Inhaler for the administration of an anticholinergic
Abstract
An inhaler for administration of powdered preparations containing tiotropium, wherein the inhaler displays a flow resistance of 0.01-0.1 √{square root over (kPa)} min/L and comprises a housing, a deck with air inlet ports and a screen secured by a screen housing, an inhalation chamber connected to the deck on which there is a push button provided with two sharpened pins and movable counter to a spring, a mouthpiece which is connected to the housing, the deck and a cover via a spindle to enable the cover to be flipped open or shut, and three holes with diameters below 1 mm in a central region of the deck around a capsule chamber and underneath the screen housing and screen.
Claims
exact text as granted — not AI-modified1 . An inhaler for an inhalable powder, wherein the inhaler comprises: a housing, a deck in which there are air inlet ports and which is provided with a screen secured by a screen housing, an inhalation chamber connected to the deck on which there is a push button provided with two sharpened pins and movable counter to a spring, a mouthpiece which is connected to the housing, the deck, and a cover via a hinge spindle to enable it to be flipped open or shut, and three holes with diameters below 1 mm in the central region around the capsule chamber and underneath the screen housing and screen, wherein the inhaler has a reduced width in the range between the deck and the housing near to the hinge spindle, which forms the entrance slit for the air, and the inhaler displays a flow resistance of about 0.01 to 0.1 √{square root over (kPa)} min/L.
2 . The inhaler according to claim 1 , wherein the inhalable powder contains tiotropium is in an amount of 0.001% to 5%, in admixture with a physiologically acceptable excipient with an average particle size of between 10 μm to 500 μm.
3 . The inhaler according to claim 1 , wherein the inhaler has a flow resistance of about 0.02 to 0.06 √{square root over (kPa)} min/L.
4 . The inhaler according to claim 2 , wherein the inhaler has a flow resistance of about 0.02 to 0.06 √{square root over (kPa)} min/L.
5 . The inhaler according to claim 1 , wherein the tiotropium is a chloride, bromide, iodide, methanesulfonate, p-toluenesulfonate, or methylsulfate salt.
6 . The inhaler according to claim 2 , wherein the tiotropium is a chloride, bromide, iodide, methanesulfonate, p-toluenesulfonate, or methylsulfate salt.
7 . The inhaler according to claim 3 , wherein the tiotropium is a chloride, bromide, iodide, methanesulfonate, p-toluenesulfonate, or methylsulfate salt.
8 . The inhaler according to claim 4 , wherein the tiotropium is a chloride, bromide, iodide, methanesulfonate, p-toluenesulfonate, or methylsulfate salt.
9 . The method according to claim 5 , wherein the tiotropium is crystalline tiotropium bromide monohydrate.
10 . The method according to claim 6 , wherein the tiotropium is crystalline tiotropium bromide monohydrate.
11 . The method according to claim 7 , wherein the tiotropium is crystalline tiotropium bromide monohydrate.
12 . The method according to claim 8 , wherein the tiotropium is crystalline tiotropium bromide monohydrate.
13 . An inhalation kit comprising:
(a) an inhaler according to claim 1 ; and (b) an inhalable powder containing tiotropium.
14 . The inhalation kit according to claim 13 , wherein the inhalable powder containing tiotropium is in an amount of 0.001% to 5%, in admixture with a physiologically acceptable excipient with an average particle size of between 10 μm to 500 μm.
15 . The inhalation kit according to claim 13 , wherein the inhaler has a flow resistance of about 0.02 to 0.06 √{square root over (kPa)} min/L.
16 . The inhalation kit according to claim 14 , wherein the inhaler has a flow resistance of about 0.02 to 0.06 √{square root over (kPa)} min/L.
17 . The inhalation kit according to claim 13 , wherein the tiotropium is a chloride, bromide, iodide, methanesulfonate, p-toluenesulfonate, or methylsulfate salt.
18 . The inhalation kit according to claim 14 , wherein the tiotropium is a chloride, bromide, iodide, methanesulfonate, p-toluenesulfonate, or methylsulfate salt.
19 . The inhalation kit according to claim 15 , wherein the tiotropium is a chloride, bromide, iodide, methanesulfonate, p-toluenesulfonate, or methylsulfate salt.
20 . The inhalation kit according to claim 16 , wherein the tiotropium is a chloride, bromide, iodide, methanesulfonate, p-toluenesulfonate, or methylsulfate salt.
21 . The inhalation kit according to claim 17 , wherein the tiotropium is crystalline tiotropium bromide monohydrate.
22 . The inhalation kit according to claim 18 , wherein the tiotropium is crystalline tiotropium bromide monohydrate.
23 . The inhalation kit according to claim 19 , wherein the tiotropium is crystalline tiotropium bromide monohydrate.
24 . The inhalation kit according to claim 20 , wherein the tiotropium is crystalline tiotropium bromide monohydrate.
25 . A method for the administration of an inhalable powder containing tiotropium, the method comprising using an inhaler according to claim 1 .
26 . A method for the administration of an inhalable powder containing tiotropium, the method comprising using an inhalation kit according to claim 13 .Join the waitlist — get patent alerts
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