Search Results (1,277)

Bovine viral diarrhea virus (BVDV), a globally persistent pathogen, causes bovine viral diarrhea-mucosal disease (BVD-MD), a contagious bovine disease posing significant pressures on both public health and economic development. Baicalin (BA), a flavonoid derived from Scutellaria baicalensis, exhibits broad antiviral activities but suffers from poor aqueous solubility and low bioavailability, limiting its therapeutic potential against BVDV. To address this limitation, we developed BA-loaded poly (ethylene gly-col)-poly (lactic-co-glycolic acid) (PEG-PLGA) nanoparticles (BA-PEG-PLGA NPs). While autophagy and NLRP3 inflammasome activation have been individually implicated in viral pathogenesis, their functional crosstalk during BVDV infection remains uncharacterized. Herein, we evaluated the antiviral efficacy of BA-PEG-PLGA NPs through integrated in vitro and in vivo experiments. We employed quantitative polymerase chain reaction (qPCR), transcriptome sequencing, Western blot analysis, immunofluorescence microscopy, flow cytometry, and enzyme-linked immunosorbent assay (ELISA) to investigate the mechanisms by which BA and BA-PEG-PLGA NPs combat bovine viral diarrhea virus (BVDV) infection. We found that both free BA and BA-PEG-PLGA NPs effectively attenuated BVDV replication in vitro and in vivo; notably, the nano-formulation exhibited superior efficacy. Mechanistically, BA and its nano-formulation restored autophagy homeostasis, suppressed ROS overproduction, and blocked NLRP3 inflammasome activation and pyroptotic cell death effects comparable to the specific NLRP3 inhibitor MCC950. These findings establish the autophagy–NLRP3/pyroptosis axis as a critical pathogenic mechanism in BVDV infection and reveal that nano-formulated baicalin represents an antiviral strategy by coordinately targeting this axis. This work not only provides a translatable nanomedicine approach for BVDV control but also expands the mechanistic understanding of flavonoid-based interventions in viral inflammatory diseases. Full article

The conducted study was focused on the development of a new type of polymer blends intended for additive manufacturing applications, in particular, the material extrusion method (MEX). The developed materials were prepared from recycled poly(ethylene terephthalate) and amorphous copolymers poly(ethylene terephthalate-glycol) (PETG), and poly(cyclohexylenedimethyl terephthalate-glycol) (PCTG). The basic blend systems were additionally modified with POE-g-GMA impact modifier (IM) during the reactive extrusion process. The main aim of the work was to assess the effectiveness of using composite additives and their influence on the mechanical and thermomechanical parameters of the tested systems. To prepare the composites, selected polymer blends were modified with 10% of talc (T) and carbon fibers (CF). The properties evaluation includes the mechanical/thermomechanical testing, thermal analysis and structural observations. The accuracy of printing was measured using optical scanning methods. The test results indicate that even the relatively small amount of the CF filler could lead to a significant increase in tensile modulus from reference 1.6 GPa to 2.9 GPa; the same improvement applies to strength values, where the CF-modified materials reached 45 MPa, compared to the reference 31 MPa. The heat deflection tests (0.455 MPa) after annealing revealed the maximum HDT of around 170 °C for both types of CF-modified materials. The Vicat test results were also favorable for annealed materials. Considering that the Vicat/HDT results after the 3D-printing process usually reach around 70 °C, the performed heat treatment strongly enhanced the heat resistance for most of the prepared blends. The performed studies revealed that for most of the prepared materials, the brittleness was a common drawback for both MEX-printed and injection-molded materials. Full article

Physiologically relevant in vitro intestinal models are essential for studying key physiological processes, including barrier function, drug screening and gut-microbiota interactions. However, conventional 2D culture systems often fail to recapitulate structural and functional complexity. Here, we aimed to validate a 3D bioelectronic transmembrane platform, previously used for monitoring human intestinal epithelium and vascular endothelium, for modeling the rat small intestinal barrier in vitro. The device integrates a poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) scaffold supporting co-cultures of rat intestinal epithelial cells (IEC-6) and rat fibroblasts (208F), enabling real-time monitoring of barrier formation through electrical measurements using electrochemical impedance spectroscopy (EIS). Barrier formation was monitored over 21 days and exhibited a time-dependent increase in barrier resistance. The 3D platform was compared with traditional 2D insert-based cultures and ex vivo rat tissue using an Ethylene Glycol Tetraacetic Acid (EGTA)-induced calcium switch assay to evaluate barrier disruption and recovery. EGTA treatment and removal induced reversible barrier disruption in the 3D in vitro and ex vivo models, whereas 2D in vitro cultures showed limited recovery. These findings demonstrate that the 3D platform more faithfully recapitulates native tissue architecture and function, closely paralleling ex vivo responses. Our study highlights the importance of validating advanced 3D in vitro models and establishes this bioelectronic platform as a robust tool for drug screening, barrier studies, and preclinical gastrointestinal research. Full article

Background: Hyaluronic acid (HA) hydrogels are the most widely used injectable fillers for facial rejuvenation. A new generation of HA fillers crosslinked with poly(ethylene glycol) diglycidyl ether (PEGDE) has been developed to enhance cohesiveness, tissue integration, stability, and longevity while minimizing swelling and immunogenicity. Owing to their distinct viscoelastic properties, PEGDE-crosslinked HA fillers may require product-specific selection and adapted injection techniques. Objective: The objective of this study is to provide practical, expert-based recommendations for the safe and effective use of PEGDE-crosslinked HA hydrogels in facial aesthetic treatments. Methods: A multidisciplinary panel of nine Italian experts in aesthetic medicine, each with more than 15 years of experience using HA fillers, developed consensus recommendations based on clinical practice and available evidence. A pre-meeting questionnaire informed structured discussions during a face-to-face meeting held in Paris in January 2024. The nominal group technique was applied, with consensus defined as agreement by at least 80% of panel members. Results: Consensus was reached on product selection, injection planes, delivery devices, techniques, and typical treatment volumes for PEGDE-HA hydrogels across multiple facial regions, including the forehead, temples, midface, nasolabial folds, chin, jawline, and lips. Recommended injection techniques included microbolus, macrobolus, and retrograde linear threading, with placement ranging from superficial subcutaneous to supraperiosteal planes depending on the anatomical area and clinical indication. Typical injection volumes generally ranged from 0.1 to 0.5 mL per side. Optional ultrasound mapping was considered beneficial in selected high-risk or superficial procedures to improve anatomical safety. Conclusions: These expert consensus recommendations provide practical guidance for clinicians using PEGDE-crosslinked HA hydrogels in facial rejuvenation. Tailoring product characteristics to injection depth, technique, and regional anatomy may help optimize clinical outcomes and procedural safety. Future research priorities include prospective comparative studies with other crosslinking technologies, standardized reporting of adverse events, long-term outcome registries, and further evaluation of ultrasound-guided injection strategies. Full article

Polymeric microspheres synthesized via Pickering emulsion polymerization offer structural tunability, making them attractive platforms for dye adsorption. This study investigates the adsorption behavior of methylene blue onto two classes of polymeric microspheres—poly(methacrylic acid) crosslinked with ethylene glycol dimethacrylate (PM), containing both micro- and nanopores, and poly(methacrylic acid) crosslinked with divinylbenzene (PD), containing only nanopores. The adsorption kinetics were modeled using a dual-process approach that distinguishes between diffusion-controlled transport and surface-controlled kinetic adsorption. We quantified the relative contributions of these mechanisms and correlated them with particle architecture. In the PM particles, diffusion plays a significant role in smaller particles with larger macropores, enabling methylene blue to penetrate the interior. As the particle size increased and macroporosity decreased, adsorption becomes increasingly dominated by surface kinetics. In contrast, PD particles —which lack macropores—showed the opposite trend: smaller particles were primarily governed by fast surface adsorption, while in larger particles, diffusion through nanopores became increasingly relevant. Correlation analysis between adsorption rate constants and structural parameters such as particle diameter and pore sizes revealed strong, opposing trends. In PD particles, a near-perfect inverse correlation was observed between the diffusion and kinetic components, indicating competitive suppression, where the dominance of one mechanism limited the contribution of the other. These results demonstrated that internal pore architecture played a central role in controlling the adsorption mechanism. Tuning particle size and porosity allowed deliberate control over the balance between diffusion and surface kinetics, enabling the rational design of microparticle adsorbents with tailored uptake behavior for water purification and dye removal applications. Full article

Background/Objectives: Current clinical evidence suggests that cannabidiol (CBD) demonstrates therapeutic potential in the management of chronic pain, particularly in conditions involving inflammation. However, its therapeutic potential is severely limited by poor oral bioavailability, extensive first-pass metabolism, and the need for frequent high-dose administration, which compromises patient adherence and tolerability. Long-acting injectable (LAI) delivery systems offer a strategy to overcome these limitations by providing sustained plasma concentrations and reducing dosing frequency. This study aimed to develop and optimise CBD-loaded poly (lactic-co-glycolic acid) (PLGA) microspheres for LAI delivery and to evaluate poly(2-ethyl-2-oxazoline) (POx) as a functional and biocompatible alternative to the conventionally used poly (ethylene glycol) (PEG). Methods: CBD-loaded microspheres were prepared using emulsion–solvent evaporation technique. The formulations were optimised based on entrapment efficiency (EE), drug loading (DL), particle size distribution, surface morphology, thermal behaviour, in vitro release kinetics, and cytocompatibility using NIH 3T3 fibroblasts. Multiple in vitro release methodologies, including dialysis bag, shaking-flask, and USP Apparatus IV, were evaluated to identify the most discriminative and practical approach for long-term release assessment. Results: The optimised POx-based microspheres demonstrated superior control over particle size, yielding significantly smaller and more uniform particles compared with PEG-based microspheres (124 ± 1.47 µm vs. 218 ± 13.5 µm, respectively). Differential scanning calorimetry (DSC) confirmed molecular dispersion of CBD within the polymer matrix. In vitro release studies demonstrated sustained drug release over 20 days. Conclusions: POx represents a promising alternative to PEG for the formulation of CBD-loaded PLGA microspheres, offering enhanced physicochemical stability and biological compatibility. This platform supports the development of safe and effective long-acting injectable CBD therapies and consideration of POx as an alternative to PEG. Full article

Articular cartilage, a highly specialised and avascular tissue, exhibits limited regenerative potential following trauma or degenerative conditions such as osteoarthritis (OA). Conventional surgical interventions, including microfracture and autologous chondrocyte implantation (ACI), have shown limited long-term efficacy due to donor site morbidity and restricted cell proliferation. In this context, mesenchymal stromal cells (MSCs) have emerged as a promising alternative owing to their multipotency, self-renewal capacity, and low immunogenicity. While bone marrow (BM) remains the traditional source of MSCs, recent studies have reported that peripheral blood-derived mesenchymal stromal cells (PB-MSCs) may possess chondrogenic, osteogenic, and adipogenic potential comparable to that of BM-derived MSCs. PB-MSCs can be harvested through minimally invasive methods, thereby avoiding the complications associated with BM aspiration. Experimental evidence indicates that PB-MSCs exhibit strong cell viability, proliferative potential, and the ability to synthesise cartilage-specific extracellular matrix proteins, such as type II collagen and sulphated glycosaminoglycans, within three-dimensional scaffolds. Immunophenotypically, PB-MSCs express mesenchymal markers including CD29, CD44, CD90, and CD105 while lacking hematopoietic markers CD34 and CD45. Flow cytometry analyses reveal that CD105⁺ populations increase following cryopreservation, highlighting their clinical utility. In contrast to these experimentally defined PB-MSCs, the term peripheral blood stem cells (PBSCs) is used in clinical studies to describe heterogeneous, non-cultured peripheral blood-derived cell preparations, typically enriched in hematopoietic stem and progenitor cells following granulocyte colony-stimulating factor (G-CSF) mobilisation, without full mesenchymal characterisation. In vitro studies confirm successful tri-lineage differentiation, whereas in vivo investigations have demonstrated effective cartilage regeneration using PB-based clinical approaches, including postoperative intra-articular administration of hyaluronic acid (HA) combined with PBSCs, as well as implantation of PBSCs covered with a collagen membrane. Furthermore, advancements in biomaterial engineering, such as poly(ethylene glycol)–cysteine–arginine–glycine–aspartic acid (PEG-CRGD) hydrogels, have enhanced PB-MSC adhesion, proliferation, and chondrogenic differentiation while promoting immunomodulation through M2 macrophage polarisation. Despite these promising outcomes, the available evidence remains limited and heterogeneous, with substantial variability in cell definitions, experimental models, and clinical study designs, which currently constrains definitive conclusions regarding clinical efficacy. Future research should focus on optimising isolation protocols, understanding molecular pathways governing PB-MSC chondrogenesis, and standardising clinical applications. Overall, PB-MSCs represent a viable, less invasive, and translationally relevant cell source for cartilage regeneration and regenerative orthopaedic therapies Full article

Cellulose dissolution solvents have been developed for the fabrication of regenerated cellulose (RC) films, which are known for their high optical transparency, excellent barrier properties, and biodegradability. In this study, three types of aqueous dissolution systems, including glycol ether/sodium hydroxide (NaOH), poly(ethylene glycol) (PEG)/NaOH, and urea/NaOH aqueous systems, were investigated to compare their effects on lignocellulosic microfine (LCMF) solutions and the resulting regenerated cellulose films. The dissolution yields of LCMFs in these solvents ranged from 77.0% to 85.0%. The incorporation of glycol-based co-solvents in NaOH significantly influenced the transparency (over 70% of transparency) of the regenerated LCMF films. The use of a high molecular weight of co-solvent (PEG) especially resulted in enhanced stability of the LCMF solutions, as evidenced by higher inherent viscosities and the minimal viscosity change over 30 days compared to glycol ether/NaOH and urea/NaOH systems. Furthermore, the films regenerated from the PEG/NaOH solvent showed the lowest shrinkage (19.4%) and the highest mechanical strength (47.8 MPa), followed by the glycol ether/NaOH and urea/NaOH systems. These results confirm that the type of co-solvent in cellulose dissolution systems influences the composition, coagulation behavior, and drying characteristics of regenerated LCMF films, affecting their mechanical performance. This study provides insights into the effective utilization of lignocellulosic materials for the efficient fabrication of regenerated cellulose. Full article

The development of bioplastics, such as poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV), as sustainable alternatives to petroleum-based plastics, requires efforts to reduce their economic and environmental impacts. Aqueous Two-Phase System (ATPS) represents a sustainable alternative to isolate PHBV, as it is water-based. A polyethylene glycol (PEG8000)/phosphate salts-based ATPS was employed as a sustainable approach to isolate and purify PHBV produced by the haloarchaeon Haloferax mediterranei. The Taguchi design method was used to optimise an ATPS, integrating variables such as the concentration of commercial PEG8000 and phosphate salts, extraction temperature, system pH, and biomass-to-system volume ratio. Results revealed a maximum PHBV recovery of 80% with a purity of 93% under the following conditions: 20% of PEG8000, 20% of phosphate salts, pH of 7, 50 °C, and a 1:100 ratio. Furthermore, the potential recycling of ATPS components was studied to reduce the overall cost of the biopolymer isolation procedure. However, a significant decrease in the PHBV recovery was observed (52% when using recycled components). Finally, the use of PEG8000 from ethylene glycol (EG) polymerisation, aimed at the valorisation of EG obtained from other industrial processes, yielded comparable recovery and purity of PHBV (78% and 89%, respectively). Full article

Hydrogel fluorescent microspheres function as versatile tracers with applications spanning across biomedicine, complex plasma systems, hydrodynamics, and drug delivery. However, the controlled release of fluorescent material in hydrogel microspheres is challenging to achieve. The fluorescent hydrogel microsphere (namely poly(ethylene glycol) diacrylate@rhodamine B-tannic acid, PEGDA@RhB-TA) was fabricated by incorporating tannic acid and RhB into PEGDA microspheres. The stable encapsulation and responsive release of RhB can be achieved by leveraging the non-covalent interactions between TA and RhB. RhB was stably encapsulated within PEGDA microspheres through noncovalent interactions (hydrophobic interactions, hydrogen bonding, π–π, and ion–π interactions) between RhB and TA. Both molecular dynamics simulations by GROMACS and experimental results confirmed the noncovalent binding mechanisms between RhB and TA. The microspheres retained RhB following 24 h immersion in a highly concentrated salt solution (1 M NaCl) and exhibited minimal RhB release (7.1%) under heating at 80 °C for 24 h. However, PEGDA@RhB-TA microspheres underwent rapid RhB release in a 50% v/v ethanol–water solution, liberating 73% of the encapsulated dye within 24 h. TA within the PEGDA@RhB-TA microsphere acts as a molecular lock by forming non-covalent interactions with RhB, significantly enhancing the stability of encapsulated RhB, and enabling the responsive release of RhB under specific conditions. Upon introduction into a microfluidic chip, PEGDA@RhB-TA microspheres enable the calculation of flow velocity through position tracking using high-speed camera imaging and fluorescence microscopy. These microspheres overcome the dual challenges of tracer stability and controlled release, making them suitable for fluid tracing and measuring flow rates. Full article

A bisphenol-A-free lignin hydrogel platform with programmable network density is reported. Lignin was crosslinked with poly(ethylene glycol) diglycidyl ether (PEGDGE) and sorbitol polyglycidyl ether (SPE) via epoxide ring-opening to generate hydrogel networks spanning eleven PEGDGE/SPE ratios. A single compositional lever—the SPE fraction—allowed the predictable densification of the network, translating into a monotonic shift in swelling and viscoelastic/mechanical responses. Importantly, the well-performing hydrogel (LS₁P₉) coupled swelling ratio with adsorption functionality, removing 72% methylene blue from water under the tested conditions. This work positions lignin as more than a passive filler: it serves as an active phenolic macromonomer for designing sustainable, multifunctional hydrogels. Full article

Poly(ethylene glycol) (PEG) has long stood as the prevailing standard in drug delivery, celebrated for its capacity to enhance solubility, extend circulation, and improve pharmacological performance. Nevertheless, the emergence of anti-PEG antibodies, accelerated clearance, and limited biodegradability increasingly undermine its role as a universal solution. In response, a new generation of polymers has been developed to address these shortcomings, offering the potential to sustain or surpass PEG’s benefits while mitigating immunogenicity, improving biocompatibility, and enabling finer control over therapeutic fate. This review examines current research to articulate a coherent perspective on the replacement of PEG, tracing how advances in polymer design are reshaping the foundations of targeted drug delivery. Taken together, these developments signal not only a corrective to the limitations of PEG but also a broader paradigm shift toward safer, more versatile, and clinically translatable systems that define the next frontier in precision therapeutics. Full article

Hyperelastic models for the deformation of hydrogels were evaluated as alternatives to the widely used neo-Hookean model. Poly(ethylene glycol diacrylate) (PEGDA) was synthesized via photopolymerization, with precursor molecular weights from 700 to 4000 Da and synthesis concentrations between 5 and 30 wt% in water. Hydrogels are often modeled as neo-Hookean solids; this model holds only over a limited strain range. To model deformation over a broader range and seek additional insight into gel network structures, the Mooney–Rivlin, Ogden, Rubinstein–Panyukov, and Localization models were applied to uniaxial compression data and their fits assessed against “Mooney plots” of reduced stress versus the inverse extension ratio. The Ogden model best fits the stress–strain curves to higher ratios and the reduced stress plots over the broadest range of formulations. The Localization and Rubinstein–Panyukov models fit well above c*, the overlap concentration, capturing low-strain behavior and the observed maxima under compression in Mooney plots. The Mooney–Rivlin model fit the stress–strain curves but was unable to fit the reduced stress plots. The Localization and Rubinstein–Panyukov model parameters suggest that entanglements play a significant role at all concentrations, with their contribution decreasing as the network concentration increases. This demonstrates the potential of using two-parameter models to understand the deformation of hydrogels. Full article

Biodegradable electrospun nanofibrous scaffolds (BENS) have emerged as a highly advanced class of wound dressings owing to their close structural and morphological resemblance to the native extracellular matrix and their tunable physicochemical and mechanical characteristics. However, the successful translation of electrospun wound-healing platforms from laboratory concepts to clinically viable products necessitates a quantitative understanding of how formulation and processing variables dictate scaffold architecture, mechanical performance, and antibacterial functionality. In this study, hydrophobic poly(ε-caprolactone) (PCL) and hydrophilic poly(ethylene glycol) (PEG35000) were blended at different weight ratios and fabricated into electrospun nanofibrous scaffolds, with amoxicillin trihydrate (AMX) incorporated as a model antibacterial agent. Blank and drug-loaded systems were systematically characterized with respect to solution rheology, fiber morphology, thermal behavior, crystallinity, mechanical performance, surface wettability, and antibacterial activity. Quantitative correlation analyses and statistical comparisons revealed that solution viscosity is a strong predictor of mechanical response, while PEG fraction governs baseline stiffness and crystallinity in a non-linear manner. AMX loading acted as a secondary structural modifier, producing statistically significant increases in stiffness and wettability, accompanied by reduced crystallinity and concentration-dependent antibacterial efficacy. Among the investigated formulations, a PCL: PEG ratio of 3:1 provided the most balanced mechanophysical profile for effective drug incorporation. These findings establish validated structure–property–function relationships that support the rational design of electrospun antibacterial wound dressings. Full article

This study investigated the chemical recycling of poly(ethylene terephthalate) (PET) fiber residues from two sources—high-molar mass mooring ropes and low-molar mass textile-grade fibers—to produce functional oligomers. Glycolysis was carried out using polyethylene glycol (PEG400) as the depolymerizing agent, and two catalysts were assessed, zinc acetate and lithium octoate, with the latter reported on for the first time in this application. Reactions were performed for 180 min under mechanical stirring, inert atmosphere, reflux, and controlled heating. The resulting oligomers were characterized by Fourier-transform infrared spectroscopy (FTIR), hydroxyl and acidity indices, and thermogravimetric analysis (TGA). Both PET feedstocks showed high reactivity toward glycolysis. Monitoring the reactions by acidity index indicated that conversion reached equilibrium at approximately 120 min. ATR-FTIR confirmed the formation of ester and hydroxyl groups, consistent with oligomer structures. Glycolysis of PET derived from mooring ropes produced oligoesters with hydroxyl values of 228 and 242 mgKOH/g for zinc acetate and lithium octoate, respectively, and molar masses of 1296 and 1338 g/mol for zinc acetate and lithium octoate, respectively. These values are suitable for subsequent syntheses such as polyester polyol production. Full article