear stain improved the visibility of the structural details of the ECM. Morphological details in FCM were equivalent or even superior to frozen sections in most analyzed categories. The addition of FGFCF to the conventional staining protocol improves the assessment of the ECM and analysis of fibrosis. The rapid staining protocol is compatible with an application in intraoperative microscopy.

Rapid ion pair-based surfactant-assisted liquid-liquid microextraction with solidification of floating organic drop for simultaneous spectrophotometric determination of selected anionic dyes in food samples

Ion pair-based surfactant-assisted liquid-liquid microextraction with solidification of floating organic drops has been developed to extract Allura red (AR), tartrazine (TAR), and fast green (FG) prior to spectrophotometric determination. Cetyltrimethylammonium bromide (CTAB) was employed as ion-pairing agent to enhance the hydrophobic behavior of anionic dyes. 1-undecanol and ethanol were used as the extraction and dispersion solvents, respectively. The dyes were quantitatively extracted in the presence of KCl (0.15 mol L−1) at pH 4.0. The method exhibits wide linearity (15.0–1500.0 μg L−1 for AR, 35.0–2000.0 μg L−1 for TAR, and 3.0–1200.0 μg L−1 for FG) with preconcentration factors of 19.6, 20.1, and 19.9, respectively. The detection limit was 3.7. 9.5, and 0.83 μg L−1 for AR, TAR, and FG, respectively. The relative standard deviation did not exceed 2.1 %. The procedure was applied for the determination of these dyes in food samples.

Rational design of amine-terminated terephthalate in bismuth metal-organic framework for boosting sunlight-catalytic removal of organic pollutants

BackgroundBismuth-based metal-organic frameworks (Bi-MOFs) have garnered significant interest in energy and environment-related applications. Here, we report a Bi-MOFs synthesized by amino terephthalic acid (Bi-MOF (ATP)) and Bi-MOF (CAU-17), the developed Bi-MOF (ATP) shows exceptional photocatalytic efficiency in degrading both cationic and anionic pollutants, crystal violet (CV) fast green (FG) under solar light exposure. MethodsThe CAU-17 and Bi-MOF (ATP) were prepared by the solvothermal method. However, only the Bi-MOF (ATP) ability to absorb visible spectrum and degradation of pollutants can be attributed to several factors, including the diminished particle sizes, mitigated recombination of charge carriers, oxidation of nitrogen during photocatalytic reactions, and a favorable bandgap of positioning within the visible spectrum. Significant findingsThe Mott-Schottky plot and electron paramagnetic resonance analyses confirmed a Bi-MOF (ATP) generated free radicals (·O2‾). The remarkable photocatalytic degradation of CV and FG can achieve 92 % and 95 %, respectively. Notably, the catalyst retains robust stability throughout reusability assessments, maintaining its degradation efficiency without compromising the integrity of its crystalline structure and morphology. This study sheds light on the promising potential of Bi-MOFs (ATP) as effective photocatalysts for pollution under solar light.

Acid Treatment on Bentonite Clay for the Removal of Fast Green FCF Dye from Aqueous Solution

ABSTRACTThe bentonite clay has been activated by acid treatment and utilized as a lower‐cost and eco‐friendly adsorbent required to remove Fast Green FCF dye from the aqueous solution. At first acid activated bentonite clay minerals were analyzed by various analytical techniques like Fourier Transform Infrared Spectroscopy (FTIR), x‐ray diffraction (XRD), and x‐ray fluorescence (XRF) analysis. The batch adsorption research was performed to investigate the Fast Green FCF dye adsorption onto the acid‐treated (Bent) bentonite clay. Sorption studies investigated the impacts of adsorbent dosage, initial pH, and time of contact on Fast Green FCF color elimination. The adsorption capacity decreased as the pH was above 7 and then remained almost the same after a pH value of 9. At acidic conditions (below pH value 7), the capacity of adsorption diminished by a decrease in the pH of the solution. The results indicated that the maximum capacity of adsorption has been obtained at an adsorbent dosage of 0.1 g. As the dosage of the adsorbent was improved, several active sites that were available at the time of the dye adsorption increased. As a result, the dye percentage that was removed from the clay increased. Besides these, adsorption kinetics, adsorption equilibrium isotherm, and thermodynamics studies have been also conducted. While studying the adsorption kinetics pseudo‐2nd‐order kinetics has been seen to be more appropriate as compared to pseudo‐1st‐order model. The experimental findings indicated that the attachment of the dye to the clay surface followed the “Langmuir adsorption” isotherm rather than the Freundlich adsorption isotherm with a monolayer coverage of 18.93 mg/g. From the thermodynamics study, it was revealed that the process of adsorption takes place instantly at high temperatures.

Monitoring Photo-Fenton and Photo-Electro-Fenton process of contaminants emerging concern by a gas diffusion electrode using Ca10-xFex-yWy(PO4)6(OH)2 nanoparticles as heterogeneous catalyst

The catalytic performance of modified hydroxyapatite nanoparticles, Ca10-xFex-yWy(PO4)6(OH)2, was applied for the degradation of methylene blue (MB), fast green FCF (FG) and norfloxacin (NOR). XPS analysis pointed to the successful partial replacement of Ca by Fe. Under photo-electro-Fenton process, the catalyst Ca4FeII1·92W0·08FeIII4(PO4)6(OH)2 was combined with UVC radiation and electrogenerated H2O2 in a Printex L6 carbon-based gas diffusion electrode. The application of only 10 mA cm−2 resulted in 100% discoloration of MB and FG dyes in 50 min of treatment at pH 2.5, 7.0 and 9.0. The proposed treatment mechanism yielded maximum TOC removal of ∼80% and high mineralization current efficiency of ∼64%. Complete degradation of NOR was obtained in 40 min, and high mineralization of ∼86% was recorded after 240 min of treatment. Responses obtained from LC-ESI-MS/MS are in line with the theoretical Fukui indices and the ECOSAR data. The study enabled us to predict the main degradation route and the acute and chronic toxicity of the by-products formed during the contaminants degradation.

UV–visible spectroscopic exploratory insight into the long term photo-stability of the fast green FCF dye-fructose-sodium lauryl sulphate-NaOH electrolyte based photogalvanic cell

Photo-galvanic cells are organo-inorganic chemical based devices. These cells use chemicals like photo-sensitizer(s), reductant(s), surfactant(s), alkali, solvent, and electrodes. Photo-decay and sacrifice of the chemical materials is imminent leading to the limited electrical output, efficiency and life of these cells. For realizing practical applications, the scalability of electrical output and stability of these devices is of utmost importance. Therefore, the long term photo-stability of Fast Green FCF dye-Fructose-Sodium lauryl sulphate (SLS)-NaOH electrolyte based cells has been studied in present work. The electrical output of the cell has been monitored over long period of time. Further, the photo-stability of electrolyte has been determined and analyzed spectroscopically. It has been observed that the Fast Green FCF dye-Fructose-SLS-NaOH photogalvanic cell device is capable of producing power even after decay of electrolyte. In early 24 h, about 90.54 % of dye degradation is observed. The cell is capable of giving current with even left out concentration ∼0.2 × 10−4 M (i.e., 9.46 % of initial concentration) of sensitizer. Further, the photo-degradation products (organic sulfonates) of FCF dye and SLS are also potential candidates for current generation. Cell charged in sunlight is capable of generating current even after cutting-off the illumination of electrolyte.

A novel ceramic modified carbon based sensor for ultrasensitive electro-sensing of fast green FCF analysis: An advancement in toxic dye detection

Fast Green FCF (FG) is categorised as a triarylmethane dye, which has been associated with a rise of sarcoma, respiratory complications, inhibition of neurotransmitter release, and skin irritation. The incorporation of Yttria-Stabilized-Zirconia (YSZ) and Molybdenum Disulfide (MoS2) nanoparticles in the modification of a carbon paste electrode (YSZ/MoS2@CPE) facilitated the investigation of FG. The sample was characterised using scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy (SEM-EDX) and X-ray diffraction (XRD). Material performance was evaluated using electrochemical impedance spectroscopy (EIS). The FG compound was subjected to experimentation under various phosphate buffer conditions, employing the techniques of Cyclic voltammetry (CV) and square wave voltammetry (SWV). The ideal pH for achieving the most favourable outcomes was determined to be 6.0, within 0.2 V–1.1 V potential. The utilisation of the diffusion electrode technique was employed to investigate the impact of various parameters on the electrochemical properties. The quantitative assessment of FG was conducted using SWV within the concentration between 0.1 and 10 µM, demonstrating a linear relationship. The values for the limit of detection (LOD) and limit of quantification (LOQ) were established at 0.7 × 10−9 M and 2.3 × 10−9 M, which were found to be lowest compared to the earlier reports. The application of this novel methodology yielded successful results in quantifying FG levels in both biological and water samples with a recovery of 97.29 %–98.48 %.

Comparison of the protective effect of the upper zone of the growth plate and unique cartilage matrix-associated protein with hyaluronic acid and corticosteroids on an experimental rat osteoarthritis model.

This study sought to compare the protective effect of the upper zone of the growth plate and unique cartilage matrix-associated protein (UCMA) with hyaluronic acid (HA) and corticosteroids (CS) in a rat model of osteoarthritis (OA). In the experimental animal study, 40 adult male rats were randomly assigned into five groups: control, monosodium iodoacetate (MIA) + vehicle (MIA+V), MIA+HA, MIA+CS, and MIA+UCMA. The OA model was induced by an intra-articular MIA injection to the right knee, and intra-articular injections into the right knee were performed on the treatment groups seven times every three days for 21 days. The knee joints were taken for histopathology and immunohistochemistry (IHC) analyses after the rats were sacrificed. All sections were stained with hematoxylin-eosin, safranin O and fast green FCF, and toluidine blue, and bone morphogenetic protein 2 (BMP-2) and nuclear factor-kappa B (NF-κB) expressions were analyzed with IHC. The Mankin scoring was utilized to determine the histopathological changes in the joint tissues. Mankin score was significantly higher in the MIA group compared to the control group. Histopathologically, in the UCMA-, HA-, and CS-treated groups, degenerations in the articular cartilage were milder than in the MIA+V group. Mankin score was found to be decreased significantly in the UCMA-, HA-, and CS-treated groups compared to the MIA group. Furthermore, IHC analyses revealed that NF-κB and BMP-2 expressions elevated in the MIA-induced OA model, while they were downregulated after UCMA, HA, and CS treatments. Our data revealed that UCMA could be used as a potential protective molecule in the prevention and treatment of OA. Furthermore, the protective effect of UCMA was similar to HA and CS, and its possible beneficial roles against OA may be linked to the reduced BMP-2 and NF-κB levels. Further experimental research would make significant contributions to a better understanding of the therapeutic effect of UCMA on degenerative cartilage tissues.

Revealing the interface chemistry of polyaniline grafted biomass via statistical modeling of multi-component dye systems: optimization, kinetics, thermodynamics, and adsorption mechanism.

The growing need to examine the adsorption capabilities of innovative materials in real-world water samples has encouraged a shift from single to multicomponent adsorption systems. In this study, a novel composite, PANI-g-SM was synthesized by covalently grafting a lignocellulosic biomass, Saccharum munja (SM) with polyaniline (PANI). The as-synthesized composite was investigated for the simultaneous adsorption of cationic (Methylene Blue (MB); Crystal Violet (CV)) and anionic dyes (Reactive Red 35 (RR); Fast Green FCF (FG)) from four single components and two binary systems, MB + RR and CV + FG. Further, the effect and interaction of pH (2-11), dosage (0.01-0.04g/10mL), and initial concentration (0.0313 to 0.1563mmol/L) on the elimination of dyes by PANI-g-SM were studied through a novel design of Box-Behnken of Response Surface Methodology (RSM) technique which was found to be highly useful for revealing the chemistry of interfaces in multi-component systems. The extended Langmuir model for the binary system indicated the presence of synergism, as result the maximum monolayer adsorption capacity increased by 44.44%, 645.83%, 67.88%, and 441.07% for MB, RR, CV, and FG dye, respectively. Further, the adsorption process mainly followed a pseudo-second-order kinetic model, and the thermodynamic studies revealed the exothermic nature of adsorption for RR and FG dye while endothermic for MB and CV dye, respectively with varying from - 1.68 to - 6.12kJ/mol indicating the spontaneity of the process. Importantly, the efficacy of the composite was evaluated for the treatment of textile industry effluent highlighting its potential as an adsorbent for wastewater treatment.

Single-Dose Radial Extracorporeal Shock Wave Therapy Modulates Inflammation During Meniscal Tear Healing in the Avascular Zone

Background: Extracorporeal shock wave therapy (ESWT) promotes tissue healing by modulating inflammation, which has implications for meniscal tear healing in the avascular zone. Purpose: To evaluate the effects of a single dose of radial ESWT on the healing process and inflammation of the meniscus and knee joints after meniscal tears in the avascular zone. Study Design: Controlled laboratory study. Methods: Avascular tears were induced in the medial meniscus (MM) of 72 Sprague-Dawley rats. One week postoperatively, the rats received a single session of radial ESWT with a Power+ handpiece (ESWT group; n = 36) or with a fake handpiece (sham-ESWT group; n = 36). The rats were then euthanized at 2, 4, or 8 weeks postoperatively. The MMs were harvested for analysis of healing (hematoxylin-eosin, safranin O–Fast Green, and collagen type 2 staining) and inflammation (interleukin [IL]-1β and IL-6 staining). Lateral menisci and synovia were obtained to evaluate knee joint inflammation (enzyme-linked immunosorbent assay of IL-1β and IL-6). Cartilage degeneration was assessed in the femurs and tibial plateaus using safranin O–Fast Green staining. Results: The ESWT group showed significantly better meniscal healing scores than the sham-ESWT group at 4 (P = .0066) and 8 (P = .0050) weeks postoperatively. The IL-1β level was significantly higher in the sham-ESWT group than in the ESWT group at 2 (MM: P = .0009; knee joint: P = .0160) and 8 (MM: P = .0399; knee joint: P = .0001) weeks. The IL-6 level was significantly lower in the sham-ESWT group than in the ESWT group at 2 (knee joint: P = .0184) and 4 (knee joint: P = .0247) weeks but higher at 8 weeks (MM: P = .0169; knee joint: P = .0038). The sham group had significantly higher osteoarthritis scores than the ESWT group at 4 (tibial plateau: P = .0157) and 8 (femur: P = .0048; tibial plateau: P = .0359) weeks. Conclusion: A single dose of radial ESWT promoted meniscal tear healing in the avascular zone, modulated inflammatory factors in the menisci and knee joints in rats, and alleviated cartilage degeneration. Clinical Relevance: Radial ESWT can be considered a potential option for improving meniscal tear healing in the avascular zone because of its ability to modulate inflammation.

Comparative study of the photogalvanics of Sudan-I, Rhodamine-B, Fast Green FCF, Brilliant Cresyl Blue, Naphthol Green B, and chlorophyll ‘a’ photosensitizers at natural sunlight illumination intensity

Photogalvanic cells provide a route for simultaneous solar power and storage. The synthetic and natural photosensitizers having absorption in different spectral regions have been studied at natural sun intensity for simultaneous solar power and storage. The dye sensitizers [Sudan-I (SUD); Rhodamine-B (RHD); Fast Green FCF (FCF); Brilliant Cresyl Blue (BCB); Naphthol Green B (NGB)], and chlorophylls present in aqueous crude spinach extract (SPE) have been used. The observed power and efficiency for various sensitizers are respectively as- 610.8 μW, 7.63% for SUD; 620.1 μW, 7.75% for RHD; 654 μW, 8.17% for SPE; 661 μW, 8.26% for BCB; 649.6 μW, 8.12% for FCF; 625.8 μW, 7.82% for NGB; 596.2 μW, 7.45% for mixed NGB+FCF+BCB; 595.4 μW, CE 7.44% for mixed NGB + FCF + BCB + SPE; 587.6 μW, 7.34% for mixed NGB + FCF +BCB + SPE + RHD; and 639.6 μW, 7.99% for mixed NGB + FCF +BCB + SPE + RHD + SUD. The photogalvanic cell performance as the current, potential, and power for various photo sensitizer(s) is practically same at natural sun intensity as well. The power storage capacity of the various photosensitizer (s) may be different.

Synthesis of a Magnetic Nanostructured Composite Sorbent Only from Waste Materials.

Water pollution is a big problem for the environment, and thus depollution, especially by adsorption processes, has garnered a lot of interest in research over the last decades. Since sorbents would be used in large quantities, ideally, they should be cheaply prepared in scalable reactions from waste materials or renewable sources and be reusable. Herein, we describe a novel preparation of a range of magnetic sorbents only from waste materials (sawdust and iron mud) and their performance in the adsorption of several dyes (methylene blue, crystal violet, fast green FCF, and congo red). The preparation is performed in a hydrothermal process and is thus easily scalable and requires little sophisticated equipment. The magnetic nanostructured materials were analyzed using FTIR, VSM, SEM/EDX, XRD, and XPS. For crystal violet as a pollutant, more in-depth adsorption studies were performed. It was found that the best-performing magnetic sorbent had a maximum sorption capacity of 97.9 mg/g for crystal violet (methylene blue: 149.8 mg/g, fast green FCF: 52.2 mg/g, congo red: 10.5 mg/g), could be reused several times without drastic changes in sorption behavior, and was easily separable from the solution by simply applying a magnet. It is thus envisioned to be used for depollution in industrial/environmental applications, especially for cationic dyes.

Simultaneous Preconcentration of Fast Green FCF and Rhodamine B Using Deep Eutectic Solvent and Determination via High-Performance Thin Layer Chromatography

The aim of the current investigation is the development of a green, quick, easy, and accurate method for simultaneous preconcentration of fast green FCF (FG) and rhodamine B (Rh B) using a deep eutectic solvent (DES). Then, the high-performance thin layer chromatography (HPTLC) technique was used for the determination of analytes. Decanoic acid and tetrabutylammonium bromide were chosen as the components of DES. HPTLC analysis was performed on an aluminum plate silica gel 60 F254. Methanol-ammonia and ethyl acetate were selected as the mobile phase. Scanning of the plates was accomplished by scanner 3. Effective parameters on the preconcentration process such as concentration of salt, volume of DES, stirrer time, and pH were investigated via central composite design (CCD). Data validation demonstrated good repeatability. The limit of detection for FG and Rh B was obtained as 0.08 and 0.01 µg·mL−1, respectively. The enrichment factor for FG and Rh B was achieved as 7.43 and 10.77, respectively. The linear ranges for FG and Rh B were acquired as 0.10–1.20 and 0.05–1.20 µg·mL−1, respectively. The preconcentration factor for both analytes was 21.66. Finally, the proposed method was successfully used for the quantitation of FG and Rh B in pastille and lipstick.

Magnetic solid-phase extraction of Fast Green dye based on magnetic nanoparticles (GO/Co3O4/Fe3O4) prepared by photo-irradiation method

The magnetic nanoparticles (MNPs) of (GO/Co3O4/Fe3O4) were synthesized, characterized, and then utilized to prepare magnetic solid-phase extraction (MSPE), introducing a new method for the determination of Fast Green dye coupled with UV–visible spectrophotometry. The results demonstrated that Fast Green dye was adsorbed on GO/Co3O4/Fe3O4 MNPs and was released using 1 mL of 0.01 N NaOH. Under optimal conditions, the linear range was 0.5–6 mg/L and the limit of detection (LOD) was 0.2648. The high values of the preconcentration factor (25) and enhancement factor (10.5789) indicate that the MSPE process has concentrated the Fast Green dye by 25 times and made it 10.5789 times more sensitive. This highlights the successful extraction and concentration of Fast Green dye into a small volume of 1 mL of 0.01 N NaOH through the MSPE process. Furthermore, the GO/Co3O4/Fe3O4 MNPs sorbent exhibited reusability for up to five cycles. The application of greenness assessment tools (AES, GAPI, and AGREE) confirmed that MSPE can be considered a green chemistry method.

Development of Highly Efficient Heterogeneous Fe3O4‐Biochar Nanocomposite as Fenton‐like Catalysts for Degradation of Fast Green

AbstractIron oxide and its carbon‐containing biochar have shown efficiencies in Fenton oxidation reactions in recent years. Though magnetic biochar composites have been reported, developing facile, environment‐friendly methods with appropriate activity remains challenging. Removing dye traces from aqueous solutions is a prime concern under water scarcity issues at different levels. We developed a catalyst of biochar with magnetite for dye remediation. Magnetite is homogeneously loaded on biochar surfaces to form Fe3O4‐biochar to efficiently activate H2O2 to achieve hydroxyl radicals. This catalyst degrades Fast green dye efficiently around 89.3 % within 60 min with the optimum reaction conditions of 15 mM Fast Green dye, pH=4, 30 mg of Fe3O4‐biochar and 25 mM of H2O2. The composite shows around 41 % increase in the degradation rate after incorporating the Fe3O4 on biochar. The prepared Fe3O4‐biochar composite can be easily recycled without significant activity loss for five successive degradation reactions. The reported study provided a direction to prepare newer Fenton catalysts from sustainable sources for the degradation of organic dyes in water and overcame individual limitations of Fe3O4 and biochar.

Clock gene Per1 regulates rat temporomandibular osteoarthritis through NF-κB pathway: an in vitro and in vivo study

PurposeTemporomandibular joint osteoarthritis (TMJOA) is a common disease that negatively affects the life quality of human beings. Circadian rhythm acts an important role in life activities. However, whether the clock genes are rhythmic expressed in mandibular condylar chondrocytes, or the clock genes have an effect on the progression of TMJOA remains unknown. In this study, we aim to explore expression of clock genes and regulatory mechanism of TMJOA in rat mandibular condylar chondrocytes.MethodsAfter synchronized by dexamethasone, the expression of core clock genes Per1, Per2, Clock, Cry1, Cry2 and Bmal1 and cartilage matrix degrading factor gene Mmp13 were analyzed in mandibular condylar chondrocytes every 4 h with RT-qPCR. The mandibular condylar chondrocytes were stimulated with IL-1β, and expression of Per1, Mmp13, P65 and p-P65 was assessed by RT-qPCR and Western blot. Sh-Per1 lentivirus was used to assess the effect of clock gene Per1 in IL-1β-induced chondrocytes, and expression of Mmp13, P65 and p-P65 was measured. After establishing a rat TMJOA model using unilateral anterior crossbite (UAC), micro-CT, H & E, Alcian Blue & Nuclear Fast Red and Safranin O & Fast Green, cartilage thickness was utilized to assess the damage of cartilage and subchondral bone. Immunohistochemistry of PER1, MMP13 and P65 was performed in condylar sections.ResultsAll core clock genes and Mmp13 were rhythmically expressed. And Mmp13 expression curve was closed in phase and amplitude with Per1. After stimulation with IL-1β, the expression of MMP13, PER1 and P65 and ratio of p-P65/P65 increased in condylar chondrocytes. After Per1 was down-regulated in condylar chondrocytes, the expression of MMP13 and P65 and ratio of p-P65/P65 decreased. Compared with the condyles of Sham group, the bony parameters of UAC group were significantly worse. The thickness of cartilage in UAC group significantly reduced. The modified Mankin scores and the expression of PER1, MMP13 and P65 in cartilage of UAC group significantly increased compared with Sham group.ConclusionCore clock genes and Mmp13 are rhythmic expressed in rat mandibular condylar chondrocytes. PER1 can regulate the expression of MMP13 through NF-κB pathway in IL-1β-induced mandibular condylar chondrocytes.

A highly efficient NiCo2O4 decorated g-C3N4 nanocomposite for screen-printed carbon electrode based electrochemical sensing and adsorptive removal of fast green dye.

Herein, we demonstrate the preparation and application of NiCo2O4 decorated over a g-C3N4-based novel nanocomposite (NiCo2O4@g-C3N4). The prepared material was well characterized through several physicochemical techniques, including FT-IR, XRD, SEM, and TEM. The electrochemical characterizations via electrochemical impedance spectroscopy show the low electron transfer resistance of NiCo2O4@g-C3N4 owing to the successful incorporation of NiCo2O4 nanoparticles on the sheets of g-C3N4. NiCo2O4@g-C3N4 nanocomposite was employed in the fabrication of a screen-printed carbon electrode-based innovative electrochemical sensing platform and the adsorptive removal of a food dye, i.e., fast green FCF dye (FGD). The electrochemical oxidation of FGD at the developed NiCo2O4@g-C3N4 nanocomposite modified screen-printed carbon electrode (NiCo2O4@g-C3N4/SPCE) was observed at an oxidation potential of 0.65V. A wide dual calibration range for electrochemical determination of FGD was successfully established at the prepared sensing platform, showing an excellent LOD of 0.13µM and sensitivity of 0.6912 µA.µM-1.cm-2 through differential pulse voltammetry. Further, adsorbent dose, pH, contact time, and temperature were optimized to study the adsorption phenomena. The adsorption thermodynamics, isotherm, and kinetics were also investigated for efficient removal of FGD at NiCo2O4@g-C3N4-based adsorbents. The adsorption phenomenon of FGD on NiCo2O4@g-C3N4 was best fitted (R2 = 0.99) with the Langmuir and Henry model, and the corresponding value of Langmuir adsorption efficiency (qm) was 3.72mg/g for the removal of FGD. The reaction kinetics for adsorption phenomenon were observed to be pseudo-second order. The sensitive analysis of FGD in a real sample was also studied.

Fabrication of the new p-Co3O4/n-AgI hetero-junction and its solar photo-degradation of the fast green FCF

This work examines the heterogeneous advanced oxidation for the photodegradation of fast green FCF a recalcitrant dye on the novel hetero-junction Co3O4/AgI. The spinel Co3O4 synthesized by sol-gel route was characterized by thermal analysis (TG), FTIR, XRD, SEM, BET, diffuse reflectance and photo-electrochemically; AgI was synthesized by precipitation. Electrons in Co3O4-CB (-1.06 VSCE) excited by sunlight are injected into AgI-CB (-0.90 VSCE). The hetero-junction p-Co3O4/n-AgI brings important changes in the photo-catalytic properties, thus facilitating the rapid transfer of electron-hole (e−/h+) pairs and significantly improving the photoactivity. Some physical parameters like the pH, photocatalyst dose, CFC concentration as a function of illumination time have been studied. After 90 min, 20 mg/L of fast green FCF disappeared under optimal conditions (pH ∼8, 25 °C, p-Co3O4/n-AgI (Wt. %: 1/1) at a dose of 1 mg/mL) upon natural sunlight. The photodegradation kinetic of fast green FCF, measured spectrophotometrically and by total organic carbon (TOC) showed that the oxidation follows a first-order model with a half catalytic life of 41 min.