US20180243523A1 - Controlling flow of exhaled breath during analysis - Google Patents
Controlling flow of exhaled breath during analysis Download PDFInfo
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- US20180243523A1 US20180243523A1 US15/899,582 US201815899582A US2018243523A1 US 20180243523 A1 US20180243523 A1 US 20180243523A1 US 201815899582 A US201815899582 A US 201815899582A US 2018243523 A1 US2018243523 A1 US 2018243523A1
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- 238000004458 analytical method Methods 0.000 title description 11
- 239000012491 analyte Substances 0.000 claims abstract description 23
- 238000000034 method Methods 0.000 claims description 16
- 238000011144 upstream manufacturing Methods 0.000 claims description 8
- 230000000717 retained effect Effects 0.000 claims description 2
- MWUXSHHQAYIFBG-UHFFFAOYSA-N Nitric oxide Chemical compound O=[N] MWUXSHHQAYIFBG-UHFFFAOYSA-N 0.000 description 12
- 239000007789 gas Substances 0.000 description 6
- 238000010586 diagram Methods 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 230000005856 abnormality Effects 0.000 description 2
- 208000006673 asthma Diseases 0.000 description 2
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- 238000013461 design Methods 0.000 description 2
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- 238000005259 measurement Methods 0.000 description 2
- 230000004962 physiological condition Effects 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical group [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- 102100030497 Cytochrome c Human genes 0.000 description 1
- 108010075031 Cytochromes c Proteins 0.000 description 1
- 206010061218 Inflammation Diseases 0.000 description 1
- 206010023126 Jaundice Diseases 0.000 description 1
- 206010025476 Malabsorption Diseases 0.000 description 1
- 208000004155 Malabsorption Syndromes Diseases 0.000 description 1
- 230000001154 acute effect Effects 0.000 description 1
- 230000003466 anti-cipated effect Effects 0.000 description 1
- 150000001720 carbohydrates Chemical class 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
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- 238000003745 diagnosis Methods 0.000 description 1
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- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 230000004054 inflammatory process Effects 0.000 description 1
- 238000007726 management method Methods 0.000 description 1
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Images
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/08—Bellows; Connecting tubes ; Water traps; Patient circuits
- A61M16/0816—Joints or connectors
- A61M16/0841—Joints or connectors for sampling
- A61M16/085—Gas sampling
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/08—Measuring devices for evaluating the respiratory organs
- A61B5/0803—Recording apparatus specially adapted therefor
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/08—Measuring devices for evaluating the respiratory organs
- A61B5/082—Evaluation by breath analysis, e.g. determination of the chemical composition of exhaled breath
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B5/00—Measuring for diagnostic purposes; Identification of persons
- A61B5/08—Measuring devices for evaluating the respiratory organs
- A61B5/097—Devices for facilitating collection of breath or for directing breath into or through measuring devices
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/0003—Accessories therefor, e.g. sensors, vibrators, negative pressure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/0057—Pumps therefor
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/06—Respiratory or anaesthetic masks
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/20—Valves specially adapted to medical respiratory devices
- A61M16/208—Non-controlled one-way valves, e.g. exhalation, check, pop-off non-rebreathing valves
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/483—Physical analysis of biological material
- G01N33/497—Physical analysis of biological material of gaseous biological material, e.g. breath
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/0003—Accessories therefor, e.g. sensors, vibrators, negative pressure
- A61M2016/0027—Accessories therefor, e.g. sensors, vibrators, negative pressure pressure meter
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M2205/00—General characteristics of the apparatus
- A61M2205/33—Controlling, regulating or measuring
- A61M2205/3331—Pressure; Flow
Definitions
- This invention resides in the field of systems and methods for the analysis of exhaled breath.
- Analyses of exhaled breath from human subjects are of value in many applications, including the diagnosis and management of several physiological conditions.
- a change in the nitric oxide (NO) concentration in the exhaled breath of a person suffering from asthma can indicate a change in the level of inflammation in the airway of the person, which in turn can indicate an increase in the likelihood of an asthma attack.
- Another component of exhaled breath whose concentration can be correlated with a physiological abnormality is carbon monoxide, a rise in which can be an early indication of the onset of hemolytic jaundice.
- a still further example is hydrogen, whose rise can indicate malabsorption of carbohydrate.
- the one that is the most difficult to control in most cases is the flow rate of the exhaled breath of the subject through the analytical device.
- a crude method in the prior art for controlling the breath flow rate is a verbal instruction from the clinician performing the analysis to the subject, calling for the subject to breathe out faster or slower to correct deviations from the design rate for the analyzer. This method is limited by the subject's ability to adjust the flow rate, particularly when the subject is a child, and is generally impractical for trace gas analyses over a wide range of concentration.
- An alternative is to include a variable flow resistance in the analyzer and altering the resistance to correct for the deviations.
- a device that incorporates this capability is disclosed in Moilanen, E., et al., U.S. Pat. No.
- the present invention resides in apparatus for exhaled breath analysis that includes a housing constructed to receive exhaled breath directly from a subject, a flow-through passage within the housing for the travel of the exhaled breath, an analyte sensing element in the flow-through passage, and a pump or pump system to control the rate at which the subject exhales into the housing and to cause the exhaled breath to flow through the passage at a controlled rate.
- the invention can be used for the analysis of a variety of gaseous analytes, including those in trace amounts, and is of particular interest the quantification of NO.
- FIG. 1 is a diagram of the components of an analytical device embodying the features of the present invention.
- FIG. 2 is a diagram of the components of a second analytical device embodying the features of the present invention.
- FIG. 3 is a diagram of the components of a third analytical device embodying the features of the present invention.
- FIG. 1 represents a network 10 of components that constitute the functional parts of an analytical device in accordance with the invention.
- the device itself can be a mask or similar device that can be worn by, or otherwise mounted to, the user, either directly or through a mouthpiece, in a manner that will capture the breath exhaled by the user.
- Exhaled breath enters the device at an inlet 11 .
- the pressure of the exhaled breath is detected by a pressure sensor 12 in the device with an operating range appropriate to the anticipated range of breath pressure. In one embodiment, this range is 5 to 20 cm of water (approximately 0.45 to 1.8 psig), the lower limit of this range being the pressure necessary to close the velum of the typical user and the upper limit a pressure at which the typical user will feel discomfort.
- the pump 13 can operate in various ways. For example, when the pressure detected by the sensor rises to a threshold value, which may be the lower limit of the above range, the pump 13 can be actuated by a signal from the pressure sensor, and as exhalation into the device continues and the pressure eventually drops below the lower limit, the pump can be de-actuated (turned off).
- a suitable pump is Model No. UNMP50 of KNF Neuberger, Inc., Trenton, N.J., USA. This pump has a free-flow capacity of 66.7 cm 3 /s, a maximum vacuum of 400 mbar (63 cm H 2 O), and a maximum continuous pressure of 0.5 bar (79 cm H 2 O).
- the pump is preferably sufficiently resistant to inlet pressure to maintain a substantially constant flow rate despite changes in the subject's mouth pressure across the range of interest.
- the pump can be equipped with closed-loop control using the pressure sensor 12 for feedback.
- An optional component in the flow path of the breath through the device is a flow resistor 14 which in this embodiment is positioned downstream of the pressure sensor 12 and upstream of the pump 13 .
- a second flow resistor 15 is included in the flow path as well, downstream of the first resistor 14 but still upstream of the pump 13 .
- the flow resistor or resistors will assist in limiting the flow to a desired flow rate, which may for example be 50 cm 3 /s, and in increasing the pressure in the user's mouth, throat, or air passages.
- a flow resistor is a fixed orifice in the form of a round aperture having a diameter of approximately 0.11 cm.
- Flow resistors of other types will be readily apparent to those skilled in the art and can be used in place of an orifice. Flow resistors can serve to tune the system to the specifications of the pump 13 .
- the first resistor offers a resistance which will be designated herein by the symbol R i .
- the flow path downstream of the first resistor 14 in this embodiment is divided into two streams—a main stream 16 and a side stream 17 . These streams will also be referred to herein as a primary stream and a secondary stream, respectively.
- the second resistor 15 resides in the main stream 16 and offers a resistance which will be designated here by the symbol R p , which can be variable or fixed. Examples of variable resistors are motor-controlled needle valves, solenoid-controlled needle valves, manual needle valves, and pinch-tube valves, all of which also offer resistance to the flow.
- An example of a fixed resistor is a non-variable orifice.
- a side stream valve 18 which is preferably a shut-off, i.e., open/close, valve and a resistor 19 to allow flow into or prevent flow from entering the side stream, and to thereby control the flow distribution between the two streams.
- a shut-off valve suitable for this application is a solenoid valve; other examples will be readily apparent to those skilled in the art.
- the side stream valve 18 can be opened to allow breath flow to occur in parallel through the main and side streams.
- the valve may for example be set to open at 7 seconds after the start of exhalation flow into the device, and to remain open until 10 seconds after the start of exhalation flow. Under this protocol, all exhaled breath will pass through the main stream 16 for the first seven seconds of the test, then through both the main and side streams 16 , 17 for the next three seconds.
- the side stream 17 contains an analyte sensor 21 that detects the level of the analyte (NO or otherwise) in the exhaled breath passing through the side stream.
- the analyte sensor 21 may also offer flow resistance and eliminate the need for a separate side stream resistor 19 .
- the side stream resistor 19 is incorporated into the analyte sensor 21 .
- the side stream valve 18 can also serve to provide the flow resistance in the side stream, and accordingly the side stream resistor 19 can be incorporated into the valve 18 .
- flow resistance in the side stream is designated herein by the symbol R s .
- the side stream can contain other components, such as a carbon dioxide scrubber (not shown).
- a check valve 22 is included in the side stream to prevent backflow.
- a constant flow rate of exhaled breath through the device 10 can be maintained in any of several ways.
- One way is to use a main stream resistor 15 whose resistance R p is variable while the side stream resistor 19 has a non variable resistance R s .
- the main stream resistor may have a value of R p1 when the side stream valve 18 is closed, and be programmed or set to change to a value of R p2 when the side stream valve 18 is open.
- the values of R p1 and R p2 can be chosen so that the sum of the flow rates through the main stream 16 and the side stream 17 when the side stream valve 18 is open will equal the flow rate through the main stream 16 when the side stream valve 18 is closed.
- the choice of resistance levels for R p1 and R p2 may be influenced in part by the resistance from other components in the flow stream, such as the other resistors, valves, and sensors, as well as the voltage and capacity of the pump.
- the main stream 16 and side stream 17 recombine into a single passage 23 upstream of the device outlet 24 . Since the pump 13 is positioned downstream of the point where the main stream 16 and side stream 17 recombine, the pump 13 controls the overall flow of the system rather than each stream individually. The placing of the pump 13 downstream of the sensor 12 also avoids the risk of contaminating the sensor with the pump effluent.
- ⁇ P denotes the pressure drop across the pump 13 .
- R i denotes the resistance offered by the first (upstream) resistor 14 .
- R p denotes the resistance offered by the main stream resistor 15 .
- R s denotes the resistance offered by the side stream components 19 , 21 , and 22 .
- V denotes the total flow rate of exhaled breath through the device.
- Example 1 Operating Parameters Parameter Side Stream Valve 18 Closed Side Stream Valve 18 Open ⁇ P 32 cm H 2 O 32 cm H 2 O R i 0.4 cm H 2 O/cm 3 /s 0.4 cm H 2 O/cm3/s R p 0.24 cm H 2 O/cm 3 /s (R p1 ) 0.29 cm H 2 O/cm 3 /s (R p2 ) R s (infinite) 1.5 cm H 2 O/cm 3 /s V 50 cm 3 /s 50 cm 3 /s 50 cm 3 /s
- the two values of R p are chosen to maintain a constant flow rate of 50 cm 3 /s throughout the test, with a flow rate of 8 cm 3 /s through the analyte sensor 21 , i.e., a main stream to side stream flow ratio of 42:8, when the side stream valve is open.
- breath will flow through the side stream at a rate of 8 cm 3 /s, while the remainder will flow at 42 cm 3 /s through the main stream 16 .
- the resistance from all resistors remains constant while the pump flow rate is varied.
- This configuration utilizes a variation in the pressure drop across the pump to compensate for the change in the overall flow path resistance that occurs when the side stream is opened.
- Example 2 Operating Parameters Parameter Side Stream Valve 18 Closed Side Stream Valve 18 Open ⁇ P 34.3 cm H 2 O 32 cm H 2 O R i 0.4 cm H 2 O/cm 3 /s 0.4 cm H 2 O/cm 3 /s R p 0.29 cm H 2 O/cm 3 /s 0.29 cm H 2 O/cm 3 /s R s (infinite) 1.5 cm H 2 O/cm 3 /s V 50 cm 3 /s 50 cm 3 /s 50 cm 3 /s
- FIG. 2 represents a system 31 containing two pumps rather than a single pump, although still within the scope of the invention. Similar to the system 10 depicted in FIG. 1 , exhaled breath enters the system 31 of FIG. 2 at a single inlet 32 and leaves at a single outlet 33 , and the system divides into a main stream 34 and a side stream 35 at a dividing junction 36 , the two streams recombining at a downstream junction 37 .
- the first pump 38 is in the main stream 34 downstream of the junction 36 where the two streams are first formed, and the second pump 39 is in the side stream 35 .
- the second pump 39 can compensate for variations in the flow resistance 41 through the side stream, particularly when the resistance is in the analyte sensor 42 .
- the second pump 39 also permits independent flow rates to be established for the main stream 34 and the side stream 35 .
- the independent flow rates can be configured by software or on a real-time basis, without exchanging the components.
- the second pump 39 is downstream from the analyte sensor 42 so that the pump effluent does not interfere with the signal emitted by the sensor 42 .
- the dual-pump system of FIG. 2 can utilize resistors that offer variable resistance as well as variable-speed pumps.
- a side stream valve 43 is shown in the dual-pump system.
- the side stream valve 43 can be eliminated by using the second pump 39 itself to open and close the side stream to flow.
- FIG. 3 A further variation is shown in FIG. 3 , where the junction 37 at which the main and side streams are recombined ( FIG. 2 ) has been eliminated, and the main and side streams 34 , 35 vent separately through separate outlets 51 , 52 , respectively.
- a side stream as shown in each of the Figures herein offers various advantages.
- the flow rate of exhaled breath passing through the analyte sensor can be reduced and a small analyte sensor, particularly one that responds quickly to the analyte due to its small size, can thereby be used.
- the flow rate through the side stream can thus be limited to a rate within a range of 5 cm 3 /s to 11 cm 3 /s, or in certain embodiments a range of 6 cm 3 /s to 10 cm 3 /s, or a range of 7 cm 3 /s to 9 cm 3 /s.
- a portion of the breath passing through the entire device can be retained in the region of the sensor for an extended contact time to incubate the sample and sensor prior to the measurement.
- a typical incubation time may be 1 minute.
- the sensor can then be removed for analysis or measurement. Incubation is of value for sensors that respond too slowly to produce a real-time analysis of a moving stream.
- the placement of the analyte sensor in a side stream allows the user to pass multiple cycles of breath across the sensor before flow through the device as a whole is stopped.
- a sensor that has a volume of 5.0 cm 3 and a side stream that accommodates a breath flow of 8.0 cm 3 /s
- leaving the side stream open for 3.0 seconds will cause 24.0 cm 3 of breath to cross the sensor before the final 5.0 cm 3 is trapped in the side stream.
- Examples of periods of time during which the side stream is left open are periods of 1 to 10 seconds in duration, 1 to 7 seconds in duration, and 1 to 5 seconds in duration. This is useful for flushing the sensor prior to the analysis, thereby purging the sensor of extraneous gases with which the sensor was in contact prior to the analysis.
- the start of flow through the side stream can also be delayed for selected intervals following the start of the flow of exhaled breath through the device as a whole, for reasons of flushing or equilibration.
- the opening of the side stream will be delayed for an interval of between 5 second and 9 seconds after the start of flow of exhaled breath through the device, and in certain other embodiments, the interval will be between 6 seconds and 8 seconds.
- the optimum interval for a child may differ from the optimum interval for an adult.
- the side stream shut-off valve With the inclusion of the side stream shut-off valve, a separate side stream pump, or both, the side stream allows the system to be operated in a mode that can be termed a “stopped-flow operation.” Stopping the flow allows the system to create a stable testing environment that can be maintained for a much longer period than is possible in a flowing system. As noted above, a one-minute static exposure time is illustrative, although much longer or shorter exposure times can be used as well.
- trace gas denotes gases whose concentrations are below 1 part per million (on a volume basis), and preferably, depending on the significance of the analyte and the range within which variations can indicate a particular physiological condition or the onset of such a condition, below 300 parts per billion, below 200 parts per billion, or below 100 parts per billion. All concentrations herein, unless otherwise noted, are by volume.
- the invention is of particular interest in conjunction with a sensor consisting of cytochrome c in a sol-gel xerogel to measure NO.
- the pump can be placed upstream of the juncture where the flow passage is divided into two streams, and when using either one pump or two, the pump(s) can be placed upstream of the sensor. Further variations and embodiments of the invention will be readily apparent to those skilled in the art.
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Abstract
The flow rate of a gaseous sample of exhaled breath through an analytical device is controlled by a pump, and in certain embodiments two pumps. Placement of the analyte sensor in a secondary stream branching off of the primary stream through the device offers further control over the manner, duration, and quantity of the breath that is placed in contact with the sensor.
Description
- This is a divisional application of U.S. patent application Ser. No. 14/592,974, filed Jan. 9, 2015, which is a divisional of U.S. patent application Ser. No. 11/348,943, filed Feb. 6, 2006, now U.S. Pat. No. 8,932,230, which is a continuation-in-part of U.S. patent application Ser. No. 11/053,047, filed Feb. 7, 2005, now abandoned, the contents of which are hereby incorporated herein by reference.
- This invention resides in the field of systems and methods for the analysis of exhaled breath.
- Analyses of exhaled breath from human subjects are of value in many applications, including the diagnosis and management of several physiological conditions. A change in the nitric oxide (NO) concentration in the exhaled breath of a person suffering from asthma, for example, can indicate a change in the level of inflammation in the airway of the person, which in turn can indicate an increase in the likelihood of an asthma attack. Another component of exhaled breath whose concentration can be correlated with a physiological abnormality is carbon monoxide, a rise in which can be an early indication of the onset of hemolytic jaundice. A still further example is hydrogen, whose rise can indicate malabsorption of carbohydrate. These gases are typically present in trace amounts, notably at concentrations in the parts per billion (ppb) range, and concentration changes that are still within trace amounts can indicate abnormalities before they can be detected at the parts per million range.
- The utility and reliability of an analyzer for exhaled breath are limited by fluctuations in temperature, humidity, and breath flow, any of which can interfere with and influence the analytical result. Interference due to these factors is especially acute when the analyzer is used for measuring trace amounts of the analyte. Thus, any device that seeks to quantify analytes in trace amounts in exhaled breath must minimize the effect of these factors or compensate for their presence.
- Among these factors, the one that is the most difficult to control in most cases is the flow rate of the exhaled breath of the subject through the analytical device. A crude method in the prior art for controlling the breath flow rate is a verbal instruction from the clinician performing the analysis to the subject, calling for the subject to breathe out faster or slower to correct deviations from the design rate for the analyzer. This method is limited by the subject's ability to adjust the flow rate, particularly when the subject is a child, and is generally impractical for trace gas analyses over a wide range of concentration. An alternative is to include a variable flow resistance in the analyzer and altering the resistance to correct for the deviations. A device that incorporates this capability is disclosed in Moilanen, E., et al., U.S. Pat. No. 6,733,463 BI, issued May 11, 2004. The device in the Moilanen et al. patent contains a mechanical, electrically controlled throttle that is controlled by a signal from a mass flow meter inside the device. Unfortunately, the Moilanen et al. device is complex, requiring multiple components under feedback control.
- The present invention resides in apparatus for exhaled breath analysis that includes a housing constructed to receive exhaled breath directly from a subject, a flow-through passage within the housing for the travel of the exhaled breath, an analyte sensing element in the flow-through passage, and a pump or pump system to control the rate at which the subject exhales into the housing and to cause the exhaled breath to flow through the passage at a controlled rate. The invention can be used for the analysis of a variety of gaseous analytes, including those in trace amounts, and is of particular interest the quantification of NO.
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FIG. 1 is a diagram of the components of an analytical device embodying the features of the present invention. -
FIG. 2 is a diagram of the components of a second analytical device embodying the features of the present invention. -
FIG. 3 is a diagram of the components of a third analytical device embodying the features of the present invention. - While the invention is susceptible to a variety of constructions, the features defining the invention and its novelty are best understood by a detailed review of specific embodiments. Three such embodiments are shown in the Figures and described below.
-
FIG. 1 represents anetwork 10 of components that constitute the functional parts of an analytical device in accordance with the invention. The device itself can be a mask or similar device that can be worn by, or otherwise mounted to, the user, either directly or through a mouthpiece, in a manner that will capture the breath exhaled by the user. Exhaled breath enters the device at aninlet 11. The pressure of the exhaled breath is detected by apressure sensor 12 in the device with an operating range appropriate to the anticipated range of breath pressure. In one embodiment, this range is 5 to 20 cm of water (approximately 0.45 to 1.8 psig), the lower limit of this range being the pressure necessary to close the velum of the typical user and the upper limit a pressure at which the typical user will feel discomfort. Thepump 13 can operate in various ways. For example, when the pressure detected by the sensor rises to a threshold value, which may be the lower limit of the above range, thepump 13 can be actuated by a signal from the pressure sensor, and as exhalation into the device continues and the pressure eventually drops below the lower limit, the pump can be de-actuated (turned off). One example of a suitable pump is Model No. UNMP50 of KNF Neuberger, Inc., Trenton, N.J., USA. This pump has a free-flow capacity of 66.7 cm3/s, a maximum vacuum of 400 mbar (63 cm H2O), and a maximum continuous pressure of 0.5 bar (79 cm H2O). The pump is preferably sufficiently resistant to inlet pressure to maintain a substantially constant flow rate despite changes in the subject's mouth pressure across the range of interest. In an alternative design, the pump can be equipped with closed-loop control using thepressure sensor 12 for feedback. - An optional component in the flow path of the breath through the device is a
flow resistor 14 which in this embodiment is positioned downstream of thepressure sensor 12 and upstream of thepump 13. In certain embodiments of the invention, asecond flow resistor 15 is included in the flow path as well, downstream of thefirst resistor 14 but still upstream of thepump 13. The flow resistor or resistors will assist in limiting the flow to a desired flow rate, which may for example be 50 cm3/s, and in increasing the pressure in the user's mouth, throat, or air passages. One example of a flow resistor is a fixed orifice in the form of a round aperture having a diameter of approximately 0.11 cm. Flow resistors of other types will be readily apparent to those skilled in the art and can be used in place of an orifice. Flow resistors can serve to tune the system to the specifications of thepump 13. - The first resistor offers a resistance which will be designated herein by the symbol Ri. The flow path downstream of the
first resistor 14 in this embodiment is divided into two streams—amain stream 16 and aside stream 17. These streams will also be referred to herein as a primary stream and a secondary stream, respectively. Thesecond resistor 15 resides in themain stream 16 and offers a resistance which will be designated here by the symbol Rp, which can be variable or fixed. Examples of variable resistors are motor-controlled needle valves, solenoid-controlled needle valves, manual needle valves, and pinch-tube valves, all of which also offer resistance to the flow. An example of a fixed resistor is a non-variable orifice. Included in theside stream 17 is aside stream valve 18, which is preferably a shut-off, i.e., open/close, valve and aresistor 19 to allow flow into or prevent flow from entering the side stream, and to thereby control the flow distribution between the two streams. An example of a shut-off valve suitable for this application is a solenoid valve; other examples will be readily apparent to those skilled in the art. After a selected period of time from the start of the exhale, theside stream valve 18 can be opened to allow breath flow to occur in parallel through the main and side streams. The valve may for example be set to open at 7 seconds after the start of exhalation flow into the device, and to remain open until 10 seconds after the start of exhalation flow. Under this protocol, all exhaled breath will pass through themain stream 16 for the first seven seconds of the test, then through both the main and 16, 17 for the next three seconds.side streams - The
side stream 17 contains ananalyte sensor 21 that detects the level of the analyte (NO or otherwise) in the exhaled breath passing through the side stream. Theanalyte sensor 21 may also offer flow resistance and eliminate the need for a separateside stream resistor 19. In the representation of such an embodiment inFIG. 1 , theside stream resistor 19 is incorporated into theanalyte sensor 21. Theside stream valve 18 can also serve to provide the flow resistance in the side stream, and accordingly theside stream resistor 19 can be incorporated into thevalve 18. In general, flow resistance in the side stream is designated herein by the symbol Rs. Optionally, the side stream can contain other components, such as a carbon dioxide scrubber (not shown). Acheck valve 22 is included in the side stream to prevent backflow. - A constant flow rate of exhaled breath through the
device 10 can be maintained in any of several ways. One way is to use amain stream resistor 15 whose resistance Rp is variable while theside stream resistor 19 has a non variable resistance Rs. The main stream resistor may have a value of Rp1 when theside stream valve 18 is closed, and be programmed or set to change to a value of Rp2 when theside stream valve 18 is open. The values of Rp1 and Rp2 can be chosen so that the sum of the flow rates through themain stream 16 and theside stream 17 when theside stream valve 18 is open will equal the flow rate through themain stream 16 when theside stream valve 18 is closed. The choice of resistance levels for Rp1 and Rp2 may be influenced in part by the resistance from other components in the flow stream, such as the other resistors, valves, and sensors, as well as the voltage and capacity of the pump. - In the embodiment shown in
FIG. 1 , themain stream 16 andside stream 17 recombine into asingle passage 23 upstream of the device outlet 24. Since thepump 13 is positioned downstream of the point where themain stream 16 andside stream 17 recombine, thepump 13 controls the overall flow of the system rather than each stream individually. The placing of thepump 13 downstream of thesensor 12 also avoids the risk of contaminating the sensor with the pump effluent. - One example of a set of values for the pump pressure drop, the flow rate through the device as a whole, and the various resistances for a flow rate of 50 cm3/s through the device is listed in Table I below. In this example, the resistance in the main stream Rp is variable while the remaining resistances Ri and Rs are constant. The symbols used in Table I and the succeeding tables are as follows:
- ΔP denotes the pressure drop across the
pump 13. - Ri denotes the resistance offered by the first (upstream)
resistor 14. - Rp denotes the resistance offered by the
main stream resistor 15. - Rs denotes the resistance offered by the
19, 21, and 22.side stream components - V denotes the total flow rate of exhaled breath through the device.
-
TABLE I Example 1: Operating Parameters Parameter Side Stream Valve 18 ClosedSide Stream Valve 18Open ΔP 32 cm H2O 32 cm H2O Ri 0.4 cm H2O/cm3/s 0.4 cm H2O/cm3/s Rp 0.24 cm H2O/cm3/s (Rp1) 0.29 cm H2O/cm3/s (Rp2) Rs (infinite) 1.5 cm H2O/cm3/s V 50 cm3/s 50 cm3/s - In the example above, the two values of Rp (Rp1 and Rp2) are chosen to maintain a constant flow rate of 50 cm3/s throughout the test, with a flow rate of 8 cm3/s through the
analyte sensor 21, i.e., a main stream to side stream flow ratio of 42:8, when the side stream valve is open. To achieve this flow ratio, the ratio of Rp2 to Rs will be 8/42=0.29, and to assure that the same flow rate will occur when the side stream valve is closed, the ratio of Rp1 to Rp2 is 42/50=0.84. Thus, when theside stream 17 is open during the final three seconds of exhalation, breath will flow through the side stream at a rate of 8 cm3/s, while the remainder will flow at 42 cm3/s through themain stream 16. - In a second example, the resistance from all resistors remains constant while the pump flow rate is varied. This configuration utilizes a variation in the pressure drop across the pump to compensate for the change in the overall flow path resistance that occurs when the side stream is opened. The ratio of the resistance Rp at the
main resistor 15 and the resistance Rs at theside stream resistor 19 is again 8/42=0.29, as in Example 1. -
TABLE II Example 2: Operating Parameters Parameter Side Stream Valve 18 ClosedSide Stream Valve 18 OpenΔP 34.3 cm H2O 32 cm H2O Ri 0.4 cm H2O/cm3/s 0.4 cm H2O/cm3/s Rp 0.29 cm H2O/cm3/s 0.29 cm H2O/cm3/s Rs (infinite) 1.5 cm H2O/cm3/s V 50 cm3/s 50 cm3/s -
FIG. 2 represents asystem 31 containing two pumps rather than a single pump, although still within the scope of the invention. Similar to thesystem 10 depicted inFIG. 1 , exhaled breath enters thesystem 31 ofFIG. 2 at asingle inlet 32 and leaves at asingle outlet 33, and the system divides into amain stream 34 and aside stream 35 at a dividingjunction 36, the two streams recombining at adownstream junction 37. Thefirst pump 38 is in themain stream 34 downstream of thejunction 36 where the two streams are first formed, and thesecond pump 39 is in theside stream 35. Thesecond pump 39 can compensate for variations in theflow resistance 41 through the side stream, particularly when the resistance is in theanalyte sensor 42. Thesecond pump 39 also permits independent flow rates to be established for themain stream 34 and theside stream 35. The independent flow rates can be configured by software or on a real-time basis, without exchanging the components. In the embodiment shown inFIG. 2 , thesecond pump 39 is downstream from theanalyte sensor 42 so that the pump effluent does not interfere with the signal emitted by thesensor 42. - As in the single-pump embodiment of
FIG. 1 , the dual-pump system ofFIG. 2 can utilize resistors that offer variable resistance as well as variable-speed pumps. Aside stream valve 43 is shown in the dual-pump system. Alternatively, theside stream valve 43 can be eliminated by using thesecond pump 39 itself to open and close the side stream to flow. A further variation is shown inFIG. 3 , where thejunction 37 at which the main and side streams are recombined (FIG. 2 ) has been eliminated, and the main and 34, 35 vent separately throughside streams 51, 52, respectively.separate outlets - The use of a side stream as shown in each of the Figures herein (
element 17 ofFIG. 1 andelement 35 ofFIGS. 2 and 3 ) offers various advantages. With the 21, 42 positioned in the side stream, the flow rate of exhaled breath passing through the analyte sensor can be reduced and a small analyte sensor, particularly one that responds quickly to the analyte due to its small size, can thereby be used. The flow rate through the side stream can thus be limited to a rate within a range of 5 cm3/s to 11 cm3/s, or in certain embodiments a range of 6 cm3/s to 10 cm3/s, or a range of 7 cm3/s to 9 cm3/s. This can be done while flow through the main stream occurs at a higher rate, such as for example 40 cm3/s to 45 cm3/s. Furthermore, a portion of the breath passing through the entire device can be retained in the region of the sensor for an extended contact time to incubate the sample and sensor prior to the measurement. A typical incubation time may be 1 minute. The sensor can then be removed for analysis or measurement. Incubation is of value for sensors that respond too slowly to produce a real-time analysis of a moving stream. Still further, the placement of the analyte sensor in a side stream allows the user to pass multiple cycles of breath across the sensor before flow through the device as a whole is stopped. For example, with a sensor that has a volume of 5.0 cm3 and a side stream that accommodates a breath flow of 8.0 cm3/s, leaving the side stream open for 3.0 seconds will cause 24.0 cm3 of breath to cross the sensor before the final 5.0 cm3 is trapped in the side stream. Examples of periods of time during which the side stream is left open are periods of 1 to 10 seconds in duration, 1 to 7 seconds in duration, and 1 to 5 seconds in duration. This is useful for flushing the sensor prior to the analysis, thereby purging the sensor of extraneous gases with which the sensor was in contact prior to the analysis. The start of flow through the side stream can also be delayed for selected intervals following the start of the flow of exhaled breath through the device as a whole, for reasons of flushing or equilibration. In certain embodiments of the invention, for example, the opening of the side stream will be delayed for an interval of between 5 second and 9 seconds after the start of flow of exhaled breath through the device, and in certain other embodiments, the interval will be between 6 seconds and 8 seconds. The optimum interval for a child may differ from the optimum interval for an adult.analyte sensor - With the inclusion of the side stream shut-off valve, a separate side stream pump, or both, the side stream allows the system to be operated in a mode that can be termed a “stopped-flow operation.” Stopping the flow allows the system to create a stable testing environment that can be maintained for a much longer period than is possible in a flowing system. As noted above, a one-minute static exposure time is illustrative, although much longer or shorter exposure times can be used as well.
- The system and configurations described herein can be used for the analysis of many different analytes in exhaled breath, including gases that are present only in trace quantities, such as NO. For purposes of this specification and the appended claims, the expression “trace gas” denotes gases whose concentrations are below 1 part per million (on a volume basis), and preferably, depending on the significance of the analyte and the range within which variations can indicate a particular physiological condition or the onset of such a condition, below 300 parts per billion, below 200 parts per billion, or below 100 parts per billion. All concentrations herein, unless otherwise noted, are by volume. The invention is of particular interest in conjunction with a sensor consisting of cytochrome c in a sol-gel xerogel to measure NO. Sensors of this type and related technology are disclosed in the following pending U.S. patent applications, published U.S. patent applications, and issued U.S. patents: U.S. patent application Ser. No. 11/053,046, filed Feb. 7, 2005; U.S. patent application Ser. No. 11/053,253, filed Feb. 5, 2005; US 2004-0017570 A1, published Jan. 29, 2004 (application Ser. No. 10/334,625, filed Dec. 30, 2002); US 2005-0053549 A1, published Mar. 10, 2005 (application Ser. No. 10/659,408, filed Sep. 10, 2003); US 2005-0083527 A1, published Apr. 21, 2005 (application Ser. No. 10/767,709, filed Jan. 28, 2004); U.S. Pat. No. 5,795,187, issued Aug. 18, 1998; and U.S. Pat. No. 6,010,459, issued Jan. 4, 2000. The disclosures of all patents and patent applications cited in this specification are hereby incorporated herein by reference.
- The foregoing is offered primarily for purposes of illustration, and variations can be made without departing from the scope of the invention. The locations of the pumps, for example, can vary. When a single pump is used, the pump can be placed upstream of the juncture where the flow passage is divided into two streams, and when using either one pump or two, the pump(s) can be placed upstream of the sensor. Further variations and embodiments of the invention will be readily apparent to those skilled in the art.
Claims (28)
1-14. (canceled)
15. An apparatus for detecting an analyte in exhaled breath, said apparatus comprising a housing having a flow-through passage and adapted to receive exhaled breath from a subject, an analyte sensing element responsive to said analyte retained in said flow-through passage, and pump means for drawing said exhaled breath from a subject and through said flow-through passage at a controlled rate.
16. The apparatus of claim 15 wherein said pump means is downstream of said analyte sensing element in said flow-through passage.
17. The apparatus of claim 15 further comprising a pressure sensor arranged to detect the pressure of exhaled breath entering said flow-through passage.
18. The apparatus of claim 15 further comprising flow resistance means in said conduit.
19. The apparatus of claim 15 wherein said flow-through passage comprises a primary passage and a secondary passage branched off from said primary passage.
20. The apparatus of claim 19 wherein said analyte sensing element is in said secondary passage.
21. The apparatus of claim 19 wherein said flow-through passage divides into said primary passage and said secondary passage at an upstream junction in said flow-through passage and said secondary passage recombines with said primary passage at a downstream junction in said flow-through passage.
22. The apparatus of claim 19 wherein said flow-through passage divides into said primary passage and said secondary passage at an upstream junction in said flow-through passage and said primary and secondary passages are vented separately.
23. The apparatus of claim 21 wherein said pump means comprises a single pump downstream of said downstream junction.
24. The apparatus of claim 19 wherein said pump means comprises a first pump in said primary passage and a second pump in said secondary passage.
25. The apparatus of claim 21 wherein said pump means comprises a first pump in said primary passage and a second pump in said secondary passage.
26. The apparatus of claim 19 further comprising a shut-off valve arranged to allow or prevent flow through said secondary passage.
27. The apparatus of claim 19 further comprising a check valve in said side passage.
28. The apparatus of claim 18 wherein said flow resistance means is an orifice.
29. The apparatus of claim 18 wherein said flow resistance means is a variable flow resistor.
30. The apparatus of claim 19 further comprising a first flow resistor in said primary passage and a second flow-resistor in said secondary passage.
31. The apparatus of claim 30 wherein said first flow resistor is a variable flow resistor.
32. A method for determining the amount of an analyte in exhaled breath from a subject, said method comprising drawing exhaled breath from said subject through a flow-through device at a constant flow rate by use of a pump integrated with said flow-through device, said flow-through device comprising a sensing element responsive to said analyte.
33. The method of claim 32 further comprising detecting the pressure of exhaled breath thus drawn into said flow-through device.
34. The method of claim 32 wherein said flow-through device comprises a primary passage and a secondary passage with said sensing element in said secondary passage, and said method further comprises dividing exhaled breath thus drawn into said flow-through device into a primary stream through said primary passage and a secondary stream through said secondary passage.
35. The method of claim 34 comprising drawing said exhaled breath through said primary passage and said secondary passage by a single pump.
36. The method of claim 34 comprising drawing said exhaled breath through said primary passage and said secondary passage by a separate pump in each of said passages.
37. The method of claim 34 wherein said flow-through device comprises a shut-off valve in said secondary stream, and said method further comprises retaining a sample of said exhaled breath in contact with said sensing element in said secondary stream for a selected period of time.
38. The method of claim 34 comprising drawing said exhaled breath through said secondary stream at a flow rate of 5 cm3/s to 11 cm3/s.
39. The method of claim 34 comprising drawing said exhaled breath through said primary stream at a flow rate of 40 cm3/s to 45 cm3/s.
40. The method of claim 37 further comprising opening said shut-off valve to allow flow through said secondary passage at an interval of between 5 seconds and 9 seconds after the start of flow of exhaled breath through said device.
41. The method of claim 40 further comprising maintaining said flow through said secondary passage for a duration of between 1 second and 10 seconds.
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| US15/899,582 US20180243523A1 (en) | 2005-02-07 | 2018-02-20 | Controlling flow of exhaled breath during analysis |
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| US11874286B1 (en) | 2016-05-16 | 2024-01-16 | Hound Labs, Inc. | System and method for target substance identification |
| US11426097B1 (en) | 2018-10-17 | 2022-08-30 | Hound Labs, Inc. | Rotary valve assemblies and methods of use for breath sample cartridge systems |
| US11890090B1 (en) * | 2018-10-17 | 2024-02-06 | Hound Labs, Inc. | Rotary valve assemblies and methods of use for breath sample cartridge systems |
| US11821821B1 (en) | 2019-01-31 | 2023-11-21 | Hound Labs, Inc. | Noninvasive point of care biomarker detection from breath samples |
| US11977086B2 (en) | 2019-03-21 | 2024-05-07 | Hound Labs, Inc. | Biomarker detection from breath samples |
| US11933731B1 (en) | 2020-05-13 | 2024-03-19 | Hound Labs, Inc. | Systems and methods using Surface-Enhanced Raman Spectroscopy for detecting tetrahydrocannabinol |
| US11806711B1 (en) | 2021-01-12 | 2023-11-07 | Hound Labs, Inc. | Systems, devices, and methods for fluidic processing of biological or chemical samples using flexible fluidic circuits |
| DE102022127681A1 (en) * | 2022-10-20 | 2024-04-25 | Corscience Gmbh & Co. Kg | Method and device for measuring gas samples in the bypass flow and medical device |
Also Published As
| Publication number | Publication date |
|---|---|
| JP5491598B2 (en) | 2014-05-14 |
| NO20074073L (en) | 2007-09-05 |
| US20060178592A1 (en) | 2006-08-10 |
| JP2013037005A (en) | 2013-02-21 |
| ATE518479T1 (en) | 2011-08-15 |
| US8932230B2 (en) | 2015-01-13 |
| EP1850748B1 (en) | 2011-08-03 |
| EP1850748A4 (en) | 2009-05-06 |
| US20060195040A1 (en) | 2006-08-31 |
| US20150126887A1 (en) | 2015-05-07 |
| AU2006212828B2 (en) | 2011-02-10 |
| WO2006086323A1 (en) | 2006-08-17 |
| US9919123B2 (en) | 2018-03-20 |
| AU2006212828A1 (en) | 2006-08-17 |
| JP2008530532A (en) | 2008-08-07 |
| CA2596452C (en) | 2012-09-11 |
| CA2596452A1 (en) | 2006-08-17 |
| EP1850748A1 (en) | 2007-11-07 |
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