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This study investigates the impacts of bismuth and tin on the production of CH4 and volatile fatty acids in a microbial electrosynthesis cell with a continuous CO2 supply. First, the impact of several transition metal ions (Ni2+, Fe2+, Cu2+, Sn2+, Mn2+, MoO42−, and Bi3+) on hydrogenotrophic and acetoclastic methanogenic microbial activity was evaluated in a series of batch bottle tests incubated with anaerobic sludge and a pre-defined concentration of dissolved transition metals. While Cu is considered a promising catalyst for the electrocatalytic conversion of CO2 to short chain fatty acids such as acetate, its presence as a Cu2+ ion was demonstrated to significantly inhibit the microbial production of CH4 and acetate. At the same time, CH4 production increased in the presence of Bi3+ (0.1 g L−1) and remained unchanged at the same concentration of Sn2+. Since Sn is of interest due to its catalytic properties in the electrochemical CO2 conversion, Bi and Sn were added to the cathode compartment of a laboratory-scale microbial electrosynthesis cell (MESC) to achieve an initial concentration of 0.1 g L−1. While an initial increase in CH4 (and acetate for Sn2+) production was observed after the first injection of the metal ions, after the second injection, CH4 production declined. Acetate accumulation was indicative of the reduced activity of acetoclastic methanogens, likely due to the high partial pressure of H2. The modification of a carbon-felt electrode by the electrodeposition of Sn metal on its surface prior to cathode inoculation with anaerobic sludge showed a doubling of CH4 production in the MESC and a lower concentration of acetate, while the electrodeposition of Bi resulted in a decreased CH4 production. [ABSTRACT FROM AUTHOR]

• Production of Gag-Spike VLPs using suspension serum-free HEK 293 cells. • Purification of VLPs by ultracentrifugation, tangential flow filtration and affinity chromatography. • Incorporation of SARS-CoV-2 components into Gag-Spike VLPs. • Evaluation of humoral and cellular responses to Gag-Spike VLPs through mouse studies. The virus-like particle (VLP) platform is a robust inducer of humoral and cellular immune responses; hence, it has been used in vaccine development for several infectious diseases. In the current work, VLPs carrying SARS-CoV-2 Spike (S) protein (Wuhan strain) with an HIV-1 Gag core were produced using suspension HEK 293SF-3F6 cells by transient transfection. The Gag was fused with green fluorescent protein (GFP) for rapid quantification of the VLPs. Five different versions of Gag-Spike VLPs (Gag-S-VLPs) consisting of Gag-S alone or combined with other SARS-CoV-2 components, namely Gag-S-Nucleocapsid (N), Gag-S-Matrix (M), Gag-S-Envelope (E), Gag-S-MEN, along with Gag alone were produced and processed by clarification, nuclease treatment, concentration by tangential flow filtration (TFF) and diafiltration. A pilot mouse study was performed to evaluate the immunogenicity of the Gag-S-VLPs through the measurement of the humoral and/or cellular responses against all the mentioned SARS-CoV-2 components. Antibody response to Spike was observed in all variants. The highest number of Spike-specific IFN-γ + T cells was detected with Gag-S-VLPs. No induction of antigen-specific cellular responses to M, N or E proteins were detected with any of the Gag-S, M, E/or N VLPs tested. Therefore, the Gag-S-VLP, by reason of consistently eliciting strong antigen-specific cellular and antibody responses, was selected for further evaluation. The purification process was improved by replacing the conventional centrifugation by serial microfiltration in the clarification step, followed by Spike-affinity chromatography to get concentrated VLPs with higher purity. Three different doses of Gag-S-VLP in conjunction with two adjuvants (Quil-A or AddaVax) were used to assess the dose-dependent antigen-specific cellular and antibody responses in mice. The Gag-S-VLP adjuvanted with Quil-A resulted in a stronger Spike-specific cellular response compared to that adjuvanted with AddaVax. A strong spike neutralisation activity was observed for all doses, independent of the adjuvant combination. [ABSTRACT FROM AUTHOR]

Antimicrobial peptides (AMPs) offer a great promise in designing new therapeutics due to their ability to interfere in bacterial growth by penetrating the cell wall. The overuse of antibiotics has resulted into antibiotic-resistant bacteria and AMPs could be an alternative to circumvent this resistance. Chitosan nanocrystals (ChsNCs) are rod-shaped polysaccharide-based nanomaterials, formed by deacetylation of seafood waste. They possess primary amino groups on the surface of the nanoparticles which can be as used a scaffold due to the built-in morphology and ease in functionalization. Here, we developed a new methodology to functionalize ChsNCs with amino acids and peptides by using fundamentals of solid phase peptide synthesis. The resulting functionalized rod-shaped nanomaterials were characterized using nuclear magnetic resonance (NMR), dynamic light scattering (DLS), zeta potential measurements and microscopy imaging. This synthetic strategy could be used in designing ChsNC-based nanomaterials to target specific cells by attaching bioactive peptides to the nanomaterial surface. [Display omitted] [ABSTRACT FROM AUTHOR]

Carbon Nanotubes (CNTs), single-, double-, and multiwalled can be easily suspended up to 10 mg/ml in biocompatible carboxymethylcellulose or κ-carrageenan as these polymers are envisioned to wrap themselves around CNTs effectively forming aqueous solutions. Glucose oxidase was used as a model to show the biocompatibility and stability of the entrapped enzyme in a κ-carrageenan-CNT network. [ABSTRACT FROM AUTHOR]

A biosensor for arsenite has been developed using molybdenum-containing arsenite oxidase, prepared from the chemolithoautotroph NT-26 that oxidizes arsenite to arsenate. The enzyme was galvanostatically deposited for 10 min at 10 μA onto the active surface of a multiwalled carbon nanotube modified glassy carbon electrode. The resulting biosensor enabled direct electron transfer, i.e., effecting reduction and then reoxidization of the enzyme without an artificial electron-transfer mediator. Arsenite was detected within 10 s at an applied potential of 0.3 V with linearity up to 500 ppb and a detection limit of 1 ppb. The biosensor exhibited excellent reproducibility, 2% at 95% confidence interval for 12 repeated analyses of 25 ppb arsenite. Copper, a severe interfering species commonly found in groundwater, did not interfere, and the biosensor was applicable for repeated analysis of spiked arsenite in tap water, river water, and a commercial mineral water. [ABSTRACT FROM AUTHOR]

Boron doped diamond (BDD) macro- and microelectrodes were modified by electrodeposition of platinum nanoparticles using a multipotential step electrodeposition technique and used for the oxidative determination of arsenite, As(III). The formation of Pt nanoparticles was evident from cyclic voltammetry measurement, whereas AFM and SEM revealed the size and size distribution of deposited Pt nanoparticles. Raman spectroscopy illustrated a correlation between the typical BDD signature and the number of platinum deposition cycles, linear sweep voltammetry performed with the modified BDD microelectrode outperformed its macrocounterpart and resulted in very low detecting currents with enhanced signal-to-noise ratios. With linearity up to 100 ppb and a detection limit of 0.5 ppb, the electrochemical system was applicable for processing tap and river water samples. Over 150 repetitive runs could be performed, and electrochemical etching of platinum allowed the reuse of the BDD microelectrode. The presence of copper and chloride ions, the two most severe interferents at levels commonly found in groundwater, did not interfere with the assay. [ABSTRACT FROM AUTHOR]

Metal nanoparticles (Pt, Au, or Cu) together with multi-walled and single-walled carbon nanotubes (MWCNT and SWCNT) solubilized in Nafion have been used to form nanocomposites for electrochemical detection of trinitrotoluene (TNT) and several other nitroaromatics. Electrochemical and surface characterization by cyclic voltammetry, AFM, TEM, SEM, and Raman spectroscopy confirmed the presence of metal nanoparticles on CNTs. Among various combinations tested, the most synergistic signal effect was observed for the nanocomposite modified glassy carbon electrode (GC) containing Cu nanoparticles and SWCNT solubilized in Nafion. This combination provided the best sensitivity for detecting TNT and other nitroaromatic compounds. Adsorptive stripping voltammetry for TNT resulted in a detection limit of 1 ppb, with linearity up to 3 orders of magnitude. Selectivity toward the number and position of the nitro groups in different nitroaromatics was very reproducible and distinct. Reproducibility of the TNT signal was within 7% (n = 8) from one electrode preparation to another, and the response signal was stable (±3.8% at 95% confidence interval) for 40 repeated analyses with 10 min of preconditioning. The Cu-SWCNT-modified GC electrode was demonstrated for analysis of TNT in tap water, river water, and contaminated soil. [ABSTRACT FROM AUTHOR]

A flow analysis electrochemical system has been developed, characterized, and optimized for the determination of arsenite (As(III)). Sensitivity was significantly improved by the electrochemical deposition of gold nanoparticles on a dual glassy carbon electrode, which was inserted into a cross-flow thin-layer electrochemical celL The electrochemical system was linear up to 15 ppb with a detection limit of 0.25 ppb. Gold deposition was evident from cyclic voltammetry measurements, whereas atomic force microscopy and scanning electron microscopy revealed the size and distribution of deposited gold nanoparticles. The size and density of the nanoparticles were related to the gold salt concentration, deposition time, and potential as well as the electrode position. The response to arsenite was directly related to the frequency, increment, and amplitude of the square wave voltammetry as well as the deposition time and potential. Estimated reproducibility was ± 1.1% at 95% confidence interval for 40 repeated analyses of 8 ppb arsenite during continuous analysis. The reproducibility was far superior if the electrochemical reduction of arsenite was performed in nitric acid instead of hydrochloric or sulfuric acid. The electrochemical system was applicable for analysis of spiked arsenic in mineral water containing a significant amount of various ion elements. [ABSTRACT FROM AUTHOR]

Abstract: The capabilities of using boron-doped diamond (BDD) thin films as electrode materials for analysis of the 16 US Environmental Protection Agency (EPA) priority polyaromatic hydrocarbons (PAHs) after a liquid chromatographic separation were evaluated. The BDD electrode was able to detect all 16 PAHs with high sensitivity due to the low background current and wide potential window. The method provided detection limits ranging from 12–40nM (3–10ppb) and repeatable results over consecutive analysis. Calibration curves were linear up to at least 10μM for all PAHs. The work shows the promising use of diamond as an amperometric detector in high performance liquid chromatography (HPLC), especially for PAHs and other hydrophobic aromatic compounds. [Copyright &y& Elsevier]

Pt-Zn porphyrin nanocomposites have been synthesized using zinc porphyrin and dihydrogen hexachloroplatinate in the presence of light and ascorbic acid. TEM and AFM imaging revealed that Pt nanoparticles with an average diameter of ∼3.5 nm were embedded within the Zn porphyrin matrix. The glassy carbon electrode was modified with Nafion-stabilized Pt-Zn porphyrin nanocomposites and used for dehalogenation of carbon tetrachloride, chloroform, pentachlorophenol, chlorobenzene, and hexachlorobenzene as five test models. The Pt-Zn porphyrin nanocomposite-modified electrode exhibited catalytic activity for the reduction of organohalides at - 1.0 V versus Ag/AgCl. Raman signatures confirmed the dehalogenation of chlorobenzene by the nanocomposite-modified electrode. The above two aliphatic and three aromatic organohalides had detection limits of 0.5 μM with linearity up to 8 μM. The modified electrode was good for at least 80 repeated measurements of 4 μM chlorobenzene with a storage stability of 1 month at room temperature. The deactivation of the electrode activity was associated with the loss of platinum nanoparticles from the nanocompos- ite structure. [ABSTRACT FROM AUTHOR]

Copper (Cu) nanoparticles (4–8 nm in diameter), prepared by using sodium borohydride to reduce copper dodecyl sulfate (Cu(DS)2), were used with single-wall carbon nanotubes (SWCNTs) to fabricate electrochemical sensors. Nafion, a perfluorosulfonated polymer, was able to solubilize SWCNTs and displayed interactions with Cu nanoparticles to form a network, connecting Cu nanoparticles to a glassy carbon (GC) or Cu electrode surface. Cyclic voltammetry confirmed an electrical contact through SWCNTs between Cu nanoparticles and the GC backing whereas TEM micrographs illustrated the deposition of Cu nanoparticles on the carbon nanotubes. The response time and the detection limit (S/N=3) of the sensor for glucose were 10 s and 250 nM, respectively, i.e. a four-fold increase in the sensitivity compared to a bare Cu disk electrode. The response to interferents, such as acetaminophen, ascorbic acid and uric acid was suppressed in the presence of the SWCNT/Cu nanoparticle composite. [Copyright &y& Elsevier]

Platinum nanoparticles with a diameter of 2-3 nm were prepared and used in combination with single-wall carbon nanotubes (SWCNTs) for fabricating electrochemical sensors with remarkably improved sensitivity toward hydrogen peroxide. Nafion, a perfluorosulfonated polymer, was used to solubilize SWCNTs and also displayed strong interactions with Pt nanoparticles to form a network that connected Pt nanoparticles to the electrode surface. TEM and AFM micrographs illustrated the deposition of Pt nanoparticles on carbon nanotubes whereas cyclic voltammetry confirmed an electrical contact through SWCNTs between Pt nanoparticles and the glassy carbon (GC) or carbon fiber backing. With glucose oxidase (GOx) as an enzyme model, we constructed a GC or carbon fiber microelecirode-based biosensor that responds even more sensitively to glucose than the GC/GOx electrode modified by Pt nanoparticles or CNTs alone. The response time and detection limit (S/N =3) of this biosensor was determined to be 3 s and 0.5 μM, respectively. [ABSTRACT FROM AUTHOR]

A simple method is described for the construction of a glucose biosensor with good reproducibility. After electrochemical etching, the sensing tip of an etched platinum microelectrode was insulated using a synthetic rubber dip coating. The insulating layer was then heat-cured, leading to a small exposed area at the very end of the etched Pt tip, as confirmed by scanning electron microscopy. Phenol and 2-allylphenol were electropolymerized to form an extra insulating layer that effectively retained glucose oxidase (GOX) on the sensing tip of the electrode. On the basis of cyclic voltammetry measurements, the apparent radius of the biosensor tip was estimated to be between 10 and 500 nm, depending on GOX loading. With operational and storage stabilities over 3 weeks, the glucose biosensor prepared using optimal GOX concentration (10 mg/mL) exhibited a picoamperometric current response within ∼2 s and a detection limit of 20 µM with excellent reproducibility. [ABSTRACT FROM AUTHOR]

In this study, CO 2 conversion to acetate and CH 4 was achieved in a flow-through laboratory-scale microbial electrosynthesis (MES) cell composed of a 3D conductive polylactic acid (cPLA) lattice cathode with electrodeposited metal electrocatalyst coatings. The MES cell with a bare cPLA cathode showed the poorest performance with the lowest H 2 and CH 4 production rates and low Coulombic efficiency. This was ascribed to a poor electrocatalytic activity of cPLA towards H 2 production and high electrode resistivity. When the cPLA electrode was modified with metal coatings, the CH 4 , acetate and H 2 production rate increased significantly, with the following trend: cPLA < Ni < NiFe < NiFeMn. The better performance of the metal-coated cPLA in terms of CH 4 production was attributed to the lower electrical resistance, enhanced H 2 production and enhanced electron transfer between the cathode and the biofilm. At the cell potential of 2.8 V, the best-performing NiFeMn cPLA cathode showed stable production of CH 4 (50 ± 6 mL d−1), acetate (185 ± 27 mg d−1), and H 2 (545 ± 175 mL d−1) at close to 100% Coulombic efficiency. [Display omitted] • Conductive polylactate (cPLA) lattice cathode developed for microbial electrosynthesis. • CH 4 , acetate, and H 2 continuously produced in a microbial electrosynthesis (MES) cell. • Electrodeposition of Ni, Fe, and Mn increased cPLA performance by up to 80%. • NiFeMn cPLA showed best performance with nearly 100% Coulombic efficiency. [ABSTRACT FROM AUTHOR]

The world is currently facing a global health crisis due to the rapid increase in antimicrobial-resistant bacterial infections. One of the most concerning pathogens is Acinetobacter baumannii, which is listed as a Priority 1 pathogen by the World Health Organization. This Gram-negative bacterium has many intrinsic antibiotic resistance mechanisms and the ability to quickly acquire new resistance determinants from its environment. A limited number of effective antibiotics against this pathogen complicates the treatment of A. baumannii infections. A potential treatment option that is rapidly gaining interest is "phage therapy", or the clinical application of bacteriophages to selectively kill bacteria. The myoviruses DLP1 and DLP2 (vB_AbaM-DLP_1 and vB_AbaM-DLP_2, respectively) were isolated from sewage samples using a capsule minus variant of A. baumannii strain AB5075. Host range analysis of these phages against 107 A. baumannii strains shows a limited host range, infecting 15 and 21 for phages DLP1 and DLP2, respectively. Phage DLP1 has a large burst size of 239 PFU/cell, a latency period of 20 min, and virulence index of 0.93. In contrast, DLP2 has a smaller burst size of 24 PFU/cell, a latency period of 20 min, and virulence index of 0.86. Both phages show potential for use as therapeutics to combat A. baumannii infections. [ABSTRACT FROM AUTHOR]

Cationic nanomaterials are promising candidates for the development of effective antibacterial agents by taking advantage of the nanoscale effects as well as other exceptional physicochemical properties of nanomaterials. In this study, carboxylated cellulose nanocrystals (cCNCs) derived from softwood pulp were coated with cationic poly(diallyldimethylammonium chloride) of varying molecular weights. The resulting cationic carboxylated cellulose nanocrystals coated with poly(diallyldimethylammonium chloride) (cCNCs–PDDA) nanomaterials were characterized for their structural and morphological properties using Fourier transform infrared spectroscopy, dynamic light scattering, zeta potential, elemental analysis, transmission electron microscopy, and thermogravimetric analysis. Cationic cCNCs–PDDA were investigated for their antibacterial properties against Gram-positive Staphylococcus aureus and Gram-negative Escherichia coli 23934 and Pseudomonas aeruginosa using a bacterial lawn growth inhibition assay. cCNC–PDDA materials displayed marked antibacterial activity, particularly against Gram-positive Staphylococcus aureus. Overall, our results indicated that cCNCs–PDDA could be a potential candidate for antibacterial applications such as antibacterial surfaces or coatings. [ABSTRACT FROM AUTHOR]

To unlock nature's potential for functional biomaterials, many efforts have been devoted to isolating the nanocrystalline domains within the supramolecular structure of polysaccharides. Yet, low reactivity and yield in aqueous systems along with excessive solvent usage hinders its development. In this report, the first solvent‐free pathway to access carboxylated chitin and cellulose nanocrystals with excellent mass balance is described, relying on a new method coined high‐humidity shaker aging (HHSA). The method involves a mild grinding of the polysaccharide with ammonium persulfate followed by an aging phase under high‐humidity and on a shaker plate. Insights into the mechanism were uncovered, which highlighted the unique role of high humidity to afford a gradual uptake of water by the material up to deliquescence when the reaction is complete. This process was then validated for direct synthesis of nanocrystals from biomass sources including crab and soft wood pulp. [ABSTRACT FROM AUTHOR]

To unlock nature's potential for functional biomaterials, many efforts have been devoted to isolating the nanocrystalline domains within the supramolecular structure of polysaccharides. Yet, low reactivity and yield in aqueous systems along with excessive solvent usage hinders its development. In this report, the first solvent‐free pathway to access carboxylated chitin and cellulose nanocrystals with excellent mass balance is described, relying on a new method coined high‐humidity shaker aging (HHSA). The method involves a mild grinding of the polysaccharide with ammonium persulfate followed by an aging phase under high‐humidity and on a shaker plate. Insights into the mechanism were uncovered, which highlighted the unique role of high humidity to afford a gradual uptake of water by the material up to deliquescence when the reaction is complete. This process was then validated for direct synthesis of nanocrystals from biomass sources including crab and soft wood pulp. [ABSTRACT FROM AUTHOR]

The article focuses on the immobilization of antibodies and enzymes on aminopropyltriethoxysilane (APTES)-functionalized bioanalytical platforms for biosensing and diagnostic devices. It discusses the role of immobilization strategies and their impact on sensitivity, detection limit and operational and storage stability. It further reflects on the advantages of APTES biosensors in analytical applications including easy preparation, stable monolayers and uniform immobilization surface.

A continuous online technique based on electric cell-substrate impedance sensing (ECIS) was demonstrated for measuring the concentration and time response function of fibroblastic V79 cells exposed to nanomaterials such as quantum dots (QDs) and fluorescent gold nanoparticles. The half-inhibition concentration, (ECIS50), the required concentration to attain 50% inhibition of the cytotoxic response, was estimated from the response function to ascertain cytotoxicity during the course of measurement. The ECIS50 values agreed well with the results obtained using the standard neutral red assay. Cadmium selenide quantum dots showed direct cytoxicity with the ECIS assay. For the cadmium telluride quantum dots, significant toxicity could be assigned to free cadmium, although additional toxicity could be attributed to the QDs per se. The QDs synthesized with indium gallium phosphide and the fluorescent gold nanoparticles were not cytotoxic. [ABSTRACT FROM AUTHOR]

• %Amylose of pea flours had a good correlation with %starch (r = -0.990, p < 0.001). • %Amylose showed positive correlations with %protein and %dietary fiber (p < 0.001). • A higher amylose content increased starch gelatinization temp. of pea flours. • Pea flours with more amylose needed higher heating temp. to give viscosity and gel. • %Amylose increased %resistant starch but did not influence protein digestibility. In this study, ten pea flours covering a broad range of amylose content (37.2–77.6 %, dsb) were characterized for functional and nutritional properties. As the amylose contents increased, the starch contents of the pea flours showed a downward trend (r = -0.990, p < 0.001 in Pearson correlation) but their protein and total dietary fiber contents exhibited an upward trend (r = 0.915, p < 0.001 and r = 0.885, p < 0.001, respectively). A greater amylose content tended to increase starch gelatinization temperatures of the pea flours, which thus required a higher cooking temperature for pasting viscosity development and subsequent gel formation. An increased amylose level reduced in vitro starch digestibility of the cooked pea flours (r = -0.944, p < 0.001) but did not influence in vitro protein digestibility. The insightful findings will be valuable for utilizing the diverse pea lines to create new flour, starch, and protein ingredients. [ABSTRACT FROM AUTHOR]

[Display omitted] • Three cathode materials were compared for CH 4 and acetate bioelectrosynthesis. • Carbon felt cathode showed the highest CH 4 production per cathode volume. • Conductive polymer cathode promoted acetate and ethanol production. • Cathode material selection affects biofilm activity and bioelectrosynthesis pathways. This study compares carbon felt (CF), granular activated carbon (GAC), and a conductive acrylonitrile butadiene styrene (cABS) polymer cathodes for CH 4 and acetate production in a microbial electrosynthesis (MES) cell. At an applied voltage of 2.8 V and continuous CO 2 flow, the CF biocathode MES cell showed the highest CH 4 production rate of 1420 ± 225 mL V c -1 d-1 (V c = cathode volume), also producing acetate at a rate of 710 ± 110 mg V c -1 d-1. The volumetric rates of acetate and CH 4 production decreased when using the GAC cathode (720 ± 94 mL V c -1 d-1 and 236 ± 65 mg V c -1 d-1, respectively). When the cABS cathode was used, the CH 4 production declined to 250 ± 35 mL V c -1 d-1, while the acetate production increased to 1105 ± 130 mg V c -1 d-1. The biocatalytic activity of cABS increased after in-situ electrodeposition of Ni and Fe, resulting in a current increase from 205 mA to 380 mA accompanied by increasing acetate and ethanol production (1405 mg V c -1 d-1 and 240 mg V c -1 d-1, respectively), while the CH 4 production decreased. The cABS cathode showed the highest specific (per surface area) activity for acetate and CH 4 production. [ABSTRACT FROM AUTHOR]

An improved enzyme-linked immunosorbent (ELISA) assay using one-step antibody immobilization has been developed for the detection of human fetuin A (HFA), a specific biomarker for atherosclerosis and hepatocellular carcinoma. The anti-HFA formed a stable complex with 3-aminopropyltriethoxysilane (APTES) by ionic and hydrophobic interactions. The complex adsorbed on microtiter plates exhibited a detection range of 4.9 pg mL-1 to 20 ng mL-1 HFA, with a limit of detection of 7 pgmL-1. Furthermore, an analytical sensitivity of 10 pg mL-1 was achieved, representing a 51-fold increase in sensitivity over the commercial sandwich ELISA kit. The results obtained for HFA spiked in diluted human whole blood and plasma showed the same precision as the commercial kit. When stored at 4°C in 0.1 Mphosphate-buffered saline (PBS, pH 7.4), the anti-HFA bound microtiter plates displayed no significant decrease in their functional activity after two months. The new ELISA procedure was extended for the detection of C-reactive protein, human albumin and human lipocalin-2 with excellent analytical performance. [ABSTRACT FROM AUTHOR]

Nanocrystalline cellulose (NCC), a rigid rod-like nanoscale material, can be produced from cellulosic biomass in powder, liquid, or gel forms by acid and chemical hydrolysis. Owing to its unique and exceptional physicochemical properties, the incorporation of a small amount of NCC into plastic enhances the mechanical strength of the latter by several orders of magnitudes. Carbohydrate-based NCC poses no serious environmental concerns, providing further impetus for the development and applications of this green and renewable biomaterial to fabricate lightweight and biodegradable composites and aerogels. Surface functionalization of NCC remains the main focus of NCC research to tailor its properties for dispersion in hydrophilic or hydrophobic media. It is of uttermost importance to develop tools and protocols for imaging of NCC in a complex matrix and quantify its reinforcement effect. [ABSTRACT FROM AUTHOR]

Abstract: Graphene, graphene oxide, sulfonated graphene, and sulfonated graphene oxide (SGO) have been prepared, characterized and tested for the dehydration of xylose to furfural in water. In particular, SGO was proven to be a rapid and water-tolerant solid acid catalyst even at very low catalyst loadings down to 0.5wt.% vs xylose, maintaining its initial activity after 12 tested repetitions at 200°C, with an average yield of 61% in comparison to 44% for the uncatalyzed system. Raman spectroscopy, energy dispersive X-ray spectroscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy, 13C solid state nuclear magnetic resonance spectroscopy, Fourier transform infrared spectroscopy and surface area analysis suggested that the aryl sulfonic acid groups were the key active sites for high temperature production of furfural in water. They were more thermally stable under the reaction conditions and acidic than other functional groups attached to the graphene surface. [Copyright &y& Elsevier]

Abstract: The reinforcement effect of carbon nanotubes (CNTs) has been examined as a function of their loading and aspect ratio in poly(vinyl alcohol) (PVA) based hybird fibers. Lignosulfonic acid sodium salt (LSA) was used to disperse CNTs to produce consistently high CNT loaded PVA-LSA-CNT hybrid fibers using an electrospinning process. The elastic modulus of individual fibers was measured using atomic force microscopy. The presence of CNTs significantly increased the average elastic modulus of PVA-LSA-CNT fibers compared to PVA-LSA fibers. The elastic modulus, however, exhibited no fiber diameter dependency. Transmission electron microscopy (TEM) was used to determine the loading and the aspect ratio of CNTs in each hybrid fiber. The CNT loading in PVA-LSA-CNT fibers varied widely due to non-uniform CNT dispersion and displayed no relationship with the elastic modulus. Our results also demonstrated that the average value of CNT aspect ratio significantly affected the elastic modulus of the hybrid fibers. Such a result was in agreement with theoretical prediction in which the stress transfer efficiency in a composite matrix is strongly dependent on the CNT aspect ratio. [Copyright &y& Elsevier]

N-Acetyltyramine was Synthesized and electropolymerized together with a negatively charged sulfobutylether-β-cyclodextrin on a boron-doped diamond (BDD) electrode followed by the electropolymerization of pyrrole to form a stable and permselective film for selective dopamine detection. The selectivity and sensitivity of the formed layer-by-layer film was governed by the sequence of deposition and the applied potential. Raman results showed a decrease in the peak intensity at 1329 cm-1 (sp3), the main feature of BDD, upon each electrodeposition step. Such a decrease was correlated well with the change of the charge-transfer resistance derived from impedance data, i.e., reflecting the formation of the layer-by-layer film. The polycrystalline BDD surface became more even with lower surface roughness as revealed by scanning electron and atomic force microscopy. The modified BDD electrode exhibited rapid response to dopamine within 1.5-2 s and a low detection limit of 4-5 nM with excellent reproducibility. Electroactive interferences caused by 4-dihydroxyphenylalanine, 3,4-dihydroxyphenylacetic acid, ascorbic acid, and uric acid were completely eliminated, whereas the signal response of epinephrine and norepinephrine was significantly suppressed by the permselective film. [ABSTRACT FROM AUTHOR]

This study demonstrated the removal of selenite and selenate in flow-through permeable bioelectrochemical barriers (microbial electrolysis cells, MECs). The bioelectrochemical barriers consisted of cathode and anode electrode compartments filled with granular carbon or metallurgical coke. A voltage of 1.4 V was applied to the electrodes to enable the bioelectrochemical removal of selenium species. For comparison, a similarly designed permeable anaerobic biobarrier filled with granular carbon was operated without voltage. All biobarrier setups were fed with water containing up to 5,000 µg L−1 of either selenite or selenate and 70 mg L−1 of acetate as a source of organic carbon. Significant removal of selenite and selenate was observed in MEC experimental setups, reaching 99.5–99.8% over the course of the experiment, while in the anaerobic biobarrier the removal efficiency did not exceed 88%. By simultaneously operating several setups and changing operating parameters (selenium species, influent Se and acetate concentrations, etc.) we demonstrated enhanced removal of Se species under bioelectrochemical conditions. ga1 • Selenate and selenite removal in a flow-through bioelectrochemical barrier was demonstrated. • Anaerobic treatment resulted in 85% Se removal efficiency. • A 1.4 V applied voltage coupled with acetate addition enhanced selenate and selenite removal. • Up to 99.5% selenate and selenite removal achieved in the bioelectrochemical system. [ABSTRACT FROM AUTHOR]

Polysaccharides have been shown to have immunomodulatory properties. Modulation of the immune system plays a crucial role in physiological processes as well as in the treatment and/or prevention of autoimmune and infectious diseases. Cellulose nanocrystals (CNCs) are derived from cellulose, the most abundant polysaccharide on the earth. CNCs are an emerging class of crystalline nanomaterials with exceptional physico-chemical properties for high-end applications and commercialization prospects. The aim of this study was to design, synthesize, and evaluate the cytotoxicity of a series of biocompatible, wood-based, cationic CNCs as potential immunomodulators. The anionic CNCs were rendered cationic by grafting with cationic polymers having pendant +NMe3 and +NH3 moieties. The success of the synthesis of the cationic CNCs was evidenced by Fourier transform infrared spectroscopy, dynamic light scattering, zeta potential, and elemental analysis. No modification in the nanocrystals rod-like shape was observed in transmission electron microscopy and atomic force microscopy analyses. Cytotoxicity studies using three different cell-based assays (MTT, Neutral Red, and LIVE/DEAD®) and three relevant mouse and human immune cells indicated very low cytotoxicity of the cationic CNCs in all tested experimental conditions. Overall, our results showed that cationic CNCs are suitable to be further investigated as immunomodulators and potential vaccine nanoadjuvants. [ABSTRACT FROM AUTHOR]