Inhalation device for powdered drugs
10828433 ยท 2020-11-10
Assignee
Inventors
- Martin Herder (Bad Homburg, DE)
- Gerhard Ludanek (Bad Homburg, DE)
- Ingo Mett (Bad Homburg, DE)
- Joachim Schmidt (Bad Homburg, DE)
Cpc classification
A61M2206/16
HUMAN NECESSITIES
A61M15/0093
HUMAN NECESSITIES
A61M15/0095
HUMAN NECESSITIES
International classification
Abstract
The invention refers to an inhalation device for powdered drugs to be received by a patient by an inhalation-caused air stream, comprising at least one powder reservoir, metering means for repeatedly metering a powder dose from the reservoir, a transportation mechanism for moving said metering means from a filling position for receiving a powder dose into an emptying position for releasing said powder dose into a powder channel, at least one activating device for manual operation by the patient being operatively connected to said transportation mechanism such that upon operation a single powder dose is being metered, said activating device comprising a dosage key (5) acting on said transportation mechanism when actuated by the patient. According to the invention, said transportation mechanism furthermore comprises a dosage lever (6) acting on said metering means, said dosage lever (6) being locked in the inhalation position of said metering means after said dosage key (5) has been properly pressed down by the patient. The dosage lever (6) in the inhalation position engages a trigger member and is releasable by actuation of the trigger member. The trigger member comprises at least one cam surface and the dosage lever (6) engages the cam surface tangentially in said locked inhalation position.
Claims
1. An inhalation device for powdered drugs to be received by a patient by an inhalation-caused air stream, comprising: at least one powder reservoir, metering means for repeatedly metering a powder dose from the reservoir, a transportation mechanism for moving said metering means from a filling position for receiving a powder dose into an emptying position for releasing said powder dose into a powder channel, at least one activating device for manual operation by the patient, said activating device being operatively connected to said transportation mechanism such that upon operation a single powder dose is being metered, said activating device comprising a dosage key acting on said transportation mechanism when pressed by the patient, said transportation mechanism comprising a dosage lever acting on said metering means, wherein the dosage key and the dosage lever are provided by distinct components which are pivotable relative to each other, wherein said dosage lever locked in an inhalation position of said metering means when said dosage key is depressed to a fully depressed position by the user whereby the device is ready for inhalation, wherein said dosage lever in the inhalation position is locked in the inhalation position of said metering means by engagement with a trigger member, and, upon inhalation, is released from engagement with the trigger member by actuation of the trigger member, wherein the dosage lever comprises a fastening hook having a planar contact surface, wherein the trigger member comprises at least one cam surface which is a curved surface, and that the planar contact surface of the fastening hook engages said curved surface tangentially in the locked inhalation position.
2. The inhalation device according to claim 1, further comprising at least one powder disintegration means, wherein said metering means and said transportation mechanism are arranged within a dosing compartment and said disintegration means is arranged in a powder discharge compartment, and wherein said dosing compartment is completely sealed against said powder discharge compartment.
3. The inhalation device according to claim 1, wherein said dosage lever is locked in a middle position when said dosage key is depressed to less than the fully depressed position by the user and released prior to the fastening hook engaging the curved surface of the trigger member, and wherein, when in the locked middle position, the dosage lever is releasable from the locked middle position only upon the dosage key being subsequently depressed to the fully depressed position by the user to lock the dosage lever in the inhalation position.
4. The inhalation device according to claim 1, wherein the planar contact surface of the fastening hook and the curved surface of the trigger member face each other when the device is ready for inhalation.
5. The inhalation device according to claim 1, wherein said trigger member comprises an inhalation-operated valve in an air duct communicating with said powder channel.
6. The inhalation device according to claim 5, wherein said inhalation-operated valve includes a flap which fulfils a pivot movement upon inhalation, said cam surface being provided on the flap or on a pivot shaft of the flap.
7. The inhalation device according to claim 6, wherein the valve chamber is sealed against the housing so as to define said dosing compartment and said powder discharge compartment.
8. The inhalation device according to claim 1, wherein triggering of the dosage lever is achieved by a pivot motion of the cam surface.
9. The inhalation device according to claim 8 comprising a main structural support member defining a valve chamber as well as a support for a housing including at least two shells.
Description
(1) In the following the invention is disclosed by way of example with reference to accompanying drawings in which:
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(26) The inhaler 1 shown in
(27) The reservoir 2 is sealingly covered by a lid 4 as can be seen from
(28) The powder medicament can be received by a patient by means of an air stream caused by the user, i.e. induced by suction. Therefore, the inhaler further comprises an activating device for manual engagement by the patient in the form of a dosage key 5 being connected to a transportation mechanism including a dosage lever 6 and a locking lever 7. The dosage lever 6 acts on a dosage slide 8 as a metering means being moveable from a filling position for receiving a powder dose into an emptying position for releasing said powder dose into a powder groove 16a of a cyclone 16 for deagglomeration of the powder in the cyclone 16. From the powder groove 16a the patient can inhale the powdered drug through a mouthpiece 10 via an air stream generated by the patient. If not in use, the mouthpiece 10 is protected from dirt by a mouthpiece cover 11. The mouthpiece cover 11 is secured to the inhaler housing fixedly, i.e. non-detachable.
(29) The powder groove 16a of the cyclone 16 forms a part of a powder channel through the cyclone 16 which functions as a disintegration means as this is known from the art. The powder medicament to be received by the patient may be in form of an adhesive mixture. Adhesive mixtures consist of relatively large crystals, generally -lactose-monohydrid, carrying the micronised drug particles on their surface. In the disintegration system, the dry powder will be deagglomerated for releasing the drug particles from the powder formulation. The cyclone 16, i.e. the disintegration means, generally includes an air circulation chamber as well as several air supply channels which enter the circulation chamber tangentially so that a circular air flow pattern is created inside the circulation chamber. So the total respiratory flow through the inhaler does include a transportation airflow for traversing the powder dose in the powder groove and dragging the powder into the circulation chamber, a cyclone air flow which tangentially enters the circulation chamber as well as eventually a bypass airflow for creating a so-called sheath flow of clean air. A possible design for the disintegration means is for instance disclosed in the international patent publication WO 03/000325 the disclosure of which is herewith fully incorporated by reference. The disintegration means in the following in a rather simplified form is referred to as a cyclone. In a also rather simplified form in the following the air path from the powder groove 16a to the mouthpiece opening is referred to as powder channel. It is, however, to be understood that the term powder channel does not necessarily refer to one distinct single powder channel but rather to a channel system as explained above.
(30) As this can be taken from
(31) The heart of the inhaler 1 is formed by a valve chamber 15 including the cyclone 16 and a cartridge body 3a.
(32) Manual operation of the inhaler 1 by a patient functions via dosage key 5 which on depression by the patient against the biasing force of a dosage key spring 17 acts on a dosage lever 6 which is connected to the dosage slide 8 (see
(33) Dosage slide 8 is slidably moveable within dosage slide passage 18 extending below the reservoir 2 within the cartridge body 3a, as this for instance can be seen from
(34) The dosage slide 8 (metering means) includes a dosage cavity 19 for receiving a metered dose of a powdered drug.
(35) It should be mentioned that the cartridge body 3a not only defines the reservoir 2 for receiving the powdered drug but also defines a dosage slide passage 18 extending below the reservoir 2 as well as a housing for receiving counting and indexing means as this is described hereinafter more detailed.
(36) The dosage slide 8 is shown in
(37) In this position shown in
(38) The flap valve 22 according to a first embodiment in more detail is shown in
(39) As this can be seen also from
(40) A rear side view of the flap valve 22 is for instance shown in
(41) On the rear side of the first leg 22c of the flap 22a, a latching rib 47 is provided which may be engaged by the fastening hook 23 of the dosage lever 6 in the inhalation position. The fastening hook 23 of the dosage lever 6 at its leading end is provided with a barbed projection 50 which has a sloping face 51. The flap valve 22 includes a flap valve lever 31 integrally formed with said shaft 22b. The distal end of the flap valve lever 31 is provided with a deflector surface 53. Upon actuation of the dosage key 5 and subsequent actuation and downward movement of the dosage lever 6, a corresponding deflector surface 53 of a latch 29 integrally formed with the hook 23 of the dosage lever 6 gets into abutment with the deflector surface 53 of the flap valve lever 31. The flap valve lever 31 as well as the hook of the dosage lever are thereby both being slightly deflected, i.e. bent aside and snap back in their initial position upon further downward movement of the hook 23 of the dosage lever 6. Upon further downward movement of the hook 23, the sloping face 51 of the barbed projection 50 abuts one edge of the latching rib 47. Thereby the hook 23 is bent aside due to the resilience of its material and snaps back behind the latching rib 47 in its end position thereby engaging the flap valve 22 and being releasable by an inhalation-triggered pivoting movement of the flap valve 22.
(42) As this can particularly seen from
(43) Another embodiment of the flap valve 22 is shown in
(44) The flap valve 22 according to this embodiment comprises a relatively simple flat flap 22a which is not bent or angled in itself.
(45) As this can be taken from
(46) The shaft 22b of the flap valve 22 (see for instance
(47) In the area of the cut out portion 24 of the shaft 22b, the shaft 22b has only a semi-circle cross-section, the leading end of the fastening hook 23 engages the remainder of the cross-section of the shaft only tangentially and only in a very limited surface area (line contact) so that the contact force between the shaft 22b and the fastening hook 23 is almost independent from the tolerances of the components. Due to this design, in particular due to the fact that a planar contact surface of the fastening hook 23 contacts a curved surface area of the remainder of the cross section of the shaft 22b, the required triggering forces are only subject to minor variations so that triggering of the flap valve 22 is fairly reproducible. Only a slight rotation/pivoting movement of the shaft 22b and the flap 22a will set the fastening hook 23 free so that the dosage lever 6 may swing upwards driven by the force of the dosage lever spring 25, thereby finishing the inhalation cycle.
(48) A perspective view of the dosage key 5 is shown in
(49) Said dosage key 5 includes an actuator blade 27 being formed as a flexible arm/leg also integrally formed with the dosage key 5 and extending downwards in the mounting position shown in
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(51) Upon depression of the dosage key 5, the actuator blade 27 moves downwards and engages the beveled edge 28 of the valve chamber such that the actuator blade 27 due its inherent flexibility is deflected/bent from a first position shown in
(52) In the following the double dosing prevention mechanism of the inhaler according to the invention will be described, first referring to the first embodiment of the flap valve 22 according to the invention.
(53) As this has been mentioned before, the dosage lever 6 in the area of its trailing end (left hand side in
(54) It is again referred to
(55) In the event the dosage key 5 will be pressed and released too early, i.e. prior to the engagement of the fastening hook 23 into the latching rib 47 of the flap valve 22, latch 29 of the dosage lever 6 upon upward movement of the dosage lever 6 will abut said mechanical stop 30 of the flap valve lever 31. Accordingly, the dosage lever 6 locks into the flap valve 22 in a middle position. This middle position lock provides a double dosing prevention mechanism. In this middle position lock, i.e. first locked position, the relationship of lever is such that the forces required for releasing the dosage lever 6 can not be brought up simply by inhalation. If the dosage lever 6 does not lock into flap valve 22 in the end position, e.g. when the dosage key 5 is not pressed all the way down, the dosage lever 6 will not return to its initial starting position, i.e. will be locked in the middle position. Accordingly, no additional powder dose will be released from the reservoir 2. The dosage lever 6 and the dosage slide 8 will only return into their starting position after inhalation-triggered actuation of the flap valve 22, thereby releasing the fastening hook 23 of the dosage lever 6.
(56) A double-dosing prevention mechanism is also provided with the design of the flap valve 22 of the second embodiment according to
(57) Dosage lever 6 includes a cam-like actuating element 33 which upon each actuation moves a counter slide 34 of the cartridge so that a counter ring 35 of the cartridge is moved by one count towards a lower dose. The degree of the cartridge's content is accordingly visible in a display window 36 of the cartridge body 3a indexing the fill status of the cartridge. Details of the counter slide 34 acting on the counter ring 35 may be taken from
(58) As this also can be taken from
(59) The counter slide 34 is moveable back and forth within a sliding channel 44 of the cartridge body 3a. The cam-like actuating element 33 of the dosage lever 6 extends into the sliding channel 44 and into a recess 45 of the horizontally extending part of the counter slide 34. Engagement of the actuating element 33 with the counter slide 34 transforms a pivoting movement of the actuating element 33 into a linear movement of the counter slide 34.
(60) Upon depression of the dosage key 5, the dosage lever will be pivoted such that the actuating element 33 is pivoted towards the left hand side in
(61) As this can be seen from
(62) The dosage key 5 is also freely moveable against the biasing force of the dosage key spring 17 as shown in
(63) The counter ring 35 includes a notch 41 being engageable by a tongue 42 of the locking lever 7.
(64) The notch is arranged on the counter ring 35 such that, after a pre-determined number of doses has been delivered, the locking lever 7 engages the notch in the counter ring with a pivoting movement caused by the action of spring leg 40 actuated by the dosage key 5. Upon upward movement of the locking lever 7, the blocking arm 39 of the locking lever 7 is pushed forward (towards the mouthpiece 10) and engages the dosage key 5 in its lowest position such that the dosage key 5 stays blocked in its lowest position after the last inhalation. It is impossible to perform another activation of the empty device.
(65) As this can be seen from
(66) Apart from the indexing means in the form of the counter ring, the device includes another inhalation control window 48 indexing whether the device is ready for inhalation or not. The inhalation control window shows for instance a green-colored flag in the event the device is ready for inhalation. This is because in the activated status of the inhaler 1a green colored tab 49 of the dosage lever 6 covers a red colored flag in the inhalation control window 48. The reset of the device from the inhalation position into the starting position takes place during inhalation by means of an airflow upon inhalation. Flap valve 22 is deflected thus releasing the dosage lever 6 as this has been described in detail before.
(67) In order to ensure leak tightness of the air duct 9, the shells 12 and 13 may be sealed against valve chamber 15 by means of one or more sealing ribs which extend around valve chamber 15. The sealing rib may be in form of a thermoplastic elastomer which has been co-injection molded with valve chamber 15. Alternatively, the sealing rib 52 may be designed as a resilient ring which has been mounted into a sealing groove during assembly of the inhaler.
(68) In a particularly preferred embodiment of the inhaler according to the invention, the shells 12 and 13 are sealed against the valve chamber by a labyrinth seal which completely extends around the valve chamber 15, so that the valve chamber 15 including the cyclone 16 and the powder groove 16a is effectively sealed against the dosing compartment of the inhaler. The labyrinth seal is provided by a sealing rib 52 completely extended around the valve chamber 15 and in the assembled state of the inhaler 1 engaging a corresponding sealing groove in the shells 12 and 13. This sealing assists in keeping the triggering forces for the flap valve 22 as reproducible as possible. The bandwidth for the required triggering forces normally corresponds to an air flow variation of 30 l/min for the suction to be applied by the patient. Sealing the valve chamber of the inhaler 1 against the shells 12, 13 remarkably reduces this variation in required air flow for triggering the flap valve 22. Accordingly, this design avoids the possibility of sucking an air flow through the inhaler which bypasses the powder channel and/or the air duct 9.
REFERENCE NUMERALS
(69) 1 inhaler 2 reservoir 3 cartridge 3a cartridge body 4 lid 5 dosage key 6 dosage lever 7 locking lever 8 dosage slide 9 air duct 10 mouthpiece 11 mouthpiece cap 12, 13 shells 14 cover 15 valve chamber 16 cyclone 16a powder groove 17 dosage key spring 18 dosage slide passage 19 dosage cavity 20 opening 21 opening 22 flap valve 22a flap 22b shaft of flap valve 22c first leg of flap valve 22d second leg of flap valve 22e third leg of flap valve 23 fastening hook 24 cut-out portion 25 dosage lever spring 26 tongue member 27 actuator blade 28 beveled edge 29 latch 30 mechanical stop 31 flap valve lever 32 spring of flap valve 33 actuating element 34 counter slide 35 counter ring 36 display window 37 teeth 38 locking ratchet 39 blocking arm 40 spring leg 41 notch 42 tongue 43 pawl 44 sliding channel 45 recess 46 leading end of dosage lever 47 latching rib 48 inhalation control window 49 tab 50 barbed projection 51 sloping face 52 sealing rib 53 deflector surface 53 deflector surface 54 bearing surface 55 actuation rib