US3676073A - Alveolar breath volumetric analysis for alcohol - Google Patents

Alveolar breath volumetric analysis for alcohol Download PDF

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US3676073A
US3676073A US35139A US3676073DA US3676073A US 3676073 A US3676073 A US 3676073A US 35139 A US35139 A US 35139A US 3676073D A US3676073D A US 3676073DA US 3676073 A US3676073 A US 3676073A
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alcohol
breath
bag
tube
balloon
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Manley J Luckey
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MANLEY J LUCKEY
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    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/483Physical analysis of biological material
    • G01N33/497Physical analysis of biological material of gaseous biological material, e.g. breath
    • G01N33/4972Determining alcohol content
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S436/00Chemistry: analytical and immunological testing
    • Y10S436/90Breath testing
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/20Oxygen containing
    • Y10T436/203332Hydroxyl containing
    • Y10T436/204165Ethanol
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/25Chemistry: analytical and immunological testing including sample preparation
    • Y10T436/25375Liberation or purification of sample or separation of material from a sample [e.g., filtering, centrifuging, etc.]
    • Y10T436/255Liberation or purification of sample or separation of material from a sample [e.g., filtering, centrifuging, etc.] including use of a solid sorbent, semipermeable membrane, or liquid extraction
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10TTECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
    • Y10T436/00Chemistry: analytical and immunological testing
    • Y10T436/25Chemistry: analytical and immunological testing including sample preparation
    • Y10T436/25875Gaseous sample or with change of physical state

Definitions

  • a breath sampling kit and method for sampling breath are described for sampling the quantity of alcohol in a fixed quantity of breath without elaborate apparatus.
  • a test subject inflates an inelastic bag of predetermined volume connected in bypassing relation to an elastic container such as a balloon.
  • the volume of the bag is such as to accommodate the nonalveolar breath of the test subject.
  • the balloon is inflated with the alveolar breath.
  • the balloon is then deflated through a sample tube in which a solid material is contained and inflates a second inelastic bag, the volume of which bears a fixed relation to 1 milliliter of blood so that upon subsequent analysis the quantity of alcohol in the blood is determined directly.
  • the solid material in the tube adsorbs alcohol in the breath and keeps it trapped for later extraction and analysis.
  • the alcohol is extracted from the solid by water or other solvent for alcohol passed through the solid, and the solid material is selected for reversibly adsorbing the alcohol and being substantially insoluble in the extracting solvent so as not to interfere with subsequent analysis, silica gel being particularly preferred.
  • alcoholic intoxication is directly related to blood alcohol content and that the blood alcohol content is determinable by the content of alcohol present in the persons breath derived from the alveolae.
  • the alveolae are the small bulbs in the lung wherein oxygenation of the blood and transfer of impurities from the blood to inhaled air takes place.
  • This invention provides for ready determination of a persons blood alcohol content by accurately extracting the alcohol vapor present in a known volume of alveolar breath.
  • the apparatus is inexpensive and readily adapted for field use so that the person being tested need not be taken to a central testing facility and there is no need for taking blood or urine samples.
  • a breath sampling kit comprising a first tube connected to an inflatable bag having a fixed volume and to an elastic bag having a variable volume.
  • the second tube is also connectable to a third inflatable bag having a fixed volume for accumulating a sample from the elastic bag bearing a known relation to a volume of alveolar breath.
  • a preferred method of employing the sampling kit comprises inflating the first bag for accommodating nonalveolar breath, followed by inflation of the elastic bag to capture alveolar breath.
  • the elastic bag is then deflated through the tube containing the means for reversibly adsorbing alcohol and into the third bag having a fixed volume.
  • the alcohol adsorbed in the second tube is extracted therefrom by a solvent such as water in which the means for adsorbing alcohol is insoluble and the extracted solution is analyzed in a conventional manner to determine alcohol content.
  • FIG. 1 illustrates means for obtaining an alveolar breath sample after bypassing non-alveolar breath according to principles of this invention
  • FIG. 2 illustrates means for extracting alcohol from the breath sample
  • FIG. 3 illustrates a sample collection tube
  • FIG. 4 illustrates a means for connecting one of the bags which is illustrated in FIG. 1 to a tube
  • FIG. 5 illustrates a technique for extracting alcohol from the tube of FIG. 3.
  • FIG. 1 illustrates a portion of breath sampling apparatus constructed according to principles of this invention.
  • a mouthpiece 10 which is preferably made of substantially inert vinyl tubing which is somewhat flexible. Inserted within the tubing forming the mouthpiece 10 is a short length of intermediate tubing 11 which may, for example, be about 2 /2 inches long. The opposite end of the intermediate tube 11 is inserted into a second short length of vinyl tubing 12 which serves as an outlet.
  • the intermediate tube 11 is preferably made of a relatively rigid material such as, for example, polyethylene, for ready connection to the moreflexible tubes 10 and 12 forming the mouthpiece and the outlet respectively.
  • a notch or hole 14 in a side of the intermediate tube 11 provides fluid communication from the interior of this tube to the interior of the bag.
  • FIG. 4 A convenient and inexpensive way of interconnecting the interior tube 11, bag 13 and outlet tube 12 is illustrated in FIG. 4.
  • the intermediate tube 11 is contained within the bag 13 before the latter is heat sealed, and thereafter the inside tube 11 is manually gripped through the flexible walls of the bag 13, and the end is inserted within the end of the flexible and stretchable vinyl tube 12.
  • This carries a portion of the wall of the bag 13 between the two tubes so that the bag is tightly gripped therebetween.
  • there is a shearing action when the two tubes are so assembled which ruptures the wall of the bag in the region of the end of the tube 11 so that there is fluid communication between the two tubes 11 and 12 having the wall of the bag sandwiched therebetween. If assembly alone does not rupture the wall, a pointed object through the tube 12 will suflice.
  • This subassembly of the apparatus of this invention is readily and economically made since it is only necessary to cut short lengths of vinyl tubing for the inlet and the outlet 12, cut a short length of polyethylene tubing 11, cut, drill or punch a notch or hole 14 in the side of this latter tubing, and insert the piece in an open bag 13 of polyethylene.
  • This latter bag 13 is conveniently made from a length of polyethylene sheet tubing about two inch diameter by heat sealing one end, inserting the piece of tubing 11 and heat sealing the opposite end all in rapid succession.
  • the intermediate tube 11 can then quickly be inserted in the vinyl tubes 10 and 12 to complete the subassembly.
  • an elastic container 15 such as an ordinary rubber balloon, is connected to the outlet tube 12.
  • the balloon may inflate very slightly until an elastic resistance to inflation is encountered.
  • the breath is diverted through the hole 14 so as to inflate the bag 13 until it reaches its final fixed volume.
  • the balloon 15 is inflated against its elastic resistance in its usual manner.
  • the first volume of breath is that contained in the nose, mouth, and tracheal and bronchial passages, and this air is not normally in equilibrium with the alcohol content of the blood.
  • the alveolar air is in intimate gas exchange relation with the blood in the alveolae and the alcohol vapor content of the alveolar air is in equilibrium with the alcohol content of the blood.
  • the measurement of alcohol content of the alveolar air is, therefore, an accurate measure of the alcohol content of the blood. It is necessary, however, to avoid the bronchial air in taking a sample since this is not in equilibrium with the blood and would give a fallacious alcohol content.
  • the bag 13 therefore, has a fixed volume of about 1,000 milliliters which is suflicient to accommodate all of the air that may be present in the nose, mouth, and tracheal and bronchial passages of a normal person so that the only portion of non-alveolar breath that reaches the balloon 15 is that first small portion needed to inflate the balloon to its rest volume prior to any substantial elastic inflation of the balloon.
  • the balloon 15 is then inflated solely with alveolar breath, and when so inflated, the air in the balloon 15 is about 95% alveolar air and 5% non-alveolar After inflation, the balloon 15 is then transferred to a sample tube 17, as seen in FIG. 2, while the balloon is still inflated.
  • the balloon 15 is then permitted to deflate under the urging of its elastic walls through the sample tube 17 into an inflatable bag 18 having a fixed final volume and made of an inextensible material such as sheet polyethylene.
  • the volume of the inextensible bag 18 is slightly over 2200 milliliters, so that when the breath passes from the balloon 15 through the sample tube 17 to the bag 18, 2100 milliliters of alveolar breath passes through the sample tube for alcohol extraction.
  • the bag 18 is sealed to a short length of vinyl tubing 19 by a short length of plastic tube 20 inserted therein from the inside of the bag 18 in substantially the same manner the tubing 11 is sealed to the bag 13 and vinyl tubing 12, as illustrated hereinabove in FIG. 4.
  • the sample collecting tube 17 is further illustrated in longitudinal cross-section in FIG. 3 and comprises a glass tube 22 within the center of which is positioned a small volume of granular material 23, hereinafter described in greater detail.
  • a short wad of glass wool 24 is provided at each end of the volume of granular material 23 to prevent it from escaping and a small loop 25 of plastic, such as polyethylene, is pressed into the glass tube 22 to hold the wads of glass wool 24 in position.
  • the granular material 23 is preferably molecular sieve grade of silica gel such as, for example, grade 28 silica gel available from W. R. Grace Company, Baltimore, Md., in a size range of 20 to 40 mesh.
  • silica gel is preferred since it is inexpensive, substantially inert and insoluble in water, and readily absorbs or adsorbs alcohol vapor, other similar molecular sieve materials can be employed so long as they adsorb alcohol vapor from the breath and reversibly release alcohol to an extracting medium. It is preferred that the granular material 23 have a greater aflinity for water than for alcohol so that the alcohol vapor adsorbed as breath passes through the granular material is readily released when eluted with water.
  • Silica gel is advantageous since it is also substantially insoluble in alcohols other than ethyl alcohol, hexane, xylene, ketones, aldehydes and the like which may also be used to elute alcohol for analysis.
  • magnesium perchlorate for example, is soluble in water and the alcohol is removed by dissolving the solid material used to extract alcohol from breath. The dissolved salts must then be removed or otherwise accounted for in chemical analysis since they interfere with accurate determination of alcohol content, particularly it popular spectrophotometric techniques are employed.
  • the glass tube 22 is preferably sealed at the ends by plastic plugs 26 both prior to and after use to prevent adsorption of unwanted materials by the silica gel and to prevent loss of alcohol from the silica gel after use.
  • the sample tube 17 After a sample has been colletced in the sample tube 17, it is disconnected from the balloon 15 and bag 18 and the plugs 26 are reinstalled in the ends for transport of the sample tube to a laboratory for analysis.
  • the balance of the apparatus is sufliciently inexpensive to be discarded after use.
  • the sample tube 17 reaches the laboratory, the alcohol is removed from the silica gel by passing a solvent, preferably water, through the gel.
  • a solvent preferably water
  • the concentration of alcohol in the water collected in the flask is then exactly one-half the concentration of alcohol in the blood (since the alcohol is from 2100 ml. of alveolar breath).
  • a greater or lesser quantity of water in the range of from one to ten milliliters can be employed for eluting the alcohol or other solvents, headspace analysis or a hot gas extraction stream can be employed if desired.
  • the packing density of the granular material 23 and glass wool 24 varies slightly from Sample tube to sample tube so that the flow rate of gas through the silica gel would vary depending on the pressure applied by the balloon 15. It is desirable to have a substantially reproducible flow of breath from the balloon 15 through the sample tubes 17 in order that the flow rate is not too high so as to pass breath without opportunity for full absorption of the alcohol vapor. It is also found that the elastic properties of the balloons 15 vary from balloon to balloon.
  • the flow resistance is normally Within a relatively limited range from tube to tube and the tubes can then be sorted into batches having substantially similar flow resistance.
  • the balloons 15 are inflated to a uniform pressure in the course of manufacture in order to sort these according to the pressure applied as they deflate. While the balloon 15 is inflated at a constant pressure during the course of manufacture, a pair of indicia 21 are marked on the side of the balloon at a preselected distance apart. Thereafter, when the balloon is reinflated so that the distance between the marks is again the preselected distance, the balloon pressure is reproduced.
  • Balloons can, therefore, be calibrated to selected inflation pressures for matching with calibrated sample tubes 17 so that a preselected flow rate of gas from the balloon through the sample tube can be reproducibly obtained in each kit.
  • Employing a balloon not only assures a uniform flow pressure through the sample tube but also permits repeated tries to take a sample of a persons breath if he attempts some devious ways of avoiding a sample of alveolar breath. It also provides an opportunity to obtain a full 2100 milliliters of alveolar breath if it is not obtained upon the first exhalation.
  • duplicate samples can be taken by providing a pair of sample tubes 17 in the kit, and the inextensible bags and balloon can be deflated and reused by the same person.
  • a method for sampling the blood alcohol content of a person including the steps of:
  • An expendable sampling kit for obtaining a breath sample for alcohol analysis comprising:
  • a first tube having an end breath inlet and an end outlet and an aperture in a side intermediate the ends;
  • a second tube having an end inlet and an end outlet
  • molecular sieve means in the second tube for adsorbing alcohol from a persons breath and being insoluble in a solvent for alcohol;
  • kits as defined in claim 4 wherein the means for adsorbing alcohol comprises granular silica gel.
  • a first piece of flexible tubing having an end surrounding an end of the rigid tubing and having a portion of the wall of the first fixed volume inflatable bag therebetween for sealing the bag to the tube;
  • a second piece of flexible tubing having an end surrounding an end of the substantially rigid tubing and having a portion of the wall of the first fixed volume inflatable bag therebetween for sealing the bag to the tube.

Abstract

A BREATH SAMPLING KIT AND METHOD FOR SAMPLING BREATH ARE DESCRIBED FOR SAMPLING THE QUANTITY OF ALCOHOL IN A FIXED QUANTITY OF BREATH WITHOUT ELEBORATE APPARATUS. ACCORDING TO THIS ARRANGEMENT, A TEST SUBJECT INFLATES AN INELASTIC BAG OF PREDETERMINED VOLUME CONNECTED IN BYPASSING RELATION TO AN ELASTIC CONTAINER SUCH AS A BALLOON. THE VOLUME OF THE BAG IS SUCH AS TO ACCOMODATE THE NONALVEOLAR BREATH OF THE TEAST SUBJECT. AFTER THE BAG IS FILLED, THE BALLOON IS INFLATED WITH THE ALVEOLAR BREATH. THE BALLOON IS THEN DEFLATED THROUGH A SAMPLE TUBE IN WHICH A SOLID MATERIAL IS CONTAINED AND INFLATES A SECOND INELASTIC BAG, THE VOLUME OF WHICH BEARS A FIXED RELATION TO 1 MILLITIER OF BLOOD SO THAT UPON SUBSEQUENT ANALYSIS THE QUANTITY OF ALCOHOL IN THE BLOOD IS DETERMINED DIRECTLY. THE SOLID MATERIAL IN THE TUBE ADSORBS ALCOHOL IN THE BREATH AND KEEPS IT TRAPPED FOR LATER EXTRACTION AND ANALYSIS. THE ALCOHOL IS EXTRACTED FROM THE SOLID BY WATER OF OTHER SOLVENT FOR ALCOHOL PASSED THROUGH THE SOLID, AND THE SOLID MATERIAL IS SELECTED FROM REVERSIBLY ADSORBING THE ALCOHOL AND BEING SUBSTANTIALLY INSOLUBLE IN THE EXTRACTING SOLVENT SO AS NOT TO INTERFERE WITH SUBSEQUENT ANALYSIS, SILICA GEL BEING PARTICULARLY PREFERRED.

Description

July 11, 1972 LUCKEY 3,676,073
ALVEOLAR BREATH VOLUMETRIC ANALYSIS FOR ALCOHOL Filed May 6. 1970 United States Patent O 3,676,073 ALVEOLAR BREATH VOLUMETRIC ANALYSIS FOR ALCOHOL Manley J. Luckey, 7252 Osbun Road, San Bernardino, Calif. 92404 Filed May 6, 1970, Ser. No. 35,139 Int. Cl. G01n 33/16 U.S. Cl. 23-232 R 7 Claims ABSTRACT OF THE DISCLOSURE A breath sampling kit and method for sampling breath are described for sampling the quantity of alcohol in a fixed quantity of breath without elaborate apparatus. According to this arrangement, a test subject inflates an inelastic bag of predetermined volume connected in bypassing relation to an elastic container such as a balloon. The volume of the bag is such as to accommodate the nonalveolar breath of the test subject. After the bag is filled, the balloon is inflated with the alveolar breath. The balloon is then deflated through a sample tube in which a solid material is contained and inflates a second inelastic bag, the volume of which bears a fixed relation to 1 milliliter of blood so that upon subsequent analysis the quantity of alcohol in the blood is determined directly. The solid material in the tube adsorbs alcohol in the breath and keeps it trapped for later extraction and analysis. The alcohol is extracted from the solid by water or other solvent for alcohol passed through the solid, and the solid material is selected for reversibly adsorbing the alcohol and being substantially insoluble in the extracting solvent so as not to interfere with subsequent analysis, silica gel being particularly preferred.
BACKGROUND This invention is related to U.S. Pat. 3,437,449 entitled Breath Alcohol Determination by M. J. Luckey, and involves substantial improvements over the invention described and claimed therein.
It is well established that alcoholic intoxication is directly related to blood alcohol content and that the blood alcohol content is determinable by the content of alcohol present in the persons breath derived from the alveolae. The alveolae are the small bulbs in the lung wherein oxygenation of the blood and transfer of impurities from the blood to inhaled air takes place. This invention provides for ready determination of a persons blood alcohol content by accurately extracting the alcohol vapor present in a known volume of alveolar breath. The apparatus is inexpensive and readily adapted for field use so that the person being tested need not be taken to a central testing facility and there is no need for taking blood or urine samples.
There is present in 2,100 milliliters of alveolar breath of the average person, the same weight of alcohol vapor as there is in 1 milliliter of that persons blood. This relation is employed in the present invention to yield a simple effective economical and accurate method and apparatus for rapidly and easily determining the weight percentage of alcohol in the blood of a person being tested.
In other breath alcohol testing, it is often necessary to transport the test subject to a central station in which a breath testing unit is located. This is necesary since the breath testing equipment is relatively expensive and cannot be provided in each and every patrol unit. This is undesirable since in remote areas a long time and distance may be required to reach the testing apparatus and during this time the ofiicer may be out of service. In practice of this invention, there is provided a volumetric technique 3,676,073 Patented July 11, 1972 ice for alcohol sampling with a central laboratory determination of the alcohol content with precision. The sampling of the persons breath is, however, done if desired at a remote sampling location for later analysis. The sampling kit is inexpensive and several kits can be carried in each patrol unit.
BRIEF SUMMARY OF THE INVENTION Thus, in practice of this invention according to a preferred embodiment there is provided a breath sampling kit comprising a first tube connected to an inflatable bag having a fixed volume and to an elastic bag having a variable volume. A second tube having means therein for reversibly absorbing alcohol, and insoluble in solvent for alcohol, is selectably connectable to the elastic bag. The second tube is also connectable to a third inflatable bag having a fixed volume for accumulating a sample from the elastic bag bearing a known relation to a volume of alveolar breath.
A preferred method of employing the sampling kit comprises inflating the first bag for accommodating nonalveolar breath, followed by inflation of the elastic bag to capture alveolar breath. The elastic bag is then deflated through the tube containing the means for reversibly adsorbing alcohol and into the third bag having a fixed volume. The alcohol adsorbed in the second tube is extracted therefrom by a solvent such as water in which the means for adsorbing alcohol is insoluble and the extracted solution is analyzed in a conventional manner to determine alcohol content.
DRAWINGS Other features and attendant advantages of the present invention will be better understood by reference to the following detailed description of a presently preferred embodiment when considered in connection with the accompanying drawings wherein:
FIG. 1 illustrates means for obtaining an alveolar breath sample after bypassing non-alveolar breath according to principles of this invention;
FIG. 2 illustrates means for extracting alcohol from the breath sample;
FIG. 3 illustrates a sample collection tube;
FIG. 4 illustrates a means for connecting one of the bags which is illustrated in FIG. 1 to a tube; and
FIG. 5 illustrates a technique for extracting alcohol from the tube of FIG. 3.
Throughout the drawings like reference numerals refer to like parts.
DESCRIPTION FIG. 1 illustrates a portion of breath sampling apparatus constructed according to principles of this invention. As provided in this preferred embodiment, there is a mouthpiece 10 which is preferably made of substantially inert vinyl tubing which is somewhat flexible. Inserted within the tubing forming the mouthpiece 10 is a short length of intermediate tubing 11 which may, for example, be about 2 /2 inches long. The opposite end of the intermediate tube 11 is inserted into a second short length of vinyl tubing 12 which serves as an outlet. The intermediate tube 11 is preferably made of a relatively rigid material such as, for example, polyethylene, for ready connection to the moreflexible tubes 10 and 12 forming the mouthpiece and the outlet respectively.
An inextensible inflatable bag 13,-preferably of sheet polyethylene or the like, is sealed between the mouthpiece 10 and intermediate tube 11 and between the intermediate tube 11 and the exit or outlet tube 12 so that the only communication with the interior of the bag is through the mouthpiece or outlet. A notch or hole 14 in a side of the intermediate tube 11 provides fluid communication from the interior of this tube to the interior of the bag.
A convenient and inexpensive way of interconnecting the interior tube 11, bag 13 and outlet tube 12 is illustrated in FIG. 4. According to this arrangement, the intermediate tube 11 is contained within the bag 13 before the latter is heat sealed, and thereafter the inside tube 11 is manually gripped through the flexible walls of the bag 13, and the end is inserted within the end of the flexible and stretchable vinyl tube 12. This carries a portion of the wall of the bag 13 between the two tubes so that the bag is tightly gripped therebetween. In addition, there is a shearing action when the two tubes are so assembled, which ruptures the wall of the bag in the region of the end of the tube 11 so that there is fluid communication between the two tubes 11 and 12 having the wall of the bag sandwiched therebetween. If assembly alone does not rupture the wall, a pointed object through the tube 12 will suflice.
This subassembly of the apparatus of this invention is readily and economically made since it is only necessary to cut short lengths of vinyl tubing for the inlet and the outlet 12, cut a short length of polyethylene tubing 11, cut, drill or punch a notch or hole 14 in the side of this latter tubing, and insert the piece in an open bag 13 of polyethylene. This latter bag 13 is conveniently made from a length of polyethylene sheet tubing about two inch diameter by heat sealing one end, inserting the piece of tubing 11 and heat sealing the opposite end all in rapid succession. The intermediate tube 11 can then quickly be inserted in the vinyl tubes 10 and 12 to complete the subassembly.
When the subassembly is used, an elastic container 15, such as an ordinary rubber balloon, is connected to the outlet tube 12. Thus, when a test subject first blows into the mouthpiece 10, the balloon may inflate very slightly until an elastic resistance to inflation is encountered. Thereupon, the breath is diverted through the hole 14 so as to inflate the bag 13 until it reaches its final fixed volume. Thereafter, the balloon 15 is inflated against its elastic resistance in its usual manner.
When a person commences to exhale, the first volume of breath is that contained in the nose, mouth, and tracheal and bronchial passages, and this air is not normally in equilibrium with the alcohol content of the blood. The alveolar air, however, is in intimate gas exchange relation with the blood in the alveolae and the alcohol vapor content of the alveolar air is in equilibrium with the alcohol content of the blood. The measurement of alcohol content of the alveolar air is, therefore, an accurate measure of the alcohol content of the blood. It is necessary, however, to avoid the bronchial air in taking a sample since this is not in equilibrium with the blood and would give a fallacious alcohol content.
The bag 13, therefore, has a fixed volume of about 1,000 milliliters which is suflicient to accommodate all of the air that may be present in the nose, mouth, and tracheal and bronchial passages of a normal person so that the only portion of non-alveolar breath that reaches the balloon 15 is that first small portion needed to inflate the balloon to its rest volume prior to any substantial elastic inflation of the balloon. After the non-alveolar breath is bypassed to the bag 13, the balloon 15 is then inflated solely with alveolar breath, and when so inflated, the air in the balloon 15 is about 95% alveolar air and 5% non-alveolar After inflation, the balloon 15 is then transferred to a sample tube 17, as seen in FIG. 2, while the balloon is still inflated. The balloon 15 is then permitted to deflate under the urging of its elastic walls through the sample tube 17 into an inflatable bag 18 having a fixed final volume and made of an inextensible material such as sheet polyethylene. The volume of the inextensible bag 18 is slightly over 2200 milliliters, so that when the breath passes from the balloon 15 through the sample tube 17 to the bag 18, 2100 milliliters of alveolar breath passes through the sample tube for alcohol extraction. The bag 18 is sealed to a short length of vinyl tubing 19 by a short length of plastic tube 20 inserted therein from the inside of the bag 18 in substantially the same manner the tubing 11 is sealed to the bag 13 and vinyl tubing 12, as illustrated hereinabove in FIG. 4.
The sample collecting tube 17 is further illustrated in longitudinal cross-section in FIG. 3 and comprises a glass tube 22 within the center of which is positioned a small volume of granular material 23, hereinafter described in greater detail. A short wad of glass wool 24 is provided at each end of the volume of granular material 23 to prevent it from escaping and a small loop 25 of plastic, such as polyethylene, is pressed into the glass tube 22 to hold the wads of glass wool 24 in position.
The granular material 23 is preferably molecular sieve grade of silica gel such as, for example, grade 28 silica gel available from W. R. Grace Company, Baltimore, Md., in a size range of 20 to 40 mesh. Although silica gel is preferred since it is inexpensive, substantially inert and insoluble in water, and readily absorbs or adsorbs alcohol vapor, other similar molecular sieve materials can be employed so long as they adsorb alcohol vapor from the breath and reversibly release alcohol to an extracting medium. It is preferred that the granular material 23 have a greater aflinity for water than for alcohol so that the alcohol vapor adsorbed as breath passes through the granular material is readily released when eluted with water. Silica gel is advantageous since it is also substantially insoluble in alcohols other than ethyl alcohol, hexane, xylene, ketones, aldehydes and the like which may also be used to elute alcohol for analysis.
Previously reactive materials such as magnesium perchlorate have been employed for extracting alcohol vapor from breath. This is not entirely satisfactory, however, since magnesium perchlorate, for example, is soluble in water and the alcohol is removed by dissolving the solid material used to extract alcohol from breath. The dissolved salts must then be removed or otherwise accounted for in chemical analysis since they interfere with accurate determination of alcohol content, particularly it popular spectrophotometric techniques are employed.
As illustrated in FIG. 3, the glass tube 22 is preferably sealed at the ends by plastic plugs 26 both prior to and after use to prevent adsorption of unwanted materials by the silica gel and to prevent loss of alcohol from the silica gel after use.
After a sample has been colletced in the sample tube 17, it is disconnected from the balloon 15 and bag 18 and the plugs 26 are reinstalled in the ends for transport of the sample tube to a laboratory for analysis. The balance of the apparatus is sufliciently inexpensive to be discarded after use. When the sample tube 17 reaches the laboratory, the alcohol is removed from the silica gel by passing a solvent, preferably water, through the gel. As illustarted schematically in FIG. '5, a small funnel 28 is inserted in one end of the sample tube 17 and a small amount of water is poured through to collect in a flask 29, in which the other end of the sample tube 17 is inserted.
It is generally preferred to elute the alcohol from the silica gel with about two milliliters of water since the concentration of alcohol in the water collected in the flask is then exactly one-half the concentration of alcohol in the blood (since the alcohol is from 2100 ml. of alveolar breath). If desired, however, a greater or lesser quantity of water in the range of from one to ten milliliters can be employed for eluting the alcohol or other solvents, headspace analysis or a hot gas extraction stream can be employed if desired. Once the alcohol is extracted from the silica gel in a solvent, it can be analyzed by any conventional technique well known in the art, such as gravirnetric, titrimetric, spectrophotometric, gas chromatographic or the like.
The packing density of the granular material 23 and glass wool 24 varies slightly from Sample tube to sample tube so that the flow rate of gas through the silica gel would vary depending on the pressure applied by the balloon 15. It is desirable to have a substantially reproducible flow of breath from the balloon 15 through the sample tubes 17 in order that the flow rate is not too high so as to pass breath without opportunity for full absorption of the alcohol vapor. It is also found that the elastic properties of the balloons 15 vary from balloon to balloon.
Therefore, in the process of manufacturing the sample collection kits, it is desirable to measure the flow of gas through each sample collection tube 17 built to determine the flow resistance. The flow resistance is normally Within a relatively limited range from tube to tube and the tubes can then be sorted into batches having substantially similar flow resistance. Likewise, the balloons 15 are inflated to a uniform pressure in the course of manufacture in order to sort these according to the pressure applied as they deflate. While the balloon 15 is inflated at a constant pressure during the course of manufacture, a pair of indicia 21 are marked on the side of the balloon at a preselected distance apart. Thereafter, when the balloon is reinflated so that the distance between the marks is again the preselected distance, the balloon pressure is reproduced. Balloons can, therefore, be calibrated to selected inflation pressures for matching with calibrated sample tubes 17 so that a preselected flow rate of gas from the balloon through the sample tube can be reproducibly obtained in each kit. Employing a balloon not only assures a uniform flow pressure through the sample tube but also permits repeated tries to take a sample of a persons breath if he attempts some devious ways of avoiding a sample of alveolar breath. It also provides an opportunity to obtain a full 2100 milliliters of alveolar breath if it is not obtained upon the first exhalation. All that need be done is to prevent air from leaving the partly inflated balloon, compress the inelastic bag 13 to remove air from it, reinflate the inelastic bag 13 to remove non-alveolar breath, and then proceed to further inflate the balloon to obtain a full 2100 milliliter sample.
If desired, duplicate samples can be taken by providing a pair of sample tubes 17 in the kit, and the inextensible bags and balloon can be deflated and reused by the same person.
Although only one embodiment of this invention has been described and illustrated herein, many modifications and variations will be apparent toone skilled in the art. Thus, for example, instead of using a balloon 15 having a single inlet which is successively connected to the sample taking subassembly illustrated in FIG. 1 and the sample retention subassembly illustrated in FIG. 2, a balloon having separate inlet and outlet, and a check valve to prevent reverse gas flow can be employed in the same manner as illustrated in the aforementioned US. Pat. 3,437,449. Many other variations and modifications will be apparent to one skilled in the art.
What is claimed is:
1. A method for sampling the blood alcohol content of a person including the steps of:
inflating a flexible inextensible container of preselected volume with a persons breath; sequentially thereafter and substantially continuously therewith inflating a flexible elastic container with the persons breath so that the elastic container contains a principal proportion of alveolar breath;
passing breath from the elastic container through a vessel including an alcohol vapor extracting medium substantially insoluble in a solvent for alcohol and into a second inelastic container having a preselected volume;
removing extracted alcohol from the medium with a solvent in which the medium is substantially insoluble; and
quantitatively analyzing the solvent for contained alcohol.
2. A method as defined in claim 1 wherein the alcohol vapor extracting medium comprises silica gel.
3. A method as defined in claim 2. wherein the breath is passed through the silica gel at a controlled rate by the steps of:
calibrating the flow resistance of the silica gel;
calibrating the inflation characteristics of the elastically extensible bag; and
matching the flow resistance characteristics and the inflation characteristics to obtain a preselected flow rate.
4. An expendable sampling kit for obtaining a breath sample for alcohol analysis comprising:
a first tube having an end breath inlet and an end outlet and an aperture in a side intermediate the ends;
a first fixed volume inflatable bag sealed to the first tube with the aperture inside the bag;
a second tube having an end inlet and an end outlet;
molecular sieve means in the second tube for adsorbing alcohol from a persons breath and being insoluble in a solvent for alcohol;
an elastically extensible inflatable bag;
means for connecting the elastically extensible bag to the outlet of the first tube and the inlet of the second tube;
a second fixed volume inflatable bag; and
means for connecting the second fixed volume bag to the outlet of the second tube, whereby non-alveolar breath first applied to the end breath inlet of the first tube inflates the first fixed volume bag and alveolar breath sequentially thereafter inflates the elastically extensible bag, breath flows from the elastically extensible bag through the second tube into the second fixed volume bag for exposing a fixed volume of alveolar breath to the molecular sieve means for adsorbing alcohol.
5. A kit as defined in claim 4 wherein the means for adsorbing alcohol comprises granular silica gel.
6. A kit as defined in claim 5 wherein the first tube comprises:
a first piece of substantially rigid tubing having an aperture in one side thereof;
a first piece of flexible tubing having an end surrounding an end of the rigid tubing and having a portion of the wall of the first fixed volume inflatable bag therebetween for sealing the bag to the tube; and
a second piece of flexible tubing having an end surrounding an end of the substantially rigid tubing and having a portion of the wall of the first fixed volume inflatable bag therebetween for sealing the bag to the tube.
7. A kit as defined in claim '5 wherein the gas flow resistance of the contents of the second tube is matched with the elastic properties of the elastically extensible bag for obtaining a preselected gas flow rate therethrough.
References Cited UNITED STATES PATENTS 3,223,488 12/1965 Luckey 2'3-254 3,464,186 9/1969 Hankison et al. 55387 X 3,544,273 12/1970 McConnaughey 23-254 MORRIS O. WOLK, Primary Examiner R. M. REESE, Assistant Examiner
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JPS55163455A (en) * 1979-03-19 1980-12-19 Draegerwerk Ag Method of and apparatus for measuring alcohol content in breathing of subject
US4481297A (en) * 1982-05-13 1984-11-06 Owens-Illinois, Inc. Vapor detection tube and method of testing for a vapor
EP0133326A2 (en) * 1983-06-27 1985-02-20 Diversified Medical Technologies, Inc. Disposable breath analyzer
US4579826A (en) * 1983-09-30 1986-04-01 Bolton Craig E Method and device for analyzing human breath
US4671298A (en) * 1984-11-26 1987-06-09 Meridian Medical Corporation Isothermal rebreathing apparatus and method
EP0279069A2 (en) * 1986-12-22 1988-08-24 Abbott Laboratories Method and device for ketone measurement
US4863610A (en) * 1987-06-11 1989-09-05 Campbell Brian D Scraping, collecting & eluting apparatus for thin layer chromatography and method for its use
US4871675A (en) * 1984-11-23 1989-10-03 Jiri Coupek Storage container of samples for analysis
WO1990009572A1 (en) * 1989-02-02 1990-08-23 The United States Of America, Represented By The Secretary, United States Department Of Commerce Breath sampler
US5081871A (en) * 1989-02-02 1992-01-21 The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Breath sampler
US5122341A (en) * 1990-10-17 1992-06-16 Carrier Corporation Device for gas contaminant tester training
JPH05503182A (en) * 1989-12-15 1993-05-27 ベーリンガー マンハイム コーポレーション Regulated branch power supply
US5328664A (en) * 1991-09-24 1994-07-12 Ponsy Jacques Sarl Contralco Prepackaged fluid test system for determining levels of a substance
US5834626A (en) * 1996-11-29 1998-11-10 De Castro; Emory S. Colorimetric indicators for breath, air, gas and vapor analyses and method of manufacture
EP0957350A2 (en) * 1998-05-11 1999-11-17 Siemens Aktiengesellschaft Device for taking samples of gaseous analytes
US20030235515A1 (en) * 2002-06-21 2003-12-25 Fike Randall Stuart Encapsulated sorbent tube
US20050180893A1 (en) * 2004-02-17 2005-08-18 Handly Robert A. Centerless ground thermal desorption tube and method without frit
US20070004995A1 (en) * 2005-06-30 2007-01-04 Horn Jeffrey L Swab device and kit for the delivery of blood clotting materials to a wound site
US20090044597A1 (en) * 2005-06-25 2009-02-19 Frank Kvasnik Breath sampling device
USD777315S1 (en) * 2010-08-30 2017-01-24 Quintron Instrument Company, Inc. Evacuated air chamber
US20170086447A1 (en) * 2014-09-16 2017-03-30 The United States Of America As Represented By The Secretary Of The Army Carbon dioxide source for arthropod vector surveillance
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* Cited by examiner, † Cited by third party
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JPS55163455A (en) * 1979-03-19 1980-12-19 Draegerwerk Ag Method of and apparatus for measuring alcohol content in breathing of subject
US4481297A (en) * 1982-05-13 1984-11-06 Owens-Illinois, Inc. Vapor detection tube and method of testing for a vapor
EP0133326A2 (en) * 1983-06-27 1985-02-20 Diversified Medical Technologies, Inc. Disposable breath analyzer
EP0133326A3 (en) * 1983-06-27 1985-04-03 Diversified Medical Technologies, Inc. Disposable breath analyzer
US4579826A (en) * 1983-09-30 1986-04-01 Bolton Craig E Method and device for analyzing human breath
US4871675A (en) * 1984-11-23 1989-10-03 Jiri Coupek Storage container of samples for analysis
US4671298A (en) * 1984-11-26 1987-06-09 Meridian Medical Corporation Isothermal rebreathing apparatus and method
EP0279069A2 (en) * 1986-12-22 1988-08-24 Abbott Laboratories Method and device for ketone measurement
EP0279069A3 (en) * 1986-12-22 1990-01-17 Abbott Laboratories Method and device for ketone measurement
US5071769A (en) * 1986-12-22 1991-12-10 Abbott Laboratories Method and device for ketone measurement
EP0598262A3 (en) * 1986-12-22 1994-10-05 Abbott Lab Breath-sampling device for measuring breath component levels.
EP0598262A2 (en) * 1986-12-22 1994-05-25 Abbott Laboratories Breath-sampling device for measuring breath component levels
US4863610A (en) * 1987-06-11 1989-09-05 Campbell Brian D Scraping, collecting & eluting apparatus for thin layer chromatography and method for its use
WO1990009572A1 (en) * 1989-02-02 1990-08-23 The United States Of America, Represented By The Secretary, United States Department Of Commerce Breath sampler
US5081871A (en) * 1989-02-02 1992-01-21 The United States Of America As Represented By The Secretary Of The Department Of Health And Human Services Breath sampler
JPH05503182A (en) * 1989-12-15 1993-05-27 ベーリンガー マンハイム コーポレーション Regulated branch power supply
US5122341A (en) * 1990-10-17 1992-06-16 Carrier Corporation Device for gas contaminant tester training
US5328664A (en) * 1991-09-24 1994-07-12 Ponsy Jacques Sarl Contralco Prepackaged fluid test system for determining levels of a substance
US5834626A (en) * 1996-11-29 1998-11-10 De Castro; Emory S. Colorimetric indicators for breath, air, gas and vapor analyses and method of manufacture
EP0957350A2 (en) * 1998-05-11 1999-11-17 Siemens Aktiengesellschaft Device for taking samples of gaseous analytes
EP0957350A3 (en) * 1998-05-11 2001-11-07 Siemens Aktiengesellschaft Device for taking samples of gaseous analytes
US7566421B2 (en) * 2002-06-21 2009-07-28 Prism Analytical Technologies, Inc. Encapsulated sorbent tube
US20030235515A1 (en) * 2002-06-21 2003-12-25 Fike Randall Stuart Encapsulated sorbent tube
US20050180893A1 (en) * 2004-02-17 2005-08-18 Handly Robert A. Centerless ground thermal desorption tube and method without frit
US20090044597A1 (en) * 2005-06-25 2009-02-19 Frank Kvasnik Breath sampling device
US7856863B2 (en) * 2005-06-25 2010-12-28 Sensam Limited Breath sampling device
US20070004995A1 (en) * 2005-06-30 2007-01-04 Horn Jeffrey L Swab device and kit for the delivery of blood clotting materials to a wound site
USD777315S1 (en) * 2010-08-30 2017-01-24 Quintron Instrument Company, Inc. Evacuated air chamber
US10495552B2 (en) 2014-06-27 2019-12-03 Pulse Health Llc Breath analysis system
US20170086447A1 (en) * 2014-09-16 2017-03-30 The United States Of America As Represented By The Secretary Of The Army Carbon dioxide source for arthropod vector surveillance
WO2019177644A1 (en) * 2018-03-15 2019-09-19 Chris Marsh Sample capture assembly for an aldehyde analysis system and method of use

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