Acid Methyl Ester Research Articles

Impact of chronic psychological stress on platelet membrane fatty acid composition in a rat model of type 1 diabetes Mellitus

BackgroundChronic stress and diabetes mellitus are highly associated with oxidative stress and inflammation, resulting in cell membrane disruption and platelet activity. This study aims to evaluate the impact of chronic psychological stress on the composition of the platelet phospholipid membrane and platelet activation in type 1 diabetes mellitus (T1DM).MethodsWe enrolled 35 mature healthy female Wistar rats and randomly divided them into 4 groups, namely the control group (n = 9), stress group (n = 10), T1DM group (n = 8), and T1DM + Stress group (n = 8). The Wistar rats were treated in different experimental conditions for 28 days while being provided free access to feed and water. The concentration of corticosterone in blood serum and hair samples was measured using a competitive enzyme-linked immunosorbent assay. Gas chromatography-mass spectrometry was conducted to identify the methyl esters of fatty acids (FAs) in the platelet phospholipid membrane. A quantitative determination of 11-dehydro-thromboxane B2 in the blood serum was also performed using a competitive enzyme-linked immunosorbent assay.ResultsAfter 28 days, the concentration of corticosterone in blood serum (ng/mL) was observed to be higher in the stress group as compared to the T1DM and T1DM + Stress groups (P = 0.031 and P = 0.008, respectively). The percentage of C 16:0 FA in the platelet membrane was greater in the T1DM + Stress group, but its levels of C 20:1 omega (ω) 9 FA, including C 18:3ω3 FA, C 20:5ω3 FA, and the total sum of ω3 FAs, were lower as compared to the control group (P = 0.016; P = 0.016; P = 0.031; P = 0.016, P = 0.031). The concentration of 11-dehydro-thromboxane B2 in blood serum (pg/mL) was observed to be higher in the stress group than in rats with T1DM (P = 0.063).ConclusionChronic psychological stress is related to higher levels of corticosterone, saturated FAs acids in the platelet membrane, and greater platelet activation. This study proves how a low percentage of unsaturated fatty acids in the DM and stress groups indicates the disturbing impact of the oxidative/inflammatory environment to lipid metabolism and neuroendocrine response.

Phytochemical Screening and Gas Chromatography-Mass Spectrometry Analysis of Bioactive Compounds Present in Stem Bark of <i>Picralima nitida </i>(stapf)

Over the years, traditional societies and ethnic nationalities have engaged plants with medicinal properties for the treatment of a range of diseases without any scientific knowledge of it inherent bioactive compounds that are responsible for its medicinal and pharmacological potentials. The aim of this study is to screen for the presence of phytochemical constituents and to identify the bioactive compounds domicile in the stem bark of <i>Picralima nitida </i>by the use of Gas Chromatography - Mass Spectrometry. The result of the quantitative investigation of the stem bark extract of <i>P. nitida</i> showed the presence of some phytochemical compounds such as saponins (3.22%), alkaloids (2.43%), flavonoids (6.05%) tannins (6.25%), oxalate (12.70%), phytate (2.87%), anthracene glycosides (2.14%) and cyanogenic glycosides (1.37%). Eleven (11) different bioactive compounds were recognized in the stem bark extract of <i>P. nitida</i> by Gas Chromatography - Mass Spectrometry analysis. The percentage of major bioactive compounds were vitamin E (69.31%), Cis-Myrtanol (5.57%), Octadecanoic acid methyl ester (4.52%), 11-Octadecenoic acid methyl ester (4.42%), 9-Methyl-2-phenyl-9H-imidazo (1,2-a) benzimidazole (3.70%), Pentadecanoic acid 14-methyl- methylester (3.21%) and 7,9-Dimethyl-6H-Indolo (2,3-b) quinoxaline (3.11%). From these findings, it could be concluded that <i>P. nitida </i>stem bark is rich in various bioactive compounds which possess antioxidant, laxative and other diverse medicinal properties. Therefore, it can be recommended as a plant of phytomedicinal value.

Design, synthesis, in silico, and in vitro evaluation of novel benzyloxybenzene substituted (S)-α-amino amide derivatives as cholinesterases and monoaminoxidases inhibitor.

In this study, a series of novel benzyloxybenzene substituted (S)-α-amino acid methyl esters and their amide derivatives were synthesized and evaluated for their inhibitory actions against acetylcholinesterase(AChE), butyrylcholinesterase(BChE), monoamine oxidase A(MAO-A), and monoamine oxidase B(MAO-B). The synthetic strategy was based on starting from benzyl bromide (5) and 4-hydroxybenzaldehyde (6). The reaction of 5 and 6 in the presence of K2 CO3 gave benzyloxybenzaldehyde 7. Benzyloxybenzene substituted (S)-α-amino acid methyl esters 11, 12, 13, (±)-19, and (±)-20 were obtained from the reaction of L-amino acid methyl esters with benzyloxybenzaldehyde (7) followed by in situ reduction with NaBH4 . The reaction of (S)-11, (S)-12, 13, (±)-19, and (±)-20 with excess ammonia gave amides (S)-14, (S)-15, 16, (±)-21, and (±)-22. The in vitro inhibitory activities of compounds against MAO-A,MAO-B, AChE, and BChEwere investigated. Within the α-amino acid methyl ester series, 13 (21.32 ± 0.338 µM) showed selectivity by inhibiting the MAO-B better than MAO-A. 13 emerged as the most active member of this series, exhibiting a 12-fold selectivity for MAO-B. 14 (4.501 ± 0.295 µM) demonstrated a pronounced selectivity for MAO-A over MAO-B, with a selectivity ratio of 110-fold. In addition, it was determined that compound 15 (95.65 ± 3.09 µM) had high selectivity for BChE inhibition. 21was demonstrated the most potent inhibition (18.36 ± 1.36 µM) against AChE.

PbS QDs and rGO-decorated PbS QDs induced optical properties variations on P3HT:PC61BM composite thin films

PbS QDs and PbS QDs decorated with reduced graphene (rGO) are prepared by hot-injection method using PbO and hexamethyldisilathiane (HMDS) as Pb and S sources, respectively. PbS QDs and PbS QDs:rGO are used as an addition to poly(3-hexylthiophene-2,5-diyl):phenyl-C61-butyric acid methyl ester (P3HT:PC61BM) composite. The effect of their addition on the morphological, topographical and optical properties of spin-coated P3HT:PC61BM thin films are investigated. These additions tune the films to be more homogenous and more flatness as investigated in terms of field scanning electron microscope. The topographical properties of the films are explored by atomic force microscope. The results show decreasing in the grain size and the surface roughness in P3HT:PbSQDs:PC61BM film compared to other composites films. The optical properties of the films are studied over the spectral range 200–2500 nm. On one hand, the absorption coefficient of different films is computed and the optical band gap of the films is found to decrease after addition of PbS QDs and PbS QDs:rGO. On the other hand, the refractive index of the films is explained according to the single-oscillator model to get the dispersion parameters. In addition, the lattice dielectric constant and the ratio of the free-carriers concertation to their effective mass are evaluated.

Unraveling the inhibitory potential of fatty acids from Cola lepidota seed against monoclonal antibody Fab fragment (9F8) (3VG0) leptin antagonism and restoration of ‘satiety’ in obesity condition: insight from quantum chemical analysis, pharmacokinetics, and molecular docking

Abstract Obesity represents a significant global health issue that continues to escalate in prevalence. Interestingly, there is a less explored connection between obesity and compromised leptin function. Prior studies have highlighted the limited availability of drugs to address this issue hence, the relentless struggle against obesity persists and the need to develop new therapeutic strategies becomes necessary. In the present study, fatty acids from the seed of Cola lepidota were utilized to prevent antibody Fab fragment (9F8) (3VG0), an antagonist of leptin from binding to the leptin pocket of the human obesity receptor (ObR) thereby restoring ‘satiety’. This study is the first to investigate the effect of plant derived fatty acids from C. lepidota seed for the purpose of reversing leptin resistance in obesity condition. Our research employed experimental GCMS extraction technique and theoretical FT-IR and UV–vis analysis and compared result with those reported in literature. All computational methodologies were carried out within the framework of density functional theory (DFT) at the B3LYP/6-311++G(d,p) level of theory while molecular docking and pharmacokinetics studies were employed to investigate the biological activities and druglikeness of the compounds. Result shows that linoleic acid (LA), methylhexadecanoate (HXD), ocatadecanoic acid methyl ester (ODA) and Bis(2-ethylhexyl) phthalate (BISP) recorded energy gaps of 2.8216 eV, 7.4230 eV, 7.4244 eV, and 5.5849 eV respectively, suggesting that LA is the most reactive while BISP is the most stable as they recorded lowest and highest energy gaps respectively. The dipole moment (μ) result shows that LA recorded the highest dipole moment at 6.1119 Debye (D) indicating that it has the highest polarizability capacity. The order of polarizability is LA > BISP > HXD > ODA. The visualized electron localization function result shows that the red regions are electron rich, followed by yellow region then green and finally blue region. Electron density was distributed within the O and H atoms of the molecules indicating strong electronegativity nature of oxygen and hydrogen atoms of the compounds. LA, ODA and HXD absorbed light at the vacuum level UV region while BISP absorbed light at the UV visible region. The compounds exhibited C–H and C–O stretching vibrations except for ODA that lacks the C–O functional group. The compounds exhibited biological activities with the target receptor protein (leptin antagonist) with bis(-2ethylhexyl) phthalate (BISP) having a docking score of −4.4 kcal/mol and containing the highest number of favorable hydrogen bond interactions with LYS41, PRO42, GLN44, GLY43 residues along the polypeptide L chain and PRO173 along the polypeptide H chain of the receptor. These interactions predominantly induced conformational changes in the amino acid sequence of the protein, thereby disrupting its three-dimensional structure and mitigating the antagonistic effects at the leptin binding domain (LBD) of the human obesity receptor (ObR), thus, effectively reversing leptin resistance in obese condition. Importantly, the pharmacokinetics revealed favorable drug-like properties with no toxicity effects with respect to hepatotoxicity, immunotoxicity, cytotoxicity, mutagenicity, carcinogenicity and did not also penetrate the blood-brain barrier (BBB) or exhibit clearance delays. The therapeutic strategy presented in this study is highly thoughtful and capable of recording huge success in obesity management, thereby reducing the burden of obesity on other chronic diseases. Therefore, these compounds have positioned themselves as promising agents in leptin resistance reversal and obesity management, warranting significant interest as potential drug candidates.

The Simulation of Ester Lubricants and Their Application in Weak Gel Drilling Fluids.

To enhance the performance and reduce the amount of ester-based lubricants used in weak gel drilling fluids, a shear dynamics simulation under extreme pressure conditions was employed to refine the formulation of the base oil and pressure additives. The simulation results were validated using fatty acid methyl, ethyl, and butyl esters. Fatty acid methyl ester demonstrated the lowest temperature increase and the highest load-bearing capacity post-shear. The four-ball friction test revealed that methyl oleate had a coefficient of friction of 0.0018, approximately a third of that for butyl oleate, confirming the simulation's accuracy. By using methyl oleate as the base oil and oleamide as the pressure-resistant component, the optimal shear stress was achieved with a 10% addition of oleamide. A lubricant composed of 90% methyl oleate and 10% oleamide was tested and showed a coefficient of friction of 0.03 when 0.5% was added to bentonite slurry, indicating a strong lubricating film. Adding 1% of this lubricant to a low gel drilling fluid system did not affect its rheological properties, and the gel structure remained stable after seven days of aging. Field tests at the Fu86-3 well in the Jiangsu Oilfield of Sinopec confirmed that adding 1% of the ester-based lubricant to the drilling fluid significantly improved drilling efficiency, reduced drag by an average of 33%, and increased the drilling rate to 22.12 m/h. This innovation effectively prevents drilling complications and successfully achieves the objectives of enhancing efficiency.

Characterization of flavor quality deterioration of postharvest Chinese bayberry (Myrica rubra cv. Dongkui) at different storage temperatures

The present study characterized the flavor quality deterioration of ‘Dongkui’ Chinese bayberry (Myrica rubra) stored at different temperatures. The fruit were stored at 0 °C, 4 °C, 10 °C and 20 °C for 12 d. The quality deterioration was characterized by combining human sensory evaluation and artificial sensory evaluation, which included e-nose and e-tongue. The sensory quality deterioration was characterized in the aspects of taste strength, bitterness, and odor, in which the odor was found to be most related to the sensory quality deterioration. In the artificial sensory evaluation, 12 e-nose sensors showed differential responses with the elongation of storage time and temperature. Based on the human sensory evaluation and the response values of the 12 e-nose sensors, the stored fruit were classified, with those stored at 20 °C for 2 d or longer and those stored at 10 °C for 7 d or longer classified as “off-flavored” fruit. The artificial neural network (ANN) model verified the classification. A total of 27 volatile compounds were identified by HS-SPME–GC–MS. Eight differential volatiles were screened out with p < 0.05 and variable importance in projection (VIP) > 1 by orthogonal partial least squares discriminant analysis (OPLS-DA). Among these volatiles, (Z)-3-hexenoic acid methyl ester and (E,E)-2,4-hexadienal decreased, while octanoic acid, acetaldehyde, ethanol, phenylethyl alcohol, 2-pentylfuran and benzaldehyde increased in the deteriorated fruit.

Predicting the bioactive compounds of Lentinula edodes and elucidating its interaction with genes associated to obesity through network pharmacology and in-vitro cell-based assay

Mushrooms are traditionally used for various medicinal purposes in traditional oriental medicine. The Japanese and Chinese are familiar with the medicinal macro fungus Lentinula edodes (Shiitake mushroom). This study aims to evaluate the role of chemical compounds from L. edodes using network pharmacology and in-vitro studies for management of Obesity. Bioactive compounds in extracts of L. edodes were identified by GC-MS analysis. Compounds were later screened for their drug-like property by Lipinski's rule. In addition, public databases (SEA, STP, Omim and DisGenet) were searched to identify genes associated with selected molecules and obesity, as well as genes that overlap obesity target genes with genes related to L. edodes. Additionally, analysis was performed using Enrichr KG to predict the disease targets of L. edodes. Finally, network was constructed between the overlapping genes and bioactive molecules using Rstudio. Further in-vitro studies were carried out using 3T3-L1 cell line. The genes related to the selected compounds and obesity were identified and overlapped. The disease targets of L. edodes was predicted by enrichment analysis and was found to be linked to obesity. Furthermore, the hub gene was found to be fatty acid amide hydrolase, and the key bioactive compound was hexadecanoic acid methyl ester. The in-vitro cell culture studies confirmed the inhibition of adipogenesis in mushroom extract-treated 3T3-L1 cells and the augmentation of adiponectin. The study suggests that the hub gene fatty acid amide hydrolase might alleviate obesity by inhibiting arachidonoyl ethanolamide signaling, which would enhance the action of fatty acid amide hydrolase and limit appetite in L. edodes extract.

Effect of citric acid on cell membrane structure and function of Issatchenkia terricola WJL-G4.

This study aimed to investigate the changes of cell membrane structure and function of Issatchenkia terricola under citric acid by performing physiological analysis. The membrane integrity, surface hydrophobicity, structure, fluidity, apoptosis, and fatty acid methyl esters composition of I. terricola WJL-G4 cells were determined by propidium iodide staining, microbial adhesion to hydrocarbon test, transmission electron microscopy analysis, fluorescence anisotropy, flow cytometry, and gas chromatography-mass, respectively. The results showed that with the increasing of citric acid concentrations, the cell vitality, membrane integrity, and fluidity of I. terricola reduced; meanwhile, apoptosis rate, membrane permeable, hydrophobicity, and ergosterol contents augmented significantly. Compared to control, the activities of Na+, K+-ATPase, and Ca2+, Mg2+-ATPase increased by 3.73-fold and 6.70-fold, respectively, when citric acid concentration increased to 20g l-1. The cells cracked and their cytoplasm effused when the citric acid concentration reached 80g l-1. I. terricola could successfully adjust its membrane structure and function below 60g l-1 of citric acid. However, for citric acid concentrations above 80g l-1, its structure and function were dramatically changed, which might result in reduced functionality.

Fluorinated organic ammonium salt passivation for high-efficiency and stable inverted CsPbI2Br perovskite solar cells.

All-inorganic CsPbI2Br inverted perovskite solar cells (PSCs) have drawn increasing attention because of their outstanding thermal stability and compatible process with tandem cells. However, relatively low open circuit voltage (Voc) has lagged their progress far behind theoretical limits. Herein, we introduce phenylmethylammonium iodide and 4-trifluoromethyl phenylmethylammonium iodide (CFPMAI) on the surface of a CsPbI2Br perovskite film and investigate their passivation effects. It is found that CFPMAI with a -CF3 substituent significantly decreases the trap density of the perovskite film by forming interactions with the under-coordinated Pb2+ ions and effectively suppresses the non-radiative recombination in the resulting PSC. In addition, CFPMAI surface passivation facilitates the optimization of energy-level alignment at the CsPbI2Br perovskite/[6,6]-phenyl C61 butyric acid methyl ester interface, resulting in improved charge extraction from the perovskite to the charge transport layer. Consequently, the optimized inverted CsPbI2Br device exhibits a markedly improved champion efficiency of 14.43% with a Voc of 1.12V, a Jsc of 16.31 mA/cm2, and a fill factor of 79.02%, compared to the 10.92% (Voc of 0.95V) efficiency of the control device. This study confirms the importance of substituent groups on surface passivation molecules for effective passivation of defects and optimization of energy levels, particularly for Voc improvement.

Optimization of methyl ester synthesis using gas/liquid phase pulsed discharge plasma in a novel oscillatory slug flow reactor

In the present research, an innovative oscillatory slug flow reactor (OSFR) under the treatment of gas–liquid phase pulsed discharge plasma was developed for biodiesel production. The main goal was continuous production of high quality biodiesel at low temperature and pressure. Experimental tests were carried out under the influence of four main operating parameters including applied voltage, molar ratio, reactant flow rate, and catalyst concentration. The response surface method was employed to optimize experimental tests. The results showed that the proposed technology provided 94% production efficiency under the optimal conditions of voltage 19.4 kV, molar ratio 6.4, flow rate 2.7 ml/s, and catalyst 0.9 wt. %. According to the statistical analysis, increasing the applied voltage and reducing the flow rate have a strong effect on the Fatty Acid Methyl Ester yield, while the concentration of potassium hydroxide and methanol have less effect on the overall efficiency. In addition, the characteristics of the produced biodiesel were in accordance with ASTM D6751 standards. Surprisingly, the optimal energy consumption in this system was 95 kJ/l, which is more economically viable. In general, this study showed that the combined system of gas/liquid phase plasma in the OSFR reactor has a high synergistic potential for the transesterification reaction.

Utilization of Dairy Waste Scum Oil for Microwave-Assisted Biodiesel Production over KOH-Waste Eggshell based Calcium Oxide Catalyst

The sustainability can be maintained by utilizing the available waste as feedstock and catalysts such as dairy and eggshell waste respectively for biodiesel production. In this study, the calcium oxide (CaO) synthesized from calcined eggshell was doped with potassium hydroxide (KOH-ECaO) via wet impregnation method and analyzed the catalyst performance on biodiesel production from dairy waste scum oil (DWSO) via microwave-assisted transesterification. The catalyst was characterized by X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR), Scanning Electron Microscopy equipped with Energy Dispersive X-ray (SEM-EDX), Brunauer-Emmett-Teller (BET) and Thermogravimetric analysis (TGA). The fatty acid methyl ester (FAME) contents were deduced by Gas Chromatography-Mass Spectrometry (GC-MS). The KOH-ECaO catalyst shows good potential based on the characterization analysis such as high pore size (25.5 nm) which is supported by SEM pattern analysis. The highest biodiesel production (75%) was obtained at optimum reaction parameters conditions. The optimized conditions were discovered to be 3 wt.% of catalyst, 16:1 of methanol to oil molar ratio, reaction temperature of 65°C and 15 minutes of reaction time as microwave provided faster reaction for the transesterification. These innovative results showed that KOH-ECaO could enhance the biodiesel production from DWSO which encourage the usage of waste for wealth product.

Investigating the Quality and Purity Profiles of Olive Oils from Diverse Regions in Selçuk, İzmir.

The Selçuk district of Izmir is one of the most essential regions in terms of olive oil production. In this study, 60 olive oil samples were obtained from five different locations (ES: Eski Şirince Yolu, KK: Kınalı Köprü, AU: Abu Hayat Üst, AA: Abu Hayat Alt, and DB: Değirmen Boğazı) in the Selçuk region of Izmir during two (2019-2020 and 2020-2021) consecutive cropping seasons. Quality indices (free acidity, peroxide value, p-Anisidine value, TOTOX, and spectral absorption at 232 and 270 nm) and the fatty acid, phenolic, and sterol profiles of the samples were determined to analyze the changes in the composition of Selcuk olive oils according to their growing areas. When the quality criteria were analyzed, it was observed that KK had the lowest FFA (0.11% oleic acid, PV (6.66 meq O2/kg), p-ANV (11.95 mmol/kg), TOTOX (25.28), and K232 (1.99) values and K270 had the highest value. During the assessment of phenolic profiles, the ES group exhibited the highest concentration of the phenolic compound p-HPEA-EDA (oleocanthal), with a content of 93.58 mg/kg, equivalent to tyrosol. Upon analyzing the fatty acid and sterol composition, it was noted that AU displayed the highest concentration of oleic acid (71.98%) and β-sitosterol (87.65%). PCA analysis illustrated the distinct separation of the samples, revealing significant variations in both sterol and fatty acid methyl ester distributions among oils from different regions. Consequently, it was determined that VOOs originating from the Selçuk region exhibit distinct characteristics based on their geographical locations. Hence, this study holds great promise for the region to realize geographically labeled VOOs.

Chaenomelin, a New Phenolic Glycoside, and Anti-Helicobacter pylori Phenolic Compounds from the Leaves of Salix chaenomeloides.

Salix chaenomeloides Kimura, commonly known as pussy willow, is a deciduous shrub and tree belonging to the Salicaceae family. The genus Salix spp. has been known as a healing herb for the treatment of fever, inflammation, and pain relief. The current study aimed to investigate the potential bioactive natural products from S. chaenomeloides leaves and evaluate their antibacterial activity against Helicobacter pylori. A phytochemical investigation of the ethanol (EtOH) extract of S. chaenomeloides leaves led to the isolation of 13 phenolic compounds (1-13) from the ethyl acetate (EtOAc) fraction, which showed antibacterial activity against H. pylori strain 51. The chemical structure of a new phenolic glycoside, chaenomelin (1), was established by a detailed analysis of 1D and 2D (1H-1H correlation spectroscopy (COSY), heteronuclear single-quantum coherence (HSQC), and heteronuclear multiple-bond correlation (HMBC)) nuclear magnetic resonance (NMR), high-resolution electrospray ionization mass spectroscopy (HR-ESIMS), and chemical reactions. The other known compounds were identified as 5-O-trans-p-coumaroyl quinic acid methyl ester (2), tremulacin (3), citrusin C (4), benzyl 3-O-β-d-glucopyranosyl-7-hydroxybenzoate (5), tremuloidin (6), 1-[O-β-d-glucopyranosyl(1→2)-β-d-glucopyranosyl]oxy-2-phenol (7), arbutin cinnamate (8), tremulacinol (9), catechol (10), 4-hydroxybenzaldehyde (11), kaempferol 3-rutinoside (12), and narcissin (13), based on the comparison of their NMR spectra with the reported data and liquid chromatography/mass spectrometry (LC/MS) analysis. The isolated compounds were evaluated for antibacterial activity against H. pylori strain 51. Among the isolates, 1-[O-β-d-glucopyranosyl(1→2)-β-d-glucopyranosyl]oxy-2-phenol (7) and arbutin cinnamate (8) exhibited antibacterial activity against H. pylori strain 51, with inhibitions of 31.4% and 33.9%, respectively, at a final concentration of 100 μM. These results were comparable to that of quercetin (38.4% inhibition), which served as a positive control. Generally, these findings highlight the potential of the active compounds 7 and 8 as antibacterial agents against H. pylori.

Novel benzene sulfonamides with acetylcholinesterase and carbonic anhydrase inhibitory actions.

A series of benzene sulfonamides 15-26 were synthesized and determined for their in vitro and in silico inhibitory profiles towardacetylcholinesterase (AChE) and carbonic anhydrases (CAs). Commercially available 3,4-dimethoxytoluene was reacted with chlorosulfonic acid to furnish benzene sulfonyl chloride derivatives. The reaction of substituted benzene sulfonyl chloride with some amines also including (±)-α-amino acid methyl esters afforded a series of novel benzene sulfonamides. In this study, the enzyme inhibition abilities of these compounds were evaluated against AChE and CAs. They exhibited a highly potent inhibition ability on AChE and -CAs (Ki values are in the range of 28.11 ± 4.55 nM and 145.52 ± 28.68 nM for AChE, 39.20 ± 2.10 nM to 131.54 ± 12.82 nM for CA I, and 50.96 ± 9.83 nM and 147.94 ± 18.75 nM for CA II). The present newly synthesized novel benzene sulfonamides displayed efficient inhibitory profiles against AChE and CAs, and it is anticipated that they may emerge as lead molecules for some diseases including glaucoma, epilepsy, and Alzheimer's disease.

Hybrid Organic-Inorganic ZnO/PCBM Electron Transport Layer with Organic Lead Halide Perovskite Solar Cell Materials CH3NH3PbIX2, X is Cl or I

An experimental investigation has been undertaken to explore a variety of properties of organic perovskite solar cells (OPSCs) that are distinct in their photovoltaic response. In this study, OPSCs were constructed using zinc oxide, ZnO and [6,6]-phenylC[Formula: see text]-acid methyl ester, PCBM, as electron transfer materials (ETM), poly(3-hexylthiophene), P3HT, as hole transport material (HTM), and CH3NH3PbIX2 as a photosensitizer, where X is either Cl or I. The structural and optical characteristics of the ETM and HTM layers and the perovskite materials of OPSCs were investigated. The [Formula: see text]–[Formula: see text] and [Formula: see text]–[Formula: see text] curves of each solar cell prepared in OPSCs were measured using an integrated cell tester. This comprises a photovoltaic [Formula: see text]–[Formula: see text] measurement system and a solar simulation system. As a result of these results, the OPSC’s performance is evaluated. The calculations in this work suggest that the highest power conversion efficiency (PCE = 6.31%) was achieved in photovoltaic devices using CH3NH3PbI3 as the effective absorber layer and ZnO with PCBM as the ETM layer. At a light intensity of 100 mW/cm2, each OPSC cell was performed. Under the same conditions, the [Formula: see text]–[Formula: see text] curves were evaluated for each OPSC device. By improving the selection of organic and inorganic active materials in the ETM layer, OPSC performance may be improved.

Evaluation of Fatty Acid Methyl Esters (FAME) as a Green Alternative to Common Solvents in Conservation Treatments

This study investigates the potential of fatty acid methyl esters (FAME) as environmentally sustainable alternatives to traditional solvents for the removal of low-polarity materials commonly found in cultural heritage artefacts. Recognizing the environmental and health concerns associated with conventional solvents, this research focuses on FAME to remove low/non-polarity or non-polar substances used in cultural heritage preservation. Laboratory samples coated with low molecular synthetic resins (LMW) such as Regalrez 1094 and microcrystalline wax were treated with FAME applied in gel to prevent solvent–substrate interactions. Photographic documentation under UV-vis light, optical microscope observations, and spectrocolorimetric analysis were used for assessing surface “cleanness”, while FTIR-ATR spectroscopy was used to detect possible residue from treatment. Moreover, SEM analysis was used for a better understanding of the results. The best results were obtained using FAME base on methyl stearate according to Hansen-RED.

Chemical Characterization, Phenolic Compounds Quantification, and Assessment of Antioxidant and Anti-Acetylcholinesterase Activities of Byrsonima sericea DC fruits.

Byrsonima sericea is a species native to Brazil that is widely used in traditional medicine. The seed ethanol extract (SEE) had the highest content of total phenols (179.35 mg GAE g-1 extract) and flavonoids (10.42 mg QE g-1 extract) and was the most active in relation to antioxidant activity (DPPH: IC50 =4.25 μg mL-1 and ABTS: IC50 =4.82 μg mL-1 ). The peel/pulp ethanol extract (PEE) had the best anticholinesterase activity (IC50 =6.02 μg mL-1 ). Chromatographic investigation identified gallic acid, isoquercitrin, quercetin and amentoflavone in SEE, and gallic acid, isoquercitrin, quercetin and rutin in PEE. Six fatty acid methyl esters and seven triterpenes were identified, highlighting oleic acid in the seed hexane extract (61.85 %) and in the peel/pulp hexane extract (52.61 %), and betulin in the peel/pulp hexane extract (5.25 %). The substances and biological activities identified in B. sericea characterize this fruit as a functional food for future studies.

Efficient and robust ultrathin porous carbon encapsulated Ni–Sn intermetallic compounds derived from metal–organic frameworks for in-situ aqueous phase deoxygenation of fatty acid methyl esters

Deoxygenation of fatty acid esters in aqueous phase using in-situ generated H2 has emerged as a promising approach to producing sustainable diesel-like hydrocarbons. In this study, we employed a solvothermal method to synthesize novel Ni–Sn metal–organic frameworks (MOFs) with a homogeneous distribution of Ni and Sn elements. Subsequently, various Ni–Sn intermetallic compounds (IMCs) encapsulated with a porous carbon layer (<3 nm) (Ni–Sn IMC@C) were prepared through the facile pyrolysis of metal–organic frameworks under a controlled N2 atmosphere. Applying methyl palmitate as model reactant and methanol as hydrogen donor, Ni3Sn2 IMC@C gives approximately 100% conversion and 93% yield towards n-C15 and n-C16 alkanes at 330 °C, without significant deactivation during the recycling for five times. The deoxygenation pathway is dominated by decarbonylation (DeCO) on Ni–Sn IMCs. In Ni–Sn IMCs, the oxophilic nature of Sn, along with its charge transfer with Ni, enhances the adsorption of an η2(C, O)-aldehyde configuration. The strategic isolation of adjacent Ni by Sn effectively inhibits methanation and C–C bond hydrolysis, reducing H2 consumption and increasing carbon yield. Moreover, the ultrathin porous carbon encapsulation not only prevents the loss and sintering of Ni3Sn2 IMC under harsh hydrothermal condition but also mitigates mass transfer limitation. Surface oxidation of Ni3Sn2 IMC, particularly the formation of SnO2, is detrimental to deoxygenation. Additionally, Ni3Sn2 IMC@C exhibits high hydrocarbon yields (>89.6%) in in-situ aqueous phase deoxygenation of methyl laurate, methyl stearate and methyl oleate. These findings highlight the remarkable potential of MOF-derived catalysts for hydrothermal deoxygenation.

Effective surface passivation for stable and high-performance inverted CsPbI2Br perovskite solar cells with efficiency over 15%

Inverted CsPbI2Br perovskite solar cells (PSCs) still suffer from substantially non-radiative recombination losses at the perovskite interface, which limits the future advancement of CsPbI2Br perovskite-based single- and multi-junction photovoltaic cells. Interfacial defect passivation of perovskite films is an effective approach for enhancing the performance of PSCs. In this study, we introduce thiophene halide salts with different side groups on the surface of CsPbI2Br films to passivate the inorganic perovskite film and investigate their passivation effects. Our studies show that the 2-thiophenemethylammonium iodide (TM) passivator with –CH2NH3I side group effectively mitigates the trap density of the perovskite film by forming coordination bonding with Pb2+ ions, thus significantly inhibiting the non-radiative recombination in the resulting PSC. In addition, after the TM treatment, the better energy-level alignment between the CsPbI2Br/[6,6]-Phenyl C61 butyric acid methyl ester (PCBM) interface is achieved, thus enhancing the charge extraction from perovskite to the charge transport layer. The resulting inverted CsPbI2Br device demonstrates a significantly enhanced champion efficiency of 15.07% with a Voc of 1.16 V, Jsc of 16.42 mA/cm2, and FF of 79.11%, compared to the 11.19% efficiency of the control device, and maintains >97% of the initial efficiency after being stored for over 1700 h in N2 atmosphere. This work confirms the importance of substituent groups on surface passivation molecules for effective passivation of defects and optimization of energy levels, particularly for Voc improvement.