Search Results (92)

Bone graft substitutes are extensively investigated for addressing critical-size bone defects; however, their efficacy is limited by inadequate bone regeneration and subpar handling properties. Herein, we compared the bone regenerative capacity of CaO–SiO₂–P₂O₅–B₂O₃-based bioactive glass (BGS-7) macrobeads with that of β-tricalcium phosphate (β-TCP) beads and evaluated their performance when incorporated into hydrogels to improve their handling properties. BGS-7 macrobeads were fabricated via alginate crosslinking and heat treatment, and their physicochemical properties and microstructures were characterized. In a rabbit calvarial defect model, BGS-7 macrobeads, heat-treated at 600 and 800 °C, exhibited superior bone bridging and degradation than size-matched β-TCP macrobeads. To further evaluate their regenerative potential, critical-size defects (6 mm diameter × 10 mm depth) were created in the rabbit femoral condyle. To enhance clinical applicability, BGS-7 beads were incorporated into cellulose-based hydrogels and implanted into the defects. Radiographic and histomorphometric analyses demonstrated that bone formation and stable fixation achieved with hydrogel formulations containing BGS-7 microbeads and Laponite were more pronounced than those with BGS-7 beads alone. The findings suggest that BGS-7 macrobeads, particularly when combined with microbead- and Laponite-containing hydrogels, represent a promising bone graft substitute with improved regenerative and handling properties compared with using BGS-7 beads alone. Full article

The replacement of polyvinylidene fluoride (PVDF) with environmentally friendly binders offers potential advantages in the development of aqueous lithium-ion batteries (ALIBs) and flow batteries (FBs) incorporating solid charge carriers (so-called solid boosters). This study investigates the electrochemical stability of ethyl cellulose and cross-linked gluten as substitutes for PVDF in LiMn₂O₄ (LMO) cathodes for aqueous Li-ion battery electrodes and solid boosters for FBs. The millimetre-scaled solid booster beads must be easily produced on a large scale, and at the same time, their charging and discharging must be reversible over long durations under electrolyte tank conditions. The binders were tested under standardized conditions for discharge capacity and cycling stability. Our results demonstrate that ethyl cellulose and cross-linked gluten can rival the electrochemical stability of PVDF, maintaining initial discharge capacities near 100 mAh g⁻¹ at 0.2 C for LMO cathodes and exhibiting reasonable capacity retention over hundreds of cycles. This work supports the feasibility of sustainable electrode processing, provides promising directions for scalable, eco-friendly electrode fabrication methods, and highlights promising binder candidates for use in aqueous energy storage systems. Full article

In 2024, the global average temperature reached 1.55 °C above the pre-industrial level for the first time. However, we could still keep the long-term global average temperature below 2 °C if all possible measures are taken to mitigate greenhouse gases. It is widely accepted that methane (CH₄) mitigation can slow global warming in the near term. Among all approaches toward this goal, the utilization of aerobic methanotrophs, which are natural catalysts for the conversion of CH₄, emerges as a promising solution. Previously, we identified a candidate for CH₄ mitigation, Methylotuvimicrobium buryatense 5GB1C, which exhibits a greater growth rate and CH₄ consumption rate than other known methanotrophs at 500 ppm CH₄. In this study, we address aspects of the practical applications of this methanotroph for CH₄ mitigation. We first examined temperature and medium conditions to optimize M. buryatense 5GB1C growth at 500 ppm CH₄. The results show that M. buryatense 5GB1C has a broad optimal temperature range for growth at 500 ppm, from 15 °C to 30 °C, and that its growth rate is consistently improved by 20–30% in 10-fold-diluted medium. Next, to demonstrate the feasibility of CH₄ removal at low concentrations by this methanotroph, we applied it in a laboratory-scale packed-bed column reactor for the treatment of 500 ppm CH₄ and tested different packing materials. The column reactor experiments revealed a maximum elimination capacity of 2.1 g CH₄ m⁻³ h⁻¹ with 2 mm cellulose beads as the packing material. These results demonstrate that with further technological innovation, this methanotroph has the potential for real-world methane mitigation. Full article

Synthetic dyes are increasingly relevant pollutants due to their widespread use and discharge into water bodies. This study examines how the solution pH affects the morphology of chitosan–cellulose cryogel (Ch-C-EGDE) and its impact on dye transport to adsorption sites. Adsorption tests with dyes Y5, R2, and B1 over a pH range of 2–12 revealed optimal performance at pH 2.5. High hydronium ion concentrations significantly improved adsorption capacities (945–1605 mg/g), with a hierarchy B1 > R2 > Y5 at 250 mg/L initial concentration. The dependence of the dye adsorption on the acidic pH of the solution suggests that there is a mechanism of adsorption by electrostatic forces due mainly to the protonation of the amino group (NH₃⁺). During the dye adsorption studies, a decrease in the diameter of the cryogel beads was observed, as well as a possible “zipper effect” in the pores of the Ch-C-EGDE cryogel beads, which depends on the pH at which the anionic molecules of the dyes attract the positively charged chitosan-based adsorbent walls, which physically closes the pores and results in a decrease in pore size as well as a geometric and/or load-bearing impediment. The experimental data fitted well with the pseudo-second-order kinetic models and the Sips isotherm model, indicating multilayer and heterogeneous adsorption behavior. In the Sips model, a value of n > 1 was obtained, which confirms favorable adsorption conditions and suggests strong dye-adsorbent material interactions, especially at higher dye concentrations. Full article

A metal-ion-free method was developed to prepare κ-carrageenan/cellulose hydrogel beads for efficient cationic dye removal. The beads were fabricated using a mixture of 1-ethyl-3-methylimidazolium acetate and N,N-dimethylformamide as the solvent system, followed by aqueous ethanol-induced phase separation. This process eliminated the need for metal-ion crosslinkers, which typically neutralize anionic sulfate groups in κ-carrageenan, thereby preserving a high density of accessible binding sites. The resulting beads formed robust interpenetrating polymer networks. The initial swelling ratio reached up to 28.3 g/g, and even after drying, the adsorption capacity remained over 50% of the original. The maximum adsorption capacity for crystal violet was 241 mg/g, increasing proportionally with κ-carrageenan content due to the higher surface concentration of anionic sulfate groups. Kinetic and isotherm analyses revealed pseudo-second-order and Langmuir-type monolayer adsorption, respectively, while thermodynamic parameters indicated that the process was spontaneous and exothermic. The beads retained structural integrity and adsorption performance across pH 3–9 and maintained over 90% of their capacity after five reuse cycles. These findings demonstrate that κ-carrageenan/cellulose hydrogel beads prepared via a metal-ion-free strategy offer a sustainable and effective platform for cationic dye removal from wastewater, with potential for heavy metal ion adsorption. Full article

Background/Objectives: Long-acting injections (LAIs) are innovative drug delivery systems that improve patient compliance by maintaining therapeutic drug levels over extended periods. Micro- and nanosuspensions are commonly used in LAIs to enhance bioavailability, but their thermodynamic instability poses challenges, including particle aggregation and growth. This study aimed to evaluate the impact of two helping processes—vehicle thermal treatment and high-shear homogenization—on the stability and manufacturing efficiency of aripiprazole monohydrate (AM) suspensions. Methods: AM suspensions containing sodium carboxymethyl cellulose (CMCNa), mannitol and disodium phosphate in water for injections (WFIs) were prepared using a combination of thermal treatment of the vehicle solution, high-shear homogenization and bead milling. Four manufacturing variants were tested to assess the influence of these processes on particle size distribution (PSD), viscosity and stability during a 3-month accelerated stability study. Molecular weight changes in CMCNa from thermal treatment were analyzed using size exclusion chromatography with multiangle scattering (SEC-MALS), and PSD was measured using laser diffraction. Results: Thermal treatment of the vehicle solution had minimal impact on CMCNa molecular weight, preserving its functionality. High-shear homogenization during bead milling significantly reduced particle aggregation, resulting in improved PSD and reduced viscosity. Synergistic effects of the two helping processes used in one manufacturing process were observed, which led to superior stability and minimal changes in PSD and viscosity during storage. Batches without the helping processes exhibited increased particle size and viscosity over time, indicating reduced suspension stability. Conclusions: Incorporating vehicle thermal treatment and high-shear homogenization during bead milling enhances the stability and manufacturing efficiency of AM suspensions. These findings underscore the importance of optimizing laboratory-scale processes to ensure the quality and safety of pharmaceutical suspensions. Full article

Hydrogel-based adsorbents have gained increasing recognition in recent years due to their promising potential for pollutant removal. However, conventional hydrogels often suffer from low mechanical strength over prolonged use. Therefore, this study explores the incorporation of silica extracted from bamboo culm (Dendrocalamus asper) to enhance the mechanical stability of hydrogel beads composed from carboxymethyl cellulose (CMC), chitosan (CS), and magnetite ferrofluid (Fe₃O₄), through cross-linking. We hypothesize that silica enhances the mechanical properties of magnetite hydrogel beads without compromising their adsorption capacity. The extracted silica was confirmed with FTIR and EDS analysis. The synthesized CMC-CS-Fe₃O₄-Si hydrogel beads were characterized using FTIR and SEM. Its stability was assessed through dry weight loss measurements, while its adsorption efficiency was evaluated using batch adsorption experiments. The silica-incorporated hydrogel exhibited enhanced mechanical and thermal stability under various pH and temperature conditions, without negatively affecting its adsorption performance, achieving maximum adsorption capacities of 53.00 mg/g for Cr (VI) and 85.06 mg/g for Cu (II). Desorption and regeneration studies confirmed the reusability of the hydrogel for more than four cycles. Overall, the interaction between the hydrogel and silica resulted in excellent adsorption performance, improved mechanical properties, and long-term reusability, making this a promising hydrogel adsorbent for wastewater remediation. Full article

This study evaluated the use of brewer’s spent yeast (BSY) as an adsorbent for tannins from a chestnut shell extract (CS tannin extract). This extract was derived from an alkaline treatment (5% NaOH (v/v)) to recover cellulosic material from chestnut shells and needed valorization. Various BSY treatments, including lyophilization, immobilization in calcium alginate beads, and alkaline and acid treatments, were tested to identify which had the best tannin adsorption capacity. The results highlight BSY’s potential as a system to valorize tannins from this treatment solution. Full article

Microalgae have emerged as a sustainable and efficient source of protein, offering a promising alternative to conventional animal and plant-based proteins. Species such as Arthrospira platensis and Chlorella vulgaris contain protein levels ranging from 50% to 70% of their dry weight, along with a well-balanced amino acid profile rich in essential amino acids such as lysine and leucine. Their cultivation avoids competition for arable land, aligning with global sustainability goals. However, the efficient extraction of proteins is challenged by their rigid cell walls, necessitating the development of optimized methods such as bead milling, ultrasonication, enzymatic treatments, and pulsed electric fields. These techniques preserve functionality while achieving yields of up to 96%. Nutritional analyses reveal species-dependent digestibility, ranging from 70 to 90%, with Spirulina platensis achieving the highest rates due to low cellulose content. Functionally, microalgal proteins exhibit emulsifying, water-holding, and gel-forming properties, enabling applications in baking, dairy, and meat analogs. Bioactive peptides derived from these proteins exhibit antioxidant, antimicrobial (inhibiting E. coli and S. aureus), anti-inflammatory (reducing TNF-α and IL-6), and antiviral activities (e.g., Dengue virus inhibition). Despite their potential, commercialization faces challenges, including regulatory heterogeneity, high production costs, and consumer acceptance barriers linked to eating habits or sensory attributes. Current market products like Spirulina-enriched snacks and Chlorella tablets highlight progress, but food safety standards and scalable cost-effective extraction technologies remain critical for broader adoption. This review underscores microalgae’s dual role as a nutritional powerhouse and a source of multifunctional bioactives, positioning them at the forefront of sustainable food and pharmaceutical innovation. Full article

This study investigated the effects of combining sodium alginate (ALG) with various natural hydrocolloids on the microstructure and release behaviors of microbeads. The encapsulation solutions were prepared at a 1:1 (w/w) ratio with ALG as the control and carrageenan (CAR), locust bean gum (LBG), acacia gum (ACA), pectin (PEC), and carboxymethyl cellulose (CMC) as experimental groups. Each formulation contained 0.2% (w/v) tartrazine and was extruded into a CaCl₂ solution for bead production. Encapsulation efficiency varied across formulations, with the lowest in the control (ALG-ALG) and highest in ALG-CAR and ALG-CMC, reaching 74% and 78%, respectively. The microbead sizes ranged from 2.07 to 3.48 mm, with the lowest particle diameter observed in ALG-ACA composites. Surface analysis showed smooth and uniform microbeads in the control (ALG-ALG), while ALG-LBG microbeads were rougher. Release kinetics were assessed using various models, with the Higuchi model best describing the release for most formulations (highest R² values). Tartrazine release followed pseudo-Fickian behavior in all formulations, with slower release in ALG-ACA and faster release in ALG-LBG microbeads. This study fills a gap in understanding how the incorporation of different natural hydrocolloids influences both the encapsulation efficiency and release dynamics of alginate-based microbeads, providing valuable insights for applications in food and pharmaceutical industries. Full article

Iron oxide-based nanoparticles, such as magnetic nanoparticles (MNPs), have gained significant attention in the area of drug delivery due to their unique magnetic properties, allowing for precise targeting and controlled release of therapeutic agents. Several successful research studies were reported with combinations of magnetic nanoparticles and polysaccharides such as sodium alginate, chitosan, cellulose, etc. The presented research work is based on synthesising MNPs via the co-precipitation method and their successful encapsulation within alginate beads, serving as a promising drug delivery system for aceclofenac, a model drug. The physical and chemical characteristics of both the prepared magnetite nanoparticles and the aceclofenac-loaded MNPs alginate beads were thoroughly examined using scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), Fourier-transform infrared spectroscopy (FTIR), powder X-ray diffraction (PXRD), and vibrating sample magnetometry (VSM). Furthermore, a drug release study was conducted to evaluate the release kinetics of aceclofenac from the prepared MNP alginate beads. The magnetic characteristics of magnetite and MNP beads shed light on the potential application of novel drug delivery systems for magnetically targeted therapeutic interventions. The present research offers valuable insights into the development of magnetic nanoparticle-based drug carriers, paving the way for enhanced drug delivery strategies in the field of pharmaceutical sciences. Full article

Cellulose microgel beads fabricated using the dropping technique suffer from structural irregularity and mechanical variability. This limits their translation to biomedical applications that are sensitive to variations in material properties. Ionic salts are often uncontrolled by-products of this technique, despite the known effects of ionic salts on cellulose assembly. In this study, the coagulation behavior of cellulose/salt solutions was explored as a way to combat these challenges. An ionic salt (NaCl) was added to a cellulose solution (cellulose/NaOH/urea) prior to coagulation in a hydrochloric acid bath. Quantification of the bead geometry and characterization of the pore architecture revealed that balancing the introduction of salt with the resultant solution viscosity is more effective at reducing structural variability and diffusion limitations than other pre-gelling techniques like thermal gelation. Three-dimensional visualization of the internal pore structure of neat cellulose, thermo-gel, and salt-gel beads revealed that adding salt to the solution is the most effective way to achieve 3-D structural uniformity throughout the bead. Coupled with nanoindentation, we confirmed that the salt produced during coagulation plays a critical role in mechanical variability, and that adding salt to the solution before dropping into the coagulation bath completely screens this effect, producing uniform microgel beads with reproducible mechanical properties. Full article

According to environmental concerns related to water pollution, this study aims to develop a novel hydrogel bead as a biocompatible and efficient adsorbent by integrating bacterial cellulose-activated carbon (BCAC) and montmorillonite (MT) in alginate hydrogel (ALG). The ionotropic gelation method was applied to the fabrication of BCAC/MT/ALG hydrogel beads. The BCAC/MT/ALG hydrogel bead exhibited significantly higher tensile strength, Young’s modulus, and thermal stability, with ~1.4 times higher adsorption uptake of methylene blue (MB) from aqueous solution as compared to the pristine ALG bead. The textural properties, including specific surface area and porosity, were beneficial to accommodate the size of cationic MB as the target molecule. This resulted in a remarkable MB adsorption uptake of 678.2 mg/g at pH 7 and 30 °C. The adsorption isotherm showed the best fit for the nonlinear Redlich-Peterson isotherm model. Experimental adsorption data were well-described by the pseudo-second order kinetic model, with R² values reaching 0.997. In addition, the adsorbent bead demonstrated easy regeneration with high reusability with approximately 75% of MB removal after being used for six cycles. Therefore, BCAC/MT/ALG bead represents an eco-friendly, cost-effective, and highly efficient adsorbent for MB removal from water and could potentially be used for removal of a wide range of cationic dye pollutants from wastewater. Full article

Core–shell nanostructures are powerful platforms for the development of novel nanoscale drug delivery systems with sustained drug release profiles. Coaxial electrospinning is facile and convenient for creating medicated core–shell nanostructures with elaborate designs with which the sustained-release behaviors of drug molecules can be intentionally adjusted. With resveratrol (RES) as a model for a poorly water-soluble drug and cellulose acetate (CA) and PVP as polymeric carriers, a brand-new electrospun core–shell nanostructure was fabricated in this study. The guest RES and the host CA molecules were designed to have a reverse gradient distribution within the core–shell nanostructures. Scanning electron microscope and transmission electron microscope evaluations verified that these nanofibers had linear morphologies, without beads or spindles, and an obvious core–shell double-chamber structure. The X-ray diffraction patterns and Fourier transform infrared spectroscopic results indicated that the involved components were highly compatible and presented in an amorphous molecular distribution state. In vitro dissolution tests verified that the new core–shell structures were able to prevent the initial burst release, extend the continuous-release time period, and reduce the negative tailing-off release effect, thus ensuring a better sustained-release profile than the traditional blended drug-loaded nanofibers. The mechanism underlying the influence of the new core–shell structure with an RES/CA reverse gradient distribution on the behaviors of RES release is proposed. Based on this proof-of-concept demonstration, a series of advanced functional nanomaterials can be similarly developed based on the gradient distributions of functional molecules within electrospun multi-chamber nanostructures. Full article

Biofumigation was proposed as an alternative to synthetic pesticides for the disinfection of agricultural soils, in view of the biocidal effect of isothiocyanates (ITCs) released by some vegetal species, like Brassicaceae. However, biofumigation also presents limitations; thus, a novel and viable alternative could be the direct introduction of ITCs into agricultural soils as components loaded into biodegradable hydrogels. Thus, in this work, ITCs-based microemulsions were developed, which can be loaded into porous polymer-based hydrogel beads based on sodium alginate (ALG) or sodium carboxymethyl cellulose (CMC). Three ITCs (ethyl, phenyl, and allyl isothiocyanate) and three different surfactants (sodium dodecylsulfate, Brij 35, and Tween 80) were considered. The optimal system was characterized with attenuated ATR-FTIR spectroscopy and differential scanning calorimetry to study how the microemulsion/gels interaction affects the gel properties, such as the equilibrium water content or free water index. Finally, loading and release profiles were studied by means of UV–Vis spectrophotometry. It was found that CMC hydrogel beads showed a slightly more efficient profile of micelles’ release in water with respect to ALG beads. For this reason, and due to the enhanced contribution of Fe(III) to their biocidal properties, CMC-based hydrogels are the most promising in view of the application on real agricultural soils. Full article