CA2136679A1 - Device for inhalation - Google Patents
Device for inhalationInfo
- Publication number
- CA2136679A1 CA2136679A1 CA002136679A CA2136679A CA2136679A1 CA 2136679 A1 CA2136679 A1 CA 2136679A1 CA 002136679 A CA002136679 A CA 002136679A CA 2136679 A CA2136679 A CA 2136679A CA 2136679 A1 CA2136679 A1 CA 2136679A1
- Authority
- CA
- Canada
- Prior art keywords
- chamber
- terized
- charac
- air inlet
- channel
- Prior art date
- Legal status (The legal status 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 status listed.)
- Abandoned
Links
- 239000003814 drug Substances 0.000 claims abstract description 35
- 229940079593 drug Drugs 0.000 claims abstract description 34
- 239000000126 substance Substances 0.000 claims abstract description 4
- 230000001681 protective effect Effects 0.000 claims description 15
- 230000007246 mechanism Effects 0.000 claims description 8
- 239000002274 desiccant Substances 0.000 claims description 7
- 230000004888 barrier function Effects 0.000 claims description 6
- 230000015572 biosynthetic process Effects 0.000 claims description 5
- 210000002105 tongue Anatomy 0.000 claims description 5
- IHQKEDIOMGYHEB-UHFFFAOYSA-M sodium dimethylarsinate Chemical class [Na+].C[As](C)([O-])=O IHQKEDIOMGYHEB-UHFFFAOYSA-M 0.000 claims description 4
- 238000000034 method Methods 0.000 abstract description 4
- 239000000843 powder Substances 0.000 description 15
- 210000003811 finger Anatomy 0.000 description 10
- 230000000694 effects Effects 0.000 description 7
- 239000002245 particle Substances 0.000 description 7
- 238000010276 construction Methods 0.000 description 6
- 238000005516 engineering process Methods 0.000 description 4
- 230000033001 locomotion Effects 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 230000036961 partial effect Effects 0.000 description 4
- 230000002829 reductive effect Effects 0.000 description 4
- 230000008901 benefit Effects 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000007664 blowing Methods 0.000 description 2
- 239000002775 capsule Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 238000000926 separation method Methods 0.000 description 2
- 230000001133 acceleration Effects 0.000 description 1
- 238000009825 accumulation Methods 0.000 description 1
- 239000013543 active substance Substances 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 238000005054 agglomeration Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 230000001174 ascending effect Effects 0.000 description 1
- 210000003323 beak Anatomy 0.000 description 1
- 210000000621 bronchi Anatomy 0.000 description 1
- 150000001768 cations Chemical class 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000007599 discharging Methods 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000013583 drug formulation Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000000265 homogenisation Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 210000004072 lung Anatomy 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 230000001007 puffing effect Effects 0.000 description 1
- 230000000241 respiratory effect Effects 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 210000003813 thumb Anatomy 0.000 description 1
- 238000011144 upstream manufacturing Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES 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
- A61M15/00—Inhalators
- A61M15/0065—Inhalators with dosage or measuring devices
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES 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
- A61M2202/00—Special media to be introduced, removed or treated
- A61M2202/06—Solids
- A61M2202/064—Powder
Abstract
The device for inhalation of a powdery, pharmacologically active drug consists of a supply container (3) for the drug (4), a manually actuated metering unit for providing a portioned-off quantity of inhalation substance which is picked up by the air current drawn in during inhalation and is swirled, an air inlet channel (9), a swirl chamber (W), and a connection channel (8) between the swirl chamber (W) and the metering unit, as well as a mouth-piece channel issuing from the swirl chamber (W). The metering unit here consists of a metering drum (D) which has, in its interior (5), a supply container (3) for the drug. Furthermore, the air inlet channel (9) and the connection channel (8) are arranged in such a way that they run towards each other in a V-shape. During a metering procedure, a portioned-off quantity of drug for inhalation present in the shape of a dome is provided in each case at the apex of the two air channels (8) and (9) running towards each other in a V-shape.
(Fig. 1)
(Fig. 1)
Description
~13667~
DEVICE FOR INHALATION
The invention relates to a device for inhalation of a powdery, pharmacologically active drug, consisting of a supply container for the drug, a manually actuated metering unit for providing a portioned-off quantity of inhalation substance which is picked up by the air current drawn in during inhalation and is swirled, an air inlet channel, a swirl chPmher, and a connection channel between the swirl chamber and the metering unit, as well as a mouthpiece channel issuing from the swirl chPmher.
A device of this type is known from DE-OS (German Published Specification) 4 004 904. The drug supply is kept ready there at the periphery of the metering drum and is readjusted radially. The interior of the metering drum contains a control device for active discharge of the portioned-off inhalation quantity of drug from radially outwardly directed, open metering recesses. For this purpose, slides forming the base of the metering recesses, which are arranged distributed at uniform angles, are centrally cam-controlled. The outlay in this regard is considerable, especially since the control mechanism is released by an actuation key taking up almost the whole of one longitudinal side of the device.
Air inlet channel and connection channel run at an obtuse angle and tangent to the metering drum, this air course continuing via a swirl chamber, formed as a secondary cavity, essentially straight as far as the other end of the device. The drug transfer point lies near the open intake end and the substance can easily fall out there unused. In addition, the metered inhalation quantities of drug can add up as a result of the forced emptying of the metering recess; this can therefore lead to a dangerous overdose. In terms of volume, only a fraction of the Le A 30 002-Foreiqn Countries - 1 -213~79 device designed in pocket format remains for holding asupply. The method of handling is not clear.
The object of the invention is to design a device of the generic type which, being of simplified construction, is more advantageous and safer to use, in particular also to improve the device in terms of flow technology, and to keep the effect constant by means of complete discharge of the portioned-off inhalation quantity of drug.
This object is achieved by the invention specified in Claim 1.
The claims subsequent thereto present further advantageous embodiments of the device according to the in~ention.
As a result of such an embodiment, a device of the generic type is obtained which is of simplified construction and of improved usefulness and safety. The mechanical outlay is greatly reduced. No coordination between press button movement and inhalation is needed.
The quantity is brought into the position ready for dispensing without any rush. The user can concentrate on inhaling the active substance. The inhaler is designed in concrete terms such that the metering device consists of a metering drum, the supply container for the drug being arranged in the interior of the metering drum, and that the air inlet channel and the connection chAnnel run towards each other in a V-shape and towards a portioned-off quantity of drug present in the shape of a dome and provided by the metering drum at the apex of the two air channels. The interior of the metering drum is now used for forming a supply. Its content is kept in motion. It comes by the shortest route into the position ready for dispensing. Discharging with no residues remaining behind takes place there. As a result of the stated orientation Le A 30 002-Foreiqn Countries - 2 -21~6b79 - and sequence of the operational areas, it is not possible for any particles to fall back. The suction stream impacts first on the V apex and flows into the exactly positioned and portioned-off, exposed heap of the drug.
The zone presented in a dome-shape is quickly carried off, swirled and dispersed and, upon inhalation, reaches the target site. The drug is sucked counter to the effect of gravity. Incorrect holding is practically ruled out since the position of the metering drum suggests the correct handling, and it is readily apparent to the user that the mouthpiece channel situated at the other, upper, end is the transfer bridge. In addition, a potential for an overdose cannot build up; a non-inhaled inhalation quantity disappears in the direction of the supply. It is not added to by the next indexing step. An advantage in terms of flow technology proves to be the fact that the connection channel runs radially with respect to the metering drum. It is thus optimally suited to its function as acceleration channel with increasing abate-ment towards the top. In order to create a sufficiently large transfer area to the swirl ch~mher, which acts as a dwell-time chamber on the access side, the inhaler is advantageously designed such that the connection channel widens towards the swirl chamber, and the trace line of the one wall lies essentially radially with respect to the centre of the swirl chamber, and that of the other wall runs essentially tangentially thereto. This leads to a flow which promotes swirling and which defines the direction of rotation. As regards the outlet mouthpiece channel, the construction in this case is chosen such that the mouthpiece channel runs at an obtuse angle with respect to the connection channel, and the trace line of the one wall is aligned approximately tangentially, and that of the other wall approximately radially, with respect to the centre of the swirl chamber. A continuous cross-sectional widening (also in the transverse width) is also expediently made use of in this respect (realiz-Le A 30 002-Foreiqn Countries - 3 -213~679 ation of the diffusor effect sought). As regards the design of the air inlet channel, the procedure in this case is that the trace line of the inner wall and the trace line of the outer wall of the air inlet channel are aligned in secant formation with respect to the metering chamber. Suction opening and air outlet opening of the device are thus at a sufficient spatial distance from each other. As regards the design of the metering drum, this is continued such that it has a rotary sleeve equipped with portion apertures. The portion apertures arranged in a uniform angular distribution dip into the powder supply on account of the mixing-drum-like rotation of the metering drum, without causing pressing etc. The metering is correct in terms of volume, including the penultimate portion and, if appropriate, the final portion. Also, on account of the use of the drum move-ment, there is no agglomeration of the drug. It is further proposed that the rotary sleeve is formed by the circumferential wall of a pot, the base of which forms a rotary purchase. The correspondingly outwardly accessible rotary grip is extremely easy to use and direct. In order to obtain a defined position of the dome, that is to say of the metered quantity of the portioned-off drug, a catch mechanism deter~ining the direction of rotation is allocated to the device between rotary sleeve and housing. As regards the rotary bearing of the metering drum and the obtainment of constantly uniform inhalation quantities of drug, it proves advantageous that the rotary sleeve enclosed by an outer wall is underpinned, over a partial angle area, by an inner wall section which, in the area of the V apex, forms the base of the portion ch~mher formed by in each case one of the aper-tures. In this context it is additionally advantageous that the transverse walls of the apertures run in a wedge formation to the centre of the metering drum. This leads, as regards the transverse walls, to a convexly curved, trapezoidal trough as portion chamber which widens at the Le A 30 002-Foreiqn Countries - 4 -V apex side, in other words towards the top. A further development of the invention lies in the fact that, issuing from the base of the pot and/or the housing, loosening fingers protrude into the metering drum. They form a type of stirrer which, operating actively or statically, optimizes the loosening of the powdery drug (formulation). In order to eliminate the moisture which cannot be completely prevented, the base of the pot or the inner side of a housing-filling lid is allocated a drying agent chamber, which would be equipped as approp-riate. Such a filling lid can be formed at the same time as a viewing glass. A good suction effect is achieved by arranging transversely directed air inlet slots at the intake end of the air inlet channel. The suction opening is thus prevented from being blocked, for example by loosely carried coins, etc. The grid-like design of the air inlet is also useful to the extent that no foreign particles, such as dust etc., can be sucked in. Such air inlet slots are expediently provided on both broad sides of the device housing. They lie in such a way that, when the inhaler is being handled, they cannot easily be closed over; in any case one or the other side remains open. The device is further characterized by a dividing gusset for the path of the air sucked in. Thus, a Y-channel is formed in practice on the suction side. In theevent of incorrect use (blowing instead of sucking), in order to prevent the discharge of the powdery drug, the air inlet slots are allocated exhalation barrier tongues.
Thus, on puffing, no respiratory air moisture reaches into the inside of the inhaler device, which is to be kept as completely dry as possible. These can be simple valve flaps. The abovementioned dividing gusset can be used for fitting them, as is explained in the relevant part of the description. For correct handling it is thus expedient for the air inlet slots to reach approximately to the height of the centre of the swirl chamber. They are in this way sufficiently raised from the base area Le A 30 002-Foreiqn ~ountries - 5 -~136~7g and cannot in practice be closed off by the hand of the user. One embodiment which is similarly useful for the purpose of correct handling is achieved by means of a finger depression lying approximately underneath the swirl chamber on the device housing. The finger depres-sion at the same time provides a rest for the lower lip of the user, without the mouthpiece needing to have a projection exceeding the overall cross-section of the housing. A beak structure is obtained which is advan-tageous to use. The whole thing can in this case becovered by a protective cap engaging over the housing.
The protective cap can be held on the housing in a simple manner by means of clamping, snap locking etc., so that the device can be released only by deliberately pulling on the protective cap. To this extent, account is also taken of the relevant hygienic requirements. In order also to eliminate moisture present in the mouthpiece area during periods when the device is not in use, the protec-tive cap is also allocated a drying agent chamber. A
further improvement which is favourable particularly in terms of production technology is that all air channels and the swirl chamber are incorporated in a support structure which can be enclosed by two housing shells and in which the metering drum is also mounted, the housing shells forming the covering for the air channels and the swirl chamber. In addition, provision can be made for the support structure to form the stand for the device when it is designed as a st~n~;ng unit, the shoulder of the support structure forming a push-on limit stop for the protective cap. Finally, a feature of the channel struc-ture which is of interest in terms of flow technology is that the wall section of the swirl chamber directed towards the upper end of the connection channel has a smaller curvature and consequently assumes a signif-icantly flatter course, and a central passage of theswirl chamber is arranged eccentric to the said wall section. This "flattening" of the upper semicircle has Le A 30 002-Foreiqn Countries - 6 -2136~79 the surprising effect that a tendency towards settling, which can generally be observed there, is essentially reduced or practically no longer occurs. Instead of a purely circular flow path, there is a relatively ascending flow path with a stronger flow effect, which reliably entrains the particles which have a tendency to adhere.
The following additional advantages are achieved with the invention:
- The inhaler is also suitable for drug formulations with poor flow or which have a tendency to cake. As a result of the simultaneous homogenization upon each metering operation, any powder bridges present are broken up and loosened.
- It has moreover been found that in the event of slight deviations from the prescribed use position the metering accuracy is not appreciably impaired;
i.e. slight deviations from the use position are not critical in respect of the metering accuracy. After the metering, i.e. after actuation of the metering drum, the inhalation can take place in any desired position.
- On account of the construction being amenable to injection-moulding and on account of the small number of necessary components, the inhaler can be produced cost-effectively and economically in large batch quantities.
- The particular flow design downstream of the dis-charge from a portion chamber in the metering drum has the result that a high proportion of respirable powder particles is generated.
Le A 30 002-Foreiqn Countries - 7 -~13~7~
The subject matter of the invention is discussed in greater detail hereinbelow on the basis of an exemplary embodiment which is illustrated in the drawings, in which:
Fig. 1 shows the device for inhalation of a powdery drug, in partial vertical section along line I-I
in Fig. 2, and with the protective cap in full section, Fig. 2 shows the section along line II-II in Fig. 1, 0 Fig. 3 shows a support structure, contributing to the channel structure etc, of the housing shown in isolated representation in a side view, Fig. 4 shows the section along line IV-IV in Fig. 3, Fig. 5 shows the section along line V-V in Fig. 3, rep-resenting the dividing gusset, which divides the suction path, as well as the exhalation barrier, Fig. 6 shows the support structure in isolated represen-tation, viewed from the other broad side, Fig. 7 shows the section along line VII-VII in Fig. 6, 0 Fig. 8 shows the section along line VIII-VIII in Fig. 6, representing the seat for the catch mechanism, Fig. 9 shows an inside view towards the right-hand shell of the housing, Fig. 10 shows the section along line X-X in Fig. 9, Fig. 11 shows the section along line XI-XI in Fig. 9, Le A 30 002-Foreign Countries - 8 -~136~79 Fig. 12 shows an inside view towards the left-hand shell of the housing, Fig. 13 shows the section along line XIII-XIII in Fig.
12, Fig. 14 shows the section along line XIV-XIV in Fig.
12, Fig. 15 shows the metering drum in isolated representation, as viewed into the pot cavity, Fig. 16 shows the section along line XVI-XVI in Fig.
15, Fig. 17 shows the metering drum in isolated representation, as viewed towards its rotary grip, Fig. 18 shows the detail of the catch mechanism facing the metering-drum side, Fig. 19 shows an enlargement of the V apex area forming the portion chA~her, and Fig. 20 shows the section along line XX-XX in Fig. 19.
The device designed as a pocket appliance, referred to hereinbelow as inhaler 1, has, in accordance with Figs. 1 and 2, a long rectangular, flat housing 2 designed in pocket format. Its head area contains a so-called dispersing part I and its foot area contains a metering part II. In the description which follows it is assumed that the inhaler 1 is situated in a vertical plane which corresponds to the drawing plane in the figures, i.e. as represented in Figs. 1 to 2, the dispersing part I is arranged above the metering part II.
Le A 30 002-Foreiqn Countries - 9 -The metering part II comprises a supply container 3 which is filled with a powdery drug 4 (formulation).
The supply container 3 is formed by the interior 5 of a metering drum D. The metering drum D is mounted rotatably in the housing 2 and can be actuated directly by hand from the outside. It is situated in the foot area of the inhaler 1 and in terms of volume utilizes almost the whole width of the housing 2. The geometric, horizontal axis of rotation of the metering drum D is designated x-x (Fig. 2).
Situated above the metering drum D, which serves for providing a portioned-off inhalation quantity of drug, there is a swirl chamber W.
The swirl chamber continues into an upwardly directed mouthpiece M which, at the highest point of its beak-shaped structure, forms an outlet opening 6 fitting the mouth.
When it is being used, the inhaler is held in such a way that the metering part II is situated at the bottom and the dispersing part I with the mouthpiece M is situated at the top (use position). This position also corresponds to the representation chosen in Fig. 1 and Fig. 2.
Thus, metering drum D, swirl chamber W and mouthpiece channel 7, which connects the swirl chamber W and the outlet opening 6 to each other and forms, with its surround, the mouthpiece M, in practice lie vertically one above the other in the use position of the inhaler 1.
The powdery particles are therefore conveyed from the bottom upwards during inhalation.
Issuing from the swirl chamber W is a downwardly directed connection channel 8. The latter is joined, in the area Le A 30 002-Foreiqn Countries - 10 -~136679 Oc the provision of a predetermined (portioned-off) inhalation quantity of drug, to an air inlet channel 8 leading to the outside.
Air inlet channel 9 and connection channel 8 run in a V-shape towards each other and towards the periphery of the metering drum D. This forms an acute-angled channel structure (about 50), at the V-shaped apex area of which the exactly metered quantity of powder removed from the supply container 3 is exposed to the suction air stream so as to be discharged. For this purpose, the metering drum D has portion chambers 11 open towards the channel side. As a result of the circular curvature of the metering drum D, the portioned-off drug (formulation) is prepared as a layer bulging in the direction counter to the cause of the bend. The resulting dome shape of the drug can be cleared off and out in a manner particularly favourable in flow terms. The convex curvature pointing in the direction of a channel-dividing point 12 of the channels 8 and 9 is particularly clear from Fig. 19.
There, the additional height y (indicated in the chord centre), resulting from the curvature of the chamber 11, of the radial R directed towards the centre Z' of the metering drum D can be clearly seen. The centre Z' lies on the abovementioned geometric axis of rotation x-x.
As is clear from Figs. 1, 2, 12 to 14, 16, and in particular 19, a portion chamber 11 is formed by an aperture 14 in a rotary sleeve 15 of the metering drum D
designed as a pot. According to Fig. 1, four apertures 14 are distributed uniformly about the circumference of the rotary sleeve 15. The apertures 14 are delimited by side walls 13 which are bevelled in such a way that the apertures 14 taper towards the centre Z' of the metering drum D. The bevel angle lies at 45 to the shortest connection between inner and outer surface of the metering drum wall. The transverse walls 13 give the Le A 30 002-Foreiqn Countries - 11 -213~679 portion chamber 11 the shape of a trapezoidal, outwardly opening, curved trough of considerably greater length than width.
The rotary sleeve 15 is mounted rotatably between an annular wall 16 and a likewise annular wall section 17 extending through a curve angle of approximately 180.
The approximately semicircular, web-shaped wall section 17 is in this case arranged in such a way that, on the one hand, at the zenith of the metering drum D it extends beyond the V-shaped apex area of the air channels 8 and 9 to such a degree that at no point is there a through-connection between the air channels 8 and 9 and the supply container 3, and, on the other hand, at the lower end it leaves the foot area of the rotary sleeve 15 free (see Fig. 1). The annular wall 16 and the wall section 17 are integrally formed on the housing 2. The bearing of the rotary sleeve can be improved by means of an approx-imately 1 to 2 mm high bearing collar which extends in a continuation of the said wall section 17 through the remaining circumference angle and is likewise integrally formed on the housing 2. In this way the circumferential surface of the rotary sleeve 15 can be guided with precision in the annular gap between the annular wall 16 and the wall section 17, including the said bearing collar. The annular wall 16 has an inlet window 18 opposite the channel-dividing point 12 of the air channels 8 and 9. The side surfaces 19 of the inlet window 18 are bevelled such that they are flush with the side surfaces 13 of the portion chamber 11 when this portion ch~her 11 is situated exactly under the inlet window 18. As long as a portion chamber 11 is situated within the angle range of the wall section 17, the outer surface of the wall section 17 functions as a base 16 for the trough-shaped portion chamber 11. For this reason, the height of the web-shaped wall section 17 is dimen-sioned slightly greater than the width of the aperture Le A 30 002-Foreiqn Countries - 12 -~13~679 14. Upon a further rotation of the metering sleeve 15 in the clockwise direction, i.e. after the portion chamber 11 under the inlet window 18 has advanced beyond the right upper end of the wall section 17, the base of the portion chamber 11 is open, so that it is once again in cnmmlln;cation with the interior 5 and with the supply container 3.
The channel-dividing point 12 directed approximately towards the transverse centre of the portion chamber 11 lies at a distance from the wall section 17 lying underneath, which distance amounts to approximately half the transverse ~ n.~ion of the V-apex end of the connection channel 8 and air inlet channel 9. This leads to a high flow velocity in the area of the bend, with the result that the portion chAmher 11 filled with the powdery drug is emptied without leaving residues behind upon inhalation, even in a critical position of the inhaler.
Whereas the said wall section 17 in the area of the V
apex functions with its outer surface as a base 16, in the area of the rising portion chamber, upstream in the clockwise direction, it shields from the inside the inhalation quantity, taken from the powder supply, of the next aperture 14 from the supply container. In Fig. 1 this portion chamber is situated in a "9 o'clock" pos-ition, while the portion chamber ready for inhalation is in a "12 o'clock" position. The charging of a portion chamber 11 is effected by means of the associated aper-ture 14 being pushed forwards under the powder supply 4 upon further rotation of the metering sleeve 15 (in Fig.
1 approximately in a zone from "4 o'clock" to "7 o'clock"), this portion chamber 11 thus filling with the powder. Upon further rotation of the metering sleeve 15, this portion chamber comes into the asc~n~;ng area between "6 o'clock" and "9 o'clock". In this area the Le A 30 002-Foreign Countries - 13 -21~5 79 quantity of the inhalation dose in the portion chamber is protected by the shielding effect of the wall section 17, the lower end of which functions as a stripper, so that any inwardly directed surplus powder is scraped off. In 5 this way an exact inhalation dose with reproducible powder density is achieved.
The wall section 17 leaves a good 180 open to the interior 5 of the supply container 3. The rotary sleeve 15 acts as a rotary slide. If the metered inhalation 10 quantity is not removed, then upon further rotation of the metering drum D it returns automatically to the supply, in other words to the supply container 3.
Quantity accumulation is not possible. This important advantage results from the vertical orientation of the 15 functional members.
The circumferential wall of the rotary sleeve 15 of the pot-shaped metering drum D merges outwardly into a pot base 20 which closes the supply container 3 and on the outside of which an easily accessible turning knob 21 is 20 arranged (see in particular Fig. 16 and Fig. 17).
The metering drum D has a catch mechanism 22 which is designed for rotation in the clockwise direction. The main component of this mechanism is a radially movable locking pin 23 which is loaded by a compression spring 24 25 in the engagement direction. The opposite catch means consist of opposite catches 25 which lie on the circumference of the rotary sleeve 15 and of the metering drum D and which are positioned in such a way that the ready-to-dispense position of the portion chamber 11 is 30 obtained exactly step by step. The opposite catch 25 is equipped with edges which are such that, when the catch is intentionally overcome, the metering drum D locked in the respective ready-to-dispense position can be rotated further, while a rotation in the opposite direction is Le A 30 002-Foreiqn Countries - 14 -~136679 not readily possible on account of a steeper edge. A
reversal of the direction of rotation is of course possible if the device is to be designed specially for left-handed users.
The actual catch depression of the opposite catch 25 is designated in Fig. 18 by 26, the steeper edge by 27, and the less inclined edge, which can be overcome if so intended, by 28. The opposite catch 27 lies in a flange section of the rotary sleeve 15 having a thickened wall and lying nearer the pot base 20 of the metering drum D.
Arranged on the pot base 20, parallel to the axis of rotation of the metering drum D and distributed uniformly about the circumference, are a plurality of loosening fingers 29 which project into the powder supply and whose radial distance from the centre is chosen such that, upon rotation, they scrape along the back of the wall section 17, so that no powder can settle there. According to Fig. 1, one loosening finger 29 is arranged, as seen in the clockwise direction, directly behind each aperture 14 (leading). Alternatively, or in addition to this, the loosening fingers can be arranged stationary on the housing 2, in which case the drum movement is similarly used for loosening the powder.
Situated in the centre of the base 20, likewise on the inner side thereof, that is to say projecting into the supply container 3, is a drying agent chamber 30. This is, for example, a capsule which can be secured by means of a clip fastening and whose base is perm~hle to water vapour. Clip lugs 31 engaging over the edges serve to hold the capsule in position.
The inhaler housing 2 consists of two housing shells 32 and 33 of U-shaped cross-section. The two shells 32 and 33 enclose, in sandwich fashion, a support structure 34 Le A 30 002-Foreiqn Countries - 15 -~13~679 as core part, in which there are accommodated, as main components, the connection channel 8, the air inlet channel 9 with flow separation at the inlet side, the swirl chamber W, the mouthpiece channel 7, a circular recess 35 for the mounting of the metering drum D, and the catch mechanism 22. The air channels 7, 8, 9 are incorporated into the support structure 34 in the form of groove-like depressions of approximately rectangular cross-section, and the air chambers are incorporated into the support structure 34 in the form of essentially circular recesses, and they are closed off and covered by the housing shells 32 and 33. This construction guaran-tees a sufficient mechanical stability, even when the support structure 34 is designed with relatively thin walls (e.g. about 5 mm) for reasons of reducing weight.
The support structure 34 is represented in Figs. 3 to 7, the right-hand housing shell 32, as viewed according to Fig. 2, is shown in Figs. 9 to 11 in isolated representation, and the left-hand housing shell 33 is shown in Figs. 12 to 14. Ridges moulded integrally on the inner sides of the shell abut against each other via their end faces and against oppositely directed ridges of the support structure 34 which is held between them. The ~-nner of fastening the parts can be based on a clamping technique; an adhesive bo~;ng or ~herm~l bonding is also conceivable, unless it is desired that the housing 2 should be able to be taken apart completely or partially for cleaning purposes and refilling purposes. In this case the usual traditional fastening means are to be preferred, such as screwing etc.
The connection channel 8 is aligned in the support structure 34 in such a way that it runs essentially radially to the metering drum D. While it tapers slightly in this direction, it widens continuously in the opposite direction. The extent to which the connection channel 8 Le A 30 002-Foreiqn Countries - 16 -~136679 widens towards the swirl chamber is shown clearly in Fig.
1 and Fig. 3. It can also be seen from these that the trace line of the one channel wall a runs radically with respect to the centre Z' of the circular swirl chamber W
5 and that the trace line of the other wall b runs tangentially with respect to the swirl chamber. The connection channel 8 and swirl chamber W thus present an outline which can be likened to a whistle. The swirl chamber is designed in two parts, and the two chamber 10 parts, the dwell-time chamber 36 and the outlet chamber 37, lie alongside each other, viewed perpendicular to the housing shells 32 and 33, and csmmlln;cate with each other via a central, transversely directed, circular passage 38. A saliva guard is formed by means of this 15 arrangement. It has been found that a settlement or adhesion of the powder in the dwelltime chamber 36 and the outlet ch~mher 37 can be substantially avoided if the volume of the chambers is reduced by inwardly directed impressions in the housing shells 32 and 33. The circular 20 outlet chamber 37, while forming the abovementioned whistle profile, continues upwards into the mouthpiece channel 7. The mouthpiece channel 7 running at an obtuse angle to the connection channel 8 is designed in such a way that the trace line of one wall c is directed 25 tangentially, and that of the other wall d approximately radially, with respect to the centre Z'' of the swirl chamber W. Halfway along its length the wall c has a bend for the purpose of forming a slight narrowing towards the outside.
30 The air inlet channel 9 is aligned in such a way that the trace line of the inner wall e, leading to the channel-dividing point 12, and that of the outer wall f of the air inlet channel 9 are aligned in a secant formation with respect to the metering drum D.
Le A 30 002-Foreiqn Countries - 17 -~136-~79 The inhalation air is sucked in from the outside and through the air inlet channel 9 via air inlet slots 39.
Half of the air inlet slots are arranged on the housing shell 32 and the other half on the opposite housing shell 33, so that the suction air stream is divided into two partial streams before entry into the air inlet chAnnel 9. For this purpose, a splitting of the air inlet channel 9 is provided for in the support structure 34. The splitting is obtained by means of a dividing gusset 40 which combines the partial streams sucked in from both broad sides of the device into one suction stream (see Fig. 1 and Figs. 3 to 6). Whereas the outlet chAmher of the swirl chamber W is circular, the dwell-time chamber 36 has a shape deviating from a circular cross-section.
As can be seen from Fig. 3, the wall section 36' facing towards the upper end of the connection channel 8 has a slighter curvature and, consequently, a significantly flatter course than does the greater part of the dwell-time chamber 36. The central passage of the swirl chamber W is arranged eccentrically relative to this flattened part 36'.
This "flattening" leads surprisingly to a better removal of powdery drug which may possibly have settled.
The distinct flattening extends over only the upper semi-circle of the swirl chamber W; the lower half, which is interrupted by the upper end of the connection chAnnel 8, is circular, that is to say concentric with respect to the centre Z'' of the swirl chamber W.
In order to prevent the discharge of the inhalation quantity of drug in the event of incorrect operation of the inhaler 1, that is to say when blowing instead of sucking, two exhalation barrier tongues 41 are arranged in the flow path of the dividing gusset 40 in the area of the air inlet (see Fig. 5). They act as nonreturn valves, Le A 30 002-Foreiqn Countries - 18 -~13~7~
with the inside edge of the air inlet slots 39 forming the corresponding valve seat surface. Such an exhalation barrier tongue 41 is of simple construction and consists of a rubber or plastic strip section of appropriate flexibility. The latter is simply placed over the div-iding gusset 40 of triangular cross-section and is clamped to the wall of the support 2 in a retaining slot 41a. The point of the dividing gusset 40 is directed downwards.
The function of the exhalation barrier tongues 41 is also assured from the point of view of ergonometrics, since the inlet slots 39 reach only to about the height of the centre Z'' of the swirl chamber W. The air inlet slots 39 thus lie in the head area of the inhaler 1, while the foot area thereof is free for gripping. Fig. 1 in particular also shows a beak-like configuration of the said head of the inhaler 1. The mouthpiece M tapers continuously to the free end, while at the other end a finger depression 42 is provided beside and essentially underneath the swirl chP~her W. Not only is the use of the inhaler 1 facilitated in this way, but the correct handling thereof is also suggested. When the inhaler is being used, the lower lip of the user rests on the side surface of the mouthpiece above the finger depression 42.
The said finger depression 42 is designed such that the thumb can be placed comfortably thereon.
A protective cap 43 engaging over the inhaler 1 is used in the interest of hygiene (see Fig. 6). It likewise has, in the lid area, a drying agent chamber 44 which is accommodated in the space remaining free between protective cap 43 and mouthpiece M. The protective cap 43 is recessed in the area of the turning knob 21 (recess 45).
Le A 30 002-Foreiqn Countries - 19 -~13~b 79 An upper, level shoulder 46 of a stand 47 formed integrally on the support structure 34 serves as a limit stop for the protective cap 43. The shell walls are slightly flared in this area, so that the lower edge of the protective cap 43 is held secure by means of a clamping fit.
The protective cap 43 engages over the broad sides and narrow sides of the housing 2 which are formed by the shells 32 and 33, and also over the upper end face of said housing.
On the broad side lying opposite the turning knob 21, the supply container 3 has a transparent, disc-shaped section 48 as viewing window (see Fig. 2). In this way the powder content can be checked. The said viewing window at the same time acts as a filling lid. The latter could also serve as for the support static loosening fingers 29, if this version were to be constructed. The drying agent chamber 30 described could also be situated on the inner side of the filling lid.
The functioning of the inhaler 1 is, in brief, as foll-ows: The air sucked in through the air inlet channel 9 flows, upon inhalation, into the portion chamber 11 filled with the metered quantity and carries the drug 4 into the upwardly directed flow path, i.e. into the connection channel 8. The the flow velocity decreases as it passes into the area of the swirl chamber W lying above. Here the air current passes into the dwell-time chamber 36, with decreasing velocity and counter to the force of gravity of the particles, and from there crosses transversely through the central passage 38, with further deceleration, into the outlet chamber 37. The powder/air mixture finally reaches the foot area of the mouthpiece channel 7, which acts as dispersing chamber. From the adjoining diffusor, which is formed by the upper end of Le A 30 002-Foreiqn Countries - 20 -the mouthpiece channel 7, the medicament passes via the outlet opening 6 to the target site (bronchi, lung). The flow path in the dispersing part I resembles two succes-sive loops of the same direction of rotation.
By virtue of the continuous decrease in the flow velocity as far as the outlet opening 6 on the mouthpiece channel 7, the likelihood of impact separation of relatively small particles in the throat area is greatly reduced.
Le A 30 002-Foreiqn Countries - 21 -
DEVICE FOR INHALATION
The invention relates to a device for inhalation of a powdery, pharmacologically active drug, consisting of a supply container for the drug, a manually actuated metering unit for providing a portioned-off quantity of inhalation substance which is picked up by the air current drawn in during inhalation and is swirled, an air inlet channel, a swirl chPmher, and a connection channel between the swirl chamber and the metering unit, as well as a mouthpiece channel issuing from the swirl chPmher.
A device of this type is known from DE-OS (German Published Specification) 4 004 904. The drug supply is kept ready there at the periphery of the metering drum and is readjusted radially. The interior of the metering drum contains a control device for active discharge of the portioned-off inhalation quantity of drug from radially outwardly directed, open metering recesses. For this purpose, slides forming the base of the metering recesses, which are arranged distributed at uniform angles, are centrally cam-controlled. The outlay in this regard is considerable, especially since the control mechanism is released by an actuation key taking up almost the whole of one longitudinal side of the device.
Air inlet channel and connection channel run at an obtuse angle and tangent to the metering drum, this air course continuing via a swirl chamber, formed as a secondary cavity, essentially straight as far as the other end of the device. The drug transfer point lies near the open intake end and the substance can easily fall out there unused. In addition, the metered inhalation quantities of drug can add up as a result of the forced emptying of the metering recess; this can therefore lead to a dangerous overdose. In terms of volume, only a fraction of the Le A 30 002-Foreiqn Countries - 1 -213~79 device designed in pocket format remains for holding asupply. The method of handling is not clear.
The object of the invention is to design a device of the generic type which, being of simplified construction, is more advantageous and safer to use, in particular also to improve the device in terms of flow technology, and to keep the effect constant by means of complete discharge of the portioned-off inhalation quantity of drug.
This object is achieved by the invention specified in Claim 1.
The claims subsequent thereto present further advantageous embodiments of the device according to the in~ention.
As a result of such an embodiment, a device of the generic type is obtained which is of simplified construction and of improved usefulness and safety. The mechanical outlay is greatly reduced. No coordination between press button movement and inhalation is needed.
The quantity is brought into the position ready for dispensing without any rush. The user can concentrate on inhaling the active substance. The inhaler is designed in concrete terms such that the metering device consists of a metering drum, the supply container for the drug being arranged in the interior of the metering drum, and that the air inlet channel and the connection chAnnel run towards each other in a V-shape and towards a portioned-off quantity of drug present in the shape of a dome and provided by the metering drum at the apex of the two air channels. The interior of the metering drum is now used for forming a supply. Its content is kept in motion. It comes by the shortest route into the position ready for dispensing. Discharging with no residues remaining behind takes place there. As a result of the stated orientation Le A 30 002-Foreiqn Countries - 2 -21~6b79 - and sequence of the operational areas, it is not possible for any particles to fall back. The suction stream impacts first on the V apex and flows into the exactly positioned and portioned-off, exposed heap of the drug.
The zone presented in a dome-shape is quickly carried off, swirled and dispersed and, upon inhalation, reaches the target site. The drug is sucked counter to the effect of gravity. Incorrect holding is practically ruled out since the position of the metering drum suggests the correct handling, and it is readily apparent to the user that the mouthpiece channel situated at the other, upper, end is the transfer bridge. In addition, a potential for an overdose cannot build up; a non-inhaled inhalation quantity disappears in the direction of the supply. It is not added to by the next indexing step. An advantage in terms of flow technology proves to be the fact that the connection channel runs radially with respect to the metering drum. It is thus optimally suited to its function as acceleration channel with increasing abate-ment towards the top. In order to create a sufficiently large transfer area to the swirl ch~mher, which acts as a dwell-time chamber on the access side, the inhaler is advantageously designed such that the connection channel widens towards the swirl chamber, and the trace line of the one wall lies essentially radially with respect to the centre of the swirl chamber, and that of the other wall runs essentially tangentially thereto. This leads to a flow which promotes swirling and which defines the direction of rotation. As regards the outlet mouthpiece channel, the construction in this case is chosen such that the mouthpiece channel runs at an obtuse angle with respect to the connection channel, and the trace line of the one wall is aligned approximately tangentially, and that of the other wall approximately radially, with respect to the centre of the swirl chamber. A continuous cross-sectional widening (also in the transverse width) is also expediently made use of in this respect (realiz-Le A 30 002-Foreiqn Countries - 3 -213~679 ation of the diffusor effect sought). As regards the design of the air inlet channel, the procedure in this case is that the trace line of the inner wall and the trace line of the outer wall of the air inlet channel are aligned in secant formation with respect to the metering chamber. Suction opening and air outlet opening of the device are thus at a sufficient spatial distance from each other. As regards the design of the metering drum, this is continued such that it has a rotary sleeve equipped with portion apertures. The portion apertures arranged in a uniform angular distribution dip into the powder supply on account of the mixing-drum-like rotation of the metering drum, without causing pressing etc. The metering is correct in terms of volume, including the penultimate portion and, if appropriate, the final portion. Also, on account of the use of the drum move-ment, there is no agglomeration of the drug. It is further proposed that the rotary sleeve is formed by the circumferential wall of a pot, the base of which forms a rotary purchase. The correspondingly outwardly accessible rotary grip is extremely easy to use and direct. In order to obtain a defined position of the dome, that is to say of the metered quantity of the portioned-off drug, a catch mechanism deter~ining the direction of rotation is allocated to the device between rotary sleeve and housing. As regards the rotary bearing of the metering drum and the obtainment of constantly uniform inhalation quantities of drug, it proves advantageous that the rotary sleeve enclosed by an outer wall is underpinned, over a partial angle area, by an inner wall section which, in the area of the V apex, forms the base of the portion ch~mher formed by in each case one of the aper-tures. In this context it is additionally advantageous that the transverse walls of the apertures run in a wedge formation to the centre of the metering drum. This leads, as regards the transverse walls, to a convexly curved, trapezoidal trough as portion chamber which widens at the Le A 30 002-Foreiqn Countries - 4 -V apex side, in other words towards the top. A further development of the invention lies in the fact that, issuing from the base of the pot and/or the housing, loosening fingers protrude into the metering drum. They form a type of stirrer which, operating actively or statically, optimizes the loosening of the powdery drug (formulation). In order to eliminate the moisture which cannot be completely prevented, the base of the pot or the inner side of a housing-filling lid is allocated a drying agent chamber, which would be equipped as approp-riate. Such a filling lid can be formed at the same time as a viewing glass. A good suction effect is achieved by arranging transversely directed air inlet slots at the intake end of the air inlet channel. The suction opening is thus prevented from being blocked, for example by loosely carried coins, etc. The grid-like design of the air inlet is also useful to the extent that no foreign particles, such as dust etc., can be sucked in. Such air inlet slots are expediently provided on both broad sides of the device housing. They lie in such a way that, when the inhaler is being handled, they cannot easily be closed over; in any case one or the other side remains open. The device is further characterized by a dividing gusset for the path of the air sucked in. Thus, a Y-channel is formed in practice on the suction side. In theevent of incorrect use (blowing instead of sucking), in order to prevent the discharge of the powdery drug, the air inlet slots are allocated exhalation barrier tongues.
Thus, on puffing, no respiratory air moisture reaches into the inside of the inhaler device, which is to be kept as completely dry as possible. These can be simple valve flaps. The abovementioned dividing gusset can be used for fitting them, as is explained in the relevant part of the description. For correct handling it is thus expedient for the air inlet slots to reach approximately to the height of the centre of the swirl chamber. They are in this way sufficiently raised from the base area Le A 30 002-Foreiqn ~ountries - 5 -~136~7g and cannot in practice be closed off by the hand of the user. One embodiment which is similarly useful for the purpose of correct handling is achieved by means of a finger depression lying approximately underneath the swirl chamber on the device housing. The finger depres-sion at the same time provides a rest for the lower lip of the user, without the mouthpiece needing to have a projection exceeding the overall cross-section of the housing. A beak structure is obtained which is advan-tageous to use. The whole thing can in this case becovered by a protective cap engaging over the housing.
The protective cap can be held on the housing in a simple manner by means of clamping, snap locking etc., so that the device can be released only by deliberately pulling on the protective cap. To this extent, account is also taken of the relevant hygienic requirements. In order also to eliminate moisture present in the mouthpiece area during periods when the device is not in use, the protec-tive cap is also allocated a drying agent chamber. A
further improvement which is favourable particularly in terms of production technology is that all air channels and the swirl chamber are incorporated in a support structure which can be enclosed by two housing shells and in which the metering drum is also mounted, the housing shells forming the covering for the air channels and the swirl chamber. In addition, provision can be made for the support structure to form the stand for the device when it is designed as a st~n~;ng unit, the shoulder of the support structure forming a push-on limit stop for the protective cap. Finally, a feature of the channel struc-ture which is of interest in terms of flow technology is that the wall section of the swirl chamber directed towards the upper end of the connection channel has a smaller curvature and consequently assumes a signif-icantly flatter course, and a central passage of theswirl chamber is arranged eccentric to the said wall section. This "flattening" of the upper semicircle has Le A 30 002-Foreiqn Countries - 6 -2136~79 the surprising effect that a tendency towards settling, which can generally be observed there, is essentially reduced or practically no longer occurs. Instead of a purely circular flow path, there is a relatively ascending flow path with a stronger flow effect, which reliably entrains the particles which have a tendency to adhere.
The following additional advantages are achieved with the invention:
- The inhaler is also suitable for drug formulations with poor flow or which have a tendency to cake. As a result of the simultaneous homogenization upon each metering operation, any powder bridges present are broken up and loosened.
- It has moreover been found that in the event of slight deviations from the prescribed use position the metering accuracy is not appreciably impaired;
i.e. slight deviations from the use position are not critical in respect of the metering accuracy. After the metering, i.e. after actuation of the metering drum, the inhalation can take place in any desired position.
- On account of the construction being amenable to injection-moulding and on account of the small number of necessary components, the inhaler can be produced cost-effectively and economically in large batch quantities.
- The particular flow design downstream of the dis-charge from a portion chamber in the metering drum has the result that a high proportion of respirable powder particles is generated.
Le A 30 002-Foreiqn Countries - 7 -~13~7~
The subject matter of the invention is discussed in greater detail hereinbelow on the basis of an exemplary embodiment which is illustrated in the drawings, in which:
Fig. 1 shows the device for inhalation of a powdery drug, in partial vertical section along line I-I
in Fig. 2, and with the protective cap in full section, Fig. 2 shows the section along line II-II in Fig. 1, 0 Fig. 3 shows a support structure, contributing to the channel structure etc, of the housing shown in isolated representation in a side view, Fig. 4 shows the section along line IV-IV in Fig. 3, Fig. 5 shows the section along line V-V in Fig. 3, rep-resenting the dividing gusset, which divides the suction path, as well as the exhalation barrier, Fig. 6 shows the support structure in isolated represen-tation, viewed from the other broad side, Fig. 7 shows the section along line VII-VII in Fig. 6, 0 Fig. 8 shows the section along line VIII-VIII in Fig. 6, representing the seat for the catch mechanism, Fig. 9 shows an inside view towards the right-hand shell of the housing, Fig. 10 shows the section along line X-X in Fig. 9, Fig. 11 shows the section along line XI-XI in Fig. 9, Le A 30 002-Foreign Countries - 8 -~136~79 Fig. 12 shows an inside view towards the left-hand shell of the housing, Fig. 13 shows the section along line XIII-XIII in Fig.
12, Fig. 14 shows the section along line XIV-XIV in Fig.
12, Fig. 15 shows the metering drum in isolated representation, as viewed into the pot cavity, Fig. 16 shows the section along line XVI-XVI in Fig.
15, Fig. 17 shows the metering drum in isolated representation, as viewed towards its rotary grip, Fig. 18 shows the detail of the catch mechanism facing the metering-drum side, Fig. 19 shows an enlargement of the V apex area forming the portion chA~her, and Fig. 20 shows the section along line XX-XX in Fig. 19.
The device designed as a pocket appliance, referred to hereinbelow as inhaler 1, has, in accordance with Figs. 1 and 2, a long rectangular, flat housing 2 designed in pocket format. Its head area contains a so-called dispersing part I and its foot area contains a metering part II. In the description which follows it is assumed that the inhaler 1 is situated in a vertical plane which corresponds to the drawing plane in the figures, i.e. as represented in Figs. 1 to 2, the dispersing part I is arranged above the metering part II.
Le A 30 002-Foreiqn Countries - 9 -The metering part II comprises a supply container 3 which is filled with a powdery drug 4 (formulation).
The supply container 3 is formed by the interior 5 of a metering drum D. The metering drum D is mounted rotatably in the housing 2 and can be actuated directly by hand from the outside. It is situated in the foot area of the inhaler 1 and in terms of volume utilizes almost the whole width of the housing 2. The geometric, horizontal axis of rotation of the metering drum D is designated x-x (Fig. 2).
Situated above the metering drum D, which serves for providing a portioned-off inhalation quantity of drug, there is a swirl chamber W.
The swirl chamber continues into an upwardly directed mouthpiece M which, at the highest point of its beak-shaped structure, forms an outlet opening 6 fitting the mouth.
When it is being used, the inhaler is held in such a way that the metering part II is situated at the bottom and the dispersing part I with the mouthpiece M is situated at the top (use position). This position also corresponds to the representation chosen in Fig. 1 and Fig. 2.
Thus, metering drum D, swirl chamber W and mouthpiece channel 7, which connects the swirl chamber W and the outlet opening 6 to each other and forms, with its surround, the mouthpiece M, in practice lie vertically one above the other in the use position of the inhaler 1.
The powdery particles are therefore conveyed from the bottom upwards during inhalation.
Issuing from the swirl chamber W is a downwardly directed connection channel 8. The latter is joined, in the area Le A 30 002-Foreiqn Countries - 10 -~136679 Oc the provision of a predetermined (portioned-off) inhalation quantity of drug, to an air inlet channel 8 leading to the outside.
Air inlet channel 9 and connection channel 8 run in a V-shape towards each other and towards the periphery of the metering drum D. This forms an acute-angled channel structure (about 50), at the V-shaped apex area of which the exactly metered quantity of powder removed from the supply container 3 is exposed to the suction air stream so as to be discharged. For this purpose, the metering drum D has portion chambers 11 open towards the channel side. As a result of the circular curvature of the metering drum D, the portioned-off drug (formulation) is prepared as a layer bulging in the direction counter to the cause of the bend. The resulting dome shape of the drug can be cleared off and out in a manner particularly favourable in flow terms. The convex curvature pointing in the direction of a channel-dividing point 12 of the channels 8 and 9 is particularly clear from Fig. 19.
There, the additional height y (indicated in the chord centre), resulting from the curvature of the chamber 11, of the radial R directed towards the centre Z' of the metering drum D can be clearly seen. The centre Z' lies on the abovementioned geometric axis of rotation x-x.
As is clear from Figs. 1, 2, 12 to 14, 16, and in particular 19, a portion chamber 11 is formed by an aperture 14 in a rotary sleeve 15 of the metering drum D
designed as a pot. According to Fig. 1, four apertures 14 are distributed uniformly about the circumference of the rotary sleeve 15. The apertures 14 are delimited by side walls 13 which are bevelled in such a way that the apertures 14 taper towards the centre Z' of the metering drum D. The bevel angle lies at 45 to the shortest connection between inner and outer surface of the metering drum wall. The transverse walls 13 give the Le A 30 002-Foreiqn Countries - 11 -213~679 portion chamber 11 the shape of a trapezoidal, outwardly opening, curved trough of considerably greater length than width.
The rotary sleeve 15 is mounted rotatably between an annular wall 16 and a likewise annular wall section 17 extending through a curve angle of approximately 180.
The approximately semicircular, web-shaped wall section 17 is in this case arranged in such a way that, on the one hand, at the zenith of the metering drum D it extends beyond the V-shaped apex area of the air channels 8 and 9 to such a degree that at no point is there a through-connection between the air channels 8 and 9 and the supply container 3, and, on the other hand, at the lower end it leaves the foot area of the rotary sleeve 15 free (see Fig. 1). The annular wall 16 and the wall section 17 are integrally formed on the housing 2. The bearing of the rotary sleeve can be improved by means of an approx-imately 1 to 2 mm high bearing collar which extends in a continuation of the said wall section 17 through the remaining circumference angle and is likewise integrally formed on the housing 2. In this way the circumferential surface of the rotary sleeve 15 can be guided with precision in the annular gap between the annular wall 16 and the wall section 17, including the said bearing collar. The annular wall 16 has an inlet window 18 opposite the channel-dividing point 12 of the air channels 8 and 9. The side surfaces 19 of the inlet window 18 are bevelled such that they are flush with the side surfaces 13 of the portion chamber 11 when this portion ch~her 11 is situated exactly under the inlet window 18. As long as a portion chamber 11 is situated within the angle range of the wall section 17, the outer surface of the wall section 17 functions as a base 16 for the trough-shaped portion chamber 11. For this reason, the height of the web-shaped wall section 17 is dimen-sioned slightly greater than the width of the aperture Le A 30 002-Foreiqn Countries - 12 -~13~679 14. Upon a further rotation of the metering sleeve 15 in the clockwise direction, i.e. after the portion chamber 11 under the inlet window 18 has advanced beyond the right upper end of the wall section 17, the base of the portion chamber 11 is open, so that it is once again in cnmmlln;cation with the interior 5 and with the supply container 3.
The channel-dividing point 12 directed approximately towards the transverse centre of the portion chamber 11 lies at a distance from the wall section 17 lying underneath, which distance amounts to approximately half the transverse ~ n.~ion of the V-apex end of the connection channel 8 and air inlet channel 9. This leads to a high flow velocity in the area of the bend, with the result that the portion chAmher 11 filled with the powdery drug is emptied without leaving residues behind upon inhalation, even in a critical position of the inhaler.
Whereas the said wall section 17 in the area of the V
apex functions with its outer surface as a base 16, in the area of the rising portion chamber, upstream in the clockwise direction, it shields from the inside the inhalation quantity, taken from the powder supply, of the next aperture 14 from the supply container. In Fig. 1 this portion chamber is situated in a "9 o'clock" pos-ition, while the portion chamber ready for inhalation is in a "12 o'clock" position. The charging of a portion chamber 11 is effected by means of the associated aper-ture 14 being pushed forwards under the powder supply 4 upon further rotation of the metering sleeve 15 (in Fig.
1 approximately in a zone from "4 o'clock" to "7 o'clock"), this portion chamber 11 thus filling with the powder. Upon further rotation of the metering sleeve 15, this portion chamber comes into the asc~n~;ng area between "6 o'clock" and "9 o'clock". In this area the Le A 30 002-Foreign Countries - 13 -21~5 79 quantity of the inhalation dose in the portion chamber is protected by the shielding effect of the wall section 17, the lower end of which functions as a stripper, so that any inwardly directed surplus powder is scraped off. In 5 this way an exact inhalation dose with reproducible powder density is achieved.
The wall section 17 leaves a good 180 open to the interior 5 of the supply container 3. The rotary sleeve 15 acts as a rotary slide. If the metered inhalation 10 quantity is not removed, then upon further rotation of the metering drum D it returns automatically to the supply, in other words to the supply container 3.
Quantity accumulation is not possible. This important advantage results from the vertical orientation of the 15 functional members.
The circumferential wall of the rotary sleeve 15 of the pot-shaped metering drum D merges outwardly into a pot base 20 which closes the supply container 3 and on the outside of which an easily accessible turning knob 21 is 20 arranged (see in particular Fig. 16 and Fig. 17).
The metering drum D has a catch mechanism 22 which is designed for rotation in the clockwise direction. The main component of this mechanism is a radially movable locking pin 23 which is loaded by a compression spring 24 25 in the engagement direction. The opposite catch means consist of opposite catches 25 which lie on the circumference of the rotary sleeve 15 and of the metering drum D and which are positioned in such a way that the ready-to-dispense position of the portion chamber 11 is 30 obtained exactly step by step. The opposite catch 25 is equipped with edges which are such that, when the catch is intentionally overcome, the metering drum D locked in the respective ready-to-dispense position can be rotated further, while a rotation in the opposite direction is Le A 30 002-Foreiqn Countries - 14 -~136679 not readily possible on account of a steeper edge. A
reversal of the direction of rotation is of course possible if the device is to be designed specially for left-handed users.
The actual catch depression of the opposite catch 25 is designated in Fig. 18 by 26, the steeper edge by 27, and the less inclined edge, which can be overcome if so intended, by 28. The opposite catch 27 lies in a flange section of the rotary sleeve 15 having a thickened wall and lying nearer the pot base 20 of the metering drum D.
Arranged on the pot base 20, parallel to the axis of rotation of the metering drum D and distributed uniformly about the circumference, are a plurality of loosening fingers 29 which project into the powder supply and whose radial distance from the centre is chosen such that, upon rotation, they scrape along the back of the wall section 17, so that no powder can settle there. According to Fig. 1, one loosening finger 29 is arranged, as seen in the clockwise direction, directly behind each aperture 14 (leading). Alternatively, or in addition to this, the loosening fingers can be arranged stationary on the housing 2, in which case the drum movement is similarly used for loosening the powder.
Situated in the centre of the base 20, likewise on the inner side thereof, that is to say projecting into the supply container 3, is a drying agent chamber 30. This is, for example, a capsule which can be secured by means of a clip fastening and whose base is perm~hle to water vapour. Clip lugs 31 engaging over the edges serve to hold the capsule in position.
The inhaler housing 2 consists of two housing shells 32 and 33 of U-shaped cross-section. The two shells 32 and 33 enclose, in sandwich fashion, a support structure 34 Le A 30 002-Foreiqn Countries - 15 -~13~679 as core part, in which there are accommodated, as main components, the connection channel 8, the air inlet channel 9 with flow separation at the inlet side, the swirl chamber W, the mouthpiece channel 7, a circular recess 35 for the mounting of the metering drum D, and the catch mechanism 22. The air channels 7, 8, 9 are incorporated into the support structure 34 in the form of groove-like depressions of approximately rectangular cross-section, and the air chambers are incorporated into the support structure 34 in the form of essentially circular recesses, and they are closed off and covered by the housing shells 32 and 33. This construction guaran-tees a sufficient mechanical stability, even when the support structure 34 is designed with relatively thin walls (e.g. about 5 mm) for reasons of reducing weight.
The support structure 34 is represented in Figs. 3 to 7, the right-hand housing shell 32, as viewed according to Fig. 2, is shown in Figs. 9 to 11 in isolated representation, and the left-hand housing shell 33 is shown in Figs. 12 to 14. Ridges moulded integrally on the inner sides of the shell abut against each other via their end faces and against oppositely directed ridges of the support structure 34 which is held between them. The ~-nner of fastening the parts can be based on a clamping technique; an adhesive bo~;ng or ~herm~l bonding is also conceivable, unless it is desired that the housing 2 should be able to be taken apart completely or partially for cleaning purposes and refilling purposes. In this case the usual traditional fastening means are to be preferred, such as screwing etc.
The connection channel 8 is aligned in the support structure 34 in such a way that it runs essentially radially to the metering drum D. While it tapers slightly in this direction, it widens continuously in the opposite direction. The extent to which the connection channel 8 Le A 30 002-Foreiqn Countries - 16 -~136679 widens towards the swirl chamber is shown clearly in Fig.
1 and Fig. 3. It can also be seen from these that the trace line of the one channel wall a runs radically with respect to the centre Z' of the circular swirl chamber W
5 and that the trace line of the other wall b runs tangentially with respect to the swirl chamber. The connection channel 8 and swirl chamber W thus present an outline which can be likened to a whistle. The swirl chamber is designed in two parts, and the two chamber 10 parts, the dwell-time chamber 36 and the outlet chamber 37, lie alongside each other, viewed perpendicular to the housing shells 32 and 33, and csmmlln;cate with each other via a central, transversely directed, circular passage 38. A saliva guard is formed by means of this 15 arrangement. It has been found that a settlement or adhesion of the powder in the dwelltime chamber 36 and the outlet ch~mher 37 can be substantially avoided if the volume of the chambers is reduced by inwardly directed impressions in the housing shells 32 and 33. The circular 20 outlet chamber 37, while forming the abovementioned whistle profile, continues upwards into the mouthpiece channel 7. The mouthpiece channel 7 running at an obtuse angle to the connection channel 8 is designed in such a way that the trace line of one wall c is directed 25 tangentially, and that of the other wall d approximately radially, with respect to the centre Z'' of the swirl chamber W. Halfway along its length the wall c has a bend for the purpose of forming a slight narrowing towards the outside.
30 The air inlet channel 9 is aligned in such a way that the trace line of the inner wall e, leading to the channel-dividing point 12, and that of the outer wall f of the air inlet channel 9 are aligned in a secant formation with respect to the metering drum D.
Le A 30 002-Foreiqn Countries - 17 -~136-~79 The inhalation air is sucked in from the outside and through the air inlet channel 9 via air inlet slots 39.
Half of the air inlet slots are arranged on the housing shell 32 and the other half on the opposite housing shell 33, so that the suction air stream is divided into two partial streams before entry into the air inlet chAnnel 9. For this purpose, a splitting of the air inlet channel 9 is provided for in the support structure 34. The splitting is obtained by means of a dividing gusset 40 which combines the partial streams sucked in from both broad sides of the device into one suction stream (see Fig. 1 and Figs. 3 to 6). Whereas the outlet chAmher of the swirl chamber W is circular, the dwell-time chamber 36 has a shape deviating from a circular cross-section.
As can be seen from Fig. 3, the wall section 36' facing towards the upper end of the connection channel 8 has a slighter curvature and, consequently, a significantly flatter course than does the greater part of the dwell-time chamber 36. The central passage of the swirl chamber W is arranged eccentrically relative to this flattened part 36'.
This "flattening" leads surprisingly to a better removal of powdery drug which may possibly have settled.
The distinct flattening extends over only the upper semi-circle of the swirl chamber W; the lower half, which is interrupted by the upper end of the connection chAnnel 8, is circular, that is to say concentric with respect to the centre Z'' of the swirl chamber W.
In order to prevent the discharge of the inhalation quantity of drug in the event of incorrect operation of the inhaler 1, that is to say when blowing instead of sucking, two exhalation barrier tongues 41 are arranged in the flow path of the dividing gusset 40 in the area of the air inlet (see Fig. 5). They act as nonreturn valves, Le A 30 002-Foreiqn Countries - 18 -~13~7~
with the inside edge of the air inlet slots 39 forming the corresponding valve seat surface. Such an exhalation barrier tongue 41 is of simple construction and consists of a rubber or plastic strip section of appropriate flexibility. The latter is simply placed over the div-iding gusset 40 of triangular cross-section and is clamped to the wall of the support 2 in a retaining slot 41a. The point of the dividing gusset 40 is directed downwards.
The function of the exhalation barrier tongues 41 is also assured from the point of view of ergonometrics, since the inlet slots 39 reach only to about the height of the centre Z'' of the swirl chamber W. The air inlet slots 39 thus lie in the head area of the inhaler 1, while the foot area thereof is free for gripping. Fig. 1 in particular also shows a beak-like configuration of the said head of the inhaler 1. The mouthpiece M tapers continuously to the free end, while at the other end a finger depression 42 is provided beside and essentially underneath the swirl chP~her W. Not only is the use of the inhaler 1 facilitated in this way, but the correct handling thereof is also suggested. When the inhaler is being used, the lower lip of the user rests on the side surface of the mouthpiece above the finger depression 42.
The said finger depression 42 is designed such that the thumb can be placed comfortably thereon.
A protective cap 43 engaging over the inhaler 1 is used in the interest of hygiene (see Fig. 6). It likewise has, in the lid area, a drying agent chamber 44 which is accommodated in the space remaining free between protective cap 43 and mouthpiece M. The protective cap 43 is recessed in the area of the turning knob 21 (recess 45).
Le A 30 002-Foreiqn Countries - 19 -~13~b 79 An upper, level shoulder 46 of a stand 47 formed integrally on the support structure 34 serves as a limit stop for the protective cap 43. The shell walls are slightly flared in this area, so that the lower edge of the protective cap 43 is held secure by means of a clamping fit.
The protective cap 43 engages over the broad sides and narrow sides of the housing 2 which are formed by the shells 32 and 33, and also over the upper end face of said housing.
On the broad side lying opposite the turning knob 21, the supply container 3 has a transparent, disc-shaped section 48 as viewing window (see Fig. 2). In this way the powder content can be checked. The said viewing window at the same time acts as a filling lid. The latter could also serve as for the support static loosening fingers 29, if this version were to be constructed. The drying agent chamber 30 described could also be situated on the inner side of the filling lid.
The functioning of the inhaler 1 is, in brief, as foll-ows: The air sucked in through the air inlet channel 9 flows, upon inhalation, into the portion chamber 11 filled with the metered quantity and carries the drug 4 into the upwardly directed flow path, i.e. into the connection channel 8. The the flow velocity decreases as it passes into the area of the swirl chamber W lying above. Here the air current passes into the dwell-time chamber 36, with decreasing velocity and counter to the force of gravity of the particles, and from there crosses transversely through the central passage 38, with further deceleration, into the outlet chamber 37. The powder/air mixture finally reaches the foot area of the mouthpiece channel 7, which acts as dispersing chamber. From the adjoining diffusor, which is formed by the upper end of Le A 30 002-Foreiqn Countries - 20 -the mouthpiece channel 7, the medicament passes via the outlet opening 6 to the target site (bronchi, lung). The flow path in the dispersing part I resembles two succes-sive loops of the same direction of rotation.
By virtue of the continuous decrease in the flow velocity as far as the outlet opening 6 on the mouthpiece channel 7, the likelihood of impact separation of relatively small particles in the throat area is greatly reduced.
Le A 30 002-Foreiqn Countries - 21 -
Claims (24)
1. Device for inhalation of a powdery, pharmacolog-ically active drug, consisting of a supply container (3) for the drug (4), a manually actuated metering unit for providing a portioned-off quantity of inhalation substance which is picked up by the air current drawn in during inhalation and is swirled, an air inlet channel (9), a swirl chamber (W), and a connection channel (8) between the swirl chamber (W) and the metering unit, as well as a mouthpiece channel (7) issuing from the swirl chamber (W), characterized in that the metering unit consists of a metering drum, the supply container (3) for the drug being arranged in the interior (5) of the metering drum D, and that the air inlet channel (9) and the connection channel (8) run towards each other in a V-shape and towards a portioned-off quantity of drug present in the shape of a dome and provided by the metering drum D at the apex of the two air channels (8) and (9).
2. Device according to Claim 1 or especially according thereto, characterized in that the connection chan-nel (8) runs radially with respect to the metering drum (D).
3. Device according to one or more of the preceding claims or especially according thereto, charac-terized in that the connection channel (8) widens towards the swirl chamber (W), and the trace line of the one wall (a) lies essentially radially with respect to the centre (Z'') of the swirl chamber (W) and that of the other wall (b) runs essentially tangentially thereto.
Le A 30 002-Foreign Countries - 22 -
Le A 30 002-Foreign Countries - 22 -
4. Device according to one or more of the preceding claims or especially according thereto, charac-terized in that the mouthpiece channel (7) runs at an obtuse angle with respect to the connection channel (8), and the trace line of one wall (c) is directed approximately tangentially, and that of the other wall (d) approximately radially, with respect to the centre (Z'') of the swirl chamber (W).
5. Device according to one or more of the preceding claims or especially according thereto, charac-terized in that the trace lines of the inner wall (e) and outer wall (f) of the air inlet channel (9) are directed in secant formation with respect to the metering drum (D).
6. Device according to one or more of the preceding claims or especially according thereto, charac-terized in that the metering drum (D) has a rotary sleeve (15) equipped with portion apertures (14).
7. Device according to one or more of the preceding claims or especially according thereto, charac-terized in that the rotary sleeve (15) is formed by the circumferential wall of a pot, on the base (18) of which a turning knob (21) is arranged.
8. Device according to one or more of the preceding claims or especially according thereto, charac-terized by a catch mechanism (22), determining the direction of rotation, between rotary sleeve (15) and housing (2) of the device.
9. Device according to one or more of the preceding claims or especially according thereto, charac-terized in that the rotary sleeve (15) is surrounded by an annular wall 16 and is underpinned, over a Le A 30 002-Foreign Countries - 23 -partial angle range, by an inner wall section (17) which, in the area of the V apex (10), forms the base of the portion chamber (11) formed by in each case one of the apertures (14).
10. Device according to one or more of the preceding claims or especially according thereto, charac-terized in that the transverse walls (13) of the apertures (14) run in a wedge formation in the direction of the centre (Z') of the metering drum (D).
11. Device according to one or more of the preceding claims or especially according thereto, charac-terized in that, issuing from the base (18) of the pot and/or from the housing (2), loosening fingers (29) protrude into the metering drum (D).
12. Device according to one or more of the preceding claims or especially according thereto, charac-terized in that a drying agent chamber (30) is allocated to the base (20) of the pot or to the inner side of a housing-filling lid.
13. Device according to one or more of the preceding claims or especially according thereto, charac-terized in that transversely directed air inlet slots (39) are arranged at the intake end of the air inlet channel (9).
14. Device according to one or more of the preceding claims or especially according thereto, charac-terized in that the air inlet slots (39) are prov-ided on both broad sides of the device housing (2).
15. Device according to one or more of the preceding claims or especially according thereto, charac-Le A 30 002-Foreign Countries - 24 -terized by a dividing gusset (40) in the flow path of the air inlet channel (9).
16. Device according to one or more of the preceding claims or especially according thereto, charac-terized in that the air inlet slots (39) are allo-cated exhalation barrier tongues (41).
17. Device according to one or more of the preceding claims, characterized in that the air inlet slots (39) are arranged in the head area of the inhaler and reach to about the height of the centre Z'' of the swirl chamber (W).
18. Device according to one or more of the preceding claims, characterized in that a finger depression (42) is arranged on the inhaler housing (2) below the swirl chamber (W).
19. Device according to one or more of the preceding claims or especially according thereto, charac-terized by a protective cap (43) engaging over the housing (2).
20. Device according to one or more of the preceding claims or especially according thereto, charac-terized by a drying agent chamber (44) allocated to the protective cap (43).
21. Device according to one or more of the preceding claims, characterized in that the channels (7, 8, 9) and the swirl chamber (W) are accommodated in a support structure (34) which can be enclosed by two housing shells (32, 33) and in which the metering drum (D) is also mounted, the housing shells (32, 33) forming the covering for the channels (7, 8, 9) and the swirl chamber (W).
Le A 30 002-Foreign Countries - 25 -
Le A 30 002-Foreign Countries - 25 -
22. Device according to one or more of the preceding claims, characterized in that the swirl chamber (W) is formed by a dwell-time chamber (36) and by a discharge chamber (37) which are connected to each other via a central passage (38), and in that a mouthpiece channel (7) acting as dispersing chamber adjoins the discharge chamber (37).
23. Device according to one or more of the preceding claims, characterized in that the support structure (34) has a stand (47), the shoulder (46) of which forms a push-on limit stop on which the protective cap (43) can be securely clamped.
24. Device according to one or more of the preceding claims, characterized in that the wall section (36') of the dwell-time chamber (36) directed towards the upper end of the connection channel (8) has a smaller curvature than the remaining part of the dwell-time chamber (36) and is consequently flatt-ened at the point of transfer into the dwell-time chamber (36), and in that the central passage (38) in the dwell-time chamber (36) is arranged eccentrically relative to the flattened wall section (36').
Le A 30 002-Foreign Countries - 26 -
Le A 30 002-Foreign Countries - 26 -
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4340768A DE4340768A1 (en) | 1993-11-30 | 1993-11-30 | Inhalation device |
| DEP4340768.4 | 1993-11-30 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2136679A1 true CA2136679A1 (en) | 1995-05-31 |
Family
ID=6503794
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002136679A Abandoned CA2136679A1 (en) | 1993-11-30 | 1994-11-25 | Device for inhalation |
Country Status (33)
| Country | Link |
|---|---|
| US (1) | US5505196A (en) |
| EP (1) | EP0661070B1 (en) |
| JP (1) | JP3293722B2 (en) |
| CN (1) | CN1106303A (en) |
| AT (1) | ATE180173T1 (en) |
| BG (1) | BG61432B1 (en) |
| BR (1) | BR9404786A (en) |
| CA (1) | CA2136679A1 (en) |
| CO (1) | CO4180610A1 (en) |
| CZ (1) | CZ285105B6 (en) |
| DE (2) | DE4340768A1 (en) |
| DK (1) | DK0661070T3 (en) |
| EE (1) | EE03138B1 (en) |
| ES (1) | ES2131619T3 (en) |
| FI (1) | FI945591A (en) |
| GR (1) | GR3030323T3 (en) |
| HR (1) | HRP940932B1 (en) |
| HU (1) | HU217046B (en) |
| IL (1) | IL111782A (en) |
| LV (1) | LV11281B (en) |
| NO (1) | NO944574L (en) |
| NZ (1) | NZ264992A (en) |
| PE (1) | PE31795A1 (en) |
| PH (1) | PH30706A (en) |
| PL (1) | PL175953B1 (en) |
| RO (1) | RO112953B1 (en) |
| RU (1) | RU2138303C1 (en) |
| SI (1) | SI0661070T1 (en) |
| SK (1) | SK280351B6 (en) |
| SV (1) | SV1994000068A (en) |
| TW (1) | TW281632B (en) |
| YU (1) | YU68594A (en) |
| ZA (1) | ZA949467B (en) |
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| FI95441C (en) * | 1994-05-31 | 1996-02-12 | Leiras Oy | Inhaler drug chamber |
| DE19518810A1 (en) * | 1995-05-26 | 1996-11-28 | Bayer Ag | Nasal applicator |
| DE19522415C2 (en) * | 1995-06-21 | 2003-12-04 | Sofotec Gmbh & Co Kg | Drug powder cartridge with integrated dosing device and powder inhaler with means for actuating the dosing device of the drug powder cartridge |
| ES2168488T3 (en) * | 1995-06-21 | 2002-06-16 | Sofotec Gmbh & Co Kg | PHARMACEUTICAL POWDER CARTRIDGE WITH INTEGRATED DOSING DEVICE AND INHALER FOR POWDERED MEDICINES. |
| JP3317823B2 (en) * | 1995-08-11 | 2002-08-26 | 株式会社ユニシアジェックス | Dosing device |
| SE9700938D0 (en) * | 1997-03-14 | 1997-03-14 | Astra Ab | Powder inhaler II and a method of construction thereof |
| US6073629A (en) * | 1997-09-25 | 2000-06-13 | Norton Healthcare Ltd. | Inhaler spacer |
| GB9720283D0 (en) * | 1997-09-25 | 1997-11-26 | Norton Healthcare Ltd | Inhaler spacer |
| DE19825434C2 (en) * | 1998-01-30 | 2002-03-28 | Ig Spruehtechnik Gmbh | Inhaler for powdered medication |
| SI20363A (en) * | 1998-01-30 | 2001-04-30 | Ig Spruehtechnik Gmbh & Co.Kg | Inhalation apparatus for powder medications |
| SE9801114D0 (en) * | 1998-03-30 | 1998-03-30 | Astra Ab | Inhalation device |
| DE19817417A1 (en) * | 1998-04-18 | 1999-10-21 | Pfeiffer Erich Gmbh & Co Kg | Dispenser for media, especially powder |
| DE60019920T2 (en) * | 1999-06-05 | 2006-02-23 | Innovata Biomed Ltd., St. Albans | ADMINISTRATION SYSTEM FOR MEDICAMENTS |
| EP1220700B1 (en) | 1999-10-06 | 2003-04-09 | Eckardt, Angela | Breathing-controlled inhalation device for dry powder |
| US6427688B1 (en) * | 2000-02-01 | 2002-08-06 | Dura Pharmaceuticals, Icn. | Dry powder inhaler |
| AU2001234005B2 (en) * | 2000-02-28 | 2006-01-19 | Pharmakodex Limited | Improvements in or relating to the delivery of oral drugs |
| EP1177806A1 (en) * | 2000-08-04 | 2002-02-06 | The Technology Partnership Public Limited Company | Dry powder inhaler |
| FI20010538A0 (en) * | 2001-03-16 | 2001-03-16 | Orion Corp | The powder inhaler |
| WO2003020197A1 (en) * | 2001-09-05 | 2003-03-13 | Vectura Limited | Improvements in or relating to the delivery of oral drugs |
| US7258118B2 (en) * | 2002-01-24 | 2007-08-21 | Sofotec Gmbh & Co, Kg | Pharmaceutical powder cartridge, and inhaler equipped with same |
| DE10202940A1 (en) | 2002-01-24 | 2003-07-31 | Sofotec Gmbh & Co Kg | Cartridge for a powder inhaler |
| JP2005527508A (en) * | 2002-03-07 | 2005-09-15 | ヴェクトゥラ リミテッド | Rapid melting multiparticulate formulation for oral delivery |
| US6985798B2 (en) * | 2002-05-10 | 2006-01-10 | Oriel Therapeutics, Inc. | Dry powder dose filling systems and related methods |
| US6889690B2 (en) | 2002-05-10 | 2005-05-10 | Oriel Therapeutics, Inc. | Dry powder inhalers, related blister devices, and associated methods of dispensing dry powder substances and fabricating blister packages |
| US7677411B2 (en) * | 2002-05-10 | 2010-03-16 | Oriel Therapeutics, Inc. | Apparatus, systems and related methods for processing, dispensing and/or evaluatingl dry powders |
| US7118010B2 (en) * | 2002-05-10 | 2006-10-10 | Oriel Therapeutics, Inc. | Apparatus, systems and related methods for dispensing and /or evaluating dry powders |
| EP1535349B1 (en) * | 2002-06-27 | 2014-06-25 | Oriel Therapeutics, Inc. | Apparatus, systems and related methods for processing, dispensing and/or evaluating non-pharmaceutical dry powders |
| DE10300032B3 (en) * | 2003-01-03 | 2004-05-27 | E. Braun Gmbh | Inhaler for powdered medicament has pivoted inhalation tube which shuts off powder supply when in out-of-use position, and doses powder into airflow when in use |
| EP1488819A1 (en) | 2003-06-16 | 2004-12-22 | Rijksuniversiteit te Groningen | Dry powder inhaler and method for pulmonary inhalation of dry powder |
| US7377277B2 (en) * | 2003-10-27 | 2008-05-27 | Oriel Therapeutics, Inc. | Blister packages with frames and associated methods of fabricating dry powder drug containment systems |
| US7451761B2 (en) * | 2003-10-27 | 2008-11-18 | Oriel Therapeutics, Inc. | Dry powder inhalers, related blister package indexing and opening mechanisms, and associated methods of dispensing dry powder substances |
| UA93031C2 (en) | 2004-07-16 | 2011-01-10 | Алміралл, С.А. | inhaler for powdered medicaments, pharmaceutical powder cartridge for use with the inhaler and method for inhaler use |
| DE102004041524B4 (en) * | 2004-08-27 | 2013-03-21 | Sanofi Sa | Inhaler for powdery, in particular medicinal substances |
| AU2007224178B2 (en) * | 2006-03-03 | 2013-03-07 | Stc.Unm | Dry powder inhaler with aeroelastic dispersion mechanism |
| WO2007123945A2 (en) * | 2006-04-21 | 2007-11-01 | Aradigm Corporation | Mechanical single dose intrapulmonary drug delivery devices |
| UA95506C2 (en) * | 2006-12-22 | 2011-08-10 | Альміраль, С.А. | Inhalation device for powder drugs |
| WO2009046215A2 (en) * | 2007-10-02 | 2009-04-09 | Lab International Srl | Safety and abuse deterrent improved device |
| JP5570996B2 (en) | 2007-12-14 | 2014-08-13 | エアロデザインズ インコーポレイテッド | Delivery of aerosolizable foodstuffs |
| EP2498848A2 (en) | 2009-11-12 | 2012-09-19 | Stc.Unm | Dry powder inhaler with flutter dispersion member |
| US8561609B2 (en) | 2010-12-07 | 2013-10-22 | Respira Therapeutics, Inc. | Dry powder inhaler |
| US10463815B2 (en) | 2012-02-21 | 2019-11-05 | Respira Therapeutics, Inc. | Inhaler to deliver substances for prophylaxis or prevention of disease or injury caused by the inhalation of biological or chemical agents |
| DE102014005646B4 (en) | 2014-01-30 | 2016-05-12 | Klaus-Dieter Beller | Powder inhaler and powder inhalation kit |
| HU230619B1 (en) * | 2014-12-30 | 2017-04-28 | Tamás Kókai | Unit for micronizing and dosing solid agents |
| CN107427650A (en) | 2015-01-14 | 2017-12-01 | 瑞必治公司 | Powder process for dispersing and device |
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| GB1392945A (en) * | 1972-08-23 | 1975-05-07 | Fisons Ltd | Inhalation device |
| ES506585A0 (en) * | 1980-10-30 | 1982-09-01 | Riker Laboratories Inc | A DEVICE TO FACILITATE THE ORAL INHALATION OF MEDICINES IN THE FORM OF POWDER |
| FI69963C (en) * | 1984-10-04 | 1986-09-12 | Orion Yhtymae Oy | DOSERINGSANORDNING |
| SE453566B (en) * | 1986-03-07 | 1988-02-15 | Draco Ab | POWDER INHALATOR DEVICE |
| US5176132A (en) * | 1989-05-31 | 1993-01-05 | Fisons Plc | Medicament inhalation device and formulation |
| US5113855A (en) * | 1990-02-14 | 1992-05-19 | Newhouse Michael T | Powder inhaler |
| DE4004904A1 (en) * | 1990-02-16 | 1990-09-13 | Gerhard Brendel | DRUM APPLICATOR |
| GB9015522D0 (en) * | 1990-07-13 | 1990-08-29 | Braithwaite Philip W | Inhaler |
| GB9026025D0 (en) * | 1990-11-29 | 1991-01-16 | Boehringer Ingelheim Kg | Inhalation device |
| AU650953B2 (en) * | 1991-03-21 | 1994-07-07 | Novartis Ag | Inhaler |
| US5243970A (en) * | 1991-04-15 | 1993-09-14 | Schering Corporation | Dosing device for administering metered amounts of powdered medicaments to patients |
| DE4211475A1 (en) * | 1991-12-14 | 1993-06-17 | Asta Medica Ag | POWDER INHALATOR |
-
1993
- 1993-11-30 DE DE4340768A patent/DE4340768A1/en not_active Withdrawn
-
1994
- 1994-11-07 TW TW083110256A patent/TW281632B/zh active
- 1994-11-11 EE EE9400248A patent/EE03138B1/en unknown
- 1994-11-14 HR HRP4340768.4A patent/HRP940932B1/en not_active IP Right Cessation
- 1994-11-17 EP EP94118118A patent/EP0661070B1/en not_active Expired - Lifetime
- 1994-11-17 ES ES94118118T patent/ES2131619T3/en not_active Expired - Lifetime
- 1994-11-17 DE DE59408283T patent/DE59408283D1/en not_active Expired - Fee Related
- 1994-11-17 DK DK94118118T patent/DK0661070T3/en active
- 1994-11-17 AT AT94118118T patent/ATE180173T1/en not_active IP Right Cessation
- 1994-11-17 SI SI9430240T patent/SI0661070T1/en unknown
- 1994-11-23 US US08/344,049 patent/US5505196A/en not_active Expired - Fee Related
- 1994-11-24 YU YU68594A patent/YU68594A/en unknown
- 1994-11-25 JP JP31428894A patent/JP3293722B2/en not_active Expired - Fee Related
- 1994-11-25 NZ NZ264992A patent/NZ264992A/en unknown
- 1994-11-25 PH PH49454A patent/PH30706A/en unknown
- 1994-11-25 CA CA002136679A patent/CA2136679A1/en not_active Abandoned
- 1994-11-28 PL PL94306024A patent/PL175953B1/en unknown
- 1994-11-28 CO CO94054150A patent/CO4180610A1/en unknown
- 1994-11-28 FI FI945591A patent/FI945591A/en unknown
- 1994-11-28 IL IL111782A patent/IL111782A/en not_active IP Right Cessation
- 1994-11-28 RO RO94-01906A patent/RO112953B1/en unknown
- 1994-11-29 RU RU94042242A patent/RU2138303C1/en active
- 1994-11-29 CZ CZ942945A patent/CZ285105B6/en not_active IP Right Cessation
- 1994-11-29 HU HU9403425A patent/HU217046B/en not_active IP Right Cessation
- 1994-11-29 BR BR9404786A patent/BR9404786A/en not_active Application Discontinuation
- 1994-11-29 BG BG99220A patent/BG61432B1/en unknown
- 1994-11-29 SV SV1994000068A patent/SV1994000068A/en unknown
- 1994-11-29 SK SK1453-94A patent/SK280351B6/en unknown
- 1994-11-29 PE PE1994255989A patent/PE31795A1/en not_active Application Discontinuation
- 1994-11-29 ZA ZA949467A patent/ZA949467B/en unknown
- 1994-11-29 NO NO944574A patent/NO944574L/en not_active Application Discontinuation
- 1994-11-30 LV LVP-94-229A patent/LV11281B/en unknown
- 1994-11-30 CN CN94112878A patent/CN1106303A/en active Pending
-
1999
- 1999-05-27 GR GR990401410T patent/GR3030323T3/en unknown
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| FZDE | Discontinued |