BRPI0618188B1 - Processo de montagem de um dispositivo de liberação de um medicamento - Google Patents
Processo de montagem de um dispositivo de liberação de um medicamento Download PDFInfo
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- BRPI0618188B1 BRPI0618188B1 BRPI0618188-0A BRPI0618188A BRPI0618188B1 BR PI0618188 B1 BRPI0618188 B1 BR PI0618188B1 BR PI0618188 A BRPI0618188 A BR PI0618188A BR PI0618188 B1 BRPI0618188 B1 BR PI0618188B1
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- 238000000034 method Methods 0.000 title claims abstract description 24
- 239000003814 drug Substances 0.000 title abstract description 20
- 229940079593 drug Drugs 0.000 title abstract description 15
- 238000005259 measurement Methods 0.000 claims abstract description 19
- 239000000443 aerosol Substances 0.000 claims description 5
- 238000004519 manufacturing process Methods 0.000 claims description 5
- 238000012377 drug delivery Methods 0.000 claims description 3
- 238000002347 injection Methods 0.000 claims description 2
- 239000007924 injection Substances 0.000 claims description 2
- 238000005070 sampling Methods 0.000 claims 3
- 239000007788 liquid Substances 0.000 abstract description 18
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 174
- -1 EGFR inhibitors Substances 0.000 description 82
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- 150000002148 esters Chemical class 0.000 description 27
- 150000003839 salts Chemical class 0.000 description 16
- YEESKJGWJFYOOK-IJHYULJSSA-N leukotriene D4 Chemical compound CCCCC\C=C/C\C=C/C=C/C=C/[C@H]([C@@H](O)CCCC(O)=O)SC[C@H](N)C(=O)NCC(O)=O YEESKJGWJFYOOK-IJHYULJSSA-N 0.000 description 12
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 10
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 10
- 241000711981 Sais Species 0.000 description 9
- 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 8
- 239000005557 antagonist Substances 0.000 description 8
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- 229940121647 egfr inhibitor Drugs 0.000 description 7
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- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 6
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- 239000012453 solvate Substances 0.000 description 6
- 125000004343 1-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C([H])([H])[H] 0.000 description 5
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- 108700015053 epidermal growth factor receptor activity proteins Proteins 0.000 description 5
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- YOHYSYJDKVYCJI-UHFFFAOYSA-N n-[3-[[6-[3-(trifluoromethyl)anilino]pyrimidin-4-yl]amino]phenyl]cyclopropanecarboxamide Chemical compound FC(F)(F)C1=CC=CC(NC=2N=CN=C(NC=3C=C(NC(=O)C4CC4)C=CC=3)C=2)=C1 YOHYSYJDKVYCJI-UHFFFAOYSA-N 0.000 description 5
- JWVCLYRUEFBMGU-UHFFFAOYSA-N quinazoline Chemical compound N1=CN=CC2=CC=CC=C21 JWVCLYRUEFBMGU-UHFFFAOYSA-N 0.000 description 5
- 101100296720 Dictyostelium discoideum Pde4 gene Proteins 0.000 description 4
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- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 4
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 4
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- NMJORVOYSJLJGU-UHFFFAOYSA-N methane clathrate Chemical compound C.C.C.C.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O.O NMJORVOYSJLJGU-UHFFFAOYSA-N 0.000 description 3
- 235000021317 phosphate Nutrition 0.000 description 3
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 3
- SNTWKPAKVQFCCF-UHFFFAOYSA-N 2,3-dihydro-1h-triazole Chemical compound N1NC=CN1 SNTWKPAKVQFCCF-UHFFFAOYSA-N 0.000 description 2
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 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
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 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
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 2
- 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 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
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 description 2
- 150000001242 acetic acid derivatives Chemical class 0.000 description 2
- 239000000043 antiallergic agent Substances 0.000 description 2
- 229940065524 anticholinergics inhalants for obstructive airway diseases Drugs 0.000 description 2
- 239000001569 carbon dioxide Substances 0.000 description 2
- 229910002092 carbon dioxide Inorganic materials 0.000 description 2
- 239000000812 cholinergic antagonist Substances 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 159000000011 group IA salts Chemical class 0.000 description 2
- TWBYWOBDOCUKOW-UHFFFAOYSA-N isonicotinic acid Chemical class OC(=O)C1=CC=NC=C1 TWBYWOBDOCUKOW-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
- 150000002942 palmitic acid derivatives Chemical class 0.000 description 2
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- 125000005547 pivalate group Chemical group 0.000 description 2
- 159000000001 potassium salts Chemical class 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 229940124530 sulfonamide Drugs 0.000 description 2
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 2
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- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 description 2
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- MCKJPJYRCPANCC-XLXYOEISSA-N (8s,9s,10r,11s,13s,14s,17r)-11,17-dihydroxy-10,13-dimethyl-3-oxo-7,8,9,11,12,14,15,16-octahydro-6h-cyclopenta[a]phenanthrene-17-carboxylic acid Chemical compound O=C1C=C[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(O)=O)[C@@H]4[C@@H]3CCC2=C1 MCKJPJYRCPANCC-XLXYOEISSA-N 0.000 description 1
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- CAGUIFXDKYSGJN-UHFFFAOYSA-N 2-(hydroxymethyl)-4-[1-hydroxy-2-[7-(3-phenylpropoxy)heptylamino]ethyl]phenol Chemical compound C1=C(O)C(CO)=CC(C(O)CNCCCCCCCOCCCC=2C=CC=CC=2)=C1 CAGUIFXDKYSGJN-UHFFFAOYSA-N 0.000 description 1
- XBUSQTCUZRYVMT-UHFFFAOYSA-N 2-hydroxy-5-[1-hydroxy-2-[2-[4-[(2-hydroxy-2-phenylethyl)amino]phenyl]ethylamino]ethyl]benzaldehyde Chemical compound C=1C=C(O)C(C=O)=CC=1C(O)CNCCC(C=C1)=CC=C1NCC(O)C1=CC=CC=C1 XBUSQTCUZRYVMT-UHFFFAOYSA-N 0.000 description 1
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- 125000000175 2-thienyl group Chemical group S1C([*])=C([H])C([H])=C1[H] 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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- RTLJQOLVPIGICL-UHFFFAOYSA-N 4-[2-(tert-butylamino)-1-hydroxyethyl]-2-(methylsulfonylmethyl)phenol Chemical compound CC(C)(C)NCC(O)C1=CC=C(O)C(CS(C)(=O)=O)=C1 RTLJQOLVPIGICL-UHFFFAOYSA-N 0.000 description 1
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- QJARANVHKUKWBO-UHFFFAOYSA-N 4-[2-[[4-(benzimidazol-1-yl)-2-methylbutan-2-yl]amino]-1-hydroxyethyl]-3-fluorophenol;4-[2-[[4-(benzimidazol-1-yl)-2-methylbutan-2-yl]amino]-1-hydroxyethyl]-2-[(4-methoxyphenyl)methylamino]phenol Chemical compound C1=NC2=CC=CC=C2N1CCC(C)(C)NCC(O)C1=CC=C(O)C=C1F.C1=CC(OC)=CC=C1CNC1=CC(C(O)CNC(C)(C)CCN2C3=CC=CC=C3N=C2)=CC=C1O QJARANVHKUKWBO-UHFFFAOYSA-N 0.000 description 1
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- LSLYOANBFKQKPT-DIFFPNOSSA-N 5-[(1r)-1-hydroxy-2-[[(2r)-1-(4-hydroxyphenyl)propan-2-yl]amino]ethyl]benzene-1,3-diol Chemical compound C([C@@H](C)NC[C@H](O)C=1C=C(O)C=C(O)C=1)C1=CC=C(O)C=C1 LSLYOANBFKQKPT-DIFFPNOSSA-N 0.000 description 1
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- IOVGROKTTNBUGK-SJCJKPOMSA-N ritodrine Chemical compound N([C@@H](C)[C@H](O)C=1C=CC(O)=CC=1)CCC1=CC=C(O)C=C1 IOVGROKTTNBUGK-SJCJKPOMSA-N 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
- 229960002052 salbutamol Drugs 0.000 description 1
- 229950001879 salmefamol Drugs 0.000 description 1
- 229960004017 salmeterol Drugs 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229950010289 soterenol Drugs 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 description 1
- 125000000446 sulfanediyl group Chemical group *S* 0.000 description 1
- HGKLFYLYWZXWPO-UHFFFAOYSA-N sulfo benzoate Chemical class OS(=O)(=O)OC(=O)C1=CC=CC=C1 HGKLFYLYWZXWPO-UHFFFAOYSA-N 0.000 description 1
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 description 1
- 229950007862 sulfonterol Drugs 0.000 description 1
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 description 1
- 229950008418 talipexole Drugs 0.000 description 1
- 229940095064 tartrate Drugs 0.000 description 1
- 229960004558 terguride Drugs 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 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
- 229960000278 theophylline Drugs 0.000 description 1
- 229940124597 therapeutic agent Drugs 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
- 229960000257 tiotropium bromide 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
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 229960000575 trastuzumab Drugs 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
- 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
Images
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
- A61M11/00—Sprayers or atomisers specially adapted for therapeutic purposes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61J—CONTAINERS SPECIALLY ADAPTED FOR MEDICAL OR PHARMACEUTICAL PURPOSES; DEVICES OR METHODS SPECIALLY ADAPTED FOR BRINGING PHARMACEUTICAL PRODUCTS INTO PARTICULAR PHYSICAL OR ADMINISTERING FORMS; DEVICES FOR ADMINISTERING FOOD OR MEDICINES ORALLY; BABY COMFORTERS; DEVICES FOR RECEIVING SPITTLE
- A61J1/00—Containers specially adapted for medical or pharmaceutical purposes
- A61J1/14—Details; Accessories therefor
- A61J1/20—Arrangements for transferring or mixing fluids, e.g. from vial to syringe
- A61J1/22—Arrangements for transferring or mixing fluids, e.g. from vial to syringe with means for metering the amount of fluid
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05B—SPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
- B05B11/00—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use
- B05B11/01—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use characterised by the means producing the flow
- B05B11/02—Membranes or pistons acting on the contents inside the container, e.g. follower pistons
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05B—SPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
- B05B11/00—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use
- B05B11/01—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use characterised by the means producing the flow
- B05B11/10—Pump arrangements for transferring the contents from the container to a pump chamber by a sucking effect and forcing the contents out through the dispensing nozzle
- B05B11/1001—Piston pumps
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05B—SPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
- B05B11/00—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use
- B05B11/01—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use characterised by the means producing the flow
- B05B11/10—Pump arrangements for transferring the contents from the container to a pump chamber by a sucking effect and forcing the contents out through the dispensing nozzle
- B05B11/1042—Components or details
- B05B11/105—Sealing arrangements around pump actuating stem
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05B—SPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
- B05B11/00—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use
- B05B11/01—Single-unit hand-held apparatus in which flow of contents is produced by the muscular force of the operator at the moment of use characterised by the means producing the flow
- B05B11/10—Pump arrangements for transferring the contents from the container to a pump chamber by a sucking effect and forcing the contents out through the dispensing nozzle
- B05B11/109—Pump arrangements for transferring the contents from the container to a pump chamber by a sucking effect and forcing the contents out through the dispensing nozzle the dispensing stroke being affected by the stored energy of a spring
- B05B11/1091—Pump arrangements for transferring the contents from the container to a pump chamber by a sucking effect and forcing the contents out through the dispensing nozzle the dispensing stroke being affected by the stored energy of a spring being first hold in a loaded state by locking means or the like, then released
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F04—POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
- F04B—POSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS
- F04B53/00—Component parts, details or accessories not provided for in, or of interest apart from, groups F04B1/00 - F04B23/00 or F04B39/00 - F04B47/00
- F04B53/16—Casings; Cylinders; Cylinder liners or heads; Fluid connections
- F04B53/162—Adaptations of cylinders
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F04—POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
- F04B—POSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS
- F04B53/00—Component parts, details or accessories not provided for in, or of interest apart from, groups F04B1/00 - F04B23/00 or F04B39/00 - F04B47/00
- F04B53/16—Casings; Cylinders; Cylinder liners or heads; Fluid connections
- F04B53/162—Adaptations of cylinders
- F04B53/164—Stoffing boxes
Landscapes
- Engineering & Computer Science (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
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- Heart & Thoracic Surgery (AREA)
- Anesthesiology (AREA)
- Hematology (AREA)
- Pulmonology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biophysics (AREA)
- Pharmacology & Pharmacy (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Infusion, Injection, And Reservoir Apparatuses (AREA)
- Medicinal Preparation (AREA)
- Containers And Packaging Bodies Having A Special Means To Remove Contents (AREA)
- Medical Preparation Storing Or Oral Administration Devices (AREA)
- Nozzles (AREA)
- Medicines Containing Plant Substances (AREA)
- Fire-Detection Mechanisms (AREA)
- Measurement Of The Respiration, Hearing Ability, Form, And Blood Characteristics Of Living Organisms (AREA)
- Steroid Compounds (AREA)
- Catching Or Destruction (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Description
- -beta miméticos com corticosteróides, inibidores de PDE4, inibidores de EGFR ou antagonistas de LTD4,
- -anticolinérgicos com beta miméticos, corticosteróides, inibidores de PDE4, inibidores de EGFR ou antagonistas de LTD4,
- -corticosteróides com inibidores de PDE4, inibidores de EGFR ou antagonistas de LTD4
- -inibidores de PDE4 com inibidores de EGFR ou antagonistas de LTD4
- -inibidores de EGFR com antagonistas de LTD4.
3- (4-{6-[2-hidróxi-2-(4-hidróxi-3-hidroximetilfenil) etil amino] hexilóxi} butil) benzil sulfonamida
5-[2-(5,6-dietil indan-2-il amino)-1-hidróxi etil]-8-hidróxi-1H-quinolin-2-ona
4- hidróxi-7-[2-{[2-{[3-(2-feniletóxi) propil] sulfonil} etil] amino} etil]-2 (3H) benzotiazolona
1 -(2-flúor-4-hidroxifenil)-2-[4-(1-benzimidazolil)-2-metil-2-butil amino] etanol
1 -[3-(4-metoxibenzilamino)-4-hidroxifenil]-2-[4-(1-benzimidazolil)-2-metil-2-butil amino] etanol
1-[2H-5-hidróxi-3-oxo-4H-1,4-benzoxazin-8-il]-2-[3-(4-N,N-dimetilaminofenil)-2-metil-2-propil amino] etanol
1 -[2H-5-hidróxi-3-oxo-4H-1,4-benzoxazin-8-il]-2-[3-(4-metóxi fenil)-2-metil-2-propil amino] etanol
1 -[2H-5-hidróxi-3-oxo-4H-1,4-benzoxazin-8-il]-2-[3-(4-n-butiloxifenil)-2-metil-2-propil amino] etanol
1 -[2H-5-hidróxi-3-oxo-4H-1,4-benzoxazin-8-il]-2-{4-[3-(4-metoxifenil)-1,2,4-triazol-3-il]-2-metil-2-butilamino} etanol
5- hidróxi-8-(1-hidróxi-2-isopropil amino butil)-2H-1,4-benzoxazin-3-(4H)-ona
1 -(4-amino-3-cloro-5-trifluormetilfenil)-2-t-butil amino) etanol
6- hidróxi-8-{1-hidróxi-2-[2-(4-metoxifenil)-1,1 -dimetiletilamino] etil}-4H-benzo [1,4] oxazin-3-ona
1.1 -dimetil etil amino] etil}-4H-benzo[1,4] oxazin-3-ona de etil éster de ácido 6-hidróxi-8-{1-hidróxi-2-[2-(4-fenóxi acético)
1.1 -dimetil etil amino] etil}-4H-benzo[1,4] oxazin-3-ona de ácido 6-hidróxi-8-{1-hidróxi-2-[2-(4-fenoxiacético)
8-{2-[1,1-dimetil-2-(2,4,6-trimetil fenil) etil amino]-1-hidroxietil}-6-hidróxi-4H-benzo[1,4] oxazin-3-ona
6-hidróxi-8-{1-hidróxi-2-[2-(4-hidroxifenil)-1,1 -dimetil etil amino]etil}-4H-benzo [1,4] oxazin-3-ona
6-hidróxi-8-{1-hidróxi-2-[2-(4-isopropil fenil)-1,1 -dimetil etil amino] etil}-4H-benzo[1,4] oxazin-3-ona
8-{2-[2-(4-etil fenil)-1,1 -dimetil etil amino]-1-hidróxi etil}-6-hidróxi-4H-benzo[1,4] oxazin-3-ona
8-{2-[2-(4-etoxifenil)-1,1 -dimetil etil amino]-1-hidróxi etil}-6-hidróxi-4H-benzo [1,4] oxazin-3-ona
ácido 4-(4-{2-[2-hidróxi-2-(6-hidróxi-3-oxo-3,4-diidro-2H-benzo[1,4] oxazin-8-il) etil amino]-2-metil propil} fenóxi) butírico
8-{2-[2-(3,4-difluorfenil)-1,1 -dimetiletilamino]-1-hidróxi etil}-6-hidróxi-4H-benzo [1,4] oxazin-3-ona
1 -(4-etoxicarbonil amino-3-ciano-5-fluorfenil)-2-(t-butil amino) etanol 2- hidróxi-5-(1-hidróxi-2-{2-[4-(2-hidróxi-2-fenil etil amino) fenil] etil amino} etil) benzaldeído
N-[2-hidróxi-5-(1-hidróxi-2-{2-[4-(2-hidróxi-2-feniletilamino) fenil] etil amino} etil) fenil] formamida
8-hidróxi-5-(1-hidróxi-2-{2-[4-(6-metoxibifenil-3-il amino) fenil] etil amino} etil)-1H-quinolin-2-ona
8-hidróxi-5-[1-hidróxi-2-(6-fenetilaminohexilamino) etil]-1H-quinolin-2-ona
5-[2-(2-{4-[4-(2-amino-2-metilpropóxi) fenil amino] fenil} etil amino)-1-hidroxietil]-8-hidróxi-1H-quinolin-2-ona
[3-(4-{6-[2-hidróxi-2-(4-hidróxi-3-hidroximetilfenil) etil amino] hexilóxi} butil)-5-metil fenil] uréia
4-(2-{6-[2-(2,6-dicloro benzilóxi) etóxi] hexilamino}-1-hidróxi etil)-2-hidróxi metil fenol
3- (4-{6-[2-hidróxi-2-(4-hidróxi-3-hidroximetilfenil) etil amino] hexilóxi} butil) benzenossulfonamida
3- (3-{7-[2-hidróxi-2-(4-hidróxi-3-hidroximetilfenil) etil amino] heptilóxi} propil) benzeno sulfonamida
4- (2-{6-[4-(3-ciclopentanossulfonil fenil) butóxi] hexil amino}-1-hidróxi etil)-2-hidróxi metil fenol
N-adamantan-2-il-2-(3-{2-[2-hidróxi-2-(4-hidróxi-3-hidroximetilfenil) etilamino] propil} fenil) acetamida
opcionalmente em forma racêmica, como enantiômeros, diastereômeros ou como sais, solvatos ou hidratos farmacologicamente aceitáveis. São preferidos sais selecionados do grupo consistindo em cloridrato, bromidrato, iodidrato, hidrossulfato, hidrofosfato, hidrometano sulfonato, hidronitrato, hidromaleato, hidroacetato, hidrocitrato, hidrofumarato, hidrotartarato, hidrooxalato, hidrossuccinato, hidrobenzoato, e hidro-p-toluenossulfonato.
tropenol éster de metobrometo de ácido 2,2-difenil
propiônico
escopinéster de metobrometo de ácido 2,2-difenil
propiônico
escopinéster de metobrometo de ácido 2-flúor-2,2-difenil
acético
tropenol éster de metobrometo de ácido 2-flúor-2,2-difenil
acético
tropenol éster de metobrometo de ácido 3,3’,4,4’-tetraflúor
benzílico
scopino éster de metobrometo de ácido 3,3’,4,4’-tetraflúor
benzílico
tropenol éster de metobrometo de ácido 4,4’-difluorbenzílico scopino éster de metobrometo de ácido 4,4’-difluorbenzílico tropenol éster de metobrometo de ácido 3,3’-difluorbenzílico scopino éster de metobrometo de ácido 3,3’-difluorbenzílico tropenol éster de metobrometo de ácido 9-hidroxifluoren-9-
carbônico
tropenol éster de metobrometo de ácido 9-fluorfluoren-9-
carbônico
escopino éster de metobrometo de ácido 9-hidróxi fluoren-9-carbônico
escopino éster de metobrometo de ácido 9-flúor fluoren-9-
carbônico
tropenol éster de metobrometo de ácido 9-metil fluoren-9-
carbônico
escopino éster de metobrometo de ácido 9-metil fluoren-9-
carbônico
ciclopropil tropino éster de metobrometo de ácido benzílico ciclopropil tropino éster de metobrometo de ácido 2,2-difenil
propiônico
ciclopropil tropino éster de metobrometo de ácido 9-hidróxi xa nte no-9-carbôni co
ciclopropil tropino éster de metobrometo de ácido 9-metil fluoreno-9-carbônico
ciclopropil tropino éster de metobrometo de ácido 9-metil xa nte no-9-carbôni co
ciclopropil tropino éster de metobrometo de ácido 9-hidróxi fluoreno-9-carbônico
metil éster ciclo propil tropino éster de metobrometo de ácido 4,4’-diflúor benzílico
tropenol éster de metobrometo de ácido 9-hidroxixanteno-9-
carbônico
scopino éster de metobrometo de ácido 9-hidroxixanteno-9-
carbônico
tropenol éster de metobrometo de ácido 9-metilxanteno-9-
carbônico
scopino éster de metobrometo de ácido 9-metilxanteno-9-
carbônico
tropenol éster de metobrometo de ácido 9-etilxanteno-9-
carbônico tropenol éster de metobrometo de ácido 9-difluormetil xa nte no-9-carbôni co
escopino éster de metobrometo de ácido 9-hidroximetil xa nte no-9-carbôni co
Exemplos de corticosteróides preferidos que podem ser mencionados incluem Beclometasona, Betametasona, Budesonida, Butixocorte, Ciclesonida, Deflazacorte, Dexametasona, Etiprednol, Flunisolida, Fluticasona, Loteprednol, Mometasona, Prednisolona, Prednisona, Rofleponida, Triamcinolona, RPR-106541, NS-126, ST-26 e
(S)-flúor metil éster de ácido 6,9-diflúor-17-[(2-furanil carbonil) óxi]-11 -hidróxi-16-metil-3-oxo-androsta-1,4-dien-17-
carbotiônico
(S)-(2-oxotetraidrofuran-3S-il) éster de ácido 6,9-diflúor-11-hidróxi-16-metil-3-oxo-17-propioniloxiandrosta-1,4-dieno-17-carbotiônico
cianometil éster de ácido 6a, 9a-diflúor-11 β-hidróxi-16a-metil-3-oxo-17a-(2,2,3,3-tetrametilciclopropilcarbonil) óxi androsta-1,4-dieno-^-carboxílico
opcionalmente em forma racêmica, como enantiômeros, diastereômeros ou como sais, solvatos ou hidratos farmacologicamente aceitáveis. Exemplos de sais e derivados preferidos são sais alcalinos, isto é, sais de sódio ou potássio, sulfobenzoatos, fosfatos, isonicotinatos, acetatos, dicloroacetatos, propionatos, diidrogenofosfatos, palmitatos, pivalatos ou furoatos.
- - N-(3,5-dicloro-1-oxo piridin-4-il)-4-difluormetóxi-3-ciclopro-pilmetoxibenzamida
- - (-)p-[(4aR*,10bS*)-9-etóxi-1,2,3,4,4a,10b-hexaidro-8-me-tóxi-2-metil benzo[s][1,6] naftiridin-6-il]-N,N-diisopropil benzamida
- - (R)-(+)-1-(4-bromo benzil)-4-[(3-ciclo pentilóxi)-4-metóxi fenil]-2-pirrolidona
- - 3-(ciclo pentilóxi-4-metóxi fenil)-1-(4-N’-[N-2-ciano-S-metil isotioureído] benzil)-2-pirrolidona
- - ácido cis-[4-ciano-4-(3-ciclopentilóxi-4-metoxifenil) ciclo hexan-1-carbônico]
- - 2-carbometóxi-4-ciano-4-(3-ciclopropilmetóxi-4-difluorme-toxifenil) ciclo hexan-1-ona
- - cis-[4-ciano-4-(3-ciclopropilmetóxi-4-difluormetoxifenil) ciclohexan-1-ol]
- - [4-(3-ciclopentilóxi-4-metoxifenil) pirrolidin-2-ilideno] acetato de (R)-(+)-etila
- - [4-(3-ciclopentilóxi-4-metoxifenil) pirrolidin-2-ilideno] acetato de (S)-(+)-etila
- - 9-ciclopentil-5,6-diidro-7-etil-3-(2-tienil)-9H-pirazol[3,4-c]-1.2.4- triazol[4,3-a] piridina
- - 9-ciclo pentil-5,6-diidro-7-etil-3-(t-butil)-9H-pirazol[3,4-c]-
- 1.2.4- triazol[4,3-a] piridina
opcionalmente em forma racêmica, como enantiômeros, diastereômeros ou como sais, solvatos ou hidratos farmacologicamente aceitáveis. São preferidos sais selecionados do grupo consistindo em cloridrato, bromidrato, iodidrato, hidrossulfato, hidrofosfato, hidrometano sulfonato, hidronitrato, hidromaleato, hidroacetato, hidrocitrato, hidrofumarato, hidrotartarato, hidrooxalato, hidrossuccinato, hidrobenzoato, e hidro-p-toluenossulfonato.
- - ácido 1-(((R)-(3-(2-(6,7-diflúor-2-quinolinil) etenil) fenil-3-(2-(2-hidróxi-2-propil) fenil) tio) metilciclopropanoacético,
- - ácido 1-(((1-(R)-3-(3-(2-(2,3-diclorotieno[3,2-b] piridin-5-il)-(E)-etenil) fenil)-3-(2-(1-hidróxi-1-metil etil) fenil) propil) tio) metil) ciclopropanoacético
- - ácido [2-[[2-(4-t-butil-2-tiazolil)-5-benzofuranil] oximetil] fenil] acético
opcionalmente em forma racêmica, como enantiômeros, diastereômeros ou como sais, solvatos ou hidratos farmacologicamente aceitáveis. São preferidos sais selecionados do grupo consistindo em cloridrato, bromidrato, iodidrato, hidrossulfato, hidrofosfato, hidrometano sulfonato, hidronitrato, hidromaleato, hidroacetato, hidrocitrato, hidrofumarato, hidrotartarato, hidrooxalato, hidrossuccinato, hidrobenzoato, e hidro-p-toluenossulfonato. Ainda exemplos para sais opcionalmente preferidos e derivados são sais alcalinos, isto é, sais de sódio ou potássio, sulfo benzoatos, fosfatos, isonicotinatos, acetatos, propionatos, diidrogeno fosfatos, palmitatos, pivalatos ou furoatos.
- - 4-[(3-cloro-4-flúor fenil) amino]-6-{[4-(morfolin-4-il)-1-oxo-2-buten-1-il] amino}-7-ciclopropilmetoxiquinazolina
- - 4-[(3-cloro-4-flúor fenil) amino]-6-{[4-(n,N-dietil amino)-1-oxo-2-buten-1-il] amino}-7-ciclopropilmetoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{[4-(N,N-dimetil amino)-1-oxo-2-buten-1-il] amino}-7-ciclopropilmetoxiquinazolina
- - 4-[(R)-(1-feniletil) amino]-6-{[4-(morfolin-4-il)-1-oxo-2-buten-1-il] amino}-7-ciclopentiloxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{[4-((R)-6-metil-2-oxo morfolin-4-il)-1-oxo-2-buten-1-il] amino}-7-ciclopropilmetoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{[4-((R)-6-metil-2-oxo mo-rfolin-4-il)-1-oxo-2-buten-1-il] amino}-7-[(S)-(tetraidrofurano-3-il) óxi] quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{[4-((R)-2-metoximetil-6-oxo-morfolin-4-il)-1-oxo-2-buten-1-il] amino}-7ciclopropilmetoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-[2-(SS)-6-metil-2-oxo-morfolin-4-il) etóxi]-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-({4-[N-(2-metoxietil)-N-metil amino]-1-oxo-2-buten-1-il} amino)-7-ciclopropilmetoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{[4-(N,N-dimetilamino)-1-oxo-2-buten-1-il] amino}-7-ciclo pentiloxiquinazolina
- - 4-[(R)-(1-feniletil) amino]-6-{[4-(N,N-bis-(2-metoxietil) ami-no)-1-oxo-2-buten-1-il] amino}-7-ciclopropilmetoxiquinazolina
- - 4-[(R)-(1-feniletil) amino]-6-({4-[N-(2-metoxietil)-N-etil amino]-1-oxo-2-buten-1-il} amino)-7-ciclopropilmetoxiquinazolina
- - 4-[(R)-(1-feniletil) amino]-6-({4-[N-(2-metoxietil)-N-me-tilamino]-1-oxo-2-buten-1-il} amino)-7-ciclopropilmetoxiquinazolina
- - 4-[(R)-(1-feniletil)amino]-6-({4-[N-(tetraidropiran-4-il)-N-me-tilamino]-1-oxo-2-buten-1-il} amino)-7-ciclopropilmetoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{[4-(N,N-dimetil amino)-1-oxo-2-buten-1-il] amino}-7-((R)-tetraidro furan-3-ilóxi) quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{[4-(N,N-dimetil amino)-1-oxo-2-buten-1-il] amino}-7-((S)-tetraidro furan-3-ilóxi) quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-({4-[N-(2-metoxietil)-N-metil amino]-1-oxo-2-buten-1-il} amino)-7ciclo pentilóxi quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{[4-(N-ciclopropil-N-metil amino)-1-oxo-2-buten-1-il] amino}-7-ciclopentiloxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{[4-(N,N-dimetil amino)-1-oxo-2-buten-1-il] amino}-7-[(R)-(tetraidro furan-2-il) metóxi] quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{[4-(N,N-dimetil amino)-1-oxo-2-buten-1-il] amino}-7-[(S)-(tetraidro furan-2-il) metóxi] quinazolina
- - 4-[(3-etinil fenil) amino]-6,7-bis-(2-metóxi etóxi) quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-7-[3-(morfolin-4-il) propilóxi]-6-[(vinilcarbonil) amino] quinazolina
- - 4-[(R)-(1-feniletil) amino]-6-(4-hidróxi fenil)-7H-pirrol[2,3-d] pirimidina
- - 3-ciano-4-[(3-cloro-4-fluorfenil) amino]-6-{[4-(N,N-dime-tilamino)-1-oxo-2-buten-1-il] amino}-7-etóxi quinolina
- - 4-{[3-cloro-4-(3-fluorbenzilóxi) fenil] amino}-6-(5-{[(2-meta-nossulfonil etil) amino] metil} furan-2-il) quinazolina
- - 4-[(R)-(1-feniletil) amino]-6-{[4-((R)-6-metil-2-oxo morfolin-4-il)-1-oxo-2-buten-1-il] amino}-7-metóxi quinazolina
- - 4-[(3-cloro-4-fluorfenil)amino]-6-{[4-(morfolin-4-il)-1-oxo-2-buten-1-il] amino}-7-[(tetraidro furan-2-il) metóxi] quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-({4-[N,N-bis-(2-metoxietil) amino]-1-oxo-2-buten-1-il} amino)-7-[(tetraidro furan-2-il) metóxi] quinazolina
- - 4-[(3-etinil fenil) amino]-6-{[4-(5,5-dimetil-2-oxo morfolin-4-il)-1-oxo-2-buten-1-il] amino} quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-[2-(2,2-dimetil-6-oxo mor-folin-4-il) etóxi]-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-[2-(2,2-dimetil-6-oxomorfolin-4-il) etóxi]-7-[(R)-(tetraidrofuran-2-il) metóxi] quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-7-[2-(2,2-dimetil-6-oxo morfolin-4-il) etóxi]-6-[(S)-tetraidrofuran-2-il) metóxi] quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{2-[4-(2-oxo morfolin-4-il) piperidin-1-il] etóxi}-7-metóxi quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-[1-(t-butiloxicarbonil) pipe-ridin-4-ilóxi]-7-metóxi quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(trans-4-aminociclohexan-1-ilóxi)-7-metóxi quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(trans-4-metanossulfo-nilamino ciclo hexan-1-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(tetraidropiran-3-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(1-metilpiperidin-4-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{1-[(morfolin-4-il) carbonil] piperidin-4-ilóxi)-7-metóxi quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{1-[(metoximetil) carbonil] piperidin-4-ilóxi}-7-metóxi quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(piperidin-3-ilóxi)-7-meto-xiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-[1-(2-acetilaminoetil) pipe-ridin-4-ilóxi]-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(tetraidropiran-4-ilóxi)-7-etoxi-quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-((S)-tetraidrofuran-3-ilóxi)-7-hidroxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(tetraidropiran-4-ilóxi)-7-(2-metoxietóxi) quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{trans-4-[(dimetilamino) sulfonil amino] ciclo hexan-1-ilóxi}-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{trans-4-[(morfolin-4-il) carbonilamino] ciclohexan-1-ilóxi}-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{trans-4-[(morfolin-4-il) sulfonilamino] ciclohexan-1-ilóxi}-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(tetraidropiran-4-ilóxi)-7-(2-acetilaminoetóxi) quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(tetraidropiran-4-ilóxi)-7-(2-metanossulfonilaminoetóxi) quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{1-(piperidin-1-il) carbonil] piperidin-4-ilóxi}-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(1-aminocarbonil metilpi-peridin-4-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(cis-4-{N-[(tetraidro piran-4-il) carbonil]-N-metil amino} ciclo hexan-1-ilóxi)-7-metóxi quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(cis-4-{N-[(morfolin-4-il) carbonil]-N-metilamino} ciclohexan-1-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(cis-4-{N-[(morfolin-4-il) sulfonil]-N-metilamino} ciclohexan-1-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(trans-4-etanossulfo-nilamino ciclohexan-1-ilóxi)-7-metóxi quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(1-metanossulfonil pipe-ridin-4-ilóxi)-7-etoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(1-metanossulfonil pipe-ridin-4-ilóxi)-7-(2-metoxietóxi) quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-[1-(2-metoxiacetil) pipe-ridin-4-ilóxi]-7-(2-metoxietóxi) quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(cis-4-acetilamino ciclo-hexan-1-ilóxi)-7-metóxi quinazolina
- - 4-[(3-etinilfenil) amino]-6-[1-(t-butilóxi carbonil) piperidin-4-ilóxi]-7-metóxi quinazolina
- - 4-[(3-etinilfenil) amino]-6-(tetraidro piran-4-ilóxi]-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(cis-4-{N-[(piperidin-1-il) carbonil]-N-metil amino} ciclo hexan-1-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(cis-4-{N-[(4-metil pipe-razin-1-il) carbonil]-N-metil amino} ciclohexan-1-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{cis-4-[(morfolin-4-il) carbonil amino] ciclohexan-1-ilóxi}-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{1-[2-(2-oxo pirrolidin-1-il) etil] piperidin-4-ilóxi}-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil)amino]-6-{1-[(morfolin-4-il)carbonil] piperidin-4-ilóxi}-7-(2-metoxietóxi) quinazolina
- - 4-[(3-etinilfenil) amino]-6-(1-acetil piperidin-4-ilóxi)-7-metoxi-quinazolina
- - 4-[(3-etinilfenil) amino]-6-(1-metilpiperidin-4-ilóxi)-7-metoxiquinazolina
- - 4-[(3-etinil fenil) amino]-6-(1-metanossulfonil piperidin-4-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(1-metilpiperidin-4-ilóxi)-7-(2-metoxietóxi) quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(1-isopropiloxicarbonil piperidin-4-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(cis-4-metil amino ciclohexan-1-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil)amino]-6-{cis-4[N-(2-metoxiacetil)-N-metil amino] ciclo hexan-1-ilóxi}-7-metoxiquinazolina
- - 4-[(3-etinilfenil) amino]-6-(piperidin-4-ilóxi)-7-meto-xiquinazolina
- - 4-[(3-etinilfenil) amino]-6-[1-(2-metóxi acetil) piperidin-4-ilóxi]-7-metoxiquinazolina
- - 4-[(3-etinilfenil) amino]-6-{1-[(morfolin-4-il) carbonil] pipe-ridin-4-ilóxi}-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{1-[(cis-2,6-dimetil mo-rfolin-4-il) carbonil] piperidin-4-ilóxi}-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{1-[(2-metilmorfolin-4-il) carbonil] piperidin-4-ilóxi}-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{1-[(S,S)-(2-oxa-5-aza-biciclo [2.2.1] hept-5-il) carbonil] piperidin-4-ilóxi}-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{1-[(N-metil-N-2-meto-xietilamino) carbonil] piperidin-4-ilóxi}-7-metóxi quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(1-etilpiperidin-4-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{1-[(2-metoxietil) carbonil] piperidin-4-ilóxi}-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-{1-[(3-metoxipropil amino) carbonil] piperidin-4-ilóxi}-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-[cis-4-(N-metanossulfonil-N-metil amino) ciclohexan-1-ilóxi]-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-[cis-4-(N-acetil-N-me-
- tilamino) ciclohexan-1-ilóxi]-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(trans-4-metilamino ciclohexan-1-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-[trans-4-(N-metano-ssulfonil-N-metilamino) ciclohexan-1-ilóxi]-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(trans-4-dimetilamino-ciclohexan-1-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(trans-4-{N-[(morfolin-4-il) carbonil]-N-metil amino} ciclohexan-1-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-[2-(2,2-dimetil-6-oxomo-rfolin-4-il) etóxi]-7-[(S)-(tetraidrofuran-2-il) metóxi] quinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(1-metanossulfonil piperidin-4-ilóxi)-7-metoxiquinazolina
- - 4-[(3-cloro-4-fluorfenil) amino]-6-(1-ciano piperidin-4-ilóxi)-7-metoxiquinazolina
opcionalmente em forma racêmica, como enantiômeros, diastereômeros ou como sais, solvatos ou hidratos farmacologicamente aceitáveis. São preferidos sais selecionados do grupo consistindo em cloridrato, bromidrato, iodidrato, hidrossulfato, hidrofosfato, hidrometanossulfonato, hidronitrato, hidromaleato, hidroacetato, hidrocitrato, hidrofumarato, hidrotartarato, hidrooxalato, hidrossuccinato, hidrobenzoato, e hidro-p-toluenossulfonato.
Claims (7)
- Processo de montagem de um dispositivo (1) de liberação de um medicamento, particularmente na forma de um aerossol (A), com precisão de medição aperfeiçoada,
caracterizado pelo fato de que são providos, pelo menos, um primeiro e um segundo componente, que são colocados em ajuste selado um com o outro ou posicionados um contra o outro,
sendo que o primeiro componente é produzido em lotes, sendo que pelo menos uma grandeza significante do primeiro componente de cada lote é determinada somente por amostragem randômica,
sendo que pelo menos uma grandeza significante decisiva para todos os primeiros componentes do respectivo lote é determinada a partir de, pelo menos, uma grandeza significante,
sendo que o segundo componente é dividido em grupos que diferem por, pelo menos, uma grandeza essencial dos segundos componentes,
sendo que dependendo da, pelo menos, uma grandeza significante decisiva, é selecionado um grupo ajustando à respectiva grandeza significante decisiva e, portanto, o respectivo lote é selecionado,
sendo que um primeiro componente de um lote é combinado com um segundo componente de um grupo correspondente a este lote, de modo a obter um selo ideal entre estes dois componentes de modo a aperfeiçoar a precisão de medição, e estes dois componentes são movidos um em relação ao outro para o processo de liberação. - Processo, de acordo com a reivindicação 1, caracterizado pelo fato de que os primeiros componentes são moldados por injeção e/ou os primeiros componentes são selos conformados (5), preferivelmente em forma de anel, particularmente O-rings e/ou uma dimensão relacionada à ferramenta, volume e/ou a compressibilidade dos primeiros componentes é ou são determinados como grandeza ou grandezas significantes.
- Processo, de acordo com a reivindicação 1 ou 2, caracterizado pelo fato de que o valor médio e o desvio padrão são detectados ou determinados como grandezas significantes, e/ou que o valor médio e o desvio padrão são usados como grandezas essenciais para divisão nos grupos.
- Processo, de acordo com qualquer uma das reivindicações 1 a 3, caracterizado pelo fato de que o segundo componente têm, cada um, um recesso (6), particularmente um ressalto ou ranhura, para acomodação do primeiro componente e preferivelmente forma um tubo guia para um pistão (4), sendo que uma dimensão relacionada à ferramenta, particularmente a profundidade e/ou largura, do recesso é usada como grandeza essencial para divisão nos grupos.
- Processo, de acordo com qualquer uma das reivindicações 1 a 4, caracterizado pelo fato de que o segundo componente, são produzidos com diferentes grandezas essenciais, e em particular onde a diferença entre as grandezas essenciais de diferentes grupos é maior que a tolerância de fabricação, e/ou os segundos componentes são produzidos em lotes, a grandeza essencial dos segundos componentes em cada lote sendo determinada somente por amostragem randômica e a partir desta a grandeza essencial para todos os segundos componentes do respectivo lote é determinado para a divisão nos grupos.
- Processo, de acordo com qualquer uma das reivindicações 1 a 5, caracterizado pelo fato de que o dispositivo (1) compreende, em adição aos primeiro e segundo componentes, pelo menos ainda um componente, particularmente um pistão (4), que é selado pelo primeiro componente, e/ou um anel suporte (7) para segurar axialmente o primeiro componente ao segundo componente preferivelmente, sendo que um componente adicional, particularmente o pistão (4), é produzido em lotes e pelo menos uma grandeza significante, tal como o diâmetro, é determinada somente através de amostragem randômica de cada lote, mais preferencialmente sendo pelo menos uma ou mais grandezas significantes, particularmente dimensões relacionadas à ferramenta, de ainda componente ou componentes, particularmente o diâmetro do pistão (4) e/ou o comprimento axialmente efetivo do anel suporte (3), é ou são determinados e em consideração como ainda grandezas significantes em adição à decisiva grandeza significante quando selecionando o grupo de ajuste.
- Processo, de acordo com qualquer uma das reivindicações 1 a 6, caracterizado pelo fato de que o grupo de ajuste é selecionado de modo que a grandeza significante decisiva junto com opcionalmente pelo menos ainda uma grandeza significante de ainda um componente e junto com a grandeza(s) essencial conduzem a um valor alvo, particularmente um desejado nível de enchimento de um recesso através de um selo e/ou .
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PE (1) | PE20070673A1 (pt) |
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PT (1) | PT1942967E (pt) |
RS (1) | RS52469B (pt) |
SI (1) | SI1942967T1 (pt) |
TW (1) | TWI382859B (pt) |
UA (1) | UA95928C2 (pt) |
UY (1) | UY29897A1 (pt) |
WO (1) | WO2007051536A1 (pt) |
ZA (1) | ZA200802540B (pt) |
Families Citing this family (17)
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US8061350B2 (en) * | 2006-06-02 | 2011-11-22 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Process and device for dosing pharmaceutical agents |
EP2534957B1 (en) | 2007-12-14 | 2015-05-27 | AeroDesigns, Inc | Delivering aerosolizable products |
US8950394B2 (en) | 2010-01-12 | 2015-02-10 | Dance Biopharm Inc. | Preservative-free single dose inhaler systems |
US20130269684A1 (en) * | 2012-04-16 | 2013-10-17 | Dance Pharmaceuticals, Inc. | Methods and systems for supplying aerosolization devices with liquid medicaments |
US9283333B2 (en) | 2010-07-16 | 2016-03-15 | Boehringer Ingelheim International Gmbh | Filter system for use in medical devices |
CN102172504B (zh) * | 2011-01-31 | 2013-12-18 | 中国人民解放军防化指挥工程学院 | 一种液体有机物雾化气化装置 |
EP2694220B1 (de) | 2011-04-01 | 2020-05-06 | Boehringer Ingelheim International GmbH | Medizinisches gerät mit behälter |
ITMO20120219A1 (it) * | 2012-09-17 | 2014-03-18 | Giuseppe Maffei | Apparecchiatura per il trasferimento di fluidi biomedicali tra recipienti ospedalieri |
EP3202709B1 (de) | 2016-02-04 | 2019-04-10 | Boehringer Ingelheim microParts GmbH | Abformwerkzeug mit magnethalterung |
CN108057150B (zh) | 2016-11-06 | 2021-04-27 | 微邦科技股份有限公司 | 高压液体传输装置的组装方法 |
PL3697541T3 (pl) | 2017-10-18 | 2023-09-04 | Softhale Nv | Uszczelnienie dla urządzenia do inhalacji |
CN109745603B (zh) * | 2017-11-06 | 2021-05-28 | 微邦科技股份有限公司 | 流体输送装置 |
CN210785807U (zh) * | 2019-09-19 | 2020-06-19 | 苏州天健云康信息科技有限公司 | 雾化器 |
JP7689140B2 (ja) * | 2020-03-18 | 2025-06-05 | ベーリンガー インゲルハイム マイクロパーツ ゲゼルシャフト ミット ベシュレンクテル ハフツング | 分注デバイスを組み立てる方法及び分注デバイス |
GB2602102A (en) * | 2020-12-18 | 2022-06-22 | Merxin Ltd | Micropump having a sealing ring |
GB2636685A (en) * | 2023-05-25 | 2025-07-02 | Merxin Ltd | Micropump having a polyolefin sealing element |
WO2025073892A1 (en) * | 2023-10-04 | 2025-04-10 | Invox Belgium Nv | High-pressure medical pumping device and inhalation device |
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Publication number | Priority date | Publication date | Assignee | Title |
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DE1058440B (de) * | 1956-12-31 | 1959-05-27 | Wilhelm Waldherr | Spruehventil |
US3401849A (en) * | 1966-05-24 | 1968-09-17 | Robert L. Weber | Low force metering valve |
SG45171A1 (en) * | 1990-03-21 | 1998-01-16 | Boehringer Ingelheim Int | Atomising devices and methods |
EP0846011A1 (en) * | 1995-08-18 | 1998-06-10 | Pharmasol Limited | Spray applicator |
DE19536902A1 (de) * | 1995-10-04 | 1997-04-10 | Boehringer Ingelheim Int | Vorrichtung zur Hochdruckerzeugung in einem Fluid in Miniaturausführung |
JPH1163225A (ja) * | 1997-08-08 | 1999-03-05 | Yamaha Motor Co Ltd | ピストンリング |
GB0101944D0 (en) * | 2001-01-25 | 2001-03-07 | Bacon Raymond J | Dispenser |
EP1426662A1 (de) * | 2002-12-06 | 2004-06-09 | Boehringer Ingelheim International GmbH | Kolbenpumpsystem |
US6983630B2 (en) * | 2003-07-09 | 2006-01-10 | Kaba Ilco Corp. | Programmable cylinder lock system |
DE102004009435A1 (de) * | 2004-02-24 | 2005-12-08 | Boehringer Ingelheim International Gmbh | Zerstäuber |
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2005
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