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Publication numberUS2953132 A
Publication typeGrant
Publication dateSep 20, 1960
Filing dateOct 27, 1955
Priority dateOct 27, 1955
Publication numberUS 2953132 A, US 2953132A, US-A-2953132, US2953132 A, US2953132A
InventorsCyrus R Broman, Theodore H Gewecke, John W Richter
Original AssigneeBaxter Laboratories Inc
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Parenteral solution equipment
US 2953132 A
Abstract  available in
Images(1)
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Claims  available in
Description  (OCR text may contain errors)

Sept. 20, 1960 J. W. RICHTER ETAL PARENTERAL SOLUTION EQUIPMENT Filed Oct. 27, 1955 John M Richter Theodore H Geucakt Cyrus E. Bram-M.

IN V EN TORS BY Mom: flr-rorney PARENTERAL SOLUTION EQUIPMENT John W. Richter, Niles, Theodore H. Gewecke, Glenview, and Cyrus R. Broman, Evanston, 111., assignors to Baxter Laboratories, Inc., Morton Grove, Ill.

Filed Oct. 27, 1955, Ser. No. 543,129

2 Claims. Cl. 128-272) This invention relates -to parenteral solution equipment and the method of using same and, more particularly, to container equipment adapted to unite parenteral medicaments just prior to administration thereof.

Inasmuch as parenteral solutions are commonly used in surgical procedures, they have been found to provide convenient vehicles for supplemental medication. Where, for example, the surgeon desires to administer a parenteral anesthetic, skeletal muscle relaxant, antibiotic, or the like, and a parenteral solution regimen such as saline is also contemplated, it is distinctively advantageous to combine the two. This eliminates the need for making an additional vein puncture which is oftentimes painful and inconvenient.

To achieve the foregoing, we have invented parenteral solution equipment including a container for the supplemental medication which is adapted to introduce the medicine into an already provided parenteral solution bottle, the introduction being performed under substantially aseptic conditions and without loss of the medicine which is usually expensive and carefully controlled in quantity.

The invention set forth in this application constitutes an improvement in the structure disclosed in John W. Richters application Serial No. 536,140. Essentially, the additive vial structure described in that application includes a container closed by a flexible diaphragm whereby flexing of the diaphragm causes a pumping action which permits transfer of liquid into and out of the container. A

Inasmuch as the parenteral solution bottle into which the contents of the additive vial are introduced is generally provided with an internal pressure less than atmospheric, a problem is presented in that the sub-atmospheric pressure bottle tends to exert an unusually strong pull upon the flexible diaphragm of the supplemental medication device when the two are interconnected. Then, when it is attempted to pull the supplemental medication device away from the parenteral solution bottle to achieve the desired pumping action by reversely flexing the diaphragm, a strong pull must be exerted that might well result in disconnecting the device from the bottle and bring about a loss of the devices contents. The present invention is designed to meet the foregoing problem and overcome the described difliculties.

Our invention will be explained in conjunction with the accompanying drawing in which Fig. 1 is a perspective view of the container of our invention in combination with a parenteral solution bottle; Fig. 2 is an enlarged cross-sectional view of the container of Fig. 1; and Fig. 3 is a view similar to Fig. 2 but showing the container in operative condition.

Referring now to the drawing and, in particular, to Fig. 1, the numeral designates generally a container for a supplemental medicament which also might be termed as additive vial. Vial 10 includes a glass container 11 having a mouth at one end. Closing the mouth nited States Patent Patented Sept. 20, 1960 Bottle 14 is provided with. rubber stopper 16 mounted in its neck and provided with an annular flange 16a overlying the upper lip of bottle 14. Securing stopper 16 in the neck portion of the bottle 14 is clamping ring 17 which is rolled on in a conventional fashion. An annular bead (not shown) of bottle 14 provides the anchoring means for clamping ring 17. Overlying stopper 16 is frangible rubber disc 18.

Extending through stopper 16 is a solution outlet passage (not shown but indicated by vacuum dimple 19 in disc 1%). Vacuum dimple 19 is evidence that a sub-atmospheric pressure exists within bottle 14.

Also extending through stopper 16 is a second passage constituting an air inlet to bottle 14 during administration of solution 15. Mounted in this second passage and extending inwardly of bottle 14 is air tube 20. When solution 15 is to be administered, bottle 14 is mounted in mouth-downward fashion by means of a suspension device consisting of bail 21 and band 22 so that air tube 21' permits air to enter bottle 14 to replace solution 15 discharged through the outlet passage of stopper 16.

When it is desired to supplement solution 15 with a medicament of the character hereinbefore described or with one that is relatively unstable when provided in a solution form, it is merely necessary to insert the dispensing closure pontion 12 of medicament containing vial 10 into the outlet passage of stopper 16.

In Fig. 2, dispensing closure 12 is seen to include a cap-like plug generally designated 23 which covers the mouth of container 11. In the embodiment shown, the body of plug 23 is provided with an arched diaphragm portion 24 and a depending annular skirt 25 which permits convenient positioning of plug 23 in the mouth of container 11. Plug 23 is also provided with an annular upstanding shoulder-26 which, in combination with the annular bead 27 of container 11, permits securement of plug 23 to container 11 by clamping ring 13. This securement is readily achieved by providing ring 13 in the form of a metal collar and rolling the lower edge as at 13a to grip head 27.

Diaphragm portion 24 is provided with a centrally positioned aperture 28 which permits outflow of supplemental medicament 29. In the embodiment shown in Fig. 2, aperture or passage 28 is closed by hinged valve 28a which is provided integral with diaphragm portion 24.

Integral with diaphragm portion 24 and extending outwardly therefrom is a neck-like portion 30. Necklike portion 30 is positioned about aperture 28 and is adapted to receive dispensing spout 31 and hold the same in a substantially airtight grip achieved by integral male threads 31a. Prior to use of the thus assembled container 10, we provide a protector cap as indicated at 32 to close off the puncturing end of spout 31. We also provide annular flange 31b on spout 31 to serve as a gripping means for insertion and removal of spout 31 from the outlet passage of a parenteral solution bottle stopper.

The use of the container 10 can be appreciated with a consideration of Fig. 1 wherein the spout 31 of container 10 is shown positioned above the dispensing closure portion of a parenteral solution bottle prior to insertion therein. Spout 31 can be adapted to puncture any frangible closure means overlying stopper 16 such as disc 18 in the event such closure means is not removed prior to use. After spout 31 is inserted into stopper 16, thereby communicating the interior of container 10 with that of bottle 14, medicament 29 can be forced downwardly through aperture 28 and the bore of spout 31 merely by pumping container 10. The pumping action referred to involves a relative longitudinal movementof container with respect to the larger-'parenteral solution bottle so as to cause resilient diaphragm portion 24 to flex, thereby varying the internal volume of container 10. e

i is lowermost.

We have discovered that the effect of the vacuum in container 14 after vial 10 has been attached can be overcome by filleting or thickening that portion of plug 23 at the juncture between diaphragm portion 24 and annular skirt 25 as at 24a. Thus,- there is provided a heavy and relatively non-flexing annular portion that rests against the side and upon the top of .the rim of container 10 which causes plug 23 to'assume its static position shown in Fig. 2' whenever it has been flexed as shown in Fig. 3. V v V The arched, or steeply pitched diaphragm portion 24, as indicated specifically at 24b also urges a return to the structure of Fig. 2 after the diaphragm portion 24 has been doubled back substantially upon itself, as illustrated in Fig. 3. This return, therefore, is achieved irrespective of the influence of vacuum generally existing within bottle 14.

In contrast to the desirable result obtained by the structural features of plug 23 described above, the provision of a plug with a flat diaphragm portion would result in ;a tendency of the diaphragm to remain in the doubled backfposition of Fig. 3 under the influence of the vacuum in bottle 14. In addition, the arched diaphragm portion 24, the wall portions of which are extended upwardly in almost a vertical plane, permits the achievement of another new result-the substantial variation of the internal volume of vial 10 without having to flex diaphragm portion outwardly.

of vial 10 from bottle 14 during pumping. In the embodiment shown, it is only necessary to push vial 10 downwardly toward bottle 14 to achieve pumping, the vial returning to its normal or static position without the 7 need for exerting a pulling force.

7 Operation Once spout 31 has been inserted into the outlet pas- Thus, we have fur-. ther minimized the possibility of accidental disengagement sage indicated by dimple 19 as outlined above, it is 7 only necessary to thrust down lightly on vial 10 to cause medicament 29 to be forced, out of vial 10 into bottle 14.

V The same downward movement causesneck-like portion 'vial 10 is essentially a closed container untilcommunh cation between it and bottle 14 is established;

The above procedureis followed when medicament 29 is a liquid, and in the event all medicament is not forced into bottle. 14 by one'thrust, subsequent relative move-.

ment of vial '10 with respect to bottle 14 causes the remaining medicament to flow through spout 30 into bottle 14. We prefer to refer to this as a pumping action since the inward flexing of diaphragm 24 results in a smaller 4 7 internal volume in vial 10 .with'an attendant increase in pressure. 7

In an analogous fashion, medicament 29, if a solid, can be transferred. Such may be the case where it is impossible to provide certain drugs in a stable liquid form. When medicament 29 is a solid, it can be transferred by inverting the united containers so that the additive vial Thrusting vial 10 upwardly causes valve 28a to open andsolution 29- from bottle 14 to run into vial 10. Upon reinversion. of the united containers, solution-borne solid medicament 29 can be pumped ou of vial 10 as set forth above with respect: to the operation involving a medicament originally. provided in liquid form.

The foregoing detailed description has been given for clearness of understanding only and no unnecessary limitations are to be inferred therefrom.

We claim; i V

1. In adevice for adding asupplemental medicine to a parenteral solution container, a vial having an open mouth providing a closurc-supportinglip andhaving an external bead about said-mouth, a resilient closure over said mouthhaving an edge portion supported on said lip and having an outwardly arched flexible central portion, said closure also having an inwardly depending annular skirt receivedwithin the open mouth of said ivial, a juncture between said 7 central portionandsaid skirt being filleted to providea relatively thick non-flexing skirt and a relatively thin central portionwhereby the central portion is induced to return to its nit-flexed condition after being flexed, an aperture in said central portion and an outwardly extending integral tubular projection about said aperture, a rigid puncturing spout in said projection, and a circular metal clamping ring engaging said bead and said edge portion to seal said closure to said vial, said outwardly arched central portion being generally dome-shaped inwardly and outwardly thereof and providing an annular portion between said, tubular projection and said closure edge portion, said annular portion being deformable upon movement of said spout inwardly of said vial, said annular portion, when so deformed, being generally folded on itself and thereby being elfective to urge said spout outwardly of said vialt 2; The structure of claim 1 in which said edge portion is equipped with an upwardly extending generally rounded annular shoulder that, with saidoutwardly arched central portion, provides acircular recess in which one edge of said clamping ring is received.

Patent Citations
Cited PatentFiling datePublication dateApplicantTitle
US180036 *Mar 16, 1876Jul 18, 1876 Improvement in lubricating attachments for oil-bottles
US1152601 *Nov 5, 1909Sep 7, 1915Harold N CarpenterFountain-pen filler.
US2143661 *Feb 23, 1938Jan 10, 1939Schrader Arthur WDispensing head for collapsible tubes
US2461620 *Nov 1, 1946Feb 15, 1949Wright Ray CDispensing closure cap
US2557917 *Aug 11, 1945Jun 19, 1951Eagle Chemical CompanyDispenser having a resilient wall diaphragm flow controller, actuated by a reciprocating dispensing nozzle
US2638613 *Jul 27, 1948May 19, 1953Gunther Roland ECombination receptacle closure and dispensing device
US2664085 *Jun 15, 1950Dec 29, 1953Abbott LabVenoclysis equipment
US2667986 *Dec 22, 1951Feb 2, 1954Harold N PerelsonSelf-sealing dispensing device
DK57882A * Title not available
FR59880E * Title not available
Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3066833 *May 25, 1960Dec 4, 1962Baxter Don IncContainer with closure having a retractable spout
US3125092 *Jun 30, 1961Mar 17, 1964 Infusion flask
US3206080 *Jul 23, 1962Sep 14, 1965Abbott LabDispensing assembly
US3938520 *Jun 10, 1974Feb 17, 1976Abbott LaboratoriesTransfer unit having a dual channel transfer member
US4020839 *Feb 26, 1976May 3, 1977Parke, Davis & CompanyMedicament-dispensing package
US4128098 *Dec 6, 1976Dec 5, 1978American Hospital Supply CorporationValved spike transfer device
US4300404 *Sep 10, 1979Nov 17, 1981Becton, Dickinson And CompanyLiquid specimen container
US4475914 *Aug 30, 1982Oct 9, 1984Merck & Co., Inc.Medicament container and transfer device
US4610374 *Oct 29, 1984Sep 9, 1986Dougherty Brothers CompanyApparatus for mixing flowable materials in sealed containers
US4927605 *Apr 22, 1987May 22, 1990Wadley Technologies, Inc.Specimen collection and sampling container
US5429803 *Apr 18, 1991Jul 4, 1995Lamina, Inc.Liquid specimen container and attachable testing modules
US5549585 *Jul 1, 1994Aug 27, 1996Abbott LaboratoriesGelling treatment for suction drainage system
US5702019 *Sep 27, 1995Dec 30, 1997Becton Dickinson France S.A.Vial having resealable membrane assembly activated by a medical delivery device
US5871110 *Sep 13, 1996Feb 16, 1999Grimard; Jean-PierreTransfer assembly for a medicament container having a splashless valve
US5873872 *Sep 17, 1996Feb 23, 1999Becton Dickinson And CompanyMultipositional resealable vial connector assembly for efficient transfer of liquid
US5925029 *Sep 25, 1997Jul 20, 1999Becton, Dickinson And CompanyMethod and apparatus for fixing a connector assembly onto a vial with a crimp cap
US6003566 *Feb 26, 1998Dec 21, 1999Becton Dickinson And CompanyVial transferset and method
US6003702 *Sep 27, 1995Dec 21, 1999Becton Dickinson France, S.A.Vial with resealable connector assembly having a membrane and a multi-configuration fluid access device
US6090093 *Sep 25, 1997Jul 18, 2000Becton Dickinson And CompanyConnector assembly for a vial having a flexible collar
US6168037Aug 4, 1997Jan 2, 2001Becton Dickinson France, S.A.Resealable vial with connector assembly having a membrane and pusher
US6189580Dec 6, 1999Feb 20, 2001Becton, Dickinson And CompanyVial transferset and method
US6209738Oct 20, 1999Apr 3, 2001Becton, Dickinson And CompanyTransfer set for vials and medical containers
US6213994Sep 25, 1997Apr 10, 2001Becton Dickinson France, S.A.Method and apparatus for fixing a connector assembly onto a vial
US6378576Jun 7, 2001Apr 30, 2002Becton Dickinson And CompanyVial transferset and method
US6378714Oct 20, 1999Apr 30, 2002Becton Dickinson And CompanyTransferset for vials and other medical containers
US6382442Oct 8, 1998May 7, 2002Becton Dickinson And CompanyPlastic closure for vials and other medical containers
US6571837Jan 23, 2001Jun 3, 2003Becton Dickinson France S.A.Transfer set for vials and medical containers
US6626309Oct 5, 2000Sep 30, 2003Becton Dickinson France S.A.Transfer set
US6681946Sep 20, 2000Jan 27, 2004Becton, Dickinson And CompanyResealable medical transfer set
US6787634Feb 2, 1999Sep 7, 2004Medisup International, N.V.Recognizes the extracellular domain of the human ifn-r and which has neutralizing capacity against the biological properties of human type i-ifn.
US6904662Apr 24, 2001Jun 14, 2005Becton, Dickinson And CompanyMethod of sealing a cartridge or other medical container with a plastic closure
US6945417Nov 26, 2003Sep 20, 2005Becton, Dickinson And CompanyResealable medical transfer set
US6957745Jan 29, 2002Oct 25, 2005Becton, Dickinson And CompanyTransfer set
US7179465Apr 14, 2004Feb 20, 2007Medarex, Inc.Monoclonal antibodies against the interferon receptor, with neutralizing activity against type 1 interferon
US7465451Dec 27, 2006Dec 16, 2008Medarex, Inc.Monoclonal antibodies against the interferon receptor, with neutralizing activity against type I interferon
EP0765651A1 *Sep 9, 1996Apr 2, 1997Becton Dickinson and CompanyVial with resealable connector assembly having a membrane and a multiconfiguration fluid access device
Classifications
U.S. Classification604/414, 222/406, 141/329, 604/111
International ClassificationA61J1/00, A61J1/20
Cooperative ClassificationA61J2001/201, A61J1/2089
European ClassificationA61J1/20B