WO2023226590A1 - 代谢物检测装置、尿不湿和护理系统 - Google Patents

代谢物检测装置、尿不湿和护理系统 Download PDF

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Publication number
WO2023226590A1
WO2023226590A1 PCT/CN2023/085439 CN2023085439W WO2023226590A1 WO 2023226590 A1 WO2023226590 A1 WO 2023226590A1 CN 2023085439 W CN2023085439 W CN 2023085439W WO 2023226590 A1 WO2023226590 A1 WO 2023226590A1
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metabolite
sensing
coil
processing unit
unit
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PCT/CN2023/085439
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English (en)
French (fr)
Inventor
谢继权
谢俊达
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深达创芯(深圳)科技有限公司
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Publication of WO2023226590A1 publication Critical patent/WO2023226590A1/zh

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    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/02Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance
    • G01N27/04Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance
    • G01N27/12Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance of a solid body in dependence upon absorption of a fluid; of a solid body in dependence upon reaction with a fluid, for detecting components in the fluid
    • G01N27/121Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance of a solid body in dependence upon absorption of a fluid; of a solid body in dependence upon reaction with a fluid, for detecting components in the fluid for determining moisture content, e.g. humidity, of the fluid
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/42Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators with wetness indicator or alarm
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/84Accessories, not otherwise provided for, for absorbent pads
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/02Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance
    • G01N27/04Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance
    • G01N27/041Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance of a solid body
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/02Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance
    • G01N27/04Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance
    • G01N27/048Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance for determining moisture content of the material
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/02Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance
    • G01N27/04Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance
    • G01N27/06Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance of a liquid
    • G01N27/08Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance of a liquid which is flowing continuously
    • G01N27/10Investigation or analysis specially adapted for controlling or monitoring operations or for signalling
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/02Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance
    • G01N27/04Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance
    • G01N27/12Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance of a solid body in dependence upon absorption of a fluid; of a solid body in dependence upon reaction with a fluid, for detecting components in the fluid
    • G01N27/125Composition of the body, e.g. the composition of its sensitive layer
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N27/00Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
    • G01N27/02Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance
    • G01N27/04Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance
    • G01N27/12Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating impedance by investigating resistance of a solid body in dependence upon absorption of a fluid; of a solid body in dependence upon reaction with a fluid, for detecting components in the fluid
    • G01N27/128Microapparatus
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/42Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators with wetness indicator or alarm
    • A61F2013/424Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators with wetness indicator or alarm having an electronic device
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/42Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators with wetness indicator or alarm
    • A61F2013/427Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators with wetness indicator or alarm pH indicator
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/84Accessories, not otherwise provided for, for absorbent pads
    • A61F2013/8473Accessories, not otherwise provided for, for absorbent pads for diagnostic purposes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61FFILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
    • A61F13/00Bandages or dressings; Absorbent pads
    • A61F13/15Absorbent pads, e.g. sanitary towels, swabs or tampons for external or internal application to the body; Supporting or fastening means therefor; Tampon applicators
    • A61F13/84Accessories, not otherwise provided for, for absorbent pads
    • A61F2013/8476Accessories, not otherwise provided for, for absorbent pads with various devices or method
    • A61F2013/8479Accessories, not otherwise provided for, for absorbent pads with various devices or method including electric or magnetic devices

Definitions

  • the present invention relates to the technical field of diaper detection, and in particular to a metabolite detection device, diaper and nursing system.
  • Diapers, diapers, sanitary napkins, nursing pads and other diapers are widely used for infants, women, and people with incontinence.
  • Diapers are made of flexible substrates such as PI, PET, nylon, and non-woven fabrics.
  • the absorbent part is usually in a long strip shape and is used to absorb or adhere metabolites when worn to prevent metabolites from leaking.
  • a metabolite detection device applied to diapers, the metabolite detection device includes:
  • the sensing module includes a sensing unit, a signal conditioning chip and a first coil connected in sequence.
  • the sensing unit is used to sense metabolites and generate corresponding multiple sensing signals.
  • the signal conditioning chip is used to Process each of the sensing signals to respectively generate corresponding conditioning signals, and transmit a plurality of the conditioning signals to the first coil for transmission;
  • the processing module includes a connected second coil and a data processing unit.
  • the second coil is electromagnetically coupled to the first coil to wirelessly transmit energy and data.
  • the second coil is used to receive a plurality of the modulations. processing signals, and transmitting a plurality of the conditioning signals to the data processing unit, where the data processing unit is configured to obtain metabolite information according to the plurality of conditioning signals.
  • the sensing unit includes a plurality of sensors, the sensors are arranged on the diffusion path of metabolites, and each sensor is used to generate a corresponding sensing signal;
  • the signal conditioning chip is configured with multiple sensing channel interfaces, and each of the sensing channel interfaces is used to connect a corresponding sensor.
  • the signal conditioning chip is configured with an updateable signal conditioning algorithm, and the signal conditioning algorithm is set corresponding to the types of multiple sensors in the sensing unit.
  • the signal conditioning chip is also configured with preset identity identification information
  • the signal conditioning chip when the signal conditioning chip transmits a plurality of the conditioning signals to the first coil for transmission, the signal conditioning chip is also used to transmit the identity identification information to the first coil for transmission, So that the processing unit establishes a mapping relationship between the metabolite information and the identity information.
  • the data processing unit is further configured to generate and send a data acquisition instruction through the second coil;
  • the signal conditioning chip is further configured to receive the data acquisition instruction via the first coil and transmit the conditioning signal back to the data processing unit in response to the data acquisition instruction.
  • the sensing unit includes:
  • a plurality of humidity sensors respectively located at different sensing points on the metabolite diffusion path, each of the humidity sensors is used to sense the humidity of the sensing point and generate a corresponding humidity sensing signal;
  • the data processing unit is further configured to determine a metabolite type based on the humidity sensed by each humidity sensor, and the metabolite type includes liquid metabolites and non-liquid metabolites.
  • the sensing unit includes:
  • At least one temperature sensor is provided on the metabolite diffusion path, and the temperature sensor is used to sense the temperature of the sensing point and generate a corresponding temperature sensing signal;
  • the data processing unit is further configured to determine a metabolite type according to the temperature sensed by the temperature sensor, and the metabolite type includes liquid metabolites and non-liquid metabolites.
  • the sensing unit includes:
  • Liquid-phase metabolite sensor located in the biochemical reaction zone of the diaper, is used to sense the liquid flowing into the biochemical reaction zone from the liquid siphon channel of the diaper, and generate corresponding liquid-phase biochemical sensing Signal;
  • the data processing unit is also used to obtain liquid phase biochemical information corresponding to the liquid phase biochemical sensing signal.
  • the sensing unit includes a gas phase metabolite sensor and a gas latch structure covering the gas phase metabolite sensor, the gas latch structure is used to latch the gas in the metabolite, The gas phase metabolite sensor is used to sense the latched gas and generate a corresponding gas phase biochemical sensing signal;
  • the data processing unit is also used to obtain gas phase biochemical information corresponding to the gas phase biochemical sensing signal.
  • the processing module further includes at least one of an operating unit, an indication unit and a power management unit, wherein:
  • the operation unit is connected to the data processing unit, and is used to receive an activation operation input by the user and generate an activation signal accordingly, and transmit the activation signal to the data processing unit;
  • the instruction unit is connected to the data processing unit, and is used to receive the instruction signal output by the data processing unit, and to instruct the user according to the status information carried by the instruction signal.
  • the status information carried by the instruction signal includes The metabolite status information, sensing module status information and processing unit status at least one of the state information;
  • the power management unit is connected to the data processing unit and used to provide power to the data processing unit.
  • a diaper including:
  • At least one inner core layer is provided between the surface layer and the bottom layer;
  • Sensing layer the sensing layer is provided between the surface layer and the bottom layer, and at least one inner core layer is provided between the sensing layer and the bottom layer;
  • the sensing module in the metabolite detection device is located on the sensing layer, and the processing module in the metabolite detection device is located outside the bottom layer.
  • the inner core layer is not provided on the coupling path between the first coil and the second coil in the metabolite treatment device.
  • a portion of the inner core layer is provided on the coupling path between the first coil and the second coil in the metabolite treatment device;
  • the processing unit is also used to obtain the electromagnetic coupling efficiency on the coupling path, and obtain the metabolite absorption amount of the inner core layer according to the electromagnetic coupling efficiency.
  • it also includes:
  • a storage bag connected to the outside of the bottom layer, is used to accommodate the processing module.
  • the storage bag is provided with an opening, and a switch structure is provided at the opening.
  • the switch structure is used to expose when opened.
  • the opening is used to put in or take out the processing module through the opening, and the switch structure is also used to close the opening when closed to prevent the processing module from coming out during operation.
  • the holding bag is provided at a position corresponding to the first coil in the sensing module.
  • the position is such that the coupling path between the second coil and the first coil is the shortest.
  • a system of care that includes:
  • a mobile terminal includes a first wireless transmission unit
  • the diaper processing module further includes a second wireless transmission unit, the second wireless transmission unit is connected to the data processing unit and is used to send the metabolite information to the third terminal of the mobile terminal.
  • a wireless transmission unit and receives control instructions from the first wireless transmission unit.
  • a cloud server is also included, the mobile terminal is further used to send the metabolite information to the cloud server, and the cloud server is used to store and analyze the received metabolite information.
  • the metabolite detection device of the above embodiment includes a sensing module and a processing module.
  • the sensing module includes a sensing unit, a signal conditioning chip and a first coil connected in sequence.
  • the processing module includes a connected second coil and a data processing unit.
  • the signal conditioning chip establishes wireless communication between the sensing unit and the data processing unit through the first coil and the second coil, effectively reducing the connection length of the line and simplifying the complexity of the line.
  • the first coil and the second coil can transmit energy through wireless coupling, in the sensing module, the energy received wirelessly from the first coil can be directly used to power the sensing unit, signal conditioning chip and other devices. Based on the above power supply method, there is no need to install batteries and other structures in the sensing module, thereby simplifying the structure of the sensing module and thus the overall structure of the diaper.
  • Figure 1 is a schematic system structure diagram of a metabolite detection device according to an embodiment
  • Figure 2 is one of the schematic diagrams of a sensor according to an embodiment
  • Figure 3 is a schematic diagram of the humidity change curve of semi-solid metabolites according to an embodiment
  • Figure 4 is a schematic diagram of the humidity change curve of liquid metabolites according to an embodiment
  • Figure 5 is a second schematic diagram of a sensor according to an embodiment
  • Figure 6 is a schematic diagram of the position of a humidity sensor according to an embodiment
  • Figure 7 is a third schematic diagram of a sensor according to an embodiment
  • Figure 8 is a schematic cross-sectional view of a liquid-phase metabolism sensor according to an embodiment
  • Figure 9 is a schematic structural diagram of a processing module according to an embodiment
  • Figure 10 is a schematic cross-sectional view of a diaper according to an embodiment
  • Figure 11 is a second schematic cross-sectional view of a diaper according to an embodiment
  • Figure 12 is a schematic structural diagram of a nursing system according to an embodiment.
  • Sensing module 100; Sensing unit: 110; Signal conditioning chip: 120; First coil: 130; Processing module: 200; Second coil: 210; Data processing unit: 220; Operating unit: 230; Indicating unit: 240 ;Power management unit: 250; Second wireless transmission unit: 260; Surface layer: 11; Bottom layer: 12; Inner core layer: 13; Sensing layer: 14.
  • first, second, etc. used in this application may be used herein to describe various elements, but these elements are not limited by these terms. These terms are only used to distinguish one element from another element.
  • a first resistor may be referred to as a second resistor, and similarly, the second resistor may be referred to as a first resistor, without departing from the scope of the present application.
  • the first resistor and the second resistor are both resistors, but they are not the same resistor.
  • connection in the following embodiments should be understood as “electrical connection”, “communication connection”, etc. if the connected circuits, modules, units, etc. have the transmission of electrical signals or data between each other.
  • FIG 1 is a schematic system structure diagram of a metabolite detection device according to an embodiment.
  • the metabolite detection device of this embodiment is applied to diapers.
  • the metabolite detection device includes a sensing module. 100 and processing module 200.
  • the sensing module 100 includes a sensing unit 110, a signal conditioning chip 120 and a first coil 130 connected in sequence.
  • the sensing unit 110 is used to sense metabolites and generate corresponding multiple sensing signals.
  • the sensing unit 110 may include multiple sensors, which are disposed on the diffusion path of metabolites, and each of the sensors is used to generate a corresponding sensing signal.
  • the signal conditioning chip 120 is used to process each of the sensing signals to respectively generate corresponding conditioning signals, and transmit a plurality of the conditioning signals to the first coil 130 for transmission.
  • the signal conditioning chip 120 can have a signal modulation function.
  • the signal conditioning chip 120 may also have at least one of functions such as digital-to-analog conversion, non-volatile storage, simple logic operations, and wireless modulation.
  • the processing module 200 includes a connected second coil 210 and a data processing unit 220.
  • the second coil 210 is electromagnetically coupled to the first coil 130 to wirelessly transmit energy and data.
  • the second coil 210 is used to receive multiple signals. the conditioning signals, and transmits a plurality of the conditioning signals to the data processing unit 220.
  • the signal conditioning chip 120 may send data to the processing module 200 at a certain interval, or the signal conditioning chip 120 may perform data return in response to the acquisition instruction of the processing module 200.
  • the data processing unit 220 is configured to obtain metabolite information according to a plurality of conditioning signals. Specifically, the metabolite information may include but is not limited to metabolite type.
  • the processing module 200 may determine the sensing result of the sensing point based on the conditioning signal, and then determine the metabolite type based on the sensing result.
  • a signal conditioning chip 120 is disposed therebetween, and the signal conditioning signal controls the first coil 130 to transmit and receive signals.
  • the wired connection between the sensing unit 110 and the processing module 200 is converted into a wireless connection, thereby reducing the connection length of the circuit and simplifying the complexity of the circuit.
  • the processing module 200 since the circuit connection between the processing module 200 and the signal conditioning chip 120 is omitted, the processing module 200 does not need to be provided with a connector for circuit connection. Therefore, the rigid reinforcing plate can be removed, the reinforcing process is omitted, and the roll process is easier to handle, thus saving material and process costs and improving processing efficiency.
  • the first coil and the second coil can transmit energy through wireless coupling, in the sensing module, the energy received wirelessly from the first coil can be directly used to power the sensing unit, signal conditioning chip and other devices. Based on the above power supply method, there is no need to install batteries and other structures in the sensing module, thereby simplifying the structure of the sensing module and thus the overall structure of the diaper.
  • the signal conditioning chip 120 is configured with multiple sensing channel interfaces, and each of the sensing channel interfaces is used to connect a corresponding the sensor. It can be understood that the sensing channel interface can be designed according to needs, so it is easier to adapt to the situation when the number of sensors increases. Moreover, since the signal conditioning chip 120 is small in size, adding a sensing channel interface will not have a great impact on the overall space occupied by the device. It is understandable that when the number of sensors increases to sense more data, compatibility can be achieved by simply changing the connection relationship between the sensors and the sensing channel interface. The method is simple and easy to implement, and is more conducive to the development of metabolite detection devices. Function expansion.
  • the signal conditioning chip 120 is configured with an updateable signal conditioning algorithm, and the signal conditioning algorithm is set corresponding to the types of multiple sensors in the sensing unit 110 . That is, only the signal conditioning algorithm needs to be updated in the signal conditioning chip 120 to achieve richer signal conditioning functions. Therefore, there is no need to update the hardware structure of the signal conditioning chip 120, and only a simple software algorithm update is required to complete the product update iteration.
  • the signal conditioning chip 120 is also configured with preset identity information.
  • the signal conditioning chip 120 has a storage function to record the identification information of each diaper.
  • the identity information includes but is not limited to diaper ID information and other information.
  • the signal conditioning chip 120 transmits a plurality of the conditioning signals to the first coil 130 for transmission, the signal conditioning chip 120 is also used to transmit the identity identification information to the first coil. 130 Send, so that the processing unit establishes a mapping relationship between the metabolite information and the identity information.
  • the processing module 200 can determine the correspondence between the metabolite information and the signal conditioning chip 120 .
  • the user name, diaper wearing time, etc. corresponding to each metabolite information can also be learned, thereby facilitating traceability and data analysis. .
  • the data processing unit 220 is further configured to generate and send a data acquisition instruction through the second coil 210 .
  • the signal conditioning chip 120 is also configured to receive the data acquisition instruction via the first coil 130, and in response to the data acquisition instruction, return the conditioning signal to the data processing unit 220. It is understandable that users have a need to open the mobile terminal APP and check the current usage of diapers to determine whether the diapers need to be replaced. Therefore, by setting the above functions, real-time data can be obtained, thereby providing accurate information to users and improving the user experience.
  • FIG. 2 is a schematic diagram of a sensor according to an embodiment.
  • the sensing unit 110 includes a plurality of humidity sensors, and the plurality of humidity sensors are disposed on the base material of the sensing layer 14 .
  • the base material is a flexible material to fit the user's body, and conductive lines are embedded in the base material to transmit sensing signals of each sensor.
  • a plurality of humidity sensors are respectively arranged at different sensing points on the metabolite diffusion path. Each of the humidity sensors is used to sense the humidity of the sensing point and generate a corresponding humidity sensing signal.
  • the number of humidity sensors can be 5 to 10, which can be determined according to the size of the diaper.
  • the data processing unit 220 is further configured to determine a metabolite type based on the humidity sensed by each of the humidity sensors.
  • the metabolite type includes liquid metabolites and non-liquid metabolites.
  • the processing module 200 can obtain growth status information based on the sensing results of each sensor, and determine the metabolite type based on the growth status information.
  • the growth status information is used to represent the growth of the sensing results of each sensing point over time. For example, it may include the humidity growth rate, the maintenance time for the humidity to remain within the preset humidity range after the humidity increases, and the maintenance time for the humidity to remain within the preset range after the humidity increases. conditions within the temperature range, etc.
  • the processing module 200 is also configured to determine the type of metabolite to be a liquid metabolite if the humidity growth rate of at least one sensing point is greater than a rate threshold.
  • the rate threshold can be determined based on the empirical value of the humidity growth rate when the liquid metabolite diffuses in the inner core layer of the diaper.
  • the processing module 200 may also be configured to determine that the metabolite type is a semi-solid metabolite if the maintenance time of at least one sensing point is greater than the first time threshold; and/or if the maintenance time of any sensing point If it is less than the second time threshold, it is determined to be a liquid metabolite.
  • semi-solid metabolites refer to stools containing liquid in metabolites, which may be loose stools, for example.
  • the first time threshold can be determined according to the user's usual urination time, for example, it can be greater than or equal to the user's longest urination time. Since liquid metabolites are quickly absorbed by the inner core layer of the diaper after being excreted, its humidity can only be maintained through continued urination. Since the semi-solid metabolite contains liquids such as the liquid in the metabolite, and the liquid in the metabolite will not be quickly and completely absorbed by the inner core layer of the diaper, the humidity at the sensing point will be maintained for a period of time. .
  • FIG. 3 is a schematic diagram of the humidity change curve of a semi-solid metabolite according to an embodiment.
  • Curve l1 is a time change curve
  • curve l2 is a humidity value change curve of a semi-solid metabolite.
  • the liquid metabolite may be, for example, liquid, blood, etc. among the metabolites.
  • the second time threshold may also be determined based on the user's usual urination time, which may be less than or equal to the longest urination time, for example. It can be understood that if the maintenance time of at least one sensing point is less than the first time threshold, that is, less than the user's normal urination time, it can be indicated that the maintenance of the humidity at the sensing point is caused by urination, and therefore the type of metabolite can be determined at this time For liquid metabolites.
  • Figure 4 is a schematic diagram of the humidity change curve of the liquid metabolite according to an embodiment. Refer to Figure 4. Curve l3 is a time change curve, and curve l4 is a humidity value change curve of the liquid metabolite. Wherein, the first time threshold and the second time threshold may be equal.
  • FIG. 5 is a second schematic diagram of a sensor according to an embodiment.
  • the The sensing unit 110 includes at least one temperature sensor.
  • the temperature sensor is disposed on the metabolite diffusion path.
  • the temperature sensor is used to sense the temperature of the sensing point and generate a corresponding temperature sensing signal.
  • the sensing unit 110 includes three temperature sensors.
  • the data processing unit 220 is further configured to determine a metabolite type according to the temperature sensed by the temperature sensor, and the metabolite type includes liquid metabolites and non-liquid metabolites.
  • the growth status information may also include a maintenance time within a preset temperature range after the humidity increases.
  • the processing module 200 is also configured to: if the growth status information of at least one humidity sensing point meets the preset condition, the adjacent humidity sensing point If the temperature of the temperature sensing point gradually decreases, the metabolite type is determined to be a semi-solid metabolite. It can be understood that when the metabolite is a semi-solid metabolite, since the liquid in the metabolite will not be quickly and completely absorbed by the inner core layer of the diaper, its humidity will be maintained within a certain range after excretion. In addition, the temperature will slowly decrease after it is discharged, instead of continuing to rise or remain within a certain temperature range like continuous urination.
  • the type of metabolite can be determined to be a semi-solid metabolite.
  • the data processing unit 220 is further configured to determine a target number according to the humidity, where the target number is the number of sensing points whose humidity is greater than the second humidity threshold, and determine the metabolic amount according to the target number.
  • the second humidity threshold may be the humidity of the inner core layer of the diaper when the liquid metabolite is excreted into the inner core layer of the diaper. It can be understood that if the humidity of the sensing point is greater than the second humidity threshold, it means that there is liquid metabolite at the sensing point. By reasonably setting the distance between the sensing points, the number of sensing points exposed to the liquid metabolite is equal to The metabolic amount corresponds one to one, so that the corresponding metabolic amount can be obtained according to the number of sensing points.
  • FIG. 6 is a schematic diagram of the position of the humidity sensor according to an embodiment.
  • each humidity sensor is arranged in a one-to-one correspondence at the humidity sensing points A, B, C, D, E, F, and G, and can be based on each sensing point.
  • the points divide the penetration areas L1-L4, where the areas of the penetration areas L1-L4 increase sequentially.
  • the liquid excrement is located in area L1, and the corresponding metabolic volume of area L1 can be 20 ml.
  • the liquid excrement is located in area L2, and the corresponding metabolic volume of area L2 can be 40 ml.
  • the metabolic volume corresponding to area L2 can be 40ml, and the metabolic volume corresponding to area L4 can be 120ml. Therefore, in this embodiment, the corresponding metabolic amount can be determined according to the target quantity. This method is simple and can effectively measure the metabolic amount.
  • the metabolic amount in order to determine the metabolic amount, can be further determined by obtaining the excretion time of liquid metabolites during the user's excretion process, combined with the excretion volume per unit time.
  • the excretion time is the time interval between the time when the user starts excretion and the time when the user ends excretion.
  • the start time of excretion can be characterized by the increase time of the humidity of the user's urinary excretion sensing point. Since liquid excrement is quickly absorbed after being discharged, the humidity at the sensing point will decrease if the discharge stops. Therefore, the end of excretion time can be characterized by the decay time of the humidity of the user's urinary excretion sensing point.
  • the humidity of the sensing point increases sharply at the growth moment, so it can be determined according to whether the growth rate of the humidity at the target sensing point reaches the growth threshold.
  • the humidity at the sensing point at the decay moment will sharply attenuate, so it can be determined according to whether the attenuation rate reaches The attenuation threshold is determined.
  • the collected humidity can have a time stamp, so that the growth and decay moments can be determined based on it.
  • the temperature sensor is also used to sense at least the temperature of the temperature sensing point where the user excretes stool, and transmits it to the processing module 200 through the signal conditioning chip 120.
  • At least one sensor is disposed at the temperature sensing point to Sensing the humidity of the temperature sensing point
  • the processing module 200 is also used to determine that the type of metabolite is solid-state metabolism if the temperature of the temperature sensing point changes due to temperature rise and the humidity of the adjacent humidity sensing point is less than the first humidity threshold.
  • the first humidity threshold may be less than or equal to the maximum humidity of the inner core layer of the diaper when solid metabolites are excreted into the inner core layer of the diaper.
  • the temperature of the first sensing point changes, it indicates that there is a metabolite at the first sensing point.
  • the humidity of the first sensing point is less than the first humidity threshold, it indicates that it is a solid-state metabolite, where solid-state metabolism
  • the object may be, for example, dried feces.
  • the temperature sensor is also used to sense the temperature of multiple sensing points on the inner core layer of the diaper corresponding to each excretion site of the user when the diaper is worn, and the data processing unit 220 further use It is used to determine the temperature diffusion information based on the temperature, and determine the metabolite type based on the temperature diffusion information.
  • the temperature diffusion information is used to characterize the order in which temperature changes occur at each sensing point. Specifically, if the temperature diffusion information shows that the temperature changes successively from the sensing point at the pee to the sensing point at the stool, the metabolite type is determined to be a liquid metabolite.
  • the metabolite type is determined to be a non-liquid metabolite. It can be understood that the specific type of metabolites can be determined based on the excretion location and diffusion of the metabolites.
  • Liquid metabolites may include liquid or blood in the metabolites, and non-liquid metabolites may include solid metabolites, such as dry metabolites. Stool may also include semi-solid metabolites, such as loose stools.
  • FIG. 7 is a third schematic diagram of a sensor according to an embodiment.
  • the sensing unit 110 further includes a liquid phase metabolite sensor.
  • a liquid-phase metabolite sensor is disposed in the biochemical reaction zone of the diaper, used to sense the liquid flowing into the biochemical reaction zone from the liquid siphon channel of the diaper, and generate a corresponding liquid-phase biochemical sensing signal.
  • the data processing unit 220 is also used to obtain liquid phase biochemical information corresponding to the liquid phase biochemical sensing signal.
  • the liquid-phase metabolism sensor is designed with a separate liquid siphon channel and a biochemical reaction zone to ensure the detection of multiple metabolites, so that the detection results are not affected by the droplet channel and signals between each other.
  • the substances that can be detected include but are not limited to pH value, glucose, dopamine, uric acid, ascorbic acid, galactose, ketone bodies, leukocytes, protein, occult blood, K+ ions, Na+ ions, iodide ions, calcium ions, iron ions, zinc ions , nitrite, etc.
  • FIG. 8 is a schematic cross-sectional view of a liquid-phase metabolism sensor according to an embodiment. Referring to FIG.
  • the sensitive material layer of the liquid-phase sensor is provided at each sensing point on the substrate for specific reactions of metabolic substances. generate electrical signals.
  • a separation layer is provided between two adjacent sensitive material layers to separate the adjacent sensitive material layers and construct a siphon channel to latch the liquid in the metabolites.
  • a hydrophilic membrane layer is provided on the partition, and the hydrophilic membrane layer is used to absorb the liquid in the metabolites, thereby introducing the liquid into the siphon channel.
  • the entrance of the siphon channel for liquid phase component analysis is realized by drilling holes in the hydrophilic membrane layer.
  • liquid phase component analysis needs to establish a stable reaction zone to ensure that the liquid in the metabolites in the reaction zone is sufficient during the detection time, otherwise the liquid in the metabolites may be absorbed by the diaper.
  • the inner core layer is sucked away and cannot meet the needs of biochemical testing.
  • the above structure provides a stable reaction zone.
  • the liquid in the metabolites enters the reaction zone through siphoning and is detected by the sensitive material layer in the reaction zone, thereby realizing liquid phase analysis.
  • the sensing unit 110 includes a gas phase metabolite sensor and a gas latch structure covering the gas phase metabolite sensor.
  • the gas latch structure is used to latch the gas phase metabolite sensor. Gases in metabolites, the gas phase metabolite sensor is used to sense the latched gas and generate corresponding gas phase biochemical sensing signals.
  • the data processing unit 220 is also used to obtain gas phase biochemical information corresponding to the gas phase biochemical sensing signal. Similar to the siphon channel, the gas latch structure can establish a stable reaction zone to ensure that the gas in the reaction zone is relatively stable within the detection time. Otherwise, the gas in the metabolites will volatilize and cannot meet the needs of biochemical detection.
  • gas phase analysis substances include (but are not limited to) ammonia gas, hydrogen sulfide, hydrogen, skatole, etc.
  • FIG. 9 is a schematic structural diagram of the processing module 200 according to an embodiment.
  • the processing module 200 further includes at least one of an operating unit 230 , an indication unit 240 and a power management unit 250 .
  • the operation unit 230 is connected to the data processing unit 220 and is configured to receive an activation operation input by a user, generate an activation signal accordingly, and transmit the activation signal to the data processing unit 220 .
  • the activation signal may be that when the processing module 200 is placed in the holding bag, the processing module 200 can automatically detect the sensing module 100 and send an activation signal to the sensing module 100 to establish communication with the sensing module 100. Thereby obtaining the ID information, production time, configuration information, etc. of the sensing module 100. Information such as whether it has been used.
  • the instruction unit 240 is connected to the data processing unit 220, and is used to receive the instruction signal output by the data processing unit 220, and to instruct the user according to the status information carried by the instruction signal, and the status information carried by the instruction signal is
  • the information includes at least one of the metabolite status information, sensing module 100 status information, and processing unit status information.
  • the metabolite status information refers to the number of excretions, usage time, whether the detection index exceeds the set value, etc.
  • the sensing module 100 status information refers to the switch status of the sensor, the electromagnetic coupling status of the coil, etc.
  • the processing unit status information refers to the processing Whether the module 200 is working normally, whether the power of the processing module 200 is normal, etc.
  • the indication unit 240 can when the amount of liquid metabolites metabolize exceeds the set warning value, Output warning information to remind the user to replace.
  • the warning information may be a sound signal.
  • the power management unit 250 is connected to the data processing unit 220 and is used to provide power to the data processing unit 220 .
  • FIG. 10 is a schematic cross-sectional view of a diaper according to an embodiment.
  • the diaper includes a surface layer 11, a bottom layer 12, and at least one inner core layer 13. and sensing layer 14, an inner core layer 13 is shown in the figure.
  • the surface layer 11 is close to the user's skin, and the bottom layer 12 is far away from the user's skin.
  • the inner core layer 13 is provided between the surface layer 11 and the bottom layer 12.
  • the inner core layer 13 can also be called an absorption layer and is used to absorb metabolites.
  • the sensing layer 14 is disposed between the surface layer 11 and the bottom layer 12 , and at least one core layer 13 is disposed between the sensing layer 14 and the bottom layer 12 .
  • the sensing layer 14 can be disposed between the first inner core layer 13 and the surface layer 11 , or the sensing layer 14 can be disposed between the first inner core layer 13 and the surface layer 11 .
  • the sensing layer 14 can also be disposed between the second inner core layer 13 and the third inner core layer 13, or the sensing layer 14 can be disposed between the third inner core layer 13 and the third inner core layer 13.
  • the distance between the inner core layer 13 and the bottom layer 12 is not limited in this embodiment.
  • the sensing module 100 in the metabolite detection device is located on the sensor
  • the sensing layer 14 that is, the sensing unit 110 , the signal conditioning chip 120 and the first coil 130 in the metabolite detection device are all provided on the sensing layer 14 .
  • the processing module 200 in the metabolite detection device is disposed outside the bottom layer 12 , that is, the second coil 210 and the data processing unit 220 in the metabolite detection device are both disposed outside the bottom layer 12 .
  • the processing module 200 is arranged on the side away from the user's skin, which can be used to replace the processing module 200 at any time, or to prevent metabolites from flowing into the processing module 200 and affecting the operation of the processing module 200 .
  • a portion of the inner core layer 13 is provided on the coupling path between the first coil 130 and the second coil 210 in the metabolite treatment device.
  • the processing unit is also used to obtain the electromagnetic coupling efficiency on the coupling path, and obtain the metabolite absorption amount of the inner core layer 13 according to the electromagnetic coupling efficiency. It can be understood that the hygroscopic state of the inner core layer 13 will affect the electromagnetic coupling efficiency. Therefore, the designed algorithm can also be used to determine the amount of metabolites and whether the diaper needs to be changed.
  • Figure 11 is a second schematic cross-sectional view of a diaper according to an embodiment.
  • the coupling path between the first coil 130 and the second coil 210 in the metabolite treatment device The inner core layer 13 is not provided on. It can be understood that if the inner core layer 13 is not provided on the coupling path, the influence of the hygroscopic state of the inner core layer 13 on the electromagnetic coupling efficiency can be avoided, thereby effectively preventing the first coil 130 from being damaged when the diaper has not been changed for a long time.
  • the connection with the second coil 210 is unstable or even disconnected. Therefore, in this embodiment, by arranging the above structure, the reliability of communication can be effectively ensured.
  • the diaper further includes a holding bag.
  • the accommodation bag is connected to the outside of the bottom layer 12 for accommodating the processing module 200.
  • the accommodation bag is provided with an opening, and a switch structure is provided at the opening.
  • the switch structure is used to open the The opening is exposed to put in or take out the processing module 200 through the opening, and the switch structure is also used to close the opening when closed to prevent the processing module 200 from coming out during operation.
  • the processing The module 200 is installed into a new diaper storage bag, thereby reducing the user's cost of use.
  • the diaper according to the embodiment of the present application does not need to perform operations such as alignment of the connecting wire when disassembling and assembling the processing module 200, thereby improving the convenience of disassembly and assembly.
  • the software function of the processing module 200 can also be upgraded so that the diaper can support richer detection and analysis functions. It is understandable that based on the wireless connection method, after the software function upgrade, there is no need to The hardware structure of the module 200 such as pins and connecting lines is improved, thereby effectively improving the functional scalability of the processing module 200 without excessively increasing the cost.
  • the accommodation bag is provided at a corresponding position of the first coil 130 in the sensing module 100, so that the coupling path between the second coil 210 and the first coil 130 is Shortest.
  • FIG. 12 is a schematic structural diagram of a nursing system according to an embodiment.
  • the nursing system includes a mobile terminal and the aforementioned diaper.
  • the mobile terminal includes a first wireless transmission unit
  • the diaper processing module 200 also includes a second wireless transmission unit 260 (refer to Figure 9).
  • the second wireless transmission unit 260 is connected to the data processing unit 220 for sending
  • the metabolite information is sent to the first wireless transmission unit of the mobile terminal, and the control instructions from the first wireless transmission unit are received.
  • the processing module 200 in the diaper serves as the host and sends the monitoring data to the APP of the mobile terminal through the wireless transmission unit.
  • the APP of the mobile terminal can obtain the data sent by the processing module 200, process the data and display it on the UI interface of the APP to realize user viewing, feedback and other functions.
  • the nursing system also includes a cloud server
  • the The mobile terminal is also used to send the metabolite information to the cloud server
  • the cloud server is used to store and analyze the received metabolite information.
  • the mobile terminal APP can also forward the acquired data to the cloud, thereby realizing cloud storage of data and richer analysis and application decision-making functions, thus improving the flexibility of the use process.

Abstract

一种代谢物检测装置、尿不湿和护理系统,代谢物检测装置应用于尿不湿,包括:传感模块(100),包括依次连接的传感单元(110)、信号调理芯片(120)和第一线圈(130),传感单元(110)用于对代谢物进行感测并生成对应的多个传感信号,信号调理芯片(120)用于对各传感信号进行处理以分别生成对应的调理信号,并将多个调理信号传输至第一线圈(130)进行发送;处理模块(200),包括连接的第二线圈(210)和数据处理单元(220),第二线圈(210)与第一线圈(130)电磁耦合连接,以无线传输能量和数据,第二线圈(210)用于接收多个调理信号,并将多个调理信号传输至数据处理单元(220),数据处理单元(220)用于根据多个调理信号获取代谢物信息。

Description

代谢物检测装置、尿不湿和护理系统 技术领域
本发明涉及尿不湿检测技术领域,特别是涉及一种代谢物检测装置、尿不湿和护理系统。
背景技术
尿不湿、纸尿裤、卫生巾、护理垫等尿不湿广泛用于婴幼儿、女性和大小便失禁等人群,尿不湿由PI、PET、尼龙、无纺布等柔性基材制备而成,其吸收部通常为长条形状,用于在穿戴时吸收或粘附代谢物,以防止代谢物泄露。
为了识别代谢物类型,通常会在尿不湿内设置多种传感器,而为了将各传感器都连接至处理器进行数据的处理和分析,就会导致走线数量过多,从而提升了线路的复杂性,加大了质量把控难度。
发明内容
基于此,有必要提供一种线路简单的代谢物检测装置、尿不湿和护理系统。
一种代谢物检测装置,应用于尿不湿,所述代谢物检测装置包括:
传感模块,包括依次连接的传感单元、信号调理芯片和第一线圈,所述传感单元用于对代谢物进行感测并生成对应的多个传感信号,所述信号调理芯片用于对各所述传感信号进行处理以分别生成对应的调理信号,并将多个所述调理信号传输至所述第一线圈进行发送;
处理模块,包括连接的第二线圈和数据处理单元,所述第二线圈与所述第一线圈电磁耦合连接,以无线传输能量和数据,所述第二线圈用于接收多个所述调 理信号,并将多个所述调理信号传输至所述数据处理单元,所述数据处理单元用于根据多个所述调理信号获取代谢物信息。
在其中一个实施例中,
所述传感单元包括多个传感器,所述传感器设于代谢物的扩散路径上,各所述传感器分别用于产生一个对应的所述传感信号;
所述信号调理芯片被配置有多个传感通道接口,各所述传感通道接口分别用于连接一个对应的所述传感器。
在其中一个实施例中,所述信号调理芯片被配置有可更新的信号调理算法,所述信号调理算法与所述传感单元中的多个所述传感器的类型对应设置。
在其中一个实施例中,所述信号调理芯片还被配置有预设的身份标识信息;
其中,当所述信号调理芯片将多个所述调理信号传输至所述第一线圈进行发送时,所述信号调理芯片还用于将所述身份标识信息传输至所述第一线圈进行发送,以使所述处理单元建立所述代谢物信息与所述身份标识信息之间的映射关系。
在其中一个实施例中,所述数据处理单元还用于生成并经所述第二线圈发送数据获取指令;
所述信号调理芯片还用于经所述第一线圈接收所述数据获取指令,并响应于所述数据获取指令回传所述调理信号至所述数据处理单元。
在其中一个实施例中,所述传感单元包括:
多个湿度传感器,分别设于代谢物扩散路径上的不同感测点,各所述湿度传感器分别用于感测所在感测点的湿度并生成对应的湿度传感信号;
其中,所述数据处理单元还用于根据各所述湿度传感器传感到的湿度确定代谢物类型,所述代谢物类型包括液态代谢物和非液态代谢物。
在其中一个实施例中,所述传感单元包括:
至少一个温度传感器,设于所述代谢物扩散路径上,所述温度传感器用于感测所在感测点的温度并生成对应的温度传感信号;
其中,所述数据处理单元还用于根据所述温度传感器传感到的温度确定代谢物类型,所述代谢物类型包括液态代谢物和非液态代谢物。
在其中一个实施例中,所述传感单元包括:
液相代谢物传感器,设于所述尿不湿的生化反应区,用于感测由所述尿不湿的液体虹吸通道流入所述生化反应区的液体,并生成对应的液相生化传感信号;
其中,所述数据处理单元还用于获取与所述液相生化传感信号对应的液相生化信息。
在其中一个实施例中,所述传感单元包括气相代谢物传感器和包覆所述气相代谢物传感器的气体锁存结构,所述气体锁存结构用于锁存所述代谢物中的气体,所述气相代谢物传感器用于感测锁存的气体并生成对应的气相生化传感信号;
其中,所述数据处理单元还用于获取与所述气相生化传感信号对应的气相生化信息。
在其中一个实施例中,所述处理模块还包括操作单元、指示单元和电源管理单元中的至少一个,其中:
所述操作单元,与所述数据处理单元连接,用于接收用户输入的激活操作并对应的生成激活信号,传输所述激活信号至所述数据处理单元;
所述指示单元,与所述数据处理单元连接,用于接收所述数据处理单元输出的指示信号,并根据所述指示信号携带的状态信息对用户进行指示,所述指示信号携带的状态信息包括所述代谢物状态信息、传感模块状态信息和处理单元状 态信息中的至少一个;
所述电源管理单元,与所述数据处理单元连接,用于对所述数据处理单元进行供电。
一种尿不湿,包括:
表层;
底层;
至少一个内芯层,设于所述表层与所述底层之间;
传感层,所述传感层设于所述表层与所述底层之间,且所述传感层与所述底层之间设有至少一个所述内芯层;
如上述的代谢物检测装置,所述代谢物检测装置中的传感模块设于所述传感层,且所述代谢物检测装置中的处理模块设于所述底层的外侧。
在其中一个实施例中,所述代谢物处理装置中的第一线圈与第二线圈之间的耦合路径上不设置所述内芯层。
在其中一个实施例中,所述代谢物处理装置中的第一线圈与第二线圈之间的耦合路径上设置有部分所述内芯层;
其中,所述处理单元还用于获取所述耦合路径上的电磁耦合效率,并根据所述电磁耦合效率获取所述内芯层的代谢物吸收量。
在其中一个实施例中,还包括:
容置袋,连接于所述底层的外侧,用于容置所述处理模块,所述容置袋设有开口,且所述开口处设有开关结构,所述开关结构用于在打开时暴露所述开口,以经所述开口放入或取出所述处理模块,所述开关结构还用于在关闭时封闭所述开口,以防止所述处理模块在工作过程中脱出。
在其中一个实施例中,所述容置袋设于所述传感模块中的第一线圈的对应 位置,以使所述第二线圈与所述第一线圈之间的耦合路径最短。
一种护理系统,包括:
移动终端,包括第一无线传输单元;
上述的尿不湿,所述尿不湿的处理模块还包括第二无线传输单元,所述第二无线传输单元与数据处理单元连接,用于发送所述代谢物信息至所述移动终端的第一无线传输单元,并接收来自所述第一无线传输单元的控制指令。
在其中一个实施例中,还包括云端服务器,所述移动终端还用于发送所述代谢物信息至所述云端服务器,所述云端服务器用于对接收到的所述代谢物信息进行存储和分析。
上述实施例的代谢物检测装置包括传感模块和处理模块,传感模块包括依次连接的传感单元、信号调理芯片和第一线圈,处理模块包括连接的第二线圈和数据处理单元,通过设置信号调理芯片,并经第一线圈和第二线圈建立传感单元与数据处理单元之间的无线通信,有效减小了线路的连接长度,简化了线路的复杂性。而且,由于第一线圈和第二线圈可以通过无线耦合的方式传输能量,在传感模块中,就可以直接由第一线圈无线接收到的能量对传感单元、信号调理芯片等器件的供电。基于上述供电方式,传感模块中可以无需设置电池等结构,从而简化了传感模块的结构,进而简化了尿不湿的整体结构。
附图说明
为了更清楚地说明本申请实施例或传统技术中的技术方案,下面将对实施例或传统技术描述中所需要使用的附图作简单地介绍,显而易见地,下面描述中的附图仅仅是本申请的一些实施例,对于本领域普通技术人员来讲,在不付出创造性劳动的前提下,还可以根据这些附图获得其他的附图。
图1为一实施例的代谢物检测装置的系统结构示意图;
图2为一实施例的传感器示意图之一;
图3为一实施例的半固态代谢物的湿度变化曲线示意图;
图4为一实施例的液态代谢物的湿度变化曲线示意图;
图5为一实施例的传感器示意图之二;
图6为一实施例的湿度传感器的位置示意图;
图7为一实施例的传感器示意图之三;
图8为一实施例的液相代谢传感器处的剖视示意图;
图9为一实施例的处理模块的结构示意图;
图10为一实施例的尿不湿的剖视示意图之一;
图11为一实施例的尿不湿的剖视示意图之二;
图12为一实施例的护理系统的结构示意图。
元件标号说明:
传感模块:100;传感单元:110;信号调理芯片:120;第一线圈:130;处理模块:200;第二线圈:210;数据处理单元:220;操作单元:230;指示单元:240;电源管理单元:250;第二无线传输单元:260;表层:11;底层:12;内芯层:13;传感层:14。
具体实施方式
为了便于理解本申请,下面将参照相关附图对本申请进行更全面的描述。附图中给出了本申请的实施例。但是,本申请可以以许多不同的形式来实现,并不限于本文所描述的实施例。相反地,提供这些实施例的目的是使本申请的公开内容更加透彻全面。
除非另有定义,本文所使用的所有的技术和科学术语与属于本申请的技术领域的技术人员通常理解的含义相同。本文中在本申请的说明书中所使用的术语只是为了描述具体的实施例的目的,不是旨在于限制本申请。
可以理解的是,本申请所使用的术语“第一”、“第二”等可在本文中用于描述各种元件,但这些元件不受这些术语限制。这些术语仅用于将第一个元件与另一个元件区分。举例来说,在不脱离本申请的范围的情况下,可以将第一电阻称为第二电阻,且类似地,可将第二电阻称为第一电阻。第一电阻和第二电阻两者都是电阻,但其不是同一电阻。
可以理解的是,以下实施例中的“连接”,如果被连接的电路、模块、单元等相互之间具有电信号或数据的传递,则应理解为“电连接”、“通信连接”等。
在此使用时,单数形式的“一”、“一个”和“所述/该”也可以包括复数形式,除非上下文清楚指出另外的方式。还应当理解的是,术语“包括/包含”或“具有”等指定所陈述的特征、整体、步骤、操作、组件、部分或它们的组合的存在,但是不排除存在或添加一个或更多个其他特征、整体、步骤、操作、组件、部分或它们的组合的可能性。同时,在本说明书中使用的术语“和/或”包括相关所列项目的任何及所有组合。
图1为一实施例的代谢物检测装置的系统结构示意图,本实施例的代谢物检测装置应用于尿不湿,参考图1,在本实施例中,所述代谢物检测装置包括传感模块100和处理模块200。
其中,传感模块100包括依次连接的传感单元110、信号调理芯片120和第一线圈130。所述传感单元110用于对代谢物进行感测并生成对应的多个传感信号。所述传感单元110可以包括多个传感器,所述传感器设于代谢物的扩散路径上,各所述传感器分别用于产生一个对应的所述传感信号。所述信号调理芯片 120用于对各所述传感信号进行处理以分别生成对应的调理信号,并将多个所述调理信号传输至所述第一线圈130进行发送。具体地,信号调理芯片120可以具有信号调制功能,例如可以将传感单元110输出的本身比较微弱的信号进行放大增强,也可以对信号的电压范围不符合后续模块的电压输入要求的信号进行电压调节,还可以对信号以外的噪声进行滤除,从而输出较为干净的调理信号。信号调理芯片120还可以具有数模转换、非易失性存储、简单的逻辑运算以及无线调制等功能中的至少一个。
处理模块200包括连接的第二线圈210和数据处理单元220,所述第二线圈210与所述第一线圈130电磁耦合连接,以无线传输能量和数据,所述第二线圈210用于接收多个所述调理信号,并将多个所述调理信号传输至所述数据处理单元220。可以理解的是,在使用过程中,可以是信号调理芯片120间隔一定时长就发送一次数据给处理模块200,也可以是信号调理芯片120响应于处理模块200的获取指令进行数据回传,本实施例不做限定。所述数据处理单元220用于根据多个所述调理信号获取代谢物信息。具体地,代谢物信息可以包括但不限于代谢物类型,处理模块200接收到调理信号后,可以根据调理信号确定感测点的感测结果,进而根据感测结果判定代谢物类型。
在本实施例中,相较于相关技术中将传感单元110直接通过线路连接至处理模块200,在其间设置一信号调理芯片120,并由信号调理信号控制第一线圈130进行信号收发,可以将传感单元110与处理模块200的有线连接转化成无线连接,从而减小了线路的连接长度,简化了线路的复杂性。此外,由于处理模块200与信号调理芯片120之间省去了线路连接,处理模块200不需要设置用于线路连接的连接头。因此,可以去掉了刚性补强板,省去了补强工艺,更易处理成卷工艺,因此节省了物料和工艺成本,提高了加工效率。同时大大提升了用户在 使用装配时的便利性,传感模块功能扩展方便。而且,由于第一线圈和第二线圈可以通过无线耦合的方式传输能量,在传感模块中,就可以直接由第一线圈无线接收到的能量对传感单元、信号调理芯片等器件的供电。基于上述供电方式,传感模块中可以无需设置电池等结构,从而简化了传感模块的结构,进而简化了尿不湿的整体结构。
在其中一个实施例中,当所述传感单元110包括多个传感器时,所述信号调理芯片120被配置有多个传感通道接口,各所述传感通道接口分别用于连接一个对应的所述传感器。可以理解的是,传感通道接口可以根据需求设计,因此更容易适配于传感器数量增多的情形。而且,由于信号调理芯片120的体积较小,增加传感通道接口对器件整体占用空间也不会造成太大影响。可以理解的是,当传感器数量增加以感测更多的数据时,仅需改变传感器与传感通道接口之间的连接关系即可实现兼容,方法简单且易于实施,更加利于代谢物检测装置的功能扩展。
在其中一个实施例中,所述信号调理芯片120被配置有可更新的信号调理算法,所述信号调理算法与所述传感单元110中的多个所述传感器的类型对应设置。也即,仅需在信号调理芯片120中进行信号调理算法的更新,即可实现更加丰富的信号调理功能。因此,无需更新信号调理芯片120的硬件结构,只需要进行简单的软件算法更新,就能完成产品的更新迭代。
在其中一个实施例中,所述信号调理芯片120还被配置有预设的身份标识信息。相应地,信号调理芯片120具有存储功能,以记录每一片尿不湿的身份标识信息。其中,身份标识信息包括但不限于尿不湿的ID信息等信息。其中,当所述信号调理芯片120将多个所述调理信号传输至所述第一线圈130进行发送时,所述信号调理芯片120还用于将所述身份标识信息传输至所述第一线圈130 进行发送,以使所述处理单元建立所述代谢物信息与所述身份标识信息之间的映射关系。在本实施例中,处理模块200可以确定代谢物信息与信号调理芯片120之间的对应关系。而且,若建立了信号调理芯片120的身份标识信息与用户使用信息之间的对应关系,还能够获悉每一个代谢物信息对应的用户名称、尿不湿的穿戴时间等,从而便于追溯和数据分析。
在其中一个实施例中,所述数据处理单元220还用于生成并经所述第二线圈210发送数据获取指令。所述信号调理芯片120还用于经所述第一线圈130接收所述数据获取指令,并响应于所述数据获取指令,回传所述调理信号至所述数据处理单元220。可以理解的是,用户存在打开移动终端的APP并查询尿不湿当前的使用情况的需求,以确定是否需要更换尿不湿。因此,通过设置上述功能,可以获取即时的数据,从而提供准确的信息给用户,提升用户的使用体验。
图2为一实施例的传感器示意图之一,参考图2,在其中一个实施例中,所述传感单元110包括多个湿度传感器,多个湿度传感器均设置于传感层14的基材上。基材为柔性材料,以贴合用户的身体,且基材中埋设有导电线路,以传输各传感器的传感信号。多个湿度传感器分别设于代谢物扩散路径上的不同感测点,各所述湿度传感器分别用于感测所在感测点的湿度,并生成对应的湿度传感信号。其中,湿度传感器的数量可以为5个至10个,具体可以根据尿不湿的尺寸确定。其中,所述数据处理单元220还用于根据各所述湿度传感器传感到的湿度确定代谢物类型,所述代谢物类型包括液态代谢物和非液态代谢物。具体地,处理模块200可以根据各传感器的感测结果获取增长状态信息,并根据增长状态信息确定代谢物类型。增长状态信息用于表征各感测点的感测结果随时间的增长情况,例如可包括湿度增长速率、湿度增大后维持在预设湿度范围内的维持时间、湿度增大后维持在预设温度范围内的情况等。
一示例性地,处理模块200还用于若至少一个感测点的湿度增长速率大于速率阈值,则判定代谢物类型为液态代谢物。其中,速率阈值可根据液态代谢物在尿不湿的内芯层扩散时的湿度增长速率经验值进行确定。另一个示例性地,处理模块200还可用于若至少一个感测点的维持时间大于第一时间阈值,则判定代谢物类型为半固态代谢物;和/或若任一感测点的维持时间小于第二时间阈值,则判定为液态代谢物。其中,半固态代谢物指的带有代谢物中的液体的大便,例如可为稀便。可以理解的是,第一时间阈值可根据用户通常的持续排尿时间进行确定,例如可大于或等于用户的最长排尿时间。由于液态代谢物排出后会迅速被尿不湿的内芯层吸收,因此,其湿度只可能在持续排尿的情况下才得以保持。而由于半固态代谢物带有代谢物中的液体等液体,且其内的代谢物中的液体不会迅速被尿不湿的内芯层完全吸收,因此会使得感测点的湿度维持一段时间。若至少一个感测点的维持时间超过了第一时间阈值,即超过了用户正常排尿时间,则表明该感测点湿度的维持不是由排尿情况引起,而是由半固态代谢物引起的,因此此时可判定代谢物类型为半固态代谢物。图3为一实施例的半固态代谢物的湿度变化曲线示意图,参考图3,其中曲线l1为时间变化曲线,曲线l2为半固态代谢物的湿度值变化曲线。液态代谢物可例如为代谢物中的液体、血液等,第二时间阈值也可根据用户通常的持续排尿时间进行确定,例如可小于或等于最长排尿时间。可以理解的是,若至少一个感测点的维持时间小于第一时间阈值,即小于用户正常排尿时间,则可表明该感测点湿度的维持由排尿情况引起,因此此时可判定代谢物类型为液态代谢物。图4为一实施例的液态代谢物的湿度变化曲线示意图,参考图4,其中,曲线l3为时间变化曲线,曲线l4为液态代谢物的湿度值变化曲线。其中,第一时间阈值和第二时间阈值可相等。
图5为一实施例的传感器示意图之二,参考图5,在其中一个实施例中,所 述传感单元110包括至少一个温度传感器,温度传感器设于所述代谢物扩散路径上,所述温度传感器用于感测所在感测点的温度并生成对应的温度传感信号。在图5所示的实施例中,传感单元110包括三个温度传感器。其中,所述数据处理单元220还用于根据所述温度传感器传感到的温度确定代谢物类型,所述代谢物类型包括液态代谢物和非液态代谢物。
具体地,增长状态信息还可包括湿度增大后维持在预设温度范围内的维持时间,处理模块200还用于若至少一个湿度感测点的增长状态信息满足预设条件的同时,相邻的温度感测点的温度逐渐减小,则判定代谢物类型为半固态代谢物。可以理解的是,当代谢物为半固态代谢物时,由于其内的代谢物中的液体不会迅速被尿不湿的内芯层完全吸收,因此排泄后其湿度会维持在某一范围,此外其排出后温度会慢慢降低,而不会像持续排尿的情况会继续上升或维持在某一温度范围。因此,对于某一感测点,若该感测点的湿度增大后维持在预设湿度范围内,同时该感测点的温度逐渐减小,则可判定代谢物类型为半固态代谢物。
在其中一个实施例中,数据处理单元220还用于根据湿度确定目标数量,目标数量为湿度大于第二湿度阈值的感测点数量,并根据目标数量确定代谢量。其中,第二湿度阈值可为液态代谢物排泄至尿不湿的内芯层时尿不湿的内芯层的湿度。可以理解的是,若感测点的湿度大于第二湿度阈值,则说明该感测点有液态代谢物,通过合理设置各感测点的间距,使得接触到液态代谢物的感测点数量与代谢量一一对应,从而可根据感测点数量得到对应的代谢量。
图6为一实施例的湿度传感器的位置示意图,参考图6,各湿度传感器分别一一对应设置于湿度感测点A、B、C、D、E、F、G,并可基于各感测点划分出渗透区域L1-L4,其中渗透区域L1-L4的区域面积依次增大。当只有一个感测点接触到液态排泄物时,液态排泄物位于区域L1内,区域L1对应的代谢量可为20ml。 当有三个感测点接触到液态排泄物时,液态排泄物位于区域L2内,区域L2对应的代谢量可为40ml。以此类推,区域L2对应的代谢量可为40ml,区域L4对应的代谢量可为120ml。因此,在本实施例中,根据目标数量则可确定对应的代谢量,该方法简单,且能够有效测得代谢量。
在一些实施例中,为了确定代谢量,还可通过获取用户排泄过程中液态代谢物的排泄时间,结合单位时间排泄体积进一步确定代谢量。其中,排泄时间为用户开始排泄时刻和结束排泄时刻之间的时间间隔,开始排泄时刻可用用户小便排泄感测点的湿度的增长时刻来表征。由于液态排泄物排出后会被快速吸收,若停止排泄,感测点的湿度则会降低。因此,结束排泄时刻可用用户小便排泄感测点的湿度的衰减时刻来表征。其中,增长时刻感测点的湿度急剧增大,因此可根据目标感测点的湿度的增长率是否达到增长阈值来确定,衰减时刻感测点的湿度会急剧衰减,因此可根据衰减率是否达到衰减阈值来确定。其中,采集到的湿度可带有时间戳,从而可根据其判定增长时刻和衰减时刻。
在其中一个实施例中,温度传感器还用于至少传感用户大便排泄处的温度感测点的温度,并通过信号调理芯片120传输至处理模块200,至少一个传感器设置在温度感测点,以传感温度感测点的湿度,处理模块200还用于若温度感测点的温度发生升温变化,且相邻的湿度感测点的湿度小于第一湿度阈值,则判定代谢物类型为固态代谢物。可以理解的是,第一湿度阈值可小于或等于固态代谢物排泄至尿不湿的内芯层时,尿不湿的内芯层的最大湿度。若第一感测点的温度发生升温变化,则表明第一感测点有代谢物,同时若第一感测点的湿度小于第一湿度阈值,则表明其为固态代谢物,其中,固态代谢物可例如为干便。
在其中一个实施例中,温度传感器还用于感测尿不湿在穿戴状态下,对应用户各排泄处的尿不湿的内芯层上的多个感测点的温度,数据处理单元220还用 于根据温度确定温度扩散信息,并根据温度扩散信息判定代谢物类型。其中,温度扩散信息用于表征各感测点发生升温变化时的顺序。具体地,若温度扩散信息为由小便处感测点向大便处感测点相继发生升温变化,则确定代谢物类型为液态代谢物。若温度扩散信息为由大便处感测点向小便处感测点相继发生升温变化,则确定代谢物类型为非液态代谢物。可以理解的是,根据代谢物的排泄位置及扩散情况,可判定代谢物的具体类型,其中,液态代谢物可包括代谢物中的液体或血液,非液态代谢物可包括固态代谢物,例如干便,还可包括半固态代谢物,例如稀便。
图7为一实施例的传感器示意图之三,参考图7,在其中一个实施例中,所述传感单元110还包括液相代谢物传感器。液相代谢物传感器设于所述尿不湿的生化反应区,用于感测由所述尿不湿的液体虹吸通道流入所述生化反应区的液体,并生成对应的液相生化传感信号。其中,所述数据处理单元220还用于获取与所述液相生化传感信号对应的液相生化信息。
具体地,所述液相代谢传感器设计有单独的液体虹吸通道和生化反应区,用于保证多种代谢物的检测,使得检测结果不受液滴流道和相互之间信号的影响。其中,可以检测的物质包括但不限于pH值,葡萄糖,多巴胺,尿酸,抗坏血酸,半乳糖,酮体,白细胞,蛋白质,隐血,K+离子,Na+离子,碘离子,钙离子,铁离子,锌离子,亚硝酸盐等。具体地,图8为一实施例的液相代谢传感器处的剖视示意图,参考图8,液相传感器的敏感材料层设于基材上的各感测点处,用于代谢物质发生特定反应产生电信号。相邻的两块敏感材料层之间设置有隔层,用于间隔相邻的敏感材料层并构建虹吸通道,以锁存代谢物中的液体。隔层上设有亲水膜层,亲水膜层用于吸收代谢物中的液体,从而将液体导入虹吸通道。在图8所示的实施例中,液相成分分析的虹吸通道入口通过在亲水膜层打孔来实 现。可以理解的是,液相成分分析需要建立一个稳定的反应区,从而保证在检测时间内,反应区内的代谢物中的液体是充足的,否则代谢物中的液体可能会被尿不湿的内芯层吸走,不能满足生化检测的需求。上述结构提供了一个稳定的反应区,代谢物中的液体通过虹吸作用进入到反应区,被反应区的敏感材料层检测到,从而实现液相分析。
继续参考图7,在其中一个实施例中,所述传感单元110包括气相代谢物传感器和包覆所述气相代谢物传感器的气体锁存结构,所述气体锁存结构用于锁存所述代谢物中的气体,所述气相代谢物传感器用于感测锁存的气体并生成对应的气相生化传感信号。其中,所述数据处理单元220还用于获取与所述气相生化传感信号对应的气相生化信息。与虹吸通道类似地,气体锁存结构能够建立一个稳定的反应区,从而保证在检测时间内,反应区内的气体是相对稳定的,否则代谢物中的气体挥发,不能满足生化检测的需求。上述结构提供了一个稳定的反应区,代谢物中的气体由气体锁存结构固定在反应区,被反应区的敏感材料层检测到,从而实现气相分析;气相分析物质包括(但不限于)氨气、硫化氢、氢气、粪臭素等。
图9为一实施例的处理模块200的结构示意图,参考图9,在其中一个实施例中,所述处理模块200还包括操作单元230、指示单元240和电源管理单元250中的至少一个。
具体地,所述操作单元230与所述数据处理单元220连接,用于接收用户输入的激活操作并对应的生成激活信号,传输所述激活信号至所述数据处理单元220。其中,激活信号可以为当处理模块200放入容置袋时,处理模块200能够自动检测到传感模块100,并发送激活信号至传感模块100,以建立与传感模块100之间通讯,从而获取传感模块100的ID信息、生产制造时间、配置信息、 是否已经使用过等信息。所述指示单元240与所述数据处理单元220连接,用于接收所述数据处理单元220输出的指示信号,并根据所述指示信号携带的状态信息对用户进行指示,所述指示信号携带的状态信息包括所述代谢物状态信息、传感模块100状态信息和处理单元状态信息中的至少一个。其中,代谢物状态信息是指排泄次数、使用时长、检测指标是否超出设定值等,传感模块100状态信息是指传感器的开关状态、线圈的电磁耦合状态等,处理单元状态信息是指处理模块200的工作是否正常,处理模块200的电量是否正常等。可以理解的是,为避免尿不湿液态代谢物堆积过多,从而影响尿不湿后续的吸收作用,更影响用户健康,指示单元240可当液态代谢物的代谢量超过设置的警示值时,输出警示信息以提醒用户进行更换。其中,警示信息可为声音信号。所述电源管理单元250与所述数据处理单元220连接,用于对所述数据处理单元220进行供电。
本申请实施例还提供了一种尿不湿,图10为一实施例的尿不湿的剖视示意图之一,参考图10,尿不湿包括表层11、底层12、至少一个内芯层13和传感层14,图中示出了一个内芯层13。其中,表层11靠近用户皮肤,底层12远离用户皮肤。内芯层13设于所述表层11与所述底层12之间如上述的代谢物检测装置,内芯层13也可以称为吸收层,用于吸收代谢物。所述传感层14设于所述表层11与所述底层12之间,且所述传感层14与所述底层12之间设有至少一个所述内芯层13。例如,若尿不湿包括层叠依次设置的三个内芯层13,则可以将传感层14设置在第一内芯层13与表层11之间,也可以将传感层14设置在第一内芯层13与第二内芯层13之间,也可以将传感层14设置在第二内芯层13与第三内芯层13之间,还可以将传感层14设置在第三内芯层13与底层12之间,本实施例不做限定。所述代谢物检测装置中的传感模块100设于所述传 感层14,即,代谢物检测装置中的传感单元110、信号调理芯片120和第一线圈130均设于所述传感层14。而且,所述代谢物检测装置中的处理模块200设于所述底层12的外侧,即,代谢物检测装置中的第二线圈210和数据处理单元220均设于底层12的外侧。在本实施例中,将处理模块200设置在远离用户皮肤的一侧,可以用于随时更换处理模块200,也可以方式处理模块200中流入代谢物,影响处理模块200的运行。
继续参考图10,在其中一个实施例中,所述代谢物处理装置中的第一线圈130与第二线圈210之间的耦合路径上设置有部分所述内芯层13。其中,所述处理单元还用于获取所述耦合路径上的电磁耦合效率,并根据所述电磁耦合效率获取所述内芯层13的代谢物吸收量。可以理解的是,内芯层13的吸湿状态会影响电磁耦合效率,因此,通过设计的算法也可以用于代谢物量判断,以及是否需要更换尿不湿。
图11为一实施例的尿不湿的剖视示意图之二,参考图11,在其中一个实施例中,所述代谢物处理装置中的第一线圈130与第二线圈210之间的耦合路径上不设置所述内芯层13。可以理解的是,若耦合路径上不设置内芯层13,可以避免内芯层13的吸湿状态对影响电磁耦合效率的影响,从而可以有效避免长时间未更换尿不湿时,第一线圈130与第二线圈210的连接不稳定甚至断开的情况。因此,在本实施例中,通过设置上述结构,可以有效确保通信的可靠性。
在其中一个实施例中,尿不湿还包括容置袋。容置袋连接于所述底层12的外侧,用于容置所述处理模块200,所述容置袋设有开口,且所述开口处设有开关结构,所述开关结构用于在打开时暴露所述开口,以经所述开口放入或取出所述处理模块200,所述开关结构还用于在关闭时封闭所述开口,以防止所述处理模块200在工作过程中脱出。具体地,当用户对尿不湿进行更换时,可以将处理 模块200安装至新的尿不湿的容置袋中,从而降低用户的使用成本。而且,相较于有线连接方式,本申请实施例的尿不湿在进行处理模块200的拆装时,无需进行连接线的对位等操作,从而可以提高拆装的便捷性。此外,还可以通过对处理模块200的软件功能升级,使尿不湿能够支持更加丰富的检测和分析功能,而且可以理解的是,基于无线连接的方式,在进行软件功能升级后,无需对处理模块200的pin脚、连接线等硬件结构进行改进,从而可以在不过度增大成本的前提下,有效提高处理模块200的功能扩展性。在本实施例中,通过设置容置袋,可以确保处理模块200的位置不发生过大的移动,从而确保通信过程的可靠性。而且,通过为容置袋设置带有开关结构的开口,可以避免处理模块200从容置袋中自然脱出,从而进一步提高可靠性。
在其中一个实施例中,所述容置袋设于所述传感模块100中的第一线圈130的对应位置,以使所述第二线圈210与所述第一线圈130之间的耦合路径最短。通过上述设置方式,可以使两个线圈之间的传输效率最高,从而提高通信过程的通信速率。
本申请实施例还提供了一种护理系统,图12为一实施例的护理系统的结构示意图,参考图12,护理系统包括移动终端和上述的尿不湿。移动终端包括第一无线传输单元,所述尿不湿的处理模块200还包括第二无线传输单元260(参考图9),所述第二无线传输单元260与数据处理单元220连接,用于发送所述代谢物信息至所述移动终端的第一无线传输单元,并接收来自所述第一无线传输单元的控制指令。尿不湿中的处理模块200作为主机,通过无线传输单元将监测数据发送至移动终端的APP。移动终端的APP能够获取处理模块200发送的数据,将数据处理后显示在APP的UI界面上,以实现用户的查看、反馈等功能。
继续参考图12,在其中一个实施例中,护理系统还包括云端服务器,所述 移动终端还用于发送所述代谢物信息至所述云端服务器,所述云端服务器用于对接收到的所述代谢物信息进行存储和分析。移动终端的APP还能够将获取到的数据转发至云端,从而实现数据的云端存储,以及更丰富的分析和应用决策的功能,从而提高使用过程的灵活性。
在本说明书的描述中,参考术语“有些实施例”、“其他实施例”、“理想实施例”等的描述意指结合该实施例或示例描述的具体特征、结构、材料或者特征包含于本发明的至少一个实施例或示例中。在本说明书中,对上述术语的示意性描述不一定指的是相同的实施例或示例。
以上所述实施例的各技术特征可以进行任意的组合,为使描述简洁,未对上述实施例中的各个技术特征所有可能的组合都进行描述,然而,只要这些技术特征的组合不存在矛盾,都应当认为是本说明书记载的范围。
以上所述实施例仅表达了本发明的几种实施方式,其描述较为具体和详细,但并不能因此而理解为对发明专利范围的限制。应当指出的是,对于本领域的普通技术人员来说,在不脱离本发明构思的前提下,还可以做出若干变形和改进,这些都属于本发明的保护范围。因此,本发明专利的保护范围应以所附权利要求为准。

Claims (17)

  1. 一种代谢物检测装置,其特征在于,应用于尿不湿,所述代谢物检测装置包括:
    传感模块,包括依次连接的传感单元、信号调理芯片和第一线圈,所述传感单元用于对代谢物进行感测并生成对应的多个传感信号,所述信号调理芯片用于对各所述传感信号进行处理以分别生成对应的调理信号,并将多个所述调理信号传输至所述第一线圈进行发送;
    处理模块,包括连接的第二线圈和数据处理单元,所述第二线圈与所述第一线圈电磁耦合连接,以无线传输能量和数据,所述第二线圈用于接收多个所述调理信号,并将多个所述调理信号传输至所述数据处理单元,所述数据处理单元用于根据多个所述调理信号获取代谢物信息。
  2. 根据权利要求1所述的代谢物检测装置,其特征在于,
    所述传感单元包括多个传感器,所述传感器设于代谢物的扩散路径上,各所述传感器分别用于产生一个对应的所述传感信号;
    所述信号调理芯片被配置有多个传感通道接口,各所述传感通道接口分别用于连接一个对应的所述传感器。
  3. 根据权利要求2所述的代谢物检测装置,其特征在于,所述信号调理芯片被配置有可更新的信号调理算法,所述信号调理算法与所述传感单元中的多个所述传感器的类型对应设置。
  4. 根据权利要求2所述的代谢物检测装置,其特征在于,所述信号调理芯片还被配置有预设的身份标识信息;
    其中,当所述信号调理芯片将多个所述调理信号传输至所述第一线圈进行发送时,所述信号调理芯片还用于将所述身份标识信息传输至所述第一线圈进行发送,以使所述处理单元建立所述代谢物信息与所述身份标识信息之间的映 射关系。
  5. 根据权利要求2所述的代谢物检测装置,其特征在于,所述数据处理单元还用于生成并经所述第二线圈发送数据获取指令;
    所述信号调理芯片还用于经所述第一线圈接收所述数据获取指令,并响应于所述数据获取指令回传所述调理信号至所述数据处理单元。
  6. 根据权利要求2所述的代谢物检测装置,其特征在于,所述传感单元包括:
    多个湿度传感器,分别设于代谢物扩散路径上的不同感测点,各所述湿度传感器分别用于感测所在感测点的湿度并生成对应的湿度传感信号;
    其中,所述数据处理单元还用于根据各所述湿度传感器传感到的湿度确定代谢物类型,所述代谢物类型包括液态代谢物和非液态代谢物。
  7. 根据权利要求2所述的代谢物检测装置,其特征在于,所述传感单元包括:
    至少一个温度传感器,设于所述代谢物扩散路径上,所述温度传感器用于感测所在感测点的温度并生成对应的温度传感信号;
    其中,所述数据处理单元还用于根据所述温度传感器传感到的温度确定代谢物类型,所述代谢物类型包括液态代谢物和非液态代谢物。
  8. 根据权利要求2所述的代谢物检测装置,其特征在于,所述传感单元包括:
    液相代谢物传感器,设于所述尿不湿的生化反应区,用于感测由所述尿不湿的液体虹吸通道流入所述生化反应区的液体,并生成对应的液相生化传感信号;
    其中,所述数据处理单元还用于获取与所述液相生化传感信号对应的液相生化信息。
  9. 根据权利要求2所述的代谢物检测装置,其特征在于,所述传感单元包括气相代谢物传感器和包覆所述气相代谢物传感器的气体锁存结构,所述气体锁存结构用于锁存所述代谢物中的气体,所述气相代谢物传感器用于感测锁存的气体并生成对应的气相生化传感信号;
    其中,所述数据处理单元还用于获取与所述气相生化传感信号对应的气相生化信息。
  10. 根据权利要求1所述的代谢物检测装置,其特征在于,所述处理模块还包括操作单元、指示单元和电源管理单元中的至少一个,其中:
    所述操作单元,与所述数据处理单元连接,用于接收用户输入的激活操作并对应的生成激活信号,传输所述激活信号至所述数据处理单元;
    所述指示单元,与所述数据处理单元连接,用于接收所述数据处理单元输出的指示信号,并根据所述指示信号携带的状态信息对用户进行指示,所述指示信号携带的状态信息包括所述代谢物状态信息、传感模块状态信息和处理单元状态信息中的至少一个;
    所述电源管理单元,与所述数据处理单元连接,用于对所述数据处理单元进行供电。
  11. 一种尿不湿,其特征在于,包括:
    表层;
    底层;
    至少一个内芯层,设于所述表层与所述底层之间;
    传感层,所述传感层设于所述表层与所述底层之间,且所述传感层与所述底层之间设有至少一个所述内芯层;
    如权利要求1至10任一项所述的代谢物检测装置,所述代谢物检测装置中 的传感模块设于所述传感层,且所述代谢物检测装置中的处理模块设于所述底层的外侧。
  12. 根据权利要求11所述的尿不湿,其特征在于,所述代谢物处理装置中的第一线圈与第二线圈之间的耦合路径上不设置所述内芯层。
  13. 根据权利要求11所述的尿不湿,其特征在于,所述代谢物处理装置中的第一线圈与第二线圈之间的耦合路径上设置有部分所述内芯层;
    其中,所述处理单元还用于获取所述耦合路径上的电磁耦合效率,并根据所述电磁耦合效率获取所述内芯层的代谢物吸收量。
  14. 根据权利要求11所述的尿不湿,其特征在于,还包括:
    容置袋,连接于所述底层的外侧,用于容置所述处理模块,所述容置袋设有开口,且所述开口处设有开关结构,所述开关结构用于在打开时暴露所述开口,以经所述开口放入或取出所述处理模块,所述开关结构还用于在关闭时封闭所述开口,以防止所述处理模块在工作过程中脱出。
  15. 根据权利要求14所述的尿不湿,其特征在于,所述容置袋设于所述传感模块中的第一线圈的对应位置,以使所述第二线圈与所述第一线圈之间的耦合路径最短。
  16. 一种护理系统,其特征在于,包括:
    移动终端,包括第一无线传输单元;
    权利要求11至15任一项所述的尿不湿,所述尿不湿的处理模块还包括第二无线传输单元,所述第二无线传输单元与数据处理单元连接,用于发送所述代谢物信息至所述移动终端的第一无线传输单元,并接收来自所述第一无线传输单元的控制指令。
  17. 根据权利要求16所述的护理系统,其特征在于,还包括云端服务器,所 述移动终端还用于发送所述代谢物信息至所述云端服务器,所述云端服务器用于对接收到的所述代谢物信息进行存储和分析。
PCT/CN2023/085439 2022-05-27 2023-03-31 代谢物检测装置、尿不湿和护理系统 WO2023226590A1 (zh)

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