Nonenzymatic Glucose Sensor Using Bimetallic Catalysts.

Bimetallic glucose oxidation electrocatalysts were synthesized by two electrochemical reduction reactions carried out in series onto a titanium electrode. Nickel was deposited in the first synthesis stage followed by either silver or copper in the second stage to form Ag@Ni and Cu@Ni bimetallic structures. The chemical composition, crystal structure, and morphology of the resulting metal coating of the titanium electrode were investigated by X-ray diffraction, energy-dispersive X-ray spectroscopy, X-ray photoelectron spectroscopy, and electron microscopy. The electrocatalytic performance of the coated titanium electrodes toward glucose oxidation was probed using cyclic voltammetry and amperometry. It was found that the unique high surface area bimetallic structures have superior electrocatalytic activity compared to nickel alone. The resulting catalyst-coated titanium electrode served as a nonenzymatic glucose sensor with high sensitivity and low limit of detection for glucose. The Cu@Ni catalyst enables accurate measurement of glucose over the concentration range of 0.2-12 mM, which includes the full normal human blood glucose range, with the maximum level extending high enough to encompass warning levels for prediabetic and diabetic conditions. The sensors were also found to perform well in the presence of several chemical compounds found in human blood known to interfere with nonenzymatic sensors.

Leveraging Arylboronic Acid - Cellulose Binding as a Versatile and Scalable Approach to Hydrophobic Patterning.

Paper-based analytical devices, or µPADs, have proven to be valuable bioanalytical tools for a broad range of applications. New methods for µPAD fabrication are needed, however, to facilitate their mass production at a competitive cost. To address this need, we report the use of a boronic acid-containing siloxane polymer (BorSilOx) for patterning hydrophobic barriers for µPADs. This material functions by covalently binding to hydroxyl groups in the paper substrate. It is compatible with inkjet printing or roll-to-roll (stamping) processes, as demonstrated here using three different deposition methods. BorSilOx is able to render a broad range of cellulosic materials (from paper towels to wood) hydrophobic, with contact angle measurements demonstrating superhydrophobicity in many cases. We further demonstrate the utility of the polymer in µPADs via assays for pH and glucose.

Figure-of-Merit Characterization of Hydrogen-Bond Acidic Sorbents for Waveguide-Enhanced Raman Spectroscopy.

The optical properties of several hydrogen-bond acidic sorbent materials are evaluated in situ to assess their suitability for waveguide-enhanced Raman spectroscopy (WERS) of vapor-phase organophosphonates. A number of characteristics critical to WERS are evaluated for each sorbent: infrared absorption, Raman spectral background, and the limit of detection for a test hydrogen-bond-basic analyte (dimethyl methylphosphonate, DMMP). We describe the chemical properties of the sorbents that differentiate their optical properties for sensing. Then, we introduce a sorbent figure-of-merit that quantifies these differences and provides a framework to assess the quality of newly developed sorbent materials.

Antibacterial Copper-Hydroxyapatite Composite Coatings via Electrochemical Synthesis.

Antibacterial copper-hydroxyapatite (Cu-HA) composite coatings on titanium were synthesized using a novel process consisting of two consecutive electrochemical reactions. In the first stage, HA nanocrystals were grown on titanium using the cathodic electrolytic synthesis. The HA-coated titanium was then used as the cathode in a second reaction stage to electrochemically reduce Cu2+ ions in solution to metallic Cu nanoparticles. Reaction conditions were found that result in nanoscale Cu particles growing on the surface of the HA crystals. The two-stage synthesis allows facile control of copper content in the HA coatings. Antibacterial activity was measured by culturing Escherichia coli (Gram-negative) and Staphylococcus aureus (Gram-positive) in the presence of coatings having varying copper contents. The coatings displayed copper concentration-dependent antibacterial activity against both types of bacteria, likely due to the slow release of copper ions from the coatings. The observation of antibacterial activity from a relatively low loading of copper on the bioactive HA support suggests that multifunctional implant coatings can be developed to supplement or supplant prophylactic antibiotics used in implant surgery that are responsible for creating resistant bacteria strains.

Enhanced Photocatalytic Activity of TiO2 Nanoparticles Supported on Electrically Polarized Hydroxyapatite.

Fast recombination of photogenerated charge carriers in titanium dioxide (TiO2) remains a challenging issue, limiting the photocatalytic activity. This study demonstrates increased photocatalytic performance of TiO2 nanoparticles supported on electrically polarized hydroxyapatite (HA) films. Dense and thermally stable yttrium and fluorine co-doped HA films with giant internal polarization were synthesized as photocatalyst supports. TiO2 nanoparticles deposited on the support were then used to catalyze the photochemical reduction of aqueous silver ions to produce silver nanoparticles. It was found that significantly more silver nanoparticles were produced on polarized HA supports than on depolarized HA supports. In addition, the photodegradation of methyl orange with TiO2 nanoparticles on polarized HA supports was found to be much faster than with TiO2 nanoparticles on depolarized HA supports. It is proposed that separation of photogenerated electrons and holes in TiO nanoparticles is promoted by the internal polarization of the HA support, and consequently, the recombination of charge carriers is mitigated. The results imply that materials with large internal polarization can be used in strategies for enhancing quantum efficiency of photocatalysts.

α-Calcium Sulfate Hemihydrate Nanorods Synthesis: A Method for Nanoparticle Preparation by Mesocrystallization.

The past decades have witnessed great advances in nanotechnology since tremendous efforts have been devoted for the design, synthesis, and application of nanoparticles. However, for most mineral materials such as calcium sulfate, it is still a challenge to prepare their nanoparticles, especially with uniform size and high monodispersity. In this work, we report a route to regulate the morphology and structure of α-calcium sulfate hemihydrate (α-HH) and successfully synthesize and stabilize its mesocrystals for the first time. The ellipsoidal mesocrystals in length of 300-500 nm are composed by α-HH nanoparticles arranged in the same crystallographic fashion and interspaced with EDTA. The time-dependent experiments indicate the α-HH aggregates evolve from irregular structure to mesocrystal structure with the subsequent growth of subunits and then partially fuse into single crystals. Disorganizing the mesocrystal structure before the emergence of fusion reaps α-HH nanorods in a length of 30-80 nm and a width of 10-20 nm with high monodispersion. This ingenious concept paves an alternative way for nanoparticle preparation and is readily extended to other inorganic systems.

Synthesis of poly(N-isopropylacrylamide) particles for metal affinity binding of peptides.

Temperature-sensitive poly(N-isopropylacrylamide) (PNIPAM) microgel particles with metal affinity ligands were prepared for selective binding of peptides containing the His6-tag (six consecutive histidine residues). The PNIPAM particles were copolymerized with the functional ligand vinylbenzyl iminodiacetic acid (VBIDA) through a two-stage dispersion polymerization using poly(N-vinyl pyrrolidone) (PVP) as a steric stabilizer. The resulting particles were monodisperse in size and colloidally stable over a wide range of temperature and ionic strength due to chemically grafted PVP chains. The particle size was also found to be sensitive to ionic strength and pH of the aqueous environment, likely due to the electrostatic repulsion between ionized VBIDA groups. Divalent nickel ions were chelated to the VBIDA groups, allowing selective metal affinity attachment of a His6-Cys peptide. The peptide was released upon the addition of the competitive ligand imidazole, demonstrating that the peptide attachment to the particles is reversible and selective.

Two-dimensional patterns of poly(N-isopropylacrylamide) microgels to spatially control fibroblast adhesion and temperature-responsive detachment.

Thermoresponsive poly(N-isopropyl acrylamide) (PNIPAM) microgels were patterned on polystyrene substrates via dip coating, creating cytocompatible substrates that provided spatial control over cell adhesion. This simple dip-coating method, which exploits variable substrate withdrawal speeds forming particle suspension stripes of densely packed PNIPAM microgels, while spacings between the stripes contained sparsely distributed PNIPAM microgels. The assembly of three different PNIPAM microgel patterns, namely, patterns composed of 50 µm stripe/50 µm spacing, 50 µm stripe/100 µm spacing, and 100 µm stripe/100 µm spacing, was verified using high-resolution optical micrographs and ImageJ analysis. PNIPAM microgels existed as monolayers within stripes and spacings, as revealed by atomic force microscopy (AFM). Upon cell seeding on PNIPAM micropatterned substrates, NIH3T3 fibroblast cells preferentially adhered within spacings to form cell patterns. Three days after cell seeding, cells proliferated to form confluent cell layers. The thermoresponsiveness of the underlying PNIPAM microgels was then utilized to recover fibroblast cell sheets from substrates simply by lowering the temperature without disrupting the underlying PNIPAM microgel patterns. Harvested cell sheets similar to these have been used for multiple tissue engineering applications. Also, this simple, low-cost, template-free dip-coating technique can be utilized to micropattern multifunctional PNIPAM microgels, generating complex stimuli-responsive substrates to study cell-material interactions and allow drug delivery to cells in a spatially and temporally controlled manner.

Control of α-calcium sulfate hemihydrate morphology using reverse microemulsions.

Alpha calcium sulfate hemihydrate (α-HH) is an important class of cementitious material and exhibits considerable morphology-dependent properties. In the reverse microemulsions of water/n-hexanol/cetyltrimethylammonium bromide (CTAB)/sodium dodecyl sulfonate (SDS), the morphology and aspect ratio of α-HH are successfully controlled by adjusting the mass ratio of CTAB/H(2)O and the concentration of SDS. As the ratio of CTAB/H(2)O is increased from 1.3 to 4.5, the crystal length decreases from 120 to 150 µm to 0.5-1.2 µm with the corresponding aspect ratio reduced sharply from 180 to 250 to 2-7. With increasing SDS concentration, the crystal morphology gradually changes from submicrometer-sized long column to rod, hexagonal plate, and even nanogranule. The preferential adsorption of CTAB on the side facets and SDS on the top facets contributes to the morphology control. This work presents a simple, versatile, highly efficient approach to controlling the morphology of α-HH on a large scale and will offer more opportunities for α-HH multiple applications.

Fabrication of size-tunable TiO2 tubes using rod-shaped calcite templates.

Titania tubes with tunable wall thickness were produced by the sol-gel reaction of titanium(IV) n-butoxide in the presence of rod-shaped calcite particles that act as templates. A shell of amorphous titania was deposited around the calcite particles by sol-gel synthesis. The titania was crystallized to the anatase or rutile phase by sintering at different temperatures, and then acid etching was used to remove the calcite core, leaving hollow titania tubes. The influences of several parameters on the final particle formation were investigated, including calcite templates, surfactant, the method of adding reagents, and catalyst. The average width of the prepared titania tubes ranges from nearly 100 nm to 1 microm, with wall thickness ranging from approximately 70 to 300 nm. A possible growth mechanism of the titania tubes is presented. The ability to control titania tube size and crystal structure is important for photocatalysis, photovoltaics, and other applications. The fabrication approach presented is applicable to form tubes of other oxide materials by sol-gel synthesis.

Formation of rod-shaped calcite crystals by microemulsion-based synthesis.

Novel rod-shaped calcite crystals are formed by precipitation from cetyltrimethylammonium bromide (CTAB)/1-pentanol/cyclohexane microemulsions containing calcium chloride and ammonium carbonate. The calcium carbonate initially precipitates as hexagon-shaped vaterite crystals. The vaterite crystals transform to unusual rod-shaped calcite crystals over several days. The rod-shaped calcite crystals are prismatic, with the longest crystal axis displaying (110) crystal faces. A possible mechanism of crystal growth is discussed. The elongated shape of the crystals facilitates the assembly into hierarchical structures and can allow the crystals to be used as templates for fabricating advanced materials.

Carbon dioxide emulsion assisted loading of polymer microspheres toward sustained release materials.

An organic solvent-free method for encapsulating progesterone at high loadings within micron-sized inert latex polymer beads is reported. This approach makes use of a polymeric surfactant to emulsify carbon dioxide into an aqueous latex suspension. In this way, preformed approximately 4 microm polystyrene (PS) microparticles surface-grafted with poly(N-vinylpyrrolidone) (PVP) were plasticized and swollen followed by rapid partitioning of progesterone into the polymer matrix. The as-prepared polystyrene beads incorporated over 10% progesterone by weight while maintaining their initial size and morphological uniformity. Dissolution experiments were also carried out to obtain the release profile of progesterone entrapped within the PVP/PS particles.