CA2653183A1 - Adaptateur avec raccord pour pulverisateur - Google Patents

Adaptateur avec raccord pour pulverisateur Download PDF

Info

Publication number: CA2653183A1
Authority: CA; Canada
Prior art keywords: atomizer; amino; phenyl; quinazoline; methoxy
Prior art date: 2006-06-02
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

Application number

CA002653183A

Other languages

English (en)

Inventor

Michael Markert

Michael Pieper

Hans Schmitt

Juergen Schraivogel

Thomas Trautmann

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Boehringer Ingelheim International GmbH

Original Assignee

Individual

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2006-06-02

Filing date

2007-06-01

Publication date

2007-12-13

2007-06-01 Application filed by Individual filed Critical Individual

2007-12-13 Publication of CA2653183A1 publication Critical patent/CA2653183A1/fr

Status Abandoned legal-status Critical Current

Links

230000000241 respiratory effect Effects 0.000 claims abstract description 41
239000012530 fluid Substances 0.000 claims abstract description 26
239000000443 aerosol Substances 0.000 claims abstract description 19
238000000889 atomisation Methods 0.000 claims abstract description 12
239000003814 drug Substances 0.000 claims description 13
238000003860 storage Methods 0.000 claims description 9
239000007921 spray Substances 0.000 claims description 6
239000003595 mist Substances 0.000 claims description 4
208000036366 Sensation of pressure Diseases 0.000 claims 1
230000014759 maintenance of location Effects 0.000 claims 1
-1 EGFR-inhibitors Substances 0.000 description 35
150000003839 salts Chemical class 0.000 description 24
125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 19
150000001875 compounds Chemical class 0.000 description 16
239000002253 acid Substances 0.000 description 13
FIMXSEMBHGTNKT-UHFFFAOYSA-N Scopine Natural products CN1C2CC(O)CC1C1C2O1 FIMXSEMBHGTNKT-UHFFFAOYSA-N 0.000 description 11
HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 description 10
150000004677 hydrates Chemical class 0.000 description 10
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
239000005557 antagonist Substances 0.000 description 9
239000012453 solvate Substances 0.000 description 9
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 8
229940121647 egfr inhibitor Drugs 0.000 description 7
239000007788 liquid Substances 0.000 description 7
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 5
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 5
229910019142 PO4 Inorganic materials 0.000 description 5
229940123932 Phosphodiesterase 4 inhibitor Drugs 0.000 description 5
239000013543 active substance Substances 0.000 description 5
150000001450 anions Chemical class 0.000 description 5
230000003454 betamimetic effect Effects 0.000 description 5
150000003842 bromide salts Chemical class 0.000 description 5
239000003246 corticosteroid Substances 0.000 description 5
125000005635 hydromethanesulphonate group Chemical group 0.000 description 5
239000002587 phosphodiesterase IV inhibitor Substances 0.000 description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
AFVFQIVMOAPDHO-UHFFFAOYSA-M Methanesulfonate Chemical compound CS([O-])(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-M 0.000 description 4
229940065524 anticholinergics inhalants for obstructive airway diseases Drugs 0.000 description 4
239000000812 cholinergic antagonist Substances 0.000 description 4
210000004072 lung Anatomy 0.000 description 4
239000000203 mixture Substances 0.000 description 4
235000021317 phosphate Nutrition 0.000 description 4
239000000126 substance Substances 0.000 description 4
JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 description 4
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 4
238000009423 ventilation Methods 0.000 description 4
GXAMYUGOODKVRM-UHFFFAOYSA-M 9-hydroxyfluorene-9-carboxylate Chemical compound C1=CC=C2C(O)(C([O-])=O)C3=CC=CC=C3C2=C1 GXAMYUGOODKVRM-UHFFFAOYSA-M 0.000 description 3
DTZDZCNXNYMMOW-UHFFFAOYSA-N 9-hydroxyxanthene-9-carboxylic acid Chemical compound C1=CC=C2C(C(=O)O)(O)C3=CC=CC=C3OC2=C1 DTZDZCNXNYMMOW-UHFFFAOYSA-N 0.000 description 3
PUPWRKQSVGUBQS-UHFFFAOYSA-N 9-methylfluorene-9-carboxylic acid Chemical compound C1=CC=C2C(C)(C(O)=O)C3=CC=CC=C3C2=C1 PUPWRKQSVGUBQS-UHFFFAOYSA-N 0.000 description 3
CBNOKZSYCBHRAD-UHFFFAOYSA-N 9-methylxanthene-9-carboxylic acid Chemical compound C1=CC=C2C(C)(C(O)=O)C3=CC=CC=C3OC2=C1 CBNOKZSYCBHRAD-UHFFFAOYSA-N 0.000 description 3
QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 3
QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 3
239000000808 adrenergic beta-agonist Substances 0.000 description 3
229940079593 drug Drugs 0.000 description 3
239000003112 inhibitor Substances 0.000 description 3
239000002245 particle Substances 0.000 description 3
239000010452 phosphate Substances 0.000 description 3
229910021653 sulphate ion Inorganic materials 0.000 description 3
ZMXHONJJTQSZKY-UHFFFAOYSA-N 2,2-bis(3,4-difluorophenyl)-2-hydroxyacetic acid Chemical compound C=1C=C(F)C(F)=CC=1C(O)(C(=O)O)C1=CC=C(F)C(F)=C1 ZMXHONJJTQSZKY-UHFFFAOYSA-N 0.000 description 2
YKZXWNCXGVYCKF-UHFFFAOYSA-N 2,2-bis(4-fluorophenyl)-2-hydroxyacetic acid Chemical compound C=1C=C(F)C=CC=1C(O)(C(=O)O)C1=CC=C(F)C=C1 YKZXWNCXGVYCKF-UHFFFAOYSA-N 0.000 description 2
ODELFXJUOVNEFZ-UHFFFAOYSA-N 2,2-diphenylpropanoic acid Chemical compound C=1C=CC=CC=1C(C(O)=O)(C)C1=CC=CC=C1 ODELFXJUOVNEFZ-UHFFFAOYSA-N 0.000 description 2
MAGCRYYXZYUDSY-UHFFFAOYSA-N 2-fluoro-2,2-diphenylacetic acid Chemical compound C=1C=CC=CC=1C(F)(C(=O)O)C1=CC=CC=C1 MAGCRYYXZYUDSY-UHFFFAOYSA-N 0.000 description 2
ZMPRRFPMMJQXPP-UHFFFAOYSA-N 2-sulfobenzoic acid Chemical class OC(=O)C1=CC=CC=C1S(O)(=O)=O ZMPRRFPMMJQXPP-UHFFFAOYSA-N 0.000 description 2
ULMFXAMQUGLVGA-LJQANCHMSA-N 3-[[2-methoxy-4-[(2-methylphenyl)sulfonylcarbamoyl]phenyl]methyl]-1-methyl-n-[(2r)-4,4,4-trifluoro-2-methylbutyl]indole-5-carboxamide Chemical compound C=1C=C(CC=2C3=CC(=CC=C3N(C)C=2)C(=O)NC[C@H](C)CC(F)(F)F)C(OC)=CC=1C(=O)NS(=O)(=O)C1=CC=CC=C1C ULMFXAMQUGLVGA-LJQANCHMSA-N 0.000 description 2
CVDXFPBVOIERBH-JWQCQUIFSA-N 4-[(4ar,10bs)-9-ethoxy-8-methoxy-2-methyl-3,4,4a,10b-tetrahydro-1h-benzo[c][1,6]naphthyridin-6-yl]-n,n-di(propan-2-yl)benzamide Chemical compound N([C@@H]1CCN(C)C[C@@H]1C=1C=C(C(=CC=11)OC)OCC)=C1C1=CC=C(C(=O)N(C(C)C)C(C)C)C=C1 CVDXFPBVOIERBH-JWQCQUIFSA-N 0.000 description 2
PYUGFOWNYMLROI-KPKJPENVSA-N 8-[(e)-2-[4-[4-(4-fluorophenyl)butoxy]phenyl]ethenyl]-2-(2h-tetrazol-5-yl)chromen-4-one Chemical compound C1=CC(F)=CC=C1CCCCOC(C=C1)=CC=C1\C=C\C1=CC=CC2=C1OC(C=1NN=NN=1)=CC2=O PYUGFOWNYMLROI-KPKJPENVSA-N 0.000 description 2
BHEFSGMUMYBJRZ-UHFFFAOYSA-N 9-fluorofluorene-9-carboxylic acid Chemical compound C1=CC=C2C(C(=O)O)(F)C3=CC=CC=C3C2=C1 BHEFSGMUMYBJRZ-UHFFFAOYSA-N 0.000 description 2
208000006545 Chronic Obstructive Pulmonary Disease Diseases 0.000 description 2
KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 description 2
FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 2
KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 description 2
VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
229910002651 NO3 Inorganic materials 0.000 description 2
NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical class OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical class CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
150000001242 acetic acid derivatives Chemical class 0.000 description 2
229910052783 alkali metal Inorganic materials 0.000 description 2
150000003797 alkaloid derivatives Chemical class 0.000 description 2
230000001078 anti-cholinergic effect Effects 0.000 description 2
229940125715 antihistaminic agent Drugs 0.000 description 2
239000000739 antihistaminic agent Substances 0.000 description 2
239000002585 base Substances 0.000 description 2
WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 2
CFBUZOUXXHZCFB-OYOVHJISSA-N chembl511115 Chemical compound COC1=CC=C([C@@]2(CC[C@H](CC2)C(O)=O)C#N)C=C1OC1CCCC1 CFBUZOUXXHZCFB-OYOVHJISSA-N 0.000 description 2
238000010276 construction Methods 0.000 description 2
229960001334 corticosteroids Drugs 0.000 description 2
229940052760 dopamine agonists Drugs 0.000 description 2
239000003136 dopamine receptor stimulating agent Substances 0.000 description 2
229960003133 ergot alkaloid Drugs 0.000 description 2
238000009472 formulation Methods 0.000 description 2
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 2
LMOINURANNBYCM-UHFFFAOYSA-N metaproterenol Chemical compound CC(C)NCC(O)C1=CC(O)=CC(O)=C1 LMOINURANNBYCM-UHFFFAOYSA-N 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
FSDOTMQXIKBFKJ-UHFFFAOYSA-N n-(2,5-dichloropyridin-3-yl)-8-methoxyquinoline-5-carboxamide Chemical compound C12=CC=CN=C2C(OC)=CC=C1C(=O)NC1=CC(Cl)=CN=C1Cl FSDOTMQXIKBFKJ-UHFFFAOYSA-N 0.000 description 2
DPHDSIQHVGSITN-UHFFFAOYSA-N n-(3,5-dichloropyridin-4-yl)-2-[1-[(4-fluorophenyl)methyl]-5-hydroxyindol-3-yl]-2-oxoacetamide Chemical compound C1=C(C(=O)C(=O)NC=2C(=CN=CC=2Cl)Cl)C2=CC(O)=CC=C2N1CC1=CC=C(F)C=C1 DPHDSIQHVGSITN-UHFFFAOYSA-N 0.000 description 2
229960002657 orciprenaline Drugs 0.000 description 2
150000002942 palmitic acid derivatives Chemical class 0.000 description 2
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 2
150000003013 phosphoric acid derivatives Chemical class 0.000 description 2
125000005547 pivalate group Chemical group 0.000 description 2
159000000001 potassium salts Chemical class 0.000 description 2
230000029058 respiratory gaseous exchange Effects 0.000 description 2
150000003431 steroids Chemical class 0.000 description 2
KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 2
125000000446 sulfanediyl group Chemical group *S* 0.000 description 2
230000009885 systemic effect Effects 0.000 description 2
229940095064 tartrate Drugs 0.000 description 2
JWZZKOKVBUJMES-UHFFFAOYSA-N (+-)-Isoprenaline Chemical compound CC(C)NCC(O)C1=CC=C(O)C(O)=C1 JWZZKOKVBUJMES-UHFFFAOYSA-N 0.000 description 1
XWTYSIMOBUGWOL-UHFFFAOYSA-N (+-)-Terbutaline Chemical compound CC(C)(C)NCC(O)C1=CC(O)=CC(O)=C1 XWTYSIMOBUGWOL-UHFFFAOYSA-N 0.000 description 1
NDAUXUAQIAJITI-LBPRGKRZSA-N (R)-salbutamol Chemical compound CC(C)(C)NC[C@H](O)C1=CC=C(O)C(CO)=C1 NDAUXUAQIAJITI-LBPRGKRZSA-N 0.000 description 1
LITNEAPWQHVPOK-FFSVYQOJSA-N 2(1h)-pyrimidinone, 5-[3-[(1s,2s,4r)-bicyclo[2.2.1]hept-2-yloxy]-4-methoxyphenyl]tetrahydro- Chemical compound C1=C(O[C@@H]2[C@H]3CC[C@H](C3)C2)C(OC)=CC=C1C1CNC(=O)NC1 LITNEAPWQHVPOK-FFSVYQOJSA-N 0.000 description 1
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KVVDRQDTODKIJD-UHFFFAOYSA-N 2-cyclopropylacetic acid Chemical compound OC(=O)CC1CC1 KVVDRQDTODKIJD-UHFFFAOYSA-N 0.000 description 1
BWYJJZBRYSADRP-UHFFFAOYSA-N 2-methoxyquinazoline Chemical compound C1=CC=CC2=NC(OC)=NC=C21 BWYJJZBRYSADRP-UHFFFAOYSA-N 0.000 description 1
DDYUBCCTNHWSQM-UHFFFAOYSA-N 3-(3-cyclopentyloxy-4-methoxyphenyl)-3-(1,3-dioxoisoindol-2-yl)propanamide Chemical compound COC1=CC=C(C(CC(N)=O)N2C(C3=CC=CC=C3C2=O)=O)C=C1OC1CCCC1 DDYUBCCTNHWSQM-UHFFFAOYSA-N 0.000 description 1
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UTUUPXBCDMQYRR-HSZRJFAPSA-N 4-[(2r)-2-(3-cyclopentyloxy-4-methoxyphenyl)-2-phenylethyl]pyridine Chemical compound COC1=CC=C([C@H](CC=2C=CN=CC=2)C=2C=CC=CC=2)C=C1OC1CCCC1 UTUUPXBCDMQYRR-HSZRJFAPSA-N 0.000 description 1
LIXBJWRFCNRAPA-UHFFFAOYSA-N 4-[2-(tert-butylamino)-1-hydroxyethyl]-3-chlorophenol Chemical compound CC(C)(C)NCC(O)C1=CC=C(O)C=C1Cl LIXBJWRFCNRAPA-UHFFFAOYSA-N 0.000 description 1
DAFYYTQWSAWIGS-UHFFFAOYSA-N 4-[2-[6-[2-[(2,6-dichlorophenyl)methoxy]ethoxy]hexylamino]-1-hydroxyethyl]-2-(hydroxymethyl)phenol Chemical compound C1=C(O)C(CO)=CC(C(O)CNCCCCCCOCCOCC=2C(=CC=CC=2Cl)Cl)=C1 DAFYYTQWSAWIGS-UHFFFAOYSA-N 0.000 description 1
CFBUZOUXXHZCFB-UHFFFAOYSA-N 4-cyano-4-(3-cyclopentyloxy-4-methoxyphenyl)-1-cyclohexanecarboxylic acid Chemical compound COC1=CC=C(C2(CCC(CC2)C(O)=O)C#N)C=C1OC1CCCC1 CFBUZOUXXHZCFB-UHFFFAOYSA-N 0.000 description 1
KBDAGRORIZKHHD-UHFFFAOYSA-N 4h-1,4-benzoxazin-3-one;ethyl n-[4-[2-(tert-butylamino)-1-hydroxyethyl]-2-cyano-6-fluorophenyl]carbamate Chemical compound C1=CC=C2NC(=O)COC2=C1.CCOC(=O)NC1=C(F)C=C(C(O)CNC(C)(C)C)C=C1C#N KBDAGRORIZKHHD-UHFFFAOYSA-N 0.000 description 1
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XMOAAORIXBPOCZ-UHFFFAOYSA-N 9-(difluoromethyl)xanthene-9-carboxylic acid Chemical compound C1=CC=C2C(C(=O)O)(C(F)F)C3=CC=CC=C3OC2=C1 XMOAAORIXBPOCZ-UHFFFAOYSA-N 0.000 description 1
ZRDOWGBNGIHJTG-UHFFFAOYSA-N 9-(hydroxymethyl)xanthene-9-carboxylic acid Chemical compound C1=CC=C2C(CO)(C(O)=O)C3=CC=CC=C3OC2=C1 ZRDOWGBNGIHJTG-UHFFFAOYSA-N 0.000 description 1
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DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
HUYWAWARQUIQLE-UHFFFAOYSA-N Isoetharine Chemical compound CC(C)NC(CC)C(O)C1=CC=C(O)C(O)=C1 HUYWAWARQUIQLE-UHFFFAOYSA-N 0.000 description 1
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OIGNJSKKLXVSLS-VWUMJDOOSA-N prednisolone Chemical compound O=C1C=C[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 OIGNJSKKLXVSLS-VWUMJDOOSA-N 0.000 description 1
229960004618 prednisone Drugs 0.000 description 1
XOFYZVNMUHMLCC-ZPOLXVRWSA-N prednisone Chemical compound O=C1C=C[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 XOFYZVNMUHMLCC-ZPOLXVRWSA-N 0.000 description 1
229960002288 procaterol Drugs 0.000 description 1
FKNXQNWAXFXVNW-BLLLJJGKSA-N procaterol Chemical compound N1C(=O)C=CC2=C1C(O)=CC=C2[C@@H](O)[C@@H](NC(C)C)CC FKNXQNWAXFXVNW-BLLLJJGKSA-N 0.000 description 1
229960003910 promethazine Drugs 0.000 description 1
239000003380 propellant Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
MIXMJCQRHVAJIO-TZHJZOAOSA-N qk4dys664x Chemical compound O.C1([C@@H](F)C2)=CC(=O)C=C[C@]1(C)[C@@H]1[C@@H]2[C@@H]2C[C@H]3OC(C)(C)O[C@@]3(C(=O)CO)[C@@]2(C)C[C@@H]1O.C1([C@@H](F)C2)=CC(=O)C=C[C@]1(C)[C@@H]1[C@@H]2[C@@H]2C[C@H]3OC(C)(C)O[C@@]3(C(=O)CO)[C@@]2(C)C[C@@H]1O MIXMJCQRHVAJIO-TZHJZOAOSA-N 0.000 description 1
229960002720 reproterol Drugs 0.000 description 1
WVLAAKXASPCBGT-UHFFFAOYSA-N reproterol Chemical compound C1=2C(=O)N(C)C(=O)N(C)C=2N=CN1CCCNCC(O)C1=CC(O)=CC(O)=C1 WVLAAKXASPCBGT-UHFFFAOYSA-N 0.000 description 1
229960001457 rimiterol Drugs 0.000 description 1
IYMMESGOJVNCKV-SKDRFNHKSA-N rimiterol Chemical compound C([C@@H]1[C@@H](O)C=2C=C(O)C(O)=CC=2)CCCN1 IYMMESGOJVNCKV-SKDRFNHKSA-N 0.000 description 1
IXTCZMJQGGONPY-XJAYAHQCSA-N rofleponide Chemical compound C1([C@@H](F)C2)=CC(=O)CC[C@]1(C)[C@]1(F)[C@@H]2[C@@H]2C[C@H]3O[C@@H](CCC)O[C@@]3(C(=O)CO)[C@@]2(C)C[C@@H]1O IXTCZMJQGGONPY-XJAYAHQCSA-N 0.000 description 1
229950004432 rofleponide Drugs 0.000 description 1
MNDBXUUTURYVHR-UHFFFAOYSA-N roflumilast Chemical compound FC(F)OC1=CC=C(C(=O)NC=2C(=CN=CC=2Cl)Cl)C=C1OCC1CC1 MNDBXUUTURYVHR-UHFFFAOYSA-N 0.000 description 1
229960002586 roflumilast Drugs 0.000 description 1
229960001879 ropinirole Drugs 0.000 description 1
UHSKFQJFRQCDBE-UHFFFAOYSA-N ropinirole Chemical compound CCCN(CCC)CCC1=CC=CC2=C1CC(=O)N2 UHSKFQJFRQCDBE-UHFFFAOYSA-N 0.000 description 1
HGEYJZMMUGWEOT-UHFFFAOYSA-N roxindole Chemical compound C12=CC(O)=CC=C2NC=C1CCCCN(CC=1)CCC=1C1=CC=CC=C1 HGEYJZMMUGWEOT-UHFFFAOYSA-N 0.000 description 1
229950001879 salmefamol Drugs 0.000 description 1
229960004017 salmeterol Drugs 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229950010289 soterenol Drugs 0.000 description 1
229960000195 terbutaline Drugs 0.000 description 1
229960004558 terguride Drugs 0.000 description 1
125000004192 tetrahydrofuran-2-yl group Chemical group [H]C1([H])OC([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 1
229960000278 theophylline Drugs 0.000 description 1
229950010302 tiaramide Drugs 0.000 description 1
HTJXMOGUGMSZOG-UHFFFAOYSA-N tiaramide Chemical compound C1CN(CCO)CCN1C(=O)CN1C(=O)SC2=CC=C(Cl)C=C21 HTJXMOGUGMSZOG-UHFFFAOYSA-N 0.000 description 1
LERNTVKEWCAPOY-DZZGSBJMSA-N tiotropium Chemical class O([C@H]1C[C@@H]2[N+]([C@H](C1)[C@@H]1[C@H]2O1)(C)C)C(=O)C(O)(C=1SC=CC=1)C1=CC=CS1 LERNTVKEWCAPOY-DZZGSBJMSA-N 0.000 description 1
229950003899 tofimilast Drugs 0.000 description 1
OOGJQPCLVADCPB-HXUWFJFHSA-N tolterodine Chemical compound C1([C@@H](CCN(C(C)C)C(C)C)C=2C(=CC=C(C)C=2)O)=CC=CC=C1 OOGJQPCLVADCPB-HXUWFJFHSA-N 0.000 description 1
229960004045 tolterodine Drugs 0.000 description 1
230000000699 topical effect Effects 0.000 description 1
230000002110 toxicologic effect Effects 0.000 description 1
231100000027 toxicology Toxicity 0.000 description 1
229960000575 trastuzumab Drugs 0.000 description 1
229960005294 triamcinolone Drugs 0.000 description 1
GFNANZIMVAIWHM-OBYCQNJPSA-N triamcinolone Chemical compound O=C1C=C[C@]2(C)[C@@]3(F)[C@@H](O)C[C@](C)([C@@]([C@H](O)C4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 GFNANZIMVAIWHM-OBYCQNJPSA-N 0.000 description 1
OYYDSUSKLWTMMQ-JKHIJQBDSA-N trospium Chemical class [N+]12([C@@H]3CC[C@H]2C[C@H](C3)OC(=O)C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CCCC1 OYYDSUSKLWTMMQ-JKHIJQBDSA-N 0.000 description 1
BDIAUFOIMFAIPU-UHFFFAOYSA-N valepotriate Natural products CC(C)CC(=O)OC1C=C(C(=COC2OC(=O)CC(C)C)COC(C)=O)C2C11CO1 BDIAUFOIMFAIPU-UHFFFAOYSA-N 0.000 description 1
229960004764 zafirlukast Drugs 0.000 description 1
XJBCFFLVLOPYBV-UHFFFAOYSA-N zinterol Chemical compound C=1C=C(O)C(NS(C)(=O)=O)=CC=1C(O)CNC(C)(C)CC1=CC=CC=C1 XJBCFFLVLOPYBV-UHFFFAOYSA-N 0.000 description 1
229950004209 zinterol Drugs 0.000 description 1
XJSMBWUHHJFJFV-VTIMJTGVSA-N α-dihydroergocryptine Chemical compound C([C@H]1N(C)C2)C([C]34)=CN=C4C=CC=C3[C@H]1C[C@H]2C(=O)N[C@@]1(C(C)C)C(=O)N2[C@@H](CC(C)C)C(=O)N3CCC[C@H]3[C@]2(O)O1 XJSMBWUHHJFJFV-VTIMJTGVSA-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
- A61M16/00—Devices for influencing the respiratory system of patients by gas treatment, e.g. ventilators; Tracheal tubes
- A61M16/08—Bellows; Connecting tubes ; Water traps; Patient circuits
- 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
- A61M11/00—Sprayers or atomisers specially adapted for therapeutic purposes
- A61M11/006—Sprayers or atomisers specially adapted for therapeutic purposes operated by applying mechanical pressure to the liquid to be sprayed or atomised
- A61M11/007—Syringe-type or piston-type sprayers or atomisers
- 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
- A61M15/0001—Details of inhalators; Constructional features thereof
- A61M15/0021—Mouthpieces therefor
- 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

Landscapes

Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Life Sciences & Earth Sciences (AREA)
Anesthesiology (AREA)
General Health & Medical Sciences (AREA)
Biomedical Technology (AREA)
Heart & Thoracic Surgery (AREA)
Hematology (AREA)
Veterinary Medicine (AREA)
Animal Behavior & Ethology (AREA)
Public Health (AREA)
Pulmonology (AREA)
Bioinformatics & Cheminformatics (AREA)
Emergency Medicine (AREA)
Mechanical Engineering (AREA)
Biophysics (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Medicinal Preparation (AREA)

CA002653183A 2006-06-02 2007-06-01 Adaptateur avec raccord pour pulverisateur Abandoned CA2653183A1 (fr)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
DE102006025884A DE102006025884A1 (de)	2006-06-02	2006-06-02	Adapter mit einem Anschluss für einen Zerstäuber
DE102006025884.3		2006-06-02
PCT/EP2007/055381 WO2007141201A1 (fr)	2006-06-02	2007-06-01	Adaptateur avec raccord pour pulvérisateur

Publications (1)

Publication Number	Publication Date
CA2653183A1 true CA2653183A1 (fr)	2007-12-13

Family

ID=38353123

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CA002653183A Abandoned CA2653183A1 (fr)	2006-06-02	2007-06-01	Adaptateur avec raccord pour pulverisateur

Country Status (5)

Country	Link
EP (1)	EP2023990A1 (fr)
JP (1)	JP2009538655A (fr)
CA (1)	CA2653183A1 (fr)
DE (1)	DE102006025884A1 (fr)
WO (1)	WO2007141201A1 (fr)

Cited By (16)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US7837235B2 (en)	2004-01-08	2010-11-23	Boehringer Ingelheim International Gmbh	Device for clamping a fluidic component
US9265910B2 (en)	2009-05-18	2016-02-23	Boehringer Ingelheim International Gmbh	Adapter, inhalation device, and nebulizer
US9545487B2 (en)	2012-04-13	2017-01-17	Boehringer Ingelheim International Gmbh	Dispenser with encoding means
US9724482B2 (en)	2009-11-25	2017-08-08	Boehringer Ingelheim International Gmbh	Nebulizer
US9744313B2 (en)	2013-08-09	2017-08-29	Boehringer Ingelheim International Gmbh	Nebulizer
US9757750B2 (en)	2011-04-01	2017-09-12	Boehringer Ingelheim International Gmbh	Medicinal device with container
US9827384B2 (en)	2011-05-23	2017-11-28	Boehringer Ingelheim International Gmbh	Nebulizer
US9943654B2 (en)	2010-06-24	2018-04-17	Boehringer Ingelheim International Gmbh	Nebulizer
US10004857B2 (en)	2013-08-09	2018-06-26	Boehringer Ingelheim International Gmbh	Nebulizer
US10011906B2 (en)	2009-03-31	2018-07-03	Beohringer Ingelheim International Gmbh	Method for coating a surface of a component
US10016568B2 (en)	2009-11-25	2018-07-10	Boehringer Ingelheim International Gmbh	Nebulizer
US10099022B2 (en)	2014-05-07	2018-10-16	Boehringer Ingelheim International Gmbh	Nebulizer
US10124129B2 (en)	2008-01-02	2018-11-13	Boehringer Ingelheim International Gmbh	Dispensing device, storage device and method for dispensing a formulation
US10124125B2 (en)	2009-11-25	2018-11-13	Boehringer Ingelheim International Gmbh	Nebulizer
US10195374B2 (en)	2014-05-07	2019-02-05	Boehringer Ingelheim International Gmbh	Container, nebulizer and use
US10722666B2 (en)	2014-05-07	2020-07-28	Boehringer Ingelheim International Gmbh	Nebulizer with axially movable and lockable container and indicator

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US7963955B2 (en)	1998-02-27	2011-06-21	Boehringer Ingelheim International Gmbh	Container for a medicinal liquid
EP2135632A1 (fr) *	2008-06-20	2009-12-23	Boehringer Ingelheim International Gmbh	Inhalateur
WO2014140765A1 (fr)	2013-03-15	2014-09-18	Trudell Medical International	Circuit de ventilateur, adaptateur utilisé dans le circuit de ventilateur et leurs procédés d'utilisation

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4225928A1 (de) *	1992-08-05	1994-02-10	Ritzau Pari Werk Gmbh Paul	Zerstäubervorrichtung mit Heizeinrichtung
DE19520622C2 (de) *	1995-06-06	2003-05-15	Pari Gmbh	Vorrichtung zum Vernebeln von Fluiden
US6725858B2 (en) *	2001-05-07	2004-04-27	Hudson Respiratory Care Inc.	Valved aerosol tee adapter assembly
MY136601A (en) *	2001-06-15	2008-10-31	Otsuka Pharma Co Ltd	Dry powder inhalation system for transpulmonary administration, method of manufacturing a dry powdered preparation, and use of a freeze dried composition
EP1509266B1 (fr) *	2002-05-16	2009-07-01	Boehringer Ingelheim International GmbH	Systeme comprenant une buse et un dispositif de maintien
DE10320143A1 (de) *	2003-05-06	2004-12-16	Pari GmbH Spezialisten für effektive Inhalation	Vernebleranschlussvorrichtung für Beatmungsgeräte oder dergleichen
JP2007522902A (ja) *	2004-02-24	2007-08-16	ベーリンガーインゲルハイムインターナショナルゲゼルシャフトミットベシュレンクテルハフツング	ネブライザ
DE102005029498B4 (de) *	2005-06-24	2007-08-30	Pari GmbH Spezialisten für effektive Inhalation	Inhalationstherapievorrichtung

2006
- 2006-06-02 DE DE102006025884A patent/DE102006025884A1/de not_active Withdrawn
2007
- 2007-06-01 EP EP07729782A patent/EP2023990A1/fr not_active Withdrawn
- 2007-06-01 JP JP2009512610A patent/JP2009538655A/ja active Pending
- 2007-06-01 CA CA002653183A patent/CA2653183A1/fr not_active Abandoned
- 2007-06-01 WO PCT/EP2007/055381 patent/WO2007141201A1/fr not_active Ceased

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US9027967B2 (en)	2004-01-08	2015-05-12	Boehringer Ingelheim International Gmbh	Device for clamping a fluidic component
US7837235B2 (en)	2004-01-08	2010-11-23	Boehringer Ingelheim International Gmbh	Device for clamping a fluidic component
US10124129B2 (en)	2008-01-02	2018-11-13	Boehringer Ingelheim International Gmbh	Dispensing device, storage device and method for dispensing a formulation
US10011906B2 (en)	2009-03-31	2018-07-03	Beohringer Ingelheim International Gmbh	Method for coating a surface of a component
US9265910B2 (en)	2009-05-18	2016-02-23	Boehringer Ingelheim International Gmbh	Adapter, inhalation device, and nebulizer
US9682202B2 (en)	2009-05-18	2017-06-20	Boehringer Ingelheim International Gmbh	Adapter, inhalation device, and atomizer
US10124125B2 (en)	2009-11-25	2018-11-13	Boehringer Ingelheim International Gmbh	Nebulizer
US10016568B2 (en)	2009-11-25	2018-07-10	Boehringer Ingelheim International Gmbh	Nebulizer
US9724482B2 (en)	2009-11-25	2017-08-08	Boehringer Ingelheim International Gmbh	Nebulizer
US9943654B2 (en)	2010-06-24	2018-04-17	Boehringer Ingelheim International Gmbh	Nebulizer
US9757750B2 (en)	2011-04-01	2017-09-12	Boehringer Ingelheim International Gmbh	Medicinal device with container
US9827384B2 (en)	2011-05-23	2017-11-28	Boehringer Ingelheim International Gmbh	Nebulizer
US9545487B2 (en)	2012-04-13	2017-01-17	Boehringer Ingelheim International Gmbh	Dispenser with encoding means
US10220163B2 (en)	2012-04-13	2019-03-05	Boehringer Ingelheim International Gmbh	Nebuliser with coding means
US10894134B2 (en)	2013-08-09	2021-01-19	Boehringer Ingelheim International Gmbh	Nebulizer
US10004857B2 (en)	2013-08-09	2018-06-26	Boehringer Ingelheim International Gmbh	Nebulizer
US9744313B2 (en)	2013-08-09	2017-08-29	Boehringer Ingelheim International Gmbh	Nebulizer
US11642476B2 (en)	2013-08-09	2023-05-09	Boehringer Ingelheim International Gmbh	Nebulizer
US10716905B2 (en)	2014-02-23	2020-07-21	Boehringer Lngelheim International Gmbh	Container, nebulizer and use
US10099022B2 (en)	2014-05-07	2018-10-16	Boehringer Ingelheim International Gmbh	Nebulizer
US10722666B2 (en)	2014-05-07	2020-07-28	Boehringer Ingelheim International Gmbh	Nebulizer with axially movable and lockable container and indicator
US10195374B2 (en)	2014-05-07	2019-02-05	Boehringer Ingelheim International Gmbh	Container, nebulizer and use

Also Published As

Publication number	Publication date
WO2007141201A1 (fr)	2007-12-13
JP2009538655A (ja)	2009-11-12
EP2023990A1 (fr)	2009-02-18
DE102006025884A1 (de)	2007-12-06

Publication	Publication Date	Title
JP6048767B2 (ja)	2016-12-21	アダプタ、吸入器具及びアトマイザ
CA2653183A1 (fr)	2007-12-13	Adaptateur avec raccord pour pulverisateur
JP5719291B2 (ja)	2015-05-13	吸入器
EP2445558B1 (fr)	2016-06-29	Inhalateur
CA2653422A1 (fr)	2007-12-13	Pulverisateur
US8528548B2 (en)	2013-09-10	Inhaler
CA2711547A1 (fr)	2009-07-23	Buse et inhalateur et procede de production d'une buse
US8205613B2 (en)	2012-06-26	Piston dosing pump
CA2648577A1 (fr)	2007-10-18	Inhalateur
CA2651190A1 (fr)	2007-11-15	Pulverisateur comportant un rincage de buse predose
CA2648722A1 (fr)	2007-10-25	Inhalateur pour administrer un medicament a partir d'une capsule
US9533112B2 (en)	2017-01-03	Inhaler
US9937306B2 (en)	2018-04-10	Dosage aerosols for the application of pharmaceutical formulations

Legal Events

Date	Code	Title	Description
2011-06-01	FZDE	Dead