CN214749753U - CO (carbon monoxide)2Breath isotope detector - Google Patents

CO (carbon monoxide)2Breath isotope detector Download PDF

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CN214749753U
CN214749753U CN202120765942.4U CN202120765942U CN214749753U CN 214749753 U CN214749753 U CN 214749753U CN 202120765942 U CN202120765942 U CN 202120765942U CN 214749753 U CN214749753 U CN 214749753U
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detector
laser
optical cavity
channel
expiration
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阮英恒
周静洋
杨晓云
杨晓军
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Shenzhen Dingbang Chemicals Co ltd
Shenzhen Dingbang Biotechnology Co ltd
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Shenzhen Dingbang Chemicals Co ltd
Shenzhen Dingbang Biotechnology Co ltd
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Abstract

The utility model discloses a CO2Breath isotope detector, CO2The breath isotope detector includes: the infrared laser, the optical cavity and the infrared detector are arranged in sequence; the optical cavity is provided withAn air inlet and an air outlet are arranged; at least one expiration channel communicated with the air inlet, wherein the expiration channel is used for introducing CO into the light cavity2Expiration; the air outlet channel is communicated with the air outlet; and laser emitted by the infrared laser is transmitted to the infrared detector through the optical cavity. An infrared laser is used as a light source, and CO of different isotopes2When the difference between the absorption wavelengths is small and an infrared laser is adopted, the wavelength of laser emitted by the infrared laser can be accurately controlled, so that CO of different isotopes can be accurately distinguished2Thereby improving the accuracy of the analysis.

Description

CO (carbon monoxide)2Breath isotope detector
Technical Field
The utility model relates to an expiration isotope detects technical field, what especially relates to is a CO2An exhaled isotope detector.
Background
Helicobacter pylori is one of the most common gastric pathogens in the human stomach, and is closely associated with chronic tracheitis and peptic ulcer disease. The microorganism has high urease activity, and can hydrolyze urea in gastric juice to generate carbon dioxide and ammonia gas.
Based on the activity of the urease of the body13C Urea breath test (13C-UBT) is widely used as a non-invasive diagnostic method, specifically to detect the presence of helicobacter pylori infection in the stomach, and in the prior art,13the accuracy of the urea breath test is low.
Accordingly, the prior art is yet to be improved and developed.
SUMMERY OF THE UTILITY MODEL
The to-be-solved technical problem of the present invention is to provide a CO system for overcoming the above drawbacks of the prior art2An expiratory isotope detector, aiming at solving the problems in the prior art13C, the accuracy of the urea breath test is low.
The utility model provides a technical scheme that technical problem adopted as follows:
CO (carbon monoxide)2A breath isotope detector, comprising:
the infrared laser, the optical cavity and the infrared detector are arranged in sequence; the optical cavity is provided with an air inlet and an air outlet;
at least one expiration channel communicated with the air inlet, wherein the expiration channel is used for introducing CO into the light cavity2Expiration;
the air outlet channel is communicated with the air outlet;
and laser emitted by the infrared laser is transmitted to the infrared detector through the optical cavity.
Said CO2The breath isotope detector is characterized in that the infrared laser is a quantum cascade laser.
Said CO2A breath isotope detector, wherein the wavelength of laser light emitted by the infrared laser comprises: 4874.448cm-1,4874.086cm-1And 4874.178cm-1
Said CO2Breath isotope detector wherein said CO2A breath isotope detector, further comprising:
a zero gas passage communicating with the gas inlet;
an air pump is arranged on the air-free channel.
Said CO2The breath isotope detector is characterized in that a check valve or a one-way valve is arranged on the zero gas channel.
Said CO2The breath isotope detector comprises a breath channel, an air outlet channel and a zero air channel, wherein the breath channel, the air outlet channel and the zero air channel all adopt airtight interfaces.
Said CO2The breath isotope detector is characterized in that the air inlet is positioned at one end of the optical cavity close to the infrared detector;
the air outlet is positioned at one end of the optical cavity close to the infrared laser.
Said CO2And the expiratory isotope detector is characterized in that a radiator is arranged on one side of the infrared laser, which deviates from the optical cavity.
Said CO2A breath isotope detector, wherein the infrared laser comprises: the QCL laser, the TEC controller and the LDC controller;
the TEC controller and the LDC controller are connected with the QCL laser.
Said CO2The breath isotope detector is characterized in that a pretreatment device is arranged on the breath channel.
Has the advantages that: the application adopts an infrared laser as a light source, and CO of different isotopes2When the difference between the absorption wavelengths is small and an infrared laser is adopted, the wavelength of laser emitted by the infrared laser can be accurately controlled, so that CO of different isotopes can be accurately distinguished2Thereby improving the accuracy of the analysis.
Drawings
FIG. 1 shows the CO in the present invention2The structure of the breath isotope detector is shown schematically.
Fig. 2 is a flow chart of an analysis method according to the present invention.
Description of reference numerals:
10. an infrared laser; 11. a QCL laser; 12. a TEC controller; 13. an LDC controller; 15. a heat sink; 20. an optical cavity; 21. an air inlet; 22. an air outlet; 30. an infrared detector; 40. an exhalation passage; 41. a pretreatment device; 50. an air outlet channel; 60. a zero gas channel; 61. an air pump; 62. a check valve; 70. a housing; 80. a display screen; 90. and (5) measuring and analyzing the terminal.
Detailed Description
In order to make the objects, technical solutions and advantages of the present invention clearer and clearer, the present invention will be described in further detail below with reference to the accompanying drawings and examples. It should be understood that the specific embodiments described herein are merely illustrative of the invention and are not intended to limit the invention.
Referring also to figure 1 of the drawings, in which,the utility model provides a CO2Some embodiments of a radioisotope detector.
As shown in figure 1, the utility model relates to a CO2A breath isotope detector comprising:
the infrared laser 10, the optical cavity 20 and the infrared detector 30 are arranged in sequence; the light cavity 20 is provided with a gas inlet 21 and a gas outlet 22;
at least one exhale channel 40 in communication with the air inlet 21, the exhale channel 40 for introducing CO into the light chamber 202Expiration;
an air outlet channel 50 communicated with the air outlet 22;
wherein, the laser light emitted from the infrared laser 10 propagates through the optical cavity 20 to the infrared detector 30.
It is worth noting that exhalation passageways 40 are used to introduce CO into light chamber 202Expiration, expiration channel 40 means the passage of CO2Passage of exhaled air, CO2Exhalation refers to the exhalation of the lungs containing CO2The exhalation of (2). The air outlet channel 50 is a channel through which air in the optical cavity 20 flows out. At the time of analysis, CO is added2The expired air passes from the expiration channel 40 into the optical cavity 20, and then when the laser light emitted from the infrared laser 10 passes through the optical cavity 20, CO is present in the optical cavity 202Expiration, CO2Absorbs some wavelengths of the laser light, so that the spectrum of the laser light detected by the infrared detector 30 is different from the spectrum of the laser light emitted by the infrared laser 10, and thus can be used for CO2The breath is analyzed so that CO can be analyzed2CO in exhaled breath2The composition of (1).
In particular, CO due to different isotopes in the present application2The absorption wavelengths of infrared light are different, so that CO of different isotopes can be obtained through the absorbance of different wavelengths2The larger the absorbance, the larger the amount of the component (b), and the smaller the absorbance, the smaller the amount of the component (b).
It should be noted that the present application uses the infrared laser 10 as the light source, because of CO of different isotopes2The difference between the absorption wavelengths is small, and red is usedWhen the laser 10 is used, the wavelength of the laser emitted by the infrared laser 10 can be accurately controlled, so that CO of different isotopes can be accurately distinguished2To analyze CO of different isotopes2The composition of (1).
The optical cavity 20 includes a tube, a closed lens and a cage-type optical path structure, and the closed lens and the cage-type optical path structure collimate, introduce and extract the laser. The closed lenses are two and are respectively arranged at two ends of the tube body, and the cage type light path structure is positioned between the two closed lenses.
The detection signal generated by the infrared detector 30 sensing the laser is amplified and then sent to the QCLAS analysis system, and the harmonic demodulation is realized, and the high-precision gas concentration signal is obtained through a signal processing algorithm.
A pretreatment device 41 is provided in the exhalation path 40 for CO2The exhalation is pre-processed and then passed through the exhalation passageways 40 into the optical cavity 20. The pretreatment device 41 may be for CO2Filtering and drying the breath.
In a preferred implementation manner of the embodiment of the present invention, the wavelength of the laser emitted by the infrared laser 10 includes: 4874.448cm-1,4874.086cm-1And 4874.178cm-1
In particular, the amount of the solvent to be used,12C16O16o has an absorption wavelength of 4874.448cm-113C16O16O has an absorption wavelength of 4874.086cm-112C18O16O has an absorption wavelength of 4874.178cm-1. A wavelength of 4874.448cm is obtained by the infrared detector 30-1,4874.086cm-1And 4874.178cm-1Can thereby determine the absorbance of12C16O16O、13C16O16O and12C18O16concentration (or mass) of O, thereby achieving the effect on CO2Breath was subjected to composition analysis.
In a preferred implementation manner of the embodiment of the present invention, the infrared laser 10 is a quantum cascade laser.
In particular, Quantum Cascade Lasers (QCLs) are novel unipolar semiconductor devices based on the principles of conduction band-to-band transition of electrons in semiconductor quantum wells and phonon-assisted resonant tunneling. The quantum cascade laser has the characteristics that the working wavelength has no direct relation with the band gap of the used material and is only determined by the sub-band spacing of the coupled quantum wells, so that the wavelength can be cut in a large range, and the wavelength of the emitted laser can be conveniently adjusted and controlled.
In a preferred implementation of the embodiment of the present invention, as shown in fig. 1, the CO2A breath isotope detector, further comprising:
a zero air passage 60 communicating with the air inlet 21;
an air pump 61 is arranged on the air-free passage 60.
Specifically, the zero gas channel 60 is a channel for introducing zero gas into the optical cavity 20, where the zero gas is a gas that does not absorb laser light and enters the optical cavity 20, and therefore, when the zero gas is introduced, the absorbance of the zero gas detected by the infrared detector 30 is 0. Before or after each test, zero gas may be passed from zero gas channel 60 to purge CO from optical cavity 20 through exhalation channel 40 into optical cavity 202Breath out to ensure that each test is not disturbed by other gases.
Specifically, the air pump 61 is disposed on the zero air channel 60, and the zero air in the zero air channel 60 is delivered to the optical cavity 20 by the air pump 61, so as to purge the optical cavity 20, and of course, the zero air channel 60 may be further disposed with a check valve 62 or a one-way valve, so as to prevent the air in the optical cavity 20 from flowing back to the zero air channel 60, and prevent CO from flowing back into the zero air channel 602The breath leaks, thereby ensuring the cleaning effect of the zero-air channel 60 and improving the accuracy of the analysis result.
The exhalation channel 40, the air outlet channel 50 and the zero air channel 60 all adopt airtight interfaces, and specifically, the exhalation channel 40, the air outlet channel 50 and the zero air channel 60 all adopt airtight interfaces composed of a SWAGELOK 6MM air valve and a stainless steel shell.
In a preferred implementation manner of the embodiment of the present invention, as shown in fig. 1, the air inlet 21 is located at one end of the optical cavity 20 close to the infrared detector 30; the air outlet 22 is located at one end of the optical cavity 20 close to the infrared laser 10.
Specifically, the air inlet 21 is close to the infrared detector 30 and away from the infrared laser 10, and the air outlet 22 is close to the infrared laser 10 and away from the infrared detector 30, so that when CO is present2The breath entering the optical cavity 20 through the air inlet 21 can sufficiently absorb the light with the corresponding wavelength of the laser light emitted from the infrared laser 10, that is, the laser light emitted from the infrared detector 30 passes through the optical cavity 20, and the CO is absorbed2The light with corresponding wavelength is gradually absorbed, and when the laser light propagates to the end of the optical cavity 20 close to the laser detector, the laser light and the CO which is not absorbed by the light and enters from the air inlet 212Expiratory contact to CO in laser2Light of the corresponding wavelength is sufficiently absorbed.
In a preferred implementation manner of the embodiment of the present invention, as shown in fig. 1, a heat sink 15 is disposed on one side of the infrared laser 10 away from the optical cavity 20.
Specifically, in order to improve the stability of the laser light emitted by the infrared laser 10, a heat sink 15 is disposed on a side of the infrared laser 10 away from the optical cavity 20 to dissipate heat of the infrared laser 10. The infrared laser 10 includes: QCL laser 11, TEC controller 12 and LDC controller 13 all are connected with QCL laser 11, QCL laser 11 is used for sending laser, TEC controller 12 is used for controlling the temperature, for example, when the temperature rises after TEC controller 12 controls radiator 15 work and reduces the temperature to infrared laser 10, LDC controller 13 controls operating current to the wavelength of the laser that infrared laser 10 sent.
A display screen 80 is arranged on the shell 70 of the detector, and the display screen 80 displays the real-time temperature and the real-time working current of the infrared laser 10 and can also display laser parameters. The detector is connected with a measurement and analysis terminal 90 through a USB interface, and the measurement and analysis terminal 90 can be a computer.
As shown in figure 2, the utility model discloses CO2The breath isotope detector adopts the following analysis method for analysis, and the analysis method comprises the following steps:
step (ii) ofS100, providing for taking13First gas for pre-pulmonary exhalation of C-urea and citric acid and administration13C-urea and citric acid followed by a second gas exhaled by the lungs.
In particular, two gas collections are performed in the same lung in order to detect changes in the composition of exhaled breath, which is taken by an individual13Collecting first gas exhaled from the lungs of the subject prior to the administration of the C-urea and citric acid to the subject13After the C-urea and citric acid, the second gas exhaled from the lungs of the individual is collected. Analyzing the first gas and the second gas to obtain the administration13CO produced in lungs after C-Urea and citric acid2A change in composition. If the subject is infected with helicobacter pylori, the subject is taking13The difference between the first gas and the second gas exhaled before and after C-urea and citric acid, respectively, is large because helicobacter pylori-infected individuals decompose urea and, therefore, produce13C16O16O and12C18O16o, i.e. in the second gas13C16O16O and12C18O16the amount of O is relatively large and,12C16O16the amount of O is small and the first gas is12C16O16The amount of O is relatively large and,13C16O16o and12C18O16the amount of O is small. If the individual is not infected with H.pylori, the composition of the first gas is not very different from the composition of the second gas. It should be noted that citric acid can promote the decomposition of urea, facilitating the formation13C16O16O and12C18O16O。
the exhalation from the lungs of an individual may typically be collected using a gas collection device, which may be a gas collection bag. After the first gas and the second gas are collected, the gas collecting device is connected with the expiration channel, and the first gas in the gas collecting device is introduced into the optical cavity to be analyzed to obtain first detection data.
Specifically, the13The mass of C-urea is greater than or equal to50mg, the mass of the citric acid is more than or equal to 4 g. Is taken by an individual13When C is urea and citric acid, the reaction solution is prepared,13the mass of the C-urea is more than or equal to 50mg, and the mass of the citric acid is more than or equal to 4 g.
Step S200, after the infrared laser is started, the first gas is introduced into the optical cavity from the expiration channel, so that first detection data corresponding to the first gas are obtained through the infrared detector.
It should be noted that the detection order of the first gas and the second gas can be determined as required, that is, the first gas can be detected first, and then the second gas can be detected; alternatively, the second gas may be detected first, followed by the first gas. During detection, the infrared laser is started first, and in order to ensure the stability of laser light emitted by the infrared laser, the infrared laser may be started for a preset time to be preheated, for example, for 30 minutes, so that the infrared laser reaches a stable state. Of course, background calibration may also be performed, and specifically, a background sample is used for testing to obtain background calibration data.
The first gas is then passed from the expiratory channel into the optical cavity, for example, by loading the first gas with a gas collection bag, passing the first gas from the expiratory channel into the optical cavity by pressing the gas collection bag, and contacting the laser in the optical cavity.
In background calibration or one-round test, the CO is used for removing residual gas in the optical cavity2A breath isotope detector, further comprising:
a zero gas passage communicating with the gas inlet;
an air pump is arranged on the air-free channel.
And introducing zero gas through the zero gas channel, purging the optical cavity, and emptying residual gas in the optical cavity so as to carry out the next round of test.
The step S200 includes:
step S210, starting the air pump to remove the residual air in the optical cavity.
Step S220, the first gas is introduced into the optical cavity from the expiration channel, so that first detection data corresponding to the first gas are obtained through the infrared detector.
Before the first gas is introduced, the gas pump is started to remove the residual gas in the optical cavity. For example, when zero gas is used for background calibration of the infrared laser, if the real-time data detected by the infrared detector is consistent with background calibration data when the optical cavity is purged by introducing the zero gas, it is indicated that residual gas in the optical cavity is completely removed. And then, introducing the first gas into the optical cavity, and detecting first detection data corresponding to the first gas by the infrared detector.
The first detection data includes:12C16O16the detection data of the optical fiber is O,13C16O16o probe data and12C18O16o, detection data. The first detection data may be expressed in terms of a concentration of the first gas, and the first detection data includes:12C16O16the first concentration of the oxygen is selected to be,13C16O16the first concentration of the oxygen is selected to be,12C18O16a first concentration of O.
And S300, introducing the second gas into the optical cavity from the expiration channel so as to obtain second detection data corresponding to the second gas through the infrared detector.
Specifically, the second gas is tested and passed from the exhalation channel into the optical cavity, for example, by loading the second gas with a gas collection bag, passing the second gas from the exhalation channel into the optical cavity by pressing the gas collection bag, and contacting the laser in the optical cavity.
Step S300 specifically includes:
and step S310, starting the air pump, and removing residual air in the optical cavity.
Step S320, introducing the second gas into the optical cavity from the exhalation channel, so as to obtain second detection data corresponding to the second gas through the infrared detector.
Before the second gas is introduced, the gas pump is started to remove the residual gas in the optical cavity. For example, the optical cavity is purged with zero gas to remove residual gas, i.e., the first gas tested before. And then, introducing the second gas into the optical cavity, and detecting second detection data corresponding to the second gas by the infrared detector.
The second detection data includes:12C16O16the detection data of the optical fiber is O,13C16O16o probe data and12C18O16o, detection data. The second detection data may be expressed in terms of a concentration of a second gas, and the second detection data includes:12C16O16the second concentration of the oxygen is selected from the group consisting of,13C16O16the second concentration of the oxygen is selected from the group consisting of,12C18O16a second concentration of O.
Step S400, analyzing the first detection data and the second detection data to obtain an analysis result.
Specifically, after the first detection data and the second detection data are obtained, the first detection data and the second detection data are analyzed to obtain an analysis result.
Specifically, step S400 includes:
step S410, determining according to the first detection data and the second detection data13C-DOB value and18O-DOB value.
Step S420, according to the above13C-DOB value and18and determining the analysis result according to the O-DOB value.
In particular, the amount of the solvent to be used,13C-DOB value ═ C-DOB13Second abundance of C-13A first abundance of C, wherein,13second abundance of C ═13Second concentration of C/(13Second concentration of C +12A second concentration of C),13first abundance of C ═13First concentration of C/(13First concentration of C +12First concentration of C).13Second concentration of C13C16O16The second concentration of the oxygen is selected from the group consisting of,12second concentration of C12C16O16The second concentration of the oxygen is selected from the group consisting of,13the first concentration of C is13C16O16The first concentration of the oxygen is selected to be,12the first concentration of C is12C16O16A first concentration of O.
18O-DOB value ═18Second abundance of O-18A first abundance of O, wherein,18second abundance of O ═18Second concentration of O/(18Second concentration of O +16A second concentration of O),18first abundance of O ═18First concentration of O/(18First concentration of O +16A first concentration of O).18Second concentration of O12C18O16The second concentration of the oxygen is selected from the group consisting of,16second concentration of O12C16O16The second concentration of the oxygen is selected from the group consisting of,18the first concentration of O is12C18O16The first concentration of the oxygen is selected to be,16the first concentration of O is12C16O16A first concentration of O.
To obtain13C-DOB value and18after the O-DOB value is according to13C-DOB value and18and determining the analysis result according to the O-DOB value.
Specifically, the analysis result includes: HP positive, HP negative, NUD positive and NUD negative. HP refers to helicobacter pylori, and NUD refers to non-ulcer dyspepsia.
Step S420 specifically includes:
step S421, when the13And when the C-DOB value is larger than a preset threshold value, taking HP positive as an analysis result.
Step S422, when the above13The C-DOB value is greater than a preset threshold value18When the O-DOB value is greater than 0, the NUD is positive as the analysis result.
Step S423, when the13The C-DOB value is greater than a preset threshold value18When the O-DOB value is less than or equal to 0, NUD negativity is regarded as the analysis result.
Step S424, when the13And when the C-DOB value is less than or equal to a preset threshold value, taking HP negativity as an analysis result.
Specifically, first pass through13The size of the C-DOB value judges that the HP is positive or negative,13when the C-DOB value is larger than a preset threshold value, the HP is positive,13and when the C-DOB value is less than or equal to a preset threshold value, the HP is negative. When HP is positive, the process is continued18Judging NUD positive or NUD negative according to the O-DOB value,18if the O-DOB value is more than 0, the NUD is positive,18an O-DOB value of 0 or less is NUD negative.
For taking only13Expiration when C-urea is taken, expiration when citric acid is taken alone, and administration13C-urea and citric acid were separately detected by expiration to obtain DOB values, as shown in tables 1, 2 and 3. Is taken orally13The change range of the DOB value of the exhaled air is larger during the process of C-urea and citric acid, so that the analysis and the detection are more convenient, and the accuracy is higher.
TABLE 1 administration of drugs alone13DOB value of expired air at C-Urea
09:25AM 09:55AM
CO2 3.46 3.84
13Abundance of C 10.94 -9.26
18Abundance of O 35.33 22.09
13C-DOB value -20.20
18O-DOB value -13.24
TABLE 2 DOB values of exhaled breath when only citric acid was administered
Figure BDA0003020175930000111
TABLE 3 administration of drugs13DOB value of expired air at C-Urea and citric acid
Figure BDA0003020175930000112
Figure BDA0003020175930000121
It is to be understood that the invention is not limited to the above-described embodiments, and that modifications and variations may be made by those skilled in the art in light of the above teachings, and all such modifications and variations are intended to be included within the scope of the invention as defined in the appended claims.

Claims (10)

1. CO (carbon monoxide)2A breath isotope detector, comprising:
the infrared laser, the optical cavity and the infrared detector are arranged in sequence; the optical cavity is provided with an air inlet and an air outlet;
at least one exhalation passage in communication with the air inlet, the exhalation passageThe channel is used for introducing CO into the optical cavity2Expiration;
the air outlet channel is communicated with the air outlet;
and laser emitted by the infrared laser is transmitted to the infrared detector through the optical cavity.
2. CO according to claim 12The breath isotope detector is characterized in that the infrared laser is a quantum cascade laser.
3. CO according to claim 12The breath isotope detector is characterized in that the wavelength of laser emitted by the infrared laser comprises: 4874.448cm-1,4874.086cm-1And 4874.178cm-1
4. CO according to claim 12An isotope expiration detector, wherein the CO is2A breath isotope detector, further comprising:
a zero gas passage communicating with the gas inlet;
an air pump is arranged on the air-free channel.
5. CO according to claim 42An isotope expiration detector, characterized in that,
and a check valve or a one-way valve is arranged on the zero air passage.
6. CO according to claim 42An isotope expiration detector, characterized in that,
the expiration channel, the air outlet channel and the zero air channel all adopt airtight interfaces.
7. CO according to claim 12An isotope expiration detector, characterized in that,
the air inlet is positioned at one end of the optical cavity close to the infrared detector;
the air outlet is positioned at one end of the optical cavity close to the infrared laser.
8. CO according to claim 12An isotope expiration detector, characterized in that,
and a radiator is arranged on one side of the infrared laser, which deviates from the optical cavity.
9. CO according to claim 82An isotope expiration detector, characterized in that,
the infrared laser includes: the QCL laser, the TEC controller and the LDC controller;
the TEC controller and the LDC controller are connected with the QCL laser.
10. CO according to claim 12An isotope expiration detector, characterized in that,
and a pretreatment device is arranged on the expiration channel.
CN202120765942.4U 2021-04-14 2021-04-14 CO (carbon monoxide)2Breath isotope detector Active CN214749753U (en)

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