Effective Immobilization Research Articles

Exploring Enzyme Encapsulation Efficiency in MOFs Using Eco-Friendly Approaches.

The encapsulation of protein enzymes in metal-organic frameworks (MOFs) has been recognized as an effective enzyme immobilization approach. In this study, we demonstrated the influence of enzyme amount and the isoelectric points (pI) of different enzymes on the enzyme loading capacity in both mechanochemical (ball-milling) and water-based approaches. We found that increasing enzyme amounts enhances MOF enzyme loading without compromising activity, while the MOF shell protects encapsulated enzymes from proteinase K degradation through its size-sheltering mechanism. However, an excess of enzymes can hinder the formation of ZIF-90. Moreover, enzymes with low pI values (e. g., catalase, pI 5.4) facilitate encapsulation in MOFs, whereas enzymes with high pI values (e. g., lysozyme, pI 11.35) are more challenging to encapsulate. The simulation results revealed that increasing the enzyme amounts and pI values raises the activation energy necessary for MOF formation. This study highlights the crucial role of enzyme properties in the encapsulation process within MOFs, providing valuable insights for fabricating enzyme-MOF biocomposites for diverse applications, such as protein drug delivery.

3D manipulation of small multicellular organisms in soft microtubes

Small multicellular organisms, such as C. elegans and zebrafish larvae, are essential models in biological research, but their 3D manipulation poses challenges due to their small size. Manual positioning is labor-intensive and imprecise. To address this, we developed a soft PDMS microtube that can be gently stretched and released, immobilizing organisms without anesthetization and damage. This tube enables easy rotation and adjustment of orientation, facilitating comprehensive imaging. Functionality testing showed effective immobilization as well as precise imaging and microinjection. Zebrafish larvae were successfully injected with fluorescein in the hindbrain without anesthesia. This technique offers a simple, efficient, and non-damaging method for 3D manipulation and imaging of small multicellular organisms and provides a versatile tool for biological research practices.

Organic and Inorganic Modifications to Increase the Efficiency in Immobilization of Heavy Metal (Zn) in Cementitious Composites—The Impact of Cement Matrix Pore Network Characteristics

This research investigated the properties of modified cementitious composites including water purification from heavy metal—zinc. A new method for characterizing the immobilization properties of tested modifiers was established. Several additions had their properties investigated: biochar (BC), active carbon (AC), nanoparticulate silica (NS), copper slag (CS), iron slag (EAFIS), crushed hazelnut shells (CHS), and lightweight sintered fly ash aggregate (LSFAA). The impact of modifiers on the mechanical and rheological properties of cementitious composites was also studied. It was found that considered additions had a significantly different influence over the investigated properties. The addition of crushed hazelnut shells, although determined as an effective immobilization modifier, significantly deteriorated the mechanical performance of the composite as well as its rheological properties. Modification by iron slag allowed for a significant increase in immobilization properties (five-fold compared to the reference series) without a substantial impact on other properties. The negative effect on immobilization efficiency was observed for nanoparticulate silica modification due to its sealing effect on the pore network of the cement matrix. The capillary pore content in the cement matrix was identified as a parameter significantly influencing the immobilization potential of most considered modifications, except biochar and active carbon.

Fast and label-free detection of procalcitonin in human serum for sepsis using a WTex-based extended-gate field-effect transistor biosensor

In this article, we present the first instance of depositing WTex-sensitive films with varying thicknesses (3, 4, and 5 nm) onto flexible polyimide substrates using radio-frequency sputtering. These films were used to create an extended-gate field-effect transistor (EGFET) for pH sensing and detecting procalcitonin (PCT) in the sera of patients with sepsis or bacterial infections. Among the films, the 4 nm WTex film exhibited high sensitivity (59.57 mV/pH), minimal hysteresis (∼0.8 mV), and a low drift rate (0.14 mV/h). Additionally, this WTex-based EGFET sensor retained a pH sensitivity of 59.2 mV/pH even after 180 days of operation and exhibited excellent mechanical flexibility, enduring 500 bending cycles without degradation. Moreover, PCT antibodies, activated using 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide and N-hydroxysuccinimide, were immobilized on the WTex film functionalized with 3-aminopropyl triethoxysilane. This effective immobilization enabled the specific binding of PCT antigens. The WTex-based EGFET biosensor demonstrated high sensitivity (18.12 mV/pCPCT) across a wide dynamic range (1 fg/mL to 1 μg/mL). Furthermore, the PCT concentrations in patient sera, whether from individuals with or without sepsis or bacterial infections, measured by our biosensor were comparable to results obtained using clinical enzyme-linked immunosorbent assay kits.

Rapid Assembly of Ultrafine Palladium Nanoparticle-Decorated HOF-101 Triggered by Guest Enzyme Encapsulation.

Rapid enzyme immobilization is essential for enzyme catalysis and sensing applications, yet constructing effective immobilization systems is challenging due to the need to balance enzyme activity with the properties of the surrounding framework. Herein, taking glucose oxidase (GOx) as a model, a rapid and straightforward approach was presented for synthesizing palladium nanoparticles (PdNPs)-decorated GOx encapsulated in HOF-101 nanocomposite materials (designated as PdNPs/GOx@HOF-101) through an in situ photoreduction and enzyme-triggering HOF-101 encapsulation. The enzyme's surface residues trigger the nucleation of HOF-101 around it through the hydrogen-bonded bio interface, completing the self-assembly of HOF-101 in 0.5 h. Furthermore, the biocomposites loaded with ultrafine PdNPs show satisfactory photoelectrochemical (PEC) properties. As a proof-of-concept, a PEC biosensor was constructed by utilizing PdNPs/GOx@HOF-101 as a photoactive probe, which can quickly and sensitively detect glucose and simultaneously remain stable within the circumstance of 30-60 °C and pH 4-8. These attributes pave the way for diverse applications, including improved enzyme immobilization techniques, advanced biosensors, and more efficient biocatalytic processes.

Endoxylanase Immobilized Nanoporous Silica for the Production of Xylooligosaccharides: Equilibrium Kinetics, Thermodynamic Studies, and Enzyme Characteristics

AbstractNanoporous structured silica materials, namely f‐SiO2, SBA‐15, IITM‐41, and MCM‐41 were employed as the matrices for immobilizing endoxylanase by adsorption method. The equilibrium kinetics, activation energy, and thermodynamic parameters associated with endoxylanase adsorption were investigated. Our findings revealed a two‐phase adsorption mechanism: an initial phase featuring rapid adsorption rates, succeeded by a slower phase wherein adsorption gradually progressed until equilibrium was attained. Analysis of the adsorption kinetic data indicated a better fit with the pseudo‐second‐order model, suggesting chemisorption and highlighting its temperature dependency. The calculated activation energy (Ea) values fell within the range of physisorption, indicating the involvement of both types of adsorption processes. Thermodynamic assessments confirmed that the adsorption reactions were spontaneous, feasible, and endothermic. Notably, the immobilization process did not change the optimum pH of the enzyme, while the optimum temperature shifted slightly. Furthermore, immobilized enzymes show a higher reaction rate (Vmax) than the soluble XynC. All immobilized xylanases produced xylobiose (X2) to xylohexose (X6) by hydrolyzing the xylan substrate. Recycling studies showed that up to 80 % of the yield was retained after seven cycles of reuse. Our study demonstrates the potential of nanostructured silica as an effective immobilization matrix for enzymes of industrial significance.

In-situ synthesis of 2D nanozymes-coated cellulose nanofibers on paper-based chips for portable detection of biothiols

BackgroundSimple, fast and low-cost paper-based analytical devices (PADs) have a good application prospect for point-of-care detection of GSH. However, effective immobilization of functional nanomaterials onto cellulose, as a critical factor in the construction of PADs, presents numerous difficulties and challenges. ResultsIn this study, we have developed an exceptionally straightforward and environmentally friendly synthetic approach by using ovalbumin (OVA) as a bio-mineralization template for the preparation of MnO2 nanosheets. The MnO2 nanosheets produced in the solution phase exhibited excellent intrinsic nano-enzyme activity and biodegradability. The OVA-MnO2 nanosheets can effectively oxidize Amplex red in the absence of H2O2, enabling sensitive detection of GSH with a linear range of 5 nM–10 μM and a detection limit as low as 2.8 nM. Furthermore, we utilized this method to facilitate in situ synthesis of OVA-MnO2 nanosheets directly on paper substrates. This approach eliminates the need for conventional stirring and centrifugation steps, greatly simplifying the fabrication process while reducing material usage and time expenditure. Characterization of the chemical composition and morphology confirmed the intimate growth of the 2D nano-enzymes on the cellulose fibers. Utilizing smartphone capabilities, the OVA-MnO2 nanosheet-modified PAD enabled instrument-free detection of GSH, demonstrating high sensitivity (0.74 μM) and a wide linear response range (1–1000 μM). SignificanceThe synthesis of MnO2 nanosheets directly on cellulose substrates substantially streamlines the modification workflow of PADs and reduces detection costs, offering new avenues for clinical diagnostics of relevant diseases.

Thermothelomyces thermophilus cultivated with residues from the fruit pulp industry: enzyme immobilization on ionic supports of a crude cocktail with enhanced production of lichenase.

β-Glucans comprise a group of β-D-glucose polysaccharides (glucans) that occur naturally in the cell walls of bacteria, fungi, and cereals. Its degradation is catalyzed by β-glucanases, enzymes that catalyze the breakdown of β-glucan into cello-oligosaccharides and glucose. These enzymes are classified as endo-glucanases, exo-glucanases, and glucosidases according to their mechanism of action, being the lichenases (β-1,3;1,4-glucanases, EC 3.2.1.73) one of them. Hence, we aimed to enhance lichenase production by Thermothelomyces thermophilus through the application of response surface methodology, using tamarind (Tamarindus indica) and jatoba (Hymenaea courbaril) seeds as carbon sources. The crude extract was immobilized, with a focus on improving lichenase activity, using various ionic supports, including MANAE (monoamine-N-aminoethyl), DEAE (diethylaminoethyl)-cellulose, CM (carboxymethyl)-cellulose, and PEI (polyethyleneimine)-agarose. Regarding lichenase, the optimal conditions yielding the highest activity were determined as 1.5% tamarind seeds, cultivation at 50°C under static conditions for 72h. Moreover, transitioning from Erlenmeyer flasks to a bioreactor proved pivotal, resulting in a 2.21-fold increase in activity. Biochemical characterization revealed an optimum temperature of 50°C and pH of 6.5. However, sustained stability at varying pH and temperature levels was challenging, underscoring the necessity of immobilizing lichenase on ionic supports. Notably, CM-cellulose emerged as the most effective immobilization medium, exhibiting an activity of 1.01 U/g of the derivative (enzyme plus support), marking a substantial enhancement. This study marks the first lichenase immobilization on these chemical supports in existing literature.

Synergistic effect between biochar and nitrate fertilizer facilitated arsenic immobilization in an anaerobic contaminated paddy soil

Nitrate nitrogen fertilizer was usually used to mitigate arsenic (As) release and mobilization in the anaerobic contaminated paddy soil. However, the effect of the interplay between nitrate fertilizer and biochar on As availability as well as the involved mechanism were poorly understood. Herein, the effects and mechanisms of biochar, nitrate fertilizer, and biochar-based nitrate fertilizer on the availability of As in the contaminated paddy soil were investigated via a microcosm incubation experiment. Results indicated that the application of biochar-based nitrate fertilizer significantly lessened the available As concentration in the contaminated paddy soil from 3.01 ± 0.03 (control group) to 2.24 ± 0.08 mg kg−1, which presented an immobilization efficiency of 26.6 % better than those of individual biochar (13.5 %) and nitrate fertilizer (17.6 %), exhibiting a synergistic effect. Moreover, the biochar-based nitrate fertilizer also facilitated the transformation of more toxic arsenite in the contaminated soil to less toxic arsenate. Further, biochar-based nitrate fertilizer increased soil redox potential (Eh), dissolved organic carbon, organic matter, and nitrate yet decreased soil pH and ammonium, which changed the microbial community in the soil, enhancing the relative abundance of Bacillus, Arthrobacter, and Paenibacillus. These functional microorganisms drove the coupled transformation between nitrate denitrification and Fe(II) or As(III) oxidation, favoring As immobilization in the anaerobic paddy soil. Additionally, the co-application of biochar offset the negative effect of single nitrate fertilizer on microbial community diversity. Overall, biochar-based nitrate fertilizer could be a promising candidate for the effective immobilization of As in the anaerobic paddy soil. The current research can provide a valuable reference to the remediation of As-contaminated paddy soil and the production of safe rice.

Development of polyfunctionalized biochar modified with manganese oxide and sulfur for immobilizing Hg(II) and Pb(II) in water and soil and improving soil health

Mercury (Hg) and lead (Pb) pose significant risks to human health due to their high toxicity and bioaccumulative properties. This study aimed to develop a novel biochar composite (HMB-S), polyfunctionalized with manganese dioxide (α-MnO2) and sulfur functional groups, for the effective immobilization of Hg(II) and Pb(II) from contaminated environments. HMB-S demonstrated superior adsorption capacities of 190.1 mg/g for Hg(II) and 259.9 mg/g for Pb(II), which significantly surpasses the capacities of unmodified biochar (HB) and biochar functionalized solely with Mn (HMB). Mechanistic studies revealed that the immobilization of these metals by HMB-S involved ion exchange, mineral precipitation, surface complexation, and electrostatic interactions. In soil incubation experiments, HMB-S significantly decreased the levels of extractable Hg(II) and Pb(II) compared to the control, reducing the mobility of these metals and converting 17 % of Hg(II) and 26 % of Pb(II) into less bioavailable residual forms. Pot experiments confirmed that all tested biochar materials (HB, HMB, and HMB-S) promoted spinach growth in contaminated soils, with HMB-S being the most effective at lowering Hg(II) and Pb(II) uptake by plants. Additionally, analysis of soil microbial communities indicated that HMB-S altered community composition and increased the relative abundance of metal-resistant bacteria. These findings highlight the potential of polyfunctionalized biochar HMB-S as an effective remediation strategy for Hg and Pb contamination in soil and aqueous environments.

Clean-up of wastewater discharged from zinc industry through application of zeolite 4A produced from a waste contaminated by lubricant oil components

The zeolite 4 A powders were sustainably derived from clay-based waste contaminated with the spent lubricant oil. Then, the products were used to treat the wastewater discharged from a local zinc industry. The main challenge is removal of toxic organic components from the waste and conversion of obtained precursor to the zeolite structure, simultaneously. The variation in crystallinity was studied as a function of composition, fusion temperature, aging, and recrystallization times. The zinc adsorption was found to be markedly dependent not only on sodium carbonate/waste ratio but also on aluminum hydroxide content. However, pronounced adsorption was observed over the particles fabricated through the fusion at 900 °C. The relative crystallinity, ∼32 %, is crucial for the effective immobilization of heavy metal ions like Cd2+, Ni2+, and Zn2+ from the wastewater. This level of crystallinity is achievable with the control of aging and recrystallization times, both in 3 h. The maximal zinc adsorption capacity, ∼143 mg g−1, was obtained for the particles with large pores, 48 nm, facilitating the ion diffusion into the adsorbent. On the other hand, the appropriate electrical charge surface expressed based on zeta potential, −43 mV, provided a proper condition for the electrostatic adsorption.

Kinetic features and mechanism of scorodite formation via multivalent iron source from arsenic-bearing solution

Arsenic-bearing wastes from non-ferrous metallurgy exhibit poor stability during long-term storage, and are transferred as pollutants to the atmosphere and groundwater, thereby, threatening human health and ecological security. Immobilising arsenic as scorodite crystals via a multivalent iron source (Fe(OH)3-FeSO4·7 H2O) is one effective approach for controlling arsenic pollution. However, the kinetic features and mechanisms of this method have not yet been revealed, thereby, necessitating further research. Herein, the kinetics of scorodite generation influenced by the initial pH, Fe/As ratio, Fe(III)/Fe(II) ratio, and reaction temperature were investigated. Prominent features included variations in the minimum pH, oxidation–reduction potential (ORP) platform, Fe/As ratio (1.0), and the delay or advance of scorodite generation. The complicated mechanism of scorodite formation can be divided into coordinated polymerisation, acidic Fe(OH)3 dissolution, polymer oxidation, Fe(II) oxidation, and scorodite crystallisation. The fast coordinated polymerisation of precursors ([Fe(H2O)4(H2AsO4)]nn+) in stage I resulted in a decrease in pH; Fe(OH)3@scorodite and Fe(H2O)2AsO4 basic units were formed via the oxidation of ionic Fe(III) in stage II. Furthermore, regular octahedral scorodite was generated from two sources: the crystallisation of Fe(H2O)2AsO4 basic units and Ostwald ripening of flaky scorodite from Fe(III)–As(V) precipitates at stage III. The Fe(II) in the polymers was mainly oxidised by ferric ions generated from the oxidation of ferrous ions via dissolved O2 from the oxygen gas. Fe(II) ions as carriers for transferring electrons from O2 to polymers. Scorodite formation was controlled by the oxidation of Fe(II) by oxygen gas. Overall, this study provides guidance for the effective immobilisation of arsenic wastes into scorodite via multivalent iron sources to eliminate arsenic pollution.

Label-free and sensitive detection of Citrus Bark Cracking Viroid in hop using Ti3C2Tx MXene-modified genosensor

Since the discovery of Citrus bark cracking viroid (CBCVd) in hops in 2007, affected hop-growing countries such as Slovenia and Germany have been actively pursuing efficient and easily accessible diagnostic tools that could contribute to the early detection of CBCVd in the field. In the early stages of CBCVd infection, typical symptoms or subtle signs of spread may not be evident. Detection becomes feasible only when the plant begins to display symptoms. Unfortunately, there is currently no treatment available, which requires the removal of infected plants as the only viable solution. However, this approach leads to significant economic losses on a large scale. This work demonstrates the development and study of a sensitive, selective, and label-free impedimetric genosensor for the detection of CBCVd in total RNA hop samples. The genosensor is based on a supporting glassy carbon electrode modified with streptavidin-agarose beads, which serve as an effective immobilization layer for a biotinylated single-stranded DNA capture probe. The integration of a 2D-layered Ti3C2Tx MXene into the sensing architecture resulted in a significantly improved electroanalytical performance of the genosensor. Several fabrication and operational parameters were optimized, such as the streptavidin-agarose beads deposition time, capture probe immobilization time and concentration, and sample incubation time. The optimized genosensor exhibited a limit of detection of only 0.5 fg μL⁻¹ (5.5 fmol L−1) in combination with a one-hour incubation with the denatured total RNA hop extract, thus eliminating the need for an additional and laborious amplification step.

Chemical Durability And Mechanical Properties Of Cementitious Matrices Containing Ashes Obtained After Combustion Of Waste From Moukondo Landfill In Brazzaville, Republic Of Congo.

The regular burning of solid waste in the open air and on the ground is commonplace in the Republic of Congo. Burning waste produces pollutants and ashes that can be hazardous to the soil and surrounding waters. Inadequate management of the ash generated by the open burning of household waste results in site pollution, particularly heavy metal contamination (Pb, Ni, Cr, Cu, Zn...). The aim of this study is to develop cementitious matrices containing burnt ashes that are sufficiently effective to retain the heavy metals contained in these ashes in their structure. To this end, in order to assess the chemical durability of these cementitious matrices, we carried out static leaching tests at pH=4 and 7 at 25°C in distilled water on the raw ashes firstly, and then on the 24 cementitious matrices synthesized with different ash/cement/lime ratios. The mechanical durability of the cementitious matrices was assessed using flexural and compressive strength tests. The leaching results obtained demonstrated the effective immobilization of heavy metals in cementitious matrices, whose leachates contain very low levels of heavy metals compared with those of raw ash. Flexural and compressive strength tests showed an improvement in strength from 25°C to 60°C. Several cementitious matrices doped with waste ashes show flexural strengths higher than the recommended standard for flexural strength EN1339 (5 MPa) and compressive strength X31-211 (1 MPa) after 28 days curing at 60°C

Development of a Chitin-Based Purification System Utilizing Chitin-Binding Domain and Tobacco Etch Virus Protease Cleavage for Efficient Recombinant Protein Recovery.

This study aims to develop an efficient chitin-based purification system, leveraging a novel design where the target proteins, superfolding green fluorescent protein (sfGFP) and Thermus antranikianii trehalose synthase (TaTS), fused with a chitin-binding domain (ChBD) from Bacillus circulans WL-12 chitinase A1 and a tobacco etch virus protease (TEVp) cleavage site. This configuration allows for the effective immobilization of the target proteins on chitin beads, facilitating the removal of endogenous proteins. A mutant TEVp, H-TEVS219V-ChBD, fused with the His-tag and ChBD, is employed to cleave the target proteins from the chitin beads specifically. Subsequently, fresh chitin beads are added for adsorption to remove H-TEVS219V-ChBD in the solution, thereby significantly improving the purity of the target protein. Our results confirm that this system can efficiently and specifically purify and recover sfGFP and TaTS, achieving electrophoretic-grade purity exceeding 90%. This system holds significant potential for industrial production and other applications.

Radiation stability and durability of magnesium phosphate cement for radioactive reactive metals encapsulation

The encapsulation of Radioactive Reactive Metallic Waste (RRMW) in ordinary Portland cement poses significant challenges due to its incompatibility with the alkaline environment of the matrix. To address this issue, magnesium phosphate cements (MPC) emerge as potential solutions for the safe and effective immobilisation of RRMWs. The radiation stability and durability of an optimised formulation have been examined for samples irradiated up to 1000 kGy, in particular concerning the leaching behaviour of the three main constituents of the cement hydration products, and on four artificially added elements used to simulate radionuclides commonly found in radioactive waste (caesium, strontium, europium, and cobalt). The mortars exhibited excellent leaching behaviour and a high mechanical resistance, even after irradiation, freeze-thaw cycles, and water immersion. No significant radiation-induced effects were observed in the mineralogical and microstructural properties of the mortars, thus supporting their stability at the examined doses. Having verified the compliance with the main Italian waste acceptance criteria, the results of this research represent an encouraging step for the future implementation of MPCs for RRMWs conditioning.

Sorption-spectrophotometric determination of bismuth ion (III) using immobilised xylenol orange on modified polyacrylonitrile

ABSTRACT This study presents a new sorption-spectrophotometric method for determining bismuth (III) ions using a new adsorbent for PPM-1 fibre immobilised with xylenol orange. The complex exhibited a maximum reflectance at 550 nm and absorption at 530 nm, indicating stable formation. The method demonstrated high sensitivity with a detection limit of 0.1 µg/mL and high selectivity, minimising interference from other metal ions. Optimal pH for complex formation was 1.37, with faster response and higher sensitivity in the immobilised state (detection limit 0.12 µg/mL, formation time 10 minutes). The complex adhered to the Bouguer-Lambert-Beer law within 3–42 µg/25 mL. Interferences from Cu2+, Ag+, Pd2+, and Fe3+ were reduced when the reagent was immobilised. Conductometric analysis confirmed the stable formation of the complex. Validation using model mixtures and pharmaceutical preparations showed accurate bismuth determination with an error margin of 0.005. For example, a mixture containing 25 µg of bismuth with zinc and cadmium yielded 25.20 µg, and De-nol had a found content of 49.50 µg for 50.00 µg added. IR spectroscopy confirmed complex formation with significant shifts in absorption bands. SEM and EDS analysis validated the reagent’s effective immobilisation and interaction with bismuth ions. The method provides a rapid, accurate, and environmentally friendly approach for bismuth analysis, demonstrating high reproducibility, sensitivity, and selectivity, suitable for environmental monitoring and pharmaceutical quality control.

Efficient mineralization of cadmium and arsenic by poorly crystalline CaFe-layered double hydroxide in soil: Performance and mechanism

The co-contamination of arsenic (As) and cadmium (Cd) in the environment is of most concern. In this work, poorly crystalline CaFe-layered double hydroxide (CaFe-LDH) was synthesized with a Ca-to-Fe molar ratio of 4 to ensure effective immobilization of Cd and As in soil. The application of Ca4Fe-LDH in soil remediation demonstrated that the targeted heavy metals gradually mineralized into a relatively stable oxidizable and residual state. At a soil remediation dosage of 1.6%, the availability levels of Cd and As decreased significantly, achieving stabilization efficiencies of 99% and 85.2% respectively. Cd is trapped through isomorphic substitution and dissolution-reprecipitation of calcium (Ca) laminate, resulting in the formation of CdCaFe-LDH mineralization products. As is immobilized through ion exchange with interlayer anions, redox with Fe(III), and Fe-Cd-As complexation. Moreover, the results of the characterization and density functional theoretical (DFT) calculations demonstrate that the CdCaFe-LDH formed by isomeric substitution of Ca for Cd enhanced the adsorption of As on the (110) plane of LDH, indicating that the trap mechanism of Cd and As by Ca4Fe-LDH is synergistically promoted. Overall, the above results prove that mineralization using Ca4Fe-LDH is a promising method to remediate soils combined contaminated by both Cd and As.

A high-power hybrid carbon nanotube/three-dimensional reduced graphene oxide glucose/O2 enzymatic biofuel cell

Long-lasting, high-performance enzymatic biofuel cells (EBFCs) are among the most promising candidates for renewable and green power generation. There are two main drawbacks to EBFCs: 1) short enzyme lifetime due to the enzyme's (protein) denaturation; and 2) low electron transfer efficiency as the enzyme's active site is deeply buried inside the non-conductive protein structure of the enzyme. In this study, a hybrid of carbon nanotubes (CNT) and three-dimensional graphene (3DG) was used to immobilize the glucose oxidase (GOx) on the surface of a glassy carbon electrode (GCE) to fabricate a modified bioanode in a glucose/O2 EBFC. This facile and low-cost CNT/3DG hybrid is a solution to the problems of instability, short lifespan, and poor electron transport in EBFCs. The exceptional electrocatalytic activity of the porous CNT/3DG hybrid is demonstrated by its effective immobilization of GOx and ability to collect energy from glucose oxidation by direct electron transfer (DET) while preserving the structure of the enzyme. The CNT acts like a tiny electrical wire that reaches and harvests the electron directly from the flavin adenine dinucleotide (FAD) (the redox center of GOx) and transfers it to the electrode surface, thus enhancing the performance of the EBFC. The immobilized GOx lifetime was increased to 210 days with a maximum power density of 253.36 µWcm-2 at 0.65 V. These results demonstrate the attractive capability of the CNT/3DG hybrid in the development of efficient biofuel cells and biosensors that employ enzymes in their structures.

Nalbuphine, medetomidine, and azaperone use in free‐ranging American black bears and mountain lions in Wyoming

AbstractSafe and effective chemical immobilization is a necessary component of large carnivore management and research, but laws regulating controlled substances can limit the use of many drugs by non‐veterinary personnel. NalMed‐A (40 mg/mL nalbuphine HCl, 10 mg/mL medetomidine HCl, 10 mg/mL azaperone tartrate) is a non‐controlled drug combination used to immobilize a number of free‐ranging species, but there are limited published reports of its usage by non‐veterinary personnel when immobilizing American black bears (Ursus americanus) and mountain lions (Puma concolor). Additionally, there are some safety concerns regarding anecdotal reports of spontaneous arousals occurring in large carnivores immobilized with NalMed‐A. We performed a retrospective analysis of capture forms for free‐ranging black bears (n = 34) and mountain lions (n = 7) immobilized with NalMed‐A by non‐veterinary personnel across Wyoming, USA, in 2017 and 2019–2024. Induction (x̅ ± SE) was 10.74 ± 1.16 minutes for black bears (n = 34) and 7.14 ± 1.60 for mountain lions (n = 7). Reversal was 14.21 ± 1.51 minutes for black bears (n = 28) and 10.00 ± 1.26 minutes for mountain lions (n = 5). We used non‐parametric tests (Kruskal‐Wallis, Wilcoxon rank sum) and odds ratios to examine the effect of certain parameters on induction times, redoses, and spontaneous arousals in black bears. Median induction time for black bears injected in their hind leg or rump was greater than for black bears injected in their shoulder (n = 34, W = 79.5, P = 0.045). Six black bears (18%) experienced spontaneous arousals. We recommend avoiding the hind leg and rump for dart placement in bears, and using hobbles and a muzzle for large carnivores when using NalMed‐A in a free‐ranging setting because of the risk of spontaneous arousals.