A system having a scope with a longitudinal length extending between a proximal end and a distal end includes a plurality of markers spaced along the longitudinal length. The system also includes a disassociation and positioning device that is configured to enhance unsedated transnasal endoscopic procedures by at least partially occluding the vision of a patient while enabling body cavity access, and optionally record and sense body functions such as temperature, heart rate and oxygenation of the blood stream. The system further includes a sensor integrated into the distraction device, wherein the sensor is configured to detect the markers on the longitudinal length of the scope.

Methods and apparatuses for blood glucose measurement are provided. A first glucose concentration in a body fluid of a user is detected based on a first measurement interval. A first blood glucose level of the user is determined based on the first glucose concentration. A glucose concentration measurement interval is changed from the first measurement interval to a second measurement interval according to an occurrence of an event. A second glucose concentration in the body fluid is detected based on the second measurement interval. A second blood glucose level of the user is determined based on the second glucose concentration.

Systems and methods for processing sensor data and self-calibration are provided. In some embodiments, systems and methods are provided which are capable of calibrating a continuous analyte sensor based on an initial sensitivity, and then continuously performing self-calibration without using, or with reduced use of, reference measurements. In certain embodiments, a sensitivity of the analyte sensor is determined by applying an estimative algorithm that is a function of certain parameters. Also described herein are systems and methods for determining a property of an analyte sensor using a stimulus signal. The sensor property can be used to compensate sensor data for sensitivity drift, or determine another property associated with the sensor, such as temperature, sensor membrane damage, moisture ingress in sensor electronics, and scaling factors.

Analyte sensors and methods of manufacturing same are provided, including analyte sensors comprising multi-axis flexibility. For example, a multi-electrode sensor system 800 comprising two working electrodes and at least one reference/counter electrode is provided. The sensor system 800 comprises first and second elongated bodies E1, E2, each formed of a conductive core or of a core with a conductive layer deposited thereon, insulating layer 810 that separates the conductive layer 820 from the elongated body, a membrane layer deposited on top of the elongated bodies E1, E2, and working electrodes 802′, 802″ formed by removing portions of the conductive layer 820 and the insulating layer 810, thereby exposing electroactive surface of the elongated bodies E1, E2.

Presented herein are systems, methods, and architectures related to functionalization of the metallic gates of field-effect transistors (FETs) and the use of the functionalized FETs as biochemical sensors in liquid samples. The functionalization can either be a molecularly imprinted polymer or a probe material. The functionalized FETs can be used in devices for analyte detection/quantification. In particular, the functionalized FETs are used in devices for the detection and/or quantification of cytokines (e.g. interleukin) and/or cholesterol (LDL or HDL).

A sensing device for detecting a characteristic of an analyte in a sample solution and method of making the same is provided. The device includes one or more sensors configured to measure a characteristic of an analyte in a sample. The device further includes a sample solution that contains the analyte and one or more interfering solutes, wherein the interfering solute reduces a performance characteristic of the one or more sensors. The device further includes a sensor solution in fluidic communication with the one or more sensors. The device further includes a hydrophobic barrier that separates the sample solution from the one or more sensors, wherein the hydrophobic barrier is permeable to the analyte and impermeable to the interfering solute, and wherein the hydrophobic barrier is in fluidic communication with the sample solution and the sensor solution.

A sweat sensing device is described. The sweat sensing device includes at least one swellable component. The sweat sensing device further includes a defined sweat collection area in fluid communication with the swellable component. The sweat sensing device further includes at least one first sensor for directly or indirectly measuring the dimension of the swellable component such that sweat generation rate and/or sweat volume can be calculated from the measure of dimension of the swellable component and the defined sweat collection area.

Analyte sensors and methods of manufacturing same are provided, including analyte sensors comprising multi-axis flexibility. For example, a multi-electrode sensor system 800 comprising two working electrodes and at least one reference/counter electrode is provided. The sensor system 800 comprises first and second elongated bodies E1, E2, each formed of a conductive core or of a core with a conductive layer deposited thereon, insulating layer 810 that separates the conductive layer 820 from the elongated body, a membrane layer deposited on top of the elongated bodies E1, E2, and working electrodes 802′, 802″ formed by removing portions of the conductive layer 820 and the insulating layer 810, thereby exposing electroactive surface of the elongated bodies E1, E2.

A device (154) for sensing sweat on skin (12) includes an analyte-specific sensor (166, 168) for sensing an analyte in sweat; a sweat stimulant reservoir (174, 176, 178) separated from a waste water reservoir (184) by a water-permeable, sweat-stimulant impermeable membrane (182). The waste water reservoir (184) has a wicking force that is not greater than the wicking force of the sweat stimulant reservoir (174, 176, 178). The waste water reservoir (184) removes excess water from sweat to prevent the dilution of the sweat stimulant from the sweat stimulant reservoir (174, 176, 178), thereby maintaining the effectiveness of the sweat stimulant.

A perspiration sensing system includes a sensor patch and a smart device. The sensor patch includes one or more perspiration sensing portions. The one or more perspiration sensing portions include an inlet having a predefined size to receive perspiration from a predefined number of sweat glands and an outlet for reducing back pressure. At least one perspiration sensing portion includes a channel having a colorimetric sensing material that changes color when exposed to perspiration. At least one perspiration sensing portion includes a colorimetric assay in a substrate that changes color when exposed to biochemical components of perspiration. The system further includes a smart device having a camera that can take a picture of the sensor patch and determine the volume, rate of perspiration, and/or biochemical components of the perspiration from the one or more perspiration sensing portions.