This invention relates to the field of sampling air from the lungs and specifically to the field of obtaining a sample of a person's air, including alveolar air from the alveoli of the lungs of a person.
Air from the lungs of a person can be used for many different types of testing that would otherwise require the person to undergo an invasive procedure. For example, alveolar air can be analyzed for, but not limited to, the noninvasive diagnosis of a wide variety of conditions including the noninvasive diagnosis of stomach infections related to a high incidence of ulcers, enzymatic deficiencies, and metabolic conditions and/or abnormalities. Crucial to any such testing is the ability to get an accurate sample containing a sufficient volume of air representative of true alveolar air, necessary for specific testing. A peristaltic pump is a type of positive displacement pump used for pumping a variety of fluids. The fluid is contained within a flexible tube fitted inside a circular pump casing (though linear peristaltic pumps have been made). A rotor with a number of ‘rollers’, ‘shoes’ or ‘wipers’ attached to the external circumference compresses the flexible tube. As the rotor turns, the part of tube under compression closes (or ‘occludes’) thus forcing the fluid to be pumped to move through the tube. Additionally, as the tube opens to its natural state after the passing of the cam (‘restitution’) fluid flow is induced to the pump. This process is called peristalsis and is used in many biological systems such as the gastrointestinal tract.
Because the only part of the pump in contact with the fluid being pumped is the interior of the tube, it is easy to sterilize and clean the inside surfaces of the pump. Furthermore, since there are no moving parts in contact with the fluid, peristaltic pumps are inexpensive to manufacture. Their lack of valves, seals and glands makes them comparatively inexpensive to maintain, and the use of a hose or tube makes for a relatively low-cost maintenance item compared to other pump types.
A simple to use, inexpensive, and user-friendly apparatus is desired to collect and store human breath samples, and also to accurately extract samples from the storage.
The present invention is particularly suited for transferring air samples from a container to a gas or liquid analyzer. These samples are required to be kept at very pristine conditions, with no outside air influencing sample results.
The present invention incorporates is a closed system coupled to breath collection apparatus, such as a bag. One exemplary bag is described in commonly owned U.S. Pat. No. 6,468,477. In general, the invention involves capturing the air in a vacuum state, accessing the air sample by a hollow needle, and using a peristaltic pump to take the pressure down to atmospheric level, in a completely closed system to avoid introduction of waste air or contaminants into the sample.
Although the disclosure hereof is detailed and exact to enable those skilled in the art to practice the invention, the physical embodiments herein disclosed merely exemplify the invention which may be embodied in other specific structures. While the preferred embodiment has been described, the details may be changed without departing from the invention.
Referring now to
It is preferable, though not required, that the bag is of two ply construction, the two plies sealed together. Of course, more or less plies may be used in the bag construction. The bag structure is preferably expandable, and constructed of a supple, inert, and airtight material. One such supple and airtight material that performs suitably is thin polyester film, but foil laminate and a variety of other materials could also perform suitably. It should be easily recognizable to one skilled in the art that any number of materials other than foil laminate can be used for the bag structure 10. Other examples of materials that could be used for constructing the present invention include for illustration, but not by way of limitation: Tedlar®, Saranex®, Saran®, and Teflon®. Those skilled in the art will appreciate that the material can vary widely based on the characteristics of the gases desired to be sampled. The materials chosen should be inert and exhibit relative impermeability to the gases desired to sample, and any materials chosen that are relatively permeable to the gases desired to sample would not be preferred.
Referring now to
Referring now to
It is preferred that the sample extractor operates on timed runs based on a typical flow profile shown in
Referring now to
Instead of using syringe to collect sample (
In one method of the present invention, the pump 20 can be programmable as is known in the art, in order to turn on and off and collect a predetermined volume of sample, or a operate for a predetermined amount of time. In this method, aggregate sampling can be accomplished by operating the pump 20 either continuously or at intervals until a predetermined volume is collected. The systems and methods of the present invention can be used to operate pumps 20 that are programmable or otherwise operated in a manner for turning on and off to collect aggregate samples. For instance, some sampling procedures require a predetermined volume for testing. Alternatively, concentrators are used to aggregate samples to measure for very small concentrations of sample analyte. In this manner, the programmable pump 20 can operate through flowmeter 28 and either volume or time calculations can be performed on the sample aggregation. Referring to the flow meter 28, this has been incorporated into the system so that a predetermined volume can be collected, or if less than the full volume of a container is withdrawn, concentration can be accurately determined.
Alternatively, pump 20 can be operated for a predetermined amount of time at a predetermined flow rate to result in a predetermined volume. This technique could be used to either fill a container for samples, or to send a predetermined volume of sample to the instrument for measurement (e.g., concentrators where material is adsorbed or absorbed into the concentrator). Alternatively, a predetermined amount of sample, or an aliquot can be transported positively into the analyzer 30. In a case where sample collection is required, a certain amount is pumped out over time into a sample collection bag (e.g., 10 ml every 60 minutes over 24 hours to result in a predetermined volume). This technique can be applied to any type of vessel or atmosphere that contains desired sample, and after passing through the pump 20, could result in either collection in collector 25 or analysis into analyzer 30. This technique, as opposed to displacing the sample with water or a benign gas (e.g., nitrogen) keeps the sample in its pure form, reducing the amount of contaminants introduced into the analysis.
If necessary or desirable, a chromatographic footprint can be created for ambient contaminants in the system, or pump 20 plus tube 75, and that footprint could be subtracted from the results of the analyzer 30.
A closed system is disclosed without contaminating connections or sample transfer techniques, and the present methods can be utilized to target atmospheric or non-atmospheric targets. A closed system is defined as a system not subject to the atmosphere between the situs of the target analyte and the gas or liquid analyzer.
The foregoing is considered as illustrative only of the principles of the invention. Furthermore, since numerous modifications and changes will readily occur to those skilled in the art, it is not desired to limit the invention to the exact construction and operation shown and described. While the preferred embodiment has been described, the details may be changed without departing from the invention, which is defined by the claims.
This application claims the benefit of U.S. Provisional Patent Application Ser. No. 61/132,869, filed 23 Jun. 2008 and entitled “Air Sampling Apparatus and Methods.”
Number | Name | Date | Kind |
---|---|---|---|
1191700 | Howes | Jul 1916 | A |
1467615 | Fairbanks | Sep 1923 | A |
2795223 | Stampe | Jun 1957 | A |
2893683 | Lane | Jul 1959 | A |
3303840 | Etzlinger | Feb 1967 | A |
3388705 | Grosshandler | Jun 1968 | A |
3410300 | Mondano | Nov 1968 | A |
3426745 | Farr | Feb 1969 | A |
3544273 | McConnaughey | Dec 1970 | A |
3602531 | Patry | Aug 1971 | A |
3734692 | Lucker et al. | May 1973 | A |
3777571 | Jaeger | Dec 1973 | A |
3817108 | Principe et al. | Jun 1974 | A |
3858573 | Ryan et al. | Jan 1975 | A |
3923043 | Yanda | Dec 1975 | A |
3924832 | Babcock | Dec 1975 | A |
4076044 | Schindling | Feb 1978 | A |
4161307 | Clinch et al. | Jul 1979 | A |
4327741 | Watson et al. | May 1982 | A |
4470412 | Nowacki et al. | Sep 1984 | A |
4506665 | Andrews et al. | Mar 1985 | A |
4544273 | Berndt | Oct 1985 | A |
4579826 | Bolton et al. | Apr 1986 | A |
4580556 | Kondur | Apr 1986 | A |
4585254 | Adams | Apr 1986 | A |
4587989 | Mayhew, Jr. | May 1986 | A |
4646786 | Herder et al. | Mar 1987 | A |
4671298 | Babb et al. | Jun 1987 | A |
4809692 | Nowacki et al. | Mar 1989 | A |
4821737 | Nelson | Apr 1989 | A |
4827921 | Rugheimer | May 1989 | A |
4832015 | Nowacki et al. | May 1989 | A |
4852563 | Gross | Aug 1989 | A |
4852583 | Walker | Aug 1989 | A |
4919127 | Pell | Apr 1990 | A |
4938210 | Shene | Jul 1990 | A |
4947861 | Hamilton | Aug 1990 | A |
4953547 | Poole, Jr. | Sep 1990 | A |
5012803 | Foley et al. | May 1991 | A |
5012804 | Foley et al. | May 1991 | A |
5042500 | Norlien et al. | Aug 1991 | A |
5042501 | Kenny et al. | Aug 1991 | A |
5062423 | Matson et al. | Nov 1991 | A |
5066597 | Stinson et al. | Nov 1991 | A |
5100005 | Noble et al. | Mar 1992 | A |
5137520 | Maxson et al. | Aug 1992 | A |
5140993 | Opekun, Jr. et al. | Aug 1992 | A |
5165393 | Kawaguchi | Nov 1992 | A |
5327901 | Delente | Jul 1994 | A |
5346089 | Brown et al. | Sep 1994 | A |
5432094 | Delente | Jul 1995 | A |
5467776 | Hamilton | Nov 1995 | A |
5573005 | Ueda et al. | Nov 1996 | A |
5711306 | Guilluy | Jan 1998 | A |
5834626 | De Castro et al. | Nov 1998 | A |
5957839 | Kruse et al. | Sep 1999 | A |
6019122 | Chen | Feb 2000 | A |
6368558 | Suslick et al. | Apr 2002 | B1 |
6468477 | Hamilton et al. | Oct 2002 | B1 |
6495102 | Suslick et al. | Dec 2002 | B1 |
6541272 | Mitra | Apr 2003 | B1 |
6712770 | Lin et al. | Mar 2004 | B2 |
20040157281 | Hulkower et al. | Aug 2004 | A1 |
20070066928 | Lannoy | Mar 2007 | A1 |
20080041172 | Jaffe et al. | Feb 2008 | A1 |
20080053439 | Lighton | Mar 2008 | A1 |
Number | Date | Country |
---|---|---|
4028387 | Mar 1992 | DE |
1294835 | Apr 1962 | FR |
2497686 | Jul 1982 | FR |
2230456 | Oct 1990 | GB |
9311817 | Jun 1993 | WO |
Entry |
---|
Rakow, N. A.; Suslick, K. S. “A Colorimetric Sensor Array for Odour Visualization” Nature, 2000, 406, 710-714.; Suslick, K. S.; Rakow, N. A. “Colorimetric Artificial Nose Having an Array of Dyes and Method for Artificial Olfaction”. |
Number | Date | Country | |
---|---|---|---|
20090318823 A1 | Dec 2009 | US |
Number | Date | Country | |
---|---|---|---|
61132869 | Jun 2008 | US |