NZ620334B2 - Dual chamber device - Google Patents

Dual chamber device Download PDF

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Publication number
NZ620334B2
NZ620334B2 NZ620334A NZ62033412A NZ620334B2 NZ 620334 B2 NZ620334 B2 NZ 620334B2 NZ 620334 A NZ620334 A NZ 620334A NZ 62033412 A NZ62033412 A NZ 62033412A NZ 620334 B2 NZ620334 B2 NZ 620334B2
Authority
NZ
New Zealand
Prior art keywords
chamber
barrel
plunger
distal end
composition
Prior art date
Application number
NZ620334A
Other versions
NZ620334A (en
Inventor
James Quinton Stewart Haughey
Original Assignee
Norbrook Laboratories Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from GBGB1113606.6A external-priority patent/GB201113606D0/en
Application filed by Norbrook Laboratories Limited filed Critical Norbrook Laboratories Limited
Publication of NZ620334A publication Critical patent/NZ620334A/en
Publication of NZ620334B2 publication Critical patent/NZ620334B2/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61DVETERINARY INSTRUMENTS, IMPLEMENTS, TOOLS, OR METHODS
    • A61D1/00Surgical instruments for veterinary use
    • A61D1/02Trocars or cannulas for teats; Vaccination appliances
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61DVETERINARY INSTRUMENTS, IMPLEMENTS, TOOLS, OR METHODS
    • A61D7/00Devices or methods for introducing solid, liquid, or gaseous remedies or other materials into or onto the bodies of animals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/178Syringes
    • A61M5/31Details
    • A61M5/315Pistons; Piston-rods; Guiding, blocking or restricting the movement of the rod or piston; Appliances on the rod for facilitating dosing ; Dosing mechanisms
    • A61M5/31596Pistons; Piston-rods; Guiding, blocking or restricting the movement of the rod or piston; Appliances on the rod for facilitating dosing ; Dosing mechanisms comprising means for injection of two or more media, e.g. by mixing
    • A61M2005/31598Pistons; Piston-rods; Guiding, blocking or restricting the movement of the rod or piston; Appliances on the rod for facilitating dosing ; Dosing mechanisms comprising means for injection of two or more media, e.g. by mixing having multiple telescopically sliding coaxial pistons encompassing volumes for components to be mixed
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M2250/00Specially adapted for animals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/178Syringes
    • A61M5/19Syringes having more than one chamber, e.g. including a manifold coupling two parallelly aligned syringes through separate channels to a common discharge assembly
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/178Syringes
    • A61M5/28Syringe ampoules or carpules, i.e. ampoules or carpules provided with a needle
    • A61M5/285Syringe ampoules or carpules, i.e. ampoules or carpules provided with a needle with sealing means to be broken or opened
    • A61M5/286Syringe ampoules or carpules, i.e. ampoules or carpules provided with a needle with sealing means to be broken or opened upon internal pressure increase, e.g. pierced or burst
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61MDEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
    • A61M5/00Devices for bringing media into the body in a subcutaneous, intra-vascular or intramuscular way; Accessories therefor, e.g. filling or cleaning devices, arm-rests
    • A61M5/178Syringes
    • A61M5/31Details
    • A61M5/315Pistons; Piston-rods; Guiding, blocking or restricting the movement of the rod or piston; Appliances on the rod for facilitating dosing ; Dosing mechanisms
    • A61M5/31596Pistons; Piston-rods; Guiding, blocking or restricting the movement of the rod or piston; Appliances on the rod for facilitating dosing ; Dosing mechanisms comprising means for injection of two or more media, e.g. by mixing

Abstract

dual chamber syringe comprising a first barrel defining a first chamber (12) for holding a first composition, the first chamber having at least one side wall and a distal end wall defining a dispensing nozzle (22). A second barrel defining a second chamber (14) for holding a second composition, the second chamber having at least one side wall (14) and a distal end wall, an annular seal at the distal end of the second barrel, and the at least one side wall of the second chamber defining at least one orifice proximal to the seal; and a plunger operable to drive the second barrel into the first chamber to displace the first composition out of the first chamber through the nozzle, and to bring the annular seal of the second barrel into contact with the distal end wall of the first chamber, thereby to deform the seal and permit fluid communication between each orifice in the second barrel and each flow channel, wherein the plunger is subsequently moveable into the second chamber to displace the second composition out of the second chamber through each orifice and flow channel to the nozzle. e second chamber having at least one side wall (14) and a distal end wall, an annular seal at the distal end of the second barrel, and the at least one side wall of the second chamber defining at least one orifice proximal to the seal; and a plunger operable to drive the second barrel into the first chamber to displace the first composition out of the first chamber through the nozzle, and to bring the annular seal of the second barrel into contact with the distal end wall of the first chamber, thereby to deform the seal and permit fluid communication between each orifice in the second barrel and each flow channel, wherein the plunger is subsequently moveable into the second chamber to displace the second composition out of the second chamber through each orifice and flow channel to the nozzle.

Description

Dual Chamber Device The present invention is directed to a dual chamber device for sequentially dispensing two compositions, without the compositions mixing with each other.
In some situations it may be necessary or desirable to dispense two compositions which are not mixed with one another but are delivered directly one after the other. One example is in veterinary medicine for treating infection in the udder of animals such as cattle. It is desirable to first inject an antibiotic composition to treat the infection and then to deliver a teat seal to seal the teat canal to prevent the entry of further bacteria.
Various devices and syringes with two or more chambers are known. Many are used where two compositions must be mixed together before they are delivered. Some designs employ separate barrels either adjacent to one another, or a first cylindrical barrel surrounded by an annular second barrel, with each barrel having a separate plunger. Examples can be found in and US 2004/092864. Other designs include a single barrel and plunger which divides the barrel into two chambers and a bypass passage or valve arrangement so that in certain positions of the plunger the two chambers are connected and the compositions can mix. Typical examples are shown in EP 1759728, US 2003/040701 and WO 99/17820.
Some syringes for sequential delivery of separate compositions are also known. In US 2006/224105 a complex, multi-part arrangement of syringe and valve assembly is provided. In US 6,723,074 a single barrel with a flexible 4172863-1 membrane defines a chamber for a first composition. A flexible bag contains a second composition. A plunger forces the bag against the membrane to deliver the first composition. Subsequently a piercing member breaks the bag to deliver a second composition. In US 5,102,388 a single barrel is divided into chambers by stoppers with piercing members. As a plunger is depressed fluid from a first chamber is delivered and a first stopper then pierces the adjacent stopper to allow fluid from the next chamber to be delivered and so on. These are all multi-part devices requiring a combination of materials, detailed parts, and piercing members, adding complexity and cost.
BE 1018797 describes a syringe with an outer barrel providing a first chamber and a piston providing a second chamber. A plunger drives the piston into the first chamber to dispense a liquid from the first chamber. The plunger can then be driven into the second chamber to dispense liquid from the second chamber.
The present invention provides a device comprising: a first barrel defining a first chamber for holding a first composition, the first chamber having at least one side wall and a distal end wall defining a dispensing nozzle, wherein at least one flow channel is formed in the at least one side wall and distal end wall of the first chamber, extending across the distal end wall from the at least one side wall to the nozzle in helical fashion; a second barrel defining a second chamber for holding a second composition, the second chamber having at least one side wall and a distal end wall, an annular seal at the distal end of the second barrel, and the at least one side 4172863-1 wall of the second chamber defining at least one orifice proximal to the seal; and a plunger operable to drive the second barrel into the first chamber to displace the first composition out of the first chamber through the nozzle, and to bring the annular seal of the second barrel into contact with the distal end wall of the first chamber, thereby to deform the seal and permit fluid communication between each orifice in the second barrel and each flow channel, wherein the plunger is subsequently moveable into the second chamber to displace the second composition out of the second chamber through each orifice and flow channel to the nozzle.
In this way, a single device can be provided which holds two compositions in separate chambers. The user need only operate a single plunger in order to sequentially dispense the first and second compositions, without the two compositions mixing with one another.
Preferably, a plurality of flow channels are provided, arranged in three equi-spaced groups of flow channels.
Preferably, the at least one side wall of the first and second chambers is a cylindrical wall.
This arrangement aids in efficiently delivering the second composition from the second chamber to the nozzle.
Preferably, the syringe further comprises releasable engagement means to engage the plunger with the second barrel, such that when engaged the plunger and second barrel move as one unit to drive the second barrel into the first 4172863-1 chamber, and when disengaged the plunger can move into the second chamber.
In this way, a single stroke of the plunger is operable to deliver the first composition, followed by the second composition.
Preferably, the engagement means is releasable by exerting increased force on the plunger. The engagement means may comprise cooperating structures on an inner surface of the second barrel and an outer surface of the plunger.
Thus, a simple mechanism is provided which is cost effective to manufacture and simple to operate without the user needing to operate separate release means.
Preferably, the syringe also includes a closure member to prevent leakage of the second composition from the second chamber through each orifice until the second barrel is located in the first chamber.
In this way, the second chamber can be charged with the second composition before it is engaged with the first barrel.
Preferably, the closure member comprises a tube sealingly located on the second barrel and the device further comprises retention structures to retain the tube and allow the second barrel to move through the tube into the first chamber when driven by the plunger. 4172863-1 Thus, action of the plunger also automatically moves the second barrel relative to the closure member so that each orifice is no longer closed.
Preferably, the device further comprises a releasable stop means for preventing movement of the plunger into the second chamber until the stop is released. This ensures there cannot be unintentional delivery of the second composition.
Described herein is a device comprising: a first barrel defining a first chamber for holding a first composition and a nozzle communicating with the first chamber; a second barrel defining a second chamber for holding a second composition and at least one orifice communicating with the second chamber; a plunger operable to drive the second barrel into the first chamber thereby to displace the first composition out of the first chamber through the nozzle and to bring each orifice into fluid communication with the nozzle, wherein the plunger is subsequently moveable into the second chamber to displace the second composition out of the second chamber through each orifice and the nozzle; and further comprising a releasable stop means for preventing movement of the plunger into the second chamber until the stop is released.
Described herein is a device comprising: a first barrel defining a first chamber for holding a first composition and a nozzle communicating with the first chamber; 4172863-1 a second barrel defining a second chamber for holding a second composition and at least one orifice communicating with the second chamber, a plunger operable to drive the second barrel into the first chamber thereby to displace the first composition out of the first chamber through the nozzle and to bring each orifice into fluid communication with the nozzle, wherein the plunger is subsequently moveable into the second chamber to displace the second composition out of the second chamber through each orifice and the nozzle; and further comprising a tube sealingly locatable on the second barrel so as to cover each orifice, and retention structures operable to fix the tube relative to the first barrel and allow the second barrel to pass through the tube and into the first chamber when driven by the plunger.
The present invention will now be described in detail, by way of example only, with reference to the accompanying drawings in which: Figure 1 is a cross section of a device in accordance with one embodiment of the present invention, in its starting position; Figure 2 shows the device of Figure 1 in an intermediate position after delivery of a first composition; Figure 3 shows the device of Figure 1 in a final position after removal of a releasable stop means and delivery of a second composition; 4172863-1 Figure 4 is a cross section of the outer barrel of the device of Figure 1; Figure 5 is an end view of the barrel of Figure 4; Figure 6 is a side view of the inner barrel of the device of Figure 1; Figure 7 is a cross section of the inner barrel of Figure 6; Figure 8 is an enlarged cross section of the protection ring of the device of Figure 1; Figure 9 is a side view of the plunger of the device of Figure 1; Figure 10 is a cross section of the plunger of Figure 9; and Figure 11 is an enlarged perspective view of the releasable stop means of the device of Figure 1.
As shown in Figure 1, a device 10 in accordance with one embodiment of the present invention comprises an outer barrel 12, an inner barrel 14, a plunger 16, and a protection ring 18. The device 10 also comprises a releasable stop means 80, stop 82 and cap 84.
As best seen in Figure 4, the outer barrel 12 comprises a hollow cylindrical body 20, a dispensing nozzle 22 at the distal end of the body 20 and an open proximal end surrounded by a flange 24. 4172863-1 As shown in Figure 4, the inner bore of the outer barrel 12 comprises an enlarged diameter portion 26 at the proximal end bounded by a shoulder 28, and a smaller diameter portion . In use, the enlarged diameter portion 26 receives and retains the protection ring 18 and the smaller diameter portion 30 defines a first chamber for receiving a first composition.
At the distal end of the outer barrel 12, a number of circumferentially spaced grooves 32 are formed in the inner surface of the cylindrical body 20 and the end wall 34, leading to the nozzle 22. In this example, three sets of grooves are provided. As best seen in Figure 5, the grooves 32 may extend in a converging, arcuate fashion across the end wall 34 towards the nozzle 22. These helical grooves 32 form flow channels which help the compositions to flow towards the nozzle and empty the syringe.
Referring to Figures 6 and 7, the inner barrel 14 also comprises a hollow cylindrical body 36. It has a closed distal end 38 with a central projection 40 on the outer surface and a corresponding recess 42 on the inner surface, and an open proximal end surrounded by a flange 44. The inner bore of the cylindrical body 36 includes a proximal portion 46 of slightly larger diameter and a distal portion 48 of slightly smaller diameter, joined by a shoulder 50.
The proximal portion 46 may include a flared mouth 52 at the open end to assist with locating the plunger 16. The proximal portion 46 may also include one or more axially extending ridges or grooves 53 to assist with aligning the plunger 16 as discussed further below. The distal end portion 48 may include a further reduced diameter portion 54 4172863-1 adjacent the end wall 38 to receive the distal end of the plunger 16.
As best seen in Figure 6, the outer surface of the inner barrel 14 includes a waisted portion 56 of reduced outer diameter close to the distal end. A number of circumferentially spaced orifices 58 are provided in this waisted portion 56 (see Figure 7). In this example, four equi-spaced orifices 58 are provided, but this number may be varied.
A flexible annular flange 86 is formed around the distal end of the inner barrel 14. The flange 86 projects distally, leaving an annular channel 88 between the flange 86 and the outer surface of the distal end 38. The flange 86 is sufficiently thin that it is flexible and deformable as described further below.
The protection ring 18 is shown in Figure 8 at an enlarged scale. This is initially located around the distal end of the inner barrel 14 as shown in Figure 1. The protection ring 18 comprises a tubular body 60 with a flange 62 around the proximal end. The inner surface of the body 60 and outer surface of the inner barrel 14 are provided with cooperating structures 64 such as grooves and ribs, which serve to locate the protection ring 18 on the inner barrel 14. As shown in Figure 6, on the inner barrel 14 the structures 64 are located proximally of the waisted portion 56, and the flexible flange 86 is distal of it. The protection ring 18 covers this area when located on the inner barrel 14. The structures 64 and the flexible flange 86 serve to seal the protection ring 18 against the inner barrel 14 either side 4172863-1 of the orifices 58, to prevent leakage of liquid from the inner barrel 14.
The plunger 16 is shown in Figures 9 and 10 and comprises a cylindrical body 66. The proximal end includes a flange 68 against which a user exerts pressure in order to operate the device 10. The flange 68 is illustrated relatively small and flat but in practice this may be extended and formed curved or otherwise ergonomically shaped to enhance comfort and ease of operation for a user, in a similar manner to the proximal end flange 24 of the outer barrel 12 which is preferably enlarged and curved to comfortably and securely fit a user’s fingers to help in operating the device 10.
At the distal end of the plunger 16, is a reduced diameter nose portion 72 with a central projection 74. A flexible flange 70 is formed on the outer surface of the plunger 16 around the proximal end of the nose portion 72. In a similar manner to the flexible flange 86 on the inner barrel 14, the flange 70 projects distally, leaving an annular channel between it and the nose portion. As seen in Figures 1-3, when the plunger 16 is located in the inner barrel 14, the flange 70 is deformed inwardly and forms a seal against the inner wall of the body 37, to seal the proximal end of the bore.
The outer surface of the plunger 16 may include one or more axially extending projections 90 (or ribs or grooves) to cooperate with the ribs or grooves 53 in the inner barrel 14 to align and locate the plunger 16 in the inner barrel 14.
In conjunction with engagement of flange 70 against shoulder 4172863-1 50, the plunger 16 can be clipped into the inner barrel 14 as shown in Figure 1.
A stop 82 is fitted into the open proximal end of the plunger 16 to close off the body 66, as seen in Figures 1-3.
The stop 82 comprises a tubular part 92, configured to be a push fit with the interior of the body 66, and a flange 94 which provides a larger area for a user’s thumb to press against when depressing the plunger 16 to operate the syringe 10.
A releasable stop means or clip 80 is releasably fitted around the proximal part of the body 66 of the plunger 16, as seen in Figures 1 and 2. As shown in Figure 11, the releasable stop means 80 is preferably a resilient member which is generally C-shaped in cross section, dimensioned to securely fit around the plunger 16. Ridges 96 may protrude from the releasable stop means 80 to provide gripping features, enabling a user to push the releasable stop means 80 onto the plunger 16 and to pull it off again when required.
A cap 84 is releasably clipped over the nozzle 22 of the outer barrel 12 in order to seal the device 10 and prevent leakage of fluid through the nozzle 22, and to keep the nozzle 22 clean before use, as shown in Figure 1.
When the device 10 is prepared and ready for use, a first composition is held in the outer barrel 12 in a first chamber defined by the smaller diameter portion 30. A second composition is held in the inner barrel 14 in a second chamber defined by the distal portion 48. The protection 4172863-1 ring 18 is sealingly located on the inner barrel 14 to prevent leakage of the second composition which can exit the second chamber via the orifices 58. The plunger 16 is located in the proximal portion 46 of the inner barrel 14 with the flange 70 engaged against the shoulder 50. The inner barrel 14 and protection ring 18 are located in the proximal end of the outer barrel 12 with the protection ring 18 located in the larger diameter portion 26. The releasable stop means 80 is located around a proximal portion of the plunger 16. The nozzle 22 is covered by the cap 84. The distal end of the plunger 16 is closed by the stop 82. Thus, the device 10 is in the position shown in Figure 1.
In order to deliver the first composition, a user first removes the cap 84 to expose the nozzle 22. The user then exerts pressure against the end flange 94 of the stop 82.
Since the plunger 16 is located in the inner barrel 14 by engagement of the flange 70 against shoulder 50, the plunger 16 and inner barrel 14 move as one unit into the outer barrel 12. Thus, the first composition is displaced out of the first chamber and passes through the nozzle 22 to exit the device 10.
As the inner barrel 14 and plunger 16 move into the outer barrel 12, the protection ring 18 is retained at the proximal end of the outer barrel 12 in portion 26. Thus, the inner barrel 14 and plunger 16 move as one unit through the ring 18. The flexible annular flange 86 is pressed against the inner wall of the outer barrel 12, thereby preventing leakage of the composition in the second chamber into the first chamber. When the closed distal end 38 of the inner barrel 14 reaches the distal end of the outer barrel 12, the 4172863-1 projection 40 is received in the nozzle 22 but does not completely block it. An annular chamber 98 is formed between the waisted portion 56 and the inner wall of the body 20 of the outer barrel 12. This communicates with the grooves 32 formed in the outer barrel 12. The flexible flange 86 is deformed by contact with the distal end wall of the outer barrel 12. This allows the second composition to exit the second chamber via orifices 58 and to flow via the annular channel 98 and the grooves 32 in order to reach the nozzle 22. At this point, the releasable stop means 80 prevents further movement of the plunger 16 into the inner barrel 14.
Thus, when required the user removes the releasable stop means 80 and then exerts an increased pressure on the flange 68. This forces the base of the flange 70 to pass over the shoulder 50 and allows the plunger 16 to move into the distal portion 48 of the inner barrel 14. Thus, the second composition is displaced out of the second chamber in the inner barrel, via the orifices 58 and can flow through the annular channel 98 and grooves 32 to the nozzle 22 for delivery.
This releasable stop means for preventing movement of the plunger into the second chamber can include the removable clip as shown in Figures 1 and 11 and equivalents thereof.
The releasable stop means for preventing movement of the plunger into the second chamber can also include one or more depressible flanges or one or more depressible rings on the body of the plunger; a twist lock mechanism that requires the plunger be rotated in relation to the barrel to allow further movement of the plunger into the barrel; one or more collapsible flanges or one or more collapsible rings that collapse at a significantly higher force than that required 4172863-1 to move the plunger into the barrel in the absence of such collapsible flanges or rings; one or more flanges, hinges, or rings that are attached to the side of the body of the plunger and which must be pulled away from the body of the plunger to allow the plunger to move into the barrel, such one or more flanges, hinges, or rings may remain attached to at least a portion of the body of the plunger while still allowing the plunger to move into the barrel; one or more retractable flanges or rings that may be retracted by pulling on an element located inside the body of the plunger that is attached to said flanges or rings and protrudes from inside the body of the plunger.
At the very end of the stroke, as in Figure 3, the nose 72 of the plunger 16 is located in the reduced diameter portion 54 at the distal end of the inner barrel 14 and the projection 74 is received in the recess 42.
In practise, the first composition delivered may be an antibiotic to treat mastitis in cattle and the second composition may be a teat seal. It is desirable to inject the antibiotic and then to massage the teat to ensure the medication accesses it properly, before injecting the seal.
Therefore, the releasable stop means 80 provides the advantage that the seal cannot be dispensed unintentionally and will only be deliverable when a user is ready and has removed the releasable stop means 80.
Thus, a single device can be provided which contains first and second compositions in separate chambers and does not permit them to mix, but is able to sequentially deliver both compositions by one full stroke of the plunger. 4172863-1 The term ‘comprising’ as used in this specification and claims means ‘consisting at least in part of’. When interpreting statements in this specification and claims which include the term ‘comprising’, other features besides the features prefaced by this term in each statement can also be present. Related terms such as ‘comprise’ and ‘comprised’ are to be interpreted in a similar manner. 4172863-1

Claims (8)

What we claim is:
1. A device comprising: a first barrel defining a first chamber for holding a 5 first composition, the first chamber having at least one side wall and a distal end wall defining a dispensing nozzle, wherein at least one flow channel is formed in the at least one side wall and distal end wall of the first chamber, extending across the distal end wall from the at 10 least one side wall to the nozzle in helical fashion; a second barrel defining a second chamber for holding a second composition, the second chamber having at least one side wall and a distal end wall, an annular seal at the distal end of the second barrel, and the at least one side 15 wall of the second chamber defining at least one orifice proximal to the seal; and a plunger operable to drive the second barrel into the first chamber to displace the first composition out of the first chamber through the nozzle, and to bring the annular 20 seal of the second barrel into contact with the distal end wall of the first chamber, thereby to deform the seal and permit fluid communication between each orifice in the second barrel and each flow channel, wherein the plunger is subsequently moveable into the second chamber to displace 25 the second composition out of the second chamber through each orifice and flow channel to the nozzle.
2. A device as claimed in claim 1, further comprising a plurality of flow channels arranged in three equi-spaced 30 groups of flow channels. 4172863-1
3. A device as claimed in claim 1 or claim 2, further comprising releasable engagement means to engage the plunger with the second barrel such that when engaged the plunger and second barrel move as one unit to drive the second 5 barrel into the first chamber, and when disengaged the plunger is able to move into the second chamber.
4. A device as claimed in claim 3, wherein the engagement means is releasable by exerting increased force on the 10 plunger.
5. A device as claimed in claim 3 or claim 4, wherein the engagement means comprises cooperating structures on an inner surface of the second barrel and an outer surface of 15 the plunger.
6. A device as claimed in any preceding claim, further comprising a closure member to prevent leakage of the second composition from the second barrel.
7. A device as claimed in claim 6, wherein the closure member comprises a tube sealingly located on the second barrel and the device further comprises retention structures to retain the tube and allow the second barrel to move 25 through the tube and into the first chamber when driven by the plunger.
8. A device as claimed in any preceding claim, further comprising a releasable stop means for preventing movement 30 of the plunger into the second chamber until the stop is released. 4172863-1
NZ620334A 2011-08-05 2012-08-06 Dual chamber device NZ620334B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB1113606.6A GB201113606D0 (en) 2011-08-05 2011-08-05 Dual chamber syringe
GB1113606.6 2011-08-05
PCT/GB2012/051900 WO2013021186A1 (en) 2011-08-05 2012-08-06 Dual chamber device

Publications (2)

Publication Number Publication Date
NZ620334A NZ620334A (en) 2016-01-29
NZ620334B2 true NZ620334B2 (en) 2016-05-03

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