A method includes receiving acoustic inputs; generating signal channels from the acoustic inputs; pre-processing data in the signal channels; extracting S1-S2 peaks from the pre-processed data; removing artifacts and outliers from the S1-S2 peaks; generating S1-S2 signal channels based on the S1-S2 peaks in the pre-processed signal channels; selecting two or more of the S1-S2 signal channels; and combining the selected two or more S1-S2 signal channels to produce an acoustic uterine monitoring signal.

The disclosed apparatus, systems and methods relate to ocular surface potential difference (OSPD) measurement, and in particular, to the devices, methods, and design principles allowing for such measurement and the use of the measured OSPD in various research and clinical settings.

Data collection schemes for a wound dressing and related methods are disclosed. In an embodiment, a monitor device for a wound dressing system comprises a wound dressing. The wound dressing comprises an electrode assembly. The electrode assembly comprises a plurality of electrodes including a first set of first electrodes and a second set of second electrodes. The monitor device comprises: a processor, memory and a first interface. The first interface is connected to the processor and the memory. The first interface comprises a plurality of terminals including a first terminal and a second terminal and a data collector coupled to the first terminal and the second terminal. The first terminal is configured to form an electrical connection with a first primary electrode of the first set of first electrodes and the second terminal is configured to form an electrical connection with either a first secondary electrode of the first set of first electrodes or a second primary electrode of the second set of second electrodes. The data collector comprises a data collection controller and is configured to: collect data from the plurality of terminals according to a primary data collection scheme; and collect data from the plurality of terminals according to a secondary data collection scheme, wherein the primary data collection scheme is different from the secondary data collection scheme.

Data collection schemes for a wound dressing and related methods are disclosed. In an embodiment, a monitor device for a wound dressing system comprises a wound dressing. The wound dressing comprises an electrode assembly. The electrode assembly comprises a plurality of electrodes including a first set of first electrodes and a second set of second electrodes. The monitor device comprises: a processor, memory and a first interface. The first interface is connected to the processor and the memory. The first interface comprises a plurality of terminals including a first terminal and a second terminal and a data collector coupled to the first terminal and the second terminal. The first terminal is configured to form an electrical connection with a first primary electrode of the first set of first electrodes and the second terminal is configured to form an electrical connection with either a first secondary electrode of the first set of first electrodes or a second primary electrode of the second set of second electrodes. The data collector comprises a data collection controller and is configured to: collect data from the plurality of terminals according to a primary data collection scheme; and collect data from the plurality of terminals according to a secondary data collection scheme, wherein the primary data collection scheme is different from the secondary data collection scheme.

A method includes receiving acoustic inputs; generating signal channels from the acoustic inputs; pre-processing data in the signal channels; extracting S1-S2 peaks from the pre-processed data; removing artifacts and outliers from the S1-S2 peaks; generating S1-S2 signal channels based on the S1-S2 peaks in the pre-processed signal channels; selecting two or more of the S1-S2 signal channels; and combining the selected two or more S1-S2 signal channels to produce an acoustic uterine monitoring signal.

Flexible implant for electrically recording or stimulating a nerve structure, said flexible implant comprising: a first layer of electrically insulating diamond; an electrode of electrically conductive doped diamond, in contact with the first layer of electrically insulating diamond; an electrically conductive layer in contact with the electrode and the first layer, so as to define a conductive track for the electrode; and a second layer of electrically insulating diamond, at least in contact with the electrically conductive layer and a remaining portion of the first layer, all of the above arranged such that: electrically insulating diamond/electrically conductive doped diamond sealing is provided at the electrode (3) by resumption of epitaxial growth; and the electrically conductive layer is encapsulated by the electrode (3), the first layer and the second layer, at the electrode and over the entirety of the remaining surface thereof except over an area defining an electrical contact. The implant has two faces, namely: a front face comprising one of the two layers of electrically insulating diamond, open locally, providing access to the electrode and the area defining an electrical contact; and a rear face comprising the other of the two layers of electrically insulating diamond.

Flexible implant for electrically recording or stimulating a nerve structure, said flexible implant comprising: a first layer of electrically insulating diamond; an electrode of electrically conductive doped diamond, in contact with the first layer of electrically insulating diamond; an electrically conductive layer in contact with the electrode and the first layer, so as to define a conductive track for the electrode; and a second layer of electrically insulating diamond, at least in contact with the electrically conductive layer and a remaining portion of the first layer, all of the above arranged such that: electrically insulating diamond/electrically conductive doped diamond sealing is provided at the electrode (3) by resumption of epitaxial growth; and the electrically conductive layer is encapsulated by the electrode (3), the first layer and the second layer, at the electrode and over the entirety of the remaining surface thereof except over an area defining an electrical contact. The implant has two faces, namely: a front face comprising one of the two layers of electrically insulating diamond, open locally, providing access to the electrode and the area defining an electrical contact; and a rear face comprising the other of the two layers of electrically insulating diamond.

Provided is a garment for measuring biological information having favorable conductivity and stretchability that prevent a wiring and a bonding part from being disconnected by stress or deformation when the garment is put on, taken off, or washed, while detecting a stable electrical signal. In a wiring with a stretchable electrode according to an embodiment of the present invention, the electrode includes an electrically conductive sheet including electrically conductive fine particles and a binder resin, and the wiring incudes an electrically conductive fiber structure including an electrically conductive fiber. A part of a bond between the electrode and the wiring has a peeling strength of 0.5 to 20 N/cm.

Provided is a garment for measuring biological information having favorable conductivity and stretchability that prevent a wiring and a bonding part from being disconnected by stress or deformation when the garment is put on, taken off, or washed, while detecting a stable electrical signal. In a wiring with a stretchable electrode according to an embodiment of the present invention, the electrode includes an electrically conductive sheet including electrically conductive fine particles and a binder resin, and the wiring incudes an electrically conductive fiber structure including an electrically conductive fiber. A part of a bond between the electrode and the wiring has a peeling strength of 0.5 to 20 N/cm.

Embodiments are disclosed for a method for restoring a wearable biological sensor. The method includes determining that a wearable biological marker sensor comprising a reference electrode is placed within a restoration apparatus. The restoration apparatus includes a correct reference electrode, a counter electrode, and a chloride solution. The reference electrode is in electrical contact with the correct reference electrode and the counter electrode through the chloride solution. The method additionally includes determining whether the reference electrode is degraded based on a voltage differential between the reference electrode and the correct reference electrode. The method also includes restoring the reference electrode, if the reference electrode is degraded, by applying a voltage to a circuit. The circuit includes the reference electrode and the counter electrode. Further, multiple chloride ions of the chloride solution bond with a plurality of silver atoms of the reference electrode.