United States Patent Stumpf et al.
[54] BREECH LOADED SYRINGE AND METHOD OF BREECH LOADING SAME [72] Inventors: Marvin D. Stumpl, 9301 Clarion Drive, St. Louis, Mo. 63136; Elmer A. Koenig, 1702 Ben Davis Lane, Kirkwood, Mo. 63122 [22] Filed: Sept. 23, 1969 [21] Appl. No.: 860,223
[52] US. Cl. ..12s/21s P, 53/57 [51] Int. Cl. ..A6lm 5/00 [58] Field of Search ..128/218 R, 218 P, 218 M, 220; 53/57 [56] References Cited 7 UNITED STATES PATENTS 3,391,518 7/1968 Gettig et al. ..53/37 X 3,470,671 10/1969 Gettig et al 841,701 l/l907 DeLisle 1,139,368 5/1915 Pierce ..128/218 P [451 Dec. 12, 1972 l-lein ..128/218 R Brown ..128/218 R UX Van Sickle ..128/218 P UX Ogle ..128/218 P X Von Pechmann ..128/218 R Primary Examiner-Joseph S. Reich Attorney-Donald S. Olexa, Jerome M. Teplitz and John G. Heimovics A syringe wherein a piston is moved axially through a tubular barrel to deliver liquid medicament and the like outwardly through a needle connected through an inner end of the barrel. A control is provided for selectively deforming the piston to permit the barrel to be preloaded with the liquid medicament through the breech end thereof with the piston being brought into engagement with the liquid while a fluid bypass passage is provided around the piston to the breech end of the barrel, thereby to vent air outwardly from the space between the piston and the liquid medicament during the insertion of the piston.
ABSTRACT 8 Claims, 9 Drawing Figures I PATENTEDDECIZIHR 3.705 582 SHEET 2 HP 2 I Jig- J? BREECH LOADED SYRINGE AND METHOD OF BREECII LOADING SAME BACKGROUND OF THEINVENTION 1. Field of the Invention This invention relates to syringes and in particular to piston-type syringes.
2. Description of the Prior Art In the conventional piston syringe, the filling of the syringe is effected through the needle connecting end. Such a method of filling the syringe is undesirable where the filled syringe is to be stored, such as where the syringe comprises a prefilled syringe. Further, such needle end filling is inimical to good aseptic techniques. Illustratively, it has been found that the narrow lumens of the needle or needle connector tip become clogged by the dried medicament.
One attempted method of resolving this problem has been to load the syringe through the breech end of the barrel. Such a loading of the syringe provides improved storage characteristics where air is removed from between the piston and liquid medicament upon insertion of the piston. Thus, in the prior art devices for providing such breech loading, needles, rods, valves, conical shaped sleeves, etc. have been employed to permit venting of the trapped air. Not only are such means relatively expensive, but also, such means have been found to lead to contamination of the liquid medicament.
SUMMARY OF THE INVENTION The present invention comprehends an improved syringe structure wherein the piston, during insertion through the breech end of the barrel into engagement with the previously deposited liquid medicament, is deformed so as to provide a bypass vent. The deforming means may comprise a tubular element adapted to receive the piston under compression and having a clearance with the barrel permitting movement of the inner end of the element through the breech end of the barrel into juxtaposition with the liquid medicament wherein the trapped air is vented through the clearance space between the sleeve and the barrel. Upon reaching the fully inserted position, the piston is removed from its position within the sleeve end thereby permitting the, piston to expand into sealed sliding engagement with the barrel wall. The piston may be carried on the inner end of a shaft extending from the piston to outwardly of the barrel outer end.
In one specific embodiment of the invention, the shaft extends coaxially through a tubular sleeve having a bore radially enlarged at its inner end to define a piston receiving recess. The tubular sleeve also has a recess at its outer end for receiving in nested relationship the thumb piece of the shaft. Movement between the shaft and the sleeve may be effected manually to provide the selective deformation and release of the piston.
Alternatively, the piston may be deformed by a rib element on the inner end of the sleeve which extends the length of the piston to deform an outer wall portion thereof radially inwardly and thereby form a fluid bypass passage permitting the air to be vented from the barrel during the insertion of the piston. If desired, a plurality of such rib elements may be provided to form a plurality of such bypass passages for venting during the piston insertion step.
Iii!
' air from the barrel as the piston is moved to the liquid medicament, and discontinuing the deforming of the piston upon the piston reaching the liquid medicament to cause the piston to have sealed sliding engagement with the barrel. The filling of the syringe may be effected to provide a prefilled syringe unit which may be stored for subsequent use as desired. In such case, the needle end of the syringe is maintained sealingly closed. Alternatively, the syringe will be breech filled at the time of use by the above indicated steps.
BRIEF DESCRIPTION OF THE DRAWING Other features and advantages of the invention will be apparent from the following description taken in connection with the accompanying drawing wherein:
FIG. 1 is a fragmentary enlarged front view of a syringe embodying the invention with portions broken away to illustrate the invention;
FIG. 2 is a view similar to that of FIG. 1 but illustrating the arrangement of the syringe during the piston inserting operation;
FIG. 3 is an exploded view with portions broken away illustrating the arrangement of the piston and sleeve assembly prior to insertion into the syringe barrel;
FIG. 4 is a front view of one form of sleeve thereof;
FIG. 5 is a fragmentary bottom end view thereof;
FIG. 6 is a front view of the sleeve used in the syringe shown in FIGS. 1-3, with a portion broken away to pro vide a clear illustration of the invention;
FIG. 7. is a bottom end view of the sleeve of FIG. 6;
FIG. 8 is a front view of still another modified form of sleeve thereof with a portion broken away to illus trate the invention; and
FIG. 9 is a bottom end view of the sleeve of FIG. 8.
DESCRIPTION OF THE PREFERRED EMBODIMENTS In the exemplary embodiment of the invention as disclosed in FIGS. l-3 of the drawing, a syringe generally designated 10 is shown as having a conventional tubular barrel 1 l defining a chamber l2v opening axially outwardly through anouter end 13. Theinner end 14 of the barrel 1] is provided with anoutlet 15 opening into aconnector 16 for attaching a needle, such asconventional needle 17, in fluid transfer association with the inner end of the barrel. In the illustrated embodiment, the connector comprises a conventional luer lock connector, it being understood that any suitable needle connecting means may be utilized. Prior to the installation of theneedle 17 onto theconnector 16,connector 16 may be conventionally closed by aconventional cap 18, as shown in FIGS. 2 and 3.
Thesyringe 10 may comprise a prefilled syringe wherein a body of liquid, such asliquid medicament 19, is provided in the portion 20 of thechamber 12 inwardly of apiston 21. In the illustrated embodiment, theliquid 19 is delivered into thechamber 12 through theouter end 13 in a breech loading operation. The
Inuun npiston 21 is then brought into thechamber 12 through theouter end 13 to engage theliquid 19 as shown in FIG. 2. To permit such insertion of the piston, abypass passage 22 is provided around the piston from the inner chamber portion 20 to theouter opening 13 whereby air may be vented from thechamber 12 as the piston is moved downwardly therethrough to the position of FIG. 2.
The invention comprehends the provision of thevent passage 22 by means of a tubular element, or sleeve, 23 having an outside diameter slightly smaller than the inside diameter of thebarrel 11. Thebore 24 ofsleeve 23 is stepped at 25 to define a radially enlarged innerend bore portion 26 adapted to receive thepiston 21 as shown in FIG. 2. Piston 21 is preferably formed of a resilient material, such as neoprene rubber, to permit the ready compression thereof into thebore portion 26 of thesleeve 23 as by urging the sleeve axially forward relative to thepiston 21 until the piston is encased inportion 26 as shown in FIG. 3. The piston is secured to anend connector portion 27 of ashaft 28 having anouter thumb piece 29.Shaft 28 extends coaxially through thebore 24 ofsleeve 23. As shown in FIG. 2,shaft 28 is somewhat smaller in transverse dimension than the diameter ofbore 24, permitting the ready axial movement of theshaft 28 therethrough when desired. To provide relative movement between theshaft 28 andsleeve 23 and to provide for the movement of thesleeve 23 into thebarrel 11, the outer end of the sleeve is provided with aflange 30.Flange 30 is spaced outwardly of the conventionaloutturned flange 31 of the barrel to permit the user to insert his fingers underflange 30 with his thumb onthumb piece 29 and thereby readily effect a movement of thepiston 21 inwardly from theend portion 26 when desired. Thus by maintaining thepiston 21 in contact with theliquid medicament 19 and urging thesleeve 23 outwardly, the lower end of the sleeve is withdrawn from the piston permitting the piston to expand radially into sliding sealing engagement with the barrel wall in bore portion 20' thereby to permit subsequent controlled delivery of the liquid medicament outwardly throughneedle 17 as desired.
Theflange 30 of thesleeve 23 has a recess formed in theupper surface 32 whichrecess 35 is of a size and shape to receive in nested relationship thethumb piece 29 of theshaft 28 when the shaft is fully depressed relative to thesleeve 23. In moving theshaft 28 relative to thesleeve 23 from the position of FIG. 2 to the position of FIG. 1, thethumb piece 29 will nest in therecess 35 and create the appearance of a one piece plunger unit.
In the normal use, thepiston 21 may be provided retracted withinbore portion 26 as shown in FIG. 3, permitting the movement of the assembled piston andsleeve 23 into thebarrel 11 as discussed above. However, alternatively, the piston may be mounted on theshaft end 27 inwardly of the sleeve (in the arrangement seen in FIG. 1) and inserted into theopen end 13 of thebarrel 11. The piston is then caused to move into thebore portion 26 by a combination of forces directed by the users fingers on theouter surface 32 of theflange 30 and the fluid pressure within thebore 12 ahead of thepiston 21 thereby to cause the piston to move axially into the sleeve bore end 2 6. Once the piston is fully received inbore end 26, further movement of the assembly may be effected as discussed above as the sleeve and piston structure are now disposed in the arrangement shown in FIG. 2. This method of bringing the piston into thebore end 26 at the time of assembly is advantageous where thepiston 21 is formed of a material which may take a permanent set if stored within the sleeve bore 24 for a protracted period of time. Thepiston 21,sleeve 23, andshaft 28 may, of course, be assembled together by inserting theshaft 28 through thesleeve 23, and then mounting thepiston 21 onto theinner end 27 of the shaft so that these parts occupy the relative positions shown in FIG. 1. The piston is deformed to provide a vent passage around thepiston 21 by effecting relative movement between the shaft with the piston connected thereto, and the sleeve. In the illustrated embodiment of FIGS. 1-3, such relative movement positions thepiston 21 in the sleeve boreend 26 and this effects deformation of the piston by urging peripheral portions thereof radially inwardly, the piston being retained in thebore end 26 by the inherent resiliency thereof.
Thus, thesyringe 10 provides an improved structure permitting prefilling of the syringe in an aseptic manner by a breech loading of the liquid medicament therein. As indicated above, the liquid medicament may be retained in the prefilled syringe by the subsequent installation of thepiston 21 as discussed above, whereby the piston may be brought into engagement with the upper surface of the liquid by a vented movement of the piston through the barrel, thereby maintaining the aseptic condition of the breech loaded syringe. When the syringe is to be used, thecap 18 is removed and theneedle 17 installed on theconnector 16 in the conventional manner whereupon the liquid medicament may be delivered through the needle by suitable manipulation of theshaft 28 by the usersfingers engaging flange 31 andthumb piece 29.
The invention comprehends broadly providing a means for deforming thepiston 21 during its insertion through thebore 12 to define abypass passage 22 whereby the bore '12 is vented to facilitate the movement of the piston fully to the position of FIG. 2. As discussed above, in one form, the means for forming thebypass passage 22 may comprise means for receiving the piston under compression within one end of thetubular sleeve 23. The sleeve construction is illustrated in FIGS. 6 and 7. As will be obvious to those skilled in the art, other forms of piston deforming means may be provided within the scope of the invention. Illustratively, in FIG. 4, asleeve 123 is shown to comprise a sleeve similar tosleeve 23 but having a plurality of circumferentially spacedend prongs 133 which effectively distort the piston when the piston is retracted into thespace 126 radially within the prongs. In the illustrative embodiment of FIG. 4, three such prongs are provided spaced about the axis of the sleeve. In FIGS. 8 and 9, a further modified form ofsleeve 223 is shown to comprise a sleeve having a dependingprong 223 provided with a radially inwardly projectingrib 234 which effectively distorts the piston to define an air bypass vent passage for venting the barrel during the installation of the piston.
Each of thesleeves 23, 123, and 223 is similar to the others and functions in a similar manner except as otherwise noted. In each embodiment, means are provided for deforming the piston during insertion thereof into the barrel bore to define a vent passage. The deforming means are carried on an elongated element which extends to outwardly of the barrel serving as a means for effecting a separation of the deforming 'means from the piston after the piston reaches the desired fully inserted position whereby the piston may then function in the normal manner within the barrel. As will be obvious to those skilled in the art, the element carrying the deforming means may have other configurations in addition to the tubular sleeve configuration of the illustrative embodiments. The different parts of these syringes may be made of suitable materials, such as plastics, permitting relative ease of sterilization. Thus, the syringes may comprise one-time use, prefilled syringes.
The foregoing disclosure of specific embodiments is illustrative of the broad inventive concepts comprehended by the invention.
I claim: 1. In a syringe having a tubular barrel defining a chamber opening axially through the outer end of the barrel, and a needle connecting portion at the inner end of the barrel for connecting a needle in fluid flow association with said chamber, the improvement comprising:
a resilient piston arranged to have sealing sliding engagement with the barrel in said chamber; first means secured to said piston and extending from said piston to outwardly of said outer end for moving said piston into said chamber through said outer end during insertion thereof in said barrel and for moving said piston to discharge fluid from said chamber in response to a manually applied force on said first means during operational use of the syringe; and second means carried by said first means and extending from within said chamber to outwardly of said outer end, said second means being movable in one direction relative to said first means to deform said piston for forming fluid bypass means around said piston for venting the chamber portion forward of said piston, and movable in the direction opposite said one direction relative to said first means for removing the fluid bypass means whereby the piston sealingly engages with the barrel to force fluid from said chamber through said needle connecting portion as an incident of movement of said piston in said chamber toward said inner end in response to said applied force on said first means.
2. in a syringe having a tubular barrel defining a chamber opening axially through the outer end of the barrel, and a needle connecting portion at the inner end of the barrel for connecting a needle in fluid flow association with said chamber, the improvement comprising:
a resilient piston arranged to have sealing sliding engagement with the barrel in said chamber;
first means secured to and extending from said piston to outwardly of said outer end for manipulating said piston during operational use of the syringe; and
second means carried by said first means, said first and second means being relatively movable a. for forming fluid bypass means around said piston for venting the chamber portion forward of said piston, and
b. for removing the fluid bypass means whereby the piston is in sealing engagement with the barrel to force fluid from said chamber through said needle connecting portion. as an incident of movement of said piston in said chamber toward said inner end, said second means comprising means having a tubular inner end removably receiving said piston, and means for causing axial removal of said piston from said tubular inner end, said second means having a clearance with said barrel defining said fluid bypass means to said outer end of the barrel, said second means also having an axially inner end for retaining the piston axially inwardly of said tubular end subsequent to said removal.
3. In a syringe having a tubular barrel defining a chamber opening axially through the outer end of the barrel, and a needle connecting portion at the inner end of the barrel for connecting a needle in fluid flow association with said chamber, the improvement comprising:
a resilient piston arranged to have sealing sliding engagement with the barrel in said chamber;
first means secured to and extending from said piston to outwardly of said outer end for manipulating said piston during operational use of the syringe; and
second means carried by said first means and extending from within said chamber to outwardly of said outer end, said first and second means being selectively relatively movable.
a. for forming fluid bypass means around said piston for venting the chamber portion forward of said piston, and
b. for removing the fluid bypass means whereby the piston is in sealing engagement with the barrel to force fluid from said chamber through said needle connecting portion as an incident of movement of said piston in said chamber toward said inner end in response to an applied force on said first means, said second means comprising means removably extending the length of said piston between said piston and said barrel for deforming said piston to form a plurality of fluid bypass passages between the deformed piston and the barrel which communicate with said outer end of the barrel, said passages defining said fluid bypass means, said second means comprising a plurality of angularly spaced elements providing said fluid bypass means.
4. In a syringe having a tubular barrel defining a chamber opening axially through the outer end of the barrel, and a needle connecting portion at the inner end of the barrel for connecting a needle in fluid flow association with said chamber, the improvement comprising:
a resilient piston arranged to have sealing sliding engagement with the barrel in said chamber;
first means extending from said piston to outwardly of said outer end for manipulating said piston during operational use of the syringe; and
second means carried by said first means and extending from within said chamber to outwardly of said outer end, said first and second means being selectively relatively movable a. for forming fluid bypass means around said piston for venting the chamber portion forward of said piston, and b. for removing the fluid bypass means whereby the piston is in sealing engagement with the barrel to force fluid from said chamber through said needle connecting portion as an incident of movement of said piston in said chamber toward said inner end, said second means comprising a tubular element having an axial bore provided with a portion at the inner end of said tubular element of greater diameter than other portions of said bore for receiving said piston, said tubular element removably extending the length of said piston between the piston and said barrel for deforming the piston to define said fluid bypass means between the deformed piston and the barrel which communicate with said outer end of the barrel. 5. The method of filling a syringe having a barrel with a bore open at the breech end of the barrel for receiving a liquid medicament during the filling of the syringe, and a shaft and piston assembly comprising a resilient piston for sliding sealing engagement with the barrel in the bore, and a shaft connected to the piston and responsive to an applied force thereon for moving the piston toward the inner end of the barrel to discharge the medicament from the bore during operational use of the syringe comprising the steps of:
providing said shaft and piston assembly with a relatively movable elongate member adapted to deform said piston upon movement thereof in one "Ill direction relative to said shaft; moving said elongate member in said one direction relative to said shaft to deform said piston;
inserting said piston and shaft assembly and said elongate member into the bore through the breech end thereof;
moving the shaft and piston assembly and elongate member toward the inner end of the barrel with said piston deformed to provide fluid bypass means within the barrel from a point ahead of said piston to said breech end for venting air from the barrel as said piston is moved toward the liquid medicament; and moving said elongate member in the direction opposite said one direction relative to said shaft to cause said piston to have scaled sliding engagement with the barrel.
6. The method of filling a syringe with liquid medicament of claim 5 wherein substantially the entire piston is deformed away from contact with the barrel during the step of moving the shaft and piston assembly and the elongate member toward the inner end of the barrel.
7. The method of filling a syringe with liquid medicament of claim 5 wherein only a portion of the piston is deformed away from contact with the barrel during the step of moving the shaft and piston assembly and the elongate member toward the inner end of the barrel.
8. The method of filling a syringe with liquid medicament of claim 5 wherein the step of movin said second means in said one direction relative to san first means to deform said piston is performed prior to the step of inserting said shaft and piston assembly into the breech end of the barrel, and said piston is maintained deformed by said elongate member until it is substantially moved to the liquid medicament.