Aqueous Research Articles

Berberine hydrochloride-loaded lipid-based nanoparticles ameliorate β-cell function by targeting Nrf2/NF-κB signaling pathway in alloxan-induced diabetes using a murine model: Optimization through full factorial design

Berberine hydrochloride (BH), a naturally occurring alkaloid having pleiotropic biological effects, is characterized by high water solubility, poor bioavailability, and a brief half-life. The objective of this study was to develop a liposomal formulation of BH that is more accessible and to ascertain whether its intraperitoneal administration might mitigate pancreatic tissue damage in rats that have been induced by alloxan. Rats were divided into four groups: control, alloxan, metformin, and BH-liposomes (BH-Lip). Measurements of blood glucose, insulin, pancreatic antioxidant state, and pro-inflammatory mediators were used to assess the severity of pancreatic injury in rats among all groups. According to the results, BH-Lip reduced the extent of alloxan-induced pancreatic tissue damage in rats, as demonstrated by improved HOMA-IR and HOMA-β scores, insulin, total pancreatic antioxidant capacity, and lower blood glucose levels. Furthermore, BH-Lip boosted the antioxidant transcription factor Nrf2 and downregulated the mRNA expression of pancreatic pro-inflammatory mediators, such as NF-κB and NLRP3. Moreover, immuno-histochemical labeling revealed that BH-Lip inhibited the protein transcription of caspase-3 and TNF-α in the pancreatic tissues of alloxan-treated rats. These findings provide BH-Lip as a safe substitute for traditional antidiabetics by reducing pancreatic tissue damage caused by alloxan via targeting the Nrf2/NF-κB pathway.

Removal of ivermectin from aqueous medium on chitosan-based magnetic adsorbent

This work focused on the uptake of ivermectin from aqueous media using chitosan derivative as an adsorbent material. The adsorbent was synthesized through the co-precipitation approach, controlling the iron oxide quantity on the polymer surface. FTIR, XRD, SEM, EDS, XPS, textural properties, and surface charge characterized magnetic chitosan (CS⋅Fe3O4). The adsorption efficiency was affected by different experimental conditions, especially by adsorbent dosage and ionic strength. The shifts in the FTIR spectrum of CS⋅Fe3O4 after adsorption suggest the occurrence of hydrogen bonds between the adsorbent surface and adsorbate molecules. The kinetic modeling showed that the Elovich model was well suitable to describe the kinetic data. Meantime, the Sips and Liu models described well the adsorption isotherms. The maximum adsorption capacity (81.86 mg g−1) was reached at pH 7.0 and 298 K, using an adsorbent dosage of 0.6 g L−1. Thermodynamic parameters indicated that the process was spontaneous and exothermic. The regeneration and reuse assays displayed that the recovery of adsorbent was more effective using ethyl alcohol than sodium hydroxide.

Droplet-based microfluidics for engineering shape-controlled hydrogels with stiffness gradient

Current biofabrication strategies are limited in their ability to replicate native shape-to-function relationships, that are dependent on adequate biomimicry of shape, size and spatial heterogeneity, within cell-laden hydrogels. In this study, a diffusion-based microfluidics platform is presented that meets these needs in a two-step process. In the first step, a hydrogel-precursor solution is dispersed into a continuous oil phase within the microfluidics tubing. By adjusting the dispersed and oil phase flow rates, the physical architecture of hydrogel-precursor phases can be adjusted to generate spherical and plug-like structures, as well as continuous meter-long hydrogel-precursor phases (up to 1.75 m). The second step involves the controlled introduction a small molecule-containing aqueous phase through a T-shaped tube connector to enable controlled small molecule diffusion across the interface of the aqueous phase and hydrogel-precursor. Application of this system is demonstrated by diffusing co-initiator sodium persulfate (SPS) into hydrogel-precursor solutions, where the controlled SPS diffusion into the hydrogel-precursor and subsequent photo-polymerization allows for the formation of unique radial stiffness patterns across the shape- and size-controlled hydrogels, as well as allowing the formation of hollow hydrogels with controllable internal architectures. Mesenchymal stromal cells are successfully encapsulated within hollow hydrogels and hydrogels containing radial stiffness gradient. The cells are observed to respond to the microscale spatial heterogeneity as evidenced by increased cell elongation in softer core regions of the hydrogel as compared to the peripheral stiffer hydrogel regions, as well as stiffness-dependent nuclear accumulation of the yes-associated protein mechano-regulator. Finally, breast cancer cells are found to phenotypically switch in response to stiffness gradients, causing a shift in their ability to aggregate, which may have implications for metastasis. The diffusion-based microfluidics will mimic native shape-to-function relationship and provides a platform to further study the roles of micro- and macroscale architectural features that exist within native tissues.

Synthesis, characterization and photoelectrochemical performance of Bi2Fe4O9 thin films

Mullite-type Bi2Fe4O9 has been little explored in thin film form as a photoanode for photoelectrochemical water splitting. In this study, Bi2Fe4O9 thin films have been prepared using the sol-gel technique from a simple precursor solution based on the corresponding metal salts, acetic acid, and polyvinyl alcohol. The films were deposited by dip-coating onto fluorine-doped tin oxide substrates and dried at 350 °C, repeating the dipping-drying cycle six times, and finally sintered at 600 °C. The films were characterized by GIXRD, revealing the formation of the material in its orthorhombic phase. Raman spectroscopy showed the Ag and B1g vibrational modes, validating the formation of the bismuth iron oxide. UV–Vis transmittance measurements revealed that the material exhibits two optical transitions: a direct band gap of 2.86 eV and an indirect band gap of 1.98 eV. FESEM micrographs and AFM images showed a uniform nanostructured surface morphology. The photoelectrochemical properties of the Bi2Fe4O9 films were studied using cyclic voltammetry and chronoamperometry with front side illumination, demonstrating the stability of the material in aqueous media and the generation of photocurrent in the presence of H2O2. Furthermore, results from intensity-modulated photocurrent spectroscopy (IMPS) revealed that the photocurrent is limited by both bulk and surface recombination and a short hole diffusion length.

Effect of Stearyl Methacrylate Comonomer on the Mechanical and Physical Properties of Dimethacrylate-Based Dental Resins.

This study evaluated the effect of stearyl methacrylate addition on the physical and mechanical properties of bisphenol A glycidyl methacrylate- and triethylene glycol dimethacrylate-based polymers, which are traditionally used in dental applications. Methacrylate-based monomer compositions are polymerized under the visible blue light spectrum. An analysis of double bond conversion, surface microhardness test, three-point bending test and water sorption and water solubility were tested to determine the physical and mechanical properties of the dental polymers. The results indicated that stearyl methacrylate addition up to 25 wt% reduced the water sorption of the polymers. At amounts of stearyl methacrylate higher than 25 wt%, the solubility of the polymer in water increases due to the monofunctional structure. Mechanical properties are negatively affected by the increasing stearyl methacrylate ratio. Further, the addition of stearyl methacrylate slightly increased thermal stability. As such, the amount of stearyl methacrylate in a polymer composition is critical for the optimization of its mechanical and physical properties. According to the results, the amount of stearyl methacrylate has to be between 12.5-25 wt%.

Research on compound amidohydroxysulfobetaine foamer for high-temperature and high-salinity clastic reservoirs

A high-quality foaming agent should exhibit excellent solubility in formation water and strong foaming ability, while also meeting the requirements of stability under high-temperature and high-salinity conditions, as well as low adsorption capacity. This study explores the potential of amidohydroxysulfobetaine surfactant as a foaming agent in sandstone reservoirs under specific reservoir conditions of 110 ℃ and 25.0×104 mg/L salinity. The findings indicate that compounding EHSB with a small amount of LHSB to form LA13 significantly reduces the Krafft point of EHSB. Furthermore, LA13 demonstrates outstanding solubility in 25.0×104 mg/L brine and exhibits an overall adsorption capacity on quartz sand surfaces lower than 0.6 mg/g when its concentration is below 1.0 wt%. Performance evaluation of bulk foam for LA31 at concentrations ranging from 0.05 wt% to 0.4 wt% suggests that using a foaming agent concentration of 0.05 wt% results in relatively low foaming volume and foam decay half-life; however, consistent foaming performance is observed across other concentrations, leading to highly stable foam due to the compound system's higher surface dilational modulus being the primary factor contributing to foam stability. Flow experiments reveal that the foam generated in cores with permeabilities of 46.5 mD, 185.5 mD, 632.0 mD, and 2005.3 mD exhibits a high resistance factor when the concentration of LA13 exceeds 0.1 wt%, while also demonstrating commendable gas-channeling regulation capability. Therefore, it is recommended to use LA13 as a foaming agent for field applications when its concentration surpasses 0.1 wt%. Additionally, comparing the mobility of foam formed by concentrations of 0.1 wt% and 0.2 wt% LA13 in cores with varying permeabilities shows that LA13 exhibits selective mobility regulation specifically in cores with permeabilities lower than 632.0 mD.

Hydrothermal carbonization of combined food waste: A critical evaluation of emergent products

Hydrothermal carbonization (HTC) increasingly appears as an eco-friendly method for managing food waste (FW). In this work, a combination of FW was subjected to HTC, and products were critically evaluated. This involved a lab-scale pressure reactor and optimization of HTC conditions: temperature (220–340 °C) and residence time (90–260 min) via central composite design type of response surface methodology (CCD-RSM). Results showed varying temperatures and residence time to impact the hydrochar (HC) and hydrothermal carbonization aqueous phase (HTC-AP) properties. Although HC produced through HTC exhibited lower ash content (<2%) despite higher fixed carbon (>55 %) with respect to the raw FW, the heating value of HC ranged from 19.2 to 32.5 MJ/kg. Temperature primarily influenced FW conversion, affecting carbonaceous properties. Saturated fatty acids (SFA) were found to be predominant in the HTC-AP under all tested operating conditions (77.3, 48.4, and 37.1 wt% for HTC at 340, 280, and 220 °C in 180 min, respectively). Total phosphorus recovery in HC and HTC-AP respectively peaked at 340 °C and 220 °C in 180 min. The study concludes that HTC holds promise for energy-dense biofuel production, nutrient recovery, and fostering a circular economy.

Encapsulation of resveratrol in alginate microcapsules using internal gelation technique: Fabrication, characterization and release kinetics

Resveratrol (RES) is a proven anticancer, antioxidant, anti-inflammatory, and cardioprotective compound. However, low bioavailability, poor water solubility, and sensitivity to UV light and heat limit RES's use in food applications. In this study, we aim to protect RES by encapsulating it in sodium alginate (NaAlg) matrix using internal gelation, followed by drying the moist microencapsulates using spray and freeze-drying techniques. The spray-dried microencapsulates exhibited a smaller mean diameter (5.57 ± 2.40 μm), higher encapsulation efficiency (91.32 ± 1.98%), and higher ζ-potential (−61.9 ± 2.33 mV) compared to freeze-dried microencapsulates. SEM images revealed the smooth and spherical surface of the spray-dried microencapsulates, while the freeze-dried samples exhibited irregular shapes and porous textures. FTIR results showed polyelectrolyte interactions between NaAlg, RES, and CaCO3. XRD and DSC results confirmed the incorporation of RES in the NaAlg matrix. Spray-dried microencapsulates demonstrate the highest RES retention of 80.89 ± 0.70% and 78.59 ± 0.27% after 4 h of UV light and thermal treatments, respectively. In vitro release studies showed that spray-dried microencapsulates demonstrate a delayed gastric release compared to freeze-dried microencapsulates. The release mechanism of RES from the microencapsulates was effectively described by the Shalin-Peppas model.

Preparation and Properties of Polyimide/Polysulfonamide/Polyethylene Glycol (PI/PSA/PEG) Hydrophobic Nanofibrous Membranes.

In this study, polyimide (PI) and polysulfonamide (PSA) were used as base materials, and polyethylene glycol (PEG) was added to successfully prepare PI/PSA/PEG nanofiber membranes through electrospinning technology. Subsequently, water etching was performed on the membranes, utilizing the water solubility of PEG to form the rough wrinkled structure, further enhancing the surface hydrophobicity. The experimental results showed that under the conditions of a spinning voltage of 10 kV, PI/PSA mass fraction of 15 wt.%, and PEG-to-PI/PSA mass ratio of 1/3, the obtained fiber membranes exhibit a uniform morphology (an average diameter of 0.73 µm) and excellent hydrophobicity (the initial water contact angle (WCA) reaching 130.4°). After PEG water etching, the surface of the PI/PSA/PEG hydrophobic membranes formed the rough wrinkled structure, which not only improved their mechanical properties but also further enhanced their hydrophobicity (the initial WCA increasing to 137.9°). Hence, fiber membranes are expected to have broad application prospects in fields such as waterproofing and moisture permeability.

Effects of microencapsulated phenethyl isothiocyanate on gastrointestinal cancer cells and pathogenic bacteria

Gastrointestinal cancers remain a global health burden, demanding more effective prevention and treatments. Phenethyl isothiocyanate (PEITC), a compound derived from cruciferous vegetables, stands out as a promising nutraceutical agent due to its chemopreventive and therapeutic properties. However, its therapeutic translation remains limited mainly due to its poor water solubility and rapid metabolism. Herein, we encapsulated PEITC into biocompatible chitosan-based microparticles with an extra virgin olive oil core to improve its bioavailability and stability. Pure PEITC's biocompatibility and microencapsulated PEITC's stability and antibacterial activity were evaluated. The antibacterial activity analysis showed microencapsulated PEITC as a promising antibacterial agent against gastrointestinal pathogenic bacteria (two Gram-positive and two Gram-negative). The impact of both pure and microencapsulated PEITC was assessed on gastrointestinal cancer cells (MKN45 gastric cancer and SW48 colon cancer cell lines). PEITC exhibited threshold or hormetic dose-dependent toxicity in colon fibroblasts and decreased gastric cancer cells' migration capacity, enhanced upon encapsulation into microparticles. In addition, microencapsulated PEITC induced downregulation of phosphorylated AKT, FAK, and ERK1/2 proteins, disrupting motility signaling pathways and tubulin expression. These findings suggest that the delivery of PEITC via chitosan-based microparticles holds promise as a nutraceutical delivery strategy against gastrointestinal disorders that predispose to cancer.

High-carbon-content biochar from chemical manufacturing plant sludge for effective removal of ciprofloxacin from aqueous media

Biochar is considered a promising biosorbent for harmful organic pollutants in aqueous media. However, only a limited number of biochars derived from industrial sludges have been utilized due to their problematic high ash content and heavy metal leaching. In this study, a highly effective biochar was prepared as a superabsorbent for ciprofloxacin (CIP) from chemical manufacturing plant sludge via K2CO3-activated pyrolysis, and its CIP removal behavior was evaluated. Unlike sewage sludge, chemical manufacturing plant sludge contains low SiO2, resulting in an ultra-pure carbon (95.4%) based biochar with almost negligible ash content. As the pyrolysis temperature increased from 400 to 800 °C, the ordered graphitic carbon structure transformed into an amorphous carbon phase, and most oxygen-containing groups disappeared. However, the pore size significantly decreased to ∼4.5 nm due to the corrosive carbon volatilization caused by K2CO3, resulting in an extremely large surface area of 2331.8 m2/g. Based on its large surface area and porous carbon structure, the activated biochar at 800 °C (CAB-800) exhibited an outstanding CIP adsorption capacity of 555.56 mg/g. The CIP adsorption isotherm, kinetic, and thermodynamic studies were systematically investigated. The CIP adsorption on CAB-800 was mainly attributed to π-π interactions and hydrogen bond formation, with electrostatic interactions partially contributing to the adsorption reaction. From pH 2 to 12, CAB-800 showed an excellent CIP adsorption capacity of over 316.7 mg/g, with adsorption favored under acidic conditions. Except for HCO3− and CO32−, the presence of anions and humic acids did not significantly affect CIP adsorption capacity. These results demonstrate that biochar produced from chemical manufacturing industry sludge via K2CO3 activation is a highly feasible material for the removal of CIP from aqueous media.

A Hydrogen Bonded Non-Porous Organic-Inorganic Framework for Measuring Cysteine in Blood Plasma and Endogenous Cancer Cell.

An imbalance in cysteine (Cys) levels in the cells and plasma has been identified as the risk indicator for various human diseases. The structural similarity of cysteine with its congener homocysteine and glutathione offers challenges in its measurement. Herein, we report a hydrogen-bonded organic-inorganic framework of Cu(II) (HOIF) for the selective detection of cysteine over other biothiols. The non-fluorescent HOIF showed 12-fold green emission in the presence of cysteine. The monomeric unit of HOIF is stabilized via intermolecular hydrogen bonds, resulting in a non-porous network structure. Non-interference from homocysteine, glutathione, and other competitive bio-analytes revealed explicit affinity of HOIF for cysteine. Fluorimetric titration showed a wide working concentration window (650 nM-800 μM) for measuring cysteine in an aqueous medium. The mechanistic investigation involving HRMS, EPR, and UV-vis spectroscopic studies revealed the decomplexation of HOIF with Cys, resulting in a fluorescence turn-on response from the luminescent ligand. Validation using a commercial dye, "Cysteine Green", confirmed the prospect of HOIF for early diagnostic purposes. Utilizing the fluorescence turn-on property of HOIF in the presence of cysteine, we measured cysteine quantitatively in the blood plasma samples. Bio-imaging of endogenous cysteine in cancer cells indicated the ability of HOIF to monitor the intracellular cysteine.

Bridging pyrimidine hemicurcumin and Cisplatin: Synthesis, coordination chemistry, and in vitro activity assessment of a novel Pt(II) complex

In the upcoming decades, the incidence and mortality rates of cancer are expected to rise globally, with colorectal and prostate cancers among the most prevalent types. Despite advancements in molecular targeted therapy, platinum-based chemotherapies remain the cornerstone of treatment, especially for colorectal and prostate cancer, with oxaliplatin and cisplatin being extremely effective due to their DNA-targeting capabilities. In our pursuit of new platinum-based chemotherapeutics that are potentially less toxic and more effective, we have explored the combination of the Pt-binding groups of the diaminocyclohexane ring used in oxaliplatin, with the stable amino-pyrimidine hemicurcumin moiety. This new derivative exhibit improved stability in physiological conditions and increased solubility in aqueous media, demonstrating promising effects on cell proliferation of both colorectal and prostate cells. We report herein the complete synthesis and chemical characterization in solution of the new derivative [(1R,2R)-N1-(3-(4-((E)-2-(2-Amino-6-methylpyrimidin-4-yl)vinyl)-2-methoxyphenoxy) propyl) cyclohexane-1,2-diamine] (MPYD). Our analysis includes an examination of its acid-base equilibria, speciation and stability in physiological conditions. The synthesis and in situ formation of Pt(II) complexes were investigated by nuclear magnetic resonance spectroscopy, while density functional theory calculations were employed to elucidate the chemical structure in solution. Results on the biological activity were obtained through cell viability assays on different colorectal and prostate cell lines (HCT116, HT29, PC3 and LNCaP).

Enhancing recovery of gold(III) from hydrochloric acid solutions using gemini surfactant microemulsions: The effect of spacer group

The recovery of precious metals from waste has garnered significant attention owing to their non-renewable nature and essential role in the burgeoning information industry. However, enhancing the extraction efficiency of microemulsions remains a significant challenge. In this study, three water-in-oil microemulsions were formulated using gemini surfactants with different spacers (14-OH-14, 14-SO4-14, and 14-3-14) as emulsifiers, supplemented with n-butanol as a cosurfactant, n-heptane as the oil phase, and NaCl aqueous solution as the internal aqueous phase. These microemulsions were employed for the extraction of gold(III) from hydrochloric acid solutions. The results illustrate that all three microemulsions effectively extracted gold(III) through a spontaneous, exothermic, enthalpy-driven anion-exchange mechanism, achieving notable extraction efficiency. In contrast to 14-3-14, incorporating –OH into the spacer significantly augments the positive electrostatic potential through the cationization of –OH in an HCl solution, resulting in a higher binding constant (2.43) and thereby improving the extraction efficiency. However, the presence of −SO4 diminishes the positive electrostatic potential through partial neutralization, resulting in a lower binding constant (1.17), which is detrimental to the extraction process. Response surface optimization revealed that concentrations of C(14-OH-14) and V(1-butanol) significantly influence extraction efficiency and exhibit pronounced interaction. At optimal conditions (C(14-OH-14) = 0.09 mol·L−1, V(1-butanol) = 47.41 %, R=20, and C(NaCl) = 1.57 mol·L−1), over 95.54 % of gold(III) can be extracted from actual e-waste solutions. This study offers an alternative approach for designing or selecting surfactants in microemulsion-based extraction of gold(III) from e-waste.

Molecular interaction of cyclodextrins with cellulose nanocrystals: A new venue for improving the functional properties of Pickering emulsions

The design of functional delivery systems is essential for storing and releasing active components. Inspired by the structure of Nepenthes mirabilis, cellulose nanocrystals (CNC) cooperate with cyclic α-cyclodextrins (α-CD), β-cyclodextrins (β-CD), and γ-cyclodextrins (γ-CD) to form nanocomposites at different mass ratios for the delivery the Mosla chinensis essential oils (EO)-loaded Pickering emulsions (PE), respectively. Characterization methods including FT-IR, TG, XPS, AFM, XRD, and three-phase contact angle were used to analyze the structure of the nanocomposites. The molecular docking and molecular dynamic simulation results revealed that the most hydrogen bonds were formed between β-CD and CNC, but the tendency for γ-CD and CNC to bond with hydrogen bonds was stronger in the molecular dynamic simulation. Subsequently, the physicochemical properties of emulsions stabilized by CNC/CDs nanocomposites were characterized through particle size, potential, microstructure, long-term stability, rheology, and aqueous phase distribution indexes. The results showed that the different mass ratios CNC/α-CD and CNC/β-CD nanocomposites stabilized PE had smaller droplet scales and better stability. While CNC/γ-CD nanocomposites had a negative effect on the emulsion. The in vitro release results showed that the emulsions stabilized by CNC/CDs nanocomposites had a slow-release rate for EO by diffusion. The simulated gastrointestinal release showed that CNC/β-CD-PE had the highest bioavailability. Moreover, CNC/β-CD-PE reduced the minimal inhibitory concentration of EO by a mechanism that disrupts the membrane structure of bacteria. Therefore, the introduction of β-CD may be an effective alternative in regulating the physical properties, function, and stabilization of CNC-based PE. These findings provide a scientific basis for the rational structural design of delivery systems for the encapsulated aroma molecules.

Novel Carboxymethyl Cellulose/Gelatin-Based Film Incorporated with Zein-Stabilized Lemon Essential Oil Pickering Emulsion for the Preservation of Cherries.

In this study, a zein-stabilized lemon essential oil Pickering emulsion (ZLPE) was incorporated into a carboxymethyl cellulose/gelatin (CMC/GL) composite film to develop a bio-based packaging material with bioactive properties. The average droplet size of the ZLPE was measured at 3.62 ± 0.08 μm, with a zeta potential of -31.33 ± 0.32 mV, highlighting its excellent stability. The image results of confocal laser microscopy and scanning electron microscopy validated the uniform distribution of ZLPE in the film. The incorporation of ZLPE reduced the water solubility of films by 45.90% and decreased its water vapor permeability by 22.61%, thereby enhancing its hydrophobicity. Additionally, the ZLPE-loaded film improved mechanical properties, enhanced UV-blocking capabilities, and increased thermal stability. The introduction of ZLPE led to the antioxidant activity of the CMC/GL film increasing by six times the original level and endowed it with outstanding antibacterial properties. As a result, cherries packaged with the ZLPE film demonstrated superior preservation performance and extended shelf life in the preservation experiment, exhibiting the film's potential as a food packaging material.

Discovery of potent HIV-1 NNRTIs by CuAAC click-chemistry-based miniaturized synthesis, rapid screening and structure optimization

In addressing the urgent need for novel HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs) to combat drug resistance, we employed CuAAC click chemistry to construct a diverse 312-member diarylpyrimidine (DAPY) derivative library. This rapid synthesis approach facilitated the identification of A6N36, demonstrating exceptional HIV-1 RT inhibitory activity. Moreover, it was demonstrated with EC50 values of 1.8–8.7 nM for mutant strains L100I, K103 N, Y181C, and E138K, being equipotent or superior to that of ETR. However, A6N36's efficacy was compromised against specific resistant strains (Y188L, F227L + V106A and RES056), highlighting a need for further optimization. Through scaffold hopping, we optimized this lead to develop 10c, which exhibited broad-spectrum activity with EC50 values ranging from 3.2 to 57.5 nM and superior water solubility. Molecular docking underscored the key interactions of 10c within the NNIBP. Our findings present 10c as a promising NNRTI lead, illustrating the power of click chemistry and rational design in combatting HIV-1 resistance.

Polyvinylimidazole-Based Cryogel as an Efficient Tool for the Capture and Release of Oleuropein in Aqueous Media.

A polyvinylimidazole-based cryogel is presented as a pioneering solution for efficient extraction and release of partially water-soluble polyphenols from olive byproducts. Specifically, oleuropein was used as model molecule to evaluate its recovery from water. The material merges the properties of interconnected cryogel structure in adsorbing molecules via fast diffusion flux, with the strong electrostatic interactions acted by imidazole moiety. Such cryogel achieves effective oleuropein binding likely through hydrogen bonding and π-π interactions. Comprehensive assessments of static adsorption kinetics, isotherms, and desorption kinetics underscore the cryogel's efficacy in oleuropein extraction and release, highlighting its pivotal role in valorizing olive wastewater through sustainable biotechnological applications.

Physicochemical characterization of antioxidant film based on ternary blend of chitosan and Tulsi-Ajwain essential oil for preserving walnut

This study focuses on changes in the physiochemical properties of chitosan film when incorporated with a blend of essential oils of Tulsi and Ajwain. The essential oil blend-loaded films showed a decrement in transparency. Tulsi essential oil decreased the moisture content, swelling capacity, and water solubility. However, adding Ajwain along with Tulsi essential oil led to a significant increase in these properties. Meanwhile, the water vapor transmission rate didn't change significantly due to non-polar constituents in Tulsi essential oil, except when only Ajwain essential oil was present. The mechanical properties showed that the tensile strength of films increased with the addition of Tulsi essential oil (14.95 MPa to 31.27 MPa) but decreased further with increasing Ajwain oil concentration in films (32.13 MPa to 15.89 MPa). On the other hand, an increment in percent elongation at break (8.26 % to 24.02 %) was observed due to the excellent plasticization effect of Ajwain essential oil. Antioxidant activity was observed for the Tulsi essential oil-containing films and increased significantly with adding Ajwain essential oil. Finally, walnuts were packed in the active film. The active film showed better antioxidant activity against the oxidation of oil in walnuts, which the FTIR of the packed product confirmed.

Spectrophotometric analysis and mechanistic insights investigation of a developed CT complex as colorimetric real-time sensing performance towards Fe2+ in aqueous medium

A newly developed charge transfer complex (CTC) is explored for colorimetric real-time sensing behavior towards the Fe2+ ion, as a highly selective real-time colorimetric chemosensor material. The synthesized and characterized CTC / P1, [(2HP)+(SA)−] is cheap, remarkably distinctive, and simple to manufacture. Beyond the exposure limitations, iron is also the most common cofactor in enzyme reactions, which is, therefore a crucial part of life. However, too much or not enough iron leads to anemia, liver damage, cancer, Alzheimer's disease, and Parkinson's disease. In this report, unusual sensing capacity has been reported with a relatively low detection limit of 1.247 ppb for Fe2+ ions in aqueous medium, which was lowest at 1.267 ppb in previous reports of CTC sensors. By using a static quenching process, the incredible sensing behavior of this material as a chemosensor was determined. Colorimetric sensing behavior in real-time has also been observed. The complex has been described using a variety of methods, including UV-visible and FTIR spectroscopy. In FTIR spectra, the CTC (P1) showed a change in wavenumber when compared to its reactants. Furthermore, the complex's stoichiometry was measured using UV-visible spectroscopy by taking mixture with an equimolar ratio using the straight-line approach known as the Benesi-Hildebrand equation, which was found to be 1:1. Oscillator strength (f), transition dipole moment (μEN), molar extinction coefficient (εCT), energy of interaction (ECT), and stability constant (KCT) were among the thermodynamic and physical characteristics studied. Van't Hoff's equation was used to compute other parameters such as Gibbs free energy (G°), absorptivity coefficient (ε), Resonance energy (RN), etc. [O+—H……O−] hydrogen bonding was used to depict the interaction between reactants (salicylic acid and 2-hydroxypyridine). The stability of the P1 as a function of temperature is demonstrated through TG/DTA analysis.