DRIVE ASSEMBLY FOR A MEDICAMENT DELIVERY DEVICE
20220241506 · 2022-08-04
Inventors
- Chun Chu (Taipei, TW)
- Anders Holmqvist (Värmdö, SE)
- Erika André (Saltsjö-Boo, SE)
- Pär Leander (Nacka, SE)
- Linda Odelberg (Ekerö, SE)
Cpc classification
A61M5/3157
HUMAN NECESSITIES
A61M5/2033
HUMAN NECESSITIES
A61M5/3155
HUMAN NECESSITIES
A61M2005/2026
HUMAN NECESSITIES
International classification
A61M5/20
HUMAN NECESSITIES
Abstract
A power pack for use with a medicament delivery device is presented having a plunger rod movable along a longitudinal axis; a drive spring operably connected to said plunger rod; a plunger rod sleeve arranged with holding elements for releasably holding said plunger rod with said drive spring in a tensioned state. Signal initiating elements are arranged to said plunger rod; and signal generating elements arranged to cooperate with said signal initiating elements for providing information to a user of a medicament delivery device about the movement of said plunger rod when said plunger rod sleeve has been activated to release said holding elements.
Claims
1. A notification mechanism within a medicament delivery device, where the notification mechanism comprises: a tubular proximal part having a longitudinal axis and comprising a central opening having an internal surface with an inwardly extending ledge and a longitudinal ledge that projects radially into the central opening; and a plunger rod positioned within the central opening and comprising a row of signal initiating elements and a groove positioned longitudinally along the plunger rod, wherein engagement of the longitudinal ledge and the groove rotationally locks the plunger rod with the tubular proximal part to prevent rotation of the plunger rod relative to an outer housing of the medicament delivery device, and wherein the signal initiating elements slidably engage with the inwardly extending ledge during relative axial movement between the plunger rod and the tubular proximal part such that a tactile or audible signal notification is provided to a user of the medicament delivery device.
2. The notification mechanism of claim 1, wherein the inwardly extending ledge is part of a flexible arm.
3. The notification mechanism of claim 2, wherein the inwardly extending ledge is a protrusion.
4. The notification mechanism of claim 2, wherein the flexible arm is formed from a cut-out in the tubular proximal part.
5. A notification mechanism of claim 3, wherein the flexible arm flexes radially outward away from an outer surface of the tubular proximal part when the protrusion engages with the signal initiating elements.
6. The notification mechanism of claim 1, wherein the inwardly extending ledge and the longitudinal ledge are separated by a radial distance along the inner surface of the central opening.
7. The notification mechanism of claim 1, wherein the row of signal initiating elements comprises a plurality of recesses.
8. The notification mechanism of claim 1, wherein the recesses are axially spaced wedge-shaped recesses.
9. The notification mechanism of claim 1, wherein recesses are formed as cut-outs in an outer surface of the plunger rod.
10. The notification mechanism of claim 1, wherein the signal initiating elements are equally spaced in the row to provide a constant notification frequency of the tactile or audible signals.
11. The notification mechanism of claim 1, wherein the signal initiating elements are unequally spaced in the row to provide a variable notification frequency of the tactile or audible notification signals.
12. The notification mechanism of claim 11, wherein the variable notification frequency provides notice to the user that a medicament delivery sequence is progressing.
13. The notification mechanism of claim 1, wherein the inwardly extending ledge is a protrusion formed at the end of a flexible arm that is formed from a cut-out in a surface of the tubular proximal part, where the protrusion is shaped to snap into and out of the signal initiating elements during a medicament delivery sequence.
14. The notification mechanism of claim 1, wherein the row of signal initiating elements is positioned at a distal end of the plunger rod such that the user is only notified at an end of a medicament delivery sequence.
15. The notification mechanism of claim 1, wherein the longitudinal ledge is rigidly fixed to the inner surface.
16. The notification mechanism of claim 1, wherein the signal initiating elements and the groove are positioned on an outer surface of the plunger rod such that there is a radial distance between the signal initiating elements and the groove.
17. The notification mechanism of claim 1, wherein the notification mechanism further comprises a spring that causes the relative axial movement between the plunger rod and the tubular proximal part.
18. Medicament delivery device comprising: an outer housing; a drive spring within the outer housing having a biased state and a released state; and a notification mechanism positioned within the housing and operatively associated with the drive spring, where the notification mechanism comprises: a tubular proximal part having a longitudinal axis and comprising a central opening having an internal surface with an inwardly extending ledge and a longitudinal ledge that project radially into the central opening; and a plunger rod positioned within the central opening and comprising a row of signal initiating elements and a groove positioned longitudinally along the plunger rod; wherein engagement of the longitudinal ledge and the groove rotationally locks the plunger rod with the tubular proximal part to prevent rotation of the plunger rod relative to an outer housing of the medicament delivery device, and wherein when the drive spring transitions from the biased state to the released state the signal initiating elements slidably engage with the inwardly extending ledge to produce a tactile or audible signal notification to a user of the medicament delivery device.
Description
BRIEF DESCRIPTION OF DRAWINGS
[0024] In the following detailed description of the disclosure, reference will be made to the accompanying drawings, of which
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DETAILED DESCRIPTION
[0043] A power pack 10 shown in the drawings is designed to fit into a medicament delivery device designed to deliver a dose of medicament to a patient or user. The power pack 10,
[0044] The distal end of the plunger rod holder 16 is arranged with attachment elements 32 that are designed to attach the plunger rod holder 16 to a suitable housing of the medicament delivery device. The distal end of the plunger rod holder 16 may then be arranged with an end cap 34 that fits with the housing. A drive spring 36,
[0045] Outside and coaxial with the actuator is a generally tubular actuator 46, which actuator sleeve will act as an activator of the power pack as will be described. The actuator 46 is on its inner surface arranged with inwardly directed surfaces 48 that will function as blocking elements for the holding elements as will be described. Further the inner surface of the actuator 46 is arranged with longitudinally extending recesses 50, in the embodiment two recesses 50, that are arranged on opposite sides of the inner surface. The outer surface of the actuator 46 is further arranged with guide ledges 52, where some sections of the guide ledges 52 are extending longitudinally, and some sections are arranged with an inclination in relation to a longitudinal axis L.
[0046] The device is intended to function as follows. When the power pack 10 is in its powered, ready to use state, the plunger rod 12 is pushed into the plunger rod holder 16 from the proximal end, tensioning the drive spring 36. The arms 20 of the plunger rod holder 16 then enter the recesses 14 of the plunger rod 12, thereby holding the plunger rod 12 in the tensioned state. In order for the arms 20 not to flex out of engagement with the recesses 14 of the plunger rod 12, the actuator 46 is placed outside the plunger rod holder 16, whereby the outwardly directed protrusions 24 of the arms 20 of the actuator abut the inwardly directed surfaces 48 of the actuator 46, thereby preventing radial outward movement of the arms,
[0047] The power pack 10 is then assembled with a suitable housing accommodating a medicament container, which in turn is provided with a medicament delivery member. When the power pack 10 is to be activated, preferably after a medicament delivery member has been placed at a dose delivery site, such as an injection needle penetrating the skin of a patient or user, the actuator 46 is operated, functioning as an activator. This is done by turning the actuator 46 in relation to the plunger rod holder 16. The turning may be performed in many ways, such as by an activation button operated manually by a user or by a medicament delivery member guard that is contacting the dose delivery site and is moved distally in relation to the medicament delivery device and the actuator sleeve. Appropriate elements may then cooperate with the inclined guide ledges of the actuator 46 for providing a rotation of the latter.
[0048] The turning of the actuator 46 will cause the longitudinal recesses 50 of the actuator sleeve 46 to be moved in line with the arms 20 with their outwardly directed protrusions 24,
[0049] During the movement of the plunger rod 12 in the proximal direction during the dose delivery sequence, the inwardly directed ledges 22 of the arms 20 will be in contact with and slide along the plunger rod 12,
[0050] In the embodiment shown, the row of wedge-shaped protrusions 30 extends along a majority of the length of the plunger rod 12. It is however to be understood that the row of protrusions 30 may be arranged such that they engage with the ledges 22 of the arms 20 only at the end of a dose delivery sequence or during the latter half of the dose delivery sequence for just informing the user that the dose delivery sequence is about to terminate. It is of course to be understood that the signalling elements may have other shapes for creating the desired signalling to a user. Also the length between each subsequent protrusion, and thus the frequency of the sound, or vibration, may be modified in order to vary the signalling. In this respect the frequency may be altered during the dose delivery sequence, e.g. increasing the frequency during the progress of the dose delivery sequence.
[0051] A second alternative is shown in
[0052] Further in order to ensure the relative positions between the row or rows of cut-outs and the protrusions on the arms, the plunger rod 12.sup.II is arranged with a number of laterally extending protrusions or wings 68, which wings fit into longitudinal guide slots 70 in the plunger rod sleeve 66. The guide slots 70 are further preferably arranged with stop surfaces 72 at a proximal area of the plunger rod sleeve 66. This ensures that a tensioned plunger rod 12.sup.II cannot shoot out of the plunger rod sleeve 66 during assembly of the power pack.
[0053] Further, even though it is an advantage to use the arms of the plunger rod holder not only for holding the plunger rod, but also to create the information to the user, in some instances there could be separate elements that are in contact with the rows of protrusions, causing the sound and the vibrations.
[0054] This variant is displayed in
[0055] The outer ends of the arms 88 are arranged with protrusions 92 that are to interact with an actuator 93 that in the embodiment shown has a tubular body 94 with two distally directed arms 95 slidable inside a housing 96 of a medicament delivery device. When the proximal end of the housing 96 with its extended actuator 93 is pressed against a dose delivery site, the actuator 93 will move in the distal direction and the distal ends of the arms 95 will act on the protrusions 92 and move the arms 88 of the plunger rod sleeve 82 outwardly for releasing the plunger rod 12.sup.III. Moreover, the distal end of the plunger rod 12.sup.III is provided with a number of outwardly directed guide elements 98, which guide elements 98 are designed to fit into longitudinally extending grooves 99 of the plunger rod sleeve 82 for preventing rotation of the plunger rod 12.sup.III in relation to the plunger rod sleeve 82.
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[0057] The plunger rod sleeve 100 is further arranged with signal generating elements in the form of a plurality of proximally directed arms 108 that are flexible in a generally radial direction. The free ends of the arms 108 are arranged with inwardly directed protrusions 110. The plurality of arms 108 is placed in rows after each other in the longitudinal direction of the plunger rod sleeve 100. In the embodiment shown, there are two rows of arms 108 that are placed on opposite sides. The plurality of arms 108 of the signal generating elements is to cooperate with signal initiating elements that are in the form of outwardly directed protrusions 112 on a distal area of the plunger rod 12.sup.IV. The protrusions 112 are placed such that when the plunger rod 12.sup.IV is released, the protrusions 112 will come in contact with the inwardly directed protrusions 110 of the arms 108 of the signal generating elements, causing an audible feedback that the plunger rod 12.sup.IV is moving, e.g. during a dose delivery sequence. As with the previous embodiment, if more than one row of arms 108 is used, one row may be placed offset half a step in relation to the other row, creating a higher frequency of the sounds generated.
[0058]
[0059] Further, the plunger rod 12.sup.V is arranged with a plurality of circumferentially extending, wedge-shaped, protrusions 140, being sound initiating elements. Thus, when the plunger rod 12.sup.V is released and is moved in the proximal direction by a drive spring 34 for performing a dose delivery sequence, the inclined tongues 138 will be in contact with and be tensionally biased by the passing wedge-shaped protrusions 140, hitting subsequent protrusions when leaving previous protrusions, causing tactile and audible information to the user of the ongoing sequence. Since the wedge-shaped protrusions 140 are positioned around the whole circumference of the plunger rod 12.sup.V, there is no need for guiding elements that orientate the plunger rod 12.sup.V in relation to the signal generating element, i.e. the tongues 138.
[0060] It is to be understood that the embodiment described above and shown in the drawings is to be regarded only as a non-limiting example of the disclosure and that it may be modified in many ways within the scope of the patent claims.