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EP4294255A1 - Procédé et capteur pour déterminer une concentration d'un gaz cible dans le sang d'un être vivant - Google Patents

Procédé et capteur pour déterminer une concentration d'un gaz cible dans le sang d'un être vivant

Info

Publication number
EP4294255A1
EP4294255A1 EP22701403.2A EP22701403A EP4294255A1 EP 4294255 A1 EP4294255 A1 EP 4294255A1 EP 22701403 A EP22701403 A EP 22701403A EP 4294255 A1 EP4294255 A1 EP 4294255A1
Authority
EP
European Patent Office
Prior art keywords
absorption
volume
gas
target gas
photoacoustic sensor
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP22701403.2A
Other languages
German (de)
English (en)
Inventor
Katrin Schmitt
M.SC. Christian WEBER
Jürgen WÖLLENSTEIN
Johannes KAPP
Hassan YASSINE
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Fraunhofer Gesellschaft zur Forderung der Angewandten Forschung eV
Albert Ludwigs Universitaet Freiburg
Original Assignee
Fraunhofer Gesellschaft zur Forderung der Angewandten Forschung eV
Albert Ludwigs Universitaet Freiburg
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Fraunhofer Gesellschaft zur Forderung der Angewandten Forschung eV, Albert Ludwigs Universitaet Freiburg filed Critical Fraunhofer Gesellschaft zur Forderung der Angewandten Forschung eV
Publication of EP4294255A1 publication Critical patent/EP4294255A1/fr
Pending legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/0093—Detecting, measuring or recording by applying one single type of energy and measuring its conversion into another type of energy
    • A61B5/0095—Detecting, measuring or recording by applying one single type of energy and measuring its conversion into another type of energy by applying light and detecting acoustic waves, i.e. photoacoustic measurements
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/145—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue
    • A61B5/14542—Measuring characteristics of blood in vivo, e.g. gas concentration or pH-value ; Measuring characteristics of body fluids or tissues, e.g. interstitial fluid or cerebral tissue for measuring blood gases
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B5/00—Measuring for diagnostic purposes; Identification of persons
    • A61B5/68—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient
    • A61B5/6801—Arrangements of detecting, measuring or recording means, e.g. sensors, in relation to patient specially adapted to be attached to or worn on the body surface
    • A61B5/683—Means for maintaining contact with the body
    • A61B5/6832—Means for maintaining contact with the body using adhesives
    • A61B5/6833—Adhesive patches
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/1702—Systems in which incident light is modified in accordance with the properties of the material investigated with opto-acoustic detection, e.g. for gases or analysing solids
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
    • A61B2562/00—Details of sensors; Constructional details of sensor housings or probes; Accessories for sensors
    • A61B2562/02—Details of sensors specially adapted for in-vivo measurements
    • A61B2562/0204—Acoustic sensors
    • G—PHYSICS
    • G01—MEASURING; TESTING
    • G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N21/00—Investigating or analysing materials by the use of optical means, i.e. using sub-millimetre waves, infrared, visible or ultraviolet light
    • G01N21/17—Systems in which incident light is modified in accordance with the properties of the material investigated
    • G01N21/1702—Systems in which incident light is modified in accordance with the properties of the material investigated with opto-acoustic detection, e.g. for gases or analysing solids
    • G01N2021/1704—Systems in which incident light is modified in accordance with the properties of the material investigated with opto-acoustic detection, e.g. for gases or analysing solids in gases

Definitions

  • the gases dissolved in the blood of mammals are specific to the current state of breathing. They immediately provide information about, for example, insufficient oxygen supply or a reduced respiratory rate.
  • O2 oxygen
  • CO2 carbon dioxide
  • the concentration of oxygen and carbon dioxide is typically determined directly in the exhaled air using a mask. If such a measurement using a mask is not possible or is a hindrance in everyday clinical practice, the concentration of the gases can also be determined indirectly transcutaneously, i.e. using a sensor over the skin.
  • the method according to the invention has the steps: generating electromagnetic excitation radiation with a carrier frequency, the carrier frequency being selected in such a way that the target gas and an absorption gas absorbs the excitation radiation, modulating an amplitude or the carrier frequency of the excitation radiation with a modulation frequency, illuminating an absorption path superficial of a skin of the creature with the excitation radiation, generating a sound wave by absorbing the excitation radiation in the absorption gas and detecting at least one amplitude or one phase of the sound wave as a measure of a concentration of the target gas on the absorption path.
  • the basic idea of the present invention is to detect the concentration of a target gas in the blood of a human or animal being transcutaneously with a photoacoustic process.
  • Photoacoustic methods have the potential to determine a concentration of the target gas with sufficient accuracy at low cost and yet with the required accuracy.
  • the absorption gas in particular a gas mixture containing the absorption gas
  • the excitation radiation having a frequency of its alternating electromagnetic field, i.e. a carrier frequency, which is equal to an absorption frequency of the absorption gas.
  • the absorption gas absorbs the excitation radiation.
  • the target gas is heated and, as a result, the absorption gas or the gas mixture containing the absorption gas undergoes thermal expansion.
  • the absorption distance from the skin of the living being is 5 cm or less, preferably 2 cm or less, more preferably 1 cm or less and particularly preferably 7 mm or less. Due to the underlying physiological diffusion process, the concentration of target gases from the subject's blood becomes less characteristic with increasing distance from the subject's skin. It is decisive for the implementation of the method according to the invention that the absorption section is arranged superficially from the skin in such a way that the target gas diffuses from the blood into the area of the absorption section.
  • the target gas absorbs the excitation radiation as absorption gas on the absorption path and the resulting sound wave, which propagates in the target gas, is detected.
  • the target gas and the absorption gas are identical.
  • the amplitude of the generated and detected sound wave is also directly proportional to the concentration of the target gas in the area of the absorption section and thus also dependent on the concentration of the target gas in the blood of the living being.
  • a high concentration of target gas in the absorption path results in a large amplitude sound wave. If the concentration drops, the amplitude of the sound wave decreases.
  • the detection chamber contains a predetermined and constant concentration of the absorption gas. At least the amplitude or the phase of the sound wave, which is generated due to the absorption of the excitation radiation in the absorption gas in the detection chamber, is detected.
  • the amplitude or the phase of the sound wave is dependent on the power of the excitation radiation which reaches the absorption gas in the detection chamber. Since the absorption volume is arranged in front of the detection chamber in the beam direction of the excitation radiation, each absorption of the excitation radiation in the absorption volume leads to a weakening of the power of the excitation radiation that reaches the absorption gas in the detection volume. The associated reduction in the amplitude of the sound wave detected in the detection chamber or change in its phase is then a measure of the concentration of the target gas in the absorption volume.
  • Such a two-chamber system with an absorption volume separated from the closed detection chamber can be described as an absorption spectrometer with a detector in the form of the photoacoustic detection chamber.
  • this arrangement has an absorption spectrum that is very precisely defined by the absorption gas. This results in a significantly higher sensor sensitivity and thus also a high signal-to-noise ratio and high drift stability despite the short absorption path compared to a conventional absorption spectrometer.
  • the high sensitivity of a sensor and a measurement method which are based on a two-chamber system, makes it possible to keep the length of the absorption path for the electromagnetic excitation radiation in the absorption volume very short.
  • the length of the absorption path in the sense of the present application is the geometric length of the absorption volume along a beam axis of the electromagnetic excitation radiation.
  • the absorption volume is also closed off from the source for the electromagnetic excitation radiation by a transparent element.
  • the absorption distance is defined geometrically by the perpendicular distance between the two, preferably planar, transparent elements.
  • the respective transparent element is a preferably planar pane, preferably made of glass, plastic or a semiconductor material, which is transparent to the electromagnetic excitation radiation used.
  • the dimension of the absorption volume defined by the absorption section contributes significantly to reducing the absorption volume and thus the target gas volume of the sensor.
  • a small length of the absorption section not only reduces this dimension of the absorption volume, but also allows the reduction of the other dimensions of the absorption volume. While the length of the absorption section is limited by the sensitivity of the sensor and the detection limit to be achieved, the other dimensions of the absorption volume are determined by the requirements of the optical beam path of the electromagnetic excitation radiation.
  • the absorption path is kept short, then in principle a comparatively large amount of power from the excitation radiation reaches the detection chamber. Therefore, the cross section of the absorption volume from the absorption chamber can then also be in a direction perpendicular to the absorption path and thus the beam cross-section of the excitation radiation can be reduced. The loss of performance that may be associated with this is manageable.
  • the diameter of this cross-sectional area is 10 mm or less, preferably 5 mm or less, more preferably 2 mm or less and particularly preferably 1 mm or less.
  • this is realized in that an exit facet or exit surface of the source for the radiation sits directly on the transparent element that delimits the absorption volume.
  • the arrangement of the exit facet or the exit surface of the source for the excitation radiation on the transparent element also has the advantage that, due to the reduced distance between the source and the absorption volume, a larger solid angle of the excitation radiation emerging from the source reaches the absorption volume. This despite the small cross-section of the absorption volume perpendicular to the absorption path.
  • the detection chamber with the absorption gas also defines a section of the absorption path for the excitation radiation.
  • the length of this section of the absorption path in the detection chamber is defined perpendicularly to the planar surface of the transparent element which separates the detection chamber from the absorption volume.
  • the length of the section of the absorption path in the detection chamber in the beam direction of the excitation radiation is approximately equal to the mean absorption length of the absorption gas.
  • the absorption length of the target gas within the meaning of the present application is that distance in the target gas after which the initially incident excitation radiation has been absorbed up to 1/e. If the absorption gas is CO2, then in one embodiment of the invention the length of the section of the absorption path in the detection chamber is 0.2 mm.
  • the diffusion opening has a cylindrical inner wall surface with a diameter of less than 50% of the length of the absorption section in the absorption volume, preferably with a diameter of 30% of the length of the absorption section in the absorption volume or less and particularly preferably with one Diameter of 10% of the length of the absorption path in the absorption volume or less.
  • the sensor has a collection element belonging to the target gas volume.
  • the collection element is in fluid communication with the diffusion opening so that the target gas can diffuse from the skin through the collection element into the diffusion opening.
  • the target gas and the absorption gas can be different gases as long as they are absorbing at the carrier frequency of the excitation radiation.
  • the target gas and the absorption gas are also identical in such an embodiment.
  • the absorption gas is enclosed in a closed detection chamber and the absorption section also has an absorption volume for the target gas, it is sufficient if the absorption section in the area of the absorption volume is at a distance from the skin of the living being of 5 cm or less.
  • the method according to the invention also includes the step: calculating a concentration of the target gas in the blood of the living being from the measure of the concentration of the target gas on the absorption section.
  • physiological parameters such as the diffusion rate of the target gas through the skin and design parameters of the photoacoustic sensor used to carry out the method, such as a value for the volume of the absorption volume, a.
  • the photoacoustic sensor for determining a content of a target gas in the blood of a human or animal being according to the independent claim directed to the photoacoustic sensor.
  • the photoacoustic sensor has: a source which is designed in such a way that the source generates electromagnetic excitation radiation with a carrier frequency when the photoacoustic sensor is in operation, the excitation radiation being amplitude-modulated or frequency-modulated with a modulation frequency, an absorption volume which is configured in this way is that in the operation of the photoacoustic sensor, the through a skin of the living essentially diffusing target gas distributed in the absorption volume, the source and the absorption volume being arranged and designed in such a way that during operation of the photoacoustic sensor the electromagnetic excitation radiation of the source illuminates an absorption path within the absorption volume, and a sound detector, the sound detector being set up and arranged in such a way is that when the photoacoustic sensor is in
  • the source of the electromagnetic excitation radiation may be an incoherent source such as a light emitting diode, incandescent emitter, or supercontinuum source in one embodiment, or a coherent source such as a diode laser in another embodiment.
  • the selection of the carrier frequency or the wavelength of the excitation radiation and thus the source depends on which target gas from the blood of the living being is to be detected. It goes without saying that the target gas must show absorption at the carrier frequency of the excitation radiation.
  • the modulation frequency is chosen such that a sound wave with a frequency equal to the modulation frequency can be detected using a conventional sound detector.
  • the modulation frequency is in a range from 200 Hz to 20 kHz.
  • the sound detector is an alternating pressure transducer or an alternating gas flow transducer.
  • An example of an alternating pressure transducer is a microphone, where it the specific design of the microphone is not important according to the invention.
  • An alternating pressure transducer senses a pressure change in the absorbent gas with which the transducer is in contact.
  • An alternating gas flow converter detects a change in a gas flow of a gas surrounding the converter.
  • An example of an alternating gas flow transducer is a measurement device that relies on a temperature change of a wire, with the wire being in the sound wave.
  • the photoacoustic sensor also has an evaluation device, with the evaluation device being effectively connected to the sound detector in such a way that the evaluation device generates a measurement signal during operation of the photoacoustic sensor as a measure of the concentration of the target gas in the absorption volume of the sound detector and wherein the evaluation device is set up and designed in such a way that the evaluation device calculates and outputs a concentration of the target gas in the blood of the living being from the measure of the concentration of the target gas in the absorption volume during operation of the photoacoustic sensor.
  • the photoacoustic sensor comprises a detection chamber, the detection chamber having a closed detection volume separate from the absorption volume, the detection volume of the detection chamber containing the absorption gas and the absorption gas having an absorption at the same carrier frequency as the target gas.
  • the absorption volume is closed off by a housing except for a diffusion opening, the target gas flowing into the absorption volume through the diffusion opening when the photoacoustic sensor is in operation.
  • the diffusion opening of the housing is sealed with a membrane that is permeable to the target gas. In this way, contamination of the absorption volume can be prevented during operation of the photoacoustic sensor.
  • a membrane that is permeable to the target gas.
  • the absorption volume is sealed off from the environment in a gas-tight manner by the housing, with the exception of the diffusion opening.
  • the housing is biocompatible, so that it can be brought into contact with the body, in particular the skin, of the living being without hesitation. Examples of such biocompatible materials are stainless steel, titanium and selected plastics.
  • the housing can be sterilized so that it can be used in a medical environment without hesitation and can be sterilized after use.
  • the housing can be sterilized in an autoclave.
  • the housing in addition to the absorption volume, also includes the detection chamber with the detection volume that is separate from the absorption volume and is closed off from the outside.
  • the housing also comprises the source. In a further embodiment, the housing also includes the evaluation device.
  • the photoacoustic sensor includes an interface for connecting the evaluation device to a conventional data network, in particular a LAN or WLAN interface.
  • the photoacoustic sensor includes a display for displaying a concentration of the target gas in the subject's blood.
  • the housing has a contact device, the contact device being designed and arranged in such a way that the housing with the contact device can be placed on the skin of the living being such that the diffusion opening points towards the skin.
  • the contact device forms a closed, circumferential ring around the diffusion opening.
  • a ring can be in the form of a circular ring, but can also have any other shape, for example it can be rectangular, square, polygonal or oval. It is essential that the ring encloses the diffusion opening in a closed manner. If this ring is brought into contact with the skin, the target gas can enter the absorption volume through the diffusion opening, while the rest of the housing seals the absorption volume against the environment in a gas-tight manner.
  • the contact device comprises a sealing element, the sealing element being designed in such a way that the sealing element can be used to provide a substantially gas-tight seal between the housing and the skin of the living being.
  • the sealing element is a circumferential seal that is closed around the diffusion opening, in particular a seal made of rubber or caoutchouc.
  • the sealing element is a self-adhesive ring that runs around the diffusion opening.
  • the photoacoustic sensor has a heating device, the heating device being arranged and designed in such a way that the heating device heats at least the absorption volume or the skin of the living being in the vicinity of the diffusion opening during operation of the photoacoustic sensor.
  • Such a heating element provides direct or indirect heating of the subject's skin. Warming causes increased blood flow to the skin and the tissues surrounding it, creating ideal conditions for determining the concentration of the target gas.
  • the heating device is set up in such a way that the heating device heats the skin locally to a temperature in a range from 40.degree. C. to 45.degree. C., preferably from 42.degree. Due to the increased blood flow in the tissue when the skin is heated to this temperature range, the transcutaneously measured value for the CO 2 concentration comes very close to the value of the actual CO 2 concentration in an artery section and the heated skin section.
  • the heating device is arranged in such a way that, when the sensor is in operation, it heats an area of the skin which lies beneath the diffusion opening, so that the target gas can flow through the heated skin section into the diffusion opening.
  • One of the above objects is also achieved by using a photoacoustic sensor in one of the previously described embodiments for determining the concentration of the target gas in the blood of the human or animal being.
  • the housing when using the photoacoustic sensor, is placed on the skin of the living being in such a way that the diffusion opening points in the direction of the skin.
  • At least one of the objects mentioned above is also achieved by a system with a sensor, as described above in embodiments thereof, the system during worn on the body of a human or animal being during use.
  • Such systems are also referred to as wearables.
  • Examples of a system worn on the living being's body during use are a smart watch, a digital sports watch, a piece of clothing, and a "smart care" product for monitoring a vital function.
  • Figure 1 is a schematic cross-sectional view through a first embodiment of a photoacoustic sensor for determining a concentration of a target gas in the blood of a living being.
  • FIG. 2 is a schematic cross-sectional view through a further embodiment of such a photoacoustic sensor.
  • Figure 3 is a schematic cross-sectional view through yet another embodiment of a photoacoustic sensor for determining a concentration of a target gas in the blood of a subject.
  • Figure 4 is a schematic cross-sectional view of a modification of the photoacoustic
  • the photoacoustic sensors 1 are shown in a side cross-sectional view, the photoacoustic sensors being shown during their use for detecting the concentration of a target gas. Therefore, the skin surface 2 of the skin 9 of a living being is shown schematically. The respective photoacoustic sensor 1 is placed on this skin surface 2 .
  • the concentration of CO2 as the target gas is to be detected within the meaning of the present application. Therefore, the photoacoustic sensors 1 from FIGS. 1 and 2 have a source 3 for electromagnetic excitation radiation with a wavelength in a range around 4.3 mhh, for example. CO2 absorbs the electromagnetic radiation with this carrier frequency.
  • the excitation radiation 4 emitted and radiated by the source 3 passes through an absorption path 5 in the photoacoustic sensor 1.
  • One by absorption of the excitation radiation A sound wave generated in an absorption gas is detected using a microphone 6 as a sound detector within the meaning of the present application.
  • the absorption gas and the target gas are identical.
  • an absorption gas different from the target gas could also be used in the embodiment from FIG. 1, as long as it absorbs the excitation radiation at the same carrier frequency or wavelength as the target gas.
  • the source 3 and the microphone 6 are arranged in a housing 7 . So that the excitation radiation 4 does not irradiate a wall of the housing 7 after passing through the absorption section 5 and generate an additional sound wave there, an absorber 8 is provided in the housing 7, which absorbs the excitation radiation 4 without heating and thus without thermal expansion of the material of the Wall 7, the absorber 8 or the gas absorbed. In this way, a background or interference signal due to an interaction of the excitation radiation 4 with the housing 7 Ge is avoided. Instead of being absorbed by the absorber 8, the excitation radiation 4 could also be absorbed by the housing 7 or emerge from the housing 7 through a window.
  • the housing 7 defines in its interior an absorption volume 10 and a detection volume 11 separated from this.
  • the detection volume 11 contains the carbon dioxide in a predetermined, unchangeable concentration.
  • the detection volume 11 is a closed volume separated from the absorption volume 10 and from the environment and enclosed in a detection chamber 12 .
  • a window 13 that is transparent to the excitation radiation 4 is provided inside the housing 7 .
  • the absorption section 5 is thus divided into the absorption volume 10 and the detection volume 11 , the absorption volume 10 being arranged in front of the detection volume 11 in the propagation direction of the excitation radiation 4 .
  • the excitation radiation 4 from the source 3 has an amplitude modulation with a modulation frequency of 700 Hz.
  • a sound wave with a sound frequency that is equal to the modulation frequency is generated by absorption of the excitation radiation in the absorption gas.
  • the detection chamber 12 forms an acoustic resonator.
  • this resonator When it is filled with a gas, in particular a gas mixture containing the absorption gas, this resonator has a resonant frequency.
  • This resonant frequency is equal to the modulation frequency of the excitation radiation 4 and thus the frequency in which Absorption gas generated sound wave. Due to the design of the detection chamber 12 as a resonator, the sound wave experiences an amplitude increase, which in turn improves the signal-to-noise ratio.
  • a sound wave is generated in the detection volume 11 , the amplitude of which is determined by the power of the excitation radiation 4 and the concentration of the CO 2 in the detection volume 11 .
  • the amplitude of the sound wave is detected using the microphone 6 .
  • the absorption volume 10 Since the normal ambient air always also contains CO2, when the absorption volume 10 is exposed to the ambient air, a certain proportion of the excitation radiation 4 is absorbed by the CO2 contained in the ambient air. The absorption in the absorption volume 10 reduces the power of the excitation radiation 4 available for the excitation in the detection volume 11 and the sound wave that occurs due to the absorption in the detection volume 11 reduces its amplitude.
  • the housing 7 of the photoacoustic sensor 1 has a diffusion opening 14 in the region of the absorption volume 10 through which gas can flow into the absorption volume 10 .
  • the diffusion opening 14 is surrounded in the form of a ring by a self-adhesive film 15 .
  • the photoacoustic sensor 1 is placed on the skin surface 2 of the living being's skin 9 on the self-adhesive film 15, the self-adhesive film 15 sealing the housing and thus the absorption volume 10 from the skin surface.
  • the photoacoustic sensor 1 has a display 16 with an evaluation device, with the evaluation device 16 being connected to the microphone 6 .
  • the evaluation device 16 receives measured values during operation of the photoacoustic sensor 1 and thus a measure of the amplitude of the sound wave from the microphone 6.
  • the evaluation can be made from the measure of the amplitude of the generated sound wave.
  • te worn 16 calculate a measure of the concentration of the target gas in the absorption volume 10. Since the CC>2 concentration in the ambient air can be estimated fairly accurately and the diffusion process is known as such, a measure of the concentration of the CO2 in the blood of the living being can be determined from the concentration of the CO2 in the absorption volume 10 .
  • the photoacoustic sensor 1 also has a heating device 17 .
  • the housing in the vicinity of the diffusion opening 14 can be heated with the heating device 17 . Since the housing is in thermal contact with the skin surface 2 via the very thin self-adhesive film 15, the heating device 17 also heats the skin and the surrounding tissue during the operation of the photoacoustic sensor 1.
  • the blood flow in this area of the living being is stimulated by the heating and the measurement of the concentration of the CO2 in the absorption volume 10 becomes more meaningful for the actual concentration of the CO2 in the blood.
  • FIGS. 3 and 4 each show a photoacoustic sensor 1 which is based on a two-chamber arrangement.
  • the principle of such a two-chamber arrangement has already been explained above with reference to the embodiment from FIG.
  • the two variants of FIGS. 3 and 4 have an absorption section 5 in the absorption volume 10, which is precisely defined by two planar windows 13, 18.
  • the reduced length of the absorption section 10 in the absorption chamber enables a reduction in the other dimensions of the absorption volume 10, i.e. the cross section of the absorption volume perpendicular to the absorption section 5. If the absorption section 5 is kept short, then in principle a comparatively high intensity of the electromagnetic radiation 4 passes through it Absorption volume 10 in the detection chamber 12. Therefore, the cross section of the absorption volume 10 and thus the beam cross section of the electromagnetic excitation radiation can then be reduced.
  • the absorption volume 10 has a circular cross-section, the cross-sectional area perpendicular to the absorption path 5 having a diameter of only 1 mm.
  • the target gas volume of the sensors 1 from Figures 3 and 4 also consists of the volume of the diffusion opening 14 and the volume of a collecting element 10.
  • the target gas volume of the sensors is measured from the skin surface 2 or a flat plate placed in its place.
  • the absorption volume 10 is only 0.5 microliters.
  • the target gas volume is only slightly larger.
  • the absorption volume 10 is closed off by the window 18 from the source 3 for the electromagnetic excitation radiation 4 .
  • the source 3 is thus positioned outside of the absorption volume 10 .
  • the electromagnetic excitation radiation 4 is radiated into the absorption volume 10 through the window 18 .
  • the source 3 is arranged in a source chamber 20 which is closed off from the environment but also from the absorption volume 10 .
  • the source chamber 20 is evacuated, so that the excitation radiation 4 does not experience any absorption that falsifies the measurement result before it passes through the window 18 into the absorption volume 10 .
  • the diffusion opening 14 provides the only access for gas into the absorption volume 10 ready. Minimizing the target gas volume with the absorption volume 10 and the volume of the diffusion opening 14 means that the partial pressures of the target gas in the body of the living being and in the absorption volume 10 are in equilibrium more quickly, and the time after which the arterial target gas concentration in the living being has changed reliably can be detected is reduced.
  • the largest possible surface area of the skin surface 2 must be included in the collection of the target gas, so that as much target gas as possible flows into the absorption volume 10 .
  • the senor 1 includes a collector element 22 which effectively increases the target gas collecting area of the sensor without commensurately increasing the target gas volume of the sensor.
  • the collecting element 22 is in fluid communication with the diffusion opening 14.
  • the collector element 22 is a thin, porous, and therefore gas-permeable, sheet of plastic.
  • the collecting effect of the collecting element 22 is indicated schematically.
  • the collecting element 22 is covered towards the skin surface 2 with a membrane 23 which is permeable for the target gas.

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  • Animal Behavior & Ethology (AREA)
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  • Biochemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Investigating Or Analysing Materials By Optical Means (AREA)
  • Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)
  • Investigating Or Analyzing Materials By The Use Of Ultrasonic Waves (AREA)

Abstract

La présente invention concerne un procédé pour déterminer une concentration d'un gaz cible dans le sang d'un être vivant humain ou animal. À cet effet, le procédé selon l'invention comprend les étapes suivantes qui consistent à : produire un rayonnement d'excitation électromagnétique avec une fréquence porteuse, la fréquence porteuse étant choisie de façon que le gaz cible et un gaz d'absorption absorbent le rayonnement d'excitation ; moduler une amplitude ou la fréquence porteuse du rayonnement d'excitation à l'aide d'une fréquence de modulation ; éclairer de manière superficielle une section d'absorption de surface de la peau de l'être vivant au moyen du rayonnement d'excitation ; produire une onde sonore par absorption du rayonnement d'excitation dans le gaz d'absorption ; et détecter au moins une amplitude ou une phase de l'onde sonore en tant que mesure de la concentration du gaz cible sur la section d'absorption. L'invention concerne également un capteur photoacoustique destiné à déterminer une concentration d'un gaz cible dans le sang d'un être vivant humain ou animal.
EP22701403.2A 2021-02-19 2022-01-28 Procédé et capteur pour déterminer une concentration d'un gaz cible dans le sang d'un être vivant Pending EP4294255A1 (fr)

Applications Claiming Priority (2)

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EP21158069.1A EP4046569A1 (fr) 2021-02-19 2021-02-19 Procédé et capteur de détermination d'une concentration d'un gaz cible dans le sang d'un être vivant
PCT/EP2022/051999 WO2022175058A1 (fr) 2021-02-19 2022-01-28 Procédé et capteur pour déterminer une concentration d'un gaz cible dans le sang d'un être vivant

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EP4294255A1 true EP4294255A1 (fr) 2023-12-27

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EP21158069.1A Withdrawn EP4046569A1 (fr) 2021-02-19 2021-02-19 Procédé et capteur de détermination d'une concentration d'un gaz cible dans le sang d'un être vivant
EP22701403.2A Pending EP4294255A1 (fr) 2021-02-19 2022-01-28 Procédé et capteur pour déterminer une concentration d'un gaz cible dans le sang d'un être vivant

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Publication number Priority date Publication date Assignee Title
DE102022131508A1 (de) 2022-11-29 2024-05-29 Endress+Hauser Optical Analysis, Inc. Gassensor zur Bestimmung der Konzentration zumindest eines Gases in einem Gasgemisch und Verfahren zur Bestimmung der Konzentration zumindest eines Gases in einem Gasgemisch mit einem Gassensor

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WO1985003574A1 (fr) * 1984-02-07 1985-08-15 Oskar Oehler Installation pour la detection photo-acoustique de gaz
US5933245A (en) * 1996-12-31 1999-08-03 Honeywell Inc. Photoacoustic device and process for multi-gas sensing
US7034943B1 (en) * 2000-03-03 2006-04-25 Aritron Intrumente AG Gas sensors
JP2010107414A (ja) * 2008-10-31 2010-05-13 Sonac Kk 経皮ガスの採取方法、採取装置および測定方法
US9513261B2 (en) * 2013-10-14 2016-12-06 Infineon Technologies Ag Photoacoustic gas sensor device and a method for analyzing gas
CN110333190A (zh) * 2019-07-05 2019-10-15 大连理工大学 一种扩散式光声微腔气体传感器
EP3798607B1 (fr) * 2019-08-09 2023-01-25 Sensirion AG Dispositifs de capteur de gaz photoacoustique

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WO2022175058A1 (fr) 2022-08-25
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