Container cap assembly having an enclosed penetrator

Information

  • Patent Grant
  • 6524295
  • Patent Number
    6,524,295
  • Date Filed
    Wednesday, December 20, 2000
    23 years ago
  • Date Issued
    Tuesday, February 25, 2003
    21 years ago
Abstract
A penetrator for penetrating a stopper sealing an opening in a container. The penetrator includes a stamped piece of sheet material formed to define a shank having a length. A groove extends along the length of the shank. The shank has a pointed distal. The stamped piece of sheet material further includes a bearing plate extending from the shank at a proximal end opposite the distal end of the shank.
Description




CROSS REFERENCE TO RELATED APPLICATION(S)




Not Applicable




STATEMENT REGARDING FEDERALLY SPONSORED RESEARCH OR DEVELOPMENT




Not Applicable




REFERENCE TO A MICROFICHE APPENDIX




Not Applicable




TECHNICAL FIELD




The present invention relates to closures for containers, including vials and the like, containing liquid pharmaceutical medicaments or other products. The present invention is directed to a closure for containing and delivering a pharmaceutical product. More particularly, the present invention is directed to a closure that permits the introduction and withdrawal of fluid from a container using an instrument having a blunt luer fitting or connector, such as a luer lock syringe or other fluid transfer device.




BACKGROUND OF THE INVENTION AND TECHNICAL PROBLEMS POSED BY THE PRIOR ART




Many pharmaceutical products are delivered to pharmacies in sealed containers such as glass or plastic vials, glass or plastic bottles, and flexible bags. Such containers can contain a powdered or lyophilized formulation of a pharmaceutical product that must be reconstituted prior to administration to a patient. In addition, such containers can contain a solution or suspension formulation of a pharmaceutical product that can be withdrawn from the container and administered directly to a patient, for example, by parenteral administration.




Most pharmaceutical vials are sealed by a pierceable stopper which is press-fit into the mouth of the vial to thereby isolate the contents of the vial from the vial's external environment. In order to access the pharmaceutical product within the vial, it is necessary either to pierce the stopper or to remove the stopper from the vial. However, removal of the stopper results in exposure of the pharmaceutical product to the external environment, thereby compromising the sterility and/or stability of the pharmaceutical product within the vial. For this reason, it often is preferable to access the pharmaceutical product by piercing the stopper.




A conventional syringe can be used to add a diluent to the vial and/or to withdraw liquid from the vial. The syringe has a hollow cannula or needle which is pushed through the stopper and into communication with the liquid. The syringe plunger can be depressed to dispense a diluent into the vial or pulled outwardly to draw liquid from the vial into the syringe.




The piercing of vial stoppers typically has been achieved through the use of sharp, small-bored needles. Standard hypodermic syringe needles are particularly useful for this purpose because they allow the pharmaceutical product to be aseptically withdrawn from the vial and parenterally administered directly to a patient using a single device, thereby minimizing risk of contamination of the pharmaceutical product.




While the above-described conventional system has long been used with satisfactory results, it is not without disadvantages. A fundamental disadvantage is the necessity of using a syringe with a sharp needle. This exposes the medical professional to the possibility of being accidently pricked by the syringe needle. In addition to the undesirable injury resulting from such an accidental needle prick, there may be a risk of contamination of the needle by the medical professional. If the medical professional violates safe procedures and continues to use a contaminated syringe to withdraw the liquid medicament from the vial and administer it to a patient, there is a risk of transmitting the contaminant to the patient.




In addition, if the syringe needle is used to inject the liquid medicament into a patient, there is a danger that the medical professional could accidentally be pricked by the needle following the injection of the patient. This could expose the medical professional to contamination from the patient, especially pathogens carried in blood.




In many cases it is necessary to clean the outer surface of the vial stopper prior to piercing in order to reduce the risk of infection to the patient. This requires the medical professional to perform two distinct steps in order to withdraw the pharmaceutical product from the vial.




It would be desirable to provide an improved closure system that would permit withdrawal of liquid medicament from a closed vial without requiring the use of a syringe having an exposed, sharp needle.




It would also be advantageous to provide such an improved system which can provide simple and rapid access to the liquid medicament contained within the vial.




Preferably, such an improved system should accommodate current product designs and manufacturing techniques to as great an extent as possible. Also, it would be desirable if such an improved system could be employed with conventional, luer lock syringes. Further, such an improved system should preferably accommodate the design of components that can be manufactured at very low cost, with mass production techniques, with low product reject rates, and with high reliability.




Additionally, it would be desirable if the improved design could be easily operated to establish a reliable communication between the syringe or other luer lock transfer device and the liquid medicament in the vial in a way that would minimize the possibility of interrupted withdrawal flow or reduced withdrawal flow.




Further, it would be beneficial if such an improved design could provide evidence of tampering.




The present invention provides an improved container stopper penetrator, a novel process for making a penetrator, and an improved container cap assembly with an integral stopper penetrator which can accommodate designs having the above-discussed benefits and features.




SUMMARY OF THE INVENTION




According to one aspect of the present invention, a piercing member or penetrator is provided for being disposed in a cavity of a housing over a stopper that occludes the mouth of a container. The penetrator is adapted for piercing or penetrating the stopper upon movement of the penetrator into the stopper.




In one embodiment, a penetrator is stamped from sheet metal. The sheet metal is formed to define a shank having a length, a groove extending along its length, and a pointed distal end. The sheet metal is also formed to define a bearing plate extending from the shank at an end opposite the pointed distal end. In a preferred embodiment, the sheet metal is further formed to provide at least a first guide wall extending from the shank intermediate the pointed distal end and the bearing plate.




According to a method aspect of the invention, the metal penetrator is fabricated in a number of processing steps. A plurality of progressive die stations are provided, and each die station comprises an associated complementary punch and die. A planar strip of sheet metal is indexed to incrementally advance progressively between the punches and dies. Each die station is operated after each incremental advancement of the sheet metal strip to effect relative movement between the associated punch and die so as to sever and separate regions of the strip. This process defines a bearing plate portion and a pointed shank portion of the penetrator. Preferably, an extending guide wall portion is also formed.




In a preferred form of the method, the die stations are operated to define part of the periphery of at least one of the stamped metal portions at one of the stations and to define another part of the periphery of that portion at another, downstream station. Further, some of the stations also effect deformation of the metal strip by bending the shank portion into a configuration defining a convex surface and a concave surface oriented along a longitudinal axis. Other stations effect deformation of the metal strip by bending the bearing plate portion out of the plane of the strip. Preferably, a guide wall portion is also bent into a configuration extending out of the plane of the strip to define a guide surface that is generally parallel to the longitudinal axis.




According to another aspect of the invention, another embodiment of a penetrator is molded from a plastic material as a unitary structure. The molded penetrator includes a shank molded from plastic material, and the shank has a distal end defining a point. The penetrator also has a hub at the end of the shank opposite the shank distal end. The hub is molded from the plastic material so that it is unitary with the shank, and the hub defines an upper end of the penetrator. The hub and shank together define a transfer passage extending from the upper end to the pointed distal end. The transfer passage opens from the hub at the upper end and opens from the shank at the pointed distal end.




The invention includes a third embodiment of a penetrator for a container stopper. The third embodiment of the penetrator comprises a hollow needle having a base end and a pointed distal end. The penetrator further includes a hub of plastic material molded around the needle base end. In a preferred form of the third embodiment of the penetrator, the hub has an upper, smaller diameter cylindrical portion and a lower, larger diameter cylindrical portion.




According to yet another aspect of the present invention, a cap assembly is provided for a container which has an upper portion defining a mouth occluded by a stopper having a top end. The cap assembly includes a hollow housing. The housing defines a lower end adapted to be mounted on the container, an upper end, and an internal cavity opening at the housing upper and at the housing lower end.




The cap assembly further includes a penetrator that is disposed in the housing cavity. The penetrator has a lower, pointed, distal end and has an upper end adapted to be engaged by the distal end of the transfer device male member when the transfer device is moved into the housing. The penetrator defines a fluid transfer passage extending from the penetrator upper end to the penetrator pointed distal end. The penetrator is moveable between a retracted position completely within the housing cavity and an extended position in which the penetrator projects from the housing cavity at the housing lower end.




The cap assembly also includes a removable cap disposed on, and sealingly engaged with, the exterior of the housing so as to seal the housing cavity at the housing upper end.




Finally, the cap assembly includes a ferrule disposed over a radially outwardly extending flange of the lower end of the housing. The ferrule has a skirt adapted to be received on the container around both the stopper and the upper portion of the container. The skirt is preferably metal so that it can be crimped into engagement with the upper portion of the container to hold the ferrule and housing to the container with the penetrator and cap carried by the housing.




The cap assembly provides a sterile protective covering for the container stopper.




The cap assembly can also include tamper-evident features.




The cap assembly can be manufactured reliably and at low cost.




Importantly, the cap assembly readily connects to a conventional male luer. The penetrator within the cap assembly readily pierces the vial stopper, but the distal, piercing end of the penetrator is never exposed. This eliminates or minimizes the likelihood that a medical professional will be accidently pricked by a sharp, pointed component when handling the cap assembly and withdrawing a medicament from the container.




Numerous other advantages and features of the present invention will become readily apparent from the following detailed description of the invention, from the claims, and from the accompanying drawings.











BRIEF DESCRIPTION OF THE DRAWINGS




In the accompanying drawings that form part of the specification, and in which like numerals are employed to designate like parts throughout the same,





FIG. 1

is a side elevational view of a container cap assembly of the present invention showing it installed on a vial;





FIG. 2

is a cross-sectional view of the cap assembly prior to installation on the vial;





FIG. 3

is an exploded, perspective view of the components of the cap assembly illustrated in

FIG. 2

;





FIG. 4

is a top view of the housing in the cap assembly shown in

FIG. 3

;





FIG. 5

is a cross-sectional view taken generally along the plane


5





5


in

FIG. 3

;





FIG. 6

is a cross-sectional view taken generally along the plane


6





6


in

FIG. 5

;





FIG. 7

is a cross-sectional view taken generally along the plane


7





7


in

FIG. 5

;





FIG. 8

is a front elevational view of the penetrator of the cap assembly shown in

FIG. 4

;





FIG. 9

is a bottom, plan view taken along the plane


9





9


in

FIG. 8

;





FIG. 10

is a side elevational view of the penetrator shown in

FIGS. 8 and 9

;





FIG. 11

is a cross-sectional view of the overcap of the assembly illustrated in

FIG. 4

;





FIG. 12

is a perspective view of a conventional luer lock type syringe;





FIG. 13

is a view similar to

FIG. 2

, but

FIG. 13

shows the syringe of

FIG. 12

attached to the housing of the cap assembly after removal of the overcap and shows the penetrator in the fully extended, lowered, position penetrating the stopper in the mouth of the vial;





FIG. 14

is a perspective view of a second embodiment of a penetrator that employs a needle and that may be used in the cap assembly;





FIG. 15

is a front, perspective view of a third embodiment of a penetrator that is stamped from sheet metal and that may be used in the cap assembly;





FIG. 16

is a cross-sectional perspective view of the third embodiment of the penetrator in a fully retracted position within the housing;





FIG. 17

is a rear elevational view of the third embodiment of the penetrator illustrated in

FIGS. 15 and 16

;





FIG. 18

is a top plan view of the third embodiment of the penetrator;





FIG. 19

is a cross-sectional view taken generally along the plane


19





19


in

FIG. 17

;





FIG. 20

is a cross-sectional view taken generally along the plane


20





20


in

FIG. 18

;





FIG. 21

is a cross-sectional view taken generally along the plane


21





21


in

FIG. 17

;





FIG. 22

is a cross-sectional view taken generally along the plane


22





22


in

FIG. 18

;





FIG. 23

is a simplified, fragmentary, partly diagrammatic, schematic illustration, partly in cross-section, generally showing the manner in which the third embodiment of the penetrator illustrated in

FIGS. 14-21

is formed by the apparatus of the present invention operating according to the method of the present invention:





FIG. 24

is a plan view taken generally along the plane


24





24


in

FIG. 23

;




FIG.


25


. is a fragmentary, perspective, view of a second embodiment of an overcap of the present invention shown as part of a cap assembly on a vial;





FIG. 26

is a view of the second embodiment of the overcap shown in

FIG. 25

after an upper, removable portion of the overcap has been torn away to expose the upper end of an underlying housing; and





FIG. 27

is an elevational plan view of a preferred embodiment of the penetrator depicted in FIGS.


15


-


26


.











DESCRIPTION OF THE PREFERRED EMBODIMENTS




While this invention is susceptible of embodiment in many different forms, this specification and the accompanying drawings disclose only some specific forms as examples of the invention. The invention is not intended to be limited to the embodiments so described, however. The scope of the invention is pointed out in the appended claims.




For ease of description, the components of this invention are described in the positions depicted in the accompanying drawings, and terms such as upper, lower, horizontal, etc., are used with reference to this position. It will be understood, however, that the components of this invention may be manufactured, stored, transported, used, and sold in an orientation other than the position described.




Figures illustrating the components show some mechanical elements that are known and that will be recognized by one skilled in the art. The detailed descriptions of such known elements are not necessary to an understanding of the invention, and accordingly, are herein presented only to the degree necessary to facilitate an understanding of the novel features of the present invention.




The components of this invention are intended to be used with certain other conventional instruments and/or components the details of which, although not fully illustrated or described, will be apparent to those having skill in the art and an understanding of the necessary functions of such components.




One aspect of the invention facilitates rapid and safe access to the contents stored within a sealed container. The invention is especially suitable for use with a container such as a glass or plastic vial containing a pharmaceutical product or medicament. However, it will be appreciated that other applications of the present invention are feasible, including, but not limited, applications in connection with parenteral tube sets. The pharmaceutical product may be in liquid (solution or suspension) form or in a solid form, e.g., powdered or lyophilized. The invention is especially useful with a conventional vial which is normally sealed with a rubber stopper and which is conventionally designed to be pierced by a hollow needle or cannula of a hypodermic syringe so that the contents of the vial can be diluted/reconstituted with the syringe contents and/or so that the contents of the vial can be withdrawn into the syringe for subsequent discharge into another container system or for direct administration to a patient.





FIG. 1

illustrates a container such as a conventional glass or plastic vial


30


having a cylindrical neck


32


terminating in a slightly larger diameter annular flange


34


which defines an opening or mouth


36


of the container.




The mouth of the vial


30


contains an internal, removable, resilient seal, plug or stopper


38


. The stopper


38


is typically made from rubber or other suitable elastomeric material. The stopper


38


includes a central, generally annular, plug portion


40


and an enlarged diameter head portion


42


. The head portion


42


functions as a support flange and is normally disposed on the top end surface of the container neck flange


34


. The stopper annular plug portion defines an internal recess


44


which opens downwardly toward the container contents.




The stopper


38


prevents the discharge, or removal, of the contents from the vial


30


unless and until the stopper is either removed or penetrated. In a preferred embodiment, stopper


38


does not define channels or pores therethrough, i.e., stopper


38


is not “pre-pierced”. However, the cap assembly of the present invention can be used with stoppers that define one or more channels or pores therethrough. One aspect of the present invention provides a special system for penetrating the stopper


38


to gain access to the contents of the vial


30


as explained in detail hereinafter.




The annular plug portion


40


of the conventional stopper


38


preferably has an exterior diameter which is slightly larger than the interior diameter of the mouth


36


of the container neck


32


. Typically, the stopper annular body


40


is received in the container mouth


36


in a radially, inwardly compressed condition and is retained within the container mouth


36


by frictional engagement established by the outward force of the stopper annular body portion


40


on the vial neck


32


owing to the resiliency of the stopper material.




One aspect of the present invention provides a special cap assembly


46


which has a number of functions. The cap assembly


46


covers the top of the stopper


38


as well as an upper portion of the container neck


32


to protect the stopper


38


and upper portion of the container as well as to provide a barrier to contaminant ingress.




The cap assembly


46


also functions as an additional mechanism for holding the stopper


38


and container


30


together in a sealed relationship.




Further, the cap assembly


46


permits rapid connection of the container


30


to a luer-type fluid transfer device, such as a conventional luer lock syringe (described in detail hereinafter).




Additionally, the cap assembly


46


functions to contain a pointed piercing member or penetrator and to accommodate penetration of the stopper


38


with the penetrator in a way that does not expose the medical professional or patient to a pointed or sharp component. Other advantages and features of the cap assembly


46


, as well as the detailed construction, method of fabrication, and method of use, are described in detail hereinafter.




The vial


30


can be a pharmaceutical vial of known construction. However, it will be appreciated that closure assembly


46


can be adapted to seal a wide variety of containers and devices for containing pharmaceutical or non-pharmaceutical products. The depiction herein of a pharmaceutical vial


30


is not intended to be limiting, but instead represents one useful application of the system of the present invention. The container also can be a plastic or glass bottle, a flexible bag of known construction, or a parenteral or enteral tube set. For the purposes of this disclosure, all references to the terms “container” and “vial” are intended to include, inter alia, vials, bottles, flexible containers, parenteral or enteral tube sets, and equivalents thereof.




The vial


30


is filled with product, and the stopper


38


is inserted in the mouth of the vial


30


in a separate conventional or special process, the details of which form no part of the present invention. The cap assembly


46


is initially manufactured as an assembly separate from the vial


30


and stopper


38


. After manufacture of the cap assembly


46


, and prior to its installation over the stopper


38


on the filled container


30


, the cap assembly


46


has a configuration as illustrated in cross section in FIG.


2


.




The separate components of the cap assembly


46


are illustrated in the perspective view in FIG.


3


. The cap assembly


46


includes a hollow housing


50


in which is slidably disposed a penetrator


60


. An overcap or cap


70


is provided for covering and sealing the top portion of the housing


50


. The housing


50


and penetrator


60


are preferably constructed such that they are held together by frictional forces therebetween. Ferrule


80


is provided to retain radially outwardly extending lower end


82


of housing


50


on vial


30


. Ferrule is preferably constructed of a metal material, but may be constructed of other known materials without departing from the scope of the present invention. When the assembly


46


is mounted to the top of the container


30


, the lower end


82


of the housing


50


rests either on vial


30


or on the top surface of stopper


38


, dependent upon the configuration of stopper


38


. A bottom peripheral portion of the metal ferrule


80


is crimped about the lower edge of the flange


34


of the container


30


as shown in FIG.


1


.




As shown in

FIGS. 1 and 6

, the housing lower end


82


may include a downwardly extending element such as annular seal ring


83


for engaging a top surface of the stopper


38


and effecting a leak-tight seal when the two components are held in clamping engagement by the crimped, metal ferrule


80


.




As shown in

FIGS. 3-7

, the housing


50


has an upper end


84


which is open to an internal cavity


86


. The internal cavity


86


extends through the housing


50


and opens at the lower end


82


. The housing cavity


86


defines an upper bore


88


which is open at the housing upper end


84


. The upper bore


88


preferably is frustoconical to define a luer-compatible taper (i.e., a 1.7° side taper or 3.4° included conical angle). In the preferred embodiment of the present invention, upper bore


88


is shorter in length than a conventional luer, thereby ensuring that a luer can be inserted into upper bore


88


to an extent great enough to impart the requisite degree of travel to penetrator


60


, as explained in greater detail below.




The cavity


86


also includes a lower, cylindrical bore


90


that communicates with the upper bore


88


The lower, cylindrical bore


90


opens at the housing lower end


82


. The upper bore


88


has a diameter less than the diameter of the lower, cylindrical bore


90


. This defines an annular shoulder


92


(

FIGS. 6 and 7

) adjacent the upper bore


88


within the lower, cylindrical bore


90


. The bore


90


may have a small draft angle, but is cylindrical in the preferred embodiment of the present invention.




The lower, cylindrical bore


90


includes a plurality of circumferentially spaced, interior channels


96


(

FIG. 5

) defined between ribs


98


. The housing


50


is preferably molded as a unitary structure from a plastic material such as polypropylene, and the vertical inner edges of each rib


98


are preferably provided with a draft angle (e.g., 2°) to assist in separation of the housing


90


from the mold parts. The ribs


98


function to guide the penetrator


60


as it moves downwardly to penetrate the vial stopper


38


as described in detail hereinafter. In the preferred embodiment of the present invention, ribs


98


do not extend inwardly any further than the wall of lower bore


90


.




In order to make the cap assembly of the present invention accessible by means of a locking luer, the upper exterior portion of the housing


50


preferably defines a laterally projecting formation, such as a conventional luer lock dual lead helical thread formation


100


(FIGS.


3


and


6


). The laterally projecting thread formation


100


is designed for threadingly engaging a mating thread system on an annular skirt of a luer lock-type fluid transfer device, such as a luer lock syringe (as described in detail hereinafter).




The first embodiment of the penetrator


60


(

FIGS. 8-11

) which is adapted for being received in the housing


50


is a unitary structure molded from plastic material. The penetrator


60


has a shank


102


with a point defining a pointed distal end


104


. The penetrator


60


has a hub


108


(

FIG. 8

) at the end of the shank


102


opposite the pointed distal end


104


, and the hub


108


defines the upper end of the penetrator


60


.




The penetrator


60


defines a transfer passage


110


which extends from the pointed distal end


104


through the shank


102


and through the hub


108


. As illustrated in

FIG. 2

, the transfer passage


110


comprises a lower, cylindrical bore


112


communicating with an upper, cylindrical bore


114


. The upper, cylindrical bore


114


has a diameter which is larger than the diameter of the lower, cylindrical bore


112


. The hub


108


may be characterized as defining a central, longitudinal axis


115


(FIG.


8


), and the transfer passage upper bore


114


and lower bore


112


are axially aligned on the longitudinal axis


115


.




The hub


108


of the penetrator


60


has a smaller diameter, upper, cylindrical portion


116


(

FIG. 8

) and a larger diameter lower portion


120


. Both the upper portion


116


and lower portion


120


are axially aligned along the longitudinal axis


115


of the penetrator


60


. The larger diameter lower portion


120


includes an annular bead or rib


122


(

FIGS. 2 and 3

) which has a diameter which defines the larger diameter of the lower portion


120


of the hub


108


. The hub larger diameter lower portion


120


also includes a plurality of circumferentially spaced ribs


124


. In the preferred embodiment of the present invention depicted in the accompanying figures, four circumferentially spaced ribs


124


extend axially from the bead


122


parallel to the longitudinal axis


115


of the penetrator


60


. The longitudinal lengths of the ribs


124


all terminate axially at the same distance from the bead


122


so as to define an abutment end


126


at the top end of each rib


124


. Each rib


124


also extends radially outwardly and terminates radially on the diameter of the hub lower portion


120


as established by the outer diameter of the annular bead


122


.




As shown in

FIG. 2

, the ribs


124


of the lower portion of the hub


108


are received within the larger diameter, lower cylindrical bore


90


of the housing


50


. The abutment end


126


of each rib


124


can engage the internal shoulder


92


of the housing


50


to establish an uppermost elevational position of the penetrator


60


within the housing


50


. In a preferred embodiment, the outer diameter of ring


122


is slightly larger than the nominal diameter of the housing lower bore


90


. Specifically, in one presently contemplated embodiment, the exterior diameter of the ring


122


is up to 0.004 inches greater than the nominal diameter of the housing receiving bore


90


. This establishes a slight interference fit so that the penetrator


60


can be initially maintained generally in the highest elevation shown in

FIG. 2

within the housing


50


. In this position, the pointed distal end


104


is retracted somewhat inwardly (upwardly) from the opening of the cavity


86


at the bottom end of the housing


50


.




In some manufacturing sequences, the cap assembly


46


may be stored separately until it is mounted on the vial


30


. The above-described retention features prevent the penetrator


60


from slipping out during such storage as well as during the process of mounting the cap assembly


46


on the vial


30


.




During the initial assembly of the components, the penetrator


60


must be forced upwardly into the housing cavity


86


with sufficient force to slightly compress the bead


122


radially inwardly and/or to temporarily expand the housing


50


radially outwardly. Then the penetrator


60


can be moved further inwardly (upwardly) to the elevated position wherein the penetrator bead


122


is above the upper ends of the housing ribs


98


. Preferably, the penetrator


60


is fully inserted to the elevated position illustrated in

FIG. 2

wherein the abutment ends


126


of the penetrator ribs


124


engage the housing shoulder


92


.




When the penetrator


60


is subsequently moved downwardly to pierce the container stopper


38


as described in detail hereinafter, the hub lower portion


120


, including the exterior surfaces of the ribs


124


, function as a guide wall for guiding the downward movement of the penetrator


60


through the housing cavity


86


, including along the housing bore


90


and along the inwardly projecting guide ribs


98


.




The overcap


70


is removable from the assembly


46


. The overcap


70


has an elongated, tubular configuration with a closed top end and an open bottom end. The bottom end includes a plurality of flexible tabs


130


(

FIG. 3

) which extend radially over a portion of the housing lower end


82


under the ferrule


80


when the components are assembled as shown in FIG.


2


. The overcap


70


also preferably includes a plurality of circumferentially spaced retention tabs


132


. Each retention tab


132


has a downwardly and outwardly angled camming surface


134


and has a downwardly facing retention shoulder


136


.




The metal ferrule


80


is disposed over the radially outwardly extending lower end


82


of the housing


50


. The ferrule


80


has a skirt


140


adapted to be received on the container


30


around both the stopper


38


and an upper portion of the container


30


. A lower portion of the skirt


140


can be crimped into engagement with the lower portion of the container flange


34


, as depicted in FIG.


1


.




The ferrule


80


also includes a radially inwardly extending, annular deck


142


defining a receiving aperture


144


(FIGS.


2


and


3


). The receiving aperture


144


receives the subassembly of the penetrator


60


, housing


50


, and overcap


70


. During assembly of the ferrule over the overcap


70


, the inner edge of the annular deck


142


(at the aperture


144


) engages the camming surfaces


134


on the retention lugs


132


. This temporarily deflects the annular deck


142


outwardly slightly and/or deflects the overcap


70


inwardly until the deck


142


moves downwardly past the retention shoulders


136


of the lugs


132


. It will be appreciated that lugs


132


impair the movement of ferrule


80


relative to overcap


70


during placement of the cap assembly on a container. That is, after the ferrule


80


is assembled with the other components as shown in

FIG. 2

, the ferrule


80


is able to move upwardly slightly until it engages the retention shoulders


136


on the retention lugs


132


. However, the metal ferrule


80


cannot move upwardly beyond the retention lugs


132


.




The cap assembly


46


can be assembled either manually or, preferably, by automatic assembly machinery (the details of which form no part of the present invention). The completed cap assembly


46


can then be immediately mounted on a container


30


or can be stored for later mounting on a container


30


. The components of the assembly


46


remain in the assembled condition with the penetrator


60


fully retracted within the housing


50


.




After the assembly


46


is mounted and crimped to a container


30


as shown in

FIG. 1

, the cap assembly


46


may be readily connected to a luer-type fluid transfer device, such as a luer lock syringe


150


as shown in FIG.


12


. Use of the present invention will now be described in connection with a luer lock syringe


150


. However, it will be appreciated that this description is for exemplary purposes only and that use of the present invention is not limited to a luer lock syringe.




The luer lock syringe


150


includes a barrel


152


and a telescopically received plunger


154


. The distal end of the plunger


154


includes a conventional piston or grommet


156


sealingly engaged with the interior cylindrical surface of the barrel


152


.




The distal end of the syringe


150


has a conventional annular skirt


158


which is internally threaded with a conventional luer lock dual lead helical thread system


160


. A conventional male cannula


162


projects from the distal end of the barrel


152


within the annular skirt


158


. The cannula


162


has a conventional exterior taper which reduces the exterior diameter of the cannula


162


to a minimum at the bottom, distal end of the cannula


162


. The cannula


162


defines a bore


164


which is in communication with the interior volume of the syringe barrel


152


below the syringe plunger piston


156


.




As shown in

FIG. 13

, the syringe


150


can be coupled with the container


30


. To this end, the overcap


70


(

FIG. 1

) must first be removed. This is effected by manually grasping the upper end of the overcap


70


and pulling it upwardly away from the container


30


. The tabs


130


around the bottom end of the overcap


70


are temporarily deformed downwardly and pass through the ferrule aperture


144


as the cap


70


is pulled upwardly.




Once the overcap


70


is free of the metal ferrule


80


, the overcap


70


cannot readily be placed back into position because the cap tabs


130


cannot easily be repositioned under the ferrule annular deck


142


. Thus, once the overcap


70


is removed, it cannot be readily placed back on the assembly in the properly mounted condition. Rather, the overcap


70


, once removed, will most likely be placed only loosely over the top of the housing


50


, and the cap tabs


130


at the bottom end of the overcap


70


will remain outside of, and on top of, the ferrule annular deck


142


. This will provide a visual indication that the overcap


70


has been removed from its original, properly mounted position. This provides the assembly


46


with a tamper-evident feature.




After the overcap


70


is removed, the syringe


150


is threadingly engaged with the luer lock thread system


100


on the housing


50


. The syringe thread system


160


engages the housing thread system


100


. As relative rotation is effected between the syringe


150


and the container


30


, the male member


162


of the syringe


152


moves downwardly against the upper end of the penetrator


60


. This pushes the penetrator


60


downwardly along the internal cavity in the housing


50


.




As the penetrator


60


moves downwardly within the housing


50


, the penetrator pointed distal end


104


pierces the stopper


38


and establishes communication between the interior of the container


30


and the penetrator fluid transfer passage


110


. As shown in

FIG. 13

, the upper end of the penetrator fluid transfer passage


110


is in communication with, and is generally axially aligned with, the bore


164


in the syringe cannula


162


. The syringe plunger


154


(

FIG. 12

) can then be moved outwardly within the syringe barrel


152


to reduce the pressure within the syringe and to draw the liquid from the container into the syringe. Alternatively, the syringe


152


can be initially employed to dispense a diluent or another medicament into the container. Subsequently, the mixed contents in the container


30


can be withdrawn with the syringe


150


or with a similar, but different syringe


150


.




It will be appreciated that the design of the housing bore


90


and guide ribs


98


, and the design of the penetrator hub guide ribs


124


, facilitate the downward movement of the penetrator


60


and prevent the penetrator from cocking.




The cap assembly


46


can advantageously be mounted to existing, conventional packages comprising a conventional vial


30


and conventional rubber stopper


38


.




The cap


46


is readily connected to a conventional standard luer lock syringe designed according to the conventional ISO Standard 594.




The medical professional can use the cap


46


, along with a standard luer lock syringe, to readily gain access to the contents of a vial


30


without the need for a sharp needle. Even the molded plastic penetrator


60


is entirely contained within the cap assembly


46


, and the pointed distal end


104


is never exposed where it could be contacted by medical personnel.




The cap assembly


46


has the advantage of not requiring the medical professional to swab the top of the stopper


38


or parts of the cap assembly


46


with alcohol or similar antimicrobial agent. Overcap


70


preferably provides a sterile barrier between the interior of cap


46


and the external environment of overcap


70


. The interior of cap


46


can be sterilized using known processes that form no part of the present invention.




The cap assembly


46


accommodates efficient manufacturing processes because the components can be assembled into a single unit or assembly by snap-fitting the components together and/or interference fitting the components together. The completed assembly


46


can be sterilized prior to, during, or after the final mounting of assembly


46


on the vial


30


.




The cap assembly


46


can be readily designed for industry standard size vial closures, such as 13 mm, 20 mm, and 28 mm. The assembly


46


is suitable for use with glass vials or plastic vials as well as flexible bags.




It will also be appreciated that the luer-type connection configuration of the cap assembly housing


50


may be employed with fluid transfer devices other than a luer lock syringe as discussed herein. For example, the upper end of the housing


50


of the cap assembly


46


may be connected to a suitable luer-type instrument that is part of another device or that is attached to a length of flexible tubing.





FIG. 14

illustrates a second embodiment of a penetrator


260


which may be used in the cap assembly


46


in place of the first embodiment of the penetrator


60


described above. The penetrator


260


includes a hollow needle


262


having a base end


263


and a point


264


opposite the base end


263


so as to define a pointed distal end. The penetrator


260


also includes a hub


268


molded from a plastic material around an upper portion of the hollow needle


262


so as to encapsulate the base


263


.




The hub


268


has an upper, smaller diameter cylindrical portion


270


and a lower, larger diameter cylindrical portion


274


. The upper cylindrical portion defines a bore


276


communicating with the upper end of a bore


278


defined by the hollow needle


262


.




The larger diameter cylindrical portion


272


of the hub


268


defines an annular shoulder


280


around the smaller diameter cylindrical portion


270


.




The penetrator


260


may be disposed within a cap assembly housing in substantially the same manner as the first embodiment of the penetrator


60


is disposed in the housing


50


. To this end, and with reference to

FIG. 2

, the second embodiment of the penetrator


260


is adapted to be disposed within the housing


50


so that the needle


260


extends downwardly in the same manner as does the shank


102


of the of the first embodiment penetrator


60


. The second embodiment penetrator hub


268


is adapted to be disposed within the housing upper bore


88


and within the housing lower bore


90


in substantially the same way as the hub of the first penetrator


60


as shown in FIG.


2


. In particular, the smaller cylindrical portion


270


of the second embodiment penetrator


260


is adapted to be disposed within the housing upper bore


88


, and the larger, lower cylindrical portion


274


of the hub of the second embodiment penetrator


260


is designed to be disposed within the lower bore


90


of the housing


50


. The second penetrator annular shoulder


280


is designed to engage the downwardly facing shoulder


92


of the housing


50


, and this establishes the uppermost position of the penetrator


260


.




The overcap


70


(

FIG. 3

) and metal ferrule


80


(

FIG. 3

) are assembled over the housing


50


with the penetrator


260


contained therein in the same manner as discussed above with respect to the first embodiment of the cap assembly


46


containing the penetrator


60


illustrated in

FIGS. 1-3

. The cap assembly


46


is then mounted on, and crimped to, the container


30


as previously described.




In use, after the overcap


70


(

FIG. 1

) is removed, the syringe


150


is attached to the housing


50


. The second embodiment of the penetrator


260


is adapted to be engaged by the cannula


162


(

FIG. 12

) of the syringe


150


when the syringe is threadingly engaged with the housing


50


(as shown in FIG.


13


). The second embodiment of the penetrator


260


is designed to be forced downwardly when the syringe


150


moves downwardly as the syringe is threadingly coupled to the cap assembly housing


50


. The second embodiment of the penetrator


260


is designed to pierce the stopper


38


so as to establish communication between the syringe


150


and the interior of the container


30


.




Another form of penetrator is illustrated in

FIGS. 15-22

and FIG.


27


and is designated therein generally by the reference number


360


.

FIG. 27

depicts the preferred embodiment of this form of penetrator


360


.

FIGS. 15-22

reflect an alternative embodiment of penetrator


360


. The embodiments of the penetrator


360


depicted in

FIGS. 15-22

and

FIG. 27

(hereinafter collectively referred to as “the third embodiment”) are designed to be employed in the cap assembly


46


(

FIG. 2

) in place of the first embodiment of the penetrator


60


described above.

FIG. 16

shows the third embodiment of the penetrator


360


disposed within the housing


50


of the cap assembly


46


.




The third embodiment of the penetrator


360


is stamped from a piece of sheet metal, preferably stainless steel, and formed to define a shank


362


having a groove


363


extending along the length of the shank (FIG.


15


), and having a pointed distal end


364


. A bearing plate


366


extends from the shank


362


at an end opposite the distal end


364


. Preferably, a pair of guide walls


368


extend from the shank


362


intermediate the distal end


364


and the bearing plate


366


.




The shank


362


is defined by two legs


371


and


372


oriented in a generally V-shaped configuration to define an included angle of about 60° in the preferred embodiment. In the preferred embodiment, the shank pointed distal end


364


is defined by a substantially 20° included angle on each leg as indicated by the angle S in FIG.


22


. The configuration of shank


362


and legs


371


,


372


preferably is contingent upon the characteristics, e.g., durometer hardness value, of the stopper with which the cap assembly of the present invention is used. That is, by altering the configuration of shank


362


and legs


371


,


372


, it is possible to provide for a sealing of the stopper about penetrator


360


upon expiration of a predetermined period of time. Alternatively, by altering the configuration of shank


362


and legs


371


,


372


, it is possible to prevent the sealing of the stopper about penetrator


360


during a predetermined period of time.




As best illustrated in

FIG. 19

, the shank


362


includes a first extension member


381


extending from the shank first leg


371


and includes a second extension member


382


extending from the shank second leg


372


. The extension members


381


and


382


preferably are substantially flat, substantially parallel, and extend generally laterally for each supporting one of the guide walls


368


. Each guide wall


368


is curved and substantially defines an arc of a circle.




As can be seen in

FIGS. 15

,


20


, and


21


, a support post


386


, which has a generally rectangular cross section (

FIG. 21

) extends upwardly, and at an oblique angle, from the extension member


381


. In the preferred embodiment, support post


386


is unitary with a portion of the peripheral edge of the bearing plate


366


.




In the preferred embodiment depicted in

FIG. 27

, bearing plate


366


′ does not include an aperture and is contoured to define a trough


367


along its upper surface. When bearing plate


366


is engaged by an access device such as a luer lock syringe, fluid will be able to flow around bearing plate


366


′, through trough


367


, and into the luer lock syringe. This embodiment offers advantages in that it creates an indirect flow path for fluid being withdrawn from a container with which the cap assembly of the present invention is used. In this way, the preferred embodiment substantially prevents “spraying” of fluid from the container. This is preferable due to both safety and cost considerations.




In the alternative embodiment depicted in

FIGS. 15 and 20

, the bearing plate


366


has a generally annular configuration. The bearing plate


366


has an outer peripheral margin


390


bent toward the shank distal end


364


. The bearing plate


366


also has an inner peripheral margin


392


bent toward the shank distal end


364


. In this alternative embodiment, fluid from the container can flow both through and around bearing plate


366


.




Another support post


396


extends upwardly from the second extension member


382


. The post


396


has an upper end portion


398


bent over at an angle below the bearing plate


366


to define a support for the bearing plate


366


.




The shank groove


363


defines a concave surface along one side of the shank. The other side of the shank defines a convex surface. The shank convex surface is more specifically defined by the outer surfaces of the legs


371


and


372


, and the shank concave surface is defined by the inner surfaces of the shank legs


371


and


372


. The shank legs


371


and


372


, and hence the convex and concave surfaces defined by the legs, may be characterized as being oriented along a longitudinal axis. The penetrator bearing plate


366


,


366


′ is oriented so that it is generally perpendicular to the longitudinal axis.




The stamped metal penetrator


360


is disposed in the cap assembly housing


50


so that the arcuate guide walls


368


are received within the housing lower cylindrical bore


90


(FIG.


16


). The upper edge of each guide wall


368


is adapted to engage the downwardly facing annular shoulder


92


of the housing


50


. This limits the upward movement of the penetrator


360


and positions the penetrator bearing plate


366


,


366


′ within the housing bore


88


.




The shank


362


of the penetrator


360


extends downwardly in the bore


90


past the guide ribs


98


. The guide ribs


98


define additional flow paths past portions of the penetrator


360


when the penetrator is moved downwardly to pierce the vial stopper as explained hereinafter.




Preferably, the guide ribs


98


project slightly beyond the cylindrical surface of the lower bore


90


. This provides a frictional retention means for insuring that the penetrator


360


is initially maintained in a fully retracted position within the housing


50


during assembly of the components and prior to mounting the assembly on the container


30


over the stopper


38


. Additionally, there may be a friction fit between the guide walls


368


and the bore


90


.




When the penetrator


360


is inserted into the housing


50


, the guide walls


368


are temporarily deflected radially inwardly as the penetrator


360


is pushed up into the housing from the bottom. The housing


50


may also temporarily expand radially outwardly until the lower edges of the penetrator guide walls


368


become located above the tops of the housing ribs


98


. The upper edges of the penetrator guide walls


368


are received within the bore


90


in abutting relationship with the downwardly facing annular shoulder


92


of the housing


50


.




The overcap


70


(

FIG. 3

) and metal ferrule


80


(

FIG. 3

) are assembled over the housing


50


(with the penetrator


360


contained therein) in the same manner as discussed above with respect to the first embodiment of the cap assembly


46


illustrated in

FIGS. 1-3

. The cap assembly


46


is then mounted on, and crimped to, the container


30


as previously described.




In use, after the overcap


70


(

FIG. 1

) is removed, the syringe


150


is attached to the housing


50


as previously described with reference to FIG.


13


. As the syringe


150


is screwed onto the housing


50


, the distal end of the syringe cannula


162


engages the bearing plate


366


,


366


′ of the penetrator


360


and forces the penetrator


360


to pierce the rubber stopper


38


. The rubber stopper


38


stretches around the penetrator legs


371


and


372


. The rubber stopper does not conform to the concave surface defined by the groove


363


(

FIG. 15

) between the two V-shaped legs


371


and


372


of the penetrator shank


362


. Accordingly, there is a flow path which is established along the groove


363


of the penetrator shank


362


.




When the syringe plunger


154


is withdrawn, the liquid within the vial


30


flows along groove


363


of the penetrator and through and around the bearing plate


366


,


366


′ as above-described. The aperture


393


is generally aligned with, and is in communication with, the bore


164


defined in the cannula


162


of the syringe


150


. Thus, the liquid from the vial


30


is drawn into the syringe


150


.




Because the stamped metal penetrator


360


does not have a closed, cylindrical configuration, there is a reduced tendency of penetrator


360


to core out or plug out a piece of rubber from the stopper when compared to a sharp needle on a hypodermic syringe. However, as above-discussed, the durometer hardness of the stopper and the configuration of the penetrator


360


will determine whether the stopper


360


is cored and whether the flow path created by insertion of penetrator


360


will remain open during use.




The design of the penetrator


360


accommodates economical manufacture by means of a progressive die containing multiple, in-line stations. According to one aspect of the present invention, a method is provided for making the penetrator utilizing a plurality of progressive die stations, each of which comprises an associated complementary punch and die as illustrated in

FIGS. 23 and 24

.

FIGS. 23 and 24

are provided for illustrative purposes only. One of ordinary skill in the pertinent art will recognize that variations of the process depicted in

FIGS. 23 and 24

are possible without departing from the spirit and scope of the present invention. For example, it will be appreciated that the number of stations can be varied.





FIG. 23

shows a planar strip of sheet metal


402


being indexed to incrementally advance progressively through six die stations in the direction of arrow


404


. The strip


402


is preferably type


304


or type


316


stainless steel in the form of strip stock from a roll. The first, and most upstream, die station has a punch


1


A on one side of the strip


402


and has a complementary die


1


B on the other side of the strip


402


. The associated punches and dies of the second through sixth stations are analogously designated with numbers


2


-


6


, respectively.




The associated punch and die stations are progressive, and each succeeding station functions to stamp out additional portions of the strip


402


and/or deform portions of the strip to a progressively greater extent. This is effected by operating the stations (after each incremental advancement of the sheet metal strip


402


) to effect relative movement between the associated punch and die of each station against the strip


402


. In a preferred embodiment, the punch is moved while the die and the strip


402


are stationary. In an alternative embodiment, the punches are moved in the direction of the arrow


406


(

FIG. 23

) against one side of the strip


402


, and the dies are moved in the direction of the arrow


410


against the other side of the strip


402


.




The mechanism for indexing the strip


402


may employ any suitable conventional or special indexing system, the details of which form no part of the present invention.




Similarly, the die stations may be provided in any suitable conventional or special punch press apparatus, the details of which form no part of the present invention. The specific configuration of the complementary die and punch in each station conforms to the particular severed and deformed portions of the strip


402


illustrated in each of the stations, respectively, in

FIGS. 23 and 24

.




In the preferred embodiment of the method for forming penetrator


360


of the present invention, strip


402


is introduced into two stations which consecutively punch out the perimeter of penetrator


360


. At a third station, the geometry of bearing plate


366


is formed. Upper end portion


398


is then bent upwardly, as is bearing plate


366


. Next, guide walls


368


and groove


363


are initially formed. Guide walls


368


are then refined in two separate steps. Guide walls


368


also are subjected to a “hemming” step in which their edges are curved to form corner radii. Next, the guide walls


368


are brought into their operative position. The groove is then brought into its final position in three steps. A final forming and a final cutting step are then provided.




In the alternative embodiment of the method of the present invention depicted in the accompanying figures, a portion of the strip


402


is severed in a closed path configuration so as to create a waste piece of the strip that defines a void


420


in the strip after removal of the waste piece. At the second station, the size of the void is increased by stamping out more of the strip material, and the bearing plate portion or preform


366


′ is defined, but the bearing plate portion


366


′ still remains generally in the plane of the strip


402


. A support post portion


396


′ and support post end portion


398


′ are also stamped and defined at the second station.




In the third station, a portion defining the extension member preform


382


′ and guide wall preform


368


′ are defined, but they do not yet have the final orientation or configuration of the extension member


382


and guide wall


386


shown in

FIGS. 19 and 22

. Additionally, in the third station, a lower void


422


is punched out.




The planar bearing plate portion


366


′ created in the second station is bent 90° in the fourth station so as to form the bearing plate


366


. Similarly, the support post distal end portion


398


′ formed in station two is bent about 90° out of the plane of the strip


402


in station four.




In station four, the void


422


from station three is enlarged to define a preform


364


′ for the pointed distal end


364


(shown fully formed in FIG.


15


).




Further, in station four, the preform of the other extension member portion


381


′ is formed along with the connected preform of the other guide wall portion


368


′.




In station five, one side of the penetrator shank is defined by punching further material out of the strip


402


. In addition, in station five the previously formed guide wall preforms


368


′ are further deformed into arcuate guide wall preforms


368


″, and the final orientations of the bearing plate


366


and the support post


396


are established. Also, the shank leg


372


is bent to its final angular orientation of about 60° out of the plane of the strip


402


.




At the sixth station, the remaining connecting portion of the strip


402


is severed from the penetrator


360


, and the shank leg


371


is fully defined and bent upwardly at an angle of about 60° relative to the plane of the strip


402


. At the same time, the partially formed guide wall portions


368


″ (as previously partially formed in station five) are now fully formed into the guide walls


368


in station six.




The final, formed penetrator


360


can then be routed to an appropriate apparatus (not illustrated) for assembling the penetrator


360


with the other components to form the cap assembly


46


(FIG.


1


). Any suitable conventional or special apparatus may be employed to assemble the components. The details of such an apparatus and the method of its operation form no part of the present invention.




Another embodiment of a cap assembly is illustrated in

FIGS. 25 and 26

and is designated therein generally by the reference number


546


. The cap assembly


546


has a metal ferrule


580


which, in the preferred embodiment, is substantially identical with the ferrule


80


described above with reference to the first embodiment illustrated in

FIGS. 1-3

. The ferrule


580


is disposed around the base of a cap or overcap


570


(FIG.


25


). The overcap


570


is disposed over a housing and penetrator contained therein. The housing and penetrator are not visible in

FIG. 25

, but a portion of the housing


550


is visible in

FIG. 26

wherein a portion of the overcap


570


has been removed to expose the upper portion of the housing


550


. The housing


550


is preferably identical with the housing


50


described above with reference to

FIGS. 1-5

. The penetrator is not visible within the housing


550


, but the penetrator is preferably one of the three embodiments of the penetrator


60


,


260


, or


360


described above.




The second embodiment of the overcap


570


includes an upper part


571


and a lower part


573


below the upper part


571


. The lower part


573


has a bottom end extending into the metal ferrule


580


, and the bottom end of the lower part


573


preferably has a radially extending flange (not visible) which extends under the annular deck of the metal ferrule


580


. Such a flange prevents removal of the overcap


570


from the assembly


546


after the assembly has been mounted to a container and after the metal ferrule


580


has been crimped around the bottom of the flange of the container or vial. Although the bottom end of the overcap


570


may have circumferentially spaced, radially extending tabs, such as the tabs


130


on the first embodiment of the overcap


70


as shown in

FIG. 3

, such a tab structure is not necessary in the alternate embodiment of the overcap


570


. Indeed, the bottom end of the alternate embodiment of the cap


570


may be a simple, annular flange that does not include tabs such as the tabs


130


illustrated in

FIG. 3

for the first embodiment of the overcap


70


.




Preferably, the lower part


573


of the alternate embodiment of the overcap


570


includes a radially outwardly extending retention bead


575


. This facilitates the assembly of the components. In particular, the metal ferrule


580


can be forced over the bead


575


. The metal ferrule


580


temporarily expands outwardly a slight amount or the bead


579


deflects inwardly a small amount as the ferrule moves past the bead


575


. Then, during further processing of the cap assembly


546


, the metal ferrule


580


is retained between the bead


575


and the bottom flange (not visible) on the overcap


570


.




The overcap


570


includes a circumferential tear ring


577


connecting the upper part


571


to the lower part


573


. Preferably, the overcap


570


is molded as a unitary structure from plastic material, such as polyethylene or the like. The top edge of the tear ring


577


is connected to the overcap upper part


571


with a reduced thickness of material which defines an annular groove


579


. Similarly, the bottom edge of the tear ring


577


is connected to the top of the overcap lower part


573


with a reduced thickness of material defining an annular groove


581


. The grooves


579


and


581


function as circumferential lines of weakness defining frangible connections.




Preferably, a pull tab


583


extends from the tear ring


577


. The pull tab


583


is molded as part of the unitary structure of the overcap


570


. Preferably, the pull tab


583


includes a first, vertically extending post


585


which has a bottom end directly merging with the tear ring


577


. The upper end of the post


585


merges with a stabilizing bar


587


which is connected to the top of the overcap upper part


571


with a small, generally V-shaped, frangible connecting member


591


.




The connecting member


591


is molded as an extension between the stabilizing bar


587


and the top of the overcap upper part


571


. The member


591


is unitary with both the stabilizing bar


587


and the overcap upper part


571


. The lower, pointed end of the connecting member


591


is relatively small, and is therefore easily broken away from the top of the overcap upper part


571


.




The stabilizing bar


587


may be grasped between the thumb and index finger and lifted upwardly to rupture the connection between the connecting member


591


and the top of the overcap upper part


571


. The pull tab


583


may then be pulled radially outwardly to effect separation of the tear ring


577


from the overcap upper part


571


and lower part


573


. If desired, the stabilizing bar


587


may be provided in the form of an annular pull ring.




After the tear ring


577


is torn away, the overcap upper part


571


falls away, or can be lifted away, to expose the upper portion of the housing


550


. The upper portion of the housing


550


preferably includes a conventional luer lock dual thread formation


1


,


100


for engaging a mating luer lock thread on a syringe or other suitable fluid transfer device.




It will be readily apparent from the foregoing detailed description of the invention and from the illustrations thereof that numerous variations and modifications may be effected without departing from the true spirit and scope of the novel concepts or principles of this invention.



Claims
  • 1. A closure assembly for establishing fluid communication between a fluid transfer device and a container, the container having an open end, a flange surrounding the open end, a neck portion adjacent the flange and a pierceable stopper received in and sealing the open end, the stopper having a head portion received over the container flange, the closure assembly comprising:a hollow housing having an open lower end portion adapted to be mounted on the stopper head portion in alignment with the container open end and an open upper end portion adapted to receive a fluid transfer device in sealed communication; a penetrator received in the housing, said penetrator having a pointed, distal end opposite the stopper head portion adapted to pierce the stopper and an opposed proximate end; a cap surrounding the housing, the cap including an open end having a radially outwardly extending portion extending therefrom and a closed end enclosing the upper end portion of the housing and the proximate end of the penetrator; and a ferrule surrounding the radially outwardly extending portion of the cap and the container flange, the ferrule having a radial portion disposed over said radially outwardly extending portion of said cap and a lower radial portion received in the neck portion of the container beneath the container flange securing the closure assembly to the container.
  • 2. The closure assembly in accordance with claim 1, wherein the penetrator includes a groove providing communication between the container open end and the housing when the penetrator pierces the stopper.
  • 3. The closure assembly in accordance with claim 1, wherein the housing lower end includes a downwardly extending seal ring to engage the stopper.
  • 4. The closure assembly in accordance with claim 1, wherein the penetrator further comprises a shank having a groove providing communication between the container open end and the housing when the penetrator pierces the stopper.
  • 5. The closure assembly in accordance with claim 1, wherein the cap further comprises a circumferential line of weakness for removing the closed end of the cap to expose the upper portion of the housing.
  • 6. The closure assembly in accordance with claim 1, wherein the ferrule is formed of a relatively thin malleable metal and is crimped into the container neck beneath the container flange securing the closure assembly to the container.
  • 7. The closure assembly in accordance with claim 1, wherein the open upper end of the housing further comprises a Luer connector to receive a Luer connector of a fluid transfer device.
  • 8. The closure assembly in accordance with claim 1, wherein the penetrator is reciprocally supported by an internal cavity of the housing.
  • 9. A closure assembly for establishing fluid communication between a fluid transfer device and a container, the container having an open end, a flange surrounding the open end, a reduced diameter neck adjacent the flange, and a pierceable stopper received in and sealing said container open end, the stopper having a head portion received over the container flange, the closure assembly comprising:a hollow housing having an open lower end portion adapted to be mounted to the head portion of the stopper in generally coaxial alignment with the container open end and an open upper end portion adapted to receive a fluid transfer device in sealed communication; a penetrator received within the housing reciprocally supported by an internal surface of the housing, the penetrator having a pointed, distal end deforming the head portion of the stopper and an external groove providing communication between the container and the housing when the penetrator penetrates the stopper; a cap surrounding the housing, the cap having a removable cover portion enclosing the open upper end of the housing and an upper end of the penetrator; and a ferrule surrounding a radially outwardly extending portion of the cap and the container flange, the ferrule having a radial portion received over the radially outwardly extending portion of the cap and a lower radial portion received in the container neck portion beneath the container flange securing the closure assembly to the container.
  • 10. The closure assembly in accordance with claim 9, wherein the housing lower end includes a downwardly extending seal ring to engage the stopper.
  • 11. The closure assembly in accordance with claim 9, wherein the cap further includes a circumferential line of weakness for removing the cover portion of the cap to expose the upper end of the housing.
  • 12. The closure assembly in accordance with claim 9, wherein the open upper end of the housing further comprises a Luer connector to receive a mating Luer connector of a fluid transfer device.
  • 13. The closure assembly in accordance with claim 9, wherein the ferrule is formed of a relatively thin malleable metal and is crimped into the container neck beneath the container flange securing the closure assembly to the container.
  • 14. A method of transferring a medicament between a sealed vial and a second container, the vial having an open end, a flange surrounding the open end, a neck adjacent the flange, and a pierceable stopper received in and sealing the vial open end, the stopper having a head portion received over the vial flange, said second container including a connector portion, said method comprising:mounting a closure assembly on the vial, the closure assembly including a housing having an open lower end adapted to be sealingly mounted on the stopper head portion in alignment with the vial open end and an open upper end having a connector adapted to be connected to said connector portion of said second container, a penetrator received in said housing, said penetrator having a pointed distal end, an opposed proximate end, and a groove, and a ferrule, said method including mounting said closure assembly on said vial by securing the ferrule on the neck of the vial beneath the flange with said housing sealingly engaging the stopper head portion and said penetrator coaxially aligned with the vial open end and the pointed end adjacent the stopper; attaching the connector portion of the second container to the connector on the housing, driving the penetrator pointed end through the stopper head portion, the groove in the penetrator establishing fluid communication between the vial and the second container through the housing, thereby permitting transfer of fluid from the second container to the vial or from the vial to the second container.
  • 15. The method of transferring a medicament between a sealed vial and a second container in accordance with claim 14 wherein the penetrator is reciprocally supported by an internal cavity of the housing.
  • 16. The method of transferring a medicament between a sealed vial and a second container in accordance with claim 14, wherein the closure assembly includes a cap comprising an upper part having a closed end, a lower part having an outwardly extending radial portion at an open end, said method including mounting the cap with the radial portion adjacent the open lower end portion of the housing, the cap surrounding the housing and the closed end of the cap enclosing the open upper end of the housing and the proximate end of the penetrator, the cap upper part attached to the cap lower part by a circumferential line of weakness, said method including mounting the closure assembly on the vial with the cap enclosing the housing until use, then removing the upper part of the cap by breaking the line of weakness, then attaching the second container to the housing.
  • 17. A method of securing a closure assembly on a vial and stopper assembly, the vial having an open end, a flange surrounding the open end and a reduced diameter neck portion adjacent the open end, said stopper formed of an elastomeric material and received in the vial open end, the stopper including an integral generally planar head portion overlying the vial flange, said method comprising:assembling the closure assembly on the stopper head portion, the closure assembly including a radially outwardly extending surface overlying the stopper head portion having a sealing ring projecting from the radially outwardly extending surface; securing the closure assembly on the vial stopper assembly with a ferrule formed of a malleable metal, the ferrule having an inside diameter slightly greater than an outside diameter of the vial flange and a radially inwardly extending annular portion, the method including disposing the ferrule over the closure assembly and the vial flange with the ferrule radially inwardly extending annular portion receiving the radially outwardly extending surface of the closure assembly, compressing said sealing ring projecting from the radially extending surface into the stopper head portion and crimping a lower portion of the ferrule into the vial neck beneath the vial flange.
Parent Case Info

This is a divisional of U.S. patent application Ser. No. 09/282,959, filed Apr. 1, 1999, which is a divisional of Ser. No. 08/808,330 now U.S. Pat. No. 5,891,129, filed Feb. 28, 1997.

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