Ludmila Aricov

The potential of zein gels as functional delivery platforms for resveratrol (RESV), a natural polyphenol with antiamyloidogenic action but low systemic bioavailability, is explored by a combination of spectroscopic (circular dichroism, infrared, fluorescence, UV–Vis), calorimetric (differential scanning microcalorimetry) and rheological methods. Molecular docking is also applied for mapping the interaction sites and forces between native zein and RESV. Zein–RESV interactions in solution are systematically evaluated to understand the structural changes from a soluble protein–polyphenol system to a gel network. The concentration-dependent effect of RESV on the structural and thermal stability of zein is investigated in relation to the mechanical and functional properties of zein–RESV gels. It is shown that RESV acts as a promoter of zein aggregation, with a more pronounced effect obtained at a RESV:zein 1:1 molar ratio. By increasing the α-helix content, RESV induces a more ordered zein secondary structure in solution. In gel, the three-dimensional zein network is disrupted by hydrophobic and hydrogen-bonding interactions with RESV. Fluorescence spectra of zein gels point to conformational changes upon interaction that are confirmed by infrared spectroscopy. A significant viscoelastic deformation of the gel occurs when the RESV:zein molar ratio increases to 4:1. The RESV:zein 1:1 gel network demonstrates optimal viscoelastic properties for the release of RESV, following a biphasic transition from diffusion to matrix-controlled release. The findings of this study contribute to the structural design of zein-based systems for encapsulating and delivering bioactive compounds.

Ionotropic alginate-based hydrogelation by divalent metal interaction has been employed to study the effect that different types of ions might have on gel formation. In this regard, EPR and IR spectroscopies, as well as rheology techniques, have been used to evaluate the influence of divalent cations on gel formation, and at the same time to assess host–guest interactions. Alginate was functionalized with TEMPO moieties; therefore, TEMPO-alginate system was taken as a reference. The novelty of this study consists of using a mixture of adamantyl-TEMPO-functionalized alginate and β-cyclodextrin linked through 1,3-diaminopropane to assess the host–guest interactions in functionalized gels. The properties of divalent cations considered in this study (Ba²⁺, Ca²⁺, Sr²⁺, Zn²⁺) were proven by changes in spectral parameters of paramagnetic moieties, while the viscoelastic moduli as functions of shear strain and frequency were evaluated through rheology measurements. Overall, the information obtained from these investigations has shown that the properties of the alginate gels are influenced both by the type of divalent cation used for complexation and by the host–guest interactions. The results show that the type of the cation significantly affects gel strength; therefore, Ba²⁺ forms the strongest gel, while Zn²⁺ the least resistant. Additionally, a high immobilization of the spin-labeled probes has been obtained by the addition of tosylated β-cyclodextrin in the alginate gel network containing Ba²⁺ ions.

We report a systematic investigation on the physicochemical properties of polymer systems consisting of polyvinyl alcohol (PVA) and hyaluronic acid (HA) mixed in various volume ratios (1/4, 2/3, 1/1, 3/2, and 4/1). At PVA/HA ratios above 1/1, in the presence of glutaraldehyde and divinyl sulfone as crosslinking agents, hydrogels are formed. Their swelling behavior is dependent on the polymer ratio, with the highest water uptake determined for PVA/HA 4/1. The in situ generation of reactive oxygen species (HO^• radicals) under UV-A irradiation, in the presence of riboflavin as a photoinitiator, is evidenced by electron paramagnetic resonance (EPR) spectroscopy. The diffusion of small paramagnetic molecules across the interface of two PVA/HA 4/1 gel pieces placed in direct contact reveals the occurrence of molecular exchange, which could indicate some degree of self-repair of the hydrogel network. When the paramagnetic moiety is attached to the HA polymer by spin labeling, the absence of diffusion demonstrates the stability of the crosslinked HA chains within the PVA/HA network. The structural modifications induced by crosslinking, by the presence of riboflavin, and by exposure to UV-A light, and the resulting alterations in the mechanical behavior of the hydrogels are monitored by infrared spectroscopy and rheology. Only a slight decrease in the viscoelastic moduli values is noted, indicating that the formation of HO^• radicals has minimal impact on the macroscopic properties of the hydrogels.

This study aimed to develop and characterise novel hydrogels based on natural bioactive compounds for topical antimicrobial applications. Four gel systems were formulated using different polymers, namely polyacrylic acid (Carbopol 940, CBP-G), chitosan with high and medium molecular weights (CTH-G and CTM-G), and sodium alginate (ALG-G), incorporating tinctures of Verbena officinalis and Aloysia triphylla, Laurus nobilis essential oil, and a β-cyclodextrin–clove essential oil complex. All gels displayed a homogeneous macroscopic appearance and maintained stability for over 90 days. Rheological studies demonstrated gel-like behaviour for CBP-G and ALG-G, with well-defined linear viscoelastic regions and distinct yield points, while CTM-G exhibited viscoelastic liquid-like properties. SEM imaging confirmed uniform and continuous matrices, supporting controlled active compound distribution. Thermogravimetric analysis (TG-DTA) revealed a two-step degradation profile for all gels, characterised by high thermal stability up to 230 °C and near-total decomposition by 500 °C. FTIR spectra confirmed the incorporation of bioactive compounds and products and highlighted varying interaction strengths with polymer matrices, which were stronger in CBP-G and CTH-G. Antimicrobial evaluation demonstrated that chitosan-based gels exhibited the most potent inhibitory and antibiofilm effects (MIC = 2.34 mg/mL) and a cytocompatibility assessment on HaCaT keratinocytes showed enhanced cell viability for chitosan gels and dose-dependent cytotoxicity for alginate formulations at high concentrations. Overall, chitosan-based gels displayed the most favourable combination of stability, antimicrobial activity, and biocompatibility, suggesting their potential for topical pharmaceutical use.

For decades, royal jelly achieved notoriety and became an ultra-rich ingredient with numerous pharmacological properties especially for its use in production of topical ointments and creams. A novel formulation enriched with 2% royal jelly has been developed and characterized. Rheological results highlight a gel-like behavior of the product in the packaging, as it does not flow from the costumer’s hand after application and behaves like a liquid, spreading evenly onto clean skin. A clear comparison in size distribution of pure and cream samples was noticed by dynamic light scattering analysis and completed further by Fourier transform infrared spectroscopy (FTIR-ATR) which showed off shift changes in the gel sample as compared to pure compounds. MTT assays were conducted in quintuplicate on murine fibroblasts cell line (NCTC L-929) for testing the biocompatibility of the product in the range of 50–1000 μg/mL over 24, 48 and 72 h. The designed formulation is typically intended to deliver active compounds to the skin surface and potentially into deeper layers. A molecular docking study was performed for binding mode prediction of P-gp protein residues with two ligands, quercetin and myricetin, in order to investigate their role in the internal modulation of drug transport across cell membranes within the skin.

The comonomer bisphenol A (BPA) finds applications in the plastics industry, where it is used in the production of polycarbonates, plastics, PVC, thermal paper, epoxy and vinyl ester resins, and polyurethane. The water, with which many of these materials come into contact, is one of the main sources of human exposure to BPA. When ingested or touched, BPA can damage organs, disrupt the endocrine and immune systems, generate inflammatory responses, and be involved in genotoxic processes. Therefore, the need to develop effective techniques for removing BPA from aqueous environments is imperative. This paper provides a comprehensive review regarding the effective removal of BPA from water, focusing on the performance and adsorption mechanisms of various adsorbents based on chitosan and chitosan composites. The chemical and physical factors, adsorption kinetics and models governing the adsorption process of BPA in chitosan materials are also examined. This review outlines that, despite considerable progress in the absorption of bisphenol using chitosan gels, further research is necessary to assess the efficacy of these adsorbents in treating real wastewater and in large-scale manufacture.

Hydrogels are a viable option for biomedical applications due to their biocompatibility, biodegradability, and ability to incorporate various healing agents while maintaining their biological efficacy. This study focused on the preparation and characterization of novel hybrid hydrogels enriched with the natural algae compound Ulvan for potential use in wound dressings. The characterization of the hydrogel membranes involved multiple methods to assess their structural, mechanical, and chemical properties, such as pH measurements, swelling, moisture content and uptake, gel fraction, hydrolytic degradation, protein adsorption and denaturation tests, rheological measurements, SEM, biocompatibility testing, and scratch wound assay. The hydrogel obtained with a higher concentration of Ulvan (1 mg/mL) exhibited superior mechanical properties, a swelling index of 264%, a water content of 55%, and a lower degradation percentage. In terms of rheological properties, the inclusion of ULV in the hydrogel composition enhanced gel strength, and the Alginate + PVA + 1.0ULV sample demonstrated the greatest resistance to deformation. All hydrogels exhibited good biocompatibility, with cell viability above 70% and no obvious morphological modifications. The addition of Ulvan potentiates the regenerative effect of hydrogel membranes. Subsequent studies will focus on encapsulating bioactive compounds, investigating their release behavior, and evaluating their active biological effects.

Photovoltaic (PV) solar panels suffer from efficiency losses due to the accumulation of dust on their surface during operation, as well as the loss of transparency in the top glass. The efficiency can be increased when hydrophobic films are deposited on the top glass of the solar cells. The top glass of solar cells must have three characteristics: high transmittance in the 380–750 nm range, a band gap greater than 3.2 eV and a refractive index higher than 1.23. So, the films require the same characteristics. This work presents an increase in the contact angle (related to an increase in the hydrophobic character) when Ta₂O₅ is partially substituted with ZnO. The studied films, physically deposited on glass by e-gun technology, present a non-crystalline state in the form of the X-ray patterns shown. The films have a transmission of 75%–80% in the visible range. The morphology and roughness of the coatings were evaluated by atomic force microscopy. All films show the values of the Millipore water contact angle higher than 91 degrees, leading to the acquisition of hydrophobic properties on the surface. In comparison, the substrate is hydrophilic, with an average contact angle of 53.81 ± 2.16. The hydrophobic properties and self-cleaning ability make the films recommendable for application. The band gap of the coatings was calculated with the Tauc method, and they have values of 4.5–4.6 eV.

The removal of pharmaceutical contaminants from wastewater has gained considerable attention in recent years, particularly in the advancements of hydrogel-based adsorbents as a green solution for their ease of use, ease of modification, biodegradability, non-toxicity, environmental friendliness, and cost-effectiveness. This study focuses on the design of an efficient adsorbent hydrogel based on 1% chitosan, 40% polyethylene glycol 4000 (PEG4000), and 4% xanthan gum (referred to as CPX) for the removal of diclofenac sodium (DCF) from water. The interaction between positively charged chitosan and negatively charged xanthan gum and PEG4000 leads to strengthening of the hydrogel structure. The obtained CPX hydrogel, prepared by a green, simple, easy, low-cost, and ecological method, has a higher viscosity due to the three-dimensional polymer network and mechanical stability. The physical, chemical, rheological, and pharmacotechnical parameters of the synthesized hydrogel were determined. Swelling analysis demonstrated that the new synthetized hydrogel is not pH-dependent. The obtained adsorbent hydrogel reached the adsorption capacity (172.41 mg/g) at the highest adsorbent amount (200 mg) after 350 min. In addition, the adsorption kinetics were calculated using a pseudo first-order model and Langmuir and Freundlich isotherm parameters. The results demonstrate that CPX hydrogel can be used as an efficient option to remove DCF as a pharmaceutical contaminant from wastewater.