Inverse-opal conducting polymer monoliths in microfluidic channels

Inverse opal monolithic flow-through structures of polyaniline (PANI) were achieved in microfluidic channels for lab-on-a-chip (LOC) applications. In order to achieve the uniformly porous monolith, polystyrene (PS) colloidal crystal (CC) templates were fabricated in channel. An inverse opal PANI structure was achieved on-chip, through a two-step process involving the electrochemical growth of PANI and subsequent removal of the template. The effect of electropolymerisation on these structures is discussed. It was found that growth time is critical in achieving an ordered structure with well-defined flow-through pores. This is significant in order to fabricate optimal porous PANI structures that maximise surface area of the monolith and also provide well-defined flow profiles through the micro-channel

Spectral functions at small energies and the electrical conductivity in hot, quenched lattice QCD

In lattice QCD, the Maximum Entropy Method can be used to reconstruct spectral functions from euclidean correlators obtained in numerical simulations. We show that at finite temperature the most commonly used algorithm, employing Bryan's method, is inherently unstable at small energies and give a modification that avoids this. We demonstrate this approach using the vector current-current correlator obtained in quenched QCD at finite temperature. Our first results indicate a small electrical conductivity above the deconfinement transition.Comment: 4 pages, v2: minor changes, footnote corrected, to appear in PR

Elucidation of the mode of action of a conductive polymer-based electrochemical immunosensor.

An amperometric biosensor has been developed, incorporating the electroactive polymer, polyaniline (PANI), which undergoes redox cycling, and can couple electrons directly from the enzyme active site, to the electrode surface. Construction of this sensor was achieved by electropolymerisation of polyvinylsulphonate-doped aniline onto the surface of a screen-printed carbon-paste electrode. Biomolecules could then be doped onto the surface of the polymer by electrostatic interactions with the polymer backbone. A key component in a biosensor is the recognition molecule and its immobilisation. This study investigates this process of protein immobilisation using amperometric and colorimetric techniques. Immobilisation of protein (enzyme or antibody) onto the transducer is achieved by electrostatic interactions. By applying bovine serum albumin (BSA) electrostatically at the electrode, efficient blocking of the electrode surface from the bulk solution was achieved above approximately 0.75 mg/ml. When horseradish peroxidase was immobilised on the electrode surface at various concentrations, optimal amperometric responses were achieved at approximately the same protein concentration. Determination of the number of molecules of protein immobilised on the surface of the electrode at this concentration was done using a colorimetric enzyme assay. It was found that under optimal immobilisation conditions, a protein monolayer was formed at the electrode surface. In the case of enzymes such as horseradish peroxidase (HRP), this provides simultaneous blocking of the electrode surface from bulk solution interactions as well as yielding optimal electron transfer properties

Immunoelectrochemical methods immunoelectrochemical of hormone anaylsis

Over the last decade, there has been considerable interest in the development of immunoelectrochemical assays, mainly due to the advantages offered by the combination of the selectivity of immunoassays with the great sensitivity and simplicity of modern electroanalytical techniques. However, immunoelectrochemical assays have not yet been exploited commercially, as transitions from the laboratory bench to large-scale manufacturing has proved difficult. The system described is an amperometric peroxide biosensor prepared by electrochemical deposition of horseradish peroxidase on an electroactive polymer, polyaniline. Polyaniline brings about mediatorless redox coupling between the electrode and biomolecular components attached to the surface. This assay will be the stepping-stone to developing an immunoelectrochemical method for the analysis of human chorionic gonadotropin (hCG), and other female hormones. The assay initially utilises glassy carbon electrodes for preliminary data, before being replaced with a commercially available electrode Euroflash TM, produced by Inverness Medical Limited TM. This electrode was utilised with a view to producing an electrochemical assay that complies with manufacturing requirements

Charmonium spectral functions in Nf=2 QCD

We report on a study of charmonium at high temperature in 2-flavour QCD. This is the first such study with dynamical fermions. Using an improved anisotropic lattice action, spectral functions are extracted from correlators in the vector and pseudoscalar channels. No signs of medium-induced suppression of the ground states are seen for temperatures up to 1.5T_c, while at T~2T_c there are clear signs of modifications. The current systematic and statistical uncertainties in our data, in particular the relatively coarse lattice and small volume, do not allow us to draw a firm conclusion at this stage.Comment: 6 pages, talk by JIS at Lattice 2005 (Non-zero temperature and density

Electrochemistry and application of a novel monosubstituted squarate electron-transfer mediator in a glucose oxidase-doped poly(phenol) sensor

Electrosynthetic poly(phenol) nanofilms were deposited in situ on platinum electrodes in the presence and absence of glucose oxidase. The synthesis charges and currents of the nonconducting polymer films were recorded at various applied potentials for films grown from 25–100 mM phenol concentrations. Film parameters such as the standard rate constant for film deposition, film thickness, and surface concentration of the poly(phenol) films were evaluated from the cyclic and step voltammograms of the polymerization process. A novel electron-transfer mediator consisting of monosubstituted 4-hydroxycyclobut-3-ene-1,2-dione (squarate) was used as a mediator for Pt/poly(phenol) nano-film/GOx amperometric glucose biosensors. Amperometric responses for 3-diphenylamino-4-hydroxycyclobut-3-ene-1,2- dione (diphenylaminosquarate: E°′ = of +328 mV/Ag-AgCl at pH 7.0)-mediated systems were measured by both steady-state amperometric and cyclic voltammetry. The sensor sensitivity was calculated to be 558 nA cm –2 (µM) –1

Polyaniline-silver hybrid materials for ink-jet printing

The synthesis of PANI/Ag hybrid materials has been carried out via a rapid chemical oxidative, in-situ polymerisation method, using silver nitrate and ammonium peroxydisulfate as oxidant precursors. These species react together to produce Ag2+, an oxidising intermediate which has greater oxidising power than either persulphate or Ag+ alone. The reaction thus proceeds at a much accelerated rate than that of pure PANI, approximately 6 times faster. Various characterisation techniques were used to characterise this new hybrid material, PANI-Ag. UV-vis absorption spectroscopy was used to follow the formation of polymer over time and monitor the rate at which the reaction progresses for both PANI and PANI-silver. It is evident from the absorption spectra that the polymer forms via the fully-oxidised pernigraniline state initially, before reducing back into the more stable emeraldine salt form. This process is significantly accelerated using both APS and AgNO3, as opposed to when using APS or AgNO3 alone. These new composites could potentially find use as functional materials for the printed electronics industry where new processable, hybrid materials as required for applications in sensing, memory, logic and photovoltaics

Inverse-opal conducting polymer monoliths in micro-fluidic channels.

Inverse opal monolithic flow-through structures of polyaniline (PANI) were achieved in microfluidic channels for lab-on-a-chip (LOC) applications. In order to achieve the uniformly porous monolith, polystyrene (PS) colloidal crystal (CC) templates were fabricated in channel. An inverse opal PANI structure was achieved on-chip, through a two-step process involving the electrochemical growth of PANI and subsequent removal of the template. The effect of electropolymerisation on these structures is discussed. It was found that growth time is critical in achieving an ordered structure with well-defined flow-through pores. This is significant in order to fabricate optimal porous PANI structures that maximise surface area of the monolith and also provide well-defined flow profiles through the micro-channel

EMµ: the next generation of separation science.

The extensive application of monolithic columns for HPLC is severely hindered by a lack of column-to-column reproducibility. EMμ (Electroactive Monolithic mChip) is a new concept that solves the significant reproducibility problems, as well as allowing miniaturization and improving overall efficiency through electrochemically controlled dynamic separations. This novel μchip has a micro-structured monolith fabricated from intelligent, electroactive polymer. By application of a specific potential, conducting polymers such as polyaniline (PANI) can be reproducibly grown and readily fine-tuned in terms of porosity, hydrophobicity and ionic capacity. This unique chip provides for an Electroactive Monolithic μchip capable of multi-dimensional chromatographic separations. Additionally, EMμ can exploit on-chip electrodes permitting incorporation of contactless conductivity detection (C4D). The monolith microstructuring (provided by templating) will provide reproducibility and improve efficiency by decreasing the A term of the Van Deemter equation. Furthermore, the use of these intelligent materials will enable gradient control and redox reactions to be exploited during separations of larges biomolecules