Good Reactivity Research Articles

Increased serum galectin-3 level is associated with endothelial dysfunction and cardiovascular events in patients with hypertension.

Endothelial dysfunction can lead to various harmful cardiovascular complications. The importance of galectin-3 (Gal-3) has been proposed in some cardiac diseases related to chronic inflammation. However, its role in hypertension-induced endothelial dysfunction remains unclear. We enrolled 120 patients with hypertension, assessed their baseline characteristics, and monitored their 7-year cardiovascular outcomes. We performed an enzyme-linked immunosorbent assay to measure serum Gal-3 levels. The vascular reactivity index (VRI) was examined by digital thermal monitoring. Patients with VRI <1.0, 1.0 to <2.0, and ≥2.0 were defined as having poor, intermediate, and good vascular reactivity, respectively. Among the recruited patients, 12 had poor vascular reactivity, 57 had intermediate vascular reactivity, and 51 had good vascular reactivity. Older age, higher total cholesterol levels, higher low-density lipoprotein cholesterol levels, lower estimated glomerular filtration rate, and higher Gal-3 levels were associated with poor endothelial dysfunction. Multivariate linear regression analysis showed that age and Gal-3 levels were correlated with VRI. During the 7-year follow-up period, patients with higher Gal-3 levels had more cardiovascular events. Higher Gal-3 levels are associated with endothelial dysfunction and unfavorable cardiovascular outcomes in patients with hypertension, suggesting its potential role in the hypertension-induced endothelial dysfunction.

Squaric acid derivatives with cytotoxic activity-a review.

3,4-Dihydroxycyclobut-3-ene-1,2-dione (squaric acid, SQ) is the most important representative of the oxocarbon acids family. Squaric acid derivatives can be promising pharmaceutical agents, due to their unique structural properties, from which novel drugs benefit: a planar aromatic ring, the ability to form hydrogen bonds, good reactivity and similarity with carboxylate, phosphate and amide groups. These properties make it suitable for three major applications in cancer treatment. Firstly, due to their excellent ion binding ability, the halogenated squaramides can be used as artificial ion transporters or mobile carriers to disrupt Na+/Cl- gradients in cancer cells, thus hindering lysosomal function and inducing apoptosis. Another advantage of this class is their bioisosteric properties. Such molecules have been reported to be selective inhibitors of HDACs, FAK, SNM1A, MMP and kinases, involved in tumor growth and metastasis. Finally, the cyclobutenedione moiety proves to be a great linker in complex radiopharmaceuticals, used in theranostics. Its aromaticity and good reactivity make the generation and stability of these drugs easy and efficient. Multiple derivatives containing the squamide motif have been the subject of in-vitro investigations and have demonstrated anti-cancer activity in the nanomolar range against tumor cell lines, including colorectal adenocarcinoma, breast cancer, gastric carcinoma and cervical cancer. On the other hand, squaric acid derivative-Navarixin, has already been evaluated in Phase II clinical trials for its potential efficacy in the treatment of solid tumors. In this context this review is the first looking into the potential applications of squaric acid derivatives as anticancer therapies. It analyzes experimental studies presented in articles published between 2000 and 2024.

Continuous-flow synthesis of carboxylic acids from alcohols via platinum and silicon dioxide-catalyzed hydrogen peroxide oxidation.

A continuous-flow method for the direct oxidation of alcohols to carboxylic acids is reported, employing hydrogen peroxide (H2O2) and a platinum (Pt) catalyst within a flow reactor system. This approach allows for precise control over the contact time between the reactants and the catalyst, enabling optimization of reaction conditions. By analyzing the yields of both aldehydes and carboxylic acids as a function of weight hourly space velocity (WHSV), selective synthesis of carboxylic acids was achieved without the formation of corresponding aldehydes. The Pt catalyst exhibited excellent stability, producing 25.2 g of octanoic acid from 1-octanol with a yield exceeding 96% over 210 h at a WHSV of 1.3 h-1 using a 5 mm inner diameter × 100 mm column. This Pt-catalyzed continuous-flow H2O2 oxidation method demonstrates good reactivity for a variety of alcohols, including aliphatic, aromatic, allylic, and heteroaromatic, affording the corresponding carboxylic acids in 19-98% isolated yields with water as the sole byproduct. X-ray photoelectron spectroscopy (XPS) analysis confirmed the preservation of metallic zero-valent Pt (Pt(0)) throughout the reaction.

Isoform-Specific vs Isoform-Universal Drug Targeting: A New Targeting Paradigm Illustrated by New Anti-ICAM-1 Antibodies

ABSTRACT Drug targeting can be achieved by coupling drugs or their carriers to affinity molecules, mostly antibodies (Abs), which recognize specific protein targets. However, most proteins are not expressed in an exclusive configuration but as various isoforms. Hence, selected targeting molecules may fail to target with enough efficiency in clinical trials, which is overlooked. We illustrate this by targeting ICAM-1, a cell-surface protein overexpressed in many pathologies. Most ICAM-1 targeting studies used Ab R6.5, which binds ICAM-1 domain 2 (D2). Yet, literature and our data show that D2 is frequently absent among ICAM-1 isoforms. We thus produced a battery of five new Abs (B4, B6, B11, C12, G2) and tested their ability to recognize both full-length and -D2 ICAM-1. In solution, all Abs recognized both ICAM-1 forms (from 5.3x1011 to 4.2x1012 sum intensity/well). Coating them on nanocarriers (NCs) rendered G2 specific against -D2 ICAM-1 (4.2x106 NCs/well) while other Abs kept their dual recognition (from 6.4x106 to 2.2x107 NCs/well). All Abs induced NC intracellular uptake in respective cells (from 42% to 85%) and displayed good cross-species reactivity (from 4.4x1011 to 2.6x1012 sum intensity/well). These Abs represent valuable tools to target ICAM-1 and illustrate a new targeting paradigm that may improve classical strategies.

Recombinant African swine fever virus p30-flagellin fusion protein promotes p30-specific humoral and cellular immune responses in mice.

African swine fever (ASF) is a transmissible and deadly viral disease caused by the African swine fever virus (ASFV) that has considerably affected the global pig industry. Vaccination is considered a potentially effective method to control ASF. However, live attenuated vaccines can't protect against all circulating virus isolates. Subunit vaccines can induce both cellular and humoral immune responses, but often require the addition of adjuvants. Flagellin, a stimulator of Toll-like receptor 5 (TLR5), functions as a potent adjuvant by enhancing cellular and humoral immune responses. However, its high antigenicity may cause severe systemic inflammation. In this study, an Escherichia coli expression system was used to express ASFV p30 protein (p30) fused with Salmonella Typhimurium FliCΔD2D3 (without the D2 and D3 domains of FliC). The immunological effect of p30-FlicΔD2D3 protein in mice was evaluated. Results revealed that the ASFV p30 protein and the p30-FlicΔD2D3 fusion protein were effectively expressed by the E. coli expression system. In vitro activity analysis showed that the p30-FlicΔD2D3 fusion protein could be recognized by ASFV-positive serum, had good immunoreactivity, and remarkably promoted IL-8 secretion related to TLR5 activity in HEK293-mTLR5 cells. However, p30-FlicΔD2D3 induced significantly lower levels of inflammatory factor IL-8 than that induced by wild-type flagellin. Immunization with the p30-FlicΔD2D3 fusion protein considerably promoted cellular and humoral immune responses in mice. Therefore, the p30-FlicΔD2D3 protein retained good immune reactivity and TLR5 agonist efficacy. It also enhanced humoral and cellular immune responses in mice. This work offered valuable information that will be helpful to develop ASF subunit vaccines.

Multiple Tolerization Subtractive Immunization in the Obtention of Specific Monoclonal Antibodies Against Paracoccidioides lutzii.

Paracoccidioidomycosis (PCM) is a chronic endemic mycosis in Latin America, predominantly caused by Paracoccidioides brasiliensis (Pb18) and Paracoccidioides lutzii (Pl01). Diagnosing PCM is challenging due to species-specific antigenic differences, therefore new biomarkers for accurate and rapid detection are needed. This study explores multiple tolerization subtractive immunization (MTSI) to generate monoclonal antibodies against rare or weakly expressed epitopes of Pb18 and Pl01, potentially improving PCM diagnosis. These strains were cultured to obtain cell-free antigens (CFA). MTSI involved immunizing BALB/c mice with CFA from Pb18 as a tolerogen and Pl01 as an immunogen, using Freund's adjuvant and cyclophosphamide to induce immune tolerance. The immune response was monitored via Enzyme-linked immunosorbent assay (ELISA) and Western blotting. Hybridomas were generated by fusing splenocytes from immunized mice with myeloma cells, after which clonal selection was conducted based on reactivity to Pl01 antigens. The study explores the presence of various proteins, including gp43 and Hsp60, in the protein profile of CFAs. Additionally, polyclonal antibody reactivity to Pb18 antigens was significantly reduced, suggesting that MTSI effectively promoted immunological tolerance. Followig the screening of hybridomas, clones with good reactivity to Pl01 and less reactive to Pb18 were selected. The monoclonal clones C1 and E6 exhibited potential specificity for Pl01 antigens. The effective generation of P. lutzii-specific antibodies by MTSI demonstrates this technology's promise for the development of accurate PCM diagnostic instruments. These antibodies have the potential to enhance patient outcomes and reduce the incidence of false-negative diagnoses, which could lead to better disease management.

Syngas Production by Fe2SiO4 Oxygen Carrier in Chemical Looping Partial Oxidation of Methane

Chemical looping partial oxidation of methane (CLPOM) is a low energy consumption and environmentally friendly new technology that can generate syngas. The main challenge is to find suitable oxygen carriers, which should be highly active, stable, low cost, and eco-friendly. This study found that Fe2SiO4 had good reactivity in the CLPOM process. Thermodynamic calculations were carried out by FactSage8.1 to demonstrate the feasibility of Fe2SiO4 as an oxygen carrier for CLPOM. Fe2SiO4 was prepared by the direct ball milling method and the high-temperature solid-phase synthesis method. The reaction properties of Fe2SiO4 were investigated in the fixed bed reactor. The XRD and FTIR results indicate that Fe2SiO4 can be synthesized successfully through the high-temperature solid-phase synthesis method. The results of fixed bed experiments showed that when the reaction temperature was 980 °C and the reaction time was 28 min, the XCH4 reached 87%, and the SH2 and SCO were 70% and 71%, respectively. Subsequently, 20 redox cycle experiments were conducted under the optimal reaction conditions. The results showed that Fe2SiO4 exhibited good reactivity in the first two cycles, and as the reaction progressed, the reduced oxygen carrier could not regain the lattice oxygen, leading to a decline in cyclic performance. This study demonstrates that Fe2SiO4 can couple CO2 and CH4 to produce syngas and is conducive to reducing carbon emissions.

DABCO-Intercalated α-Zirconium Phosphate as a Latent Thermal Catalyst in the Reaction of Urethane Synthesis.

The mixture of hexamethylene diisocyanate (HDI) and butanol (BuOH) with the intercalation compound of 1,4-diazabicyclo[2.2.2]octane (DABCO) with α-zirconium phosphate (α-ZrP) has been evaluated as a latent thermal catalyst at varying temperatures. α-ZrP·DABCO did not show activity at 25 °C, but showed a high level of activity at a higher temperature of 80 °C. To clarify the reaction behavior of HDI-BuOH with α-ZrP·DABCO, a viscosity value of 1200 mPa·s·g/cm2 was reached at 80 °C for 30 min. To investigate the deintercalation behavior of DABCO from the α-ZrP interlayer, it was investigated in BuOH and in HDI, respectively, under heated conditions. Interestingly, XRD patterns showed a reduction in α-ZrP·DABCO for the interlayer distance due to the deintercalation of DABCO in BuOH, while no changes associated with the deintercalation of DABCO were observed in HDI. Butanol was found to be important for the deintercalation of DABCO. To examine the reactivity of bifunctional monomers, the reaction of 1,4-butanediol (1,4-BDO) and HDI with α-ZrP·DABCO were investigated to show good reactivity at 80 °C and stability at 40 °C.

Construction of poly (styrene-divinylbenzene)@tris(4-aminophenyl)amine-p-phthalaldehyde-triethylenetetramine core-shell microspheres for the preparation of ion chromatography stationary phase

Core-shell composite microspheres are increasingly favored for the development of stationary phases due to their ability to integrate the monodispersity of inner core with the functional versatility of outer shell. In this study, poly(styrene-divinylbenzene)@(tris(4-aminophenyl)amine-p-phthalaldehyde-triethylenetetramine) (PS-DVB@TAPA-PPA-TETA) core-shell composite microspheres were constructed via an amine-aldehyde condensation reaction. The resultant microspheres were subsequently quaternized using the residual amine groups of TETA in the shell to create an effective anion-exchange stationary phase. The composite microspheres were characterized by SEM, FTIR, N2 adsorption-desorption experiment, et al. According to the results, the surface of PS-DVB microspheres was wholly covered by TAPA-PPA-TETA. The obtained PS-DVB@TAPA-PPA-TETA exhibited good reactivity, mechanical and chemical stability. The customized column exhibited good separation performance for seven conventional anions, five organic acids and three carbohydrates. The results demonstrate that PS-DVB@TAPA-PPA-TETA is a highly suitable material for the preparation of ion chromatographic stationary phase, exhibiting exceptional chemical stability and robust chromatographic performance in practical application. Finally, the customized column was successfully utilized for the determination of phosphate in waste acid sample.

Thermal and self‐curing kinetics of single pack epoxy adhesive with zeolitic imidazolate framework‐8

AbstractSingle pack epoxy adhesives, known for their simple operation process, combined with good reactivity at moderate temperatures and excellent storage stability, have gained extensive attention. An appropriate accelerator is crucial for enhancing their performance. This study demonstrates that the zinc zeolitic imidazolate framework ZIF‐8 (Zn(2‐methylimidazole)2) can effectively serve as an effective accelerator for the epoxy‐anhydride system, as evidenced by the complete exothermic curing curve obtained via differential scanning calorimetry (DSC) tests of the epoxy (A‐128) and anhydride (THPA) adhesive sample with ZIF‐8. The optimal addition amount of ZIF‐8 (0.9%) was determined by assessing the glass transition temperature (Tg) of the cured resin with varying ZIF‐8 weight fractions. Furthermore, the ideal curing conditions—gel temperature of 388.4 K, curing temperature of 416.7 K, and post‐treatment temperature of 441.9 K—were established by analyzing heating curves at different circumstances. The epoxy (A‐128) and anhydride (THPA) system with accelerator ZIF‐8 exhibited superior stability compared to the commercial accelerators like PN‐23 or DMP‐30. This is attributed to the steric hindrance and coordination bonds of ZIF‐8, indicated by a large pre‐exponential factor (A1 = 5.58 × 108) and low‐value reaction rate constant (k1 = 0.3461 × 10−3 s−1). In addition, the kinetic parameters, and an autocatalytic equation model for the epoxy (A‐128) and anhydride (THPA) system with accelerator ZIF‐8 have been derived through isothermal curing kinetics analysis.

Quantum mechanical approaches and molecular docking studies of platinum based anticancer drugs Satraplatin and picoplatin structures

The structures of the anticancer drug compounds satraplatin and picoplatin are optimized, and theoretical studies done by Density Functional Theory (DFT) to investigate the optical properties, global chemical descriptors, and band gap were calculated using the obtained Frontier molecular orbital values. The theoretically obtained data of the platinum drugs found to possess low energy gap values and low chemical hardness with high chemical softness describe that the compounds are chemically stable and most reactive. Using the molecular docking process, the binding mechanisms of the satraplatin and picoplatin drugs with cancer DNA structures were studied, and the results were analyzed. For the two drug compounds examined, satraplatin has shown the least binding energies at −5.06kcal/mol compared to picoplatin at −2.69 kcal/mol, and conformations with root mean square deviation (RMSD) values by DNA structures are less than or equal to 2.00 Å in targeting the specific DNA target residues of the reference bound ligand. The grid box was generated using the selective grid parameters using the Autodock 4.2 program. The drug molecules found to have the least binding energy value with the lowest inhibition constant implicate the good docking score towards the DNA structure by the docking studies. DFT studies also show good structural properties and chemical reactivity. From the obtained results, satraplatin and picoplatin were found to have good chemical descriptors and good binding affinity and are best suited for biological molecular targets.

Co-Catalyzed Suzuki-Miyaura Coupling of Organoboronic Acids and Alkynyl Chlorides Using Potassium Bicarbonate as Base.

Organoboronic acids, some of the most common and widely used organoboron compounds, have not yet been used in the cobalt-catalyzed cross coupling reactions, despite cobalt demonstrating good reactivity with zinc reagents, Grignard reagents, and metal organoborates that are formed by n-butyl lithium or alkaline metal alkoxide salts and organoboron esters. Herein, a highly efficient and practical cobalt-catalyzed coupling reaction of aryl/alkenyl boronic acids and alkynyl chloride under mild reaction conditions is reported. The advantages of the organoboronic acids, along with a broad functional group compatibility and the reaction's tolerance to moisture and air, enable this reaction to be a synthetically useful protocol for the construction of a C(sp2)-C(sp) bond. Lastly, the synthesis of two natural products and a key intermediate of roxadustat was effectively accomplished using the methodology to construct the critical alkynyl-aryl bond.

Redox-Activated Substrates for Enhancing Activatable Cyclopropene Bioorthogonal Reactions.

Bioorthogonal chemistry has become a mainstay in chemical biology and is making inroads in the clinic with recent advances in protein targeting and drug release. Since the field's beginning, a major focus has been on designing bioorthogonal reagents with good selectivity, reactivity, and stability in complex biological environments. More recently, chemists have imbued reagents with new functionalities like click-and-release or light/enzyme-controllable reactivity. We have previously developed a controllable cyclopropene-based bioorthogonal ligation, which has excellent stability in physiological conditions and can be triggered to react with tetrazines by exposure to enzymes, biologically significant small molecules, or light spanning the visual spectrum. Here, to improve reactivity and gain a better understanding of this system, we screened diene reaction partners for the cyclopropene. We found that a cyclopropene-quinone pair is 26 times faster than reactions with 1,2,4,5-tetrazines. Additionally, we showed that the reaction of the cyclopropene-quinone pair can be activated by two orthogonal mechanisms: caging group removal on the cyclopropene and oxidation/reduction of the quinone. Finally, we demonstrated that this caged cyclopropene-quinone can be used as an imaging tool to label the membranes of fixed, cultured cells.

Short-term mechanical properties and microstructure of coastal cement soil modified by sugarcane bagasse ash

Sugarcane bagasse ash is a kind of agricultural waste with a large quantity and good volcanic ash reactivity, it is necessary to find a way to reasonably utilize it to prevent environmental pollution caused by long-term accumulation. In this paper, the effect of sugarcane bagasse ash on the short-term mechanical properties of coastal cement soil were studied, and unconfined compressive tests and triaxial shear tests were carried out. The sugarcane bagasse ash content was set to 0 %, 1 %, 2 %, 3 %, 4 % and 5 %, respectively, the cement content was set to 5 %, and the curing age was set at 7d. The test results show that sugarcane bagasse ash can effectively improve the unconfined compressive strength and triaxial shear strength of cement soil, exhibiting a trend of increasing first and then decreasing with the increase of its content. When the sugarcane bagasse ash content is 1 %, the unconfined compressive strength reaches the maximum value of 2040 kPa, which is 56 % and 8 % higher than that of cement soil with 5 % and 7 % cement content, respectively. Compared with cement soil with 5 % cement content, the triaxial shear strength increases by 12 %∼17 %, the internal friction angle φ and cohesion c increases by 3 %∼8 % and 2 %∼11 %, respectively. The SEM test results show that the addition of bagasse ash can promote the hydration of cement to produce hydrated calcium silicate and other hydration products, fill the internal pores of the sample, and make the microstructure of the modified cement soil tend to be dense. The research results provide a reference for the application of sugarcane bagasse ash modified cement soil in practical engineering.

Iron mediated n → π* electron transitions and mid-gap states formation in CN under low-temperature secondary calcination enhances photodegradation of organic pollutants

Iron modified carbon nitride (CN) materials have attracted widespread attention from researchers in different application fields. In this paper, single atom iron anchored CN (FeCN) with mid-gap states and n → π* electron transition was synthesized through low temperature secondary calcination. The mid-gap states introduce surface states capable of trapping photogenerated electrons, enabling FeCN to absorb photons with energies lower than its intrinsic optical bandgap. 10%FeCN also exhibits distinct optical absorption above 490 nm derived from the n → π* electron transition, which expand the visible light response range of photocatalysts and enhance electron transport ability. Additionally, the Fe-Nx site enhances the separation and transmission efficiency of photoexcited charges. The prepared 10%FeCN exhibits extremely high photocatalysis and photo-Fenton activity. Mercaptobenzothiazole (MBT) degradation rate of 10%FeCN is 3.47 times higher than CN, achieving a mineralization rate of 86.7% in 100 min. Additionally, the oxytetracycline hydrochloride (OTC) degradation rate of 10%FeCN in photo-Fenton reaction is 11.9 times higher than CN. After five cycles, this catalyst still has good reactivity, indicating its good stability.

Monoclonal Antibody against Porcine LAG3 Inhibits Porcine Reproductive and Respiratory Syndrome Virus Infection

Lymphocyte activation gene 3 (LAG3) is an inhibitory receptor and the interaction between fibrinogen-like protein 1 and LAG3 can inhibit the anti-tumor effect of T cells both in vivo and in vitro, which was regarded as a new immune evasion mechanism. Porcine reproductive and respiratory syndrome (PRRS), caused by PRRSV, is an infectious disease characterized by reproductive disorders in pregnant sows and gilts and respiratory problems in pigs of all ages, seriously impacting the pig industry worldwide. In this study, monoclonal antibodies (mAbs) against porcine LAG3 (pLAG3) were developed, and one mAb (1C2) showed good reactivity with pLAG3 on PHA-activated porcine peripheral blood lymphocytes. Epitope mapping showed the epitope recognized by mAb 1C2 was located at amino acid residues 214–435 of pLAG3. LAG3 expression in the tissues of PRRSV-infected pigs was detected, using mAb 1C2 as the primary antibody, and the results revealed that PRRSV infection caused a marked increase in LAG3 expression compared to the control group. Interference of LAG3 expression on PHA-activated lymphocytes promoted PRRSV replication in the co-culture system of monocyte-derived dendritic cells and lymphocytes, whereas overexpression of LAG3 or blocking of the LAG3 signal with mAb 1C2 inhibited PRRSV replication, indicating that PRRSV infection activates the LAG3-signaling pathway, suggesting that this pathway plays an important role in PRRSV pathogenesis. The results obtained lay the foundation for subsequent research on the role of LAG3 in PRRS and other diseases with persistent infection characteristics.

Silver-Catalyzed 1,2-Thiosulfonylation of Alkenes: Development of a Nucleophilic d3-Methylthiolating Reagent.

Development of robust d3-methylthiolating reagents represents an attractive synthetic method to access deuterated molecules in the field of drug discovery. Here, we report a straightforward strategy to prepare electrophilic S-methyl-d3 arylsulfonothioates in one-step without column purification. These reagents exhibit good radical reactivity toward silver-catalyzed vicinal thiosulfonylation of alkenes or 1,6-enynes on water. As a result, simultaneous incorporation of both SCD3 and ArSO2 units into unsaturated carbon-carbon bonds with 100% atom economy has been established. Moreover, the ATRA adducts with >99% D incorporation can serve as nucleophilic d3-methylthiolating synthons via retro-Michael addition under mild basic conditions, providing a good alternative in trideuteromethylthiolating alkyl iodides to access corresponding trideuteromethyl sulfides with high efficiency.

In silico Assessment of Phytochemicals from Selected Plants as Prospective TGF‐β1 Inhibitors for Prostate Cancer Therapy

AbstractTransforming growth factor β1 (TGF‐β) is a cytokine with pleiotropic biological functions. Recently, its signaling pathway has been highlighted for its implicative paradoxical roles in prostate cancer (PCa). Suppressing downstream effects of this pathway by interfering with receptor complex formation through inhibition of the TGF‐β1 leads to its antitumor effects, illuminating the TGF‐β1 as a viable therapeutic target for PCa. Our compound library—established by a literature‐based approach that identified phytochemicals with published evidence against the TGF‐β1—was screened by employing molecular docking, density functional theory (DFT), and molecular dynamic (MD) simulations to identify TGF‐β1 inhibitors. Eight of the 24 phytochemicals docked from our compound library had a good binding affinity (ranging from −11.7 to −10 kcal/mol) to the TGF‐β1 (PDB: 1PY5). The phytochemicals displayed good stability and reactivity as revealed by the DFT analysis and a desirable pharmacokinetic profile. The top four phytochemical complexes with high binding energies maintained stability throughout the 100 ns simulation. Qualitative studies on the drug repurposing attributes of bisindolylmaleimide, flavopiridol, baicalin, and gefitinib as inhibitors of TGF‐β1 are recommended; most importantly, suggest further wet‐lab studies to corroborate these phytochemicals—SB 202190, SB 203580, silymarin, and cryptotanshinone—in TGF‐β1 targeted drug development.

Precision Electrochemical Micro-Machining of Molybdenum in Neutral Salt Solution Based on Electrochemical Analysis

Molybdenum is an important material in modern industry, widely used in extreme environments such as rocket engine nozzles and microelectrodes due to its high melting point, excellent mechanical properties, and thermal conductivity. However, as a difficult-to-machine metal, traditional machining methods struggle to achieve the desired microstructures in molybdenum. Electrochemical machining (ECM) offers unique advantages in manufacturing fine structures from hard-to-machine metals. Studies have shown that molybdenum exhibits a fast corrosion rate in alkaline or acidic solutions, posing significant environmental pressure. Therefore, this study investigates the electrochemical machining of molybdenum in neutral salt solutions to achieve high-precision microstructure fabrication. First, the polarization curves and electrochemical impedance spectroscopy (EIS) of molybdenum in NaNO3 solutions of varying concentrations were measured to determine its electrochemical reaction characteristics. The results demonstrate that molybdenum exhibits good electrochemical reactivity in NaNO3 solutions, leading to favorable surface erosion morphology. Subsequently, a mask electrochemical machining technique was employed to fabricate arrayed microstructures on the molybdenum surface. To minimize interference between factors, an orthogonal experiment was used to optimize the parameter combination, determining the optimal machining process parameters. Under these optimal conditions, an array of micro-groove structures was successfully fabricated with an average groove width of 110 μm, a depth-to-width ratio of 0.21, an aspect ratio of 9000, and a groove width error of less than 5 μm.

Kinetic and optimization study of ultrasound-assisted biodiesel production from waste coconut scum oil using porous CoFe2O4@sulfonated graphene oxide magnetic nanocatalysts: CI engine approach

In this study, CoFe2O4@sulfonated graphene oxide (SGO) heterogeneous nanocatalyst was synthesized and utilized to produce biodiesel from waste coconut scum oil (WCSO). The structural features of CoFe2O4@SGO nanocatalyst were evaluated by SEM, TEM, EDX, FTIR, XRD, CO2/TPD, VSM, and BET analyses. According to these analyses, CoFe2O4@SGO nanocatalyst has high specific surface area, suitable functional groups, and good reactivity. The highest biodiesel yield using CoFe2O4@SGO nanocatalyst in optimal conditions (MeOH/WCSO ratio = 12.41, temperature = 64.73 °C, catalyst concentration = 2.24 %, and ultrasonic time = 33.08 min) was 96.87 %. The yield of biodiesel decreased from 96.91 % to 90.17 % after six reuse cycles, which demonstrates the significant stability of CoFe2O4@SGO nanocatalyst in the transesterification process. After 7 reuse steps, XRD and CO2/TPD analyzes revealed that the catalytic activity and crystallinity of the nanocatalyst were almost retained. The kinetic behavior of biodiesel generation showed that the transesterification reaction is endothermic. Enhancing the concentration of biodiesel in the fuel mix had a positive impact on the reduction of CO and UHC emissions, as well as diesel engine parameters such as cylinder pressure, BP, EGT, BSFC, and BTE. Owing to the high biodiesel yield, significant reusability, and positive impacts on the diesel engine, CoFe2O4@SGO nanocatalyst is recommended for industrial applications.