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Publication numberUS3584770 A
Publication typeGrant
Publication dateJun 15, 1971
Filing dateJan 28, 1969
Priority dateJan 28, 1969
Publication numberUS 3584770 A, US 3584770A, US-A-3584770, US3584770 A, US3584770A
InventorsPhilip Taylor
Original AssigneePhilip Taylor
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Intravenous bottle having expandable inner receptacle
US 3584770 A
Abstract  available in
Images(2)
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Claims  available in
Description  (OCR text may contain errors)

United States Patent 72] Inventor Philip Taylor 1903 E. Moyamensing Ave., Philadelphia, Pa. 19148 [21 1 Appl. No. 794,635 [22] Filed Jan. 28, 1969 [45] Patented June 15, 1971 54] INTRAVENOUS BOTTLE HAVING EXPANDABLE INNER RECEPTACLE 6 Claims, 5 Drawing Figs.

[52] [1.5. CI 222/479, 128/214 [51] Int. Cl 867d 3/00 [50] Field of Search 128/DIG.12, 214; 222/3865, 479

[56] References Cited UNITED STATES PATENTS 2,074,223 3/1937 Horiuchi 128/214 2,409,734 10/1946 Bucher 128/214 2,673,013 3/1954 ZZZ/386.5 3,211,348 10/1965 ZZZ/386.5 3,291,151 12/1966 137/56.5 3,319,837 5/1967 222/3865 X 3,437,243 4/1969 Farnsworth 128/214 X FOREIGN PATENTS 1,097,770 5/1956 Germany ZZZ/386.5

Primary Examiner-Stanley H. Tollberg Attorney-Caesar, Rivise, Berstein and Cohen ABSTRACT: An intravenous bottle which dispenses intravenous fluids by gravity feed. The bottle includes a sterile expandable receptacle which is connected to the atmosphere via an inlet port. As the fluid for intravenous injection is dispensed from the bottle, air is drawn into the expandable receptacle. The expandable receptacle acts to prevent the contact of the air from the atmosphere with the fluid to prevent spoilage thereof.

PATENTED JUN 1 51971 SHEET 1 [IF 2 PHILIP lA/VEAITOH. T AY L 0 R Mmom 4 T TOR/VEYS.

PATENTEDJUNI 5197i 3,584,770

saw 2 UF 2 IAIVE/VTOR. PHILIP TAYLOR ATTORNEYS.

INTRAVENOUS BOTTLE HAVING EXPANDABLE INNER RECEPTACLE This invention relates generally to intravenous injections and more particularly to an intravenous bottle which prevents contamination of the fluid therein during an intravenous injection.

When making injections of a dextrous solution or other fluids for insertion into the bloodstream of a patient, an intravenous bottle containing the fluid is conventionally suspended above and adjacent to the patient. The intravenous bottle normally includes a stopper at the neck of the bottle having an inlet and an outlet port. When used in intravenous injection, the bottle is inverted so that the outlet port is connected directly to the patient via an elongated tube and the inlet port is connected to the atmosphere. Consequently, as the fluid is dispensed through the outlet port, air from the atmosphere is drawn into the inlet port in order to take up the volume ofliquid that has been removed from the bottle.

In many intravenous injections, the fluid in the bottle is dispensed over a relatively long period of time. During this period, bacteria in the air can contaminate the fluid within the bottle. In the case of dextrous solutions as well as fluids such as blood, a host environment is provided which is extremely susceptible to infection from the bacteria in the air. Even in the most sterile environments, such as hospitals, when patients are visited by friends, there is nothing to prevent the bacteria from a harmless sneeze or cough of one of the visitors from ultimately contaminating the fluid in the bottle.

One means that has been provided in order to reduce the contamination of the fluid in the bottle is a cotton insert provided at the inlet port of the intravenous bottle. There are, however, disadvantages in using a medicated cotton. The first of the disadvantages is that many forms of bacteria in the air are not fllterable. A second disadvantage is that where the cotton is packed tightly, the flow of fluid can be completely inhibited because the flow of air into the bottle is impeded which is necessary to take up the volume of liquid which has been removed. Another important disadvantage is that the use of cotton can prevent higher flow rates of the liquid into the bloodstream where it is desired or required.

It is therefore an object of the invention to overcome the aforementioned disadvantages.

Another object of the invention is to provide a new and improved intravenous bottle having a sterile expandable receptacle connected to the inlet port thereof to prevent the contact of air from the atmosphere with the fluid contained in the bottle.

Another object of the invention is to provide a new and improved intravenous bottle which maintains the sterility of the fluid therein during the dispensing thereof.

Another object of the invention is to provide a new and improved intravenous bottle which can maintain sterility of the fluid therein while dispensing the fluid quickly by gravity feed.

Still another object of the invention is to provide a new and improved intravenous bottle having a safety means for preventing too fast a flow of fluid into the blood system of a patient.

Still another object of the invention is to provide a new and improved intravenous bottle having a sterile expandable insert to prevent contamination of the fluid therein, said receptacle acting to identify the fluid being dispensed.

These and other objects of the invention are achieved by providing a vessel for dispensing fluids which easily spoil during exposure to the atmosphere. The vessel is atmospherically sealed and includes a pair of ports. One of the ports is adapted for the removal of the liquid therein. An expandable receptacle is provided which is connected to the atmosphere via the other of the ports so that as the fluid is dispensed, air is drawn into the expandable receptacle. The receptacle prevents direct contact between the atmosphere and the fluid.

Other objects and many of the attendant advantages of this invention will be readily appreciated as the same becomes better understood by reference to the following detailed description when considered in connection with the accompanying drawings wherein:

FIG. 1 is a side elevational view of an intravenous bottle embodying the invention;

FIG. 2 is an enlarged vertical sectional view of the intravenous bottle;

FIG. 3 is a view similar to FIG. 2 wherein a portion of the fluid in the intravenous bottle has been dispensed;

FIG. 4 is a side elevational view of an alternate intravenous bottle embodying the invention with portions thereof shown in section for purposes of clarity; and

FIG. 5 is a side elevational view of a second alternate intravenous bottle embodying the invention.

Referring now in greater detail to the various figures of the drawing wherein similar reference characters refer to similar parts, a liquid dispenser embodying the invention is shown generally at 20 in FIG. 1.

The intravenous bottle 20 is a conventional glass vessel having a bracket 22 connected about the periphery adjacent the bottom thereof which is connected to a wire 24 for suspension of the intravenous bottle in an inverted position.

As best seen in FIG. 2, at the opposite end of the intravenous bottle 20, a neck 26 of the bottle is provided with a rubber stopper 28 therein. Stopper 28 preferably includes a pair of ports which extend vertically through the stopper. A first port is utilized to receive a substantially rigid tube 30, which is connected via conventional intravenous tubing to the bloodstream of a patient. The stopper 28 may also comprise a stopper of the self-sealing type with the ports developed by use of an entry spike.

As best seen in FIG. 1, tube 30 is connected via a bulb 32 to flexible tubing 34 which extends to the patient. The flow through the tubing 34 is regulated by a suitable plastic pinch valve 36 which varies the opening in the tubing 34 to regulate flow. The bulb 32 enables the user to visually determine the rate offlow of fluid out ofthe bottle into the bloodstream.

As best seen in FIG. 3, the tube 30 is terminated at 38 so that the edge thereof is inclined. The inclination of edge 38 produces a sharp edge which is utilized in insertion of the tube 30 to penetrate the seal in the port of the stopper of the bottle which is provided for sealing the contents thereof. In the second of the ports, a tube 40 is provided which extends substantially centrally of the bottle. The tube 40 includes a nipple 42 at the end thereof to which an expandable receptacle 44 is attached.

The expandable receptacle 44 is basically comprised of a sterilized flexible elastomeric material and suitably comprises a balloon. The tube 40 is preferably permanently secured in the stopper 28 and terminates at the outer surface of the stopper. The port in the stopper connected to tube 40 may include a breakable seal. The seal is optional, however, since the expandable receptacle 44 is provided at the opposite end of the tube 40 and therefore seals the contents of the bottle 20 from the atmosphere.

The stopper 28 is placed into the bottle 20 after a predetermined amount of liquid is placed into the bottle. The stopper 28 normally includes a seal over the first port which is penetrable by the end 38 of the outlet tube 30.

The expandable receptacle 44 may also take the form of a collapsible or folded bag which has flexible but inelastic walls. As the air enters the bag, the bag unfolds and expands to accommodate the intake of air. Moreover, the receptacle 44 is suitably colored to identify the solution in the bottle that is being dispensed. Not only are different colored receptacles contemplated, but also different patterns (i.e. stripes, dots, etc.).

As best seen in FIG. 3, during the use of the bottle, the tube 30 is inserted in the first port of stopper 28. After the intravenous fluid is emitted via tube 30, air from the atmosphere enters tube 40 via the second port and is drawn into the expandable receptacle 44. The air which is drawn into the balloon is equal in volume to the volume of liquid 46 that has been dispensed through the tube 30.

The receptacle 44 is expanded automatically as the fluid is dispensed by gravity feed because the removal of the fluid causes the air in the vessel to occupy a larger space and thereby cause a reduced pressure therein. The atmospheric pressure in tube 40 is then larger and causes the receptacle to increase until the pressure in the bottle and the atmospheric pressure are substantially equal.

It can therefore be seen that a new and improved intravenous bottle has been provided. The inlet portion to the bottle is connected to an expandable receptacle which is expanded as the fluid is dispensed from the intravenous bottle. Since the receptacle 44 is air tight, the air cannot make contact with the fluid 46. Thus, no matter how contaminated the air about the intravenous bottle 20, the fluid 46 remains sterile throughout thereby preventing any bacterial or other infections from entering the bloodstream of the patient. Moreover, the use of colored patterns on the receptacles 44 enables quick identification of the fluid dispensed.

F IG. 4 shows an alternate embodiment of the invention. The intravenous bottle shown therein includes an alternate form of expandable receptacle 50. The intravenous bottle 20 is otherwise similar to bottle 20 shown in FIG. 1. The expandable receptacle 50 is connected to the second port of the stopper 28 via a shorter tube 52 than tube 40 in FIG. 1 so that the expandable receptacle is located closer to the stopper of the bottle. The receptacle 50 basically differs from receptacle 44 in that the receptacle includes a wall of varying thickness. That is, the uppermost portion 54 of the wall of the receptacle 50 comprises a very thin and elastic membrane which is more easily expandable than the remaining portion 56 of the wall of the receptacle. in this manner, it assures the receptacle of expanding at the top thereof so that the expansion of the receptacle cannot preclude fluid from reaching the port of the stopper 28.

In FIG. 4, the receptacle 50 is shown in full line in an intermediately expanded condition. The portion shown in phantom shows the receptacle expanded when the fluid has reached the level of dotted line 58 shown therein. The receptacle 40 facilitates the complete removal of fluid from the intravenous bottle. That is, where the intravenous bottle 20 is completely filled, there is the chance that as the fluid is completely removed in the embodiment shown in FIG. 1, the receptacle 44 may be broken because of its deformation about a rigid tube 40. In the embodiment shown in FIG. 4, the receptacle 50 more easily conforms to the shape of the bottle 20 as the fluid is dispensed.

Referring now to FIG. 5, an intravenous bottle 20 is shown utilizing an alternate inlet tube 100. The inlet tube 100 is flexible so that a pinch valve 102 may be utilized to regulate the flow of air to the receptacle 44. The valve 102 supplements valve 36 so that if either valve 36 or 102 should be inadvertently removed, the flow of fluid out of the bottle cannot be greatly increased and thereby provide a hazard to the patient. The provision of the flexible tube having a pinch valve 102 is enabled by the provision of having an expandable receptacle 44 provided within the intravenous bottle 20.

That is, where the expandable insert is not provided, it is necessary to filter the incoming air by means of cotton or other purifying filters. Thus, the flow of air therethrough is not regulatable except by compacting or loosening the cotton.

it should also be understood that the size of the port in the stopper 28 may be increased to increase the flow of fluid out of the intravenous bottle. In such a case, there is still no problem of contaminating the fluid within the bottle in that the receptacle 44 maintains a barrier between the air from the atmosphere and the fluid.

Without further elaboration, the foregoing will so fully illustrate my invention that others may, by applying current or future knowledge, readily adapt the same for use under various conditions of service.

What I claim as invention is:

1. In an intravenous bottle for dispensing fluids by gravity feed in an intravenous injection and which fluids should not be exposed to the atmosphere, said bottle having inflexible walls and being atmospherically sealed, said bottle having a pair of ports, one of said ports adapted for the removal of said liquid, an expandable receptacle within said bottle, said expandable receptacle being connected to the atmosphere via the other of said ports so that as said fluid is dispensed, air is drawn into said expandable receptacle; said receptacle is conformable to the shape of the inner surface of said bottle as it expands and contacts the same and prevents direct contact between the atmosphere and said fluid, said receptacle adapted to expand to substantially replace the dispensed fluid contents of said bottle.

2. The invention of claim 1 wherein said receptacle is color coded in accordance with the fluid dispensed.

3. The invention of claim 1 wherein said ports are provided in a stopper at the neck of said bottle. v

4. The invention of claim 1 wherein said receptacle comprises a balloon.

5. The invention of claim 1 wherein said receptacle includes an elastomeric wall which is of varying thickness to predetermine the shape as said receptacle expands.

6. The invention of claim 1 wherein a regulating valve is connected to said port adapted for the removal of said liquid and a regulating valve is also connected to said port connected to the atmosphere.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US2074223 *Nov 5, 1935Mar 16, 1937Fred T HoriuchiBlood transfusion apparatus
US2409734 *Sep 4, 1942Oct 22, 1946Swiss Firm Of G Laubscher & CoInstrument for blood transfusion
US2673013 *Dec 27, 1949Mar 23, 1954Hester Dwight HDevice for dispensing predetermined amounts of liquid from containers
US3211348 *May 21, 1964Oct 12, 1965Greer Hydraulics IncPressure vessels
US3291151 *Nov 6, 1963Dec 13, 1966Selmer M LokenFluid exchange system
US3319837 *Jan 27, 1965May 16, 1967Air Ject CorpDispensing device
US3437243 *Jun 22, 1967Apr 8, 1969Farnsworth Helen DMeans for gauging timed dosages from a dispensing container
DE1097770B *May 5, 1956Jan 19, 1961Wilhelm Stigler Dipl IngFluessigkeitsverdraengungskoerper
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3980082 *Mar 14, 1975Sep 14, 1976William MillerVenous pressure indicator
US4142657 *May 16, 1977Mar 6, 1979Wanke Ronald LDispensing closure with nonrigid follower
US4601712 *Nov 16, 1983Jul 22, 1986Gould Inc.Drip chamber
US5024663 *Feb 21, 1990Jun 18, 1991Alza CorporationSelf-contained suction pump
US6641556 *Jul 6, 1999Nov 4, 2003Respiratory Support Products, Inc.Intravenous fluid heating system
US7354427Jun 21, 2006Apr 8, 2008Icu Medical, Inc.Vial adaptor for regulating pressure
US7507227May 2, 2006Mar 24, 2009Icu Medical, Inc.Vial adaptor for regulating pressure
US7510547May 2, 2006Mar 31, 2009Icu Medical, Inc.Vial adaptor for regulating pressure
US7510548May 2, 2006Mar 31, 2009Icu Medical, Inc.Vial adaptor for regulating pressure
US7513895May 2, 2006Apr 7, 2009Icu Medical, Inc.Vial adaptor for regulating pressure
US7534238May 2, 2006May 19, 2009Icu Medical, Inc.Vial adaptor for regulating pressure
US7547300 *May 1, 2006Jun 16, 2009Icu Medical, Inc.Vial adaptor for regulating pressure
US7569043May 2, 2006Aug 4, 2009Icu Medical, Inc.Vial adaptor for regulating pressure
US7618408 *Sep 19, 2007Nov 17, 2009Yandell Marion EVial assembly and method for reducing nosocomial infections
US7645271May 2, 2006Jan 12, 2010Icu Medical, Inc.Vial adaptor for regulating pressure
US7654995 *May 2, 2006Feb 2, 2010Icu Medical, Inc.Vial adaptor for regulating pressure
US7658733May 2, 2006Feb 9, 2010Icu Medical, Inc.Vial for regulating pressure
US7789871Nov 17, 2009Sep 7, 2010Yandell Marion EVial assembly and method for reducing nosocomial infections
US7883499Mar 7, 2008Feb 8, 2011Icu Medical, Inc.Vial adaptors and vials for regulating pressure
US7887528Aug 3, 2010Feb 15, 2011Yandell Marion EVial assembly and method for reducing nosocomial infections
US7972321 *Mar 19, 2008Jul 5, 2011Icu Medical, IncVial adaptor for regulating pressure
US8206367Feb 2, 2010Jun 26, 2012Icu Medical, Inc.Medical fluid transfer devices and methods with enclosures of sterilized gas
US8267913Oct 27, 2009Sep 18, 2012Icu Medical, Inc.Vial adaptors and methods for regulating pressure
US8357137May 31, 2012Jan 22, 2013Yandell Marion EBung assembly for anti vacuum lock medical vials
US8409164Aug 19, 2009Apr 2, 2013Icu Medical, Inc.Anti-reflux vial adaptors
US8512307Dec 2, 2010Aug 20, 2013Icu Medical, Inc.Vial adaptors and vials for regulating pressure
US8523838 *Dec 10, 2009Sep 3, 2013Carmel Pharma AbConnector device
US8540692Oct 13, 2011Sep 24, 2013Icu Medical, Inc.Adaptors for removing medicinal fluids from vials
US8640930Mar 10, 2011Feb 4, 2014Diversey, Inc.Vent tube apparatus and method
US8662358Jan 31, 2011Mar 4, 2014Diversey, Inc.Liquid dispensing container and method
US8827977Nov 1, 2011Sep 9, 2014Icu Medical, Inc.Vial adaptors and methods for regulating pressure
US20100147402 *Dec 10, 2009Jun 17, 2010Carmel Pharma AbConnector Device
DE2920975A1 *May 23, 1979Nov 27, 1980Siemens AgExtrakorporal tragbares infusionsgeraet
DE4018195A1 *Jun 7, 1990Nov 28, 1991Straehle & HessElectrical conductor - is ribbon laid in strips to leave open spaces without cutting the continuous electrical wire
WO2008039686A2 *Sep 20, 2007Apr 3, 2008Yandell Marion EVial assembly and method for reducing nosocomial infections
WO2010022095A1 *Aug 18, 2009Feb 25, 2010Icu Medical, Inc.Anti-reflux vial adaptors
Classifications
U.S. Classification222/479, 604/257, 604/141, 604/199
International ClassificationA61M5/14, A61J1/00, A61J1/05
Cooperative ClassificationA61J1/1462, A61J2001/1487, A61J2001/1468, A61M5/14, A61J1/1406, A61J1/05, A61J1/18, A61J1/1475
European ClassificationA61J1/18, A61J1/14P, A61J1/14B, A61J1/14H, A61J1/05, A61M5/14