Abstract: An integrated ion-sensitive probe is provided. In an example, an ion-sensitive probe can include a semiconductor substrate and a first passive electrode attached to the semiconductor substrate. The first passive electrode can be configured to contact a solution and to provide a first electrical voltage as function of a concentration of an ion within the solution. In certain examples, a passive reference electrode can be co-located on the semiconductor substrate. In some examples, processing electronics can be integrated on the semiconductor substrate.

Abstract: Proposed is a multifunctional corrosion probe system that can sense both general corrosion and focusing corrosion of a pipe on the basis of physical changes of stacked specimens. The multifunctional corrosion probe system includes a sensing unit having a plurality of specimens and a plurality of insulating layers, which are alternately stacked, and configured to be inserted into a pipe, anode wires having first ends installed on first sides of the plurality of specimens, respectively, cathode wires having second ends installed on second sides of the plurality of specimens, respectively, a power control unit to which second ends of the plurality of anode wires and second ends of the plurality of cathode wires are connected, and a graph output unit connected with the power control unit, estimating a current that is output from the power control unit, and outputting a resistance graph and a current graph.

Abstract: The invention relates to the field of nanopores, in particular to engineered Fragaceatoxin C (FraC) nanopores and their application in analyzing biopolymers and other (biological) compounds, such as single-molecule (protein) sequencing. Provided is a system comprising oligomeric FraC nanopores comprised in a lipid bilayer, wherein the sum of the nanopore fraction in the heptameric (Type II) state and the nanopore fraction in the hexameric (Type III) state represents at least 60% of the total number of FraC nanopores.

Abstract: An apparatus for in-situ monitoring and measuring of general corrosion and localized microbiologically influenced corrosion (MIC) in a simulated environment is provided. The apparatus includes a chamber containing an electrolyte solution and a microbe specimen. The chamber includes a pair of electrical resistance (ER) probes that measure a current flowing through the electrolyte solution and a general corrosion rate on the surface of the ER probes. The chamber also includes a pair of electrochemical noise (EN) probes. The EN probes are aligned to face one another such that the EN probes measure a localized corrosion rate on the surface of the EN probes and measure the influence of gravity on MIC. The apparatus measures the general and localized corrosion rates simultaneously without polarizing the surface of the ER and EN probes.

Abstract: The device uses pulsed electric fields to prevent the growth of biofilm and the attachment of bacteria to targeted surfaces. The device sets up an electric field around or surrounding the surface itself. These pulsed electric fields disrupt biofilm formation and bacterial attachment to surfaces. The device is meant to prevent the formation of biofilm or attachment of bacteria to a surface as opposed to disinfecting the surface.

Abstract: Embodiments of the present application relate to compositions comprising a sieving component, and a surface interactive component comprising an interpenetrating polymer network that includes comprising a hydrophilic N-vinyl amide polymer and a hydrophilic acrylamide polymer. The compositions are used for separating analytes by capillary electrophoresis. Kits and methods including the compositions for separating analytes by capillary electrophoresis are also provided.

Abstract: Described herein are methods, systems and devices for rapidly detecting biomarkers in a biological sample.

Abstract: Processes for conductive material nanogap formation have been developed that include: providing a base material, wherein the base material is either solid or comprises a micropore that extends through the first layered material, and wherein the micropore comprises a top opening, a bottom opening, and a volume boundary, applying a conductive material sheet to the first layered material, wherein the conductive material sheet covers the top opening of the micropore, applying two conducting electrodes to the conductive material sheet, so that each one of the conducting electrodes is positioned on either side of the micropore, applying an etch mask that covers at least a part of the conductive material sheet, the top opening of the micropore (if present), or a combination thereof, applying a passivation layer over at least the etch mask, fabricating a hole in the passivation layer directly above the top opening of the micropore, and applying at least one voltage pulse through the at least one conducting electrode

Abstract: Systems and methods are provided for trapping and electrically monitoring molecules in a nanopore sensor. The nanopore sensor comprises a support structure with a first and a second fluidic chamber, at least one nanopore fluidically connected to the two chambers, and a protein shuttle. The protein shuttle comprises an electrically charged protein molecule, such as Avidin. The nanopore can be a Clytosolin A. A method can comprise applying a voltage across the nanopores to draw protein shuttles towards the nanopores. The ionic current through each or all of the nanopores can be concurrently measured. Based on the measured ionic current, blockage events can be detected. Each blockage event indicates a capture of a protein shuttle by at least one nanopore. Each blockage event can be detected through a change of the total ionic current flow or a change in the ionic current flow for a particular nanopore.

Abstract: An electrochemical measurement system (1) includes: an insertion mechanism (4) which is capable of moving relative to a microplate (2) having a plurality of reactors which are arrayed and which contain a respective plurality of types of solutions, the plurality of types of solutions being mixtures of a plurality of types of mother liquids in different proportions; and a microelectrode unit (19) which is attached to the insertion mechanism (4) such that the microelectrode unit (19) is capable of being inserted into the plurality of types of solutions contained in the plurality of reactors.

Abstract: A method and system for determining a concentration of one or more analytes in whole blood is provided. In one aspect of the invention, the system includes a channel configured to carry whole blood. The system further includes a light source configured to emit light on the channel. Additionally, the system includes an actuation module associable with the channel, wherein the actuation module is configured to generate a cell-free plasma layer in the channel. Furthermore, the system includes an optical module associable with the channel.

Abstract: The subject of the present invention is the sensor for the impedance measurements of the biological or chemical factor sample in the potentiostat system comprising the reference electrode RE and counting electrode CE with the electric contacts leading to the edge of the sensor in the form of the edge connector characterised in that it contains n working electrodes WEn, wherein n>2 and preferably n is in the range 2 to 256, and the reference electrode RE is common for all working electrodes WEn and the fragment thereof present by the working electrode WEn forms the measuring segment RE-CE-WEn. The subject of the invention is also the detection method of the chemical or biological factor in the sample using such a sensor.

Abstract: Disclosed is a filter and a filter case using CDI, and a water purifier and a water softener using the filter case. Specifically, the filter case comprises: a case having a cylindrical shape and including a receiving space formed therein; a first cover having an inlet formed in the center thereof and configured to close one side of the case; and a second cover having an outlet formed in the center thereof and configured to close the other side of the case.

Abstract: Methods and analyte sensors including a sensor tail comprising at least a first working electrode and a second working electrode that are spaced apart from one another along a length of the sensor tail. A first active area is disposed upon a surface of the first working electrode and a second active area is disposed upon a surface of the second working electrode, the first active area and the second active area being responsive to different analytes. A mass transport limiting membrane is deposited upon the first active area and the second active area by sequential dip coating operations, and the mass transport limiting membrane comprises a bilayer membrane portion overcoating the first active area and a homogeneous membrane portion overcoating the second active area.

Abstract: Aiming at achievement of timely installation of the cartridge, sequential execution of the pretreatment process in the order of installation of the cartridge, and individual shifting of the process to the electrophoresis process upon completion of the pretreatment process, the electrophoresis device according to the present invention includes a plurality of capillaries each filled with a separation medium, a thermostat chamber for holding the capillaries at a predetermined temperature, an irradiation detector which executes light irradiation and detection in an electrophoresis process using the capillaries, a high voltage power supply unit for voltage application to the capillaries, a liquid feeding mechanism for feeding the separation medium to the capillaries, and an autosampler for conveying containers each holding a reagent or a sample to the capillary. The voltage application to the capillaries by the high voltage power supply unit is controlled for each of the capillaries.

Abstract: Multiple enzymes may be present in the active area(s) of an electrochemical sensor to facilitate analysis of one or more analytes. The multiple enzymes may function independently to detect several analytes or in concert to detect a single analyte. One sensor configuration includes a first active area and a second active area, where the first active area has an oxidation-reduction potential that is sufficiently separated from the oxidation-reduction potential of the second active area to allow independent signal production. Some sensor configurations may have an active area overcoated with a multi-component membrane containing two or more different membrane polymers. Sensor configurations having multiple enzymes capable of interacting in concert include those in which a first enzyme converts an analyte into a first product and a second enzyme converts the first product into a second product, thereby generating a signal at a working electrode that is proportional to the analyte concentration.

Abstract: In an example, a sensing system includes a pH sensor. The pH sensor includes two electrodes and a conductive channel operatively connected to the two electrodes. A complex is attached to the conductive channel of the pH sensor. The complex includes a polymerase linked to at least one pH altering moiety that is to participate in generating a pH change within proximity of the conductive channel from consumption of a secondary substrate in a fluid that is exposed to the pH sensor. The at least one pH altering moiety is selected from the group consisting of an enzyme, a metal coordination complex, a co-factor, and an activator.

Abstract: Magnesium ion selective electrode membranes and the preparation thereof. The membranes are rendered highly selective for magnesium ions by the addition of acidic groups to the preferably PVC membrane, either by introducing a lipophilic compound comprising an acidic group covalently linked to a C4-C18 alkyl-substituted phenyl group (e.g. bis-4-octylphenyl phosphoric acid) into the membrane comprising the magnesium selective ionophore (e.g. a neutral ionophore 1,10-phenanthroline derivative) or by covalently linking an acidic (e.g. a carboxylic) group to the ionophore (e.g. a 1,10-phenanthroline derivative).

Abstract: Analyte sensors responsive at low working electrode potentials may comprise an active area upon a surface of a working electrode, wherein the active area comprises a polymer, a redox mediator covalently bonded to the polymer, and at least one analyte-responsive enzyme covalently bonded to the polymer. A specific redox mediator responsive at low potential may have a structure of wherein G is a linking group covalently bonding the redox mediator to the polymer. A mass transport limiting membrane permeable to the analyte may overcoat the active area. In some sensor configurations, the mass transport limiting membrane may comprise a membrane polymer crosslinked with a branched crosslinker comprising three or more crosslinkable groups, such as polyethylene glycol tetraglycidyl ether.

Abstract: Processes for preparing ion selective membranes are presented which have selectivity for a primary analyte (in particular magnesium) as well as another ion (in particular calcium), wherein said process comprises addition of a) an ionophore (in particular 1,10-phenanthroline), b) a lipophilic salt containing said primary analyte (in particular hemi-magnesium bis[4-octylphenyl]phosphate) and c) a lipophilic salt containing said other ion (in particular hemi-calcium bis[4-octylphenyl]phosphate). Also, ion selective membranes are presented which are prepared using said processes, in particular to membranes selective for magnesium ions. In further aspects, electrodes and potentiometric sensors are presented comprising such membranes and the use thereof for determining ion concentrations in samples.