AU2001281257A1

AU2001281257A1 - Disposable injection device

Info

Publication number: AU2001281257A1
Application number: AU2001281257A
Authority: AU
Inventors: Bruce Joseph Roser
Original assignee: Cambridge Biostability Ltd; IDEA Inc
Current assignee: Cambridge Biostability Ltd
Priority date: 2000-10-13
Filing date: 2001-08-14
Publication date: 2002-04-29
Also published as: MXPA03003256A; WO2002032484A1; KR20030040523A; EP1349597A1; JP2004511308A; ZA200302611B; PL361236A1; RU2003113524A; US6602222B1; NO20031565L; WO2002032484A9; CA2425150A1; CN1471414A; NO20031565D0

Description

DISPOSABLE INJECTION DEVICE BACKGROUND OF THE INVENTION

1. Field of the Invention

This invention relates generally to disposable injector devices and more specifically, a disposable injector device which does not require a check valve but rather, a self- contained injection capsule and spring aided delivery of medicament into subcutaneous tissue of a patient .

2. Description of the Prior Art

Vaccines and drugs in today's world, are effective in controlling disease; however, parenteral injections possess serious problems which have continued to persist since the first subcutaneous injection was performed in 1836 by Lafargue . [Aronson JK. Routes of Drug Administration: 7 Subcutaneous administration Prescriber ' s Journal 38 50-55

(1988) .] For instance, the use of a standard hollow needle attached to a syringe is not only inherently dangerous and cumbersome, but requires thirteen different steps to be completed using accepted sterile techniques.

Furthermore, only medically trained personnel can undertake this process because the chances of incorrect dilution, incorrect dose measurement or failure to use sterile techniques may lead to disaster, especially if the reconstituted drug or vaccine is stored for any length of time. Training and practice are also required for optimal dexterity and efficiency to minimize the pain of injection. Because these skills are not in abundant supply, the resultant lack of trained personnel inhibits the success of current immunization campaigns.

As early as the 1920s and 1930s, several incidents occurred involving the accidental injection of diesel fuel into the hands of engineers due to pinhole defects in high- pressure fuel lines. Fine streams of liquid under sufficient pressure behaved as a "liquid nail" and painlessly penetrated the skin. Since the 1940s, numerous designs for high-pressure liquid jet injectors loosely modeled after the principles of fuel injectors continued to be patented. However, most of πhe complex designs required precision engineering with dozens of machined parts, therefore, they are inherently expensive and complicated. To a large extent, the complexity was due to a perceived need to maintain high pressure throughout each injection as with the high-pressure fuel injectors. Scherer, on the other hand, realized in 1949 that high pressure was required only at the start of the injection in order to punch a hole or track through the tough epidermis . The remaining bulk of the injection could be subsequently infused along the track under much lower pressure. [Scherer U.S. Pat. No. 2, 704, 542 (1949) ] .

Standard high-pressure instruments, because of their complexity, were not considered disposable devices. Even though simplified designs do exist [Alchas et al EP Patent No. EP0595508 (1994)], such devices are still complex, expensive and not considered truly disposable. Instead, design improvements have mostly been directed toward production of robust and reliable heavy-duty machines capable of numerous injections at high rates for mass immunization campaigns. [Ismach US Patent No. 3,057,349 (1959), Landau U.S. Patent No. 4,266,541 (1981), U.S. Patent No. 5,746,714 (1988), D'Antonio et al PCT Patent No. 098/17322 (1998), Parsons PCT Patent No. O98/15307 (1988)]. Some of the a orementioned prior art, claim capability of 4,000 injections per hour.

Problems continued to threaten the status of jet injections when an outbreak of hepatitis B caused widespread concern in the vaccine industry. [Canter J; et al 1990. An outbreak of hepatitis B associated with jet injections in a weight reduction clinic. Arch. Intern. Med.; 150: 1923-7]. The transfer of the virus through jet injection and its mechanisms were explained at the World Health Organization (WHO) meetings. [J Lloyd. Status of Jet Injectors. SEE HYPERLINK (http://www.who.int/gpv~coldchain/Powerpoint Technec . htm and http://www.who.int/gpv~coidchain/Powerpcint Technet .htm) ] .

It appeared that high pressure occurring in the tissues, which were suddenly distended by the injection, coincided with falling pressure inside the jet injector. Ultimately, this caused a reflux flow or "sucking-back" of tissue fluid into the injector. Because of this serious drawback, single-use vials which insert into the mechanical injector were developed. [Parent du Chatelet el al Clinical immunogenici y and tolerance studies of liquid vaccines delivered by jet- injector and a new single-use cartridge (Imule) : comparison with standard syringe injection. Imule Investigators Group. Vaccine, 15: 449-58 (1987)]. Cheap, plastic, replaceable nozzles and vaccine fluid paths for mechanical injectors have also been developed. Such injectors retain the multidose vial format as in Landau U.S. Patent No. 4,966581 (1990)].

A truly disposable liquid jet injector that operated on the new principle of using modest pressure of the human hand to generate a brief pulse of high pressure has been developed. This punches a narrow track through the skin to allow the subsequent delivery of the bulk of the dose at lower pressure. (Roser, B. Disposable Injector Device U.S. Patent No. 6,102,896) . However, these designs still suffer from several disadvantages . The power derived om steady pressure of the hand, converts to a sharp pulse of _high-pressure following the structural failure of "snap tabs" or the sudden overcoming of the resistance of "snap rings." The liquid dose to be injected is located in a centrally located reservoir, and the high pressure barrel is located in the base of the injector itself which also has an injection orifice in the base. Such an invention, places demands on manufacture and assembly. Both the liquid reservoir assembly and the injector itself need sterile manufacture; engineering to withstand high pressure pulses; and a valve system to isolate the high pressure pulse from the hand activating the device. This leads to an increase in production costs .

Additionally, the completion of the power stroke is dependent upon the maintenance of hand pressure until the full dose of liquid is delivered. This leaves room for error, namely, it cannot be guaranteed that a reflex arrest of hand pressure could not occur under unusual circumstances, aborting the injection before the designed dose is delivered. A preferred solution to these problems is a self-contained injection capsule which can be driven to complete the power stroke by stored energy, thereby eliminating the need for check valves .

SUMMARY OF THE INVENTION The present invention addresses the aforementioned drawbacks, and it is also cheaper to manufacture and assemble. Furthermore, it is possible to separate the dose capsule and the power assembly, meaning injection kits could contain a single power device and multiple dose capsules. Although superficially similar to the Imule concept [Parent du Chatelet et al Clinical immunogenecity and tolerance studies of liquid vaccines delivered by jet -injector and a new single-use cartridge (Imule) : comparison with standard syringe injection. Imule Investigators Group. Vaccine, 15: 449-58 (1997)], the design of the separate injection capsule in the present invention is novel and far superior. Central to this improvement is a narrow-bore element of a plunger design, which forces a small volume of a dose under high-pressure through the skin to provide an injection track, which element forms a part of the low-pressure plunger which subsequently delivers the bulk of the dose. In addition, a fine injection orifice is incorporated into the other end of the injection capsule thereby making the entire liquid path fully self-contained. Essentially, the plunger is a two- component telescopic assembly in which a narrow plunger is centrally located concentrically in a wider plunger of annular shape. The "orifice end" of the narrow plunger tightly fits in a cylindrical cavity which formed in the central portion of the annular wide plunger. The major portion of the narrow plunger is located further from the injection orifice than the annular wide plunger, thus defining a volume of liquid in the central portions of the annular wide plunger which generates a high-pressure jet during the injection stroke.

To address the problem of lack of guaranteed completion of the power stroke, one solution is to transiently store the energy generated by hand pressure in a spring and releasing the stored energy by means of a snap device. By tensioning the spring only at the time of use, the power stroke is in minimal danger of prematurely aborting the injection. This avoids the need for storage of energy in the device while on the shelf, since doing so can lead to degradation of the material and stored energy over time, thereby reducing the shelf-life of the device.

A spring which is not under tension while stored, whether a conventional metal spring or gas spring, does not undergo material fatigue or energy leakage. Rather, maximum potential energy conferred by hand is delivered as a kinetic force, at the time of use.

BRIEF DESCRIPTION OF THE DRAWINGS Several embodiments of the invention are illustrated and described in the accompanying drawings, forming a part of the specification, wherein:

FIG. 1 is a cross-sectional view of a tabjet inj ctor device, the device consisting essentially of two parts-, a power case having a cap and central finger, and contained within the power case is an injection capsule consisting of a narrow plunger centrally located within a wide annular plunger fitted in a dosage capsule containing medicament to be inj ected.

FIGS. 2A-C are cross-sectional views of the tabjet injector device, showing in succession, the break tabs yielding and allowing the central finger of the cap to strike the narrow plunger; the continued pressure driving the narrow plunger through the wide annular plunger until the central finger of the cap strikes the top of the wide annular plunger thereby punching a track through the epidermis; and finally, the central finger of the cap driving the composite narrow and wide plungers toward the orifice to deliver the bulk of the medicament through the injection track.

FIG.3 is a cross-sectional view of a second embodiment of the tabjet injector device wherein a spring assisted holder having a cap containing a freely moveable partition and attached by means of a coil spring to the holder assists in moving the cap and central finger.

FIGS.4A-D are cross -sectional views of FIG. 3, showing in succession: the spring assisted holder moving toward the patient ' s skin thereby, tensioning the coil spring until the break tabs yield; and finally, the power stored in the tensioned coil spring causing the freely mobile partition to complete the power stroke.

FIG.5 is a cross-sectional view of a third embodiment of the tabjet injector device modified so the central finger is hollow containing a freely movable member, there being a coil spring surrounding the freely movable member.

FIGS.6A-D are cross -sectional views of FIG. 5, showing in succession: compression of the coil spring; the break tabs yielding; and the power stored in the coil spring causing the power stroke to go to completion.

FIG.7 is a cross-sectional view of a fourth embodiment which is a cocked spring injector device consisting of a cocking tab which presses on a rocking lever having a driving hole; the rocking lever rotates about a fulcrum and the central finger transmits force to a narrow plunger of the injection capsule.

FIGS .8A-D are cross-sectional views of a FIG. 7 showing in succession: the cocking tab pressing on the rocking lever thereby rotating it about the fulcrum until the cocking tab slips off the rocking lever, the released rocking lever snaps back in the opposite direction causing the rocking lever to push the narrow plunger, which then slides through the wide annular plunger punching a track through the epidermis and forming a composite plunger which finally drives toward the orifice end of the injection capsule to deliver the bulk of the medicament .

FIG.9 is a cross-sectional view of a fifth embodiment which is a re-usable jet injector power device where break tabs are replaced with snap rings enabling the power case to be re-used by replacing the injection capsule after re-cocking the power case and drawing the cap back over the base until the snap rings re-engage. DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

As can be seen in FIG 1, a tabjet injector device consists of a power case having a cap 1 and a central finger 2. The cap 1 is movable on a base 5 but is prevented from movement by break tabs 3. The base 5 contains an injection capsule made up of a narrow plunger 6 , a wide annular plunger 7, a dosage capsule 8, a narrow injection orifice 10 and an integral collar, 100 on the end of the dosage capsule 8 opposite from the injection orifice 10. The narrow plunger 6 is movable in a centrally located cylindrical space within the wide annular plunger 7. The narrow plunger 6 as well as the wide annular plunger 7 create a composite plunger situated in the dosage capsule 8. The dosage capsule 8, containing medicament 9 to be injected, has the narrow injection orifice 10 at the bottom end.

Three distinct stages of operating the tabjet injector device are identified in FIGS. 2A-C. In FIG.2A, when sufficient force is exerted on the cap 1, the break tabs 3 yield allowing the central finger 2 of the cap 1 to strike the narrow plunger 6. Continued pressure drives the narrow plunger 6, as seen in FIG.2B, through a cylindrical hole in the wide annular plunger 7 forming a single composite plunger. When the central finger 2 of the cap 1 strikes the top of the narrow plunger 6, there is a tendency for this pressure to push the annular wide plunger 7 backward out of the dosage capsule 8. This is prevented by an integral collar 100 on the end of the dosage capsule 8. This high pressure pulse phase of the power stroke shoots a narrow stream of liquid through the narrow injection orifice 10 punching a track through the epidermis of a patient. Finally, in FIG.2C, the central finger 2 of the cap 1 drives the composite plunger toward an orifice 10 to deliver the bulk of the medicament through the injection track previously punched through the epidermis. Because of this simple mechanism, the need for check valves, which confine the high pressure pulse, is eliminated, as a result greatly simplifying construction, increasing reliability and reducing costs.

FIG.3 depicts an external spring injector where the device of FIG.l is located inside a spring assisted holder consisting of a cap 11 containing a freely moveable partition 12 attached to it by means of a coil spring 13.

As seen in FIGS.4A-D, in order to operate the external spring injector, hand pressure on the cap 11 of the spring assisted holder drives the cap 11 toward the patient's skin. An integral coil spring 13 is tensioned by the hand force on the cap 11 of the spring assisted holder as it slides over the injector and is arrested by contact with the patient's skin. (FIG.4A.) At this point, the pressure exerted on the cap 11 of the injector device via the freely movable partition 12 and the coil spring 13 is sufficient to snap the break tabs 3. This causes the central finger 2 of the cap 1 to strike the narrow internal plunger 6 leading to a sharp rise in pressure in the fluid reservoir and the onset of the high pressure injection pulse (FIG.4B) and the continuing pressure caused by the coil spring 13 then drives the narrow plunger 6 through the wide annular plunger 7 to complete the high pressure injection pulse which terminates when the central finger 2 of the cap 1 strikes the wide annular plunger 7," see FIG.7C. Continuing tension on the coil spring 13 in the spring assisted holder drives the composite plunger to the end of the injection capsule thereby delivering the complete medicament dosage, see FIG.4D.

The spring device may also be a gas spring which is easily achieved by making a seal between the moveable partition 12 in the spring assisted holder and the cap 11. The volume of air inside the spring assisted holder acts as an energy store eventually achieving complete injection in a similar manner to the coil spring 13 as seen in FIGS. 3 and 4.

The device in FIG.5, an internal spring injector, has a modified central finger 14 attached to the cap 1 in order to be spring loaded. The central finger 14 is hollow and contains a freely movable member 16. Between the hollow central finger 14 and the movable member 16, is a coil spring 15. The freely movable member 16 is prevented from moving toward the orifice 10 by centrally located break tabs 17 relocated to the space above the narrow plunger 6. The coil spring 13 (in tension) of FIG. 3 and/or the coil spring 15 (in compression) of FIG. 5 can be replaced with an elastomeric spring. The elastomer can either be synthetic or natural rubber, synthetic being preferred because of the perishability problems with natural rubber.

FIGS .6A-D depict the operation of the internal spring injector. In this embodiment, tension is stored in the spring during the initial movement of the cap 1 of the injector which diverts force away from the break tabs 17 until the spring is fully compressed. At this point, hand pressure conveys directly to the break tabs 17 which ultimately give way. A combination of the release of energy stored in the coil spring 13 and the continued cap movement accomplish the injection. In FIG.6A, when sufficient force is exerted on the cap 1, the spring 15 is compressed and the break tabs 17 yield. As seen in FIG.6B, the break tabs 17 completely yield allowing the movable member 16 to hit the top of the narrow plunger 6. The narrow plunger 6 moves through the wide annular plunger 7, see FIG.6C, punching a track through the epidermis until the bottom end of the movable member 16 reaches the top of the wide annular plunger 7 forming a composite plunger. This composite plunger then continues its downward movement discharging the medicament 9 through the orifice 10 by the force of coil spring 15, see FIG.6D.

A cocked spring injector device is seen in FIG.7 and carries the additional advantage of being reusable. It has a cap 1 and integral with the cap 1 is a cocking tab 18 which presses on a rocking lever 19 with a weighted bulbous end having a driving hole 20 and a free or opposite end on which the cocking tab 18 acts . The rocking lever 19 rotates about a fulcrum 23 creating tension in a spiral spring 24 held in place against a post 22 through which the fulcrum 23 passes. The central finger 2 is at the distal end of the rocking lever 19 and has a transverse rod 21 located in the driving hole 20 which carries the weight of the central finger 2 and the narrow plunger 6 of the injection capsule, see FIG.8A.

In operating the cocked spring injector, downward pressure is exerted on the cap 1, which causes the cocking tab 18 to press downward on the free end of the rocking lever 19. This ultimately causes the rocking lever 19 to rotate about the fulcrum 23 which creates tension in the spring 24 until the cocking tab 18 slips off the free end of the rocking lever 19, see FIG.8A. The released rocking lever 19 snaps backward in the direction opposite to its rotation about the fulcrum 23 which causes the weighted end of the rocking lever 19 to push the narrow plunger 6 via central finger 2 and transverse rod 21, see FIG.8B. Continued tension in the spiral spring 24 forces the narrow plunger 6 to move through the wide annular plunger 7, see FIG. 8C, forming a composite plunger and punching a track through the epidermis. Finally the composite plunger is driven toward the orifice 10 of the injection capsule by spring tension delivering the bulk of the medicament 9 from the dosage capsule 8, see FIG.8D.

FIG.9 depicts a re-usable jet injector power case. It is quite simple to convert to the re-usable power case by redesigning the snap component . Snap rings 25 replace the break tabs enabling the power case to be re-used by replacing the injection capsule after re-cocking the power case by drawing the cap 1 back over the base 5 until the snap rings 25 re-engage .

Although specific embodiments of the invention are herein disclosed for purposes of explanation, various modifications thereof, after study of this specification, will be apparent to those skilled in the art to which the invention pertains.

Claims

WHAT IS CLAIMED IS:

1. A hand-operated injector device consisting of a cap, a plunger , a base having a cavity and outer surface, a snap means for resisting movement of the plunger and an injection capsule for injecting at least one parenteral medication through skin of a patient, wherein the improvement comprises: providing a central finger centrally located within the cap and being movable relative to the injection capsule; a narrow plunger centrally located within an annular wide plunger forming a composite plunger and forming a part of the injection capsule located within the base; and a dosage capsule having a fine injection orifice at one end and containing liquid medicament also forming a part of the injection capsule,- whereby, the narrow plunger forces a volume of medicament under high pressure to form a track through skin of the patient .

2 . The injector device according to claim 1, wherein the snap means are internally located break tabs which yield to hand pressure .

3. The injector device according to claim 2, wherein the break tabs allow the central finger of the cap to strike the narrow plunger .

4. The injector device according to claim 3, wherein continued hand pressure drives the narrow plunger through the wide annular plunger until the central finger of the cap strikes the top of the wide annular plunger so as to punch the track through the epidermis .

5. The injector device according to claim 4, wherein the central finger of the cap drives the composite narrow and wide plunger toward the orifice to deliver the bulk of the medicament through the injection track.

6. The injector device according to claim 1, wherein the device is located inside a spring assisted holder containing a freely moveable partition.

7. The injector device according to claim 6, wherein the freely moveable partition is attached to the spring assisted holder by means of a spring.

8. The injector device according to claim 7, wherein the spring is a metal coil spring.

9. The injector device according to claim 8, wherein the spring is a gas spring.

10. The injector device according to claim 7, wherein the spring assisted holder moves toward the patient's skin to tension the spring.

11. The injector device according to claim 10, wherein the spring is a coil spring and it is tensioned until the break tabs yield.

12. The injector device according to claim 11 wherein force stored in the tensioned coil spring causes the freely mobile partition to complete the power stroke thereby delivering the medicament .

13. The injector device according to claim 1, wherein the central finger is hollow.

14. The injector device according to claim 13, wherein the central finger contains a freely movable member.

15. The injector device according to claim 14, wherein the freely movable member is spring loaded.

16. The injector device according to claim 15, wherein the spring is a coil spring located between the hollow central finger and the movable member.

17. The injector device according to claim 13, wherein sufficient force is exerted on the cap thereby compressing the spring and causing the break tabs to yield.

18. The injector device according to claim 17, wherein the compressed spring forces the freely movable member to touch the top of the narrow plunger.

15

19. The injector device according to claim 18, wherein the bottom end of the narrow plunger moves through to the bottom of the wide annular plunger forming a composite plunger.

20. The injector device according to claim 19, wherein the composite plunger moves toward the orifice and discharges the medicament through the orifice by the force of the coil spring .

5 21. The injector device according to claim 1, wherein the cap contains a cocking tab.

22. The injector device according to claim 21, wherein the cocking tab presses on a rocking lever with a weighted end containing a driving hole,-

23. The injector device according to claim 22, wherein the rocking lever rotates about a fulcrum creating tension in a spiral spring .

?5

24. The injector device according to claim 23, wherein the spiral spring is held in place against a post through which the fulcrum passes .

25. The injector device according to claim 24, wherein the central finger is at the distal end of the rocking lever and has a transverse rod.

26. The injector device according to claim 25, wherein the transverse rod is located in the driving hole.

27. The injector device according to claim 26, wherein the central finger and transverse rod transmit force to the narrow

15 plunger of the injection capsule.

28. The injector device according to claim 21, wherein the cocking tab presses on the rocking lever thereby rotating it about the fulcrum until the cocking tab slips off the rocking lever .

29. The injector device according to claim 28, wherein the rocking lever snaps back in the direction opposite to its rotation about the fulcrum.

25

30. The injector device according to claim 29, wherein the weighted end of the rocking lever pushes the narrow plunger via the central finger.

31. The injector device according to claim 30, wherein the narrow plunger moves through the wide plunger forming the composite plunger.

32. The injector device according to claim 31, wherein the

J. composite plunger is driven towards the orifice of the injection capsule delivering the bulk of the medicament.

33. The injector device according to claim 1, wherein the injector device less the injection capsule is reusable.

34. The injector device according to claim 33, wherein the snap means are snap rings peripherally around the base and engaging with a commensurably shaped area on the inner surface of the cap .

35. The injector device according to claim 34, wherein the the snap rings re-engage when the cap is drawn back over the base .