Search Results (515)

This research focuses on designing polymer membranes as biocompatible materials using home-built electrospinning equipment, offering alternative solutions for tissue regeneration applications. This technological development supports cell growth on biomaterial substrates, including hepatocellular carcinoma (Hep-G2) cells. This work researches the compatibility of polymer membranes (fiber mats) made of polyvinylidene difluoride (PVDF) for possible use in cellular engineering. A standard culture medium was employed to support the proliferation of Hep-G2 cells under controlled conditions (37 °C, 4.8% CO₂, and 100% relative humidity). Subsequently, after the incubation period, electrochemical impedance spectroscopy (EIS) assays were conducted in a physiological environment to characterize the electrical cellular response, providing insights into the biocompatibility of the material. Scanning electron microscopy (SEM) was employed to evaluate cell adhesion, morphology, and growth on the PVDF polymer membranes. The results suggest that PVDF polymer membranes can be successfully produced through electrospinning technology, resulting in the formation of a dipole structure, including the possible presence of a polar β-phase, contributing to piezoelectric activity. EIS measurements, based on R_ct and C_dl values, are indicators of ion charge transfer and strong electrical interactions at the membrane interface. These findings suggest a favorable environment for cell proliferation, thereby enhancing cellular interactions at the fiber interface within the electrolyte. SEM observations displayed a consistent distribution of fibers with a distinctive spherical agglomeration on the entire PVDF surface. Finally, integrating piezoelectric properties into cell culture systems provides new opportunities for investigating the influence of electrical interactions on cellular behavior through electrochemical techniques. Based on the experimental results, this electrospun polymer demonstrates great potential as a promising candidate for next-generation biomaterials, with a probable application in tissue regeneration. Full article

Understanding the early-stage physical interactions between polymeric membranes and supersaturated salt solutions is crucial for advancing membrane-assisted crystallization (MCr) processes. In this study, we employed molecular dynamics (MD) simulations to investigate the short-term morphological response of an isotactic polypropylene (PP) membrane in contact with LiF solutions at different concentrations (5.8 M and 8.9 M) and temperatures (300–353 K), across multiple time points (0, 150, and 300 ns). These data were used as input for computational fluid dynamics (CFD) analysis to evaluate structural descriptors of the membrane, including tortuosity, connectivity, void fraction, anisotropy, and deviatoric anisotropy, under varying thermodynamic conditions. The results show subtle but consistent rearrangements of polymer chains upon exposure to the hypersaline environment, with a marked reduction in anisotropy and connectivity, indicating a more compact and isotropic local structure. Surface charge density analyses further suggest a temperature- and concentration-dependent modulation of chain mobility and terminal group orientation at the membrane–solution interface. Despite localized rearrangements, the membrane consistently maintains a net negative surface charge. This electrostatic feature may influence ion–membrane interactions during the crystallization process. While these non-reactive, short-timescale simulations do not capture long-term degradation or fouling mechanisms, they provide mechanistic insight into the initial physical response of PP membranes under MCr-relevant conditions. This study lays a computational foundation for future investigations bridging atomistic modeling and membrane performance in real-world applications. Full article

Magnetic nanoparticles (MNPs), especially iron oxide (Fe₃O₄), display distinctive superparamagnetic characteristics and elevated surface-area-to-volume ratios, facilitating improved physicochemical interactions with solutes and pollutants. These characteristics make MNPs strong contenders for use in water treatment applications. This research investigates the application of iron oxide MNPs synthesized via co-precipitation as innovative draw solutes in forward osmosis (FO) for treating synthetic produced water (SPW). The FO membrane underwent surface modification with sulfobetaine methacrylate (SBMA), a zwitterionic polymer, to increase hydrophilicity, minimize fouling, and elevate water flux. The SBMA functional groups aid in electrostatic repulsion of organic and inorganic contaminants, simultaneously encouraging robust hydration layers that improve water permeability. This adjustment is vital for sustaining consistent flux performance while functioning with MNP-based draw solutions. Material analysis through thermogravimetric analysis (TGA), scanning electron microscopy (SEM), and Fourier-transform infrared spectroscopy (FTIR) verified the MNPs’ thermal stability, consistent morphology, and modified surface chemistry. The FO experiments showed a distinct relationship between MNP concentration and osmotic efficiency. At an MNP dosage of 10 g/L, the peak real-time flux was observed at around 3.5–4.0 L/m²·h. After magnetic regeneration, 7.8 g of retrieved MNPs generated a steady flow of ~2.8 L/m²·h, whereas a subsequent regeneration (4.06 g) resulted in ~1.5 L/m²·h, demonstrating partial preservation of osmotic driving capability. Post-FO draw solutions, after filtration, exhibited total dissolved solids (TDS) measurements that varied from 2.5 mg/L (0 g/L MNP) to 227.1 mg/L (10 g/L MNP), further validating the effective dispersion and solute contribution of MNPs. The TDS of regenerated MNP solutions stayed similar to that of their fresh versions, indicating minimal loss of solute activity during the recycling process. The combined synergistic application of SBMA-modified FO membranes and regenerable MNP draw solutes showcases an effective and sustainable method for treating produced water, providing excellent water recovery, consistent operational stability, and opportunities for cyclic reuse. Full article

Extracorporeal membrane oxygenation (ECMO) is a crucial life support therapy for patients with severe cardiac and respiratory failure. However, the complications associated with venoarterial ECMO (VA-ECMO), including thrombus formation, bleeding, and hemolysis, remain significant challenges that impact patient outcomes and healthcare costs. These complications primarily arise from blood–material interactions within the ECMO circuit, necessitating the development of biocompatible materials to optimize hemocompatibility. This review provides an updated overview of the latest advancements in VA-ECMO materials, focusing on cannula, oxygenators, and centrifugal pumps. Various surface modifications, such as heparin coatings, nitric oxide-releasing polymers, phosphorylcholine (PC)-based coatings, and emerging omniphobic surfaces, have been explored to mitigate thrombosis and bleeding risks. Additionally, novel oxygenator membrane technologies, including zwitterionic polymers and endothelial-mimicking coatings, offer promising strategies to enhance biocompatibility and reduce inflammatory responses. In centrifugal pumps, magnetic levitation systems and hybrid polymer-composite impellers have been introduced to minimize shear stress and thrombogenicity. Despite these advancements, no single material has fully addressed all complications, and further research is needed to refine surface engineering strategies. This review highlights the current progress in ECMO biomaterials and discusses future directions in developing more effective and durable solutions to improve patient safety and clinical outcomes. Full article

Polyamide membranes, such as nanofiltration (NF) membranes, are widely used for water purification. However, the mechanisms of solute transport and solute rejection due to solute charge interactions with the membrane remain unclear at the molecular level. Here, we use molecular dynamics simulations to examine the transport of single-solute feeds through charged nanofiltration membranes with different membrane charge concentrations of ${\mathrm{COO}}^{-}$ and NH${}_2^{+}$ resulting from the deprotonation or protonation of polymeric end groups according to the pH level that the membrane experiences. The results show that ${\mathrm{Na}}^{+}$ and ${\mathrm{Cl}}^{-}$ solute ions are better rejected when the membrane has a higher concentration of negatively charged groups, corresponding to a higher pH, whereas ${\mathrm{CaCl}}_2$ is well rejected at all pH levels studied. These results are consistent with those of experiments performed at the same pH conditions as the simulation setup. Moreover, solute transport behavior depends on the membrane functional group distribution. When ${\mathrm{COO}}^{-}$ functional groups are concentrated at membrane feed surface, ion permeation into the membrane is reduced. Counter-ions tend to associate with charged functional groups while co-ions seem to pass by the charged groups more easily. In addition, steric effects play a role when ions of opposite charge cluster in pores of the membrane. This study reveals solute transport and rejection mechanisms related to membrane charge and provides insights into how membranes might be designed to achieve specific desired solute rejection. Full article

During radiotherapy, X-rays can deliver significant doses of ionising radiation to both cancerous and healthy tissue, often leading to undesirable side effects that compromise patient outcomes. While the cellular effects of such therapeutic X-ray exposures are well studied, the impact on extracellular matrix (ECM) proteins remains poorly understood. This study characterises the response of ECM proteins, including the major tissue components collagen I and fibronectin (FN), to X-ray doses similar to those used in clinical practice (50 Gy, as employed in breast radiotherapy, and 100 Gy), using a combination of gel electrophoresis, biochemical assays, and mass spectrometry-based peptide location fingerprinting (PLF) analysis. In purified protein solutions, 50 Gy X-ray exposure led to the fragmentation of constituent collagen I α chains. Irradiation of purified plasma FN (pFN) induced localised changes in peptide yields (detected by liquid chromatography and tandem mass spectrometry (LC-MS/MS) and PLF) and enhanced its binding to collagen I. In complex environments, such as newly synthesised fibroblast-derived ECM and mature ex vivo breast tissue, X-ray exposure induced peptide yield changes in not only collagen I and FN but also key basement membrane proteins, including collagen IV, laminin, and perlecan. Intracellular proteins associated with gene expression (RPS3, MeCP2), the cytoskeleton (moesin, plectin), and the endoplasmic reticulum (calnexin) were also found to be impacted. These X-ray-induced structural changes may impair the ECM integrity and alter cell–ECM interactions, with potential implications for tissue stiffening, fibrosis, and impaired wound healing in irradiated tissues. Full article

The electrospinning technique can produce multifunctional polymeric devices by forming solid fibers from polymer solutions under a high-voltage electric field. Variations such as concentric needles yield core/shell fibers. This study evaluates the effects of applied voltage (12.5–20 kV) and tip-to-collector distance (12.5–20 cm) on the morphology and thermochemical behavior of PLGA/PVA fibers made by coaxial electrospinning compared with casting-produced membranes and monolithic fibers. Optimal coaxial fibers (597 ± 90 nm diameter) were produced at 15 cm/12.5 kV, exhibiting a well-defined core/shell structure (PVA core: ~100 nm; PLGA shell: ~50 nm) confirmed by laser scanning confocal (core solution labeled with fluorescein) and TEM. FTIR and TGA demonstrated nearly complete solvent removal in electrospun samples versus ~10% solvent retention in cast films. XRD analysis indicated that cast films (PLGAff) exhibited minimal crystallinity (Xc ≈ 0.1%), while electrospun PLGA (PLGAe) showed cold crystallization and higher crystallinity (Tcc ≈ 90.6 °C; Xc ≈ 2.45%). DSC detected two different Tg (≈43.2 °C and 52.8 °C) in the coaxial fibers, confirming distinct polymer domains with interfacial interactions. These results establish precise processing/structure relationships for defect-free coaxial fibers and provide fundamental design principles for hybrid systems in controlled drug delivery and tissue engineering applications. Full article

Recycling extracellular polymeric substances (EPSs) from excess sludge in wastewater treatment plants has garnered significant research attention. Membrane separation offers a promising approach for EPS concentration; however, membrane fouling remains a critical challenge. Previous studies demonstrate that Ca²⁺ addition effectively mitigates membrane fouling. This study reveals that Ca²⁺ mixing modes govern membrane fouling in the dead-end ultrafiltration of both the practical EPS and model EPS [sodium algiante (SA)]. The interaction mechanisms between Ca²⁺ and the EPS under varied mixing conditions and their impact on filtration performance were systematically investigated. At a low Ca²⁺ concentration, the addition sequence critically influenced colloidal particle sizes formed via Ca²⁺-EPS interactions, altering the cake layer structure governing filtration resistance; these effects diminished at higher Ca²⁺ concentrations. In suspensions prepared by adding EPS to Ca²⁺ solution (EPS-Ca), a portion of the EPS became encapsulated within an EPS-Ca layer formed through Ca²⁺ EPS binding, reducing free EPS concentration and enlarging colloidal aggregates. This encapsulation reduced EPS-mediated membrane fouling, thereby lowering filtration resistance. Conversely, in suspensions prepared by adding Ca²⁺ to EPS solution (Ca-EPS), more complete Ca²⁺ EPS interactions formed a dense crosslinked structure with smaller colloids on membrane surfaces, intensifying fouling and resistance. Additionally, EPS-Ca exhibited higher compressibility than Ca-EPS, though both exhibited comparable filtration resistance under high-pressure conditions. These results offer critical insights into optimizing EPS ultrafiltration concentration to mitigate membrane fouling through Ca²⁺ addition strategies. Full article

Nymphaeol A (NYA) is a tetrahydroxyflavanone anchored to a hydrophobic geranyl group, isolated from different sources and a component of propolis, a complex mixture produced by honeybees and used since ancient times as a healthy drug. This complex exhibits significant antioxidant, antifungal, antibacterial, antiviral, anticancer and antimicrobial properties and NYA is one of its main components. NYA is a lipophilic molecule with two domains, one polar and one hydrophobic. NYA can be inserted into membranes, and its membrane properties depend not only on its location but also on the membrane’s lipid composition. This work uses molecular dynamics to obtain the dynamics, orientation, location and interactions of NYA in a complex biomembrane. This work shows that in an aqueous solution, NYA forms high-order aggregates where the molecules are joined together by the hydrophobic chain. In the presence of a membrane but initially located in the aqueous media, NYA is capable of inserting itself spontaneously into the membrane. Inside the membrane, NYA can be found in the monomeric form, as well as forming aggregates, tending to remain in its most extended conformation. NYA moves along the x-, y- and z-axes, with the movement along the z-axis larger than that of the membrane’s lipids. NYA forms an approximate angle of 35° perpendicular with respect to the membrane and is inserted between the phospholipid hydrocarbon chains, slightly increasing membrane fluidity. Furthermore, NYA prefers POPC and PSM but not POPE or CHOL. NYA’s location and movement within the membrane should be well-suited for its potent bioactivity. Full article

Peanut (Arachis hypogaea L.) is one of the most important oilseeds crops worldwide. Through symbiosis with the bacterium Bradyrhizobium sp., peanuts can assimilate atmospheric nitrogen, reducing the need for chemical fertilizers. However, this nitrogen fixation process is highly sensitive to environmental factors that can inhibit the early stages of symbiotic interaction. In this study, we propose the encapsulation of Bradyrhizobium sp. SEMIA6144 and the flavonoid naringin (Nar) in alginate beads to improve flavonoid stability and promote nodulation kinetics in peanuts. Three types of beads were synthesized: A (control, SEMIA6144 only); B (SEMIA6144 induced with 10 µM Nar); and C (SEMIA6144 co-entrapped with 1 mM Nar). Although Nar increased cell mortality (2-fold compared to control) and reduced metabolic activity—particularly at 1 mM—cells in beads B and C responded by altering their membrane fatty acid profile (30% and 55.5% of 18:1, respectively) leading to a reduction in saturated fatty acids (5.8% and 13.1% for 16:0 and 18:0 in B; 11.8% and 21.2% in C). Bacterial release kinetics followed a primarily Fickian diffusion model, with minor matrix–bacteria interactions in Nar-treated beads. Notably, bacterial release in peanut root exudates was 6%, 10%, and 11% higher for beads A, B, and C, respectively, compared to release in physiological solutions. Nar-beads enhanced the formation of curved root hairs, promoted bacterial colonization in root hair zones, and stimulated the appearance of rosette-like structures associated with nodule initiation. In conclusion, encapsulating Bradyrhizobium sp. SEMIA6144 with Nar in beads represents a promising strategy to improve symbiotic nitrogen fixation in peanuts. Full article

As an essential trace element in the human body, fluoride is beneficial in appropriate amounts, but excessive intake can cause serious harm. Therefore, addressing the global water pollution caused by fluoride is an urgent issue. In this study, a functional composite membrane is successfully prepared using Enteromorpha prolifera (EP) as the raw material, cinnamaldehyde (CIN) as a functional modifier, and EP-bioinduced ZrO₂ nanoparticles (NPs) as the loading material via biomimetic mineralization technology. The experimental results demonstrate that the composite membrane removes fluoride ions (F⁻) with an efficiency of over 99.9% within the concentration range of 100–400 mg/L. This excellent F⁻ removal performance is attributed to the ability of the hydroxyl groups on the surface of ZrO₂ to exchange and bind with F⁻. The formed CIN/EP-ZrO₂ composite membrane also reveals significant antibacterial activity against E. coli. In addition, the adsorption rate for methylene blue at the concentration of 5–300 mg/L reaches 99.99%, which is due to the synergistic interaction of functional groups such as hydroxyl (-OH), carboxyl (-COOH), and amino groups (-NH₂) in EP. The overall sustainability footprint (OSF) assessment exhibits that the CIN/EP-ZrO₂ composite membrane has comprehensive advantages, including a simple preparation process, low cost, high performance, and environmental friendliness. This study provides an innovative solution for the sustainable treatment of F⁻, bacteria, and dye pollution in water, showcasing significant potential for applications in environmental science. Full article

Raman spectroscopy is one of the best techniques for obtaining information concerning the physical–chemical interactions between a lipid and a solvent. Phospholipids in water are the main elements of cell membranes and, by means of their chemical and physical structures, their cells can interact with other biological molecules (i.e., proteins and vitamins) and express their own biological functions. Phospholipids, due to their amphiphilic structure, form biomimetic membranes which are useful for studying cellular interactions and drug delivery. Synthetic systems such as DPhPC-based liposomes replicate the key properties of biological membranes. Among the different models, phospholipid mimetic membrane models of lamellar vesicles have been greatly supported. In this work, a biomimetic system, a deuterium solution (50 mM) of the synthetic phospholipid 1,2-diphytanoyl-sn-glycero-3-phosphocholine (DPhDC), is studied using μ-Raman spectroscopy in a wide temperature range from −181.15 °C up to 22.15 °C, including the following temperatures: −181.15 °C, −146.15 °C, −111.15 °C, −76.15 °C, −61.15 °C, −46.15 °C, −31.15 °C, −16.15 °C, −1.15 °C, 14.15 °C, and 22.15 °C. Based on the Raman evidence, phase transitions as a function of temperature are shown and grouped into five classes, where the corresponding Raman modes describe the stretching of the (C−N) bond in the choline head group (gauche) and the asymmetric stretching of the (O−P−O) bond. The acquisition temperature of each Raman spectrum characterizes the rocking mode of the methylene of the acyl chain. These findings enhance our understanding of the role of artificial biomimetic lipids in complex phospholipid membranes and provide valuable insights for optimizing their use in biosensing applications. Although the phase stability of DPhPC is known, the collected Raman data suggest subtle molecular rearrangements, possibly due to hydration and second-order transitions, which are relevant for membrane modeling and biosensing applications. Full article

Three-finger toxins (TFTs), including neurotoxins and cytotoxins, form one of the largest families of snake venom proteins and interact with various biological targets. Neurotoxins target proteinaceous receptors while cytotoxins interact mainly with the lipids of cell membranes and to a lesser extent with carbohydrates. However, no data about the interaction of TFTs with nucleic acids can be found. To detect this interaction, we applied spectrophotometry, ion-paired HPLC and electrophoretic mobility shift assay (EMSA). Using spectrophotometry, we found that TFTs from cobra venom increased the optical density of an RNA solution in a time-dependent manner indicating toxin interaction with RNA. A decrease in the net negative charge of the RNA molecule upon interaction with neurotoxin II from cobra venom was revealed by ion-pair HPLC. EMSA showed decreased electrophoretic mobility of both RNA and DNA upon addition of different TFTs including the non-conventional cobra toxin WTX and water-soluble recombinant human three-finger protein lynx1. We suggest that the interaction with nucleic acids may be a common property of TFTs, and some biological effects of TFTs, for example, cytotoxin-induced apoptosis in cancer cell lines, may be mediated by interaction with nucleic acids. Full article

Background/Objectives: Microbial infections represent a significant threat to public health due to the emergence and spread of antimicrobial resistance. Adjunctive and alternative therapeutic strategies are explored to tackle this issue, including the use of natural or synthetic antimicrobial peptides. Previous research showed that antibody-derived peptides possess antimicrobial, antiviral, and immunomodulatory properties. This study aimed to characterize newly designed antibody-derived peptides and evaluate their effectiveness against representative strains of Staphylococcus aureus, including drug-resistant isolates. Methods: Colony-forming unit assays and confocal microscopy studies were performed to evaluate peptide activity against planktonic microbial cells. Cytotoxicity tests were performed on THP-1 human monocytic cells. Circular dichroism (CD) and nuclear magnetic resonance (NMR) were employed for the conformational characterization of peptides. Results: The half-maximal effective concentrations of the peptides against bacterial reference strains and drug-resistant isolates ranged from 0.17 to 18.05 µM, while cytotoxic effects were not observed against mammalian cells. A killing kinetics analysis and observation by confocal microscopy of the interaction between peptides and bacteria suggested a mechanism of action involving membrane perturbation. CD studies showed that all peptides predominantly exhibit a random coil arrangement in aqueous solution. NMR spectroscopy revealed that the most active peptide adopts a helical conformation in the presence of membrane mimetics. Conclusions: The structural characterization and evaluation of the newly designed peptides’ antimicrobial activity may lead to the selection of a candidate to be further studied to develop an alternative treatment against microbial infections caused by drug-resistant strains. Full article

Hydrogels (HDs) offer a promising platform for localized and sustained drug delivery. In this study, carboxymethyl chitosan (CMC)—based hydrogels were crosslinked with genipin and evaluated for the controlled release and tissue retention of suramin, a polyanionic drug with anti-inflammatory and antifibrotic properties. The influence of crosslinking density (1%, 3%, and 5%) on drug release, permeation kinetics, and retention was investigated using in vitro synthetic membranes and reconstructed human epithelial tissue models. The 1% genipin HD exhibited the highest cumulative release and drug retention (48.8 ± 6.8 μg/cm² in synthetic membranes; 24.06 ± 7.33 μg/cm² in epithelial models), along with a sustained release profile governed by first-order and Fickian diffusion kinetics. Notably, the 1% crosslinked formulation also demonstrated enhanced transmembrane flux (>140 μg/cm²/h after six hours), suggesting that lower crosslinking density favors both diffusional mobility and depot functionality. In contrast, free suramin solution displayed limited tissue interaction and minimal permeation, highlighting the role of the hydrogel matrix in regulating local bioavailability. These findings demonstrate that CMC–genipin HD can closely modulate drug delivery kinetics through crosslinking density, offering a biocompatible strategy for localized treatment of ulcerated epithelial conditions such as oral mucositis or chronic wounds. Diffusion models included a synthetic multilayer membrane (Strat-M^®) and a reconstructed human epidermis (EpiDerm™) to simulate skin-like barrier properties. Full article