Understanding how molecular additives modulate the interfacial structure and foaming behaviour of natural surfactants is essential for the design of high-performance, sustainable formulations. Here, we investigate how hydrogen-bond donor and acceptor additives - glycerol, choline chloride, and urea - modify the interfacial architecture of Quillaja saponin extract solutions. A multi-technique approach combining surface tension, interfacial dilational rheology, foam stability measurements, vibrational sum-frequency generation (SFG) spectroscopy, electrokinetic analysis, and atomistic molecular dynamics (MD) simulations reveals distinct additive-specific mechanisms at the molecular level. Using SFG spectroscopy, we resolved the additive-induced reorganisation of interfacial saponins and interfacial water molecules. Glycerol reduces the fraction of more strongly hydrogen-bonded interfacial water without altering surface tension, indicating interfacial insertion and reorientation while the overall macroscopic surface activity remains largely unchanged. In contrast, urea redistributes spectral weight toward strongly hydrogen-bonded interfacial water without significantly altering the overall surface excess of saponin, while decreasing headgroup-water contributions, thereby impairing the formation of lateral hydrogen bonds between neighbouring saponins and reducing the elasticity of the surface layer. Choline chloride induces pronounced suppression of the OH stretching band from interfacial water, consistent with charge screening and a substantial reduction of the interfacial net charge. MD simulations corroborate these findings by revealing that glycerol has more frequent contacts with the saccharide region of saponin, supporting strong interfacial cohesion. The high propensity of urea to interact with the polar residues of saponin explains the redistribution of interfacial water and headgroup hydroxyls observed in SFG spectra.

This work presents a method to encapsulate plant extracts within a binary polysaccharide carrier and to characterize the physicochemical and rheological performance of the resulting biocomposites in the context of food use. Using a starch/psyllium matrix, extracts from Sambucus nigra (SN), Aronia melanocarpa (AM), and Echinacea purpurea (EP) were effectively protected and incorporated through a stepwise workflow encompassing matrix preparation, encapsulation, structural verification, and functional assessment. SEM revealed a porous network containing uniformly distributed, extract-loaded spherical structures (~800-1500 nm), while FTIR supported the presence of hydrogen bonding and hydrophobic interactions that contributed to system stability. The prepared nanoemulsions showed shear-thinning (pseudoplastic) behavior, indicating favorable processing characteristics, whereas most physicochemical and bioactivity measurements were performed on lyophilized composites. The dried materials preserved extract-specific color signatures (ΔE > 5) and exhibited distinct thermal responses: AM produced a pronounced plasticizing effect (Tg reduced by >20 °C), while the incorporation of extracts generally delayed thermal degradation, consistent with polyphenol-starch interactions. Phase-transition behavior was also altered, with melting peaks suppressed for SN and AM and melting temperatures lowered for EP. Surface analysis indicated increased hydrophobicity and a reduced polar component of surface free energy, suggesting improved moisture barrier potential. Antioxidant capacity closely tracked total phenolic content (r > 0.94), with caffeic acid contributing strongly, particularly in EP-based systems. Antimicrobial activity depended on extract type (broad-spectrum for EP, selective for SN, minimal for AM), and the comparatively higher sensitivity of Gram-negative bacteria points to improved phenolic availability and membrane interactions upon encapsulation. Collectively, these results highlight the starch/psyllium matrix as a flexible platform for stabilizing plant extracts while enabling tunable functional attributes for functional food applications.

Intravascular biosensors have become a crucial and novel class of devices in healthcare, enabling the constant real-time monitoring of essential physiological parameters directly within the circulatory system. Recent developments in micro- and nanotechnology have relevantly improved the sensitivity, miniaturization, and biocompatibility of these devices, thereby enabling their application in precision medicine. This review summarizes the latest advances in intravascular biosensor technologies, with a special focus on glucose and oxygen level monitoring, blood pressure and heart rate assessment, and early disease diagnostics, as well as modern approaches to drug therapy monitoring and delivery systems. Key challenges such as long-term biostability, signal accuracy, and regulatory approval processes are critical considerations. Innovative strategies, including biodegradable implants, nanomaterial-functionalized surfaces, and integration with artificial intelligence, are regarded as promising avenues to overcome current limitations. This review provides a comprehensive roadmap for upcoming research and the clinical translation of advanced intravascular biosensors with a strong emphasis on their transformative impact on personalized healthcare.

Polysaccharide-based composites, such as those containing chitosan, offer significant potential due to their biodegradability, non-toxicity and membrane-forming properties. Chitosan, due to its functional groups, is ideal for nano-/microcapsule formation. Encapsulation protects bioactive components from environ-mental stress, improves physicochemical properties and enhances biological and antimicrobial activity. This research has developed a surfactant-free method to produce beeswax and olive oil nano-/microcapsules stabilized solely within a chitosan matrix without synthetic stabilisers or additional surfactants. The formation of gels and films containing these nano/micro capsules was confirmed by scanning electron microscopy (SEM). Incorporation of the nano/micro capsules into the matrix reduced the mechanical properties compared to the control sample, but significantly improved the hydrophobicity and UV barrier properties. Microbiological tests revealed mild antibacterial properties, highlighting the potential of the composites for applications in cosmetics, such as emulsions and creams, and in food technology, as coatings and packaging materials. The encapsulation process enables the straightforward integration of bioactive ingredients, thus expanding the potential applications.

The aim of this study was to develop and characterize UV-crosslinked hydrogel matrices based on polyethylene glycol diacrylate (PEGDA), gum arabic, betaine, and sodium alginate for potential bioanalytical applications. Various physicochemical analyses were performed, including pre-polymerization emulsion stability (Multiscan), FT-IR spectroscopy, swelling behavior in physiological buffers, pH monitoring, contact angle measurements, and morphological assessment via SEM and optical microscopy. The results demonstrated that both alginate content and UV exposure time significantly influence the structural and functional properties of the hydrogels. The highest swelling ratio (2.32 g/g) was observed for the formulation containing 5% sodium alginate polymerized for 5 min (5SA_5), though this sample showed mechanical fragmentation during incubation. In contrast, the most balanced performance was achieved for the 10SA_15 formulation, which maintained structural integrity and exhibited a swelling ratio of 1.92 g/g after 9 days. The contact angle analysis revealed a surface hydrophilicity range from 50° to 100°, with the lowest angle (50°) recorded for 10SA_5, indicating high surface wettability. These findings confirm the suitability of such hydrogels for biomedical applications, particularly as absorbent, stable platforms for drug delivery or wound healing.

N- and Fe-containing carbon-based materials were prepared at 600 and 700 °C via catalytic chemical vapor deposition (CCVD) with acetonitrile (as carbon and nitrogen source) with the application of metal/metal oxides generated in situ from Mg–Fe–Al hydrotalcite-like materials (HTs). The impact of synthesis temperature and transition metal (Fe) concentration in a blend of metal oxides derived from HTs on carbon deposit content and its structural ordering, nitrogen doping, location of N-containing groups in graphitic array, morphology and porosity was investigated using XRD, EA, XRF, XPS, SEM, HR-TEM, Raman and Mössbauer spectroscopy, and N2 sorption. Higher synthesis temperature and increased concentration of Fe-containing species occurring in a mixture of metal oxides derived from Mg–Fe–Al HTs enhanced the quantity of carbonaceous product, the mesopore volume and the thickness of graphitic domains occurring in the carbon materials and lowered nitrogen doping extent in carbon framework. Enhanced accessibility to active sites via pore network, as well as, improved electrical conductivity associated with increased graphitic domain thickness and reduced amorphous carbon content were found to be critical factors in their performance for oxygen reduction reaction (ORR) in alkaline electrolyte. No direct correlation between the population of N-containing species and ORR activity is observed but the presence of quaternary N appears to enhance selectivity for the 4-electron pathway. In addition, the influence of the carbon materials dispersed in polymer matrix in polycaprolactone (PCL)-based composite films on bulk (conductivity, dielectric constant) and surface (morphology, topography, roughness and water contact angle) properties was also described.

Investigating the adsorption properties of emulsifiers at water-oil interfaces enables advances in the comprehension of the mechanisms governing emulsion ageing and stabilization. The utilization of natural compounds in emulsion formulations is increasingly relevant for those applications where it is challenging to maintain a low impact on the environment and health. We report here a study on saponin and chitosan at the interface between water and medium-chain triglycerides (MCT) oil in relation to the properties of the corresponding emulsions. Complementary experimental approaches have been adopted to investigate interfacial properties and emulsion evolution, relying on drop tensiometry, optical and confocal microscopy, and light transmission/scattering analysis. In addition, molecular dynamics simulation has been undertaken as support for the interpretation of the experimental results. The multi-technique investigation adopted here enabled a better understanding of saponin adsorption properties and of the role of chitosan in emulsion evolution. In particular, the results evidence the formation of amphiphilic saponin-chitosan complexes, which adsorb at the liquid-liquid interface and improve the stability of oil-in-water emulsions. Since the system investigated mainly consists of natural compounds, the results of this work can contribute to the development of new and efficient low-impact formulations.

This study explored the synthesis and characterization of pectin-based composites containing encapsulated propolis and sea buckthorn oil. Both propolis and sea buckthorn oil are well known for their antioxidant and antimicrobial properties. To mitigate their sensitivity to environmental degradation, these compounds were encapsulated within a pectin matrix. The composites were prepared using an emulsification technique and subsequently for their physicochemical properties via scanning electron microscopy (SEM), ultraviolet-visible spectroscopy (UV-Vis), Fourier-transform infrared spectroscopy (FTIR), and differential scanning calorimetry (DSC), as well as color and mechanical testing. The results showed that freeze-dried samples exhibited heterogeneous, bubble-like structures containing nanocapsules (800-2000 nm), whereas for the film samples, the capsules were visibly embedded within the matrix. The study shows that this three-component system exhibits synergistic potential. Encapsulation significantly improved the UV barrier properties and the antioxidant activity of the nanocomposites, which demonstrated greater antioxidant capacity. Microbiological assays revealed that the pectin-based composites containing encapsulated propolis and sea buckthorn oil exhibited strong antibacterial activity, particularly against Gram-positive bacteria such as Streptococcus and Staphylococcus spp. The composites also demonstrated hydrophobic surface characteristics and reduced crystallinity, which correlates with their potential for controlled release. These results underscore the applicability of pectin-propolis-sea buckthorn oil composites as effective natural preservatives or functional ingredients in food systems, due to their high antioxidant and antimicrobial efficacy.

The authors wish to make the following corrections to this paper [...]

Nano-sized biomaterials are innovative drug carriers with nanometric dimensions. Designed with biocompatibility in mind, they enable precise drug delivery while minimizing side effects. Controlled release of therapeutic substances enhances efficacy, opening new possibilities for treating neurological and oncological diseases. Integrated diagnostic-therapeutic nanosystems allow real-time monitoring of treatment effectiveness, which is crucial for therapy personalization. Utilizing biomaterials as nano-sized carriers in conjunction with drugs represents a promising direction that could revolutionize the field of pharmaceutical therapy. Such carriers represent groundbreaking drug delivery systems on a nanometric scale, designed with biocompatibility in mind, enabling precise drug delivery while minimizing side effects. Using biomaterials in synergy with drugs demonstrates significant potential for a revolutionary impact on pharmaceutical therapy. Conclusions drawn from the review indicate that nano-sized biomaterials constitute an innovative tool that can significantly improve therapy effectiveness and safety, especially in treating neurological and oncological diseases. These findings should guide researchers towards further studies to refine nano-sized biomaterials, assess their effectiveness under various pathological conditions, and explore diagnostic-therapeutic applications. Ultimately, these results underscore the promising nature of nano-sized biomaterials as advanced drug carriers, ushering in a new era in nanomedical therapy.

Studies on bionanocomposite drug carriers are a key area in the field of active substance delivery, introducing innovative approaches to improve drug therapy. Such drug carriers play a crucial role in enhancing the bioavailability of active substances, affecting therapy efficiency and precision. The targeted delivery of drugs to the targeted sites of action and minimization of toxicity to the body is becoming possible through the use of these advanced carriers. Recent research has focused on bionanocomposite structures based on biopolymers, including lipids, polysaccharides, and proteins. This review paper is focused on the description of lipid-containing nanocomposite carriers (including liposomes, lipid emulsions, lipid nanoparticles, solid lipid nanoparticles, and nanostructured lipid carriers), polysaccharide-containing nanocomposite carriers (including alginate and cellulose), and protein-containing nanocomposite carriers (e.g., gelatin and albumin). It was demonstrated in many investigations that such carriers show the ability to load therapeutic substances efficiently and precisely control drug release. They also demonstrated desirable biocompatibility, which is a promising sign for their potential application in drug therapy. The development of bionanocomposite drug carriers indicates a novel approach to improving drug delivery processes, which has the potential to contribute to significant advances in the field of pharmacology, improving therapeutic efficacy while minimizing side effects.

In this communication, the single-element version of the fractional Maxwell model (single FMM) is adopted to quantify the observed behaviour of the interfacial dilational viscoelasticity. This mathematical tool is applied to the results obtained by the oscillating drop method for aqueous solutions of ethyl lauroyl arginate (LAE). The single FMM adequately fits the experimental results, fairly well characterizing the frequency dependence of the modulus and the inherent phase-shift angle of the complex physical quantity, i.e., the interfacial dilational viscoelasticity. Further speculations are envisaged to apply the FMM to step perturbations in the time domain, allowing for the same parameter set as in the frequency domain.

Synthetic materials alternatives are crucial for reaching sustainable development goals and waste reduction. Biomaterials and biomolecules obtained through bacterial fermentation offer a viable solution. Double-layer active UV-blocking material composed of bacterial nanocellulose as an inner layer and poly(hydroxyoctanoic acid) containing prodigiosin as an active compound was produced by layer-by-layer deposition. This study referred the new material consisted of the three components produced in sustainable manner, by bacterial activity: bacterial bio-pigment prodigiosin, bacterial nanocellulose and poly(hydroytoctanoate) - biopolymer obtained by microbial fermentations. Prior the final double layer film was produced, PHO films containing different PG concentrations as a layer in charge of the bioactivity (0.2, 0.5 and 1 wt%) was casted and systematically characterized (FTIR, DSC, XRD, wettability, SEM, transparency, mechanical tests) to optimize their properties. The formulation with the best UV-blocking properties and less toxicity effect tested using MRC5 cells was chosen as an outer layer in double-layer films production. Water contact angle measurements confirmed that hydrophilic - hydrophobic double layer film was obtained with the improved mechanical properties in comparison to the native BNC. Migration test indicated release of PG in all tested media as a consequence of bilayer formulation, while the PG release from PHO in 10 % ethanol was not detected. All findings from the study suggested this activated, UV-blocking material as a candidate with excellent potential in packaging industry.

The development of multifunctional dressing materials with beneficial properties for wound healing has become a recent focus of research. Many studies are being conducted to incorporate active substances into dressings to positively impact wound healing processes. Researchers have investigated various natural additives, including plant extracts and apiproducts such as royal jelly, to enhance the properties of dressings. In this study, polyvinylpyrrolidone (PVP)-based hydrogel dressings modified with royal jelly were developed and analyzed for their sorption ability, wettability, surface morphology, degradation, and mechanical properties. The results showed that the royal jelly and crosslinking agent content had an impact on the physicochemical properties of the hydrogels and their potential for use as innovative dressing materials. This study investigated the swelling behavior, surface morphology, and mechanical properties of hydrogel materials containing royal jelly. The majority of the tested materials showed a gradual increase in swelling ratio with time. The pH of the incubated fluids varied depending on the type of fluid used, with distilled water having the greatest decrease in pH due to the release of organic acids from the royal jelly. The hydrogel samples had a relatively homogeneous surface, and no dependence between composition and surface morphology was observed. Natural additives like royal jelly can modify the mechanical properties of hydrogels, increasing their elongation percentage while decreasing their tensile strength. These findings suggest possible future applications in various fields requiring high flexibility and elasticity.

Rapid industrial growth is associated with an increase in the production of environmentally harmful waste. A potential solution to significantly reduce pollution is to replace current synthetic materials with readily biodegradable plastics. Moreover, to meet the demands of technological advancements, it is essential to develop materials with unprecedented properties to enhance their functionality. Polysaccharide composites demonstrate significant potential in this regard. Polysaccharides possess exceptional film-forming abilities and are safe for human use, biodegradable, widely available, and easily modifiable. Unfortunately, polysaccharide-based films fall short of meeting all expectations. To address this issue, the current study focused on incorporating carbon quantum dots (CQDs), which are approximately 10 nm in size, into the structure of a starch/chitosan biocomposite at varying concentrations. This modification has improved the mechanical properties of the resulting nanocomposites. The inclusion of nanoparticles led to a slight reduction in solubility and an increase in the swelling degree. The optical characteristics of the obtained films were influenced by the presence of CQDs, and the fluorescence intensity of the nanocomposites changed due to the specific heavy metal ions and amino acids used. Consequently, these nanocomposites show great potential for detecting these compounds. Cellular viability assessments and comet assays confirm that the resulting nanocomposites do not exhibit any cytotoxic properties based on this specific analytic method. The tested nanocomposites with the addition of carbon quantum dots (NC/CD II and NC/CD III) were characterised by greater genotoxicity compared to the negative control. The positive control, the starch/chitosan composite alone, was also characterised by a greater induction of chromatin damage in mouse cells compared to a pure mouse blood sample.

In this study, a methodology for synthesizing oleogels based on linseed oil and emulsifiers, such as beeswax and Tween 20 and Tween 80, was developed. Linseed oil served as the main oil phase, while beeswax acted as a gelling and emulsifying agent. Tween compounds are non-ionic surfactants composed of hydrophobic and hydrophilic parts, allowing for the formation of a stable system with promising properties. Surface wetting analysis of the obtained oleogels, FT-IR spectroscopy, and determination of relative and absolute humidity over time, as well as optical microscope analysis and rheological analysis of the obtained oleogels, were conducted as part of the research. The results indicate that increasing the amount of Tween 20 decreases the hydrophilicity of the oleogel, while Tween 80 exhibits the opposite effect. Surface energy analysis suggests that a higher content of Tween 20 may lead to a reduction in the surface energy of the oleogels, which may indicate greater material stability. Changes in relative humidity and FT-IR spectral analysis confirm the influence of emulsifiers on the presence of characteristic functional groups in the structure of the oleogels. Additionally, microscopic analysis suggests that an emulsifier with a longer hydrophobic tail leads to a denser material structure.

Oleogels are structured materials formed by immobilizing oil within a polymer network. This study aimed to synthesize bilayer foamed oleogels using Ecogel™ as an emulsifier—a natural gelling and emulsifying agent commonly used to stabilize emulsions. Ecogel™ is multifunctional, particularly in cosmetic formulations, where it aids in creating lightweight cream gels with a cooling effect. However, the specific goal of this study was to investigate the physicochemical properties of oleogels formed with Ecogel™, Tween 80, gelatin, and glycerin. The combination of these ingredients has not been studied before, particularly in the context of bilayer foamed oleogels. The biphasic nature of the resulting materials was explored, consisting of a uniform lower phase and a foamed upper layer. Several analytical techniques were employed, including FT-IR spectrophotometric analysis, moisture content evaluation, surface wettability measurements, microscopic imaging, and rheological studies, in addition to surface energy determination. The results demonstrated that the addition of Tween 80 significantly improved the stability and rigidity of the oleogels. Furthermore, storage at reduced temperatures after synthesis enhanced the material’s stabilizing properties. These materials also showed an affinity for interacting with non-polar compounds, indicating potential applications in skincare, especially for interaction with skin lipids.

Oleogels are semi-solid materials that consist primarily of liquid oil immobilized in a network of organized structural molecules, which provide stability and maintain the oil in the desired shape. Due to their structure, oleogels can stabilize large amounts of liquid, making them excellent carriers for active substances, both lipophilic and hydrophilic. This study presents the synthesis methodology and investigations of olive oil-based oleogels, which are among the healthiest and most valuable vegetable fats, rich in unsaturated fatty acids and antioxidants such as vitamin E. Two types of surfactants were used: TWEEN 80, which lowers surface tension and stabilizes emulsions, and SPAN 80, which acts in oil-dominated phases. The oleogels were enriched with lidocaine, an active substance commonly used as a pain reliever and local anesthetic. This research characterized the obtained oleogels regarding their medical applications, paying particular attention to the influence of surfactant type and amount as well as the active substance on their physicochemical properties. Structural analyses were also conducted using Fourier transform infrared (FTIR) spectroscopy, alongside rheological and sorption studies, and the wettability of the materials was evaluated. The stability of the obtained oleogels was verified using the MultiScan MS20 system, allowing for an assessment of their potential suitability for long-term pharmaceutical applications. The results indicated that SPAN-stabilized oleogels exhibited better stability and favorable mechanical properties, making them promising candidates for medical applications, particularly in pain relief formulations.

This paper reviews the literature on various biosurfactant mixtures used to obtain foams. The interactions between different biosurfactants, biosurfactants, and synthetic surfactants, biosurfactants' interactions with various additives (as non-surface-active macromolecules or particles), and the impact of pH and ionic strength variations on adsorption processes, foamability, foam stability, and rheology are discussed. Biosurfactants are natural and synthetic compounds that can facilitate the process of foam formation and stabilisation; they are an alternative to classical surfactants. Research on such materials will allow the development of innovative foaming technologies that minimise the negative environmental effects of foaming compounds without losing the properties of the final product.