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In response to increasing concerns over food waste and safety, and the environmental impacts of traditional conservation methods, this review aims to explore the potential of bio-coatings in preserving the freshness of fruits and vegetables. Our primary objective is to provide a comprehensive analysis of recent advancements in bio-coating technologies, detailing their benefits in terms of enhancing food safety, prolonging shelf life, and reducing waste. This paper delves into various forms of bio-coatings, their applications, and their effectiveness in maintaining post-harvest quality. We further elucidate the underlying mechanisms that govern their preservation efficacy. This review is intended for researchers, industry professionals, and policy makers who are interested in sustainable preservation alternatives and their implications for food security and environmental sustainability. By the end of this review, the audience will gain a thorough understanding of the current state of bio-coating technology and its prospects in the food preservation industry.

Gel-based membranes, a fusion of polymer networks and liquid components, have emerged as versatile tools in a variety of technological domains thanks to their unique structural and functional attributes. Historically rooted in basic filtration tasks, recent advancements in synthetic strategies have increased the mechanical strength, selectivity, and longevity of these membranes. This review summarizes their evolution, emphasizing breakthroughs that have positioned them at the forefront of cutting-edge applications. They have the potential for desalination and pollutant removal in water treatment processes, delivering efficiency that often surpasses conventional counterparts. The biomedical field has embraced them for drug delivery and tissue engineering, capitalizing on their biocompatibility and tunable properties. Additionally, their pivotal role in energy storage as gel electrolytes in batteries and fuel cells underscores their adaptability. However, despite monumental progress in gel-based membrane research, challenges persist, particularly in scalability and long-term stability. This synthesis provides an overview of the state-of-the-art applications of gel-based membranes and discusses potential strategies to overcome current limitations, laying the foundation for future innovations in this dynamic field.

In this paper, a new polymeric membrane including polymers (cellulose acetate, polyethylene glycol 400), copolymer poly(4-vinylpyridine)-block-polystyrene, and TiO2 nanoparticles were synthesized by the phase inversion method. In order to investigate the presence and the influence of the TiO2 nanoparticles on the membrane matrix, a polymeric membrane without TiO2 nanoparticles was prepared by the same preparation method. The structure of the polymeric membranes was characterized by several techniques, such as Fourier transform infrared spectroscopy and scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy, thermogravimetric analysis, and impedance spectroscopy. Also, the water contact angle, water retention, and porosity were determined. The results showed that the TiO2 nanoparticles were incorporated into the pores and onto the surface of the polymeric membrane, which resulted in a more uniform structure. In addition, these polymeric membranes were tested for the removal of cadmium ions from synthetic waste-water using a laboratory-scale electrochemical separation system with a custom-built setup. The results showed that the polymeric membrane with TiO2 nanoparticles showed a high cadmium ions removal rate (95.53%), compared to the polymeric membrane without TiO2 nanoparticles (85.29%), after a 1.5 h electrochemical separation test. The final results indicated that the polymeric membranes prepared with TiO2 nanoparticles had excellent thermal stability and exhibited the best ionic conductivity. The electrochemical separation system proved that the obtained polymeric membranes effectively remove cadmium from the synthetic waste-water.

This study investigated the properties of a novel polymeric membrane based on cellulose acetate, polyethylene glycol/poly(styrene)-b-poly(4-vinylpyridine), and embedded with TiO2 nanoparticles (CA/PEG/PS154-b-P4VP381/TiO2 membrane) obtained by wet-phase inversion method. The TiO2 nanoparticles fabricated by a hydrothermal method were characterized by XRD, SEM, EDX, and UV-Vis analyses to determine the purity, morphology, and optical band gap energy. The prepared polymeric membranes with and without TiO2 nanoparticles (CA/PEG/PS154-b-P4VP381/TiO2 and CA/PEG/PS154-b-P4VP381 membranes) were characterized by FTIR, SEM, EDXS, and TGA to observe the effect of TiO2 nanoparticles added to the polymeric membrane matrix and to analyze the chemical structure, morphology, and thermal stability of the obtained polymeric membranes. The contact angle, SFE, water retention, and porosity were also determined. The results showed that adding the TiO2 nanoparticles into the polymeric membrane (CA/PEG/PS154-b-P4VP381/TiO2) significantly reduced the pore size and the water contact angle, increasing the water retention and the porosity. The lower value of the water contact angle of 15.57 ± 0.45° for the CA/PEG/PS154-b-P4VP381/TiO2 membrane indicates a pronounced hydrophilic character. The investigations performed showed that the CA/PEG/PS154-b-P4VP381/TiO2 membrane presents excellent properties and can be a promising material for water and waste-water treatment through membrane processes (e.g., electrodialysis, ultrafiltration, nanofiltration, reverse osmosis) in the future.

Depending on the concentration of the drug and/or the method of administration, drugs could be used in various ways. To take full advantage of the drug beneficial properties in oral medical interventions but also in other types of surgery, like plastic surgery, general surgery, or gynecological surgery, the drug concentration as well as the administration method itself will depend on the wound, type of surgery, and severity of the postoperative pain which can be very different. Generally, the local administration methods are recommended. Piroxicam, a nonsteroidal anti-inflammatory drug (NSAID) of the oxicam class, is generally used to relieve the symptoms of pain and inflammation. Starting from the idea of the special benefit of the interference between collagen-based materials and drug beneficial properties, our work was focused on the synthesis and characterization of new collagen-piroxicam materials. These new collagen-based materials present a good water absorption, and the piroxicam release suggests a biphasic drug release profile whereas the obtained values for the release exponent revealed a complex release mechanism including swelling, diffusion, and erosion.

Collagen-based biomaterials are increasingly explored in dentistry for their ability to deliver drugs locally and support healing. In this study, we developed chlortetracycline-loaded collagen sponges aimed at preventing postoperative infections. Five formulations were prepared by lyophilization, each with the same collagen-to-drug ratio but different glutaraldehyde (GA) concentrations: 0%, 0.25%, 0.5%, 0.75%, and 1% (w/w) relative to dry collagen. The sponges were characterized using FT-IR and UV–VIS–NIR spectroscopy, and their swelling capacity, enzymatic stability, and drug release kinetics were evaluated. Antibacterial activity was tested against Escherichia coli, Staphylococcus aureus, and Enterococcus faecalis. Statistical differences between formulations were assessed using one-way ANOVA followed by Tukey’s post hoc test (p < 0.05). All sponges released the antibiotic rapidly within the first 60 min, followed by a sustained release for up to 10 h. The non-crosslinked sponge showed the highest antimicrobial effect, while the 0.25% GA formulation offered a good balance between stability and bioactivity. While higher cross-linking enhanced structural stability, it progressively reduced antimicrobial efficacy, highlighting a crucial design trade-off. These findings underline the need to fine-tune cross-linking conditions to achieve both durability and strong antimicrobial action in collagen-based drug delivery systems for dental applications.

The present paper synthesized, characterized, and evaluated the performance of the novel biopolymeric membrane enriched with cellulose acetate and chitosan (CHI)-silver (Ag) ions in order to remove iron ion from the synthetic wastewater using a new electrodialysis system. The prepared membranes were characterized by Fourier Transforms Infrared Spectroscopy-Attenuated Total Reflection (FTIR-ATR), Thermal Gravimetric Analysis (TGA) and Differential Thermal Analysis (DSC), contact angle measurements, microscopy studies, and electrochemical impedance spectroscopy (EIS). The electrodialysis experiments were performed at the different applied voltages (5, 10, and 15 V) for one hour, at room temperature. The treatment rate (TE) of iron ions, current efficiency (IE), and energy consumption (Wc) were calculated. FTIR-ATR spectra evidenced that incorporation of CHI-Ag ions into the polymer mixture led to a polymer-metal ion complex formation within the membrane. The TGA-DSC analysis for the obtained biopolymeric membranes showed excellent thermal stability (>350 °C). The contact angle measurements demonstrated the hydrophobic character of the polymeric membrane and a decrease of it by CHI-Ag adding. The EIS results indicated that the silver ions induced a higher ionic electrical conductivity. The highest value of the iron ions treatment rate (>60%) was obtained for the biopolymeric membrane with CHI-Ag ions at applied voltage of 15 V.

We report in this paper the synthesis and characterization of a new collagen-based material. This material was obtained in a spongy form and was functionalized with an antibiotic, ciprofloxacin. The targeted applications of these kind of materials concern the post-operative prophylaxis. The in vitro tests (antimicrobial, cytotoxic, drug release) showed that sponges with a concentration of 0.75 g of ciprofloxacin per gram of collagen could be beneficial for the desired applications.

Many research studies are directed toward developing safe and efficient collagen-based biomaterials as carriers for drug delivery systems. This article presents a comparative study of the properties of new collagen sponges prepared and characterized by different methods intended for biomedical applications. The structural integrity is one of the main properties for a biomaterial in order for it to be easily removed from the treated area. Thus, the effect of combining a natural polymer such as collagen with an antimicrobial drug such as oxytetracycline or doxycycline and glutaraldehyde as the chemical cross-linking agent influences the cross-linking degree of the material, which is in direct relation to its resistance to collagenase digestion, the drug kinetic release profile, and in vitro biocompatibility. The enzymatic degradation results identified oxytetracycline as the best inhibitor of collagenase when the collagen sponge was cross-linked with 0.5% glutaraldehyde. The drug release kinetics revealed an extended release of the antibiotic for oxytetracycline-loaded collagen sponges compared with doxycycline-loaded collagen sponges. Considering the behavior of differently prepared sponges, the collagen sponge with oxytetracycline and 0.5% glutaraldehyde could represent a viable polymeric support for the prevention/treatment of infections at the application site, favoring tissue regeneration.

This study investigated the properties of a novel polymeric membrane based on cellulose acetate, polyethylene glycol/poly(styrene)-b-poly(4-vinylpyridine), and embedded with TiO[sub.2] nanoparticles (CA/PEG/PS[sub.154]-b-P4VP[sub.381]/TiO[sub.2] membrane) obtained by wet-phase inversion method. The TiO[sub.2] nanoparticles fabricated by a hydrothermal method were characterized by XRD, SEM, EDX, and UV-Vis analyses to determine the purity, morphology, and optical band gap energy. The prepared polymeric membranes with and without TiO[sub.2] nanoparticles (CA/PEG/PS[sub.154]-b-P4VP[sub.381]/TiO[sub.2] and CA/PEG/PS[sub.154]-b-P4VP[sub.381] membranes) were characterized by FTIR, SEM, EDXS, and TGA to observe the effect of TiO[sub.2] nanoparticles added to the polymeric membrane matrix and to analyze the chemical structure, morphology, and thermal stability of the obtained polymeric membranes. The contact angle, SFE, water retention, and porosity were also determined. The results showed that adding the TiO[sub.2] nanoparticles into the polymeric membrane (CA/PEG/PS[sub.154]-b-P4VP[sub.381]/TiO[sub.2]) significantly reduced the pore size and the water contact angle, increasing the water retention and the porosity. The lower value of the water contact angle of 15.57 ± 0.45° for the CA/PEG/PS[sub.154]-b-P4VP[sub.381]/TiO[sub.2] membrane indicates a pronounced hydrophilic character. The investigations performed showed that the CA/PEG/PS[sub.154]-b-P4VP[sub.381]/TiO[sub.2] membrane presents excellent properties and can be a promising material for water and waste-water treatment through membrane processes (e.g., electrodialysis, ultrafiltration, nanofiltration, reverse osmosis) in the future.