This document describes a conformable substrate that includes a hydrogel having adhesion-promoting moieties, said adhesion-promoting moieties comprising one or more catechol groups. The conformable substrate includes an array of microelectrodes bonded to the hydrogel by the adhesion-promoting moieties via the one or more catechol groups. This document also describes a method for transfer printing of an electronic structure to a hydrogel. The method includes the steps of coating a donor substrate with a film of polyacrylic acid, crosslinking the film of polyacrylic acid in a solution comprising divalent ions, patterning a microelectrode array onto the crosslinked film of polyacrylic acid, laminating an adhesive hydrogel substrate onto the donor substrate coated by the crosslinked film of polyacrylic acid comprising the patterned microelectrode array, and separating the crosslinked film of polyacrylic acid from the donor substrate in a monovalent solution.

Provided is an electrode including: a polarizable electrode layer; and a non-polarizable electrode layer laminated on the polarizable electrode layer. The non-polarizable electrode layer includes silver, silver chloride, and a corrosion inhibitor for the silver. The corrosion inhibitor is a polymer-based corrosion inhibitor.

Disclosed herein are improved neural depth probes for detection and stimulation, along with various related improved components, devices, methods, and technologies. More specifically, the devices are layered depth electrodes with at least two layers, with each of the layers containing at least one thin-film trace disposed thereon. Each of the devices can also have a plurality of layers with at least two traces on each layer and contacts coupled to each trace.

A flexible and/or stretchable structural system for transmitting electrical signal between first and second rigid portions comprises a body structure and said first and second portions arranged to said body structure. The modulus of elasticity of said first portion is lower than the corresponding modulus of elasticity of said second portion. In addition the modulus of elasticity of said body structure is lower than the corresponding modulus of elasticity of said second portion. The system comprises also an interface portion, such as e.g. an electrically conducting fabric, textile or knit, which is arranged to said body structure and between said first and second portions. The interface portion electrically connects said first and second portions. The modulus of elasticity of said interface portion is lower than the corresponding modulus of elasticity of said second portion.

Devices and methods are provided for continuous measurement of an analyte concentration. The device can include a sensor having a plurality of sensor elements, each having at least one characteristic that is different from other sensor(s) of the device. In some embodiments, the plurality of sensor elements are each tuned to measure a different range of analyte concentration, thereby providing the device with the capability of achieving a substantially consistent level of measurement accuracy across a physiologically relevant range. In other embodiments, the device includes a plurality of sensor elements each tuned to measure during different time periods after insertion or implantation, thereby providing the sensor with the capability to continuously and accurately measure analyte concentrations across a wide range of time periods. For example, a sensor system 180 is provided having a first working electrode 150 comprising a first sensor element 102 and a second working electrode 160 comprising a second sensor element 104, and a reference electrode 108 for providing a reference value for measuring the working electrode potential of the sensor elements 102, 104.

Transdermal microneedles continuous monitoring system is provided. The continuous system monitoring includes a substrate, a microneedle unit, a signal processing unit and a power supply unit. The microneedle unit at least comprises a first microneedle set used as a working electrode and a second microneedle set used as a reference electrode, the first and second microneedle sets arranging on the substrate. Each microneedle set comprises at least a microneedle. The first microneedle set comprises at least a sheet having a through hole on which a barbule forms at the edge. One of the sheets provides the through hole from which the barbules at the edge of the other sheets go through, and the barbules are disposed separately.

A method of preparation of a gold electrode, which includes the steps of: a) inkjet printing on a substrate an ink including gold nanoparticles functionalized with a compound Cap of formula (I) HS-A-Polyalkylene glycol (I), wherein A is a bound or an alkyl chain having 1 to 12 carbon atoms and wherein polyalkylene glycol is polyethylene glycol, polypropylene glycol or a mixture thereof; and b) annealing printed ink, wherein the compound Cap has an average molar mass of less than 500 g/mol, preferably an average molar mass of about 200 g/mol. Also, an electrode obtainable by the method of the invention, a sensor including the electrode and the use of the sensor.

The present disclosure discloses a textile-type multi-channel high-sensitivity sensing dry electrode plate including a body, a conductive cloth and at least one electrode connection part. The body is a sheet-shaped body. The conductive cloth is arranged on one side of the body. The conductive cloth includes at least one electrode part. The electrode connection part is arranged on the body, through the body and electrically connected to the electrode part of the conductive cloth. Moreover, the electrode connection part transmits currents onto the conductive cloth, so that the electrode part of the conductive cloth generates an effect of an electrotherapy or a thermotherapy, or both the electrotherapy and the thermotherapy simultaneously. The electrode part receives physiological electric signals transmitted by a human body and transmits the physiological electric signals back to an apparatus through the electrode connection part to perform a physiological measurement.

The present invention relates to an electrode, which is an in vivo insertable electrode, including a substrate, an electrically conductive layer formed on the substrate, a platinum black layer formed on the electrically conductive layer, a self-assembled monolayer (SAM) formed on the platinum black layer, and a lubricant layer formed on the SAM, a method of manufacturing the electrode, and a medical device including the electrode. The in vivo insertable electrode according to the present invention provides excellent electrical properties such as low impedance. Further, it shows that friction with tissue occurring when the electrode is inserted is reduced, and trauma during insertion and an immune rejection response after insertion is suppressed. Further, in the long term, it is possible to detect signals with high sensitivity throughout the entire period by preventing bioadhesion of in vivo cells, such as immune cells, and other proteins.

One aspect of the present disclosure can include an intrafascicular neural electrode. The intrafascicular neural electrode can include a microwire body having a proximal end, a distal anchoring end, and a middle portion extending between the proximal end and the distal anchoring end. The distal anchoring end can substantially match the mechanical and biological properties of the target nerve. The microwire body can have a middle anchoring portion extending between the proximal end and the distal end, wherein at least a portion of the distal end and/or the middle anchoring portion substantially match(es) the mechanical and biological properties of the target nerve. The electrode can be made of graphene. The microwire body, except for the distal anchoring end, can be coated with an insulation material, preferably with a biocompatible agent adsorbed onto the insulation material.