WO2012004512A1 - Dry-powder inhaler - Google Patents

Dry-powder inhaler Download PDF

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Publication number
WO2012004512A1
WO2012004512A1 PCT/FR2011/051579 FR2011051579W WO2012004512A1 WO 2012004512 A1 WO2012004512 A1 WO 2012004512A1 FR 2011051579 W FR2011051579 W FR 2011051579W WO 2012004512 A1 WO2012004512 A1 WO 2012004512A1
Authority
WO
WIPO (PCT)
Prior art keywords
capsule
opening
inhaler
loading opening
cover
Prior art date
Application number
PCT/FR2011/051579
Other languages
French (fr)
Inventor
Arnaud Colomb
Zakaria Sallak
Original Assignee
Valois Sas
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
Application filed by Valois Sas filed Critical Valois Sas
Priority to BR112013000401-0A priority Critical patent/BR112013000401B1/en
Priority to CN201180041251.9A priority patent/CN103079617B/en
Publication of WO2012004512A1 publication Critical patent/WO2012004512A1/en

Links

Classifications

    • 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
    • A61M15/00Inhalators
    • A61M15/0028Inhalators using prepacked dosages, one for each application, e.g. capsules to be perforated or broken-up
    • 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
    • A61M15/00Inhalators
    • A61M15/0001Details of inhalators; Constructional features thereof
    • A61M15/0021Mouthpieces therefor
    • 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
    • A61M15/00Inhalators
    • A61M15/0001Details of inhalators; Constructional features thereof
    • A61M15/0021Mouthpieces therefor
    • A61M15/0025Mouthpieces therefor with caps
    • A61M15/0026Hinged caps
    • 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
    • A61M15/00Inhalators
    • A61M15/0028Inhalators using prepacked dosages, one for each application, e.g. capsules to be perforated or broken-up
    • A61M15/003Inhalators using prepacked dosages, one for each application, e.g. capsules to be perforated or broken-up using capsules, e.g. to be perforated or broken-up
    • 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
    • A61M15/00Inhalators
    • A61M15/0028Inhalators using prepacked dosages, one for each application, e.g. capsules to be perforated or broken-up
    • A61M15/003Inhalators using prepacked dosages, one for each application, e.g. capsules to be perforated or broken-up using capsules, e.g. to be perforated or broken-up
    • A61M15/0031Inhalators using prepacked dosages, one for each application, e.g. capsules to be perforated or broken-up using capsules, e.g. to be perforated or broken-up by bursting or breaking the package, i.e. without cutting or piercing
    • 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
    • A61M2202/00Special media to be introduced, removed or treated
    • A61M2202/06Solids
    • A61M2202/064Powder

Definitions

  • the present invention relates to a dry powder inhaler.
  • Inhalers are well known in the state of the art. There are different kinds.
  • a first type of inhaler contains a reservoir receiving a multitude of doses of powder, the inhaler being provided with dosing means allowing each actuation to separate a dose of this powder from the reservoir to bring it into an expulsion conduit to to be distributed to the user.
  • Another type of inhaler consists in arranging the doses of powder in pre-dosed individual reservoirs and then opening one of these reservoirs each time the inhaler is actuated. This implementation ensures a better seal of the powder, since each dose is open at the time of its expulsion.
  • various variants have already been proposed, such as an elongated blister strip or blisters arranged on a rotating circular disk.
  • the present invention aims to provide a dry powder inhaler, which does not reproduce the aforementioned drawbacks.
  • the present invention aims to provide such an inhaler that is simple and inexpensive to manufacture and assemble, reliable of use, and limiting as much as possible the risk of contamination and / or pollution.
  • the present invention therefore relates to a dry powder inhaler, comprising a body containing a dispersion chamber, a cap pivotally mounted on said body between a closed position and an open position, said cap having a dispensing orifice through which the user inhale, the inhaler further comprising a loading opening receiving a capsule containing a dose of dry powder to inhale, said capsule having an upper portion and a lower portion separable from said upper portion, said loading opening having at least one rib clamping device for tightly holding said upper part of the capsule inserted in said loading opening, before and during the opening of said cap, said cap comprising a pin which, at the end of closing of the cap, cooperates with said upper part of the capsule held tightly in said loading opening to push it into said dispersing chamber of the inhaler.
  • said loading opening comprises three clamping ribs regularly distributed around said loading opening.
  • a plate portion is fixed on said body, said plate portion having said loading opening.
  • FIG. 1 is an exploded schematic perspective view of a dispensing device according to an advantageous embodiment of the invention
  • FIG. 2 is a schematic cross-sectional view of the device of FIG. 1, in the closed position before the first use
  • FIG. 3 is a view similar to that of FIG. 2, in the open position, with a capsule loaded in the loading opening;
  • FIGS. 4 and 5 are views similar to that of FIG. 2, during closing of the cover and opening of the capsule,
  • FIG. 6 is a view similar to that of FIG. 2, in the closed position, before inhalation,
  • FIG. 7 is a view similar to that of FIG. 6, in the closed position, during inhalation,
  • FIG. 8 is a view similar to that of FIG. 3, in the open position
  • FIGS. 9 and 10 are diagrammatic perspective views of the device of FIG. 1, respectively in the closed and open position.
  • the inhaler 100 comprises a hollow body 1 and having an upper opening and a lower opening.
  • the upper opening is at least partially closed by a plate portion 120 fixed to said body and the lower opening is closed by a closure element, such as a hatch 150, pivotally mounted on said body 1 10.
  • a sliding member 140 provided with a toothing.
  • the plate portion 120 comprises guide means, such as rails 129, cooperating with projections 149 of the sliding member 140, to guide the translational movement of said sliding member.
  • a pivoting cover 130 is assembled above said plate portion 120.
  • This cover 130 includes the dispensing orifice 131, preferably formed at a mouthpiece around which the user will place his mouth to inhale.
  • the device according to this embodiment consists of five main parts, namely the body 1 10, the part of plate 120, the sliding member 140, the cover 130 and the hatch 150. All these elements are assembled on one another by means of an axis 160 passing through a lateral opening 1 15 provided in the body 1 10, to through appropriate lateral openings 135 of the cover 130 and through a hollow cylinder 155 formed in a portion of the hatch 150. At least one toothed element 161, 162 is mounted on said axis 160 to cooperate with at least one toothing 145 provided on the sliding member 140. In the example shown, there are two toothed elements 161 and 162 mounted on the axis 160, and thus the sliding member 140 also has two sets of teeth 145 and 146, the operation of which will be described below. .
  • An appropriate fastener namely the body 1 10, the part of plate 120, the sliding member 140, the cover 130 and the hatch 150. All these elements are assembled on one another by means of an axis 160 passing through a lateral opening 1 15 provided in the body 1 10,
  • the axis 160 may be provided to releasably fix said axis 160 on said body 1 10 by assembling the different constituent parts with each other.
  • the axis 160 preferably has a particular section, for example substantially square, and the toothed elements also comprise a similar section so that they are integral in rotation with the axis 160.
  • cover 130 also includes openings 135 of similar shape so that the cover, the toothed elements and said axis 160 are integral in rotation.
  • the plate portion 120 comprises a loading opening 121, advantageously provided with at least one, preferably three positioning ribs 125, advantageously evenly distributed around said loading opening 121. These ribs make it possible to position and hold tightly a capsule 10 in the desired position.
  • the capsules 10 comprise an upper part 1 1 and a lower part 12 separable from said upper part, said ribs 125 serve to maintain said upper part 1 1 before and during the separation of said lower part 12.
  • this part plate 120 also advantageously comprises a reservoir zone 122 formed by an area provided with a plurality of holes 123 for disposing one or more reserve capsule (s). This allows the user to always have several capsules available, for example when traveling. In this case, after each use of the device, it only has to use in this capsule tank for charging the next capsule into the loading opening 121. Of course, such a capsule reservoir is not essential to the operation of the device.
  • FIG. 2 to 8 illustrate a cycle of operation of the device according to this embodiment.
  • the body 1 10 defines inside a dispersion chamber January 1 which will be intended to receive the powder after opening the capsule 10.
  • FIG. 3 shows the device after opening the cover 130.
  • the opening of the cover 130 causes rotation of the axis 160 due to the cooperation of the approximately square shape of this axis 160 with the correspondingly shaped orifices. 135.
  • This rotation of the axis 160 thus also causes a rotation of the toothed elements 161 and 162 which rotate with said axis 160.
  • a rotation of these toothed elements 161, 162 causes a lateral translation of the sliding member 140.
  • FIG. 3 shows also a capsule 10 placed inside the loading opening 121. It can be seen that the upper part 1 1 of the capsule is tightly held in the ribs 125 provided in said loading opening 121. Furthermore, the lower part 12 of the capsule passes through a first opening 141 made in said sliding member 140 and which, in the open position of the cover 130, is opposite said loading opening 121.
  • FIGS. 4 to 6 illustrate the closing phase of the cover 130 after loading the capsule 10.
  • the hatch 150 will also close and the sliding member 140 will be brought to the left in the figures by the cooperation between the toothed elements 161 and 162 and the teeth of said sliding member 140.
  • the lower portion 12 of the capsule 10 passing through the first opening 141 of said sliding member 140 a lateral displacement of this sliding member will break the lower portion 12 of the capsule 10 as shown in Figure 4.
  • the upper part 1 1 of the capsule 10 is of course held tightly in the loading opening 121, in particular by the ribs 125.
  • Figure 7 illustrates the inhalation phase.
  • the user places his mouth around the dispensing orifice 131 of the cover 130 and sucks in the direction of the arrow B, shown in FIG. 7. In doing so, he creates a stream of air inside. of the dispersion chamber 1 1 1 which will swirl the two parts of the capsules 1 1 and 12 inside said dispersion chamber 1 1 1.
  • This swirling illustrated by the arrow C in Figure 7 will allow a total emptying of said capsule parts but also a good dispersion of the powder, and in particular a deagglomeration of any clumps of powder that may have formed.
  • additional air inlets may be provided in the dispersion chamber to promote swirling of the inhalation stream.
  • the cover 130 advantageously comprises a grid 137 through which the powder will be able to pass and be expelled in the direction of the dispensing orifice 131.
  • the grid prevents the capsule parts 11, 12 from being expelled from the dispersion chamber.
  • the user then inhales the dose of powder that was initially contained in the capsule 10.
  • said dispersion chamber may have a frustoconical shape narrowing towards the dispensing orifice 131, in particular to accelerate the inhalation flow by direction of said orifice.
  • the user opens the cover 130 again, which, as before, will tilt the hatch 150 at the end of opening.
  • This tipping of the hatch 150 illustrated in Figure 8 will allow to evacuate the two parts of the capsules 1 1 and 12 empty of the dispersion chamber 1 1 1.
  • the device is ready for next use.
  • the user can close the device and wait to reopen it the next time he needs it.
  • the user is not obliged to empty empty capsule parts after each inhalation but it can of course only do when the next opening of the device when it wants to load a new capsule.
  • the hatch 150 may include one or more pins (s) 156 which snaps (s) slightly into the bottom of the body 1 10 in the closed position, to ensure a secure closure and reliable hatch 150 in the closed position.
  • Figures 1 1 and 12 show openings 1 16 formed in the bottom of the body 1 10 through which said latching lugs 156 of the hatch will be able to pass.
  • this snap is not too strong not to hinder the opening of the hatch when the user opens the hood 130.
  • Figures 9 and 10 show perspective views of the device in closed and open positions
  • Figures 1 1 and 12 are views similar to Figures 9 and 10 but partially cut away, showing the internal structure of the device in these two positions.
  • the device of the invention is therefore particularly simple and clever. It consists of a small number of parts, so it is inexpensive to manufacture and assemble. Moreover, the presence of a dispersion chamber and parts of empty capsules that swirl allow to disagglomerate the powder and thus ensure a better distribution thereof to the user during inhalation. Finally, the evacuation of empty capsule parts does not require disassembly of the device which limits the risk of pollution thereof. The lack of disassembly of the device also avoids the risk of not being able to reassemble it, or to misplace the disassembled parts, especially in children or elderly people.
  • the manipulation of the device does not require manipulating the part forming the mouthpiece around the dispensing orifice 131.
  • a specific gripping portion for handling said cover is therefore also limited.
  • the method of use of the device is very simple, the user having to move the cover between its two end positions to fully operate the device. Thus, he first opens the hood, then he inserts a capsule, he closes the hood and inhales.

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  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Anesthesiology (AREA)
  • Biomedical Technology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Hematology (AREA)
  • Life Sciences & Earth Sciences (AREA)
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  • General Health & Medical Sciences (AREA)
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  • Veterinary Medicine (AREA)
  • Medical Preparation Storing Or Oral Administration Devices (AREA)

Abstract

The invention relates to a dry-powder inhaler (100) comprising a body (110) containing a dispersion chamber (111), and a lid (130) mounted on the body such that it can pivot between a closed position and an open position, said lid including a dispensing opening (131) through which the user inhales. The inhaler also comprises a loading opening (121) which can receive a capsule (10) containing a dose of dry powder to be inhaled, said capsule (10) comprising a top portion (11), and a bottom portion (12) which can be separated from the top portion. The above-mentioned loading opening (121) comprises at least one clamping rib (125) for clampingly holding the top portion (11) of the capsule (10) inserted into the loading opening (121) before and during the opening of said capsule (10). The lid (130) comprises a lug (135) which, when the lid (130) is completely closed, engages with the top portion (11) of the capsule that is clampingly held in the loading opening (121), in order to push same into the dispersion chamber (111) of the inhaler.

Description

Inhalateur de poudre sèche  Dry powder inhaler
La présente invention concerne un inhalateur de poudre sèche. The present invention relates to a dry powder inhaler.
Les inhalateurs sont bien connus dans l'état de la technique. Il en existe différentes sortes. Un premier type d'inhalateur contient un réservoir recevant une multitude de doses de poudre, l'inhalateur étant pourvu de moyens de dosage permettant à chaque actionnement de séparer une dose de cette poudre du réservoir pour l'amener dans un conduit d'expulsion afin d'être distribué à l'utilisateur. Un autre type d'inhalateur consiste à disposer les doses de poudre dans des réservoirs individuels prédosés, puis d'ouvrir un de ces réservoirs à chaque actionnement de l'inhalateur. Cette mise en œuvre assure une meilleure étanchéité de la poudre, puisque chaque dose n'est ouverte qu'au moment de son expulsion. Pour réaliser ces réservoirs individuels, diverses variantes ont déjà été proposées, telle qu'une bande de blisters allongée ou des blisters disposés sur un disque circulaire rotatif. Tous les types d'inhalateurs décrits ci-dessus et existants présentent des avantages et des inconvénients liés à leur structure et à leur fonctionnement. Ainsi, avec certains inhalateurs, se pose le problème de la précision et de la reproductibilité du dosage à chaque actionnement. De même, l'efficacité de la distribution, c'est-à-dire la partie de la dose qui pénètre effectivement dans les poumons de l'utilisateur pour avoir un effet thérapeutique bénéfique, est également un problème qui se présente avec un certain nombre d'inhalateurs. Concernant l'ouverture des réservoirs individuels, il a été proposé de peler ou décoller la couche de fermeture. Ceci présente l'inconvénient d'une maîtrise difficile des forces à appliquer pour garantir une ouverture totale sans risquer d'ouvrir le réservoir suivant, particulièrement si les moyens d'ouverture doivent être actionnés par l'inhalation. Un autre problème qui se pose avec les inhalateurs pourvus de bande de blisters est lié au déplacement de la bande, et au stockage de la partie utilisée de la bande. Ainsi, selon la longueur de la bande et/ou l'épaisseur des blisters, un espace important peut s'avérer nécessaire et tout blocage de la bande de blisters peut empêcher le bon fonctionnement de l'inhalateur. Par ailleurs, lorsque le dispositif d'avancée de la bande tire en même temps sur l'extrémité avant de la bande pour éviter un mauvais enroulement, il peut se poser un problème au fur et à mesure des actionnements en raison notamment du diamètre de la bande usée enroulée qui augmente progressivement. Les inhalateurs multidoses et les inhalateur contenant une bande de blisters sont donc généralement des dispositifs complexes, constituées d'un grand nombre de pièces, et donc coûteux à fabriquer et à assembler. Pour réaliser des dispositifs moins complexes et donc moins coûteux, il a été proposé des inhalateurs comportant des réservoirs individuels, tels que des capsules, qui sont à charger dans l'inhalateur juste avant l'utilisation de celui-ci. L'avantage de ces dispositifs est qu'il n'est pas nécessaire de stocker l'ensemble des doses à l'intérieur de l'appareil, de sorte que celui-ci peut être de dimension réduite. Par contre, l'utilisation est plus complexe, puisque l'utilisateur est obligé de charger une capsule dans l'inhalateur avant chaque utilisation. De plus, d'autres inconvénients spécifiques à ces inhalateurs à capsules sont apparus. Ainsi, ces dispositifs sont généralement constitués de deux pièces, l'une étant pourvue de l'embout buccal. Lors de la manipulation de ces dispositifs, pour ouvrir la capsule et libérer la poudre, ou pour vider la capsule vide après inhalation, les doigts de l'utilisateur entrent généralement en contact avec l'embout buccal, ce qui peut présenter des risques de contamination. De même, pour évacuer la capsule vide, le dispositif doit généralement être démonté, ce qui expose l'intérieur du dispositif à toute pollution extérieure, susceptible d'être par la suite transmise à l'utilisateur lors d'une future inhalation. Les documents WO 2009/091780, WO 91/19524 et US-4 206 758 décrivent des dispositifs de l'art antérieur. Inhalers are well known in the state of the art. There are different kinds. A first type of inhaler contains a reservoir receiving a multitude of doses of powder, the inhaler being provided with dosing means allowing each actuation to separate a dose of this powder from the reservoir to bring it into an expulsion conduit to to be distributed to the user. Another type of inhaler consists in arranging the doses of powder in pre-dosed individual reservoirs and then opening one of these reservoirs each time the inhaler is actuated. This implementation ensures a better seal of the powder, since each dose is open at the time of its expulsion. To make these individual tanks, various variants have already been proposed, such as an elongated blister strip or blisters arranged on a rotating circular disk. All types of inhalers described above and existing have advantages and disadvantages related to their structure and operation. Thus, with some inhalers, there is the problem of accuracy and reproducibility of the dosage at each actuation. Similarly, the effectiveness of the distribution, that is, the portion of the dose that actually enters the user's lungs to have a beneficial therapeutic effect, is also a problem with a number of inhalers. Regarding the opening of the individual tanks, it has been proposed to peel or peel off the closure layer. This has the disadvantage of difficult control of the forces to be applied to ensure full opening without the risk of opening the next tank, especially if the opening means must be actuated by inhalation. Another problem that arises with inhalers provided with blister band is related to the displacement of the band, and the storage of the used part of the band. Thus, depending on the length of the strip and / or the thickness of the blisters, a large space may be necessary and any blocking of the strip of blisters can prevent the proper functioning of the inhaler. Moreover, when the advancing device of the band pulls at the same time on the front end of the band to avoid a bad winding, it can be a problem as the actuations take place, in particular because of the diameter of the band. worn band wound up gradually. Multi-dose inhalers and inhaler containing a band of blisters are therefore generally complex devices, consisting of a large number of parts, and therefore expensive to manufacture and assemble. To achieve less complex and therefore less expensive devices, it has been proposed inhalers with individual reservoirs, such as capsules, to be loaded into the inhaler just before use thereof. The advantage of these devices is that it is not necessary to store all the doses inside the device, so that it can be reduced in size. By cons, the use is more complex, since the user is obliged to load a capsule in the inhaler before each use. In addition, other disadvantages specific to these capsule inhalers have appeared. Thus, these devices are generally made of two parts, one being provided with the mouthpiece. When handling these devices, to open the capsule and release the powder, or to empty the empty capsule after inhalation, the fingers of the user generally come into contact with the mouthpiece, which may present risks of contamination . Similarly, to evacuate the empty capsule, the device must generally be disassembled, which exposes the interior of the device to any external pollution, may subsequently be transmitted to the user during a future inhalation. WO 2009/091780, WO 91/19524 and US-4 206 758 disclose devices of the prior art.
La présente invention a pour but de fournir un inhalateur de poudre sèche, qui ne reproduit pas les inconvénients susmentionnés.  The present invention aims to provide a dry powder inhaler, which does not reproduce the aforementioned drawbacks.
En particulier, la présente invention a pour but de fournir un tel inhalateur qui soit simple et peu coûteux à fabriquer et à assembler, fiable d'utilisation, et limitant autant que possible les risques de contamination et/ou de pollution. In particular, the present invention aims to provide such an inhaler that is simple and inexpensive to manufacture and assemble, reliable of use, and limiting as much as possible the risk of contamination and / or pollution.
La présente invention a donc pour objet un inhalateur de poudre sèche, comportant un corps contenant une chambre de dispersion, un capot monté pivotant sur ledit corps entre une position fermée et une position ouverte, ledit capot comportant un orifice de distribution à travers lequel l'utilisateur inhale, l'inhalateur comportant en outre une ouverture de chargement recevant une capsule contenant une dose de poudre sèche à inhaler, ladite capsule comportant une partie supérieure et une partie inférieure séparable de ladite partie supérieure, ladite ouverture de chargement comportant au moins une nervure de serrage pour maintenir de manière serrante ladite partie supérieure de la capsule insérée dans ladite ouverture de chargement, avant et pendant l'ouverture de ladite capsule, ledit capot comportant un ergot qui, en fin de fermeture du capot, coopère avec ladite partie supérieure de la capsule maintenue serrée dans ladite ouverture de chargement pour la pousser dans ladite chambre de dispersion de l'inhalateur.  The present invention therefore relates to a dry powder inhaler, comprising a body containing a dispersion chamber, a cap pivotally mounted on said body between a closed position and an open position, said cap having a dispensing orifice through which the user inhale, the inhaler further comprising a loading opening receiving a capsule containing a dose of dry powder to inhale, said capsule having an upper portion and a lower portion separable from said upper portion, said loading opening having at least one rib clamping device for tightly holding said upper part of the capsule inserted in said loading opening, before and during the opening of said cap, said cap comprising a pin which, at the end of closing of the cap, cooperates with said upper part of the capsule held tightly in said loading opening to push it into said dispersing chamber of the inhaler.
Avantageusement, ladite ouverture de chargement comporte trois nervures de serrage réparties régulièrement autour de ladite ouverture de chargement.  Advantageously, said loading opening comprises three clamping ribs regularly distributed around said loading opening.
Avantageusement, une partie de plaque est fixée sur ledit corps, ladite partie de plaque comportant ladite ouverture de chargement.  Advantageously, a plate portion is fixed on said body, said plate portion having said loading opening.
Ces caractéristiques et avantages et d'autres de la présente invention apparaîtront plus clairement au cours de la description détaillée suivante, faite en référence aux dessins joints, donnés à titre d'exemples non limitatifs, sur lesquels  These and other features and advantages of the present invention will appear more clearly in the following detailed description, with reference to the accompanying drawings, given by way of non-limiting examples, in which:
- la figure 1 est une vue schématique éclatée en perspective d'un dispositif de distribution selon un mode de réalisation avantageux de l'invention,  FIG. 1 is an exploded schematic perspective view of a dispensing device according to an advantageous embodiment of the invention,
- la figure 2 est une vue schématique en section transversale du dispositif de la figure 1 , en position fermée avant la première utilisation, - la figure 3 est une vue similaire à celle de la figure 2, en position ouverte, avec une capsule chargée dans l'ouverture de chargement, FIG. 2 is a schematic cross-sectional view of the device of FIG. 1, in the closed position before the first use, FIG. 3 is a view similar to that of FIG. 2, in the open position, with a capsule loaded in the loading opening;
- les figures 4 et 5 sont des vues similaires à celle de la figure 2, en cours de fermeture du capot et d'ouverture de capsule,  FIGS. 4 and 5 are views similar to that of FIG. 2, during closing of the cover and opening of the capsule,
- la figure 6 est une vue similaire à celle de la figure 2, en position fermée, avant inhalation,  FIG. 6 is a view similar to that of FIG. 2, in the closed position, before inhalation,
- la figure 7 est une vue similaire à celle de la figure 6, en position fermée, en cours d'inhalation,  FIG. 7 is a view similar to that of FIG. 6, in the closed position, during inhalation,
- la figure 8 est une vue similaire à celle de la figure 3, en position ouverte,  FIG. 8 is a view similar to that of FIG. 3, in the open position,
- les figures 9 et 10 sont des vues schématiques en perspective du dispositif de la figure 1 , respectivement en position fermée et ouverte, et  FIGS. 9 and 10 are diagrammatic perspective views of the device of FIG. 1, respectively in the closed and open position, and
- les figures 1 1 et 12 sont des vues schématiques en perspective découpée, respectivement en position fermée et ouverte, - Figures 1 1 and 12 are schematic views in cut perspective, respectively in closed and open position,
Les figures décrivent un mode de réalisation avantageux de l'invention. Dans ce mode de réalisation, l'inhalateur 100 comporte un corps 1 10 creux et comportant une ouverture supérieure et une ouverture inférieure. L'ouverture supérieure est au moins partiellement fermée par une partie de plaque 120 fixée sur ledit corps et l'ouverture inférieure est fermée par un élément de fermeture, tel qu'une trappe 150, monté pivotant sur ledit corps 1 10. Sous la partie de plaque 120 est interposé un organe coulissant 140 pourvu d'une denture. Avantageusement, la partie de plaque 120 comporte des moyens de guidage, tels que des rails 129, coopérant avec des projections 149 de l'organe coulissant 140, pour guider le déplacement en translation dudit organe coulissant. Un capot pivotant 130 est assemblé au-dessus de ladite partie de plaque 120. Ce capot 130 comporte l'orifice de distribution 131 , formé de préférence au niveau d'un embout buccal autour duquel l'utilisateur placera sa bouche pour inhaler. Ainsi, comme visible notamment sur la figure 1 , le dispositif selon ce mode de réalisation est constitué de cinq parties principales, à savoir le corps 1 10, la partie de plaque 120, l'organe coulissant 140, le capot 130 et la trappe 150. Tous ces éléments sont assemblés les uns sur les autres au moyen d'un axe 160 passant à travers une ouverture latérale 1 15 prévue dans le corps 1 10, à travers des ouvertures latérales appropriées 135 du capot 130 et à travers un cylindre creux 155 ménagé dans une partie de la trappe 150. Au moins un élément denté 161 , 162 est monté sur ledit axe 160 pour coopérer avec au moins une denture 145 prévue sur l'organe coulissant 140. Dans l'exemple représenté, il y a deux éléments dentés 161 et 162 montés sur l'axe 160, et donc l'organe coulissant 140 comporte également deux dentures 145 et 146, dont le fonctionnement sera décrit ci-après. Un organe de fixation appropriéThe figures describe an advantageous embodiment of the invention. In this embodiment, the inhaler 100 comprises a hollow body 1 and having an upper opening and a lower opening. The upper opening is at least partially closed by a plate portion 120 fixed to said body and the lower opening is closed by a closure element, such as a hatch 150, pivotally mounted on said body 1 10. Under the part plate 120 is interposed a sliding member 140 provided with a toothing. Advantageously, the plate portion 120 comprises guide means, such as rails 129, cooperating with projections 149 of the sliding member 140, to guide the translational movement of said sliding member. A pivoting cover 130 is assembled above said plate portion 120. This cover 130 includes the dispensing orifice 131, preferably formed at a mouthpiece around which the user will place his mouth to inhale. Thus, as can be seen in particular in FIG. 1, the device according to this embodiment consists of five main parts, namely the body 1 10, the part of plate 120, the sliding member 140, the cover 130 and the hatch 150. All these elements are assembled on one another by means of an axis 160 passing through a lateral opening 1 15 provided in the body 1 10, to through appropriate lateral openings 135 of the cover 130 and through a hollow cylinder 155 formed in a portion of the hatch 150. At least one toothed element 161, 162 is mounted on said axis 160 to cooperate with at least one toothing 145 provided on the sliding member 140. In the example shown, there are two toothed elements 161 and 162 mounted on the axis 160, and thus the sliding member 140 also has two sets of teeth 145 and 146, the operation of which will be described below. . An appropriate fastener
163 peut être prévu pour fixer de manière indémontable ledit axe 160 sur ledit corps 1 10 en assemblant les différentes parties constitutives les unes avec les autres. Comme visible sur la figure 1 , l'axe 160 a de préférence une section particulière, par exemple sensiblement carrée, et les éléments dentés comportent également une section similaire de sorte qu'ils sont solidaires en rotation avec l'axe 160. De même le capot 130 comporte également des ouvertures 135 de forme similaire de sorte que le capot, les éléments dentés et ledit axe 160 sont solidaires en rotation. La partie de plaque 120 comporte une ouverture de chargement 121 , avantageusement pourvue d'au moins une, de préférence trois nervures de positionnement 125, avantageusement réparties régulièrement autour de ladite ouverture de chargement 121 . Ces nervures permettent de positionner et de maintenir de manière serrante une capsule 10 dans la position souhaitée. En particulier, les capsules 10 comportent une partie supérieure 1 1 et une partie inférieure 12 séparable de ladite partie supérieure, lesdites nervures 125 servent à maintenir ladite partie supérieure 1 1 avant et pendant la séparation de ladite partie inférieure 12. Par ailleurs, cette partie de plaque 120 comporte également avantageusement une zone de réservoir 122 formée par une zone pourvue d'une pluralité de trous 123 permettant de disposer une ou plusieurs capsule(s) de réserve. Ceci permet à l'utilisateur d'avoir toujours plusieurs capsules à disposition, par exemple lorsqu'il voyage. Dans cette hypothèse, après chaque utilisation du dispositif, il n'a plus qu'à se servir dans ce réservoir de capsule pour charger la prochaine capsule dans l'ouverture de chargement 121 . Bien entendu, un tel réservoir de capsules n'est pas indispensable au fonctionnement du dispositif. 163 may be provided to releasably fix said axis 160 on said body 1 10 by assembling the different constituent parts with each other. As can be seen in FIG. 1, the axis 160 preferably has a particular section, for example substantially square, and the toothed elements also comprise a similar section so that they are integral in rotation with the axis 160. cover 130 also includes openings 135 of similar shape so that the cover, the toothed elements and said axis 160 are integral in rotation. The plate portion 120 comprises a loading opening 121, advantageously provided with at least one, preferably three positioning ribs 125, advantageously evenly distributed around said loading opening 121. These ribs make it possible to position and hold tightly a capsule 10 in the desired position. In particular, the capsules 10 comprise an upper part 1 1 and a lower part 12 separable from said upper part, said ribs 125 serve to maintain said upper part 1 1 before and during the separation of said lower part 12. Moreover, this part plate 120 also advantageously comprises a reservoir zone 122 formed by an area provided with a plurality of holes 123 for disposing one or more reserve capsule (s). This allows the user to always have several capsules available, for example when traveling. In this case, after each use of the device, it only has to use in this capsule tank for charging the next capsule into the loading opening 121. Of course, such a capsule reservoir is not essential to the operation of the device.
Les figures 2 à 8 illustrent un cycle de fonctionnement du dispositif selon ce mode de réalisation. En référence à la figure 2, qui montre le dispositif en position fermée avant la première utilisation, on constate que le corps 1 10 définit à l'intérieur une chambre de dispersion 1 1 1 qui sera destinée à recevoir la poudre après ouverture de la capsule 10. La figure 3 montre le dispositif après ouverture du capot 130. On constate que l'ouverture du capot 130 provoque la rotation de l'axe 160 due à la coopération de la forme environ carrée de cet axe 160 avec les orifices de forme correspondante 135 dudit capot 130. Cette rotation de l'axe 160 provoque donc également une rotation des éléments dentés 161 et 162 qui tournent avec ledit axe 160. Une rotation de ces éléments dentés 161 , 162 provoque une translation latérale de l'organe coulissant 140. En effet, comme notamment représenté sur la figure 2, la denture 165 de l'élément denté 161 est engrenée dans la denture 145 de l'organe coulissant 140. Ainsi entre les figures 2 et 3, on constate que la rotation de la denture 165 de l'élément denté va faire coulisser l'organe coulissant 140 vers la droite sur les figures. Bien entendu, il se passe la même chose de l'autre côté du dispositif avec le second élément denté 162, non visible sur les figures en coupe. Bien entendu, un seul élément denté peut être suffisant pour provoquer le déplacement dudit organe coulissant. Lors de l'ouverture du capot 130, la trappe 150 ne tourne pas avec l'axe 160. Par contre, en fin d'ouverture du capot 130, celui-ci coopère avec ladite trappe 150, et notamment avec une partie courbe 151 reliant le cylindre creux 155, qui est monté sur l'axe 160, à la partie de la trappe qui obture le fond du corps 1 10 en position de fermeture de la trappe. Cette coopération entre le capot 130 et la trappe 150 fait basculer la trappe autour dudit axe 160 vers la position ouverte représentée sur la figure 3. Ainsi, dans cette position totalement ouverte du capot 130, la trappe 150 est ouverte et l'intérieur de la chambre de dispersion 1 1 1 peut être évacué hors du dispositif. La figure 3 montre également une capsule 10 mise en place à l'intérieur de l'ouverture de chargement 121 . On constate que la partie supérieure 1 1 de la capsule est maintenue de manière serrante dans les nervures 125 prévues dans ladite ouverture de chargement 121 . Par ailleurs, la partie inférieure 12 de la capsule passe à travers une première ouverture 141 réalisée dans ledit organe coulissant 140 et qui, dans la position ouverte du capot 130, se trouve en face de ladite ouverture de chargement 121 . Figures 2 to 8 illustrate a cycle of operation of the device according to this embodiment. Referring to Figure 2, which shows the device in the closed position before the first use, it is found that the body 1 10 defines inside a dispersion chamber January 1 which will be intended to receive the powder after opening the capsule 10. FIG. 3 shows the device after opening the cover 130. It can be seen that the opening of the cover 130 causes rotation of the axis 160 due to the cooperation of the approximately square shape of this axis 160 with the correspondingly shaped orifices. 135. This rotation of the axis 160 thus also causes a rotation of the toothed elements 161 and 162 which rotate with said axis 160. A rotation of these toothed elements 161, 162 causes a lateral translation of the sliding member 140. Indeed, as shown in particular in Figure 2, the toothing 165 of the toothed element 161 is engaged in the toothing 145 of the sliding member 140. Thus between Figures 2 and 3, it is found that the rotati one of the teeth 165 of the toothed element will slide the sliding member 140 to the right in the figures. Of course, the same happens on the other side of the device with the second toothed element 162, not visible in the sectional figures. Of course, a single toothed element may be sufficient to cause the displacement of said sliding member. When opening the cover 130, the hatch 150 does not rotate with the axis 160. On the other hand, at the end of the opening of the cover 130, it cooperates with said hatch 150, and in particular with a curved portion 151 connecting the hollow cylinder 155, which is mounted on the axis 160, to the part of the hatch which closes the bottom of the body 1 10 in the closed position of the hatch. This cooperation between the cover 130 and the hatch 150 tilts the hatch about said axis 160 to the open position shown in Figure 3. Thus, in this fully open position of the cover 130, the hatch 150 is open and the inside of the 1 1 1 dispersion chamber can be evacuated out of the device. Figure 3 shows also a capsule 10 placed inside the loading opening 121. It can be seen that the upper part 1 1 of the capsule is tightly held in the ribs 125 provided in said loading opening 121. Furthermore, the lower part 12 of the capsule passes through a first opening 141 made in said sliding member 140 and which, in the open position of the cover 130, is opposite said loading opening 121.
Les figures 4 à 6 illustrent la phase de fermeture du capot 130 après chargement de la capsule 10. Ainsi, comme visible sur la figure 4, lorsque l'utilisateur referme le capot 130, la trappe 150 va également se refermer et l'organe coulissant 140 va être ramené vers la gauche sur les figures par la coopération entre les éléments dentés 161 et 162 et les dentures dudit organe coulissant 140. Or, la partie inférieure 12 de la capsule 10 passant à travers la première ouverture 141 dudit organe coulissant 140, un déplacement latéral de cet organe coulissant va casser la partie inférieure 12 de la capsule 10 comme illustré sur la figure 4. La partie supérieure 1 1 de la capsule 10 reste bien entendu maintenue de manière serrante dans l'ouverture de chargement 121 , notamment par les nervures 125. Par contre, la partie inférieure 12 va tomber dans la chambre de dispersion 1 1 1 , puisque le premier orifice 141 dudit organe coulissant 140 a un diamètre plus large que le diamètre externe de ladite partie inférieure 12 de la capsule. Ainsi, non seulement la poudre va se vider à l'intérieur de la chambre de dispersion 1 1 1 , mais la partie inférieure 12 contenant ladite poudre va tomber sur le fond de ladite chambre de dispersion 1 1 1 , pour permettre un vidage de celle- ci. Dans la position de figure 5, on constate que le capot 130 arrive juste avant sa position de fermeture. Dans cette position, un ergot 135 prévu dans ladite partie de capot 130 va coopérer avec la partie supérieure 1 1 de la capsule 10 qui est restée dans l'ouverture de chargement 121 . Ainsi, et comme clairement illustré sur les figures 5 et 6, lors de la fermeture totale du capot 130, l'ergot 135 va provoquer l'expulsion de la partie supérieure 1 1 de la capsule depuis l'ouverture de chargement 121 vers l'intérieur de la chambre de dispersion 1 1 1 . Dans cette position de la figure 6, où le dispositif est à nouveau complètement fermé, la capsule 10 a donc été cassée en deux, les deux parties supérieure 1 1 et inférieure 12 de la capsule 10 reposant dans la chambre de dispersion 1 1 1 sur le fond (formé par la trappe 150) et avec la poudre au moins partiellement expulsée hors desdites parties de capsules. Le dispositif est alors prêt pour l'inhalation. FIGS. 4 to 6 illustrate the closing phase of the cover 130 after loading the capsule 10. Thus, as can be seen in FIG. 4, when the user closes the cover 130, the hatch 150 will also close and the sliding member 140 will be brought to the left in the figures by the cooperation between the toothed elements 161 and 162 and the teeth of said sliding member 140. Now, the lower portion 12 of the capsule 10 passing through the first opening 141 of said sliding member 140, a lateral displacement of this sliding member will break the lower portion 12 of the capsule 10 as shown in Figure 4. The upper part 1 1 of the capsule 10 is of course held tightly in the loading opening 121, in particular by the ribs 125. On the other hand, the lower part 12 will fall into the dispersion chamber 1 1 1, since the first orifice 141 of said sliding member 140 has a larger diameter than the di external ameter of said lower portion 12 of the capsule. Thus, not only will the powder be emptied inside the dispersion chamber 1 1 1, but the lower part 12 containing said powder will fall on the bottom of said dispersion chamber January 1, to allow emptying of the - this. In the position of Figure 5, we see that the hood 130 just before its closed position. In this position, a lug 135 provided in said hood portion 130 will cooperate with the upper part 1 1 of the capsule 10 which has remained in the loading opening 121. Thus, and as clearly illustrated in Figures 5 and 6, during the total closure of the cover 130, the pin 135 will cause the expulsion of the upper part 1 1 of the capsule from the loading opening 121 to the inside the dispersion chamber 1 1 1. In this position of Figure 6, where the device is again completely closed, the capsule 10 has been broken in two, the two upper parts 1 1 and lower 12 of the capsule 10 resting in the dispersion chamber 1 1 1 on the bottom (formed by the hatch 150) and with the powder at least partially expelled from said capsule parts. The device is then ready for inhalation.
La figure 7 illustre la phase d'inhalation. Pour inhaler, l'utilisateur place sa bouche autour de l'orifice de distribution 131 du capot 130 et aspire dans le sens de la flèche B, représenté sur la figure 7. Ce faisant, il crée un courant d'air à l'intérieur de la chambre de dispersion 1 1 1 qui va faire tourbillonner les deux parties de capsules 1 1 et 12 à l'intérieur de ladite chambre de dispersion 1 1 1 . Ce tourbillonnement illustré par la flèche C sur la figure 7 va permettre un vidage total desdites parties de capsules mais également une bonne dispersion de la poudre, et notamment une désagglomération des éventuels amas de poudre qui auraient pu se former. Eventuellement, des entrées d'air supplémentaires peuvent être prévues dans la chambre de dispersion pour favoriser le tourbillonnement du flux d'inhalation. La poudre qui tourbillonne va alors être expulsée hors de la chambre de dispersion 1 1 1 par le flux d'inhalation à travers une seconde ouverture 142 prévue dans l'organe coulissant 140 et qui, dans cette position d'inhalation, se trouve face d'une part à la chambre de dispersion 1 1 1 et d'autre part à l'ouverture de chargement 121 . Comme visible plus clairement sur la figure 1 1 , le capot 130 comporte avantageusement une grille 137 à travers laquelle la poudre va pouvoir passer et être expulsée en direction de l'orifice de distribution 131 . La grille évite notamment que les parties de capsules 1 1 , 12 ne soient également expulsées hors de la chambre de dispersion. L'utilisateur inhale alors la dose de poudre qui était initialement contenue dans la capsule 10. Avantageusement, ladite chambre de dispersion peut avoir une forme tronconique se rétrécissant en direction de l'orifice de distribution 131 , pour notamment accélérer le flux d'inhalation en direction dudit orifice.  Figure 7 illustrates the inhalation phase. To inhale, the user places his mouth around the dispensing orifice 131 of the cover 130 and sucks in the direction of the arrow B, shown in FIG. 7. In doing so, he creates a stream of air inside. of the dispersion chamber 1 1 1 which will swirl the two parts of the capsules 1 1 and 12 inside said dispersion chamber 1 1 1. This swirling illustrated by the arrow C in Figure 7 will allow a total emptying of said capsule parts but also a good dispersion of the powder, and in particular a deagglomeration of any clumps of powder that may have formed. Optionally, additional air inlets may be provided in the dispersion chamber to promote swirling of the inhalation stream. The swirling powder will then be expelled out of the dispersion chamber 11 by the inhalation flow through a second opening 142 provided in the sliding member 140 and which, in this inhalation position, is facing the 1 part to the dispersion chamber 1 1 1 and secondly to the loading opening 121. As can be seen more clearly in FIG. 11, the cover 130 advantageously comprises a grid 137 through which the powder will be able to pass and be expelled in the direction of the dispensing orifice 131. In particular, the grid prevents the capsule parts 11, 12 from being expelled from the dispersion chamber. The user then inhales the dose of powder that was initially contained in the capsule 10. Advantageously, said dispersion chamber may have a frustoconical shape narrowing towards the dispensing orifice 131, in particular to accelerate the inhalation flow by direction of said orifice.
Après inhalation, l'utilisateur ouvre à nouveau le capot 130 ce qui, comme précédemment, va faire basculer la trappe 150 en fin d'ouverture. Ce basculement de la trappe 150 illustré sur la figure 8, va permettre d'évacuer les deux parties de capsules 1 1 et 12 vides de la chambre de dispersion 1 1 1 . Dans cette position de la figure 8, le dispositif est donc prêt pour une prochaine utilisation. Bien entendu, si cette prochaine utilisation n'est pas immédiate, l'utilisateur peut refermer le dispositif et attendre de le rouvrir la prochaine fois qu'il en a besoin. En variante, l'utilisateur n'est pas obligé de vider les parties de capsules vides après chaque inhalation mais il peut bien entendu le faire seulement lors de la prochaine ouverture du dispositif lorsqu'il veut charger une nouvelle capsule. After inhalation, the user opens the cover 130 again, which, as before, will tilt the hatch 150 at the end of opening. This tipping of the hatch 150 illustrated in Figure 8, will allow to evacuate the two parts of the capsules 1 1 and 12 empty of the dispersion chamber 1 1 1. In this position of Figure 8, the device is ready for next use. Of course, if this next use is not immediate, the user can close the device and wait to reopen it the next time he needs it. Alternatively, the user is not obliged to empty empty capsule parts after each inhalation but it can of course only do when the next opening of the device when it wants to load a new capsule.
Avantageusement, comme illustré notamment sur la figure 1 , la trappe 150 peut comporter un ou plusieurs ergot(s) de fixation 156 qui s'encliquète(nt) légèrement dans le fond du corps 1 10 en position de fermeture, pour garantir une fermeture sûre et fiable de la trappe 150 en position fermée. Les figures 1 1 et 12 montrent des ouvertures 1 16 ménagées dans le fond du corps 1 10 à travers lesquelles lesdits ergots d'encliquetage 156 de la trappe vont pouvoir passer. Bien entendu, cet encliquetage n'est pas trop fort pour ne pas gêner l'ouverture de la trappe lorsque l'utilisateur ouvre le capot 130.  Advantageously, as illustrated in particular in Figure 1, the hatch 150 may include one or more pins (s) 156 which snaps (s) slightly into the bottom of the body 1 10 in the closed position, to ensure a secure closure and reliable hatch 150 in the closed position. Figures 1 1 and 12 show openings 1 16 formed in the bottom of the body 1 10 through which said latching lugs 156 of the hatch will be able to pass. Of course, this snap is not too strong not to hinder the opening of the hatch when the user opens the hood 130.
Les figures 9 et 10 montrent des vues en perspective du dispositif en positions fermée et ouverte, et les figures 1 1 et 12 sont des vues similaires aux figures 9 et 10 mais partiellement découpées, montrant la structure interne du dispositif dans ces deux positions.  Figures 9 and 10 show perspective views of the device in closed and open positions, and Figures 1 1 and 12 are views similar to Figures 9 and 10 but partially cut away, showing the internal structure of the device in these two positions.
Le dispositif de l'invention est donc particulièrement simple et astucieux. Il est constitué d'un faible nombre de pièces, il est donc peu coûteux à fabriquer et à assembler. Par ailleurs, la présence d'une chambre de dispersion et des parties de capsules vides qui tourbillonnent permettent de désagglomérer la poudre et garantissent donc une meilleure distribution de celle-ci à l'utilisateur lors de l'inhalation. Enfin, l'évacuation des parties de capsules vides ne nécessite pas un démontage du dispositif ce qui limite les risques de pollution de celui-ci. L'absence de démontage du dispositif évite aussi les risques de ne plus pouvoir le remonter, ou d'égarer les parties démontées, notamment chez des enfants ou des personnes âgées. De plus, la manipulation du dispositif, c'est-à-dire l'ouverture et la fermeture du capot 130, n'impose pas de manipuler la partie formant l'embout buccal autour de l'orifice de distribution 131 . Eventuellement, on pourrait envisager une partie de préhension spécifique pour la manipulation dudit capot. Les risques de contamination au niveau de l'orifice de distribution 131 sont donc également limités. Le procédé d'utilisation du dispositif est donc très simple, l'utilisateur n'ayant qu'à déplacer le capot entre ses deux positions d'extrémité pour complètement actionner le dispositif. Ainsi, il ouvre d'abord le capot, puis il insère une capsule, il referme le capot et il inhale. The device of the invention is therefore particularly simple and clever. It consists of a small number of parts, so it is inexpensive to manufacture and assemble. Moreover, the presence of a dispersion chamber and parts of empty capsules that swirl allow to disagglomerate the powder and thus ensure a better distribution thereof to the user during inhalation. Finally, the evacuation of empty capsule parts does not require disassembly of the device which limits the risk of pollution thereof. The lack of disassembly of the device also avoids the risk of not being able to reassemble it, or to misplace the disassembled parts, especially in children or elderly people. Moreover, the manipulation of the device, that is to say the opening and closing of the cover 130, does not require manipulating the part forming the mouthpiece around the dispensing orifice 131. Optionally, one could consider a specific gripping portion for handling said cover. The risk of contamination at the dispensing orifice 131 is therefore also limited. The method of use of the device is very simple, the user having to move the cover between its two end positions to fully operate the device. Thus, he first opens the hood, then he inserts a capsule, he closes the hood and inhales.
Diverses modifications sont également possibles pour un homme du métier sans sortir du cadre de la présente invention tel que défini par les revendications annexées. En particulier, les diverses caractéristiques et fonctionnalités du dispositif décrites en référence aux dessins peuvent être combinées entre elles d'une quelconque façon appropriée.  Various modifications are also possible for a person skilled in the art without departing from the scope of the present invention as defined by the appended claims. In particular, the various features and functionality of the device described with reference to the drawings may be combined with each other in any suitable manner.

Claims

Revendications claims
1 . - Inhalateur de poudre sèche (100), comportant un corps (1 10) contenant une chambre de dispersion (1 1 1 ), un capot (130) monté pivotant sur ledit corps entre une position fermée et une position ouverte, ledit capot comportant un orifice de distribution (131 ) à travers lequel l'utilisateur inhale, l'inhalateur comportant en outre une ouverture de chargement (121 ) recevant une capsule (10) contenant une dose de poudre sèche à inhaler, ladite capsule (10) comportant une partie supérieur (1 1 ) et une partie inférieure (12) séparable de ladite partie supérieure, caractérisé en ce que ladite ouverture de chargement (121 ) comporte au moins une nervure de serrage (125) pour maintenir de manière serrante ladite partie supérieure (1 1 ) de la capsule (10) insérée dans ladite ouverture de chargement (121 ), avant et pendant l'ouverture de ladite capsule (10), ledit capot (130) comportant un ergot (135) qui, en fin de fermeture du capot (130), coopère avec ladite partie supérieure (1 1 ) de la capsule maintenue serrée dans ladite ouverture de chargement (121 ) pour la pousser dans ladite chambre de dispersion (1 1 1 ) de l'inhalateur. 1. - Dry powder inhaler (100), comprising a body (1 10) containing a dispersion chamber (1 1 1), a cover (130) pivotally mounted on said body between a closed position and an open position, said cover comprising a dispensing orifice (131) through which the user inhales, the inhaler further comprising a loading opening (121) receiving a capsule (10) containing a dose of dry powder to be inhaled, said capsule (10) having a portion upper (1 1) and a lower part (12) separable from said upper part, characterized in that said loading opening (121) comprises at least one clamping rib (125) for tightly holding said upper part (1 1 ) of the capsule (10) inserted in said loading aperture (121), before and during the opening of said capsule (10), said cap (130) comprising a pin (135) which, at the end of closing of the cap ( 130), cooperates with said sup the upper (1 1) of the capsule held tightly in said loading opening (121) to push it into said dispersing chamber (1 1 1) of the inhaler.
2. - Inhalateur selon la revendication 1 , dans lequel ladite ouverture de chargement (121 ) comporte trois nervures de serrage (125) réparties régulièrement autour de ladite ouverture de chargement (121 ). The inhaler according to claim 1, wherein said loading opening (121) has three clamping ribs (125) evenly distributed around said loading opening (121).
3. - Inhalateur selon l'une quelconque des revendications précédentes, dans lequel une partie de plaque (120) est fixée sur ledit corps, ladite partie de plaque (120) comportant ladite ouverture de chargement (121 ). An inhaler according to any one of the preceding claims, wherein a plate portion (120) is attached to said body, said plate portion (120) having said loading opening (121).
PCT/FR2011/051579 2010-07-07 2011-07-05 Dry-powder inhaler WO2012004512A1 (en)

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BR112013000401-0A BR112013000401B1 (en) 2010-07-07 2011-07-05 dry powder inhaler
CN201180041251.9A CN103079617B (en) 2010-07-07 2011-07-05 Dry-powder inhaler

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FR1055528A FR2962337B1 (en) 2010-07-07 2010-07-07 DRY POWDER INHALER.
FR1055528 2010-07-07

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EP3135331A1 (en) * 2012-10-02 2017-03-01 CMS Di Colosio Mauro Inhaler device
US10099021B2 (en) 2012-10-02 2018-10-16 Cms Di Colosio Mauro Inhaler device
USD852408S1 (en) 2016-02-08 2019-06-25 Nicoventures Holdings Limited Electronic cigarette
US11123501B2 (en) 2016-03-24 2021-09-21 Nicoventures Holdings Limited Electronic vapor provision system
US11213638B2 (en) 2016-03-24 2022-01-04 Nicoventures Trading Limited Vapor provision system
US11241043B2 (en) 2016-03-24 2022-02-08 Nicoventures Trading Limited Vapor provision apparatus
US11452826B2 (en) 2016-03-24 2022-09-27 Nicoventures Trading Limited Mechanical connector for electronic vapor provision system
US11524823B2 (en) 2016-07-22 2022-12-13 Nicoventures Trading Limited Case for a vapor provision device

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FR2962337A1 (en) 2012-01-13
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BR112013000401B1 (en) 2021-05-04
CN103079617B (en) 2014-10-29
CN103079617A (en) 2013-05-01

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