Fickian Diffusion Research Articles

Mechanical properties, sustained release, and oxygen scavenging properties of nanocomposite films loaded with bimetallic nanoparticles (Fe2O3/TiO2) in extra virgin olive oil.

The aim of this study was the synthesis of bimetallic nanoparticles based on Fe2O3/TiO2 and its use in the poly(lactic acid) (PLA) films as an oxygen scavenger in extra virgin olive oil (EVOO) packaging. Bimetallic nanocomposites were prepared by two different precipitation methods (precipitation with ammonia and sodium hydroxide). The characteristics of bimetallic nanoparticles precipitated with sodium hydroxide (Na-Ti0.01Fe0.048O0.08) and bimetallic nanoparticles precipitated with ammonia (NH-Ti0.01Fe0.022O0.09) were compared. Relative amounts of elements in bimetallic nanocomposites and their morphological characteristics were determined using field emission scanning electron microscopy coupled with energy-dispersive X-ray spectrometer. Porosity volume and surface area of bimetallic nanoparticles were calculated using adsorption-desorption isotherms and the Brunauer-Emmett-Teller method. The formation/characterization of bimetallic nanoparticles and their location in the matrix of PLA-based nanocomposite film was studied using X-ray diffraction and Fourier transform infrared. In nanocomposite films based on PLA, bimetallic nanoparticles lead to better oxidative stability (peroxide value, p-anisidine index, K232, and K270) of the EVOO and oxygen scavenging during storage compared to free nanoparticles. Mechanical properties of nanocomposite films were improved due to bimetallic nanoparticles, which were better for Na-Ti0.01Fe0.048O0.08. In vitro release modeling of the bimetallic nanoparticles in EVOO proved that Fickian diffusion is the dominant mechanism, and the Peleg model was the best description of the release behavior of nanoparticles.

Valorization of Agricultural By-Products (Fragaria vesca) through the Production of Value-Added Micro/Nanostructures Using Electrohydrodynamic Techniques

An innovative approach for the production of bio-micro/nanostructures with high-value compounds from agricultural by-products was studied. This research aimed to valorize bioactive compounds existing in the by-products of the plants of Fragaria vesca (wild strawberry). The particle characteristics, morphology, size, release properties, and antioxidant activity of micro/nanostructures containing the extract of by-products of the plants of Fragaria vesca or quercetin (one of the main polyphenols in the plant) were analyzed. The electrohydrodynamic (EHD) technique was utilized for encapsulation. The results showed that the morphology and size of the structures were influenced by the concentration of zein, with 10% w/v zein concentration leading to irregular and non-uniform nanostructures, while 20% w/v zein concentration resulted in a mixture of microparticles and thin fibers with an irregular surface. The type and concentration of the core material did not significantly affect the morphology of the micro/nanostructures. In vitro release studies demonstrated the controlled release of the core materials from the zein micro/nanostructures. The release profiles were analyzed using the Korsmeyer–Peppas and Weibull models, which provided insights into the release mechanisms and kinetics. The most relevant release mechanism is associated with “Fickian Diffusion”. The antioxidant activity of the structures was evaluated using an ABTS radical-scavenging assay, indicating their potential as antioxidants. In conclusion, the EHD technique enabled the successful encapsulation of Fragaria vesca by-product extract and quercetin with zein, resulting in micro/nanostructures with different morphologies.

Electrospun Fenoprofen/Polycaprolactone @ Tranexamic Acid/Hydroxyapatite Nanofibers as Orthopedic Hemostasis Dressings.

Dressings with multiple functional performances (such as hemostasis, promoting regeneration, analgesia, and anti-inflammatory effects) are highly desired in orthopedic surgery. Herein, several new kinds of medicated nanofibers loaded with several active ingredients for providing multiple functions were prepared using the modified coaxial electrospinning processes. With an electrospinnable solution composed of polycaprolactone and fenoprofen as the core working fluid, several different types of unspinnable fluids (including pure solvent, nanosuspension containing tranexamic acid and hydroxyapatite, and dilute polymeric solution comprising tranexamic acid, hydroxyapatite, and polyvinylpyrrolidone) were explored to implement the modified coaxial processes for creating the multifunctional nanofibers. Their morphologies and inner structures were assessed through scanning and transmission electron microscopes, which all showed a linear format without the discerned beads or spindles and a diameter smaller than 1.0 μm, and some of them had incomplete core-shell nanostructures, represented by the symbol @. Additionally, strange details about the sheaths' topographies were observed, which included cracks, adhesions, and embedded nanoparticles. XRD and FTIR verified that the drugs tranexamic acid and fenoprofen presented in the nanofibers in an amorphous state, which resulted from the fine compatibility among the involved components. All the prepared samples were demonstrated to have a fine hydrophilic property and exhibited a lower water contact angle smaller than 40° in 300 ms. In vitro dissolution tests indicated that fenoprofen was released in a sustained manner over 6 h through a typical Fickian diffusion mechanism. Hemostatic tests verified that the intentional distribution of tranexamic acid on the shell sections was able to endow a rapid hemostatic effect within 60 s.

Gamma radiation synthesis of hydroxyethyl cellulose/acrylic acid/CYANEX 471X hydrogel for silver ions capture from acidic nitrate medium

AbstractThe current novelty in this study is to recover silver ion with selective extractant such as cyanex 471X (triisobutylphosphine sulfide) through a clean and green method with high efficiency. Herein, a sustainable hydrogel (HEC/AAc/CX3) was fabricated from triisobutylphosphine sulfide, hydroxyethyl cellulose (HEC), and acrylic acid (AAc) using gamma irradiation polymerization and implanted for the sorption of silver Ag (I) ions from a nitrate acidic medium. Different techniques were employed for characterization of HEC/AAc/CX3 hydrogel such as FT-IR, SEM, XRD, and EDX, before and after the sorption process of Ag(I) ions. Gel content and swelling kinetics ratio of hydrogels at different irradiation doses (10, 20, 30, 40, and 50 kGy) were studied. The Fickian diffusion model results indicate that HEC/AAc/CX3 hydrogel is non-Fickian diffusion, which confirmed that the diffusion and relaxation rates are compatible and were selected for further sorption of Ag(I). The irradiated HEC/AAc/CX3 hydrogels, which contain 0.1 g of cyanex 471X, were employed for batch sorption of 100 mg/L Ag(I) from an acidic solution, and the suggested conditions were pH = 1, time = 60, and v/m = 0.05 L/g, which gives a sorption percentage of 75%. The values of thermodynamic parameters ΔH, ΔG, and ΔS were evaluated as—62.80 kJ/mol, 5 kJ/mol, and -227 J/mol, which indicate that the sorption system was exothermic and nonspontaneous in nature. The maximum adsorption capacity of irradiated HEC/AAc/CX3 for Ag(I) was found to be 12 mg. g−1 at 298 K. Furthermore, the maximum desorption percent of Ag ions from HEC/AAc/CX3 was found to be 70% and achieved with 0.5 M NH4SCN after one desorption cycle. The prepared hydrogel proved its selectivity towards silver ions with facile desorption steps and reusability cycles. Graphical Abstract

Concentration-Dependent Diffusion of Monoclonal Antibodies: Underlying Mechanisms of Anomalous Diffusion.

The development, storage, transport, and subcutaneous delivery of highly concentrated monoclonal antibody formulations pose significant challenges due to the high solution viscosity and low diffusion of the antibody molecules in crowded environments. These issues often stem from the self-associating behavior of the antibody molecules, potentially leading to aggregation. In this work, we used a dissipative particle dynamics-based coarse-grained model to investigate the diffusion behavior of IgG1 antibody molecules in aqueous solutions with 15 and 32 mM NaCl and antibody concentrations ranging from 10 to 400 mg/mL. We determined the coarse-grained interaction parameters by matching the calculated structure factor with the computational and experimental data from the literature. Our results indicate Fickian diffusion for antibody concentrations of 10 and 25 mg/mL and anomalous diffusion for concentrations exceeding 50 mg/mL. The anomalous diffusion was observed for ∼0.33 to 0.4 μs, followed by Fickian diffusion for all antibody concentrations. We observed a strong linear correlation between the diffusion behavior of the antibody molecules (diffusion coefficient D and anomalous diffusion exponent α) and the amount of aggregates present in the solution and between the amount of aggregates and the Coulomb interaction energy. The investigation of underlying mechanisms for anomalous diffusion revealed that in crowded environments at high antibody concentrations, the attractive interaction between electrostatically complementary regions of the antibody molecules could further bring the neighboring molecules closer to one another, ultimately resulting in aggregate formation. Further, the Coulomb attraction can continue to draw more molecules together, forming larger aggregates.

In-vitro dehydration kinetics coefficient of Kalifilcon A and other contact lens materials

In contact lens (CL) wear, dehydration needs to be tailored to avoid dryness and related symptoms. In this view, this work aims to assess and compare the in-vitro dehydration kinetics of five CL materials, including the newly developed Kalifilcon A CL. At 36 °C and 60% relative humidity, the in-vitro dehydration kinetics of the different CLs were compared using a gravimetric method. CLs were analyzed either after a rinse of a few seconds in preservative-free saline solution or after a 24-h incubation in the same solution. A model based on the Fick diffusion equation was employed to deduce a water kinetics coefficient, providing insights into water diffusion within the polymeric matrix. The study reveals that all materials exhibit a non-Fickian dehydration behavior, with significant differences in dehydration kinetics coefficients and dehydration rate slopes. Etafilcon A and Omafilcon A, both hydrogel CLs, exhibit a similar behavior, different compared to the pattern shown by Senofilcon A and Delefilcon A, silicone-hydrogel CLs. Notably, Kalifilcon A, despite being a silicone-hydrogel, displays a hydration behavior reminiscent of hydrogel CLs.

Analysis of the impact of reclaimed asphalt pavement agglomeration on the performance of hot-recycled asphalt pavement: A perspective on diffusion-fusion

The agglomeration of reclaimed asphalt pavements (RAP) affects the low-temperature performance and water stability of hot-recycled asphalt mixtures (HAM). To address this problem, a surface-active regeneration agent which named polyacrylamide (PAM) was employed. The effects of the coarse-grained RAP agglomeration rate, the alterations in the aged asphalt before and after the addition of PAM, and the degree of diffusion and fusion between old and new asphalt on HAM performance were investigated using macroscopic experiments, molecular dynamics simulations, Fourier-transform infrared spectroscopy (FTIR), and scanning electron microscopy (SEM). The findings revealed that the water stability of HAM first decreased and then slightly increased as the RAP agglomeration rate increased. Notably, at a 60% coarse-grained RAP agglomeration rate, the water stability of the mixture was at its poorest, accompanied by a declining low-temperature stability. Utilizing Fick's diffusion principle, in conjunction with molecular dynamics simulations, FTIR, and SEM analyses, it was observed that PAM effectively diffused and fused with the aged asphalt. This resulted in enhanced diffusion coefficients for both old and new asphalt, consequently mitigating aging effects on the aged asphalt. Furthermore, the regeneration agent facilitated the diffusion and fusion process between old and new asphalt, thereby improving HAM performance and reducing the adverse impact of coarse-grained RAP agglomeration on the road performance of thermally recycled mixtures.

A biodegradable pH-response packaging film with blueberry extract: Blown-extrusion fabrication, multifunctional activity, and kinetic investigation

This work proposed a novel strategy for manufacturing biodegradable pH-response packaging. Briefly, to minimize the amount and thermal processing times of blueberry extract (BE), ethanol-dissolved BE (≤ 3‰ w/w) was sprayed onto the starch/poly(butylene adipate-co-terephthalate) (PBAT) pellets before extrusion blowing. BE was well-integrated into the matrix, forming uniformly colored films. The films with BE exhibited superior mechanical (7.85 MPa of strength, 606.53% of elongation) and enhanced barrier capabilities against ultraviolet light, moisture, and gas. Additionally, they exhibited good antioxidant capacity (68.69%), antibacterial activity (72.40%), and maintained color stability. The film with 3‰ w/w BE presented excellent color responsiveness (ΔE⁎ ≥ 15) in the alkaline range, and successfully monitored the spoilage of shrimp. The pigments in the film had the maximum migration degree (≥ 70%) and rate in 50% ethanol simulation, following a first-order kinetic behavior dominated by Fickian diffusion. Findings supported the application of this strategy in the fabrication of starch/PBAT/BE films for pH-response intelligent packaging.

Analysis of a nonlocal diffusion model with a weakly singular kernel

We establish that for any fixed horizonδ>0, the solution of a nonlocal diffusion model with a weakly singular kernel pδ converges asymptotically to the solution of the corresponding Fickian diffusion equation. The diffusion tensor of the Fickian equation is determined by half of the covariance matrix, with pδ serving as the probability density function. Numerical experiments are performed to validate our findings. Additionally, we observe that the mean square displacement of the nonlocal diffusion model exhibits a linear relationship with respect to time t.

Direct visualization of pyrene diffusion in polyethylene and polyoxymethylene passive samplers

While passive sampling of ultra-low aqueous concentrations of hydrophobic organic compounds in environmental aqueous media has emerged as a promising analytical technique, there is a lack of good understanding of the fundamental diffusive processes. In this research, we used a fluorophore, pyrene, as a model compound to track diffusion in polymers through absorption and environmental media exchange processes. We directly tracked the penetration of pyrene into polyethylene (PE) and polyoxymethylene (POM) rods during absorption from water by sectioning the rod after different stages of absorption and observing the fluorescence signal through a microscope. Diffusion profiles of pyrene in polymers were simulated by numerical integration of Fickian diffusion. The results indicated that the uptake process in PE is governed by Fick's law and the absorption and desorption kinetics are similar in this polymer. However, the observed uptake profiles of pyrene in POM were non-Fickian and the release kinetics out of POM was slower compared to uptake into the polymer. We show that slower desorption from POM makes corrections for nonequilibrium using performance reference compounds (PRCs) problematic for deployments in water or sediment where there is significant advection. However, for static sediment deployments, the overall kinetics of exchange is controlled by slow transport through sediment and the hysteretic behavior of POM may not preclude the use of PRCs to interpret equilibrium status.

Effect of carboxylated cellulose nanocrystals on konjac glucomannan/κ-carrageenan composite hydrogels

Konjac glucomannan/κ-carrageenan (KGM/KC) composite hydrogels often fail to meet industrial requirements due to their weak mechanical properties, while nanofillers are potential materials to address this challenge by taking advantage of their nano-size and filling effects. Herein, carboxylated cellulose nanocrystals (C–CNCs) were chosen as nanofillers to regulate the properties of KGM/KC composite hydrogels, with focus on the effect of C–CNCs concentration on the morphological and physicochemical properties. Meanwhile, an in-depth exploration of the possible mechanisms was also underlying. C–CNCs were well dispersed within the KGM/KC composite matrix, which positively enhanced the mechanical strength, as well as increased the apparent viscosity and modulus of the composite hydrogel greatly when the C–CNCs concentration was 10 % (w/w). This is mainly ascribed to the enhancement of hydrogen bond interaction among the KGM, KC, and C–CNCs, which were verified by Fourier transform infrared spectroscopy. Additionally, the results of low-field nuclear magnetic resonance confirmed the presence of C–CNCs in the hydrogel matrix reduced the water mobility of the hydrogel, which improved the freeze-thaw stability of the composite hydrogel. The fitting of the Power law model (R2 > 0.98) showed that the swelling mechanism of KGM/KC composite hydrogels belonged to Fickian diffusion, and the swelling behavior could be regulated by adjusting the C–CNCs concentration. However, the excessive C–CNCs might weakened the interaction of composite hydrogels, which partially explains the reversal of the reinforcement effects seen at the lower additions of C–CNCs inclusion. These results provide a basis for the development and design of KGM/KC-based products with desirable attributes.

Fick Diffusion Coefficients in Binary Liquid Mixtures Containing Alkanes, Aromatics, Alcohols, or Acetone by Using Dynamic Light Scattering

Fick Diffusion Coefficients in Binary Liquid Mixtures Containing Alkanes, Aromatics, Alcohols, or Acetone by Using Dynamic Light Scattering

Levofloxacin loaded poly (ethylene oxide)-chitosan/quercetin loaded poly (D,L-lactide-co-glycolide) core-shell electrospun nanofibers for burn wound healing.

This study developed a new burn wound dressing based on core-shell nanofibers that co-deliver antibiotic and antioxidant drugs. For this purpose, poly(ethylene oxide) (PEO)-chitosan (CS)/poly(D,L-lactide-co-glycolide) (PLGA) core-shell nanofibers were fabricated through co-axial electrospinning technique. Antibiotic levofloxacin (LEV) and antioxidant quercetin (QS) were incorporated into the core and shell parts of PEO-CS/PLGA nanofibers, respectively. The drugs could bond to the polymer chains through hydrogen bonding, leading to their steady release for 168h. An in vitro drug release study showed a burst effect followed by sustained release of LEV and QS from the nanofibers due to the Fickian diffusion. The NIH 3T3 fibroblast cell viability of the drug loaded core-shell nanofibers was comparable to that in the control (tissue culture polystyrene) implying biocompatibility of the nanofibers and their cell supportive role. However, there was no significant difference in cell viability between the drug loaded and drug free core-shell nanofibers. According to in vivo experiments, PEO-CS-LEV/PLGA-QS core-shell nanofibers could accelerate the healing process of a burn wound compared to a sterile gauze. Thanks to the synergistic therapeutic effect of LEV and QS, a significantly higher wound closure rate was recorded for the drug loaded core-shell nanofibrous dressing than the drug free nanofibers and control. Conclusively, PEO-CS-LEV/PLGA-QS core-shell nanofibers were shown to be a promising wound healing material that could drive the healing cascade through local co-delivery of LEV and QS to burn wounds.

Improving adsorption materials properties for renewable energy-driven cooling systems

Considering addressing global warming and energy crises, this work presents an alternative cooling system based on adsorption technology. The novelty of this work lies in the improvement of the adsorption properties of the commercial adsorbent AquaSorb2000 (AS2000) for the first time by a chemical method. The AS2000 is improved by mixing with ammonium carbonate and thermally treated at 500 °C in a nitrogen gas flow. The raw AS2000 and the modified (MAS2000) adsorbents were characterized by X-ray powder diffraction, FTIR spectroscopy and N2 gas adsorption/desorption techniques. It was found that the modification led to significant surface changes. Adsorption isotherms of HFC-404A gas were investigated over AS2000 and MAS2000 adsorbents. Experimental results are fitted with Dubinin–Astakhov (D-A) and Sun-Chakraborty (S-C) equations for the isotherms and linear driving force and Fickian diffusion models for the kinetics. Moreover, the performance of the two materials is investigated for adsorption cooling systems (ADSs) using transient simulation modeling. The results showed improvement in the adsorption uptake from 0.50 kgR/kgAC of AS2000 to 0.99 kgR/kgAC of MAS2000 adsorbent. At the optimum conditions of the modified sample, the ADS performance parameters estimated by 124 W/kg specific cooling power (SCP) and 0.17 of coefficient of performance (COP) improved by 63 % and 70 %, respectively, compared to using the indicated original activated carbon material.

Preparation of celecoxib loaded bioactive glass chitosan composite hydrogels: a simple approach for therapeutic delivery of NSAIDs.

Arthritis causes inflammatory damage to joints and connective tissues. In the treatment of arthritis, precise and controlled drug delivery to the target site is among the frontline research approaches. In the present research work, celecoxib drug and bioactive glass incorporated chitosan hydrogels were fabricated by the freeze gelation method. FTIR, SEM, and TGA/DSC techniques were used to characterize the hydrogels. Different kinetic models were applied to study the drug release kinetics. The celecoxib release was mainly controlled by a Fickian diffusion process followed by the Higuchi model. Maximum 86.2 % drug entrapment was observed in 20 mg drug-loaded hydrogel and its swelling ratio was 115.5% in 28 days. Good hydrophilicity, good drug entrapment efficiency, and moderate drug release patterns of hydrogels can make them suitable for sustained drug release. The cytocompatibility of hydrogels was established by performing an MTT assay on the BHK-21 fibroblast cell line. The promising results have proved that hydrogels can be considered potential material for the slow release of anti-inflammatory drugs at the target site in arthritis.

Nitric oxide-releasing thiolated starch nanoparticles embedded in gelatin sponges for wound dressing applications

This study introduces a novel wound dressing by combining nitric oxide-releasing thiolated starch nanoparticles (NO-TS NPs) with gelatin. First, starch was thiolated (TS), and then its nanoparticles were prepared (TS NPs). Subsequently, NPs were covalently bonded to sodium nitrite to obtain NO-releasing TS NPs (NO-TS-NPs) that were incorporated into gelatin sponges at various concentrations. The resulting spherical TS NPs had a mean size of 85.42 ± 5.23 nm, which rose to 100.73 ± 7.41 nm after bonding with sodium nitrite. FTIR spectroscopy confirmed S-nitrosation on the NO-TS NPs' surface, and morphology analysis showed well-interconnected pores in all sponges. With higher NO-TS NPs content, pore size, porosity, and water uptake increased, while compressive modulus and strength decreased. Composites exhibited antibacterial activity, particularly against E. coli, with enhanced efficacy at higher NPs' concentrations. In vitro release studies demonstrated Fickian diffusion, with faster NO release in sponges containing more NPs. The released NO amounts were non-toxic to fibroblasts, but samples with fewer NO-TS NPs exhibited superior cellular density, cell attachment, and collagen secretion. Considering the results, including favorable mechanical strength, release behavior, antibacterial and cellular properties, gelatin sponges loaded with 2 mg/mL of NO-TS NPs can be suitable for wound dressing applications.

Superparamagnetic freeze-thawed PVA hydrogel for applications in tissue engineering, drug delivery and bioimaging

The prerequisite of super-paramagnetic materials in biomedical applications necessitate the optimum magnetic saturation and negligible cytotoxic characteristics. Especially, the development of super-paramagnetic hydrogels in tissue engineering has been rather a scarce documentation. In this context, the present study aims to integrate Fe2+/3+ in PVA hydrogels through repetitive freeze-thawing technique followed by lyophilisation. A detailed physiochemical characterization of the developed hydrogels has been evaluated using X-ray diffraction, TGA, Raman and XPS techniques. The binding of iron with PVA has been confirmed through FTIR analysis and magnetic measurements at room temperature ensured the super-paramagnetic nature of obtained hydrogels. The release profiles of gentamycin drug loaded PVA hydrogel showcased an 8% release in 12 h and this profile followed the non- Fickian diffusion process. The maximum tensile and compression strength of hydrogels are respectively determined as 3.2 and 4.6 MPa. The presence of Fe in the hydrogel deliberated T2 MRI imaging characteristics. In vitro test results affirmed the cell viability of more than 60% for all the hydrogels. The overall findings from the study signified the applications of FePVA hydrogels in tissue engineering applications.

Facile synthesis and polymerization of 1,4,5-oxadithiepan-2-one for disulfide-based redox-responsive drug delivery

Chemotherapeutic drugs have been shown to be promising for the treatment of tumors, however, they are associated with several disadvantages including low aqueous solubility, non-specificity, and poor plasma stability. Hence, they accumulate in the health organs and create several adverse effects. Drug encapsulated stimuli-responsive nanoparticles bearing redox-responsive disulfide linkages have emerged as promising delivery vehicle to address these limitations. A glutathione (GSH) responsive disulfide-based drug delivery system based on a polyethylene glycol methyl ether (PEGME) and a polydisulfide (PDS) diblock copolymer has been developed. The cyclic lactone containing a disulfide link, 1,4,5-oxadithiepan-2-one, was prepared using a thiol-free method utilizing the reaction of 2-bromoethyl bromoacetate with sodium disulfide. Ring-opening polymerization (ROP) of 1,4,5-oxadithiepan-2-one using 1-butanol in the presence of Sn(oct)2 generated the homopolymer PDS whereas the diblock copolymer PEGME-b-PDS was obtained when PEGME was used as a macroinitiator. In aqueous solution, PEGME-b-PDS self-assembled into spherical-shaped micelles with a hydrodynamic radius of 146 and 116 nm as measured by Field-emission Scanning Electron Microscopy (FESEM) and Dynamic Light Scattering (DLS), respectively. At pH = 7.4, a Doxorubicin (DOX) loaded PEGME-b-PDS micelle showed a cumulative release of ∼98.2, ∼9.9, and ∼1.9 % in presence of 2 mM, 2 μM DTT and in absence of DTT, respectively clearly demonstrating the redox responsiveness of the PDS block. The best fit of kinetic data using with the Korsmeyer-Peppas model suggests a Fickian diffusion as well as chain-relaxation controlled drug release process. DOX loaded micelles and free DOX displayed similar cytotoxicity towards both 4T1 and MCF-7 cells indicating that the encapsulation inside the micelle did not affect the anticancer efficacy of the drug. The drug loaded micelle showed higher cellular uptake than free DOX in both 4T1 and MCF-7 lines and lower cellular uptake than free DOX in 3T3-L1 cell lines. This polymeric micellar nanoparticle may be further exploited for encapsulation of other hydrophobic drugs.

Layered double hydroxide for slowing selenium fertilizer release and improving selenium utilization efficiency in vegetables

Selenium (Se) is a beneficial plant micronutrient, and the application of Se fertilizers can promote plant growth and enhance the Se content in crops. However, traditional soluble Se fertilizers have low utilization efficiency of Se due to adsorption or leaching. Here, selenite (SeO32−) -intercalated Mg/Al layered double hydroxide (Se-Mg/Al) for SeO32− slow-release was synthesized by co-precipitation and characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR) and X-ray photoelectron spectroscopy (XPS). Se-Mg/Al possessed a typical lamellar structure, combining with selenite by electrostatic interaction in interlayer and chemisorption on the surface. The release mechanism of selenite in distilled water from Mg/Al layered double hydroxide (Mg/Al LDH) was Fickian diffusion with gradually released 97.86% after 20 h (Over 90% within 2 h for sodium selenite). At pH range 4.0–8.0, Se-Mg/Al had a stable slow-release ability. And, the sulfate and phosphate anions could effectively trigger the release of selenite through anions exchange. The pot experiments showed that Se-Mg/Al increased Se content of vegetables, more than twice that of directly using sodium selenite. Compared with control treatment, the average stem height and fresh weight per 10 plants with Se-Mg/Al treatment improved approximately 1.48 times and 2.34 times, respectively. This work provides a feasible way for achieving crops selenium supplementation and improving selenium utilization efficiency.

Comparison of the Adsorption and Desorption Dynamics of Biological Molecules on Alginate Hydrogel Microcapsules-The Case of Sugars, Polyphenols, and Proteins.

The aim of this work was to analyze and compare the adsorption and desorption processes of carbohydrates (glucose as a model molecule), polyphenols (gallic acid as a model molecule), and proteins (bovine serum albumin, BSA as a model molecule) on alginate microcapsules. The adsorption and desorption processes were described by mathematical models (pseudo-first-order, pseudo-second-order, and Weber-Morris intraparticle diffusion model for adsorption, and first-order, Korsmeyer-Peppas, and the Higuchi model for desorption) in order to determine the dominant mechanisms responsible for both processes. By comparing the values of adsorption rate (k2) and initial adsorption rate (h0) based on the pseudo-first-order model, the lowest values were recorded for BSA (k1 = 0.124 ± 0.030 min-1), followed by glucose (k1 = 0.203 ± 0.041 min-1), while the model-obtained values for gallic acid were not considered significant at p < 0.05. For glucose and gallic acid, the limiting step of the adsorption process is the chemical sorption of substances, and the rate of adsorption does not depend on the adsorbate concentration, but depends on the capacity of the hydrogel adsorbent. Based on the desorption rates determined by the Korsmeyer-Peppas model (k), the highest values were recorded for gallic acid (k = 3.66236 ± 0.20776 g beads/mg gallic acid per min), followed by glucose (k = 2.55760 ± 0.16960 g beads/mg glucose per min) and BSA (k = 0.78881 ± 0.11872 g beads/mg BSA per min). The desorption process from alginate hydrogel microcapsules is characterized by the pseudo Fickian diffusion mechanism.