Aqueous Research Articles

Lighting up imidazole-based fluorescent chemosensor for selective discrimination of Hg2+ ions and its application in sequential detection of histidine, solid-supported extractant.

A novel turn-on fluorogenic probe based on 4-(bis(2-((2-hydroxyethyl)thio)ethyl) amino)benzaldehyde the detection of Hg2+ ions has been designed and developed. The probe BMA showed high selectivity for Hg2+ ions over the series of other tested cations in an aqueous acetonitrile medium. Only the addition of Hg2+ ions to probe BMA in aqueous acetonitrile solution (CH3CN/H2O (7:3, v/v) could induce a remarkable red shift of about 20 nm in UV-vis absorbance spectra and a dramatic fluorescent enhancement with a blue shift of 10 nm in the emission spectra. With the help of a fluorescence spectrometer, the detection limit was calculated to be 73 nM. The binding stoichiometric ratio between BMA and Hg2+ ions was found to be 1:1 by Jobs plot, which was further confirmed by 1H NMR titration, FT-IR, HR-MS, and density functional theory calculations. The probe BMA can selectively detect Hg2+ ions, with several advantages, including ultra-fast response, low detection limit, conspicuous fluorescent changes, robust anti-interference capability, and exciting reversibility. The probe BMA can also serve as a portable extractant for removing Hg2+ ions in aqueous solution and act as an efficient and practical solid-state fluorescent sensor for mercury in on-field measurements. In addition, the in situ formed BMA-Hg2+ ensemble may be used for fluorescent recognition of histidine over other common amino acids via an indicator displacement assay mechanism. The low detection limits of BMA-Hg2+ for histidine were calculated to be 0.91 µM.

Effect of cold plasma on the physicochemical characteristics of granular cold water swelling maize starch

Granular cold water swelling (GCWS) starch is a physically modified starch with several potential applications in instant foods. Recently, some studies have revealed the beneficial effects of cold plasma (CP) treatment on improving the functional properties of starch. However, the effects of CP on GCWS has not been addressed yet. Therefore, this study assessed the influence of dielectric barrier discharge (DBD) cold plasma treatment time (1, 2, 3, and 4 min) on various attributes of GCWS maize starch. Increasing the CP treatment time increased the water absorption, solubility, viscosity, and freeze-thaw stability of GCWS maize starch, while, decreased its relative crystallinity and turbidity. FTIR results indicated that the functional groups along backbone remained unchanged upon CP treatment. Morphological analysis revealed that the starch granules preserved their integrity during CP treatment. However, increasing the duration of CP treatment resulted in the formation of micro-cavities and fissures on the surface of GCWS starch granules. The textural and rheological characteristics of GCWS starch pastes were improved by CP treatment. It seems that CP treatment might lead to an interconnected structure within the starch network and reinforce the starch paste.

Study on solubility and solvation thermodynamics for the advancement of biorelevant activities of l-isoleucine and l-serine in aqueous ammonium chloride solutions in the temperature range of 288.15–308.15 K

This study investigated the dissolution behavior of l-isoleucine and l-serine in an aqueous salt solution (ammonium chloride), examining how variations in temperature and electrolyte concentration affect their solubility. We conducted careful experiments and used mathematical calculations to explore interactions at a molecular level. We observed that the structure of these amino acids and salt concentration in the aqueous medium influence their interactions, which affects dissolution. In the presence of electrolytes, l-isoleucine demonstrated a salting-out effect whereas l-serine showed a salting-in effect. This work examines the solute–solvent interactions of these solutes in aqueous ammonium chloride solutions. l-isoleucine exhibits a nonspontaneous reaction with increasing salt concentrations whereas l-serine shows spontaneous behavior. Gibbs free energy analysis revealed greater stability of l-serine. The pH and conductance measurements showed how these factors influence solution properties. This insight helps us comprehend the nature and behavior of these molecules in different situations, which could be helpful in drug formulation or protein purification in the future.

Piezoelectric-enhanced MoS2@PVDF-HFP composite for photocatalytic degradation of tetracycline

In this work, composite films of molybdenum disulfide (MoS2) with poly (vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) were fabricated using aqueous phase transformation and hydrothermal methods, aiming at efficiently degrading tetracycline hydrochloride (TC). The findings revealed that the degradation efficiency of TC by MoS2@PVDF-HFP, when subjected to a combined photocatalysis process involving a simulated pressure electric field and aeration, reached a remarkable 96.11% within 1 hour-surpassing the performance observed under individual conditions. The changes in the electron density cloud on the films surface induced by the pressure electric field and the acceleration of electron transfer rate between contact interfaces were evident. Notably, the composite films exhibited a stable performance with a TC removal rate of 90.23% after five cycles, including a relatively stable degree of mineralization. We employed Density Functional Theory (DFT) to investigate the changes in the state density of MoS2@PVDF-HFP under different conditions, such as compressive stress, tension, and no force. This further clarified the mechanism of piezoelectric coupling photocatalysis promoting induced charge transfer on the films surface. The research findings presented in this paper provide a promising avenue for the application of piezoelectric field-assisted photocatalysis in enhancing material performance.

Investigation on the interfacial and emulsion stabilized behavior of dextran/ferritin/resveratrol composite nanoparticles

Glycation of ferritin provides a viable approach to enhance its physicochemical and functional properties. However, there is limited research on the interfacial adsorption properties of glycated ferritin-based colloidal particles. Therefore, this study selected recombinant human H-chain ferritin (rHuHF), rHuHF encapsulated with resveratrol (rHuHF–Res), and rHuHF–dextran glycoconjugates loaded with resveratrol (Dex–rHuHF–Res) as emulsifiers to investigate their interfacial adsorption properties. The results revealed that Dex–rHuHF–Res exhibited superior emulsifying properties and rheological behavior. It also increased the hydrophobicity of the microenvironment around Tyr and Trp residues, while hydrogen bonds, hydrophobic force, and salt bridge were identified as the most important intermolecular interactions. Dex–rHuHF–Res exhibited the biggest contact angle and lowest interface tension, which further reduced the diffusion (Kdiff) from the aqueous phase to the interface but promoted the penetration (Kp) and rearrangement (Kr) rates at the interface. Meanwhile, the emulsion stabilized by Dex–rHuHF–Res displayed excellent freeze-thaw stability, and Dex–rHuHF–Res can be more densely accumulated at the O/W interface to form an interface layer. These findings highlight the promising application of glycated ferritin in stabilizing Pickering emulsions, and deepen our understanding of the interplay among particle interaction, interface adsorption properties, and emulsion stability.

Extraction of mucilage polysaccharides from chia seed by hydrophobic deep eutectic solvents-based three-phase partitioning system: A phase behavior-driven approach

By incorporating the hydrophobic deep eutectic solvents (DESs) into the three-phase partitioning (TPP) technique, a TPP-based method was developed to extract the chia seed polysaccharide (CSP) from chia seed. Through a single-factor experiment and response-surface model, the optimal condition for the TPP extraction was determined as DES composed of dodecanoic acid and octanoic acid in a 1:1 M ratio, (NH4)2SO4 concentration of 32.86 %, crude extract–DES ratio of 0.93 (v/v), aqueous phase pH of 4.38, extraction temperature of 35 °C, and extraction time of 10 min. The polysaccharide yield of the constructed TPP method is 8.65 %, which is higher than the conventional water extraction method (yield is 6.96 %). Molecular dynamics simulations reveal the phase behavior of proteins and polysaccharides in the TPP system, showing that noncovalent interactions play a crucial role in the TPP system. The CSP obtained by the TPP method exhibits distinctive composition, structural, physicochemical, and functional properties, leading to improved thermal stability, rheological behavior, and antioxidant performance. Compared with the traditional extraction method, efficient extraction of CSP can be achieved flexibly using the proposed TPP approach, resulting in high yield and quality of CSP, which provides a new path for the large-scale utilization of chia seed.

Aqueous fibrous membrane electrolyte for ultrathin flexible Zinc-air batteries

Membrane electrolytes are key to constructing planar energy storage devices of low thickness and high flexibility, requesting simultaneous optimization of ionic conductivity and mechanical stability. Herein, aqueous phase electrospinning (APE) was implemented to co-spin polyvinyl alcohol and pullulan polysaccharide for fabricating crosslinked fibrous membrane electrolytes. While the hydroxyl-rich polymeric backbone grafted with quaternary ammonium endows a strong hydrogen-bonding network affording a large ionic conductivity of 30.2 mS cm−1, the cellulose-braced fibrous structure manifests a high tensile strength of 4.6 MPa. What’s more, the porous structure of the membrane electrolyte with enhanced charge mobility and uniformity helps to guide homogeneous Zn plating/stripping with suppressed dendrite growth. As a result, the assembled ultrathin flexible ZAB delivers a superb round-trip energy efficiency of 59.8 %, a maximum power density of 102 mW cm−2 and a long-term cycling stability over 100 h at 5 mA cm−2. By innovating the concept and methodology of aqueous fibrous membrane electrolytes, this study opens up a new chapter on the development of solid electrolytes in aqueous battery systems for powering wearable electronics.

Co-encapsulation of probiotic bacteria and fructooligosaccharides in basil seed gum-stabilized double emulsion gels: Probiotic viability and physicochemical properties

Double emulsions (DEs) present many potential applications for encapsulating and protecting probiotics. However, their high instability limit their real applications. To improve the prolonged stability of DEs, Lacticaseibacillus rhamnosus and Lactobacillus gasseri were separately co-encapsulated together in the presence of fructooligosaccharides (FOSs) and basil seed gum (BSG) within the internal (W1) and external (W2) aqueous phases of double emulsion gels (DEGs; W1-sol/O/W2-gel). Physical properties of DEGs, and viability of probiotics during heat processing, gastrointestinal digestion and storage were evaluated. Appropriate physical stability was observed during storage for 28 d at 4 ± 2 °C. The FOSs and microorganism type showed not effect on the droplet size (10.63 to 10.47 µm). Turbidimetry, physical stability, and morphological studies revealed the formation of aggregated droplets after 3 weeks. All DEGs presented high (>90 %) encapsulation efficiency. The viability of microencapsulated probiotics over time (14.89–14.08 %) and against simulated gastrointestinal conditions was higher than that of free cells. The encapsulation of bacteria in W1 in the presence of FOSs led to a significant improvement of viability against heat (only 1.35 % to 6.83 % reduction at 72 °C). L. gasseri showed a higher stability against environmental conditions. Finally, BSG-stabilized DEGs can be considered for increasing the viability of probiotic in functional foods.

Study on the methanol aqueous phase reforming performances over Pt/CeO2 catalysts: The effect of CeO2 morphologies and oxygen vacancies

Study on the methanol aqueous phase reforming performances over Pt/CeO2 catalysts: The effect of CeO2 morphologies and oxygen vacancies

Multifunctional role of surfactant in fabricating polyamide nanofiltration membranes for Li+/Mg2+ separation

Extracting Lithium from salt-lake brines can effectively alleviate global lithium scarcity. Separating the co-existing Mg2+ ions from Li+ ions in the brines is essential. While thin-film composite (TFC) nanofiltration (NF) membrane show potential for this separation, commercial NF membranes with negatively charged surfaces fail to meet the high rejection requirement for Mg2+ ions due to the electrostatic attractions between membranes and cations. Positively charged NF membranes fabricated by interfacial polymerization (IP) between aqueous phase polyethylenimine (PEI) and hexane phase trimesoyl chloride (TMC) have shown promise for Li+/Mg2+ separation. However, lithium extraction efficiency is greatly limited by the relatively low permeance and high lithium rejection of the membrane caused by an excessively cross-linked structure. Therefore, optimizing the pore size while maintaining the positive charge of PEI/TMC-based TFC membranes is necessary. We propose adding anionic surfactants to the aqueous PEI solution to modulate PEI/TMC-based NF membrane formation. Surfactants control PEI diffusion in IP through their interactions and improve reaction uniformity at the water-hexane interface. This results in a narrow pore size distribution of the PA network. In this study, three sulfate surfactants with varying alkyl chain lengths were used to control membrane formation. Results showed that sodium n-decyl sulfate (SDES), the shortest sulfate surfactant, improved membrane performance most effectively. The optimized membrane exhibited a crumpled surface and relatively loose pore structure with narrow pore size distribution. It demonstrated a pure water permanence of 5.65 L m−2 h−1 bar−1, high MgCl2 rejection of 92.6 %, and low LiCl rejection of 21.5 %. After filtering a Mg2+ and Li+ binary mixture solution, the Mg2+/Li+ ratio decreased significantly from 40 (feed) to 3.08 (permeate). This study provides an efficient strategy for preparing PEI/TMC-based NF membranes with favorable Li+/Mg2+ separation performance.

Aqueous phase Localized Surface Plasmon Resonance based Hydrogen sensing using Mixed colloidal Ag and PdAu nanoparticles

Hydrogen sensing is critical for its role in clean energy technologies. Herein, a colloidal Ag-PdAu ternary system as an efficient Localized Surface Plasmon Resonance (LSPR)-based sensor is first proposed for H2 sensing in aqueous environments. Upon exposure to H2, the system exhibits a significant LSPR peak shift of 42 nm within just 10 min, with no observable response to N2 under identical conditions.

Surfactant Molecules and Nano Gold on HOPG: Experiment and Theory

Excessive surfactant molecules within the solution adhere to highly ordered pyrolytic graphite (HOPG) when a droplet containing gold nanorods evaporates, leading to the emergence of a unique coffee-ring pattern. The combination of surface hydrophobicity and evaporation of the aqueous phase results in a stick-slip motion, which enhances the convective hydrodynamics of suspended particles. This phenomenon initiates interactions that influence the deposition and flow dynamics inside the droplet. High-resolution scanning electron microscopy (HRSEM) does not provide significant insights into regions potentially linked to cetyltrimethylammonium bromide (CTAB) molecules, whereas the atomic force microscope (AFM) displays the presence of gold nanoparticles arranged by CTAB within specific CTAB patches. The layers forms with varying heights and gaps between them, indicating diverse adhesion of CTAB. The analytical focus lies on the quantitative assessment of CTAB molecules, stripe dimensions, and energy profiles influenced by concentration and the effective positioning of CTAB-coated gold nanorods in CTAB-covered regions. AFM examination reveals CTAB molecular stripes on HOPG, showing a binding energy of -20 kJ/mol with the surface, -10 kJ/mol for nitrogen bonding with HOPG, and a total binding energy (BE) of -60 kJ/mol, considering various contributing factors. Completely parallel aligned molecules (CPAM) exhibit higher binding energy than non-perfectly aligned molecules (NPAM) due to maximum Van der Waals (VdW) interactions, ideal electrostatic interactions, and minimal steric repulsion. The difference in binding energy between perfectly and non-perfectly aligned molecules is around 20kJ/mol, emphasizing the importance of molecular orientation. As temperature rises from 298K to 348K, the likelihood of NPAM desorption increases significantly, with the binding energy shifting from 2.5kJ/mol to 4.1kJ/mol. Temperature significantly influences the equilibrium of molecules on HOPG surfaces. The emphasis is on elucidating the alterations in energy levels during nanorod aggregation on CTAB areas compared to bare HOPG surfaces, underscoring the impact of nanorods on CTAB micelle deformation energy. Observations on the variation in CTAB desorption rates with temperature changes underscore the dynamic nature of molecular binding energy associated with surface properties, underscoring the importance of molecular configuration and energy transfers in nanoscale systems.

Engineering an oncolytic adenoviral platform for precise delivery of antisense peptide nucleic acid to modulate PD-L1 overexpression in cancer cells

Cancer immunotherapy is focused on stimulating the immune system against cancer cells by exploiting immune checkpoint mechanisms. PD-1/PD-L1 is one of the most known immune checkpoints due to the widespread upregulation of the Programmed Death Ligand 1 (PD-L1) transmembrane protein in cancer tissues. Accordingly, taking advantage of the ability of oncolytic adenoviruses (OAd) to specifically infect and kill tumor cells over healthy ones, here, we developed a targeted delivery platform based on OAd to selectively deliver in cancer cells an antisense peptide nucleic acid (PNA) targeting the PD-L1 mRNA. The antisense PNA was modified with a six-lysine tail to improve water solubility and binding affinity to the polyanionic surface of the OAd carrier. Dynamic light scattering measurements confirmed the effective binding of the PNA cargo to OAd. Flow cytometry analysis evaluated the impact on PD-L1 protein expression in A549 and SK-OV3 cancer cell lines post-incubation with the OAd/PNA system. Statistically significant PD-L1 downregulation was observed in SK-OV3 cells treated with OAd-delivered PNA, surpassing the effect of free PNA. Confocal microscopy showed the cytoplasmic localization of OAd-delivered PNA, supporting the proposed antisense mechanism for PD-L1 downregulation. This targeted delivery system holds potential for enhancing the effectiveness of cancer immunotherapy.

Hyaluronic acid act as drug self-assembly chaperone and co-assembled with celalstrol for ameliorating non-alcoholic steatohepatitis

Nanoformulations of therapeutic drugs with diverse chemical structures are often complex to produce and lack a universal synthesis approach. Herein, we demonstrate that hyaluronic acid (HA) can function as an assembly chaperone, facilitating the formulation of various chemical compounds into nanoparticles without necessitating chemical modification. As a proof of concept, celastrol-HA co-assembled nanoparticles (CHNPs) were synthesized and utilized in the multifactorial treatment of non-alcoholic steatohepatitis (NASH). By simply blending an aqueous solution of HA and celastrol, we achieved the formation of homogeneous, stable, and biocompatible nanoparticles, effectively addressing the critical issues associated with celastrol's poor water solubility and high systemic toxicity. of celastrol. Ex vivo and in vivo experiments demonstrated that CHNPs ameliorated NASH by inhibiting macrophage M1 polarization, reducing liver inflammation and lipid deposition, and improving metabolic disorders. Furthermore, CHNPs reduced systemic toxicity and enhanced the bioavailability of celastrol. The simplicity of the HA-based nanoparticles may facilitate the development of translational nanomedicines.

Advancing Photodynamic Therapy with Nano-Conjugated Hypocrellin: Mechanisms and Clinical Applications.

Hypocrellin-based photodynamic therapy (PDT) is developing as a viable cancer therapeutic option, especially when enhanced by nanoconjugation. This review investigates the methods by which nano-conjugated hypocrellin enhances therapeutic efficacy and precision when targeting cancer cells. These nanoconjugates encapsulate or covalently bind hypocrellin photosensitizers (PSs), allowing them to accumulate preferentially in malignancies. When activated by light, the nanoconjugates produce singlet oxygen and other reactive oxygen species (ROS), resulting in oxidative stress that selectively destroys cancer cells while protecting healthy tissues. We look at how they can be used to treat a variety of cancers. Clinical and preclinical studies show that they have advantages such as increased water solubility, improved tumor penetration, longer circulation times, and tailored delivery, all of which contribute to fewer off-target effects and overall toxicity. Ongoing research focuses on improving these nanoconjugates for better tumor targeting, drug release kinetics, and overcoming biological obstacles. Furthermore, the incorporation of developing technologies such as stimuli-responsive nanocarriers and combination therapies opens exciting opportunities for enhancing hypocrellin-based PDT. In conclusion, the combination of hypocrellin and nanotechnology constitutes a significant approach to cancer treatment, increasing the efficacy and safety of PDT. Future research will seek to create conjugates including hypocrellin, herceptin, and gold nanoparticles to induce apoptosis in human breast cancer cells in vitro, opening possibilities for therapeutic applications.

Enhanced chemiluminescence with sub-1 nanometer CuO-PMA nanosheets for the sensitive detection of quercetin

BackgroundChemiluminescence (CL) analysis, characterized by its simple instrumentation, high signal-to-noise ratio, wide linear range, and minimal background interference, has garnered increasing attention from researchers. Nanomaterials (NMs) have been explored to enhance CL intensity. Notably, sub-1 nanometer scale NMs are considered to hold significant untapped potential due to their size effects. The application of these sub-1 nanometer NMs in enhancing CL is anticipated to yield favorable results. Additionally, the low water solubility and bioavailability of quercetin glycosides lead to their presence in bodily fluids at only trace levels, highlighting the urgent need for efficient and rapid detection methods. ResultsIn this work, phosphomolybdic acid (PMA) was incorporated into CuO to synthesize sub-1 nanometer CuO-PMA nanosheets (SNSs) using a cluster-core co-assembly strategy. Conformational and structural characterization confirmed the successful synthesis of these nanosheets. The CuO-PMA SNSs were employed to enhance the CL emission of the luminol-H2O2 system, resulting in an increase of over 1000 times. The catalytic properties of CuO-PMA SNSs significantly facilitated the decomposition of H2O2, leading to an enhanced production of reactive oxygen species, which in turn induced the CL enhancement. Given that the antioxidant effect of quercetin would consume the reactive oxygen species generated during the catalysis, a decrease in CL intensity was anticipated. A CL sensor for quercetin detection was developed based on the CuO-PMA SNSs-luminol-H2O2 system, demonstrating a strong linear relationship (R2 = 0.9969) and a low detection limit of 0.31 nM. SignificanceThis research provides a strategy to enhance the CL intensity of the luminol-H2O2 system by using CuO-PMA SNSs, offering a highly sensitive assay for detecting quercetin concentrations. The method is characterized as a simple and cost-effective analytical strategy making CL analysis very attractive for chemical analysts.

Impact of added enzyme-treated bran on the techno-functional properties of puffed-extruded sorghum snack

Dietary fibre intake is crucial for improving human health and reducing the prevalence of diet-related non-communicable diseases. This study determines the effect of the enzyme (Viscozyme®L: a cocktail of cell wall degrading enzymes including arabanase, cellulase, β-glucanase, hemicellulase and xylanase) hydrolyzed fibre on the techno-functional properties of puffed-extruded sorghum snacks made from sorghum flour. Sorghum flour and sorghum flour mixed with untreated bran, water-incubated bran, and enzyme-treated bran were extruded using a twin-screw extruder. The puffed-extruded snacks from sorghum flour with 2-hour enzyme-treated bran showed similar expansion ratios to snacks from sorghum flour without bran. The expansion ratios of the without-bran snacks (2.80) and enzyme-treated bran-added snacks (2.77) were significantly (P<0.05) higher than those made with untreated sorghum bran (1.87). A higher expansion ratio usually results in a lighter, crispier texture and a more attractive appearance of puffed-extruded snacks, which consumers often prefer. The enzyme treatment also increased the water solubility index and decreased the water absorption index compared to snacks with untreated bran. This study explores the potential of using an enzyme-treated sorghum bran to manufacture puffed-extruded snacks comparable to those made with sorghum flour.

Magmatic initial and saturated water thresholds determine copper endowments: Insights from apatite F-Cl-OH compositions

Magmatic volatiles (H2O, F, Cl), especially water, are critical in the formation of porphyry copper deposit, for its significance as a carrier for metals. However, accurately quantifying the water contents of deep ore-forming magma remain a challenge. Here, we used apatite and forward modelling methods to reconstruct magmatic water evolution histories, with special concern on the control of initial magmatic H2O contents and water saturation threshold to porphyry mineralization. Samples investigated include granitoid rocks and apatite from highly copper-mineralized and barren localities. Generally, our research suggested that both ore-related and ore-barren magma systems are hydrous, the modeled magmatic water contents vary significantly among systems whether mineralized or not, and the major difference lies in the threshold of water saturation (6.0 wt% for barren, and up to 10.0 wt% for highly mineralized). Combined with whole rock geochemistry data (high K2O and Sr/Y contents) and modeling result (high modeled water thresholds), we think the ore-related magmas are stored at deeper depth with higher water solubility. In conclusion, we propose that the level of magmatic water saturation plays a crucial role in the formation of porphyry copper systems. Fertile magma has higher water solubility to which deeper storage depth is a critical contributing factor, and can get significantly water enriched upon saturation.

The development of functionalized alginate-based hydrogels for the management of postprandial hyperglycemia and weight reduction

Polysaccharide-derived functional food ingredients are increasingly prevalent in the food industry for their health benefits and functional versatility. Among them, sodium alginate (SA), a natural polysaccharide, is widely valued for its sustainability, renewability, non-toxic nature, and broad applicability. However, its poor water solubility has limited its use as biomedical materials and food additives. Here, we enhanced SA through carboxymethylation to produce carboxymethylated SA (CMSA), aiming to develop functional food ingredients with improved physicochemical properties for health management. The synthesized CMSA was characterized for its physical properties and ability to form a hydrogel through cross-linking with Ca2+. We assessed its encapsulation efficiency for food particles in simulated gastric and intestinal fluids and evaluated its physiological effects in a rat model. Our findings demonstrated that CMSA-based hydrogels effectively encapsulate ingredients in the stomach, reducing nutrient diffusion in the intestine, and helping to manage postprandial hypoglycemia. Additionally, the hydrogel expands in the stomach and small intestine, contributing to modest weight loss. These findings suggest that CMSA-based hydrogels offer significant potential as functional food ingredients for managing postprandial hypoglycemia and supporting weight management. The development of such gelling systems presents promising applications in both medical and nutritional sciences, offering innovative strategies for addressing diet-related health concerns.

Biodegradable MAM-based amphiphilic block copolymers: Toward efficient and eco-friendly kinetic inhibitors for methane hydrate formation

The development of low dosage hydrate inhibitors holds significant implications for the oil and gas industry. Some commercially available inhibitors, such as Luvicap EG, are derived from the lactam-containing polymer PVCap, which exhibit limited biodegradability and possess low cloud point (30-40℃), thereby constraining their practical utility. The present study successfully synthesized a series of novel amphiphilic block copolymers based on methacrylamide (MAM) by introducing biodegradable hydrophobic esters (ε-caprolactone (CL), δ-valerolactone (VL), and glycolide (GA)) onto the main chain of poly (methyl acrylamide) (PMAM), serving as KHIs. The synthesized MAM-based polymers maintain water solubility within the range of 0–98 ℃ without thermal responsiveness, effectively preventing deposition issues associated with traditional KHIs. Additionally, all MAM-based polymers demonstrated good biodegradability. The dynamics experiments have shown that PMAM homopolymers did not possess KHI effect, while the MAM-based block copolymers, especially PMAM-b-PVL, exhibited excellent performance in inhibiting hydrate nucleation. At low concentrations, the KHI effect of PMAM-b-PVL was comparable to that of the commercial KHI Luvicap EG. The in-situ Raman spectroscopy experiment further revealed the inhibition mechanism of the amphiphilic polymers, which was achieved by forming effective arrangements at the gas–liquid interface and disrupting the water structure in the interfacial region, thereby impeding the formation of hydrate cages, especially large cages. The findings provided a promising and environmentally friendly solution for the management of hydrates in the oil and gas industry