Synthesis and antimicrobial effects of highly dispersed,cellulose-stabilized silver/cellulose nanocomposites

Small, spherical silver nanoclusters were synthesised on the surface of paper as a model cellulosic fibre substrate by a standard chemical reduction method. The concentration of the silver nanoclusters on the substrate surface is roughly proportional to the initial silver salt concentration. However, there is a noticeable degree of nanocluster aggregation to larger agglomerates. The addition of small amounts of α-cellulose, carboxymethyl cellulose or aminocellulose during the synthesis of the silver/cellulose nanocomposites suppresses this aggregation and significantly increases the concentration of the silver nanoclusters on the surface of the fibres of cellulose. These small, surface-stabilised silver nanoclusters, with the desired size and morphology, deposited from aqueous solutions on the surface of cellulosic cotton fibres, show enhanced antibacterial activity against MRSA compared to that of the corresponding silver/cotton nanocomposites prepared in the absence of a cellulosic surface stabiliser.

Silver/cellulose nanocomposite fibres, prepared using a simple reduction method, exhibit significant and competitive antibacterial activity against strains of bacteria, such as MRSA, which are proving resistant to broad-spectrum antibacterial agents.     

Textile-supported silver nanoparticles as a highly efficient and recyclable heterogeneous catalyst for nitroaromatic reduction at room temperature

A novel textile-based nanosilver catalyst was prepared with a facile synthetic method. The textile-supported nanosilver (TsNS) proved to be an excellent heterogeneous catalyst for the reduction of nitroaromatics with a broad substrate scope. It can be recycled for up to 6 times without significantly compromising its catalytic efficacy. The TsNS catalyst was developed into a column reactor, demonstrating its practical application with the advantages of low cost, ease of operation and large scale synthesis capabilities. Scanning electron microscopy (SEM) showed that there were few changes to the catalyst''s surface after the reaction. Besides, inductively coupled plasma (ICP) analysis showed that few silver particles leaked, and the interactions between the nitro groups of the nitroaromatics and the nanosilver particles were characterized by X-ray photoelectron spectroscopy (XPS), which lead to the proposal of a four-step mechanism for the reduction reaction.

A novel textile-supported nanosilver (TsNS) catalyst was prepared and applied in nitroaromatic reduction with excellent activity, stability and recyclability.     

A highly active worm-like PtMo nanowire for the selective synthesis of dibenzylamines

Worm-like nanowires are among the most active nanomaterials. In this study, we report the synthesis of dibenzylamine (DBA) motifs from reductive amination of either aldehydes or nitriles catalyzed by entirely new worm-like PtMo nanowires (PtMo WNWs). Under the assistance of H₂ gas, PtMo WNWs can be prepared in a facile manner, following which, their structure and composition are characterized by TEM, XRD, XPS, etc. Upon careful optimization of reaction parameters, the as-prepared PtMo WNWs work effectively in the activation of dihydrogen molecules, and both aldehydes and nitriles can be used as starting materials to fabricate DBAs under mild and green conditions. The reaction kinetics has been investigated, which reveals that the PtMo WNWs show superior activity in the conversion of imines into amines. This study provides a practical advancement in the preparation of amines. Moreover, the protocol reported herein is feasible for the synthesis of worm-like nanostructures with designed composition for various catalytic applications.

An efficient synthetic pathway of dibenzylamine (DBA) motifs from reductive amination of either aldehydes or nitriles catalyzed by highly active worm-like PtMo nanowires.     

A reusable catalyst based on CuO hexapods and a CuO–Ag composite for the highly efficient reduction of nitrophenols

The enormous and urgent need to explore cost-effective catalysts with high efficiency has always been at the forefront of environmental protection and remediation research. This work develops a novel strategy for the fabrication of reusable CuO-based non-noble metal nanomaterials as high-efficiency catalysts. We report a facile and eco-friendly synthesis of CuO hexapods and CuO–Ag composite using uric acid as a reductant and protectant. Both exhibited high catalytic activity in the hydrogenation of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) by sodium borohydride (NaBH₄), with the CuO–Ag composite showing superior catalytic performance. Notably, the highest turnover frequency of CuO–Ag reached 7.97 × 10⁻² s⁻¹, which was much higher than numerous noble-metal nanomaterials. In addition, CuO hexapods and CuO–Ag composite were also shown to act as highly efficient and recyclable catalysts in the degeneration of 4-NP. Both CuO hexapods and the CuO–Ag composite exhibited outstanding catalytic durability, with no significant loss of activity over more than 10 cycles in the hydrogenation of 4-NP.

Schematic illustration for the process of preparing CuO hexapods and CuO–Ag composite, and their application in catalytically reducing 4-NP and K₃(Fe(CN)₆).     

Rapid and highly sensitive colloidal silver staining on cellulose acetate membrane for analysis of urinary proteins

In order to establish a rapid staining method sensitive enough to stain the protein bands on cellulose acetate membrane and suitable for the analysis of urinary proteins in healthy subjects, we conducted a detailed examination of Kovarik's method designed for the analysis of proteins in cerebrospinal fluid in detail. For purpose of our study, we changed the pH of the staining solution used in Kovarik's method to pH 4.4 by adding acetic acid. With this solution, our staining method revealed a degree of sensitivity about three times higher than that of the original method, but specific sensitivity for albumin and γ-globulin remained almost unchanged. The solution preparation we used was much more simple and the reagent much more stable than in the original method. Our method also showed better reproducibility and linearity than the original method. These results point to the suitability of this method for the analysis of low-concentration proteins, such as urinary proteins, in healthy subjects. © 1996 Wiley-Liss, Inc.     

PdAu alloy nanoparticles supported on nitrogen-doped carbon black as highly active catalysts for Ullmann coupling and nitrophenol hydrogenation reactions

Noble metal-based catalysts have been proven to be active for catalytic organic reactions. The selectivity and conversion can be improved by integration with proper carrier materials, and further modulated by tuning the composition as well as the electronic structure of the active noble metals. Compared with unsupported monometallic catalysts, the synergistic interactions between neighboring metals and the combined effects between the carrier materials and the active components often give rise to positive influences on the enhancement of the catalytic efficiency and selectivity. In this work, we report a facile process for the fabrication of nitrogen-doped carbon black (NCB) supported PdAu bimetallic nanoparticles (NPs) with a uniform dispersion and narrow size distribution. The PdAu/NCB catalyst with a Pd/Au mole ratio of 1/1 shows the highest activity towards both Ullmann coupling reactions of aryl halides and the hydrogenation reaction of nitrophenols. Moreover, this bimetallic catalyst also exhibits a superior recycling durability to that of monometallic Pd/NCB and Au/NCB catalysts. The enhanced catalytic performance of the bimetallic catalyst is mainly due to the large BET specific surface area (125.45 m² g⁻¹) and the synergy between the individual components of the catalyst.

The PdAu/NCB catalyst with a Pd/Au mole ratio of 1/1 shows the highest activity towards both Ullmann coupling reactions of aryl halides and the hydrogenation reaction of nitrophenols.     

A superhydrophilic bilayer structure of a nylon 6 nanofiber/cellulose membrane and its characterization as potential water filtration media

A bilayer structure of a nylon 6 nanofibrous membrane on a cellulose membrane has been successfully developed for water filter application. The nylon 6 nanofibrous membrane was deposited on the cellulose membrane via the electrospinning technique. The bilayer membrane properties, including mechanical strength, wettability, porosity, and microfiltration performance (flux and rejection), were thoroughly investigated. The membrane properties were studied using nylon 6 nanofibrous membranes having various fiber diameters and membrane thicknesses, which were obtained by adjusting the solution concentration and spinning time. The measurement of solution parameters, i.e., viscosity, conductivity, and surface tension, showed a strong relationship between the solution concentration and these parameters, which later changed the fabricated fiber sizes. The FTIR spectra depicted complete solvent evaporation after the electrospinning process. Smaller nanofiber diameters could improve the mechanical strength of the membranes. The porosity test showed a strong relationship between the nanofiber diameter and the pore size and pore distribution of the membranes. The water contact angle measurement showed the significant influence of the cellulose membrane on increasing the hydrophilicity of the bilayer structure, which then improved the membrane flux. The particle rejection test, using PSL sizes of 308 and 450 nm, showed high rejection (above 98%) for all sample thickness variations. Overall, the bilayer structure of the nylon 6 nanofibers/cellulose membranes showed excellent and promising performance as water filter media.

The SEM image of (a) cellulose membrane and (b) the bilayer structure of a nylon 6 nanofibrous membrane on a cellulose membrane as water filter media.     

Iron phosphide anchored nanoporous carbon as an efficient electrode for supercapacitors and the oxygen reduction reaction

Inspired by their distinctive properties, transition metal phosphides have gained immense attention as promising electrode materials for energy storage and conversion applications. The introduction of a safe and large-scale method of synthesizing a composite of these materials with carbon is of great significance in the fields of electrochemical and materials sciences. In the current effort, we successfully synthesize an iron phosphide/carbon (FeP/C) with a high specific surface area by the pyrolysis of the gel resulting from the hydrothermal treatment of an iron nitrate–phytic acid mixed solution. In comparison with the blank (P/C), the as-synthesized FeP/C appears to be an efficient electrode material for supercapacitor as well as oxygen reduction reaction (ORR) applications in an alkaline medium in a three-electrode system. In the study of supercapacitors, FeP/C shows areal capacitance of 313 mF cm⁻² at 1.2 mA cm⁻² while retaining 95% of its initial capacitance value after 10 000 cycles, while in the ORR, the synthesized material exhibits high electrocatalytic activity with an onset potential of ca. 0.86 V vs. RHE through the preferred four-electron pathway and less than 6% H₂O₂ production calculated in the potential range of 0.0–0.7 V vs. RHE. The stability is found to be better than those of the benchmark Pt/C (20 wt%) catalyst.

Synthesis of a nanoporous FeP/C material through a two-step method involving hydrothermal and carbonization processes for supercapacitors and the oxygen reduction reaction.     

A stable LnMOF as a highly efficient and selective luminescent sensor for detecting malachite green in water and real samples

A series of isostructural 3D lanthanide metal–organic frameworks (LnMOFs), with the formula n(H₃O)[Ln(L)(H₂O)]_n·nH₂O (Ln = Gd 1, Eu 2 and Tb 3, H₄L = 3,5,3′,5′-oxytetrabenzoic acid), have been successfully synthesized by solvothermal reactions. Single-crystal X-ray diffraction analysis reveals that 1–3 are constructed from wave-like Ln–carboxylate chains which are further connected by the ligands to form 3D channel-type frameworks. Further experiments suggest that 3 is thermally stable up to 322 °C and exhibits outstanding chemical stability in aqueous solutions with the pH ranging from 3 to 11. Significantly, 3 can be utilized for the first time to detect malachite green (a synthetic antibiotic to cure saprolegniasis) in aqueous media even in the presence of other interfering antibiotics, with a high sensitivity (K_sv = 8.33 × 10⁴ M⁻¹), low detection limit (DL = 0.25 μM) and good recyclability. On a more practical note, we found that the luminescence intensity of 3 showed almost no response to pH changes (pH 3–11), allowing steady sensing in real samples such as river water, simulated human serum and urine with satisfactory recoveries and RSD.

A Tb-MOF with chemical stability was synthesized. It showed excellent luminescent sensing for MG in river water, simulated serum and urine.     

Water-soluble gold nanoparticles: recyclable catalysts for the reduction of aromatic nitro compounds in water

A structure/catalytic activity study of water-soluble gold nanoparticles, stabilized by zwitterionic ligands derived from imidazolium salts, in the reduction of aromatic nitro compounds in pure water at different temperature, as well as their recyclability, was performed. Our studies indicate that the nanoparticles synthesized by an easy, fast and reproducible process, need a short characteristic induction time to restructure the surfaces and make them active. The differences observed in the catalytic activity of the nanoparticles, determined by using the typical Langmuir–Hinshelwood model, are strongly based on the degree of coverage and spatial arrangement of the imidazolium salts on them. Finally, we demonstrate that gold nanoparticles stabilized by non-traditional ligands can be an excellent choice for nitro compound degradation.

A structure/catalytic activity study of water-soluble gold nanoparticles, stabilized by zwitterionic ligands derived from imidazolium salts, in the reduction of aromatic nitro compounds in pure water, as well as their recyclability, was performed.     

Preparation and investigation of highly selective solid acid catalysts with sodium lignosulfonate for hydrolysis of hemicellulose in corncob

Saccharification of lignocellulose is a necessary procedure for deconstructing the complex structure for building a sugar platform that can be used for producing biofuel and high-value chemicals. In this study, a carbon-based solid acid catalyst derived from sodium lignosulfonate, a waste by-product from the paper industry, was successfully prepared and used for the hydrolysis of hemicellulose in corncob. The optimum preparation conditions for the catalyst were determined to be carbonization at 250 °C for 6 h, followed by sulfonation with concentrated H₂SO₄ (98%) and oxidation with 10% H₂O₂ (solid–liquid ratio of 1 : 75 g mL⁻¹) at 50 °C for 90 min. SEM, XRD, FT-IR, elemental analysis and acid–base titration were used for the characterization of the catalysts. It was found that 0.68 mmol g⁻¹ SO₃H and 4.78 mmol g⁻¹ total acid were loaded onto the catalyst. When corncob was hydrolyzed by this catalyst at 130 °C for 12 h, the catalyst exhibited high selectivity and produced a relatively high xylose yield of up to 84.2% (w/w) with a few by-products. Under these conditions, the retention rate of cellulose was 82.5%, and the selectivity reached 86.75%. After 5 cycles of reuse, the catalyst still showed high catalytic activity, with slightly decreased yields of xylose from 84.2% to 70.7%.

A novel carbon-based catalyst with high catalytic ability and xylose selectivity was prepared from sodium lignosulfonate.     

New anionic rhodium complexes as catalysts for the reduction of acetophenone and its derivatives

New anionic rhodium(iii) complexes, obtained by a simple reaction of RhCl₃ with organic chlorides (derivatives of imidazole and pyridine), have been employed as catalysts for hydrosilylation (reduction) of acetophenone derivatives. The reactions, in which 1,1,1,3,5,5,5-heptamethyltrisiloxane was a reducing agent, proceeded in a biphasic system because the above complexes are insoluble in the reaction medium. Thereby easy isolation of the complexes from post-reaction mixtures was possible after reaction completion. This is the first example of the application of rhodium complexes of this type as catalysts for ketone reduction. The complexes have shown high activity and enabled obtaining the hydrosilylation product in a very short time and in the range of low concentrations (0.1 mol%). By using FT-IR in situ analysis that enables measuring product concentrations in real time, a comparison has been made of the catalytic activity for hydrosilylation of acetophenone and methoxyacetophenone isomers shown by four rhodium complexes ([C⁺][RhCl₄⁻]) differing in cations and the most effective catalyst for this process has been distinguished.

Stable rhodium complexes were obtained in a simple way and applied as highly active catalysts for reduction of acetophenone derivatives.     

A highly sensitive and selective fluorescent probe for quantitative detection of Al3+ in food,water, and living cells

Three novel β-pinene-based fluorescent probes 2a–2c were designed and synthesized for the selective detection of Al³⁺. Probe 2a showed higher fluorescence intensity toward Al³⁺ than the other two compounds. Probe 2a determined the concentration of Al³⁺ with a rapid response time (45 s), wide pH range (pH = 1–9), excellent sensitivity (LOD = 8.1 × 10⁻⁸ M) and good selectivity. The recognition mechanism of probe 2a toward Al³⁺ was confirmed by ¹H NMR, HRMS and DFT analysis. Probe 2a was successfully used as a signal tool to quantitatively detect Al³⁺ in food samples and environmental water samples. Furthermore, probe 2a was successfully utilized to label intracellular Al³⁺, indicating its promising applications in living cells.

Probe 2a exhibiting high sensitivity, good selectivity, wide pH range, lower detection limit, and rapid detection for Al³⁺, probe 2a was applied for the successful detection of Al³⁺ in water samples, food samples and HeLa cells.     

Synthesis of non-toxic,biocompatible, and colloidal stable silver nanoparticle using egg-white protein as capping and reducing agents for sustainable antibacterial application

For nearly a decade, silver nanoparticles (AgNPs) have been the most prevalent commercial nanomaterials products widely used in different biomedical applications due to their broad-spectrum antimicrobial activity. However, their poor long-term stability in different environments, namely, pH, ionic strength, and temperature, and cytotoxicity toward mammalian cells has restricted their more extensive applications. Hence, there is urgent need to develop highly biocompatible, non-toxic, and stable silver nanoparticles for wide-ranging environments and applications. In the present study, a simple, sustainable, cost-effective and green method has been developed to prepare highly stable aqueous colloidal silver nanoparticles (AgNPs-EW) using the ovalbumin, ovotransferrin, and ovomucoid of egg-white as reducing and capping agents accomplished under the irradiation of direct sunlight. Then, we evaluated the effects of freezing–drying (lyophilization) and freeze–thaw cycles on the stability of AgNPs-EW in aqueous solution under visual inspection, transmission electron microscopy, and absorbance spectroscopy. In addition, we studied the antibacterial activity against Salmonella typhimurium and Escherichia coli, carried out biocompatibility studies on chicken blood, and tested acute, chronic toxicity in Drosophila melanogaster. The results suggest that AgNPs-EW did not aggregate upon freeze-thawing and lyophilization, thus exhibiting remarkable stability. The antibacterial activity results showed that the AgNPs-EW had the highest antibacterial activity, and the minimum inhibitory concentration (MIC) of AgNPs-EW for E. Coli and S. typhimurium were 4 and 6 μg ml⁻¹, respectively. The biocompatibility study revealed that the AgNPs-EW did not induce any hemolytic effect or structural damage to the cell membranes of chicken erythrocytes up to a concentration of 12 μg ml⁻¹. Similarly, no acute and chronic toxicity was observed on melanization, fecundity, hatchability, viability, and the duration of development in the 1^st generation of Drosophila melanogaster at the concentration range of 10 mg L⁻¹ to 100 mg L⁻¹ of AgNPs-EW, and all the flies completed their full developmental cycle. Therefore, the present study successfully demonstrated the green and sustainable preparation of non-toxic AgNPs-EW having good biocompatibility, enhanced colloidal stability, and antibacterial activity. Hence, the synthesized AgNPs-EW could be used for the development of an antimicrobial formulation for controlling microbial infection.

For nearly a decade, silver nanoparticles (AgNPs) have been the most prevalent commercial nanomaterials products widely used in different biomedical applications due to their broad-spectrum antimicrobial activity.     

Robust,highly active,and stable supported Co(ii) nanoparticles on magnetic cellulose nanofiber-functionalized for the multi-component reactions of piperidines and alcohol oxidation

The new recyclable cobalt three-core magnetic catalyst obtained by anchoring a Schiff base ligand sector and cellulose nanofiber slings on MNP (Fe₃O₄) was prepared and named as MNP@CNF@ATSM–Co(ii). Separately, MNPs and CNF have adsorbent properties of great interest. In this way, this catalyst was designed to synthesize piperidine derivatives under solvent-free conditions and alcohol oxidation reactions in EtOH as the solvent. It should be noted that this catalyst is environmentally safe and does not need an external base. This MNPs@CNF@ATSM–Co(ii) separable catalyst has been evaluated using various characterization techniques such as FT-IR, XRD, FE-SEM, EDX, EDS, ICP, TGA, DLS, HRTEM, and VSM. The catalyst was compatible with a variety of benzyl alcohols, benzaldehydes, and amines derivatives, and gave complimentary coupling products with sufficient interest for all of them. The synergistic performance of Co (trinuclear) in the catalyst was demonstrated and its different homologs such as MNPs, MNPs@CNF, MNPs@CNF@ATS–Co(ii), and MNPs@CNF@ATSM–Co(ii) were separately synthesized and applied to a model reaction, and then their catalytic activity was investigated. Also, the performance of these components for the oxidation reaction of alcohols was evaluated. The advantages of the current protocol include the use of a sustainable and safe low temperature, eco-friendly solvent no additive, and long-term stability and magnetic recyclability of the catalyst for at least five successive runs, thus following green chemistry principles. This protocol is a benign and environment-friendly method for oxidation and heterocycle synthesis. This powerful super-magnetic catalyst can use its three arms to advance the reactions, displaying its power for multi-component reactions and oxidation.

The new recyclable cobalt three-core magnetic catalyst obtained by anchoring a Schiff base ligand sector and cellulose nanofiber slings on MNP (Fe₃O₄) was prepared and named as MNP@CNF@ATSM–Co(ii).     

Gold nanoparticle decorated dithiocarbamate modified natural boehmite as a catalyst for the synthesis of biologically essential propargylamines

Here, we prepare an Au NP decorated dithiocarbamate functionalized boehmite (γ-AlO(OH)@C-NHCS₂H·Au_NPs). This stepwise synthetic method gives an efficient, cost-effective, and green heterogenous Au-based nanocatalyst for the A³-coupling preparation of the biologically essential propargylamines. Different characterization methods, including FT-IR, XRD, SEM, TEM, EDX spectra, and elemental SEM-mapping, were employed to investigate the structure of the manufactured γ-AlO(OH)@C-NHCS₂H·Au_NPs. Then we used the prepared composite as a heterogeneous gold-based nanocatalyst for the one-pot A³-coupling preparation of propargyl amines by reacting a variety of aldehydes, amines, and phenylacetylene which exhibited promising results.

Here, we prepare an Au NP decorated dithiocarbamate functionalized boehmite (γ-AlO(OH)@C-NHCS₂H·Au_NPs).     

Cerium and tin oxides anchored onto reduced graphene oxide for selective catalytic reduction of NO with NH3 at low temperatures

A series of cerium and tin oxides anchored on reduced graphene oxide (CeO₂–SnO_x/rGO) catalysts are synthesized using a hydrothermal method and their catalytic activities are investigated by selective catalytic reduction (SCR) of NO with NH₃ in the temperature range of 120–280 °C. The results indicate that the CeO₂–SnO_x/rGO catalyst shows high SCR activity and high selectivity to N₂ in the temperature range of 120–280 °C. The catalyst with a mass ratio of (Ce + Sn)/GO = 3.9 exhibits NO conversion of about 86% at 160 °C, above 97% NO conversion at temperatures of 200–280 °C and higher than 95% N₂ selectivity at 120–280 °C. In addition, the catalyst presents a certain SO₂ resistance. It is found that the highly dispersed CeO₂ nanoparticles are deposited on the surface of rGO nanosheets, because of the incorporation of Sn⁴⁺ into the lattice of CeO₂. The mesoporous structures of the CeO₂–SnO_x/rGO catalyst provides a large specific surface area and more active sites for facilitating the adsorption of reactant species, leading to high SCR activity. More importantly, the synergistic interaction between cerium and tin oxides is responsible for the excellent SCR activity, which results in a higher ratio of Ce³⁺/(Ce³⁺ + Ce⁴⁺), higher concentrations of surface chemisorbed oxygen and oxygen vacancies, more strong acid sites and stronger acid strength on the surface of the CeSn(3.9)/rGO catalyst.

A series of cerium and tin oxides anchored on graphene oxide (CeO₂–SnO_x/rGO) catalysts are synthesized for selective catalytic reduction of NO with NH₃ in the temperature range of 120–280 °C.     

N-doped graphene/CoFe2O4 catalysts for the selective catalytic reduction of NOx by NH3

In this paper, CoFe₂O₄/graphene catalysts and N-doped graphene/CoFe₂O₄ (CoFe₂O₄/graphene-_N) catalysts were prepared using the hydrothermal crystallization method for the selective catalytic reduction of NO_x by NH₃. The results of the test showed that CoFe₂O₄/graphene catalysts exhibited the best denitrification activity when the loading was at 4% and the conversion rate of NO_x reached 99% at 250–300 °C. CoFe₂O₄/graphene-_N catalysts presented a better denitrification activity at low temperature than CoFe₂O₄/graphene catalysts, and the conversion rate of NO_x reached more than 95% at 200–300 °C. The intrinsic mechanism of CoFe₂O₄/graphene-_N catalysts in promoting SCR activity was preliminarily explored. The physicochemical properties of the samples were characterized using XRD, TEM, N₂ adsorption, XPS, NH₃-TPD, and H₂-TPR. The results indicated that nitrogen doping can improve the dispersion of CoFe₂O₄, and it also increased the acidic sites and the redox performance conducive to improving the denitrification activity of the catalysts. In addition, CoFe₂O₄/graphene-_N catalysts demonstrated a better resistance to water and sulfur than CoFe₂O₄/graphene catalysts.

N-doped graphene/CoFe₂O₄ presented better denitrification activity than CoFe₂O₄/graphene due to the more uniform distribution of CoFe₂O₄ and acidic sites etc.     

Preparation of stimuli responsive microgel with silver nanoparticles for biosensing and catalytic reduction of water pollutants

Herein, we report poly(N-isopropylacrylamide/2-acrylamido-2-methylpropane sulfonic acid) microgel fabricated with silver nanoparticles. The identification of copolymerization and functional groups in the bare microgel and those fabricated with silver nanoparticles was examined by Fourier transform infrared spectroscopy. The pH and temperature sensitivity of microgels was studied using dynamic light scattering. Thermogravimetric analysis was carried out to study the thermal stability. X-Ray diffraction patterns indicated the amorphous nature of bare microgel and crystalline nature of those containing silver nanoparticles. A bathochromic shift was found in the surface plasmon resonance of silver nanoparticles present in microgel with increase in pH of the medium. Moreover, the microgel containing silver nanoparticles served as an effective catalyst for reducing the toxic nitroaromatic pollutants and carcinogenic dyes. The microgel containing silver nanoparticles also showed good capability to serve as biosensor for the detection of hydrogen peroxide.

Poly(N-isopropylacrylamide/2-acrylamido-2-methylpropane sulfonic acid) microgel was prepared and fabricated with silver nanoparticles to design a material for dual functions of catalyst and sensor.     

Characterization of SR 121463A, a highly potent and selective, orally active vasopressin V2 receptor antagonist.

SR 121463A, a potent and selective, orally active, nonpeptide vasopressin V2 receptor antagonist, has been characterized in several in vitro and in vivo models. This compound displayed highly competitive and selective affinity for V2 receptors in rat, bovine and human kidney (0.6 < or = Ki [nM] < or = 4.1). In this latter preparation, SR 121463A potently antagonized arginine vasopressin (AVP)-stimulated adenylyl cyclase activity (Ki = 0.26+/-0.04 nM) without any intrinsic agonistic effect. In autoradiographic experiments performed in rat kidney sections, SR 121463A displaced [3H]AVP labeling especially in the medullo-papillary region and confirmed that it is a suitable tool for mapping V2 receptors. In comparison, the nonpeptide V2 antagonist, OPC-31260, showed much lower affinity for animal and human renal V2 receptors and lower efficacy to inhibit vasopressin-stimulated adenylyl cyclase (Ki in the 10 nanomolar range). Moreover, OPC-31260 exhibited a poor V2 selectivity profile and can be considered as a V2/V1a ligand. In normally hydrated conscious rats, SR 121463A induced powerful aquaresis after intravenous (0.003-0.3 mg/kg) or oral (0.03-10 mg/kg) administration. The effect was dose-dependent and lasted about 6 hours at the dose of 3 mg/kg p.o. OPC-31260 had a similar aquaretic profile but with markedly lower oral efficacy. The action of SR 121463A was purely aquaretic with no changes in urine Na+ and K+ excretions unlike that of known diuretic agents such as furosemide or hydrochlorothiazide. In addition, no antidiuretic properties have been detected with SR 121463A in vasopressin-deficient Brattleboro rats. Thus, SR 121463A is the most potent and selective, orally active V2 antagonist yet described and could be a powerful tool for exploring V2 receptors and the therapeutical usefulness of V2 blocker aquaretic agents in water-retaining diseases.