Search Results (488)

Surface-imprinted polymer (SIP)-based biomimetic sensors are promising for direct whole-bacteria detection; however, the commonly used fabrication approach (micro-contact imprinting) often suffers from limited imprint density, heterogeneous template distribution, and poor reproducibility. Here, we introduce a photolithography-defined master stamp featuring E. coli mimics, enabling high-density, well-oriented cavity arrays (3 × 10⁷ imprints/cm²). Crucially, the cavity arrangement is engineered such that the SIP layer functions simultaneously as the bioreceptor and as a diffraction grating, enabling label-free optical quantification by reflectance changes without additional transduction layers. Finite-difference time-domain (FDTD) simulations are used to model and visualize the optical response upon bacterial binding. Proof-of-concept experiments using a differential two-well configuration confirm concentration-dependent detection of E. coli in PBS, demonstrating a sensitive, low-cost, and scalable sensing concept that can be readily extended to other bacterial targets by redesigning the photolithographic master. Full article

Pigment gallstones represent a heterogeneous group of concretions, classically divided into black and brown types, whose morphology and microstructure offer critical clues about their underlying pathogenesis. Gallstone formation (lithogenesis) is a complex process triggered when the physicochemical equilibrium of bile is disrupted. Background/Objectives: The spicules observed on the surface of certain black pigment gallstones have traditionally been attributed to the branching capacity of cross-linked bilirubin polymers. However, a growing body of experimental and spectroscopic evidence suggests that inorganic calcium salts, particularly calcium carbonate and calcium phosphate, play a central role in the formation of the distinctive spiculated or “coral-like” architecture. Materials and Methods: In our study, we examined a case series of 1350 consecutive patients with gallstone disease, identifying 81 patients who presented with solitary black pigment stones. We systematically explored the association between high calcium content, specifically calcium carbonate, and the occurrence of spiculated morphology. Our analyses demonstrated a robust correlation between an elevated concentration of calcium carbonate and the presence of well-defined spicules. Results: These results support the hypothesis that mineral elements, rather than organic bilirubin polymers, act as crucial determinants of the peculiar crystalline structure observed in a significant subset of pigment stones. Spiculated stones, due to their small size and sharp projections, have a higher likelihood of migrating, increasing the risk of potentially life-threatening complications, such as acute cholangitis and gallstone pancreatitis. Conclusions: Our findings, consistent with recent advanced crystallographic analyses, underscore the importance of considering mineral composition in the diagnosis and management of cholelithiasis. Understanding the factors that drive calcium carbonate precipitation is essential for developing new preventive and therapeutic strategies, aiming to modulate bile chemistry and reduce the risk of calcium-driven lithogenesis. Full article

Wood–polymer composites (WPCs) consistently garner considerable attention owing to their material versatility and sustainability, resulting in numerous review studies across diverse disciplines. Nonetheless, since a comprehensive synthesis that consolidates these disparate reviews is lacking, this study performs a meta-synthesis of review articles focused on WPCs employing a science-mapping approach enhanced by CiteSpace software. A systematic search of the Web of Science Core Collection (last updated in June 2025) was conducted, yielding 51 review-type articles selected using PRISMA screening guidelines. Network-based co-citation, clustering, and keyword analyses reveal that recent WPC research centers on three interconnected areas: (i) reinforcement and interfacial engineering, (ii) processing–structure–property relationships, and (iii) sustainability-focused design involving recycling, fire safety, thermal pretreatment, and PCM-based thermal management. Sixteen author/reference clusters and nine keyword clusters highlight well-defined knowledge communities on durability and fire safety, nano- and bio-based reinforcements, recycled and bioplastic matrices, and advanced manufacturing techniques such as co-extrusion, flat-pressing, 3D printing, and wood–polymer impregnation. Timeline and burst analyses show that mechanical performance remains the primary focus, while emerging areas include recycled/waste-derived polymers, cellulose micro- and nanofibers, moisture-resistant hybrids, and wood-based additive manufacturing for construction applications. Full article

The ongoing COVID-19 pandemic, caused by SARS-CoV-2, continues to pose major global health challenges despite extensive vaccination efforts. Variant escape, waning immunity, and reduced vaccine efficacy in immunocompromised populations underscore the urgent need for complementary antiviral therapeutics. Here, we report the design, synthesis, and biological evaluation of precision-engineered dermatan sulfate (DS)-mimetic glycopolymers as multi-targeted inhibitors of SARS-CoV-2. Guided by molecular docking and virtual screening, sulfation at the C2 and C4 positions of iduronic acid was identified as critical for binding to the viral spike protein and inhibiting host and viral enzymes, including heparanase (HPSE) and main protease (M^pro). Chemically synthesized DS disaccharides were covalently grafted onto polymer scaffolds via a post-modification strategy, yielding glycopolymers with well-defined assembly that form uniform nanoparticles under physiological conditions. Surface plasmon resonance and pseudovirus assays revealed strong binding to the viral spike protein (K_D ≈ 177 nM), potent viral neutralization, and minimal cytotoxicity. Cellular uptake studies further demonstrated efficient internalization of nanoparticles and intracellular inhibition of HPSE and M^pro. These results establish a modular, non-anticoagulant, and glycosaminoglycan-mimetic platform for the development of broad-spectrum antiviral agents to complement vaccination and enhance preparedness against emerging coronavirus variants. Full article

Mono-material multilayer polypropylene films were developed as light barrier structures through the incorporation of mineral-filled composite layers. Trilayer films with different layer arrangements were fabricated by thermocompression from polypropylene-based films containing 0, 1 and 5 wt.% of talc and kaolinite. A monolayer polypropylene film of equivalent total thickness was used as a control. Structural, thermal, mechanical, optical, and gas barrier properties were evaluated for all films fabricated. A well-defined trilayer structure was confirmed by SEM. FTIR analysis demonstrated negligible thermo-oxidation, with no thermal-degradation during processing. Improved thermal stability and a slight modification in crystallinity were evidenced by TGA and DSC, respectively. XRD revealed the predominance of the α-form crystalline phase and a preferential polymer crystal orientation associated with the particle presence. Regarding mechanical behavior, enhanced stiffness and tensile strength without loss of sealability or puncture resistance were observed. Trilayer films exhibited significantly reduced UV and visible light transmittance, while maintaining adequate translucency, making them suitable for photosensitive packaging applications. Gas permeabilities remained nearly unchanged, confirming that the barrier performances were preserved. Overall, these mono-material multilayer composites films offer a promising and recyclable alternative to conventional multi-material light barrier packaging, combining improved UV protection, mechanical robustness, and environmental compatibility. Full article

Accurate potentiometric sensing critically depends on the stability and reproducibility of the reference electrode potential. Conventional liquid-filled Ag/AgCl or calomel electrodes, though well-established, are poorly compatible with miniaturized, portable, or long-term in situ sensing devices due to electrolyte leakage, junction potential instability, and maintenance requirements. Recent advances in solid-state and membrane-based reference electrodes offer a promising alternative by eliminating the liquid junction while maintaining stable and well-defined potential. This review summarizes the advancements in polymer-based and composite reference membranes, focusing on material strategies, stabilization mechanisms, and integration approaches. Emphasis is placed on ionic-liquid-doped membranes, conducting polymers, lipophilic salts, and carbon nanomaterials as functional components enhancing interfacial stability and charge transfer. The performances of various architectures, solid-contact, liquid-junction-free, and quasi-reference systems, are compared in terms of potential drift, matrix resistance, biocompatibility, and manufacturability. Furthermore, recent developments in printed, microfluidic, and wearable potentiometric platforms demonstrate how reference membrane innovations enable reliable operation in compact, low-cost, and flexible analytical systems. The review outlines current trends, challenges, and future directions toward universal, miniaturized, and leak-free reference electrodes suitable for innovative sensing technologies. Full article

Hybrid membranes are promising alternatives for various applications, combining a continuous polymer phase with a dispersed filler phase to achieve synergistic functional benefits. The ideal fillers should possess well-defined structures and unique properties for multi-functionality, as well as being sourced from renewable, biodegradable materials for sustainability purposes. This study explored the potential of using cellulose-based renewable materials as fillers for hybrid polymer electrolyte membranes (PEMs) in fuel cells. Cellulose whiskers (CWs), known for their high crystallinity and elastic modulus, were effectively synthesized via optimized sequential alkali treatment and acid hydrolysis. Subsequent functionalization with citric acid was performed to enhance their reinforcing properties and overall performance. Initial characterization using ATR-FTIR and XRD confirmed the CWs’ structural composition, high crystallinity, and the presence of reactive groups (sulfate and hydroxyl). The functionalization process introduced new carbonyl groups (C=O), which was verified by ATR-FTIR, while maintaining high hydrophilicity. Morphological analysis revealed that the crosslinked CWs created a denser and more compact microstructure within the membrane, leading to a significant enhancement in mechanical strength. The modifications to the cellulose whiskers not only improved structural integrity but also boosted the membrane’s ion exchange capacity (IEC) and proton conductivity compared to membranes with unmodified CWs. Initial experiments demonstrated CWs’ compatibility as a filler in a polysulfone (PSU) matrix, forming hybrid membranes suitable for fuel cell applications. Full article

The removal of water pollutants with high selectivity and efficiency is still a huge challenge owing to the complex composition of contaminated water. The preparation, modification of Pickering emulsion microspheres, and their application in the adsorption and removal of non-steroidal anti-inflammatory drugs (diclofenac) in water were studied. Poly(2-(diethylamino)ethyl methacrylate-divinylbenzene), (P(DEAEMA-DVB)) microspheres were prepared by Pickering emulsion polymerization. The P(DEAEMA-DVB) polymer was modified with glycidyl trimethylammonium chloride (GTAC) and phenyl glycidyl ether (PGE) to prepare the adsorbent poly(quaternized and phenyl-functionalized) (P(QP-DVB)) with a substantial quantity of quaternary ammonium functional groups. The non-steroidal anti-inflammatory drugs in aqueous solution was mainly adsorbed by the anion exchange interaction with quaternary ammonium species. The adsorption kinetics coincided with the pseudo-second-order kinetic model, and the adsorption isotherm conformed to the Langmuir isotherm model. The optimized P(QP-DVB) particles exhibited well-defined spherical morphology and a uniform particle size distribution ranging from 15 to 30 µm. Nitrogen adsorption/desorption characterization revealed a high specific surface area of 674 m² g⁻¹ and a pore size distribution from 2 to 25 nm. In addition, the aforementioned microsphere underwent chemical regeneration and exhibits good reusability, thereby reducing both the economic costs and environmental impacts. Full article

Nanogels provide unique opportunities for stabilizing fragile enzymes through soft, hydrated polymer networks. Here, we report the development of a glutathione peroxidase (GPx)-loaded nanogel (GPxNG) engineered via a mild “grafting-to” epoxy–amine coupling strategy to enhance enzyme stability and antioxidant function. An amphiphilic copolymer composed of methacrylated 2,2,6,6-tetramethyl-4-piperidyl (PMA) and glycidyl methacrylate (GMA) was synthesized by controlled reversible addition–fragmentation chain-transfer (RAFT) polymerization using a poly(ethylene glycol) (PEG) macro-chain transfer agent (macro-CTA), yielding well-defined polymer chains with reactive epoxy groups. Covalent conjugation between polymer epoxides and GPx enzyme surface amines generated soft, PEGylated nanogels with high coupling efficiency, uniform particle sizes, and excellent colloidal stability. The engineered nanogels exhibited shear-thinning injectability, robust storage stability, and non-cytotoxic behavior in RAW 264.7 macrophages. Compared with native GPx enzyme, GPxNGs demonstrated significantly enhanced reactive oxygen species (ROS) scavenging activity, including strong inhibition of lipid peroxidation and copper-induced low-density lipoprotein (LDL) oxidation. Importantly, the nanogels preserved GPx enzyme activity after extended storage, freeze–thaw cycles, and repeated catalytic use, whereas the free enzyme rapidly lost function. This protective effect arises from the nanoscale confinement of the GPx enzyme within the flexible PEG-based network, which limits unfolding and aggregation. Overall, this work introduces a simple and biocompatible “grafting-to” nanogel platform capable of stabilizing redox-active enzymes without harsh conditions. The GPx nanogels combine high enzymatic preservation, potent antioxidant activity, and excellent handling properties, highlighting their potential as a therapeutic nanoplatform for mitigating oxidative stress-associated disorders such as atherosclerosis. Full article

Atomic force microscopy (AFM) is widely used to quantify mechanical properties, typically Young’s modulus, by fitting force–indentation data with various mathematical contact models. However, results across laboratories often diverge, and the causes remain unresolved. Here, we interrogate the methodology by which mechanical properties are defined in AFM indentation and identify key limitations of the Hertz model, the standard model for determining mechanical properties, notably that the contact radius is not directly determined, which limits the accuracy of the estimated Young’s modulus. We hypothesize that this inference systematically overestimates the true tip–sample contact, which inflates the contact area and thereby underestimates Young’s modulus. This bias is amplified under large indentation conditions, which are frequently used in soft-material studies. To isolate and clarify the issue, we focus on a well-characterized polymer, polyvinyl chloride (PVC), using it as a controlled testbed for contact radius overestimation. Our analysis is focused on the contact radius and Hertz-based extraction of Young’s modulus. We determined the contact radius and Young’s modulus using AFM with two different probes: a sphere with a 20 nm radius (SPHERE20) and a sphere with a 2 µm radius (SPHERE2000). The results were compared to macroscopic data obtained using a standard measurement (ISO 527-1:2019) of Young’s modulus. The contact was modeled using finite element analysis (FEA). The dependence of the contact radius on the indentation was compared to the Hertz model. The results from FEA fit corrected contact radius values, and it is smaller by 15.46% (SPHERE20) and 57.9% (SPHERE2000) than those calculated by the Hertz model. Full article

Atom transfer radical polymerization (ATRP) is a leading reversible deactivation radical polymerization method. It has become an emerging technology to synthesize well-defined, tailor-made polymers, promoting the development of advanced materials (e.g., bioconjugates and nanocomposites) with precisely designed and controlled macromolecular architectures. ATRP-produced polymers or polymeric materials have been successfully applied in the fields of drug delivery, tissue engineering, sample separation, environmental monitoring, bioimaging, clinical diagnostics, etc. In this review, we systematically summarize the progress of ATRP-based chemical and biological sensors in different application fields, including ion sensing, small-molecule detection, bioimaging, and signal amplification for biosensors. Finally, we briefly outline the prospects and future directions of ATRP. This review is expected to provide a fundamental and timely understanding of ATRP-based sensors and guide the design of novel materials and methods for sensing applications. Full article

Background/Objectives: Compaction of sustained release coated pellets into tablets is associated with damage to the functional coat and loss in sustained release. The influences of precompression, trilayering, and tableting rate on the compaction of sustained release coated pellets into tablets are not well defined and were herein investigated to enhance the current limited understanding of these factors. Methods: Pellets coated with acrylic polymer (AC) or ethylcellulose (EC) were combined with filler material and compacted into multi-unit pellet system (MUPS) tablets prepared using different levels of precompression, as a trilayered MUPS tablet and at different tableting rates. The physical properties of the resulting MUPS tablets were evaluated. Trilayering was achieved by adding cushioning layers at the top and bottom of the MUPS tablet to avoid direct contact of pellets with punch surfaces. Results: With precompression, slightly stronger MUPS tablets were made compared to the tablets without precompression for EC pellets but not AC pellets. However, precompression led to a slight reduction in pellet coat damage for AC pellets but not EC pellets. Trilayering led to significant reductions in pellet coat damage and significant increases in tablet tensile strength. When EC pellets were lubricated with sodium stearyl fumarate, pellet coat damage was significantly lower. Increasing the tableting rate from 20 to 100 rpm did not result in increased pellet coat damage but in significantly weaker tablets due to the shorter dwell time. Conclusions: This study provides key insights on how compaction parameters and techniques could be altered to produce better MUPS tablets. Full article

First introduced by Davidovits in the late 1970s, geopolymer binders were defined as a novel class of inorganic polymers. Then, research progressed from fundamental investigations into their structure and chemistry to a rapidly expanding body of work on construction applications. While geopolymers have attracted considerable interest for their superior performance, durability and reduced environmental footprint, their widespread adoption depends on extensive evaluation and well-defined future directions. The present paper provides a crucial and comprehensive overview of performance criteria, production parameters and future perspectives of geopolymer binders. A bibliometric trend analysis indicates that research on geopolymers has expanded markedly in recent years. From this body of literature, this paper offers priority directions for future work: standardization of diverse raw materials; development of safer, more sustainable activator systems; systematic improvement of fresh mix properties; acquisition of long-term durability data under realistic exposures; and progression toward internationally accepted test methods and design standards. These insights offer a concise roadmap for advancing geopolymer technology from a promising alternative to a widely adopted construction material. Full article

Plastics are essential in modern life but accumulate as waste. Mechanical reprocessing reduces material quality, whereas thermochemical routes require harsh conditions and are costly to upgrade. Together, these factors hinder the large-scale recovery of plastics into equivalent materials. Metal–organic frameworks provide a programmable platform where reticular design fixes porosity and positions well-defined Lewis, Brønsted, redox, and photoredox sites that can preconcentrate oligomers and align scissile bonds for activation. These attributes enable complementary pathways spanning hydrolysis, alcoholysis, aminolysis, photo-oxidation, electrocatalysis, and MOF-derived transformations, with adsorption-guided capture-to-catalysis workflows emerging as integrative schemes. In this review, we establish common figures of merit such as space–time yield, monomer selectivity and purity, energy intensity, site-normalized turnover, and solvent or corrosion footprints. These metrics are connected to design rules that involve active-site chemistry and transport through semi-crystalline substrates. We also emphasize durability under hot aqueous, alcoholic, or oxidative conditions as essential for producing polymer-grade products. Full article

Barium carbonate (BaCO₃) nanoparticles were synthesized by a facile hydrolysis route using BaCl₂ and KOH in aqueous solution, with atmospheric CO₂ as the carbonate source, without external agents. Their structural and morphological properties were investigated by XRD, ATR-FTIR, SEM, and BET, confirming the formation of a pure orthorhombic witherite phase with rod-like morphology and different surface specific areas. The crystallite size increased from 52 to 86 nm with higher precursor concentration and synthesis temperature, as predicted by a regression model correlating synthesis parameter with particle growth. When incorporated into polymer (PVC) and geopolymer (GP) matrices, BaCO₃ enhanced the photocatalytic degradation of methylene blue (MB) under solar light, with GP@Nano-BaCO₃ achieving a higher rate constant compared to PVC@Nano-BaCO₃. The results highlight that the synthesis strategy yields well-defined BaCO₃ nanoparticles with tunable structural features and promising photocatalytic potential when integrated in functional polymer matrices. Future work will address doping strategies and testing in real wastewater conditions. Overall, this synthesis strategy offers a reproducible and environmentally friendly route to BaCO₃ nanoparticles with potential applications in hybrid materials for visible light-driven environmental remediation. Full article