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Rationale: Solvent‐free sample preparation offers some advantages over solvent‐based techniques, such as improved accuracy, reproducibility and sensitivity, for matrix‐assisted laser desorption/ionization (MALDI) analysis. However, little or no information is available on the application of solvent‐free techniques for the MALDI analysis of polymer blends. Methods: Solvent‐free sample preparation by ball milling was applied with varying sample‐to‐matrix ratios for MALDI time‐of‐flight mass spectrometry analysis of various polymers, including polystyrenes, poly(methyl methacrylate)s and poly(ethylene glycol)s. The peak intensity ratios were compared with those obtained after using the conventional dried droplet sample preparation method. In addition, solvent‐assisted milling was also applied to improve sample homogeneities. Results: Depending on the sample preparation method used, different peak intensity ratios were found, showing varying degrees of suppression of the signal intensities of higher mass polymers. Ball milling for up to 30 min was required to achieve constant intensity ratios indicating homogeneous mixtures. The use of wet‐assisted grinding to improve the homogeneity of the blends was found to be disadvantageous as it caused partial degradation and mass‐dependent segregation of the polymers in the vials. Conclusions: The results clearly show that solvent‐free sample preparation must be carefully considered when applied to synthetic polymer blends, as it may cause additional problems with regard to homogeneity and stability of the blends. [ABSTRACT FROM AUTHOR]

The study investigates the heat transfer and friction factor properties of ethylene glycol and glycerol-based silicon dioxide nanofluids flowing in a circular tube under continuous heat flux circumstances. This study tackles the important requirement for effective thermal management in areas such as electronics cooling, the automobile industry, and renewable energy systems. Previous research has encountered difficulties in enhancing thermal performance while handling the increased friction factor associated with nanofluids. This study conducted experiments in the Reynolds number range of 1300 to 21,000 with particle volume concentrations of up to 1.0%. Nanofluids exhibited superior heat transfer coefficients and friction factor values than the base liquid values. The highest enhancement in heat transfer was 5.4% and 8.3% for glycerol and ethylene glycol -based silicon dioxide Nanofluid with a relative friction factor penalty of ∼30% and 75%, respectively. To model and predict the complicated, nonlinear experimental data, five machine learning approaches were used: linear regression, random forest, extreme gradient boosting, adaptive boosting, and decision tree. Among them, the decision tree-based model performed well with few errors, while the random forest and extreme gradient boosting models were also highly accurate. The findings indicate that these advanced machine learning models can accurately anticipate the thermal performance of nanofluids, providing a dependable tool for improving their use in a variety of thermal systems. This study's findings help to design more effective cooling solutions and improve the sustainability of energy systems. [ABSTRACT FROM AUTHOR]

In this study, well-known biodegradable poly [(β-butyrolactone-block-ethylene glycol methyl ether)-phthalocyanine- (β-butyrolactone-block-ethylene glycol methyl ether)] abbreviated as poly(BL-b-mEG)-Pc-poly(BL-b-mEG) copolymer was synthesised. In the first part, poly (β-butyrolactone-block-ethylene glycol methyl ether) [poly(BL-b-mEG)] block copolymer was prepared by ring-opening polymerisation (ROP) method of β-butyrolactone using poly (ethylene glycol) methyl ether. In the second part, poly(BL-b-mEG)-Pc-poly(BL-b-mEG) copolymer was obtained from the reaction poly(BL-b-mEG) block copolymer, SiPcCl2, and K2CO3. Axial binding of poly(BL-b-mEG) block copolymers to the phthalocyanine compound was achieved. The synthesised products were characterised by using multi-instruments such as1H-NMR, FT-IR, GPC, ve UV-visible. The electronic and singlet oxygen production capacity of poly(BL-b-mEG)-Pc-poly(BL-b-mEG) copolymer was investigated. [ABSTRACT FROM AUTHOR]

Molecular designs that achieve solubility of porphyrins in aqueous media are attractive for diverse applications. The presence of 4-sulfophenyl or 4-N-methylpyridinium groups at the four meso-positions is effective, but the use of fewer substituents is desirable for custom tailoring. Here, five target porphyrins (along with selected copper or zinc chelates) were prepared bearing PEG groups to understand how distinct designs affect aqueous solubility (where "PEG" refers to an oligoethylene glycol unit). One objective was to employ only one or two pegylated meso-aryl groups so that other meso-positions would be open for synthetic elaboration while retaining a compact structure. The key design features examined include (i) 2,6- versus 3,5-dipegylated aryl groups; (ii) one versus two 2,6-dipegylated aryl groups; (iii) a nonpolar versus ionizable terminus of the PEG moiety; and (iv) length of the PEG moiety. In each case, the PEG groups were attached on a porphyrin scaffold bearing one or two bis(2-propynyloxy)aryl groups. Assessment entailed octanol–aqueous solution partitioning (log P values) and aggregation over the concentration range of 0.2–200 μM. A trans-A2 free base porphyrin bearing two 2,6-dialkoxyphenyl groups equipped with methyl-terminated PEG6 groups gave ∼3 : 1 partitioning in water versus octanol but high overall solubility (at least 12 mM) in water alone; the analogous porphyrin with carboxylic acid-terminated PEG6 groups gave >100 : 1 partitioning in phosphate-buffered saline (PBS, pH 7.4). A trans-AB porphyrin bearing a single 2,6-dialkoxyphenyl group equipped with carboxylic acid-terminated PEG6 groups gave 43 : 1 partitioning in PBS versus octanol but was prone to self-aggregation at 20–200 μM in PBS alone. The results point to new molecular designs of potential value in the life sciences. [ABSTRACT FROM AUTHOR]

The construction of diverse and distinctive self‐assembled structures in water, based on the control of the self‐assembly processes of artificial small molecules, has received considerable attention in supramolecular chemistry. Cage‐like perforated vesicles are distinctive and interesting self‐assembled structures. However, the development of self‐assembling molecules that can easily form perforated vesicles remains challenging. This paper reports a lower critical solution temperature (LCST) behavior‐triggered self‐assembly property of a 4‐aminoquinoline (4‐AQ)‐based amphiphile with a tetra(ethylene glycol) chain, in HEPES buffer (pH 7.4). This property allows to form perforated vesicles after heating at 80 °C (> LCST). The self‐assembly process of the 4‐AQ amphiphile can be controlled by heating at 80 °C (> LCST) or 60 °C (< LCST). After cooling to room temperature, the selective construction of the perforated vesicles and nanofibers was achieved from the same 4‐AQ amphiphile. Furthermore, the perforated vesicles exhibited slow morphological transformation into intertwined‐like nanofibers but were easily restored by brief heating above the LCST. [ABSTRACT FROM AUTHOR]

Polyol esters are abundant bio‐based resources. Integration of polyol esters into the production chain of fine chemicals would reduce carbon emissions and improve the sustainability of the chemical industry. An efficient synthetic route to phenoxyethanols was developed through catalytic hydroxyethylation of phenols with ethylene glycol diacetate as the reagent. This method showed the potential of ethylene glycol diester as a safe and sustainable substitute for ethylene oxide, a useful but toxic reagent. A variety of phenoxyethanol esters were produced in high yield under simple catalytic conditions. Mechanistic studies revealed that the reaction underwent a neighboring group participation process. [ABSTRACT FROM AUTHOR]

A green and sustainable --COOH & --OH condensation solution polymerization method was hereby reported for FDCA-based polyesters to avoid discoloration and toxic solvents. First, taking poly(ethylene 2,5-furandicarboxylate) (PEF) as the representative of FDCA-based polyester, enabling good white appearance PEF with Mn=6.51x10³ gmol-1 from FDCA and ethylene glycol in green solvent γ-valerolactone (GVL), catalyzed by 4-dimethylaminopyridine (DMAP) and N-(3-dimethylaminopropyl)-N'-ethylcarbodiimide hydrochloride (EDC). Additionally, the molecular weight of PEF was rapidly improved (Mn >2.5x104 gmol-1) via remelting polycondensation within minutes, with the dispersity still kept relatively low dispersity (Đ<1.40). Importantly, the --COOH & --OH condensation solution polymerization method was successfully applied for the synthesis of various FDCA-based polyesters, including diols with varying carbon chain lengths (3 to 11 carbons) and cycloalkyl diols, especially the applicability of this method to diols containing C=C double bonds, which was found to exhibit low heat resistance. Lastly, assisting with 13C labeled 1,4-succinic acid and in-situ 13C-NMR, an in-depth study of the possible catalytic mechanism was proposed, by which, EDC activated FDCA, and then DMAP catalyzed it with diol to yield macromolecular chain of polyester. Overall, the results provided a green and sustainable strategy for the synthesis of FDCA-based polyesters. [ABSTRACT FROM AUTHOR]

Small‐molecule ruthenium (Ru) complexes exhibit limitations in terms of nonspecific delivery, rapid metabolism, and low tumor accumulation. Their delivery can be improved through physical encapsulation into nanocarriers via hydrophobic forces, metallophilic interactions, or π–π stacking interactions. However, delivering Ru complexes for efficient therapy is substantially hindered by potential leakage of drugs, low drug‐loading capacity, or batch‐to‐batch variations. Moreover, current metalloprodrug‐based self‐delivery systems necessitate supramolecular interactions, which are unsuitable for Ru complexes because of their octahedral structures. Herein, two self‐assembled molecular Ru drugs, Ru‐3XOEG and Ru‐PEG, are reported. Ru‐3XOEG involves a three‐arm dendritic oligo(ethylene glycol) (OEG), while Ru‐PEG involves a linear poly(ethylene glycol) (PEG) chain. Furthermore, these drugs contain an anticancer Ru moiety and a planar pyrene moiety to render hydrophobic forces and π–π stacking supramolecular interactions. Ru‐3XOEG self‐assembles into large compound micelles. Ru‐PEG self‐assembles into vesicles. These Ru‐containing self‐delivered systems exhibit well‐defined structures, high Ru loading contents, and long circulation in blood without external nanocarriers. Red light irradiation induces the release of Ru‐H2O anticancer agents and the generation of 1O2 to inhibit tumor growth. The presented design of self‐assembled molecular Ru complexes opens avenues for the concept of self‐delivered metalloprodrugs. [ABSTRACT FROM AUTHOR]

Forward osmosis (FO) using deep eutectic solvents (DESs) as the draw solution (DS) was used in liquid mining of lithium from a synthesized brine, which was used as the feed solution (FS). Two DESs (choline chloride: 2 ethylene glycol and choline chloride: 2 levulinic acid) were studied as the DS. The water flux, reverse solute flux, final lithium concentration, and physical properties of commercially available cellulose triacetate membranes were studied experimentally. The performance of the DESs as DS in FO was compared to aqueous inorganic solutions at various concentration levels. Among all the DSs studied, choline chloride: 2 ethylene glycol (ChCl: 2 EG) resulted in the highest water flux (18.25 L m−2 h−1), upgrading the concentration of lithium by up to 3.68 times. In terms of reverse solute flux, the DESs showed lower values compared to the aqueous inorganic DSs tested when the active layer of the membrane was facing the FS. The use of DESs was also found to improve the membrane hydrophilicity and roughness. Freeze concentration (FC) was subsequently used to separate and recover the water that permeated into the DS and reconcentrate the latter for reuse in FO. This work highlights the potential sustainability benefits of the use of FO in lithium extraction, as the integration of FO with green DESs offers a promising liquid mining solution to meet the increasing demand for lithium while mitigating the environmental concerns associated with its extraction. [ABSTRACT FROM AUTHOR]

0D organic–inorganic antimony halides have attracted increasing attention due to the non‐toxicity, high stability, and superior photoluminescence quantum yield (PLQY). Here, a series of hybrid antimony chlorides with the same organic cation ethyltriphenylphosphonium (Ph3EtP+), including non‐emissive (Ph3EtP)2Sb2Cl8 and nine (Ph3EtP)2SbCl5‐based emissive compounds, are synthesized and characterized. These emissive compounds are namely, the guest‐free (Ph3EtP)2SbCl5 and (Ph3EtP)2SbCl5·guest (guest = glycol, acetic acid, methanol, ethanol, n‐propanol, i‐propanol, acetone, and acetonitrile). The solvent used can alter the coordination mode of Sb because the solvation effect affects the reactivity of the anions ([SbCl4]− and Cl−), leading to the formation of either A2Sb2Cl8 or A2SbCl5. The solvents can be even incorporated into the crystal structure, where stronger interaction with [SbCl5]2− leads to higher temperature of the escape of the solvent. The guest molecules could increase the structural rigidity of [SbCl5]2− via hydrogen bonding and dipole–dipole interactions, which tends to reduce the room‐temperature photoluminescence (PL) Stokes shift and temperature‐dependent PL shift by decreasing the [SbCl5]2− deformability, along with enhanced PLQY from 81% in guest‐free to near‐unity in (Ph3EtP)2SbCl5·glycol. This work shows that targeted synthesis and diversified choices of solvents provide an efficient tool to generate steady variations in hybrid emissive materials for optoelectronics. [ABSTRACT FROM AUTHOR]

Background: Prostate cancer is a common cancer among men worldwide that has a very poor prognosis, especially when it progresses to metastatic castration-resistant prostate cancer (mCRPC). Therefore, novel therapeutic agents for mCRPC are urgently required. Because prostate-specific membrane antigen (PSMA) is overexpressed in mCRPC, targeted alpha therapy (TAT) for PSMA is a promising treatment for mCRPC. Astatine-211 (211At) is a versatile α-emitting radionuclide that can be produced using a cyclotron. Therefore, 211At-labeled PSMA compounds could be useful for TAT; however, 211At-labeled compounds are unstable against deastatination in vivo. In this study, to develop in vivo stable 211At-labeled PSMA derivatives, we designed and synthesized 211At-labeled PSMA derivatives using a neopentyl glycol (NpG) structure that can stably retain 211At in vivo. We also evaluated their biodistribution in normal and tumor-bearing mice. Results: We designed and synthesized 211At-labeled PSMA derivatives containing two glutamic acid (Glu) linkers between the NpG structure and asymmetric urea (NpG-L-PSMA ((L-Glu)2 linker used) and NpG-D-PSMA ((D-Glu)2 linker used)). First, we evaluated the characteristics of 125I-labeled NpG derivatives because 125I was readily available. [125I]I-NpG-L-PSMA and [125I]I-NpG-D-PSMA showed low accumulation in the stomach and thyroid, indicating their high in vivo stability against deiodination. [125I]I-NpG-L-PSMA was excreted in urine as hydrophilic radiometabolites in addition to the intact form. Meanwhile, [125I]I-NpG-D-PSMA was excreted in urine in an intact form. In both cases, no radioactivity was observed in the free iodine fraction. [125I]I-NpG-D-PSMA showed higher tumor accumulation than [125I]I-NpG-L-PSMA. We then developed 211At-labeled PSMA using the NpG-D-PSMA structure. [211At]At-NpG-D-PSMA showed low accumulation in the stomach and thyroid in normal mice, indicating its high stability against deastatination in vivo. Moreover, [211At]At-NpG-D-PSMA showed high accumulation in tumor similar to that of [125I]I-NpG-D-PSMA. Conclusions: [211At]At-NpG-D-PSMA showed high in vivo stability against deastatination and high tumor accumulation. [211At]At-NpG-D-PSMA should be considered as a potential new TAT for mCRPC. [ABSTRACT FROM AUTHOR]

Immobilized microorganisms technology has been explored as a promising wastewater treatment method. To further increase the activity of the immobilized microorganisms, a porous membrane which was composed of poly (lactic acid) (PLA) and poly (ethylene glycol) (PEG) was designed for microorganism encapsulation. The plane membrane and the spherical membrane were prepared respectively. The morphology, mechanical properties, nitrate permeability, and biodegradability of the plane membranes were investigated to determine an optimized formulation. And then, denitrifying bacteria was encapsulated by the spherical membrane and its denitrification performance in synthetic wastewater was explored. The mean pore size of the PLA/PEG plane membranes ranged from 2.09 ± 0.63 μm to 3.15 ± 1.32 μm. PEG stimulated interconnected pore structure of the PLA/PEG plane membrane. Compare with neat PLA membrane, the tensile strength of the PLA/50%PEG plane membrane decreased by about 53.2% and elongation at break increased by about 103.5%. Nitrate permeability attained a maximum of 188.95 ± 4.59 mg·L−1·m−2·h−1 for PLA/50%PEG plane membrane. The denitrifying active sludge enclosed with the spherical membrane showed good denitrification performance in a short start-up time. The nitrate removal rate reached 51.14% on the 4th day and 82.53% on the 17th day. This porous PLA/50%PEG membrane was good for the diffusion of substrates and nutrients, which enabled the encapsulated microorganism recovered activity in a short time. The spraying method made the microorganism encapsulation could be designed according to the different microorganisms and different user environments, which expanded the application scope of microorganism encapsulation technology. [ABSTRACT FROM AUTHOR]

Smart nanoassemblies degradable through the cleavage of acid‐labile linkages have attracted significant attention because of their biological relevance found in tumor tissues. Despite their high potential to achieve controlled/enhanced drug release, a systematic understanding of structural factors that affect their pH sensitivity remains challenging, particulary in the consruction of effective acid‐degradable shell‐sheddable nanoassemblies. Herein, the authors report the synthesis and acid‐responsive degradation through acid‐catalyzed hydrolysis of three acetal and ketal diols and identify benzaldehyde acetal (BzAA) exhibiting optimal hydrolysis profiles in targeted pH ranges to be a suitable candidate for junction acid‐labile linkage. The authors explore the synthesis and aqueous micellization of well‐defined poly(ethylene glycol)‐based block copolymer bearing BzAA linkage covalently attached to a polymethacrylate block for the formation of colloidally‐stable nanoassemblies with BzAA groups at core/corona interfaces. Promisingly, the investigation on acid‐catalyzed hydrolysis and disassembly shows that the formed nanoassemblies meet the criteria for acid‐degradable shell‐sheddable nanoassemblies: slow degradation at tumoral pH = 6.5 and rapid disassembly at endo/lysosomal pH = 5.0, while colloidal stability at physiological pH = 7.4. This work guides the design principle of acid‐degradable shell‐sheddable nanoassemblies bearing BzAA at interfaces, thus offering the promise to address the PEG dilemma and improve endocytosis in tumor‐targeting drug delivery. [ABSTRACT FROM AUTHOR]

Polymerization‐induced self‐assembly (PISA) has emerged as a scalable one‐pot technique to prepare block copolymer (BCP) nanoparticles. Recently, a PISA process, that results in poly(l‐lactide)‐b‐poly(ethylene glycol) BCP nanoparticles coined ring‐opening polymerization (ROP)‐induced crystallization‐driven self‐assembly (ROPI‐CDSA), was developed. The resulting nanorods demonstrate a strong propensity for aggregation, resulting in the formation of 2D sheets and 3D networks. This article reports the synthesis of poly(N,N‐dimethyl acrylamide)‐b‐poly(l)‐lactide BCP nanoparticles by ROPI‐CDSA, utilizing a two‐step, one‐pot approach. A dual‐functionalized photoiniferter is first used for controlled radical polymerization of the acrylamido‐based monomer, and the resulting polymer serves as a macroinitiator for organocatalyzed ROP to form the solvophobic polyester block. The resulting nanorods are highly stable and display anisotropy at higher molecular weights (>12k Da) and concentrations (>20% solids) than the previous report. This development expands the chemical scope of ROPI‐CDSA BCPs and provides readily accessible nanorods made with biocompatible materials. [ABSTRACT FROM AUTHOR]

The photoelectrochemical (PEC) conversion of organic small molecules offers a dual benefit of synthesizing value-added chemicals and concurrently producing hydrogen (H2). Ethylene glycol, with its dual hydroxyl groups, stands out as a versatile organic substrate capable of yielding various C1 and C2 chemicals. In this study, we demonstrate that pH modulation markedly enhances the photocurrent of BiVO4 photoanodes, thus facilitating the efficient oxidation of ethylene glycol while simultaneously generating H2. Our findings reveal that in a pH = 1 ethylene glycol solution, the photocurrent density at 1.23 V vs. RHE can attain an impressive 7.1 mA cm−2, significantly surpassing the outputs in neutral and highly alkaline environments. The increase in photocurrent is attributed to the augmented adsorption of ethylene glycol on BiVO4 under acidic conditions, which in turn elevates the activity of the oxidation reaction, culminating in the maximal production of formic acid. This investigation sheds light on the pivotal role of electrolyte pH in the PEC oxidation process and underscores the potential of the PEC strategy for biomass valorization into value-added products alongside H2 fuel generation. [ABSTRACT FROM AUTHOR]

We explored two methods for synthesizing Pd nanoparticles using three different carbide-derived carbon (CDC) support materials, one of which was nitrogen-doped. These materials were studied for oxygen reduction reaction (ORR) in 0.1 M KOH solution, and the resulting CDC/Pd catalysts were characterized using TEM, XRD, and XPS. The citrate method and the polyol method using polyvinylpyrrolidone (PVP) as a capping agent were employed to elucidate the impact of the support material on the final catalyst. The N-doping of the CDC material resulted in smaller Pd nanoparticles, but only in the case of the citrate method. This suggests that the influence of support is weaker when using the polyol method. The citrate method with CDC1, which is predominantly microporous, led to a higher degree of agglomeration and formation of larger particles in comparison to supports, which possessed a higher degree of mesoporosity. We achieved smaller Pd particle sizes using citrate and NaBH4 compared to the ethylene glycol PVP method. Pd deposited on CDC2 and CDC3 supports showed similar specific activity (SA), suggesting that the N-doping did not significantly influence the ORR process. The highest SA value was observed for CDC1/Pd_Cit, which could be attributed to the formation of larger Pd particles and agglomerates. [ABSTRACT FROM AUTHOR]

High-molecular-weight poly(L-lactide)-b-poly(ethylene glycol)-b-poly(L-lactide) (PLLA-PEG-PLLA) is a flexible and biodegradable bioplastic that has promising potential in flexible food packaging but it has no antibacterial ability. Thus, in this work, the effect of zinc oxide nanoparticles (nano-ZnOs) which have antimicrobial activity on various properties of PLLA-PEG-PLLA was determined. The addition of nano-ZnOs enhanced the crystallization, tensile, UV-barrier, and antibacterial properties of PLLA-PEG-PLLA. However, the crystallization and tensile properties of nanocomposite films decreased again as the nano-ZnO increased beyond 2 wt%. The nano-ZnO was well distributed in the PLLA-PEG-PLLA matrix when the nano-ZnO content did not exceed 2 wt% and exhibited some nano-ZnO agglomerates when the nano-ZnO content was higher than 2 wt%. The thermal stability and moisture uptake of the PLLA-PEG-PLLA matrix decreased and the film's opacity increased as the nano-ZnO content increased. The PLLA-PEG-PLLA/ZnO nanocomposite films showed good antibacterial activity against bacteria such as Escherichia coli and Staphylococcus aureus. It can be concluded that nano-ZnOs can be used as a multi-functional filler of the flexible PLLA-PEG-PLLA. As a result, the addition of nano-ZnOs as a nucleating, reinforcing, UV-screening, and antibacterial agent in the flexible PLLA-PEG-PLLA matrix may provide protection for both the food and the packaging during transportation and storage. [ABSTRACT FROM AUTHOR]

In this study, the stability and viscosity of four different nanoparticles are discussed in conjunction with the physical properties of these nanoparticles. The aim is to provide guidance for nanoparticle selection in future nanofluid applications. Additionally, our goal is to examine hybrid nanofluids in comparison to single nanofluids, exploring their potential benefits and evaluating their industrial applications. A two-stage approach was employed, using ethylene glycol (EG) as a base fluid, to create these nanofluids. Single nanofluids were formed with SiO2, TiO2, MWCNT, and ZnO nanoparticles at 0.1%, 0.5%, and 1% volume concentrations. Additionally, binary (SiO2–TiO2/EG), ternary (SiO2–TiO2–MWCNT/EG), and quaternary (SiO2–TiO2–MWCNT–ZnO/EG) hybrid nanofluids were formed with 0.1% volume concentrations. The dynamic viscosity of all nanofluids was evaluated over the temperature range of 20–50 °C. Analysis of nanofluids was extended by characterization studies using field emission transmission electron microscopy (FE-SEM), field emission scanning electron microscopy (FE-TEM), Zeta potential testing, and visual inspection. SiO2 nanoparticles exhibited the greatest stability, remaining in suspension for more than 28 days without sedimentation, while ZnO nanoparticles were the least stable, collapsing in < 7 days. Compared to ethylene glycol, ZnO/EG had the most increased viscosity (42.79%) at 20 °C and a 1% volume concentration. However, SiO2–TiO2–MWCNT/EG showed the largest decrease in viscosity (9.99%) at 20 °C. Hybrid nanofluids exhibit better viscosity performance compared to their base fluids and single nanofluids, enhancing the thermal efficiency of these heat transfer fluids. Additionally, this study is groundbreaking research as it emphasizes the efficiency of hybrid nanofluids as well as introducing quaternary nanofluids to the literature. [ABSTRACT FROM AUTHOR]

The study aims to investigate the performance of a thermal management system for lithium-ion batteries in electric vehicles (EVs) by utilizing a helical coiled pulsating heat pipe (HC-PHP) combined with a hybrid nanofluid consisting of Al2O3–MWCNT–ethylene glycol. The experimental investigation focuses on evaluating the effectiveness of this system under various operating conditions. The outcomes of this study will provide valuable insights into the influence of thermal management on power output, driving range, and safety of EVs. During a continuous discharge process at room temperature of 25 °C and discharge rates of 1C, 2C, and 3C, the lithium-ion battery's temperature remains below 42 °C, ensuring that it does not exceed the specified safety limit. Additionally, the maximum temperature gradient across the battery, which indicates temperature variation within the battery, remains below 2 °C. These findings demonstrate the effectiveness of the thermal management system in maintaining safe and uniform temperature distribution during high-discharge operations. The observed results provide strong evidence for the exceptional heat dissipation capabilities of the thermal management system utilizing HC-PHP and an Al2O3–MWCNT–ethylene glycol-based nanofluid. The system effectively minimizes temperature gradient and enhances thermal uniformity across the battery surface. As a result, the HC-PHP ensures optimal performance of the lithium-ion battery by maintaining temperatures within the desired range of 20–50 °C, which is crucial for its reliable operation. [ABSTRACT FROM AUTHOR]

[Display omitted] The anticancer drug doxorubicin hydrochloride (DX) shows a high solubility in aqueous media thanks to the positive charge in the ammonium group. This feature, however, affects the drug encapsulation in the hydrophobic domains of polymeric micelles (PMs) used for the targeted delivery of the drug. At basic pH, DX deprotonates but also acquires a negative charge in the phenolic groups of the anthracycline structure. Both the efficiency and the rate of encapsulation will be increased by choosing an appropriate pH such that the drug molecule is in neutral form. An optimal pH for the encapsulation of the DX in PMs based on commercial poloxamers and on the diblock copolymer methoxy-poly(ethylene glycol) 17 - b -poly(ε-caprolactone) 9 was determined by fluorescence spectroscopy, following the time evolution of both the intensity ratio of the first and the second emission bands of DX and its fluorescence lifetime, both sensitive to the environment polarity. Intracellular delivery of PMs encapsulated drug was followed by Confocal Scanning Laser Microscopy (CSLM). Cell viability was assessed with the sulforhodamine B (SRB) assay. By adjusting pH to 8.1 a high yield of incorporation of DX in the PMs was achieved coupled to an appreciable increase (one order of magnitude) in the drug encapsulation rate. In-vitro tests in selected cancer cell lines showed the slow release of the drug and a delay in the cytotoxic response in comparison to free DX as detected by CSLM and SRB assay. The proposed methodology paves the way for a greener, faster and more efficient encapsulation of DX in PMs. [ABSTRACT FROM AUTHOR]

A series of crosslinked hydrogel are developed to evaluate their applicability as efficient carriers for sustained release of ciprofloxacin (CFX) with bactericidal activity. The hydrogels are prepared from 2‐hydroxyethyl methacrylate (HEMA) and carboxymethyl‐chitosan (CMCS) using ethylene glycol dimethacrylate (EGDMA) as crosslinker to yield a semi‐interpenetrating polymer networks (semi‐IPNs) by a photoinitiated chemical method. Molecular weight and concentration of CMCS in the network are varied to optimize its properties as a wound dressing. PHEMA‐CMCS semi‐IPNs (HC‐IPNs) are characterized by their swelling ratio (Q), glass transition temperature (Tg), Young's moduli by mechanical compression submerged in water at different pHs at 37 °C, CFX delivery mimicking skin conditions, cell viability, biodegradability study and by their antibacterial activity. Results show that addition of CMCS results in pH sensitive behavior. HC‐IPNs show thermal reinforcement, and they are softer materials as compared to plain PHEMA hydrogels when submerged in water. The in vitro release of CFX suggests that the HC‐IPNs release the drug continuously up to 50 h. Unloaded HC‐IPNs show inhibition effects against Escherichia coli strain and show bacteriostatic effects against Staphylococcus aureus strain. Results suggest that HC‐IPNs probably be a potential candidate that can be applied as wound dressing for topical CFX controlled delivery. [ABSTRACT FROM AUTHOR]

In our prior paper, surface micelles with the core‐shell‐petal structure of the double hydrophilic block copolymer poly(N‐isopropylacrylamide)‐block‐poly[oligo(ethylene glycol) acrylate] (PNIPAM‐b‐POEGA) were successfully evaluated. In this work, ionic strength (under acidic conditions) and anion‐specificity effects (under neutral conditions) on the aggregation behavior of PNIPAM‐b‐POEGA at the air/water interface and the morphologies of its Langmuir–Blodgett (LB) films were systematically studied. Under acidic conditions, the salting‐out effect prevails over the electrostatic shielding effect, and the amide group shells with a slight protonation degree are covered up by the large POEGA petals. Under neutral conditions, the stretching degrees of POEGA blocks at low/moderate salt concentrations are close. At high salt concentrations, the isotherms gradually shift to large molecular areas in the order of the NaCl, Na2SO4, NaNO3, and NaSCN cases. The hysteresis degrees of the monolayers increase with the increase of salt concentrations due to the gradually increased interfacial stretching degree and compression‐induced underwater solubility of POEGA blocks. All the initial LB films of PNIPAM‐b‐POEGA exhibit isolated circular micelles with small cores. Upon compression, the LB films exhibit slightly large micelles because of the possible coalescence of some neighboring cores. [ABSTRACT FROM AUTHOR]

Poloxamers are amphiphilic block copolymers consisting of poly(ethylene glycol) (PEG) and poly(propylene glycol) segments. Their self‐assembly and interfacial properties are tied to the relative hydrophilicity and hydrophobicity of each block and can therefore be adjusted by changing block lengths. Here, a series of PEG‐polycycloether block copolymers is synthesized that have the same structure as a poloxamer, but they encompass a rigid polycyclic backbone as the hydrophobic block. A variety of polymer structures are synthesized, for example diblock or triblock architectures, with/without olefinic units, atactic or isotactic backbone, and different block lengths. Due to their amphiphilicity, self‐assembly into spherical aggregates (diameters ranging from 64 to 132 nm) at low concentrations (critical aggregation concentration as low as 0.04 mg mL−1) is observed in water. Low surface tensions (as low as 26.7 mN m−1) are observed as well as the formation of stable high internal phase emulsions (HIPEs) irrespective of the oil/water ratio. This contrasts with the properties of the commonly used poloxamers P188 or P407 and illustrates the significance of the rigid polycycloether block. These new colloidal properties offer new prospects for applications in emulsion formulations for biomedicine, cosmetics, and the food industry. [ABSTRACT FROM AUTHOR]

Ethylene glycol (EG) is an industrially important two-carbon diol used as a solvent, antifreeze agent, and building block of polymers such as poly(ethylene terephthalate) (PET). Recently, the use of EG as a starting material for the production of bio-fuels or bio-chemicals is gaining attention as a sustainable process since EG can be derived from materials not competing with human food stocks including CO2, syngas, lignocellulolytic biomass, and PET waste. In order to design and construct microbial process for the conversion of EG to value-added chemicals, microbes capable of catabolizing EG such as Escherichia coli, Pseudomonas putida, Rhodococcus jostii, Ideonella sakaiensis, Paracoccus denitrificans, and Acetobacterium woodii are candidates of chassis for the construction of synthetic pathways. In this mini-review, we describe EG catabolic pathways and catabolic enzymes in these microbes, and further review recent advances in microbial conversion of EG to value-added chemicals by means of metabolic engineering. Key points: • Ethylene glycol is a potential next-generation feedstock for sustainable industry. • Microbial conversion of ethylene glycol to value-added chemicals is gaining attention. • Ethylene glycol-utilizing microbes are useful as chassis for synthetic pathways. [ABSTRACT FROM AUTHOR]

In this work, a nanogold surface molecularly imprinted polymer spectral probe (AuNP@MIP) for selectively identifying ferrocyanide was prepared under microwave irradiation using nanogold as the core, ferrocyanide as the template ion, methacrylic acid as the monomer, and ethylene glycol dimethacrylate as the cross-linking agent. AuNP@MIP was found to produce a resonance Rayleigh scattering (RRS) peak at 370 nm. When potassium ferrocyanide (K4Fe(CN)6) was present, a AuNP@MIP-Fe(CN)6 complex was formed, producing RRSenergy transfer (RRS-ET). With an increase in ferrocyanide concentration within a certain range, the RRS intensity at 370 nm decreased linearly, and the detection range was 0.02-0.40 µmol L-1, with a detection limit as low as 0.006 µmol L-1 ferrocyanide. This new method has the advantages of simplicity, rapidity, and selectivity when applied for the determination of K4Fe(CN)6 in table salt. [ABSTRACT FROM AUTHOR]

3D bioprinting techniques have enabled the fabrication of irregular large‐sized tissue engineering scaffolds. However, complicated customized designs increase the medical burden. Meanwhile, the integrated printing process hinders the cellular uniform distribution and local angiogenesis. A novel approach is introduced to the construction of sizable tissue engineering grafts by employing hydrogel 3D printing for modular bioadhesion assembly, and a poly (ethylene glycol) diacrylate (PEGDA)‐gelatin‐dopamine (PGD) hydrogel, photosensitive and adhesive, enabling fine microcage module fabrication via DLP 3D printing is developed. The PGD hydrogel printed micocages are flexible, allowing various shapes and cell/tissue fillings for repairing diverse irregular tissue defects. In vivo experiments demonstrate robust vascularization and superior graft survival in nude mice. This assembly strategy based on scalable 3D printed hydrogel microcage module could simplify the construction of tissue with large volume and complex components, offering promise for diverse large tissue defect repairs. [ABSTRACT FROM AUTHOR]

Cyclometallated Pt(II) complexes possessing hydrophobic 2-phenylpyridine (ppy) ligands and hydrophilic acetonylacetone (acac) ligands have been investigated for their ability to detect amyloid fibrils via luminescence response. Using hen egg-white lysozyme (HEWL) as a model amyloid protein, Pt(II) complexes featuring benzanilide-substituted ppy ligands and ethylene glycol-functionalized acac ligands demonstrated enhanced luminescence in the presence of HEWL fibrils, whereas Pt(II) complexes lacking complementary hydrophobic/hydrophilic ligand sets displayed little to no emission enhancement. An amphiphilic Pt(II) complex incorporating a bis(ethylene glycol)-derivatized acac ligand was additionally found to trigger restructuring of HEWL fibrils into smaller spherical aggregates. Amphiphilic Pt(II) complexes were generally non-toxic to SH-SY5Y neuroblastoma cells, and several complexes also exhibited enhanced luminescence in the presence of Aß42 fibrils associated with Alzheimer's disease. This study demonstrates that easily prepared and robust (ppy)PtII(acac) complexes show promising reactivity toward amyloid fibrils and represent attractive molecular scaffolds for design of small-molecule probes targeting amyloid assemblies. [ABSTRACT FROM AUTHOR]

The reinforcement of mechanically‐weak hydrogels to yield composites with increased stiffness, strength, or toughness is a well‐established approach. In particular, introducing electrospun nanofibers into hydrogels is a common strategy for biomedical applications, as the resulting hierarchical structure mimics biology and allows for control over fiber diameter and alignment and tuning of mechanical properties. However, further study of the link between the constituent materials and the mechanical properties of the composite is uncommon. One potential model to understand the mechanical properties of fiber‐reinforced hydrogels involves the Halpin–Tsai equations, which relate the modulus values of the fibers and hydrogel matrix and the fiber volume fraction, to the modulus of the composite. To assess the application of this model to fiber‐reinforced hydrogels, predicted values were compared with experimental values from mechanical testing of a poly(ethylene glycol) (PEG) matrix reinforced with an electrospun polycaprolactone (PCL) fiber mat. Although the equations described these systems well in tension, providing a facile approach to identify a fiber volume fraction that will achieve a desired modulus, the Halpin–Tsai approach was less successful under compression. This study motivates additional investigation of the role of structural features of hydrogel composites in determining mechanical properties to enable design of materials for specific applications. [ABSTRACT FROM AUTHOR]

In this study, antimicrobial plasticized poly(lactic acid) (PLA) films by incorporating poly(ethylene glycol) (PEG) and methenamine (MA) were prepared by solvent casting method. We investigated the effects of different concentrations of MA on the antimicrobial properties against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) which were types of gram‐negative and gram‐positive bacteria in turn. It was determined that as the rate of MA in the PLA/PEG film enhanced, its antimicrobial activity against both bacteria also increased. As a result, the maximum inhibitory effect for E. coli was seen in MA5, MA8, and M10 films, and it reduced the bacterial population by 100%. In S. aureus, the high inhibition effect was seen in the MA8 film, and it reduced the bacterial population by 95%. Moreover, as the MA concentration increases, the thermal stability of PLA/PEG films increases and approaches the thermal decomposition temperature of neat PLA. The incorporation of 0.5% MA to this system caused a significant increase in elongation at break values. It is concluded that a minimum concentration of MA is sufficient for high flexibility compared with pure PLA. These MA containing PLA/PEG composite films have potential applications as biodegradable flexible packaging materials. [ABSTRACT FROM AUTHOR]

Bis‐carbonylimidazolide (BCI) functionalization enables an efficient synthetic strategy to generate high molecular weight segmented nonisocyanate polyurethanes (NIPUs). Melt phase polymerization of ED‐2003 Jeffamine, 4,4′‐methylenebis(cyclohexylamine), and a BCI monomer that mimics a 1,4‐butanediol chain extender enables polyether NIPUs that contain varying concentrations of hard segments ranging from 40 to 80 wt. %. Dynamic mechanical analysis and differential scanning calorimetry reveal thermal transitions for soft, hard, and mixed phases. Hard segment incorporations between 40 and 60 wt. % display up to three distinct phases pertaining to the poly(ethylene glycol) (PEG) soft segment Tg, melting transition, and hard segment Tg, while higher hard segment concentrations prohibit soft segment crystallization, presumably due to restricted molecular mobility from the hard segment. Atomic force microscopy allows for visualization and size determination of nanophase‐separated regimes, revealing a nanoscale rod‐like assembly of HS. Small‐angle X‐ray scattering confirms nanophase separation within the NIPU, characterizing both nanoscale amorphous domains and varying degrees of crystallinity. These NIPUs, which are synthesized with BCI monomers, display expected phase separation that is comparable to isocyanate‐derived analogues. This work demonstrates nanophase separation in BCI‐derived NIPUs and the feasibility of this nonisocyanate synthetic pathway for the preparation of segmented PU copolymers. [ABSTRACT FROM AUTHOR]

This study experimentally investigates the use of Meliaceae Family Extract (MFE), Annonaceae Family Extract (AFE) and the Extracts Hybrid (EH) of both plants as inhibitors of gas hydrate were compared with conventional Monoethylene glycol (MEG). 1 to 3 wt% of the inhibitors were screened on a hydrate mini flow-loop. Different plots of pressure and temperature against time, final and initial pressure against time indicate that MFE, AFE and EH outperformed MEG at different weight concentrations. At 1 wt%, MFE exhibited an outstanding inhibition efficiency of 64.65%, whereas AFE, EH and MEG record 57.58%, 58.59% and 54.55%. MFE gave an improved performance at 1 wt% compared to the other three inhibitors. At 2 wt%, the optimum efficiency was recorded by AFE with an inhibition efficiency of 72.73% while EH, MFE and MEG were 69.70%, 50.51% and 59.60%. MEG performed slightly better at 3 wt% with inhibition efficiency of 71.72% than MFE and EH with inhibition efficiency of 70.71% while AFE performed the least at 68.69%. EH generally performed better, it is locally sourced and gotten from plant families which makes it less expensive and environmentally friendly unlike MEG, which is expensive and toxic to the environment. [ABSTRACT FROM AUTHOR]

Simple Summary: In order to improve the comprehensive utilization of oil tea seed meal and increase the comprehensive economic benefits of the oil tea industry. In this paper, the low eutectic solvent was used as the extraction system, and the ultrasonic extraction method was combined with the enzymatic method to jointly extract the tea saponins. It was further purified with a large-pore adsorption resin to develop a set of environmentally friendly, energy-saving, and efficient tea saponin extraction and purification processes. On this basis, the tea saponins extracted from oil tea seed meal were further analyzed for antioxidant capacity and bacteriostatic activity. The results provided the scientific experimental basis and theoretical support for the efficient use of oil tea by-products. Tea saponins have high surface-active and biological activities and are widely used in chemicals, food, pharmaceuticals, and pesticides. Tea saponins are usually extracted using ethanol or water, but both methods have their disadvantages, including a negative impact on the environment, high energy consumption, and low purity. In this study, we explored an effective process for extracting tea saponins from tea meal using deep eutectic solvents combined with ultrasonic extraction and enzymatic techniques. The experimental results showed that a high extraction efficiency of 20.93 ± 0.48% could be achieved in 20 min using an ultrasonic power of 40% and a binary DES consisting of betaine and ethylene glycol (with a molar ratio of 1:3) at a material–liquid ratio of 1:35 and that the purity of the tea saponins after purification by a large-pore adsorption resin reached 95.94%, which was higher than that of commercially available standard tea saponin samples. In addition, the extracted tea saponins were evaluated for their antioxidant and bacteriostatic activities using chemical and biological methods; the results showed that the tea saponins extracted using these methods possessed antioxidant properties and displayed significant antibacterial activity. Therefore, the present study developed a method for using deep eutectic solvents as an environmentally friendly technological solution for obtaining high-purity tea saponins from tea meal oil. This is expected to replace the current organic solvent and water extraction process and has great potential for industrial development and a number of possible applications. [ABSTRACT FROM AUTHOR]

The article describes a green and efficient synthesis method for pyrano[2,3-c]-pyrazoles, employing DL-alpha-tocopherol methoxypolyethylene glycol succinate solution (TPGS-750-M) as a green and biodegradable surfactant in water. The utilization of water as a reaction medium and TPGS-750-M as a surfactant obviates the necessity for organic solvents, thereby enhancing the environmental sustainability of the synthesis. The compounds synthesized using this novel method was characterized using various spectroscopic techniques, including 1H-NMR, 13C-NMR, and mass spectrometry. [ABSTRACT FROM AUTHOR]

Hydrogels are of great importance for functionalizing sensors and microfluidics, and poly(ethylene glycol) dimethacrylate (PEG-DMA) is often used as a viscosifier for printable hydrogel precursor inks. In this study, 1–10 kDa PEG-DMA based hydrogels were characterized by gravimetric and electrochemical methods to investigate the diffusivity of small molecules and proteins. Swelling ratios (SRs) of 14.43–9.24, as well as mesh sizes ξ of 3.58–6.91 nm were calculated, and it was found that the SR correlates with the molar concentration of PEG-DMA in the ink (MCI) (SR = 0.1127 × MCI + 8.3256, R2 = 0.9692) and ξ correlates with the molecular weight (Mw) (ξ = 0.3382 × Mw + 3.638, R2 = 0.9451). To investigate the sensing properties, methylene blue (MB) and MB-conjugated proteins were measured on electrochemical sensors with and without hydrogel coating. It was found that on sensors with 10 kDa PEG-DMA hydrogel modification, the DPV peak currents were reduced to 92 % for MB, 73 % for MB-BSA, and 23 % for MB-IgG. To investigate the diffusion properties of MB(-conjugates) in hydrogels with 1–10 kDa PEG-DMA, diffusivity was calculated from the current equation. It was found that diffusivity increases with increasing ξ. Finally, the release of MB-BSA was detected after drying the MB-BSA-containing hydrogel, which is a promising result for the development of hydrogel-based reagent reservoirs for biosensing. [ABSTRACT FROM AUTHOR]

This study aimed to control the oral absorption of cyclosporine A (CsA) with the use of a mucosal drug delivery system (mDDS). Mucopenetrating nanocarriers (MP/NCs) and mucoadhesive nanocarriers (MA/NCs) were prepared by flash nanoprecipitation employing polystyrene‐block‐poly(ethylene glycol) and polystyrene‐block‐poly(N,N‐dimethyl aminoethyl methacrylate), respectively. Their particle distribution in the rat gastrointestinal tract were visualized by fluorescent imaging. Plasma concentrations were monitored after oral administration of CsA‐loaded MP/NCs (MP/CsA) and MA/NCs (MA/CsA) to rats. MP/NCs and MA/NCs had a particle size below 200 nm and ζ‐potentials of 4 and 40 mV, respectively. The results from in vitro experiments demonstrated mucopenetration of MP/NCs and mucoadhesion of MA/NCs. Confocal laser scanning microscopic images showed diffusion of MP/NCs in the gastrointestinal mucus towards epithelial cells and localization of MA/NCs on the surface of the gastrointestinal mucus layer. In a pH 6.8 solution, rapid and sustained release of CsA were observed for MP/CsA and MA/CsA, respectively. After oral dosing (10 mg‐CsA/kg) to rats, amorphous CsA powder exhibited a time to maximum plasma concentration (Tmax) of 3.4 h, maximum plasma concentration (Cmax) of 0.12 μg/mL, and bioavailability of 0.7%. Compared with amorphous CsA powder, MP/CsA shortened Tmax by 1.1 to 2.3 h and increased the bioavailability by 43‐fold to 30.1%, while MA/CsA prolonged Tmax by 3.4 to 6.8 h with Cmax and bioavailability of 0.65 μg/mL and 11.7%, respectively. These pharmacokinetic behaviors would be explained by their diffusion and release properties modulated by polymeric surface modification. The mDDS approach is a promising strategy for the pharmacokinetic control of orally administered CsA. [ABSTRACT FROM AUTHOR]

A responsive polymer was synthesized from polymeric chain coatings with N-(2-hydroxypropyl) methacrylamide (HPMA) and Ethylene glycol dimethyl acrylate (EGDMA) groups (MP@ p (EGDMA-co-HPMA)) and was used to adsorption/release of Cefpodoxime (CPD) from its liquid dispersions. The results revealed that magnetic polymer could effectively adsorb CPD at pH =8 at about 30 °C. Also, the adsorption of CPD on magnetic polymer was best fitted to the Langmuir model. The drug release results indicated the thermo and pH sensitivity behavior of magnetic polymer with 35% of CPD release at acidic (pH = 1.2) and 62% at alkaline (pH = 7.4) solutions. [ABSTRACT FROM AUTHOR]

• Improving the seasonal performance by increasing heat exchanger size. • R32 drop-in impacts various compressor modulation strategies in distinctive ways. • Oversizing heat exchangers has larger benefits with lower range modulation strategy. • Oversizing BPHX can yield higher performance than improving the compressor motor efficiency. • Variable speed compressor at part load conditions could experience refrigerant maldistribution. The decrease in fossil fuel reserves and high energy consumption by HVAC&R equipment require the use of compressors with better efficiencies and capacity modulation strategies. Usually, seasonal performance studies focus on compressor capacity modulation methods, however the current study explores the idea of improving the seasonal performance of two compressor modulation techniques: a two-stage and a variable speed compressor with different capacity modulation ranges by using larger condensers in an R410A water ethylene glycol chiller system. The analysis shows that oversizing the heat exchangers has larger benefits with the compressor modulation strategy with lower range. Additionally, the seasonal performance estimated according to AHRI 551/591 (2020) of a two-stage compressor with oversized condenser is higher than a basic single speed compressor with a better motor indicating that oversizing brazed plate heat exchanger (BPHX) might yield higher performance than improving the compressor motor efficiency. Due to the high global warming potential (GWP) of R410A, there is a focus on replacing it with low GWP refrigerants such as R32 to reduce CO 2 emissions. This study would also compare the performance when using R32 as a drop-in refrigerant in the two different R410A compressor capacity modulation strategies with comparable cooling capacity. When the refrigerant was changed from R410A to R32, the integrated part load value (I P L V. S I), an efficiency metric for variable speed compressor remains relatively constant at 5.5 while it increases from 3.9 to 4.4 for the two-stage compressor. It is hypothesized that low refrigerant mass flow rate (m ˙ r e f) provided by the variable speed compressor when matching the load at the lower part load conditions leads to refrigerant maldistribution in BPHX and reduced I P L V. S I. [ABSTRACT FROM AUTHOR]

Dural defects and subsequent complications, including cerebrospinal fluid (CSF) leakage, are common in both spine surgery and neurosurgery, and existing clinical treatments are still unsatisfactory. In this study, a tissue-adhesive and low-swelling hydrogel sealant comprising gelatin and o -phthalaldehyde (OPA)-terminated 4-armed poly(ethylene glycol) (4aPEG-OPA) is developed via the OPA/amine condensation reaction. The hydrogel shows an adhesive strength of 79.9 ± 12.0 kPa on porcine casing and a burst pressure of 208.0 ± 38.0 cmH2O. The hydrogel exhibits a low swelling ratio at physiological conditions, avoiding nerve compression in the limited spinal and intracranial spaces. In rat and rabbit models of lumbar and cerebral dural defects, the 4aPEG-OPA/gelatin hydrogel achieves excellent performance in dural defect sealing and preventing CSF leakage. Moreover, local inflammation, epidural fibrosis and postoperative adhesion in the defect areas are markedly reduced. Thus, these findings establish the strong potential of the hydrogel sealant for the effective watertight closure of dural defects. [ABSTRACT FROM AUTHOR]

A low-shrinkage and viscosity-reducing polycarboxylate superplasticizer was synthesized with maleic anhydride (MAH), diethylene glycol monobutyl ether, and methoxypoly (ethylene glycol) methacrylate (MPEGnMA). The surface tension, early shrinkage, cement paste performance, and application performance of concrete made with the synthesized water-reducing admixture were tested. A series of experiments were conducted to determine the optimal range of plastic viscosity coefficients for producing high-quality, fair-faced concrete with minimal surface defects. These experiments utilized both the synthesized water-reducing admixture alone and in combination with other water-reducing agents. The results showed that the synthesized water-reducing admixture had an ideal molecular structure, as confirmed by the GPC spectrum. When added to an aqueous solution, it reduced the surface tension from 72.47 mN/m to 30.56 mN/m. The 72 h shrinkage value of concrete was reduced by 20.6% compared with that of the conventional control group, effectively reducing shrinkage and adjusting the viscosity of the concrete mixture. Additionally, the influence of the plastic viscosity coefficient on the apparent voids in fair-faced concrete was investigated. This study revealed that when the plastic viscosity coefficient was between 5 and 10 Pa·s, the apparent void grade of the fair-faced concrete was simultaneously excellent and good. This water-reducing admixture helped prevent surface cracking and voids in fair-faced concrete, making it a suitable choice for producing high-quality fair-faced concrete surfaces. [ABSTRACT FROM AUTHOR]

Berberine (Ber) as a natural isoquinoline alkaloid, with a wide range of biological activities, mainly suffers from low bioavailability, decreasing its therapeutic efficacy. In this study, two novel conjugates of Ber with self-assembly property, Ber–polyethylene glycol (B–PEG) and Ber–diethylene glycol monomethyl ether (B–DG), were synthesized to investigate the effect of the anchoring part on the CMC, morphology as well as antioxidant and neuroprotective properties of the nanomicelles. The CMC increased from 1.2 μmol in B–DG to 3.0 μmol in B–PEG, measured by pendant drop. The anchored part affected greatly the shape and CMC of the self-assembled nanomicelles. A mixture of semi-spherical and cubic nanomicelles in the average hydrodynamic size of 93 nm was achieved for B–PEG, while B–DG nanomicelles were just in semispherical morphology with the hydrodynamic size of 64 nm. The antioxidant property of the nanomicelles was studied by DPPH scavenging and ferric reducing antioxidant power assays, exhibiting improved antioxidant activity of B–PEG and B–DG conjugates compared to free Ber. The neuroprotection potency of Ber was improved significantly after conjugation compared to free Ber against H2O2-induced cell death and B–PEG showed activity as level as that of the standard drug, Quercetin. Owing to the self-assembly property and interesting biological activities of the introduced amphiphilic Ber–PEG conjugate, we propose application of this nanomicelle alone, or as a promising bioactive carrier of the poorly water-soluble drugs, against neurodegenerative diseases. [ABSTRACT FROM AUTHOR]

The alkylation of 2-(4-fluorophenyl)- and 2-[3-(trifluoromethyl)phenyl]acetonitriles with 1,4-di-bromo-butane gave 1-(substituted phenyl)cyclopentane-1-carbonitriles which were hydrolyzed to the corre-sponding carboxylic acids by the action of potassium hydroxide in ethylene glycol. The resulting acids were converted to acid chlorides, and the latter reacted with N,N-dialkylaminoalkylamines, as well as with N,N-di-alkylaminoalkanols, to produce new amino amide and amino ester derivatives of 1-(4-fluorophenyl)- and 1-[3-(trifluoromethyl)phenyl]cyclopentane-1-carboxylic acids, which were characterized as hydrochlorides. The synthesized compounds were evaluated for their antiarrhythmic and anticonvulsant activities. [ABSTRACT FROM AUTHOR]

This study aimed to assess the ability of rosmarinic acid (RA) to prevent kidney stone formation in an ethylene glycol and ammonium chloride (EG/AC) model. There was an increase in diuresis in the normotensive (NTRs) and hypertensive rats (SHRs) treated with hydrochlorothiazide (HCTZ) and exposed to EG/AC, while RA restored urine volume in NTRs. The EG/AC groups exhibited lower urine pH and electrolyte imbalance; these parameters were not affected by any of the treatments. Both HCTZ+EG/AC and RA+EG/AC reduced calcium oxalate crystal formation in NTR and SHR urine. Kidney tissue analysis revealed alterations in oxidative stress and inflammation parameters in all EG/AC-receiving groups, with RA enhancing antioxidant defenses in SHRs. Additionally, crystals were found in the kidney histology of all EG/AC-exposed groups, with reduced Bowman's capsule areas in NTRs and SHRs. The NTR VEH+EG/AC group showed intense renal damage, while the others maintained their structures, where treatments with HCTZ and RA were fundamental for kidney protection in the NTRs. Docking analysis showed that RA exhibited good binding affinity with matrix metalloproteinase-9, phosphoethanolamine cytidylyltransferase, and human glycolate oxidase enzymes. The data disclosed herein underscore the importance of further research to understand the underlying mechanisms better and validate the potential of RA for clinical use. [ABSTRACT FROM AUTHOR]

In presented communication, the hybrid nanomaterial (Ethylene Glycol + Ag + CuO) flow by a stretched cylinder is numerically analyzed. Thermal characteristics are explored by thermal radiation and Newtonian heating. Flow analysis is performed via consideration of slip boundary and stagnation-point. Heat transport and flow expressions (PDEs) are converted into ODEs. In order to employ bvp4c (shooting method), the resulting ODEs are then reduced into first-order system of ODEs. Flow, heat transport rate, temperature and surface friction coefficient are examined graphically under influences of involved sundry parameters. Comparison is made among hybrid nanofluid (Ethylene Glycol + Ag + CuO), nanofluid (Ethylene Glycol + Ag) and basefluid (Ethylene Glycol) for physical quantities of interest. Velocity shows increasing behavior towards the higher value of nanoparticles volume fraction for silver and copper oxide, curvature, velocity ratio and velocity slip parameters. Higher estimations of nanoparticles volume fraction for silver and copper oxide, curvature, radiation and conjugate parameters cause intensification in fluid temperature. Skin friction is controlled against a higher velocity ratio parameter. Nusselt number decays with an increment in velocity ratio parameter while it boosts via higher nanoparticles volume fraction for silver and copper oxide and curvature parameter. Best performance is noticed for hybrid nanomaterial. [ABSTRACT FROM AUTHOR]

Dispersions of amino-functionalized silica in ethylene glycol (EG) and in aqueous glycol show excellent stability at room temperature. Stability at elevated temperatures would be much desired with respect to their potential application as heat-transfer fluids. Amino-functionalized silica was dispersed in EG and in 50–50 aqueous EG by mass. HCl and acetic acid were added to enhance the positive ζ potential. The dispersions were stored at 40, 60, 80, and 100 °C for up to 28 days, and ζ potential and apparent particle radius were studied as a function of elapsed time. The particles showed a positive ζ potential in excess of 40 mV (Smoluchowski), which remained unchanged for 28 days. Such a high absolute value of ζ potential is sufficient to stabilize the dispersion against flocculation and sedimentation. The apparent particle radius in acidified dispersions was about 70 nm, and it was stable for 28 days. The particles were larger in pH-neutral dispersions. The apparent particle radius was about 80 nm in fresh dispersions and it increased on long storage at 80 and 100 °C. [ABSTRACT FROM AUTHOR]

Currently, new clean energy storage technology must be effective, affordable, and ecologically friendly so as to meet the diverse and sustainable needs of the energy supply. In this work, NiCo-LDH containing intercalated EG was successfully prepared within 210 s using an ultrafast microwave radiation technique. Subsequently, a series of characterization and systematic electrochemical tests were conducted to analyze the composition, structure, and energy storage mechanism of the NiCo-LDH material. The Ni:Co ratio of 5:5 results in the highest capacitance value of 2156 F/g at 1 A/g and an outstanding rate performance of 86.8% capacity retention rate at 10 A/g. The results demonstrated that the unique porous structure of NiCo-LDH and large layer spacing were conducive to more electrochemical reactions. Additionally, an electrochemical test was carried out on the NiCo-LDH as a hybrid supercapacitor electrode material, with NiCo-LDH-5:5 serving as the positive electrode and activated carbon as the negative electrode, the asymmetric supercapacitor can achieve a maximum energy density of 82.5 Wh kg−1 and power density of 8000 W kg−1. The NiCo-LDH-5:5//AC hybrid supercapacitors own 81.5% cycle stability and 100% coulombic efficiency after 6000 cycles at 10 A/g. [ABSTRACT FROM AUTHOR]

The synergistic effect of drug and gene delivery is expected to significantly improve cancer therapy. However, it is still challenging to design suitable nanocarriers that are able to load simultaneously anticancer drugs and nucleic acids due to their different physico-chemical properties. In the present work, an amphiphilic block copolymer comprising a biocompatible poly(ethylene glycol) (PEG) block and a multi-alkyne-functional biodegradable polycarbonate (PC) block was modified with a number of poly(2-(dimethylamino)ethyl methacrylate) (PDMAEMA) side chains applying the highly efficient azide–alkyne "click" chemistry reaction. The resulting cationic amphiphilic copolymer with block and graft architecture (MPEG-b-(PC-g-PDMAEMA)) self-associated in aqueous media into nanosized micelles which were loaded with the antioxidant, anti-inflammatory, and anticancer drug quercetin. The drug-loaded nanoparticles were further used to form micelleplexes in aqueous media through electrostatic interactions with DNA. The obtained nanoaggregates—empty and drug-loaded micelles as well as the micelleplexes intended for simultaneous DNA and drug codelivery—were physico-chemically characterized. Additionally, initial in vitro evaluations were performed, indicating the potential application of the novel polymer nanocarriers as drug delivery systems. [ABSTRACT FROM AUTHOR]

Although the incidence of infections in orthopedic surgeries, including periprosthetic surgeries, remains low at approximately 1–2%, the number of surgeries and the incidence of drug-resistant bacteria is increasing. The cost and morbidity associated with revision surgeries are huge. More effective drug combinations and delivery methods are urgently needed. In this paper, three anti-infective drugs (vancomycin, rifampicin, and silver sulfadiazine) have been jointly and effectively electrospun in thin (0.1 mm) flexible nanofiber mats of either poly (methyl methacrylate) (PMMA) or poly (lactic-co-glycolic acid) (PLGA). The inclusion of poly (ethylene glycol) (PEG) enabled optimal drug release with a reduced water contact angle for wetting. The controlled release of these three agents from 20% PEG (w/w to polymer)-blended PMMA or PLGA nanofiber mats may allow for the prophylactical prevention of implant-related infections or provide methods to treat orthopedic infections at the time of revision surgeries. These combinations of drugs provide excellent additive or synergistic antibiotic action against a broader spectrum of bacteria than each drug alone. [ABSTRACT FROM AUTHOR]

Polymeric thin films based on polylactide with an addition of poly(ethylene glycol) as a plasticizer and flavonoids in the form of quercetin and berberine were subjected to tests that were particularly relevant from the point of view of contact with food. A comparative analysis of the effect of individual flavonoids on the antioxidative properties of tested films and blueberry storage was carried out. The influence of active compounds on the water vapor permeability, as well as UV protection, of the obtained materials was investigated. Also, the specific migration of individual flavonoids from obtained materials to food simulants in the form of acetic acid and ethyl alcohol was determined. The crucial point of this study is the storage of blueberries. The obtained results indicate that the selection of packaging, containing individual active compounds, depends on the purpose and requirements that the packaging must meet for particular types of food. [ABSTRACT FROM AUTHOR]

Poly(dimethylsiloxane) (PDMS) coatings are considered to be environmentally friendly antifouling coatings. However, the presence of hydrophobic surfaces can enhance the adhesion rate of proteins, bacteria and microalgae, posing a challenge for biofouling removal. In this study, hydrophilic polymer chains were synthesised from methyl methacrylate (MMA), Poly(ethylene glycol) methyl ether methacrylate (PEG-MA) and 3-(trimethoxysilyl) propyl methacrylate (TPMA). The crosslinking reaction between TPMA and PDMS results in the formation of a silicone-based amphiphilic co-network with surface reconstruction properties. The hydrophilic and hydrophobic domains are covalently bonded by condensation reactions, while the hydrophilic polymers migrate under water to induce surface reconstruction and form hydrogen bonds with water molecules to form a dense hydrated layer. This design effectively mitigates the adhesion of proteins, bacteria, algae and other marine organisms to the coating. The antifouling performance of the coatings was evaluated by assessing their adhesion rates to proteins (BSA-FITC), bacteria (B. subtilis and P. ruthenica) and algae (P. tricornutum). The results show that the amphiphilic co-network coating (e.g., P-AM-15) exhibits excellent antifouling properties against protein, bacterial and microalgal fouling. Furthermore, an overall assessment of its antifouling performance and stability was conducted in the East China Sea from 16 May to 12 September 2023, which showed that this silicon-based amphiphilic co-network coating remained intact with almost no marine organisms adhering to it. This study provides a novel approach for the development of high-performance silicone-based antifouling coatings. [ABSTRACT FROM AUTHOR]

In this work, comb homopolymers as well as comb-type copolymers of thermo-responsive oligo(ethylene glycol methyl ether methacrylate)s, OEGMAs, with various chain lengths (DEGMA, PEGMA500, and PEGMA950 containing 2, 9, or 19 repeating ethylene glycol units, respectively) were synthesized through free radical (co)polymerization. For the copolymers, either the functional hydrophobic glycidyl methacrylate (GMA) or the inert hydrophilic N,N-dimethylacrylamide (DMAM) were selected as comonomers. The self-assembly and thermo-responsive behavior of the products was investigated through Nile Red fluorescence probing, turbidimetry, and dynamic light scattering (DLS). Interestingly, it was found that all OEGMA-based homopolymers exhibit a tendency to self-organize in aqueous media, in addition to thermo-responsiveness. The critical aggregation concentration (CAC) increases with the number of repeating ethylene oxide units in the OEGMA macromonomers (CAC was found to be 0.003, 0.01, and 0.03% w/v for the homopolymers PDEGMA, PPEGMA500, and PPEGMA950, respectively). Moreover, the CAC of the copolymers in aqueous media is highly affected by the incorporation of hydrophobic GMA or hydrophilic DMAM units, leading to lower or higher values, respectively. Thus, the CAC decreases down to 0.003% w/v for the GMA-richest copolymer of PEGMA950, whereas CAC increases up to 0.01% w/v for the DMAM-richest copolymer of DEGMA. Turbidimetry and DLS studies proved that the thermo-sensitivity of the polymers is governed by several parameters such as the number of repeating ethylene glycol groups in the side chains of the OEGMAs, the molar percentage of the hydrophobic or hydrophilic comonomers, along with the addition of salts in the aqueous polymer solutions. Thus, the cloud point of the homopolymer PDEGMA was found at 23 °C and it increases to 33.5 °C for the DMAM-richest copolymer of DEGMA. Lastly, the formation of a hydrogel upon heating aqueous mixtures of the GMA-comprising copolymers with silica nanoparticles overnight is strong evidence of the functional character of these polymers. [ABSTRACT FROM AUTHOR]