WO2005103677A1 - Testing of breath - Google Patents

Testing of breath Download PDF

Info

Publication number
WO2005103677A1
WO2005103677A1 PCT/GB2005/001517 GB2005001517W WO2005103677A1 WO 2005103677 A1 WO2005103677 A1 WO 2005103677A1 GB 2005001517 W GB2005001517 W GB 2005001517W WO 2005103677 A1 WO2005103677 A1 WO 2005103677A1
Authority
WO
WIPO (PCT)
Prior art keywords
tube
breath
flow passage
porous body
hydrogen sulphide
Prior art date
Application number
PCT/GB2005/001517
Other languages
French (fr)
Inventor
Jacob Moses Blass
Dennis Aston
Peter Golding
Original Assignee
Westone Products Limited
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 Westone Products Limited filed Critical Westone Products Limited
Publication of WO2005103677A1 publication Critical patent/WO2005103677A1/en

Links

Classifications

    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N31/00Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods
    • G01N31/22Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods using chemical indicators
    • G01N31/223Investigating or analysing non-biological materials by the use of the chemical methods specified in the subgroup; Apparatus specially adapted for such methods using chemical indicators for investigating presence of specific gases or aerosols

Definitions

  • This invention relates to the testing of breath, and more particularly provides methods and devices for the qualitative and quantitative assessment of malodorous or bad breath.
  • Hydrogen sulphide reacts with the mercuric chloride to produce mercuric sulphide, resulting in a colour change.
  • the length of the tube, over which the colour change occurs, provides a quantitative estimate of the hydrogen sulphide content of the air.
  • a similar method can be employed for the detection of hydrogen sulphide in breath, making possible the assessment, both qualitative and quantitative, of a breath sample, to provide an indication of the degree to which it constitutes "bad breath".
  • a device is particular for use by a person who wishes to test their own breath alone e.g. at home.
  • a method of testing breath comprising passing an expired breath sample through a flow passage containing a porous body of material carrying a component which undergoes a visible colour change on reaction with hydrogen sulphide.
  • the method may be performed by a direct expiration from the lungs into the flow passage, or by capturing an expired sample, for example in an inflatable bag, and subsequently passing the sample through the flow passage.
  • a predetermined volume of breath is preferably passed through the flow passage.
  • the volume of the sample does not need to be accurately determined. Breathing through the flow passage for an approximate amount of time, for example between 5 and 15 seconds, can provide an approximate qualitative assessment.
  • the invention provides a device for use in testing breath, having a flow passage containing a porous body of material carrying a component which undergoes a visible colour change on reaction with hydrogen sulphide, the flow property of the passage being such that a gas volume of at least 500 ml passes through the porous body in 5 s when the pressure difference between the ends of the passage is 5 mmHg. Since normal out-breathing pressure (pressure of expired breath) during gentle breathing is at a pressure in the range of 1 to 5 mmHg above atmospheric pressure, this device is suitable for use in the method of testing by breathing through it. A typical volume of expired air to be passed through the device is in the range 200 to 1000 ml, which amounts to 1 or 2 normal breaths.
  • the colour change occurs progressively along the porous body as the amount of hydrogen sulphide reacted increases, so that the location of the boundary of the colour change provides a measure of the total amount of hydrogen sulphide in the air sample passed.
  • the flow passage is preferably in a tube having openable seals at each end, to protect the colour-change compound from contact with the atmosphere and moisture before the breath test.
  • the porous material carrying the colour change compound may be held between porous plugs in the tube .
  • the tube may be of glass or suitable transparent or translucent plastics material, and the seals may be flexible non-porous removable plugs or caps or adhesive peelable foils. Alternatively the seals may be breakable elements, for example glass end closures of a glass tube, which can be readily snapped off.
  • Such a glass tube, having breakable glass closures, may be enclosed within a second tube which is flexible in order to permit breakage of the glass closures, without direct contact of the user with the glass.
  • a tube may be a plastics material tube having locations of relatively high flexibility (e.g. bellows portions) permitting localised flexing of the tube to allow breakage of the glass closures.
  • the broken-off parts of the glass closures are retained within the second tube, without hindering the air flow, to avoid risk of harm to the user.
  • the preferred compound which undergoes a visible colour change on reaction with hydrogen sulphide is mercuric chloride. The reaction is H 2 S'1 + HgCl 2 ->HgS + 2HCl .
  • Suitable colour change are lead acetate (Pb (CH 3 COO) 2 ) and silver chloride (AgCl) .
  • This material is mounted on a suitable support, which provides the porous body.
  • the support may be a monolithic body, or may be in the form of a body of particles held in place within the device, for example between porous walls in a tube.
  • a suitable concentration of mercuric chloride in the porous body through which the breath sample is passed is in the range 10 ⁇ 8 to 10 "5 g/cm 3 , more preferably 5 x 10 "8 to 2.5 x 10 "6 g/cm 3 , most preferably 2.5 x 10 "7 to 1.25 x 10 "6 g/cm 3 .
  • Suitable materials of the support are silica, alumina and glass or plastics material beads of high surface area.
  • the device of the invention may be in a form of a tube which has one end suitable for the user to blow into and a second end which opens into a inflatable bag sealed to the tube.
  • the volume of the inflatable bag is suitable for receive a sample of expired breath which permits the desired measurement. This volume is preferably in the range of 200 to 1000 ml.
  • One embodiment of the device of the invention is a tube 5 cm long and 1 cm in diameter, having a volume of approximately 4 cm 3 . With a packed density of the carrier for the colour-change compound of 1, about 4 g of the substrate is loaded with an amount of mercuric chloride in the range 2xl0 ⁇ 7 g to 10 ⁇ 4 g of mercuric chloride, preferably in the range lxlO -6 to 5xl0 ⁇ 5 g.
  • Such a device containing mercuric chloride in an amount at or near the upper end of the range is suitable to give a detectable colour change for a sample on one litre of breath, containing in the range 20 parts per billion (ppb) to 6 parts per million (ppm) of hydrogen sulphide (by weight) .
  • 1 litre of air containing H 2 S at 20 ppb has a weight content of
  • the colour change caused even by 20 ppb of H 2 S is visible.
  • Fig. 1 of the accompanying drawings shows a test device of the invention.
  • Fig. 2 shows a modified part of the device of Fig. 1.
  • Fig. 3 shows alternative test devices.
  • an inflatable air-impermeable plastics material bag 1 has an open side 2 across which the bag walls are heat-sealed together along a seal line 3. Passing through the open side 2 and sealed to the bas walls is a double tube structure 4.
  • The. tube structure 4 has an outer plastics material tube 5 having apertures 6 in its ends covered by metal mesh 7.
  • held inside the tube 5 is a glass tube 8 having narrower elongated closed ends 9.
  • a porous body of particulate carrier material 11 supporting the compound which undergoes colour change on reaction with hydrogen sulphide, as described above.
  • the closed ends 9 are circumscribed by score lines 12 so that they are easily snapped off, to allow air passage through the tube 8.
  • the outer tube 5 has circumferential locations 13 of bellows-like conformation which are relatively more flexible than the remainder of the tube 5. To use the device, the user flexes the tube 5 to break off the ends 9 and then blows through the tube structure 4 to fill the bag 1 (which starts empty) with a predetermined volume of expired breath. The volume of the bag 1 when filled and the flow properties of the tube structure 4 (when open for through flow) are described above.
  • Fig. 2 shows a modified form of the glass tube 8 of Fig. 1.
  • FIGs. 3A, 3B and 3C show other forms of test devices of the invention, having the flow properties defined above.
  • Each device is a substantially rigid tube 20 of transparent plastics material containing a body 21 of particulate material, such as silica, carrying the colour change material, such as HgCl 2 , held between fixed porous plugs 22.
  • the tube has removable seals in the form ' of impermeable plugs 23 inserted into its ends to create a seal.
  • the end seals are flexible impermeable caps 24 which seal over the tube ends.
  • the end seals are peelable discs 25 of impermeable film or foil sealed by adhesive to the tube ends.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Biophysics (AREA)
  • Molecular Biology (AREA)
  • Dispersion Chemistry (AREA)
  • Analytical Chemistry (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • General Physics & Mathematics (AREA)
  • Immunology (AREA)
  • Pathology (AREA)
  • Investigating Or Analyzing Non-Biological Materials By The Use Of Chemical Means (AREA)

Abstract

A device and method for testing breath odour. An expired breath sample is passed through a device containing a material that undergoes a visible colour change on reaction with hydrogen sulphide.

Description

TESTING OF BREATH
Technical Field This invention relates to the testing of breath, and more particularly provides methods and devices for the qualitative and quantitative assessment of malodorous or bad breath.
Background Art Bad breath (halitosis) is a common social problem, but simple and effective methods for its assessment have not become available. Efforts have been made to establish testing criteria, using human testers, but this is not practical for everyday assessment. Attempts to establish instrumental methods have generally involved the use of laboratory-scale equipment, such as gas chromatographs, which are relatively expensive and cumbersome to use. See the references listed below. Hydrogen sulphide (H2S) in the breath is known to be a major cause or bad breath. Portable apparatus for measurement of the hydrogen sulphide concentration in the atmosphere is known, one manufacturer being Drager. The Drager apparatus has a tube containing mercuric chloride (HgCl2) supported on a suitable carrier. A predetermined amount of air is sucked through the tube, by a pump or a spring-loaded bellows.
Hydrogen sulphide reacts with the mercuric chloride to produce mercuric sulphide, resulting in a colour change. The length of the tube, over which the colour change occurs, provides a quantitative estimate of the hydrogen sulphide content of the air. The pressure required to draw air through this tube is about 250 mmHg (1 mHg = 133 Pa) . This device has not been proposed for use in analysis of breath.
Summary of the Invention The present inventors have realised that a similar method can be employed for the detection of hydrogen sulphide in breath, making possible the assessment, both qualitative and quantitative, of a breath sample, to provide an indication of the degree to which it constitutes "bad breath". Such a device is particular for use by a person who wishes to test their own breath alone e.g. at home. In one aspect of the invention, there is provided a method of testing breath, comprising passing an expired breath sample through a flow passage containing a porous body of material carrying a component which undergoes a visible colour change on reaction with hydrogen sulphide. The method may be performed by a direct expiration from the lungs into the flow passage, or by capturing an expired sample, for example in an inflatable bag, and subsequently passing the sample through the flow passage. In both cases, a predetermined volume of breath is preferably passed through the flow passage. However, for a qualitative assessment, the volume of the sample does not need to be accurately determined. Breathing through the flow passage for an approximate amount of time, for example between 5 and 15 seconds, can provide an approximate qualitative assessment. In a second aspect, the invention provides a device for use in testing breath, having a flow passage containing a porous body of material carrying a component which undergoes a visible colour change on reaction with hydrogen sulphide, the flow property of the passage being such that a gas volume of at least 500 ml passes through the porous body in 5 s when the pressure difference between the ends of the passage is 5 mmHg. Since normal out-breathing pressure (pressure of expired breath) during gentle breathing is at a pressure in the range of 1 to 5 mmHg above atmospheric pressure, this device is suitable for use in the method of testing by breathing through it. A typical volume of expired air to be passed through the device is in the range 200 to 1000 ml, which amounts to 1 or 2 normal breaths. Preferably the colour change occurs progressively along the porous body as the amount of hydrogen sulphide reacted increases, so that the location of the boundary of the colour change provides a measure of the total amount of hydrogen sulphide in the air sample passed. The flow passage is preferably in a tube having openable seals at each end, to protect the colour-change compound from contact with the atmosphere and moisture before the breath test. The porous material carrying the colour change compound may be held between porous plugs in the tube . The tube may be of glass or suitable transparent or translucent plastics material, and the seals may be flexible non-porous removable plugs or caps or adhesive peelable foils. Alternatively the seals may be breakable elements, for example glass end closures of a glass tube, which can be readily snapped off. Such a glass tube, having breakable glass closures, may be enclosed within a second tube which is flexible in order to permit breakage of the glass closures, without direct contact of the user with the glass. Such a tube may be a plastics material tube having locations of relatively high flexibility (e.g. bellows portions) permitting localised flexing of the tube to allow breakage of the glass closures. Preferably the broken-off parts of the glass closures are retained within the second tube, without hindering the air flow, to avoid risk of harm to the user. The preferred compound which undergoes a visible colour change on reaction with hydrogen sulphide is mercuric chloride. The reaction is H2S'1 + HgCl2->HgS + 2HCl . Other compounds which provide a suitable colour change are lead acetate (Pb (CH3COO) 2) and silver chloride (AgCl) . This material is mounted on a suitable support, which provides the porous body. The support may be a monolithic body, or may be in the form of a body of particles held in place within the device, for example between porous walls in a tube. In the case of mercuric chloride, a suitable concentration of mercuric chloride in the porous body through which the breath sample is passed is in the range 10~8 to 10"5 g/cm3, more preferably 5 x 10"8 to 2.5 x 10"6 g/cm3, most preferably 2.5 x 10"7 to 1.25 x 10"6 g/cm3. Suitable materials of the support are silica, alumina and glass or plastics material beads of high surface area. The device of the invention may be in a form of a tube which has one end suitable for the user to blow into and a second end which opens into a inflatable bag sealed to the tube. The volume of the inflatable bag is suitable for receive a sample of expired breath which permits the desired measurement. This volume is preferably in the range of 200 to 1000 ml. One embodiment of the device of the invention is a tube 5 cm long and 1 cm in diameter, having a volume of approximately 4 cm3. With a packed density of the carrier for the colour-change compound of 1, about 4 g of the substrate is loaded with an amount of mercuric chloride in the range 2xl0~7 g to 10~4 g of mercuric chloride, preferably in the range lxlO-6 to 5xl0~5 g. Such a device containing mercuric chloride in an amount at or near the upper end of the range is suitable to give a detectable colour change for a sample on one litre of breath, containing in the range 20 parts per billion (ppb) to 6 parts per million (ppm) of hydrogen sulphide (by weight) . 1 litre of air containing H2S at 20 ppb has a weight content of
H2S of 2.586 x 10"8 g, which reacts with 2.075 x 10"7 g of HgCl2. The colour change caused even by 20 ppb of H2S is visible.
Brief Description of the Drawings Fig. 1 of the accompanying drawings shows a test device of the invention. Fig. 2 shows a modified part of the device of Fig. 1. Fig. 3 shows alternative test devices.
Detailed Description of the Drawings In the device of Fig. 1, an inflatable air-impermeable plastics material bag 1 has an open side 2 across which the bag walls are heat-sealed together along a seal line 3. Passing through the open side 2 and sealed to the bas walls is a double tube structure 4. The. tube structure 4 has an outer plastics material tube 5 having apertures 6 in its ends covered by metal mesh 7. Held inside the tube 5 is a glass tube 8 having narrower elongated closed ends 9. Within the glass tube 8 and confined between fixed porous plugs 10 is a porous body of particulate carrier material 11 supporting the compound which undergoes colour change on reaction with hydrogen sulphide, as described above. The closed ends 9 are circumscribed by score lines 12 so that they are easily snapped off, to allow air passage through the tube 8. The outer tube 5 has circumferential locations 13 of bellows-like conformation which are relatively more flexible than the remainder of the tube 5. To use the device, the user flexes the tube 5 to break off the ends 9 and then blows through the tube structure 4 to fill the bag 1 (which starts empty) with a predetermined volume of expired breath. The volume of the bag 1 when filled and the flow properties of the tube structure 4 (when open for through flow) are described above. Fig. 2 shows a modified form of the glass tube 8 of Fig. 1. Between the porous plugs 10, the porous body 11 of particles carrying the mercuric chloride or other colour- change material is conical in shape, increasing in cross- sectional area in the flow direction. This increases accuracy of assessment of H2S concentration at the lower end of the detectable concentration range. Figs. 3A, 3B and 3C show other forms of test devices of the invention, having the flow properties defined above. Each device is a substantially rigid tube 20 of transparent plastics material containing a body 21 of particulate material, such as silica, carrying the colour change material, such as HgCl2, held between fixed porous plugs 22. In Fig. 3A, the tube has removable seals in the form' of impermeable plugs 23 inserted into its ends to create a seal. In Fig. 3B, the end seals are flexible impermeable caps 24 which seal over the tube ends. In Fig. 3C the end seals are peelable discs 25 of impermeable film or foil sealed by adhesive to the tube ends. References
Rosenberg (1992) J. Periodontol. 63:776-782 Shimura M (1996) J. Periodontol. 67:396-402 Suarez FL (2000) J. Dent. Res. 79 (10) : 1773-1777

Claims

1. Breath testing device comprising a flow passage containing a porous body of material carrying a component that undergoes a visible colour change on reaction with hydrogen sulphide.
2. A device according to claim 1, wherein said passage has a flow property such that a gas volume of at least 500 ml passes through the porous body in 5 s when the pressure difference between the ends of the passage is 5 mmHg.
3. A device according to claim 1 or claim 2, wherein said visible colour change occurs progressively along the porous body of material as the amount of hydrogen sulphide increases.
4. A device according to any one of claims 1 to 3, wherein the porous material carrying the colour-change compound is held between porous plugs in the tube.
5. A device according to any one of claims 1 to 4, wherein said flow passage is a tube, and openable seals are provided at each end that protect the colour-change compound from contact with the atmosphere and moisture before the breath test.
6. A device according to claim 5, wherein said tube is made of glass or a transparent or translucent plastics material.
7. A device according to claim 5 or 6, wherein the seals are flexible non-porous removable plugs or caps, or adhesive peelable foils.
8. A device according to claim 5 or 6, wherein the seals are breakable elements that can be readily snapped off.
9. A device according to claim 8, wherein said breakable elements are glass end closures of a glass tube.
10. A device according to claim 8 or 9, wherein said tube is enclosed within a flexible second tube that permits breakage of the seals without the direct contact of the user with the breakable elements.
11. A device according to claim 10, wherein said second tube is a plastics material having locations of relatively high flexibility that permit localised flexing of said second tube to allow breakage of said breakable elements.
12. A device according to claim 10 or 11, wherein the second tube retains said elements after breakage without hindering the air flow of the device.
13. A device according to any one of claims 1 to 12, wherein the component that undergoes a visible colour change on reaction with hydrogen sulphide is selected from mercuric chloride, lead acetate and silver chloride.
14. A device according to claim 13, wherein said visible colour change compound is mercuric chloride in a concentration of 10-8 to 10"5 g/cm3 in the porous body.
15. A device according to any one of claims 1 to 14 having the form of a tube that has one end suitable for the user to blow into and a second end that opens into an inflatable bag sealed to the tube.
16. A device according to claim 15, wherein said inflatable bag has a volume in the range of 200 to 1000 ml.
17. A method for testing breath, comprising the step of passing an expired breath sample through a flow passage containing a porous body of material carrying a component that undergoes a visible colour change on reaction with hydrogen sulphide
18. A method according to claim 17, wherein the breath passed through the flow passage has a predetermined total volume.
19. A method according to claim 17 or 18, wherein said expired breath is passed through a flow passage for a period of time lasting between 5 and 15 seconds.
20. A method according to any one of claims 17 to 19, wherein said breath sample is expired directly from the lungs into said flow passage.
21. A method according to any one of claims 17 to 20, wherein said expired breath sample is captured within a container and said container is used for introducing said breath sample into said flow passage.
22. A method according to claim 17, using the device according to any one of claims 1 to 16.
PCT/GB2005/001517 2004-04-20 2005-04-20 Testing of breath WO2005103677A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB0408786A GB0408786D0 (en) 2004-04-20 2004-04-20 Testing of breath
GB0408786.2 2004-04-20

Publications (1)

Publication Number Publication Date
WO2005103677A1 true WO2005103677A1 (en) 2005-11-03

Family

ID=32344069

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/GB2005/001517 WO2005103677A1 (en) 2004-04-20 2005-04-20 Testing of breath

Country Status (2)

Country Link
GB (1) GB0408786D0 (en)
WO (1) WO2005103677A1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20200064330A1 (en) * 2017-02-24 2020-02-27 Cedars-Sinai Medical Center Measurement of hydrogen sulfide during breath testing

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1092006A (en) * 1965-06-01 1967-11-22 Drager Otto H Method and apparatus for the simultaneous selective determination of hydrogen sulphide and a mercaptan in a gas mixture
GB1210295A (en) * 1967-06-29 1970-10-28 Auergesellschaft Gmbh Improvements in or relating to indicator tubes
JPS57135360A (en) * 1981-02-16 1982-08-20 Kao Corp Foul breath detecting agent
US4348358A (en) * 1980-09-25 1982-09-07 Mine Safety Appliances Company Colorimetric dosimeter
JPH01101459A (en) * 1987-10-15 1989-04-19 Naoharu Mizuno Method for deciding sulfur in sulfide and reducing sulfur oxide and implement for said decision
JPH05164753A (en) * 1991-12-11 1993-06-29 Kazuyuki Aoki Direct-reading passive monitor
JPH08224239A (en) * 1995-02-20 1996-09-03 Hideo Ueda Method for inspecting bacteria in oral cavity and apparatus for inspection therefor
WO1997005482A1 (en) * 1995-07-31 1997-02-13 The Oralife Group, Inc. A colorimetric method of detecting thiol or mercaptan compounds and its use for oral malodor determination
JPH11316223A (en) * 1998-04-30 1999-11-16 Hiroshi Oya Simple foul breath measuring instrument

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1092006A (en) * 1965-06-01 1967-11-22 Drager Otto H Method and apparatus for the simultaneous selective determination of hydrogen sulphide and a mercaptan in a gas mixture
GB1210295A (en) * 1967-06-29 1970-10-28 Auergesellschaft Gmbh Improvements in or relating to indicator tubes
US4348358A (en) * 1980-09-25 1982-09-07 Mine Safety Appliances Company Colorimetric dosimeter
JPS57135360A (en) * 1981-02-16 1982-08-20 Kao Corp Foul breath detecting agent
JPH01101459A (en) * 1987-10-15 1989-04-19 Naoharu Mizuno Method for deciding sulfur in sulfide and reducing sulfur oxide and implement for said decision
JPH05164753A (en) * 1991-12-11 1993-06-29 Kazuyuki Aoki Direct-reading passive monitor
JPH08224239A (en) * 1995-02-20 1996-09-03 Hideo Ueda Method for inspecting bacteria in oral cavity and apparatus for inspection therefor
WO1997005482A1 (en) * 1995-07-31 1997-02-13 The Oralife Group, Inc. A colorimetric method of detecting thiol or mercaptan compounds and its use for oral malodor determination
JPH11316223A (en) * 1998-04-30 1999-11-16 Hiroshi Oya Simple foul breath measuring instrument

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
PATENT ABSTRACTS OF JAPAN vol. 006, no. 233 (P - 156) 19 November 1982 (1982-11-19) *
PATENT ABSTRACTS OF JAPAN vol. 013, no. 342 (P - 908) 2 August 1989 (1989-08-02) *
PATENT ABSTRACTS OF JAPAN vol. 017, no. 566 (P - 1629) 14 October 1993 (1993-10-14) *
PATENT ABSTRACTS OF JAPAN vol. 1997, no. 01 31 January 1997 (1997-01-31) *
PATENT ABSTRACTS OF JAPAN vol. 2000, no. 02 29 February 2000 (2000-02-29) *

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20200064330A1 (en) * 2017-02-24 2020-02-27 Cedars-Sinai Medical Center Measurement of hydrogen sulfide during breath testing
US12411127B2 (en) * 2017-02-24 2025-09-09 Cedars-Sinai Medical Center Measurement of hydrogen sulfide during breath testing

Also Published As

Publication number Publication date
GB0408786D0 (en) 2004-05-26

Similar Documents

Publication Publication Date Title
US4740475A (en) Integral substance detection device and method
US4327575A (en) Monitoring apparatus and method for toxic vapors
EP2839271B1 (en) Mobile device and method for analysing breath samples
WO1993015402A1 (en) An apparatus for indicating the presence of co2 and a method of measuring and indicating bacterial activity within a container or bag
US6468477B1 (en) Sealable air sampling bag
AU2013215601A1 (en) System for measuring breath analytes
US4492673A (en) Disposable sobriety tester
US8431087B2 (en) Carbon dioxide detector having borosilicate substrate
US8420405B2 (en) Carbon dioxide detector having borosilicate substrate
JPH11503527A (en) Device that detects exhaled breath components
US8431088B2 (en) Carbon dioxide detector having borosilicate substrate
WO2005103677A1 (en) Testing of breath
US8449834B2 (en) Carbon dioxide detector having borosilicate substrate
Bergman et al. A simple gas chromatograph with an electrochemical detector for the measurement of hydrogen and carbon monoxide in the parts per million range, applied to exhaled air
US3459508A (en) Method of ascertaining the alcohol content of exhaled air,and also a testing tube for carrying out such method
CN108663503A (en) A method and system for intelligently detecting the lifespan of red blood cells
CA1157355A (en) Continuous monitor of the exposure to industrial gases and vapour contaminants
US7278291B2 (en) Trace gas sensor with reduced degradation
JPH09210875A (en) Exhalation sampling device
EP2067030A2 (en) Carbon dioxide detector having borosilicate substrate
EP0173682A1 (en) Disposable breath analyzer device and method of fabrication
EP0819940A2 (en) Method of detecting halitosis and detector for use in the method
JP3212236B2 (en) Adsorbent water absorption state detector
CA2659320A1 (en) Packaging system for testing devices
Winkel et al. Appropriate sample bags and syringes for preserving breath samples in breath odor research: a technical note

Legal Events

Date Code Title Description
AK Designated states

Kind code of ref document: A1

Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KM KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SM SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW

AL Designated countries for regional patents

Kind code of ref document: A1

Designated state(s): BW GH GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG

121 Ep: the epo has been informed by wipo that ep was designated in this application
NENP Non-entry into the national phase

Ref country code: DE

WWW Wipo information: withdrawn in national office

Country of ref document: DE

122 Ep: pct application non-entry in european phase