|Publication number||US3682168 A|
|Publication date||Aug 8, 1972|
|Filing date||Jun 10, 1970|
|Priority date||Jun 10, 1970|
|Publication number||US 3682168 A, US 3682168A, US-A-3682168, US3682168 A, US3682168A|
|Inventors||David W Deaton|
|Original Assignee||Ahldea Corp|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (3), Referenced by (22), Classifications (9)|
|External Links: USPTO, USPTO Assignment, Espacenet|
United States Patent Deaton  STERILE LIQUID ENTRAINING SYSTEM Inventor:
David W. Deaton, Dallas, Tex.
Assignee: Ahldea Corporation, Dallas, Tex. I Filed: June 10, 1970 Appl. No.: 44,929
U.s. c1.- ..128/194, 261/122 1111.01. ..A6lm 15/00 Field of Search ..239/327, 338; 12 /194, DIG.
References Cited I UNITED STATES PATENTS 2,564,400 8/1951 Hall .;....l28/173 3,052,417 9/19 2 pan ."nin .239927it [151 3,682,168 [451 Aug. 8,1972
FOREIGN PATENTS OR APPLICATIONS 604,558 7/1948 Great Britain .....l28/l88 Primary fixaminer Richard A. Gaudet Assistant Examiner-G. F. Dunne Attorney-Richards, Harris & Hubbard ABSTRACI In a sterile liquid entrain'ing system, a, liquid is fed to a vapor generator from a collapsible liquid container. Initially, the container is sterilized and is filled with a sterile liquid. Then, a vapor generator, which may Patented Aug. 8, 1972 3 Sheets-Sheet 1 INVENTOR:
DAVID W DEA TON m S wgnjzw ATTORNEYS Patented Aug. 8, 1972 3 Sheets-Sheet 2 INVENTORI DAVID W. DEA TON ATTORNE (Z Patented Aug. 8, 1972 3 Sheets-Sheet 3 FIG.
DA VID W DEA TON M m m ATIQRNEYS 1 STERILE LIQUID ENTRAINING SYSTEM BACKGROUND OF THE INVENTION In the practice of the healing arts, the remedies that are prescribed for a wide variety of ailments include the use of various gases, including oxygen, oxygen enriched air, etc. Although these gases are usually supplied in a high pressure, moisture-free state, the inhalation of a completely dry gas is generally considered to be injurious. For this reason, it is now common to employ liquid entraining systems in conjunction with the administration of medicinal gases.
At the present time two types of liquid entraining systems are in use. These include humidifiers, which traditionally generate a vapor comprising the gaseous state of a liquid, and nebulizers, which generate a vapor comprising very small liquid droplets. In the operation of both humidifiers and nebulizers, a liquid from a reservoir is transformed into a vapor, and the vapor is entrained in a medicinal gas as the gas is administered.
The reservoirs that are employed in conjunction with presently available liquid entraining systems comprise refillable plastic or glass jars. Liquid entraining system reservoirs of this type are unsatisfactory for a number of reasons. For example, hospital personnel often fail to sterilize the jars between uses. Even if a jar is sterilized, there is no guarantee that the liquid that is used to fill the jars is sterile. And, at the present time, the liquid that is withdrawn from a liquid entraining system reservoir is replaced with unfiltered room air. Microorganisms carried into a reservoir with the air can contaminate the interior of the reservoir, even though the interior was initially sterile.
Regardless of the manner in which microorganisms are introduced into'a liquid entraining system reservoir, there is ample time for the microorganisms to multiply within the reservoir. This is because modern liquid entraining systems are capable of operating for as long as eight hours before it is necessary to refill the reservoir. During the latter stages of the operation of such a liquid entraining system, microorganisms that have multiplied within the reservoir are carried out of the reservoir with the liquid, and are entrained in a medicinal gas along with the vapor that is generated from the liquid.
Obviously, the introduction of microorganisms into medicinal gases is a dangerous practice. Thus, a need exists for a liquid entraining system in which the interior of the reservoir is maintained sterile throughout the use of the system. The present invention fulfills this need, in that is comprises a liquid entraining system in which the reservoir is sterilized and filled with a sterile liquid prior to use, and in which contact between the liquid and unfiltered air is prevented during use.
SUMMARY OF THE INVENTION In accordance with the preferred embodiment of the invention, a sterile liquid entraining system includes a vapor generator and a collapsible liquid container for supplying liquid to the vapor generator. Initially, the
collapsible liquid container is sterilized and is filled a mined amount of the liquid 34 has been fed into the with a sterile liquid. During the use of the invention, the
container is collapsed as the liquid is fed from the container into the vapor generator so that the interior of mosphere. Preferably, the container is discarded when it is empty.
DESCRIPTION OF THE DRAWINGS A more complete understanding of the invention may be had by referring to the following Detailed Description when taken in conjunction with the drawings, wherein:
FIG. 1 is a front view of a collapsible liquid container in which certain portions have been broken away more clearly to illustrate certain features of the invention;
FIG. 2 is a sectional view taken along the lines 2--2 in FIG. 1 in the direction of the arrows;
FIG. 3 is a sectional view of a nebulizer assembly;
FIG. 4 is a sectional view taken along the line 44 in FIG. 3 in the direction of the arrows;
FIG. 5 is a sectional view similar to FIG. 4 showing an alternative construction of the nebulizer assembly shown in FIG. 3,
FIG. 6 is a sectional view similar to FIG. 4 showing another alternative construction of the nebulizer assembly shown in FIG. 3;
FIG. 7 is an illustration of the use of the nebulizer assembly shown in FIG. 3 in conjunction with the collapsible liquid container shown in FIG. 1;
FIG. 8 is an illustration of a humidifier assembly;
FIG. 9 is an illustration of an alternative embodiment of the humidifier assembly shown in FIG. 8, and
FIG. 10 is an illustration of the use of the humidifier assembly shown in FIG. 8 in conjunction with the collapsible liquid container'shown in FIG. 1.
DETAILED DESCRIPTION Referring now to the drawings, a sterile liquid entraining system employing the present invention is shown. Referring particularly to FIGS. 1 and 2, there is shown a collapsible liquid container 20 useful in the practice of the invention. The container 20 is formed from a sterilizable, microorganism impervious substance, for example, a poly-l-olefin, such a polyethylene, polypropylene, etc., a polyamid such as nylon, etc. The container 20 is preferably formed from flexible sheets that are joined into a flexible bag by conventional bonding techniques, such as heat sealing.
The collapsible liquid container 20 includes a main portion 22 having a support bail 24 secured to its upper end and having a nebulizer receiving port 26 and a humidifier receiving port 28 secured in its lower end. The ports 26 and 28 comprise tubes mounted between the sheets comprising the liquid container 20. In accordance with the preferred embodiment of the invention, the ports 26.and 28 are normally sealed by conventional penetrable seals 30 and 32, respectively.
Other sealing mechanisms, such as tear open strips, can be used in place of the penetrable seals 30 and 32 to close the ports 26 and 28, if desired.
container 20, the container is sealed, so that the liquid 34 remains sterile during the transportation and/or storage of the container 20.
Referring now to FIG. 3, there is shown a nebulizer 40 useful in conjunction with the collapsible liquid container 20 in the practice of the present invention. The I inlet port has a sharp tip 54 and retaining barbs 56,
and includes a liquid supply tube 58 which extenb through the port 46 to the bottom of the nebulizer chamber 44. When the nebulizer 40 isnot in use, the exterior of the liquid port 46 is maintained in a sterile condition by a cover 60.
The operating portions of the nebulizer 40 comprise e pressurized gas inlet tube 62,'a liquid delivery tube 64 and a target 66. The liquid delivery tube 64 receives liquid from the liquid supply tube 58, and directs the liquid to a liquid delivery orifice 68. The gas inlet tube 62 directs a high velocity jet of oxygen, air, or the like across the orifice 68, whereupon liquid is. drawn out of I the orifice and liquid droplets are entrained in the gas jet. a
The target 66 is supported on the housing 42 of the nebulizer 40 by a pin and hole connection 70. When the target 66 is removed, the jet flowing from the tube 62 and the liquid droplets entrained therein are directed out of the nebulizer 40 through the vapor outlet port 50. When the target 66 is positioned in the manner shown in FIG. 3, the liquid droplets entrained in the jet are directed into engagement with the target 66. The engagement of the droplets with the target 66 breaks the droplets into very small droplets having diameters ranging down to about 5 microns. The very small droplets are then directed out of the nebulizer 40 through the vapor outlet port 50. Atthe same time, a
' portion of the liquid comprising the droplets that engage the target 66 flows down-the target 66 into the bottom of the nebulizing chamber 44. -A more complete description'of the operation of nebulizers of the type shown in FIG. 3 is contained in US. Pat. No.
Referring now to FIG. 4, -the connection between the liquid supply tube 58 and the liquid delivery tube 64 is shown. In accordance with the preferred embodiment of the invention, the tube 58 is connected directly to I the-tube 64 through a crossover tube 72. A needle valve 74 is positioned in the tube 58 to control the rate of flow of liquid to the liquid delivery orifice 68, and to supply tube 58 conveys liquid to, and in which the liquid delivery tube 64 receives liquid from, the bottom of the nebulizing chamber 44. In the construction shown in FIG. 5, the nebulizer 40 includes a floating valve 78 which blocks the liquid in the bottom of the nebulin'ng chamber 44 reaches a predetermined depth. In the construction shownin FIG. 6, a check valve 80 maintains the liquid in the bottom of the nebulin'ng chamber 44 at a predetermined level by draining excess liquid from the housing 42. In both constructions, liquid flowing down the target 66 returns to the quantity of liquid in the bottom of the nebulizing chamber 44.
The use of the nebulizer 40 in conjunction with the collapsible liquid .container 20 is illustrated in FIG. 7. Initially, the cover 60 is removed from the liquid inlet port 46 of the nebulizer 40, and the exterior of the port 46 is sterilized. Then, the pointed tip 54 of the liquid inlet port 46 is forced through thepenetrable seal 30 of the nebulizer receiving port 26 until the liquid supply tube 58 of the nebulizer 40 communicates with the interior of the main portion 22 of the collapsible liquid container 20. When the nebulizer 40 is'properly positioned relative to the collapsible liquid container 20, the barbs 56 prevent outward movement of the nebulizer 40 relative to the container, and the seal 30 of the port 26 cooperates with the-exterior of the port 46 to form a seal between the nebulizer 40 and the collapsible liquid container 20. i j
Afler the nebulizer 40 and the collapsible liquid container 20 are interconnected, thepressurized gas inlet tube 62 is connected to a source of pressurized gas, and the vapor outlet port is directed to a patient through suitable hoses, tents, etc. If the nebulizer 40 is to be used in a main stream application, a source of dry gas is connected to the dry gas inlet port 48, or the port 48 is opened to the atmosphere, as required. Then, the nebulizer is operated either with or without the target 66 in place to direct a vapor to the patient through the vapor outlet port 50. When the collapsible container is empty, the nebulizer 40 is disconnected therefrom, and the container is discarded. During the use of the nebulizer 40, liquid is supplied to the nebulizer from the collapsible container 20. Due to the collapsible natureof the container 20, there is no need to admit air to the interior of the container during the withdrawal of liquid therefrom. Rather, the container 20 simply collapses as liquid isv fed to the nebulizer 40. Thus, the interior of the liquid container 20 remains sealed throughout the withdrawal of liquid so that the possibility of contamination of the liquid by micro-organisms in the atmosphere is completely 4 eliminated.
Referring now to FIG. 8, there is shown a humidifier useful in conjunction with the collapsible liquid container 20 in the practice of the present invention.The humidifier 90 comprises a relatively large diameter gas inlet cylinder 92 having a gas supply tube 94 extending to it. The upper portion 96 of the tube 92 is conical in shape and has a plurality of small diameter holes formed through it.
The humidifier 90 further includes a relatively small diameter gas outlet cylinder 98. The cylinder 98 extends axially through the cylinder 92 into communication with gas receiving tube 100, and may be integrally formed with the tube 100, if desired. The upper end 102 of the cylinder 98 is pointed and has a plurality of holes formed through it. When not in use, the gas inlet cylinder 92 and the gas outlet cylinder 98 of the hu- I outlet of the tube 58 when midifier 90 are maintained in a sterile condition by a cover 104. v 1
Referring now to FIG. 9, an alternative construction of the humidifier 90 is shown. The construction shown in FIG. 9 is identical to the construction shown in FIG. 8, except that the gas inlet cylinder 92 has a plurality of check valves 106 mounted in it. The valves 106 function to permit gas to flow out of the cylinder 92 and to prevent liquid from flowing into the cylinder 92. When the construction shown in FIG. 9 is used, the holes formed in the upper portion 96 of the cylinder 92 may be of any convenient diameter.
Referring now to FIG. 10, the use of the humidifier assembly 90 in cooperation with the collapsible liquid container is shown. Initially, the cover 104 is removed from the humidifier 90, and the exteriors of the gas outlet cylinder 98 and the gas inlet cylinder 92 are sterilized. Then, the humidifier 90 is inserted into the collapsiblecontainer 20 by forcing the upper end 102 of the gas outlet cylinder 98 through the penetra' ble seal 32 of the collapsible liquid container 20. The humidifier 90 is forced through the humidifier receiving port 28 of the collapsible liquid container 20 until the upper end 102 of the outlet tube 98 is positioned above the upper surface of the liquid 34 in the container 20. This positions the upper-portion 96 of the inlet cylinder 92 within the main portion 22 of the container 20, and the seal 32 of the port 28 and the exterior of the cylinder 92 cooperate to form a seal between the humidifier 90 and the container 20.
When the humidifier 90 is properly positioned within the collapsible liquid container 20, the tube 94 is coupled to a source of gas under pressure, and the tube 100 is directed to a patient through suitable hoses, tents, etc. Gas entering the humidifier 90 through the tube 94 flows into the interior of the container 20 through the holes formed in the upper portion 96 of the gas inlet cylinder 92. As the gas flows through the sterile liquid 34 within the container 20, the liquid is absorbed into the gas. Then, the gas flows out of the container 20 through the holes in the upper portion 102 of the outlet cylinder 98, through the outlet cylinder 98, and through the tube 100. I
Preferably, the gas that is directed to the humidifier 90 is sterilized before it is fed into the tube 94. In such a case, the interior of the collapsible liquid container 20 remains sterile throughout the operation of the humidifier; After all of the liquid within the container has been absorbed by gas flowing through the humidifier 90, the humidifier 90 is removed from the port 28, and the collapsible liquid container 20 is discarded.
From the foregoing, it will be understood that the present invention comprises a sterile liquid entraining liquid container. In the use of the invention, liquid is supplied to the vapor generator from the containerwithout exposing the liquid to the atmosphere. In this way, contamination of the liquid by microorganisms in the atmosphere is prevented. Although specific embodiments of the invention are illustrated in the drawings anddescribed herein, it will 5 be understood that the invention is not limited to the embodiments disclosed, but is capable of rearrangement, modification and substitution of parts and elements without departing from the spirit of the invenflexible and sterilizable thin walled plastic bag, said container when in operation containing an 5 amount of fluid such that an unfilled space exists in the upper portion of said container,
a humidifier assembly mounted through and supported by the walls of said plastic bag in the lower portion thereof and including 'a pressurized gas inlet member directing pressurized gas through the fluid in said container to the unfilled space therein, said gas entraining fluid while passing through the fluid, and a gas outlet member extending to the unfilled space of the container to convey humidified gas from the unfilled space to the exterior of said container, said container tending to collapse as the fluid is entained in the pressurized gas.
2. The sterile liquid entraining system according to claim 1 further including means forming a seal between the humidifier gas. inlet member and the collapsible liquid container.
3. The sterile liquid entr g system according to claim 1 wherein the gas inlet member includes means for permitting gas to flow out of the inlet member and 35 into the container and for preventing liquid from flowing out of the container and into the inlet member.
4. The sterile liquid entraining system according to claim 1 further including a gas inlet tube connected to the gas inlet member for directing a gas thereto, and a 40 gas outlet tube connected to the gas outlet member for receiving the humidified gas therefrom.
5. The sterile vapor entraining system according to claim 1 wherein the collapsible liquid container is entirely sealed except for the point of connection of the humidifier gas inlet member thereto.
7-. The humidifier of claim 1 wherein said humidifier assembly comprises:
a first relatively wide diameter, relatively short gas inlet cylinder having apertures in the end thereof for permitting gas to flow therefrom,
system including a vapor generator and a collapsible 5 asecond relatively small diameter, relatively long gas outlet cylinder extending .through said first cylinder.
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|U.S. Classification||128/200.13, 261/DIG.650, 261/122.1, 128/200.14|
|Cooperative Classification||A61M16/16, A61M16/162, Y10S261/65|