Abstract: A solid-state soil nutrient sensor comprising a sensor blade for inserting into the soil, the sensor blade comprising an electrically insulating substrate. The sensor may further comprise first and second electrodes disposed on the substrate, each electrode comprising: a sensing region located towards an end of the sensor blade inserted into the soil, and a contact region displaced away from the end of the sensor blade and electrically connected to the sensing region, for making an electrical connection to the electrode. The sensor may further comprise electrical insulation over each of the first and second electrodes between the sensing region and the contact region; a reference membrane over the sensing region of the first electrode; and a nutrient sensing membrane over the sensing region of the second electrode; and the reference and nutrient sensing membrane each comprise one or more layers of solvent-cast polymer.

Abstract: Disclosed herein is a more sensitive and accurate method of monitoring the pH of a solution, wherein the pH of the solution is quantified as a function of the electrochemical response of the solution in a two or three-electrode electrochemical cell, wherein the solution comprises a compound capable of undergoing a change in its oxidation state and/or structural conformation as a function of the pH of the solution. Also disclosed are highly accelerated methods and processes enabling analysis of specific polynucleotide sequences in a sample, e.g. a biological sample. The methods disclosed herein are, for example, useful for rapid screening of a large amount of samples in a point-of-care setting.

Abstract: The present invention relates to a method of a method of measuring a human body analyte concentration in an interstitial fluid, comprising the step of measuring a first electrical current I1 between a working electrode and a pseudo-reference electrode while applying a first potential between the working electrode and the pseudo-reference electrode, the first potential being less than a threshold potential, the magnitude of the first electrical current being greater than the magnitude of a predetermined first threshold current, and further measuring an output electrical current between the working electrode and the pseudo-reference electrode while applying a second electrical potential, the second electrical potential being greater than the first electrical potential.

Abstract: The present technology is generally directed to flow cartridges configured to measure and/or detect analytes in urine. A representative flow cartridge includes a urine inlet configured to receive urine from a patient, a flow channel fluidly coupled to the urine inlet, and sensors fluidly coupled to the flow channel that are configured to measure parameters of the urine flow. The sensors are aligned with corresponding sensing zones of the flow channel and are operable to generate sensor data based on urine flow through the sensing zones. In some embodiment, the sensor data is used to provide fluid therapy to the patient by adjusting an amount or rate of diuretic and/or hydration fluid based on the sensor data.

Abstract: A time-temperature integrating (TTi) indicator label comprises an initiator reservoir and a target reservoir, said initiator reservoir containing a pH modification system and said target reservoir comprising a pH responsive indicator. The pH responsive indicator may be photo-initiated. There is also provided a time-temperature indicator label comprising first and second reservoirs separated by a hydrogel valve, said valve allowing passage of an acid from said first reservoir to said second reservoir when the hydrogel valve is activated.

Abstract: A test microfluidic strip or cartridge comprising a blood sample collection zone, red blood cell isolation zone, lysis zone, reagents mixing zone, and sensing zone for measuring the enzymatic activity thiopurine methyltransferase is disclosed. The test strip or cartridge is disclosed to be operably connected to a metering device comprising a processor, a display and a memory card.

Abstract: A test microfluidic strip or cartridge comprising a blood sample collection zone, red blood cell isolation zone, lysis zone, reagents mixing zone, and sensing zone for measuring the enzymatic activity thiopurine methyltransferase is disclosed. The test strip or cartridge is disclosed to be operably connected to a metering device comprising a processor, a display and a memory card.

Abstract: A test microfluidic strip or cartridge comprising a blood sample collection zone, red blood cell isolation zone, lysis zone, reagents mixing zone, and sensing zone for measuring the enzymatic activity thiopurine methyltransferase is disclosed. The test strip or cartridge is disclosed to be operably connected to a metering device comprising a processor, a display and a memory card.

Abstract: A time-temperature integrating (TTi) indicator label comprises an initiator reservoir and a target reservoir, said initiator reservoir containing a pH modification system and said target reservoir comprising a pH responsive indicator. The pH responsive indicator may be photo-initiated. There is also provided a time-temperature indicator label comprising first and second reservoirs separated by a hydrogel valve, said valve allowing passage of an acid from said first reservoir to said second reservoir when the hydrogel valve is activated.

Abstract: A time-temperature integrating (TTi) indicator label comprises an initiator reservoir and a target reservoir, said initiator reservoir containing a pH modification system and said target reservoir comprising a pH responsive indicator. The pH responsive indicator may be photo-initiated. There is also provided a time-temperature indicator label comprising first and second reservoirs separated by a hydrogel valve, said valve allowing passage of an acid from said first reservoir to said second reservoir when the hydrogel valve is activated.

Abstract: A method for measuring bilirubin levels in a subject. The method can include the steps of providing a sample to be measured from the subject, wherein the sample comprises bilirubin bound to albumin; adding a release agent to the sample, the release agent configured to release the bound bilirubin from the albumin; measuring electrochemical data of the sample using an electrochemical cell; and determining a total serum bilirubin concentration of the sample using the electrochemical data. This method is capable of providing a simpler, faster, and more robust measurement when compared to traditional bilirubin assay methods.

Abstract: A method for measuring bilirubin levels in a subject. The method can include the steps of providing a sample to be measured from the subject, wherein the sample comprises bilirubin bound to albumin; adding a release agent to the sample, the release agent configured to release the bound bilirubin from the albumin; measuring electrochemical data of the sample using an electrochemical cell; and determining a total serum bilirubin concentration of the sample using the electrochemical data. This method is capable of providing a simpler, faster, and more robust measurement when compared to traditional bilirubin assay methods.

Abstract: A method for measuring bilirubin levels in a subject. The method can include the steps of providing a sample to be measured from the subject, wherein the sample comprises bilirubin bound to albumin; adding a release agent to the sample, the release agent configured to release the bound bilirubin from the albumin; measuring electrochemical data of the sample using an electrochemical cell; and determining a total serum bilirubin concentration of the sample using the electrochemical data. This method is capable of providing a simpler, faster, and more robust measurement when compared to traditional bilirubin assay methods.

Abstract: A method for measuring bilirubin levels in a subject. The method can include the steps of providing a sample to be measured from the subject, wherein the sample comprises bilirubin bound to albumin; adding a release agent to the sample, the release agent configured to release the bound bilirubin from the albumin; measuring electrochemical data of the sample using an electrochemical cell; and determining a total serum bilirubin concentration of the sample using the electrochemical data. This method is capable of providing a simpler, faster, and more robust measurement when compared to traditional bilirubin assay methods.

Abstract: A method for measuring bilirubin levels in a subject. The method can include the steps of providing a sample to be measured from the subject, wherein the sample comprises bilirubin bound to albumin; adding a release agent to the sample, the release agent configured to release the bound bilirubin from the albumin; measuring electrochemical data of the sample using an electrochemical cell; and determining a total serum bilirubin concentration of the sample using the electrochemical data. This method is capable of providing a simpler, faster, and more robust measurement when compared to traditional bilirubin assay methods.