Alginate Solution Research Articles

Fabrication of hydrogel mini-capsules as carrier systems

Conventional drug administration often results in systemic action, thus needing high dosages and leading to potentially pronounced side effects. Targeted delivery, employing carriers like nanoparticles, aims to release drugs at a target site, but only a small fraction of nanoparticles actually reaches it. Microrobots have been proposed to overcome this issue since they can be guided to hard-to-reach sites and locally deliver payloads. To enhance their functionality, we propose microrobots made as deformable capsules with hydrogel shells and aqueous cores, having the potential added advantages of biocompatibility, permeability, and stimulus-responsiveness. Endowing microrobots with deformability could allow them to navigate inside capillaries and cross barriers to finally reach the target site. In this study, we present a cost-effective method for fabricating core-shell structures without the use of organic solvents, surfactants, or extreme pH conditions unlike other techniques (e.g. Layer by Layer). The process begins with the dripping of a mixture of hydrogels, agarose and alginate, into a solution to gelate the drops into beads. After they are loaded with calcium ions at different concentrations, they are immersed in an alginate solution to form the shell. Finally, the beads are heated to let the agarose melt and diffuse out, leaving a liquid core. By varying the concentration of calcium ions, we obtain shells of different thicknesses. To estimate it, we have developed a method using the colour intensity from microscope images. This allowed us to observe that lowering the calcium ions concentration below a threshold does not lead to the formation of continuous shells. For higher concentrations, although the core may remain partially gelled, continuous shells successfully form. Therefore, our fabrication process could find applications in drug delivery, encapsulation systems, and microrobotics.

A particle-filled hydrogel based on alginate and calcium phosphate nanoparticles as bone adhesive

The clinical need for bone adhesives as an alternative to osteosynthesis is evident. However, this is a challenging problem due to the moist environment in surgical sites with bone surfaces covered with blood and biomolecules like lipids or proteins. A nanoparticle-loaded hydrogel that is based on a freeze-dried powder of silica-coated calcium phosphate/carboxymethyl cellulose nanoparticles (CaP/CMC/SiO2) and an aqueous solution of sodium alginate (2 wt%) was developed and optimized with respect to the gluing ability in air and in water. The final paste was crosslinked within about one minute by calcium ions released from the calcium phosphate nanoparticles and contained about 20 wt% nanoparticles and 80 wt% water. The mechanical properties of the hydrogel were determined by extensive rheological tests. The thixotropic pasty hydrogel can be applied with a syringe. The adhesion strength was about 84 kPa between moist bone fragments in air. The hydrogel kept fragments of cortical bone well connected for >3 months during complete submersion in water. Besides water, the material consists only of biocompatible and biodegradable components (calcium phosphate, CMC, alginate). It carries only a very low dose of these materials into the bone site (mainly calcium phosphate nanoparticles). In-vitro cell culture with hMSCs that differentiated to osteoblasts confirmed a good biocompatibility of the bone adhesive formulation.Graphical

Alginate/clinoptilolite beads as a novel adsorbent for reducing the salinity of industrial wastewater: adsorption kinetics and isotherm study

ABSTRACT Treatment and desalination of unconventional water are considered important alternatives to combat water scarcity in Tunisia. This study demonstrates a viable approach to the increasing possibility of the salinity reduction of industrial effluent through adsorption. In this work, a novel alginate complex was developed for reducing the salinity of the industrial wastewater to be reinjected and reused again within the industrial process and even in agriculture. The Calcium alginate/clinoptilolite beads (Ca-Alg/Clino beads) were prepared using sodium alginate (2%) solution and calcium chloride (4%) solution as the crosslinking agent with clinoptilolite. Batch experiments were carried out to test the adsorption capacity of the synthetised Ca-Alg/Clino beads. It was found that the salinity reduction process depends strongly on the pH, the adsorbent mass, the interaction time, and the initial salt concentration. The highest reduction efficiency and salinity reduction were achieved at pH (6-7). Batch adsorption experiments indicated that Ca-Alg/Clino beads allow an excellent salinity reduction of up to 96.83% for a dosage adsorbent/water of 2 g/L and a salinity of 6 g/L at a contact time of 20 min. The maximum adsorption capacity (qmax) was 30.1 mg/g. The optimal adsorption pH was 7. The adsorption isotherms data follow well the Langmuir model. The separation factor, RL = 0.74, indicates that the adsorption process is favourable. The kinetics data favour the pseudo-second-order model. The fabricated beads can be reused 5 times without any weight loss. This material has excellent efficiency when applied to real environmental water.

Thermo-controlled microfluidic generation of monodisperse alginate microspheres based on external gelation.

Droplet-based microfluidic systems have received much attention as promising tools for fabricating monodisperse microspheres of alginate solutions with high accuracy and reproducibility. The immediate and simple ionotropic gelation of alginate, its biocompatibility, and its tunability of mechanical properties make it a favorable hydrogel in the biomedical and tissue engineering fields. In these fields, micron-sized alginate hydrogel spheres have shown high potential as cell vehicles and drug delivery systems. Although on-chip microfluidic gelation of the produced alginate droplets is common, several challenges remain. Complicated chemical and microfabrication processes are required, and the risk of microchannel clogging is high. In the current study, we present an easy-to-use microfluidic external gelation process to produce highly spherical and monodisperse microspheres from very low-concentrated alginate-RGD solution [0.5% (w/v)]. To accomplish this, gelatin, a thermo-sensitive and inexpensive biomaterial, was incorporated into the alginate solution as a sacrificial biomaterial that mediates the off-chip external gelation of the alginate with Ca2+, and avoids droplet coalescence. Utilizing the methodology mentioned above, we successfully generated monodisperse alginate microspheres (AMs) with diameters ranging from 27 μm to 46 μm, with a coefficient of variation of 0.14, from a mixture of Arg-Gly-Asp (RGD)-modified very low viscosity alginate and gelatin. These RGD-AMs were used as microcarriers for human umbilical vein endothelial cells. The described easy-to-use and cost-effective microfluidic off-chip external gelation strategy exhibits comparable advantages to on-chip external gelation and demonstrates superiority over the latter since clogging is impossible.

Novel lattice Boltzmann method for simulation of strongly shear thinning viscoelastic fluids

AbstractThe simulation of viscoelastic liquids using the Lattice–Boltzmann method (LBM) in full three dimensions remains a formidable numerical challenge. In particular the simulation of strongly shear‐thinning fluids, where the ratio between the high‐shear and low‐shear viscosities is large, is often prevented by stability problems. Here we present a novel approach to overcome this issue. The central idea is to artificially increase the solvent viscosity which allows the method to benefit from the very good stability properties of the LBM. To compensate for this additional viscous stress, the polymer stress is reduced by the same amount. We apply this novel method to simulate two realistic cell carrier fluids, methyl cellulose and alginate solutions, of which the latter exhibits a viscosity ratio exceeding 10,000.

High precision acoustofluidic synthesis of stable, biocompatible water-in-water emulsions

Water-in-water (w/w) emulsions, comprising aqueous droplets within another continuous aqueous phase, rely on a low interfacial tension for stability. Thus far, it has been challenging to control their size and stability without the use of stabilizers. In this study, we introduce a microfluidic technique that addresses these challenges, producing stable w/w emulsions with precisely controlled size and uniformity. Results shows that using an acoustically actuated microfluidic mixer, PEG, Dextran, and alginate solutions (84.66 mPa.s viscosity difference) were homogenized rapidly, forming uniformly distributed w/w emulsions stabilized in alginate gels.The emulsion size, uniformity, and shear sensitivity can be tuned by modifying the alginate concentration. Biocompatibility was evaluated by monitoring the viability of kidney cells in the presence of emulsions and gels. In conclusion, this study not only showed emulsion formation with a high mixing efficiency exceeding 90 % for all viscosities, actuated at an optimized frequency of 1.064 MHz, but also demonstrated that an aqueous, solvent, and emulsifier-free composition exhibited remarkable biocompatibility, holding promise for precise drug delivery, cosmetics, and food applications.

Inkjet-based facile fabrication of a copper ferrocyanide-embedded magnetic alginate microadsorbent for highly enhanced cesium removal

For the first time, simple and facile fabrication of a magnetic alginate microadsorbent via piezoelectric inkjet technology was developed for the selective removal of 137Cs via magnetic separation. Through the ejection of an alginate solution containing potassium ferrocyanide and magnetic nanoparticles (MNPs) into a Cu2+ solution via an inkjet device, the fabrication of a copper ferrocyanide-embedded magnetic alginate microadsorbent (CuFC-MAM) with an average size of 39.38 μm was easily achieved in a one-pot fabrication process; here, the Cu2+ ions acted as both a cross-linker for the gelation of alginate and a Cu source for the in situ synthesis of CuFC with potassium ferrocyanide. The Cs adsorption behavior of CuFC-MAM was effectively fitted by the pseudo-second-order kinetic model and Langmuir isotherm. Owing to the increased specific surface area of CuFC-MAM, its pseudo-second-order rate constant and maximum adsorption capacity were 76.54 and 1.486 times greater than those of CuFC-embedded magnetic alginate macroadsorbents fabricated without inkjet devices. Compared with other Cs adsorbents, CuFC-MAM presented the highest maximum capacity and Kd value; these results were attributed to the high content of CuFC in CuFC-MAM (50.15%). In addition, our CuFC-MAM exhibited an excellent removal efficiency of radioactive Cs, exceeding 99% from seawater.

Effects of Coaxial Nozzle's Inner Nozzle Diameter on Filament Strength and Gelation in Extrusion-Based 3D Printing with In Situ Ionic Crosslinking.

This study systematically investigates the effects of the coaxial nozzle's inner nozzle diameter on the strength and gelation of filaments produced via extrusion-based 3D printing with in situ ionic crosslinking. In this system, bioink (sodium alginate solution) was extruded through the outer nozzle, and the ionic crosslinking solution (calcium chloride solution) was extruded through the inner nozzle. The outer nozzle diameter was fixed at 2.16 mm, and the inner nozzle diameter was varied among 1.19, 0.84, and 0.584 mm. The results indicate that, as the inner nozzle diameter decreased, filament strength decreased, and filament gelation became poorer. These findings highlight the importance of optimizing inner nozzle diameter for improved filament strength and gelation in extrusion-based 3D printing with in situ ionic crosslinking.

Microscopic mechanism of oxygen consumption inhibitor delaying the oxidation of coal

In order to inhibit the coal-oxygen complex that triggers spontaneous coal combustion, a retardant consisting of sodium alginate solution, sodium bicarbonate, inorganic salt MgCl2 and deoxidiser that can achieve multiple effects of hysteresis and oxygen depletion was developed. Taking the sulfur-containing side-chain reactive group of coal molecule -CH2-SH as the object of study, the Gaussian 16W procedure and density-functional-transfer theory (DFT) were applied to investigate the electrostatic potential and reaction tendency, oxygen adsorption capacity, front-line orbitals, natural bonding capacity, and oxygen adsorption capacity of the reactive group before and after the formation of the complexes with Na+ and Mg2+, using the solvation effect at the level of B3LYP/6-31G(d, p), respectively. The changes of electrostatic potential and reaction tendency, oxygen adsorption, front orbitals, natural bonding orbitals and charge transfer before and after the formation of complexes between -CH2-SH reactive groups and Na+, Mg2+, respectively. Comparative analysis of the interaction with oxygen before and after the formation of coordination blocking structure of coal and inorganic salts in gaseous environment, aqueous environment and retarded oxygen-depleting sodium alginate blocking solution environment, respectively. The calculated results show that the side chain of the aromatic ring of the raw coal is the active site for easy adsorption of oxygen, and the stability of the coordination blocking structure is significantly enhanced under the environment of hysteretic oxygen-depleting sodium alginate gel blocking agent, and the adsorption of oxygen before and after the coal molecule combines with Na+ and Mg2+ is the weakest under the environment of hysteretic oxygen-depleting sodium alginate gel blocking agent; The absolute value of the HOMO orbital energy increases the most, and the energy level difference (ELUMO - EHOMO) of the complexes increases the most; the natural bonding orbital analysis reveals that the lone pair of electrons of S atoms in -CH2-SH under the environment of hysteresis oxygen depletion sodium alginate gel blocker has a strong coordination effect with Na+ and Mg2+. In the hysteresis oxygen depletion sodium alginate gel resist environment, the stability of the coordination blocking structure is strengthened due to the moderateness of the dielectric constant, and its oxygen depletion also reduces the number of O2 molecules, which further reduces the adsorption and collision chances between the two, and a more desirable blocking effect can be obtained. The results reveal the micro-mechanism of the hysteresis oxygen depletion inhibitor in preventing spontaneous combustion of coal, which can provide a reference for further improving the inhibition effect of the inhibitor.

Enhanced phosphorus adsorption using modified drinking water treatment residues: A comparative analysis of powder and alginate bead forms

This study provides an analysis of the phosphorus adsorption efficacy of three modified drinking water treatment residues (MDWTRs): MDWTR-P (powdered form), MDWTR-D2, and MDWTR-D5 (alginate bead-entrapped forms with bead diameters of 2 mm and 5 mm, respectively). The preparation process involved washing and drying the drinking water treatment residue, followed by grinding and sieving to achieve particle sizes below 90 μm. The residue was then incinerated at 600 °C in oxygen-limited conditions. Subsequently, the MDWTR was formulated into alginate beads by mixing with sodium alginate and FeCl3 solutions, resulting in spherical particles of specified diameters. The evaluation of surface area, pore volume, pore size, and CHN concentration revealed that MDWTR-D5 possesses the largest surface area (284.7 m2 g−1) and highest micropore volume (0.04 cm3 g−1), indicating a greater capacity for adsorption. SEM-EDS analysis demonstrated significant compositional changes post-treatment, particularly elevated phosphorus levels, confirming effective adsorption. Metal content analysis indicated high aluminum levels in MDWTR-P and increased iron content in MDWTR-D5. Toxicity Characteristic Leaching Procedure (TCLP) and in vitro bioaccessibility (IVBA) tests confirmed the non-hazardous nature of all MDWTRs, ensuring their safety for environmental applications. Kinetic analyses using pseudo-first-order, pseudo-second-order, and intraparticle diffusion models highlighted the superior performance of MDWTR-D5, with the highest equilibrium adsorption capacity and initial adsorption rate across all tested concentrations, suggesting both high efficiency and rapid adsorption potential. Further validation using Langmuir and Freundlich isotherms revealed MDWTR-D5's highest monolayer adsorption capacity (22.88 mg g−1) and Freundlich adsorption capacity parameter (6.97 mg g−1). Statistical analysis via one-way ANOVA confirmed significant differences in phosphorus concentrations among the MDWTRs samples (p-value <0.001), consistently underscoring MDWTR-D5's superior adsorption performance. These findings highlight MDWTR-D5's potential as an effective adsorbent for phosphorus removal in wastewater treatment, emphasizing its applicability in environmental remediation strategies.

Study on Printability Evaluation of Alginate/Silk Fibroin/Collagen Double-Cross-Linked Inks and the Properties of 3D Printed Constructs.

In recent years, biological 3D printing has garnered increasing attention for tissue and organ repair. The challenge with 3D-printing inks is to combine mechanical properties as well as biocompatibility. Proteins serve as vital structural components in living systems, and utilizing protein-based inks can ensure that the materials maintain the necessary biological activity. In this study, we incorporated two natural biomaterials, silk fibroin (SF) and collagen (COL), into a low-concentration sodium alginate (SA) solution to create novel composite inks. SF and COL were modified with glycidyl methacrylate (GMA) to impart photo-cross-linking properties. The UV light test and 1H NMR results demonstrated successful curing of silk fibroin (SF) and collagen (COL) after modification and grafting. Subsequently, the printability of modified silk fibroin (RSFMA)/SA with varying concentration gradients was assessed using a set of three consecutive printing models, and the material's properties were tested. The research results prove that the addition of RSFMA and ColMA enhances the printability of low-concentration SA solutions, with the Pr values increasing from 0.85 ± 0.02 to 0.90 ± 0.03 and 0.92 ± 0.02, respectively, and the mechanical strength increasing from 0.19 ± 0.01 to 0.28 ± 0.01 and 0.38 ± 0.01 MPa; cytocompatibility has also been improved. Furthermore, rheological tests indicated that all of the inks exhibited shear thinning properties. CCK-8 experiments demonstrated that the addition of ColMA increased the cytocompatibility of the ink system. Overall, the utilization of SF and COL-modified SA materials as inks represents a promising advancement in 3D-printed ink technology.

The Preparation and Characterization of an Alginate–Chitosan-Active Bilayer Film Incorporated with Asparagus (Asparagus officinalis L.) Residue Extract

The agricultural production of asparagus generates a significant number of residues rich in bioactive compounds, most of which are wasted. In this study, active edible films with antioxidant and antibacterial properties for food packaging were developed using ethanolic extracts obtained from asparagus residues. These ethanolic extracts of asparagus residue (AspE) were incorporated (1 y 4 wt%) into sodium alginate (SA) solutions for the preparation of alginate–chitosan (SA/CS) bilayer films using the casting method, and they were characterized by optical, structural, mechanical, and thermal properties. In addition, the total phenolic and flavonoid content, antioxidant activity, and antibacterial activity were determined. The results showed that the SA/CS film with 1% AspE had better optical, structural, mechanical, and thermal properties due to its color, flexibility, and homogeneity. Both films incorporated with AspE exhibited antioxidant and antibacterial activity, with higher activity in the film with 4% AspE. However, this film showed shrinkage and surface irregularities that make its application in food packaging difficult, so the formulation with 1% AspE was considered better for this type of application. This study shows that asparagus residues can be a valuable source of bioactive compounds for the food industry, indicating the potential for the valorization of this agri-food waste.

Enhancing eco-friendly coatings: Aqueous olive leaves extract fortifies macroalgae-based packaging materials

This study incorporated bioactive compounds extracted from olive leaves (Olea europaea L.) into biodegradable films designed for preserving perishable food items like fruits and vegetables. Olive leaves, sourced from Lesvos island in Greece, yielded three aqueous extracts - OL1, OL2, and OL3 – representing different cultivated species. The antioxidant potential and phenolic compound profile of these extracts were analyzed. Subsequently, these extracts were integrated into 2% sodium alginate solutions, and the resulting mixtures were cast into 90 mm Petri dishes to form solid biofilms. Our findings reveal that the olive leaf extracts offer protection against UV–VIS radiation. Particularly, OL1 showcased the highest antioxidant capacity among the extracts examined. For the solid biofilms, various physical characteristics such as weight, diameter, density, and thickness were measured, alongside evaluating humidity, solubility in water, and water vapor permeability. The rheological properties of these solutions, influenced by temperature and extract addition, affect the viscosity, flow behavior, and gelation capacity, crucial for coating applications. Our research not only explores the impact of olive leaf extracts and glycerol as a plasticizer on biofilm solutions but also sheds light on increased opacity, reduced light absorption, and altered rheological properties. This endeavor aligns with the ongoing pursuit of sustainable packaging alternatives, emphasizing the crucial role of bioactive compounds in enhancing the functionality and eco-friendliness of biodegradable films.

Simultaneous viscoelasticity and sprayability in antimicrobial acetic acid-alginate fluid gels

Acetic acid is a promising alternative to antibiotics for topical applications, particularly burn wounds, however its site specificity and retention are impaired by poor material properties. In this study, acetic acid was investigated as both the gelling agent and antimicrobial active in alginate fluid gels. The formed microstructure was found to be directly dependent on acetic acid concentration, leading to highly tuneable material properties. At clinically relevant concentrations of 2.5–5 % acetic acid, the fluid gels were elastically dominated at rest, with viscosities up to 7 orders of magnitude greater than acetic acid alone. These material properties imparted long term surface retention and microparticle barrier function, not seen with either acetic acid or alginate solutions. Most notably, sprayability was enhanced simultaneously with the increased viscosity and elasticity due to the introduction of a discretised microstructure, leading to a remarkable tenfold increase in spray coverage. Formulation was found not to inhibit antimicrobial activity, despite the less acidic pH, with common burn wound pathogens Staphylococcus aureus and Pseudomonas aeruginosa being equally susceptible to the fluid gels as to acetic acid solutions.

Simultaneously enhancing strength and toughness of coir fiber through NaOH and sodium alginate treatment

Coir fibers are commonly subjected to alkali treatment to eliminate impurities and tune their mechanical properties. However, this process can damage the fibers’ microstructures, posing a challenge in significantly enhancing both strength and toughness simultaneously. Herein, we successfully enhanced both strength and toughness of coir fibers through a combined treatment with NaOH and sodium alginate aqueous solution. Coir fibers treated with 5 wt% NaOH solution, followed by 0.5 wt% sodium alginate solution, exhibit a tensile modulus of 2475.0 MPa, a tensile strength of 126.4 MPa, and a toughness of 30.7 MJ/m³, representing improvements of 57.1 %, 72.7 %, and 116.2 %, respectively, compared to the raw fibers. Mechanistic studies revealed that NaOH treatment effectively removes pectin, hemicellulose and lignin from coir fibers but introduces numerous defects. Sodium alginate can repair these defects by forming hydrogen bonds with the rich oxygen-containing group of coir fibers. The combined treatment also increases the crystallinity of coir fibers from 30.3 % for the raw fibers to 44.1 % by removing a large number of amorphous substances. Additionally, the combined treatment reduces the microfibril angle from ∼63.6° to ∼46.6° by elongating the helix structure and filling the gaps between helical fibers. Our cost-effective strategy not only promotes the applications of coir fibers but also provides guidance for the modification of other natural plant fibers.

A novel injectable boron doped-mesoporous nano bioactive glass loaded-alginate composite hydrogel as a pulpotomy filling biomaterial for dentin regeneration

BackgroundDifferent materials have been used as wound dressings after vital pulp therapies. Some of them have limitations such as delayed setting, difficult administration, slight degree of cytotoxicity, crown discoloration and high cost. Therefore, to overcome these disadvantages, composite scaffolds have been used in regenerative dentistry. This study aims to construct and characterize the physicochemical behavior of a novel injectable alginate hydrogel loaded with different bioactive glass nanoparticles in various concentrations as a regenerative pulpotomy filling material.MethodsAlginate hydrogels were prepared by dissolving alginate powder in alcoholic distilled water containing mesoporous bioactive glass nanoparticles (MBG NPs) or boron-doped MBG NPs (BMBG NPs) at 10 and 20 wt% concentrations. The mixture was stirred and incubated overnight in a water bath at 50 0 C to ensure complete solubility. A sterile dual-syringe system was used to mix the alginate solution with 20 wt% calcium chloride solution, forming the hydrogel upon extrusion. Then, constructed hydrogel specimens from all groups were characterized by FTIR, SEM, water uptake percentage (WA%), bioactivity and ion release, and cytotoxicity. Statistical analysis was done using One-Way ANOVA test for comparisons between groups, followed by multiple pairwise comparisons using Bonferroni adjusted significance level (p < 0.05).ResultsAlginate/BMBG loaded groups exhibited remarkable increase in porosity and pore size diameter [IIB1 (168), IIB2 (183) (µm)]. Similarly, WA% increased (~ 800%) which was statistically significant (p < 0.05). Alginate/BMBG loaded groups exhibited the strongest bioactive capability displaying prominent clusters of hydroxyapatite precipitates on hydrogel surfaces. Ca/P ratio of precipitates in IIA2 and IIB1 (1.6) were like Ca/P ratio for stoichiometric pure hydroxyapatite (1.67). MTT assay data revealed that the cell viability % of human gingival fibroblast cells have declined with increasing the concentration of both powders and hydrogel extracts in all groups after 24 and 48 h but still higher than the accepted cell viability % of (˃70%).ConclusionsThe outstanding laboratory performance of the injectable alginate/BMBGNPs (20 wt%) composite hydrogel suggested it as promising candidate for pulpotomy filling material potentially enhancing dentin regeneration in clinical applications.

Characterizations of the pullulan/sodium alginate coatings incorporated with sodium silicate and EDTA-2Na and the antifungal effect on citrus green mold

Citrus has suffered great losses from postharvest fungal diseases. The strategy of polysaccharide-based coating combined with antimicrobial salts was introduced to preserve citrus and control green mold. Sodium silicate and ethylene diamine tetraacetic acid-2Na (EDTA-2Na) (SE) were incorporated with pullulan (PUL)/sodium alginate (SA) solutions to fabricate PSA-SE systems. The results indicated that the PSA-SE films had good biocompatibility based on hydrogen bonds and showed uniform and dense. The molecular of PUL and SA were assembled through entanglement to form a network structure and the surface roughness of the PSA-SE films increased with the addition of SA. The P3SA2-SE film indicated appropriate tensile strength and elongation at break, as well as the lowest water vapor permeability. The carbon dioxide and oxygen permeability and dissolution of P3SA2-SE film were at low values. The P3SA2-SE film had the highest water contact angle (66°). With the addition of SA, the absorbance of the PSA-SE films increased, which was conducive to light blocking. The antifungal experiments revealed that the P3SA2-SE coating showed a significant effect on controlling citrus green mold, especially in Citrus sinensis Osbeck ‘Lane Late’ almost completely inhibited Penicillium digitatum (P44). This study will promote the development of citrus postharvest disease control.

Revealing the regulation mechanism of Na3V2(PO4)2O2F crystal growth in sodium alginate solution for high-performance sodium ion batteries

Na3V2(PO4)2O2F (NVPFO) attracts tremendous attention as a cathode material for sodium-ion batteries (SIBs) because of its higher capacity and structural stability. However, its inherent poor conductivity affects rate performance and long cycle performance. Herein, a special lamellar NVPFO are successfully synthesized by sodium alginate (SA) assisted hydrothermal method. SA dissolves in water to form hydrogel, due to the specific cross-linking of SA and V4+, which restricts the crystal growth of nanoparticles. Meanwhile, a conductive carbon layer for sodium ion transport channels is constructed after carbonization. Based on multidimensional experiments and density functional theory (DFT) calculations, a mechanism for formation of special lamellar NVPFO in SA solution is proposed for the first time. The results show that special lamellar morphology shortens Na+ migration path and conductive coating facilitates electronic transmission. The optimized NVPFO@C-2 has better electrochemical performance with outstanding high rate capacity (106.8 mAh g–1 at 15 C) and long-term cyclability (99.8 mAh g−1 capacity retention of 87.1 % even after 1000 cycles at 5 C).

Pilot scale manufacturing of black seed oil-loaded alginate beads; process development, and stability of thymoquinone

The approach of ionic gelation was employed at the pilot scale of the 50 kg batch size to manufacture black seed oil (BSO)-loaded alginate (ALG) beads as a natural source supplementing the main bioactive compound of BSO, i.e., thymoquinone (TQ). The BSO-ALG emulsion was prepared by initially emulsifying BSO with alginate solution at the pilot scale in two stages. The final emulsion was then dripped through 12 units of 3D-printed multi-nozzles into a curing bath containing Ca2+. The dripping flow rate was scaled up to 288 mL/min through the 3D-printed multi-nozzles (22-gauge). The characteristics of pilot scale BSO-ALG beads were similar to those produced at the lab scale; the beads were spherical with a size of 1.84–1.94 mm. The mechanical strength and loss on drying ranged from 143.6 to 172 g and 77.85–81.96 %, respectively. The production yield and encapsulation efficiency were 77.53–83.65 % and 95.36–97.9 %, respectively. Furthermore, the emulsification process did not affect TQ stability, while the curing process reduced TQ concentration from 1.51 % to 1.03 % w/w. Additionally, a substantial drop in TQ concentration in the encapsulated BSO was observed after the drying process, where it reached 0.23 % w/w. Finally, the stability of BSO-ALG beads in both wet and dried forms under real-time and accelerated conditions for 3 months revealed that beads were stable in terms of their organoleptic characteristics, size and sphericity, and loss on drying. Findings from this study enable the large-scale manufacturing of encapsulated BSO and similar bioactive compounds in ALG beads for the first time. These findings are valuable for advancing microencapsulation through ionic gelation and enhancing food preservation and safety.

Gelatin-Sodium Alginate Hydrogels Cross-Linked by Squaric Acid and Dialdehyde Starch as a Potential Bio-Ink.

Hydrogels as biomaterials possess appropriate physicochemical and mechanical properties that enable the formation of a three-dimensional, stable structure used in tissue engineering and 3D printing. The integrity of the hydrogel composition is due to the presence of covalent or noncovalent cross-linking bonds. Using various cross-linking methods and agents is crucial for adjusting the properties of the hydrogel to specific biomedical applications, e.g., for direct bioprinting. The research subject was mixtures of gel-forming polymers: sodium alginate and gelatin. The polymers were cross-linked ionically with the addition of CaCl2 solutions of various concentrations (10%, 5%, 2.5%, and 1%) and covalently using squaric acid (SQ) and dialdehyde starch (DAS). Initially, the polymer mixture's composition and the hydrogel cross-linking procedure were determined. The obtained materials were characterized by mechanical property tests, swelling degree, FTIR, SEM, thermal analysis, and biological research. It was found that the tensile strength of hydrogels cross-linked with 1% and 2.5% CaCl2 solutions was higher than after using a 10% solution (130 kPa and 80 kPa, respectively), and at the same time, the elongation at break increased (to 75%), and the stiffness decreased (Young Modulus is 169 kPa and 104 kPa, respectively). Moreover, lowering the concentration of the CaCl2 solution from 10% to 1% reduced the final material's toxicity. The hydrogels cross-linked with 1% CaCl2 showed lower degradation temperatures and higher weight losses than those cross-linked with 2.5% CaCl2 and therefore were less thermally stable. Additional cross-linking using SQ and DAS had only a minor effect on the strength of the hydrogels, but especially the use of 1% DAS increased the material's elasticity. All tested hydrogels possess a 3D porous structure, with pores of irregular shape and heterogenic size, and their swelling degree initially increased sharply to the value of approx. 1000% during the first 6 h, and finally, it stabilized at a level of 1200-1600% after 24 h. The viscosity of 6% gelatin and 2% alginate solutions with and without cross-linking agents was similar, and they were only slightly shear-thinning. It was concluded that a mixture containing 2% sodium alginate and 6% gelatin presented optimal properties after gel formation and lowering the concentration of the CaCl2 solution to 1% improved the hydrogel's biocompatibility and positively influenced the cross-linking efficiency. Moreover, chemical cross-linking by DAS or SQ additionally improved the final hydrogel's properties and the mixture's printability. In conclusion, among the tested systems, the cross-linking of 6% gelatin-2% alginate mixtures by 1% DAS addition and 1% CaCl2 solution is optimal for tissue engineering applications and potentially suitable for 3D printing.