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Biomedical subjects

Peter C Searson

Publications and source records attributed to Peter C Searson.

14 recordsLinked to original sources

Bias-dependent admittance in hybrid bilayer membranes.

Artificial bilayer membranes provide a platform for bioelectronic devices based on their structural, sensing, and transport functions. In this letter, we report on the impedance response of an engineered membrane with a lower leaflet of octadecanethiol on gold and an outer leaflet of dioleoylphosphatidylcholine with the monomeric channel protein gramicidin. This hybrid bilayer exhibits an electrical response analogous to a solid-state diode: the admittance is very low (<10(-)(7) Omega(-)(1) cm(-)(2)) over a wide potential range but increases exponentially at negative potentials.

Gold↗

Kinetics of desorption of alkanethiolates on gold.

Self-assembled monolayers (SAMs) of alkanethiols can undergo reductive desorption and oxidative re-adsorption. The Coulombic efficiency of the oxidative re-adsorption reaction is dependent on the chain length and solution pH. We show that the loss of alkanethiols from the surface after reductive desorption can be explained by a simple model that takes into account diffusion of the thiolate into the bulk solution at a rate that is determined by the bulk solubility. These results provide a quantitative basis for the determination of the loss of alkanethiols from the surface after reductive desorption.

Journal Article↗

Orientation of a nanocylinder at a fluid interface.

A nanocylinder placed on a fluid interface can assume an end-on or side-on orientation, or it can immerse itself in the surrounding bulk phases. Any of these orientations can satisfy a mechanical force balance when the particle is small enough that gravitational effects are negligible. The orientation is determined by the surface energies of the fluid-solid, fluid-vapor, and vapor-solid surfaces. A comparison of the energy of each state allows phase diagrams to be defined in terms of the scaled aspect ratio x=2L/pir and the contact angle thetao, where L and r denote the nanocylinder length and radius, respectively. Line tension can also influence the orientations by changing the equilibrium contact angle theta and by increasing the energetic cost of the contact line. Phase diagrams accounting for positive line tensions Sigma are also constructed. These phase diagrams can be divided into two classes. In the first, over some range of x and Sigma, nanocylinders can be driven from side-on to end-on orientations with increasing Sigma. This transition terminates at a triple point where the side-on, end-on, and immersed energies are the same. In the second class, there is no triple point and, for a range of Sigma values, nanocylinders of all aspect ratios x prefer an end-on orientation. In all cases, for high enough Sigma, line tension drives a wetting transition similar to that already noted in the literature for spherical particles. The zero line tension predictions are compared favorably to experiment, in which functionalized gold nanowires made by template synthesis are spread at aqueous-gas interfaces, immobilized using a gel-fixation technique, and observed by scanning electron microscopy. The small aspect ratio particles (disks) were in an end-on configuration, while the longer nanowires were in a side-on orientation, in agreement with the theory.

Journal Article↗

Single nanoporous gold nanowire sensors.

Chemisorption from the gas or liquid phase can result in a measurable resistance change in a metallic material when at least one dimension is smaller than the mean free path for electrons. Here we report on the fabrication of single nanoporous gold nanowires and demonstrate that adsorption of an alkanethiol can be monitored in real time. Single nanowire devices were fabricated by in situ etching of Au0.18Ag0.82 alloy nanowires in dilute nitric acid. The evolution of the porous structure was characterized by monitoring the resistance change and comparing to cross-sectional images. The feature size of about 10 nm is less than the mean free path for electrons in bulk gold, and hence the resistance is dominated by surface scattering. Adsorption of a monolayer of octadecanethiol onto the nanoporous gold nanowire results in a resistance change of about 3%. The sensitivity factor of 1.0x10(-16) cm2 is comparable to values reported for adsorption at ultrathin films.

Journal Article↗

Kinetics of receptor directed assembly of multisegment nanowires.

We demonstrate the receptor directed end-to-end assembly of multisegment Au/Ni/Au nanowires under agitation in ethanol. The gold end-segments were functionalized with biotin-terminated thiol thereby restricting aggregation to end-to-end attachment via an avidin linkage. On mixing biotin-terminated nanowires with avidin-terminated nanowires, the average chain length is shown to increase linearly with time. The rate constant was independent of the nanowire concentration. Kinetic Monte Carlo simulations were used to model the self-assembly process, and we show that the directed end-to-end assembly of nanowires is similar to the polycondensation of linear polymers.

Avidin↗

Quantifying electrochemical nucleation and growth of nanoscale clusters using real-time kinetic data.

Electrochemical techniques are used widely for the fabrication of nanostructured materials, yet a quantitative understanding of nucleation and growth remains elusive. Here we probe electrochemical nucleation and growth of individual nanoclusters in real time by combining current-time measurements with simultaneous video imaging. We show discrepancies between the growth kinetics measured for individual nanoclusters and the predictions of models, and we describe a significant revision to conventional models that can explain the results. This improved understanding of nucleation and growth allows a more quantitative approach to the electrochemical fabrication of nanoscale structures.

Adsorption↗

Electrochemically programmed release of biomolecules and nanoparticles.

The controlled release of molecules or nanoparticle conjugates is an important tool for a wide range of applications in science and engineering. Here we demonstrate electrochemically programmed release of biomolecules and nanoparticles immobilized on patterned gold electrodes using the thiol-gold linkage. This technique exploits the reductive desorption of self-assembled monolayers and allows both spatially controlled release and regeneration of small molecules (e.g., drugs), biopolymers (e.g., peptides, proteins, DNA), protein assemblies (e.g., viruses), and nanoparticles (e.g., particle-DNA conjugates). Fluorescence microscopy is used to image the release of avidin and nanoparticles in phosphate-buffered saline and to determine the kinetics of desorption. We also demonstrate that the electrodes can be regenerated using the same conjugation scheme.

Avidin↗

Kinetic Monte Carlo simulations of nucleation and growth in electrodeposition.

Nucleation and growth during bulk electrodeposition is studied using kinetic Monte Carlo (KMC) simulations. Ion transport in solution is modeled using Brownian dynamics, and the kinetics of nucleation and growth are dependent on the probabilities of metal-on-substrate and metal-on-metal deposition. Using this approach, we make no assumptions about the nucleation rate, island density, or island distribution. The influence of the attachment probabilities and concentration on the time-dependent island density and current transients is reported. Various models have been assessed by recovering the nucleation rate and island density from the current-time transients.

Journal Article↗

Site-selective patterning using surfactant-based resists.

Patterned SAMs of alkanethiols on gold or silver are explored as resists for electrodeposition and exhibit surprisingly rich behavior depending on the overpotential and the length of the alkane chain. At small overpotentials, SAMs are positive resists with deposition only in the surfactant-free regions. At larger overpotentials, SAMs are negative resists with preferential deposition in the SAM-modified regions. Tunable surfactant-based resists are potentially versatile tools to dictate the deposition of materials and are demonstrated as a means of creating complex, three-dimensional structures.

Journal Article↗

Influence of the reactant concentrations on the synthesis of ZnO nanoparticles.

We report on the synthesis of ZnO nanoparticles from Zn(CH3CO2)2 and NaOH in 2-propanol. Nucleation and growth are fast, and hence at longer times the particle size is controlled by coarsening. The coarsening kinetics are independent of the Zn(CH3CO2)2 concentration between 0.5 and 1.25 mM at a fixed [Zn(CH3CO2)2]:[NaOH] ratio of 0.625. The width of the size distribution was found to increase only slightly with aging time. In addition, at a fixed Zn(CH3CO2)2 concentration of 1 mM, the kinetics are independent of the [Zn(CH3CO2)2]:[NaOH] ratio between 0.476 and 0.625. The presence of water in the reaction mixture was found to only slightly affect the coarsening kinetics for water contents larger than about 20 mM. For lower water concentrations, the nucleation and growth of ZnO were very slow. It can be concluded that the synthesis method described provides a reliable source of ZnO nanoparticles due to its insensitivity to the reactant concentrations and the presence of water.

Journal Article↗

Synthesis of ZnO nanoparticles in 2-propanol by reaction with water.

We report on the synthesis of ZnO particles from Zn(CH(3)CO(2))(2) in 2-propanol as a function of the concentration of water, in the absence of a base such as NaOH. Particles with diameters of 3-5 nm are formed depending on time, temperature, and water concentration. The nucleation and growth are slower than in the presence of NaOH, and at longer times the increase in particle size is dominated by diffusion-limited coarsening. The rate constant for coarsening increases with increasing water concentration up to 150 mM, above which the rate constant is 1.1 x 10(-4) cm(3) s(-1), independent of the water concentration. The width of the particle size distribution decreases with increasing water concentration, and at 250 mM water, the full width at half-maximum of the distribution function is essentially the same as for the synthesis of ZnO using NaOH as a reactant. The temperature dependence of coarsening is determined by the bulk solubility of the ZnO nanoparticles and yields an apparent activation energy of 1.12 eV. This is significantly larger than the activation energy of 0.35 eV for coarsening of ZnO from 1 mM Zn(CH(3)CO(2))(2) in 2-propanol with 1.6 mM NaOH.

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Multifunctional nanorods for gene delivery.

The goal of gene therapy is to introduce foreign genes into somatic cells to supplement defective genes or provide additional biological functions, and can be achieved using either viral or synthetic non-viral delivery systems. Compared with viral vectors, synthetic gene-delivery systems, such as liposomes and polymers, offer several advantages including ease of production and reduced risk of cytotoxicity and immunogenicity, but their use has been limited by the relatively low transfection efficiency. This problem mainly stems from the difficulty in controlling their properties at the nanoscale. Synthetic inorganic gene carriers have received limited attention in the gene-therapy community, the only notable example being gold nanoparticles with surface-immobilized DNA applied to intradermal genetic immunization by particle bombardment. Here we present a non-viral gene-delivery system based on multisegment bimetallic nanorods that can simultaneously bind compacted DNA plasmids and targeting ligands in a spatially defined manner. This approach allows precise control of composition, size and multifunctionality of the gene-delivery system. Transfection experiments performed in vitro and in vivo provide promising results that suggest potential in genetic vaccination applications.

Cells, Cultured↗

Influence of solvent on the growth of ZnO nanoparticles.

We have synthesized ZnO nanoparticles by precipitation from zinc acetate in a series of n-alkanols from ethanol to 1-hexanol as a function of temperature. In this system, nucleation and growth are relatively fast and, at longer times, the average particle size continues to increase due to diffusion-limited coarsening. During coarsening, the particle volume increases linearly with time, in agreement with the Lifshitz-Slyozov-Wagner (LSW) model. The coarsening rate increases with increasing temperature for all solvents and increases with alkanol chain length. We show that the rate constant for coarsening is determined by the solvent viscosity, surface energy, and the bulk solubility of ZnO in the solvent.

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Coarsening of metal oxide nanoparticles.

In solution phase synthesis of nanoparticles, processes such as coarsening and aggregation can compete with nucleation and growth in modifying the particle size distribution in the system. We show that coarsening of ZnO and TiO2 nanoparticles in solution follows the Lifshitz-Slyozov-Wagner rate law for diffusion controlled coarsening originally derived for colloidal systems with micrometer-sized particles, where the average particle size cubed is proportional to time. The rate constant for growth of ZnO in propanol is in the range 10(-4)-10(-2) nm3 x s(-1) and is dependent on the precursor anion and temperature. The coarsening of TiO2 nanoparticles from aqueous Ti(IV) alkoxide solutions is slower due to the low solubility of TiO2 with the rate constant in the range 10(-5)-10(-3) nm3 x s(-1) for temperatures between 150 degrees C and 220 degrees C. Epitaxial attachment of TiO2 particles becomes significant at higher temperatures and longer times. We show that the dominant parameters controlling the coarsening kinetics are solvent, precursor salt, and temperature.

Journal Article↗