EP2773409A1 - Inhalateur et procédé de production d'un aérosol - Google Patents
Inhalateur et procédé de production d'un aérosolInfo
- Publication number
- EP2773409A1 EP2773409A1 EP12797738.7A EP12797738A EP2773409A1 EP 2773409 A1 EP2773409 A1 EP 2773409A1 EP 12797738 A EP12797738 A EP 12797738A EP 2773409 A1 EP2773409 A1 EP 2773409A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- aerosol
- filter membrane
- nozzle
- inhaler
- inhaler according
- 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.)
- Withdrawn
Links
- 239000000443 aerosol Substances 0.000 title claims description 83
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 239000012528 membrane Substances 0.000 claims abstract description 159
- 239000007921 spray Substances 0.000 claims abstract description 33
- 239000002245 particle Substances 0.000 claims description 99
- 239000011148 porous material Substances 0.000 claims description 39
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 claims description 19
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 claims description 19
- 229960002715 nicotine Drugs 0.000 claims description 19
- 239000012530 fluid Substances 0.000 claims description 17
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 16
- 235000010323 ascorbic acid Nutrition 0.000 claims description 7
- 239000011668 ascorbic acid Substances 0.000 claims description 7
- 229960005070 ascorbic acid Drugs 0.000 claims description 7
- 230000015572 biosynthetic process Effects 0.000 claims description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 6
- BSYNRYMUTXBXSQ-FOQJRBATSA-N 59096-14-9 Chemical compound CC(=O)OC1=CC=CC=C1[14C](O)=O BSYNRYMUTXBXSQ-FOQJRBATSA-N 0.000 claims description 4
- 108700031620 S-acetylthiorphan Proteins 0.000 claims description 4
- 229940071648 metered dose inhaler Drugs 0.000 claims description 3
- 238000000034 method Methods 0.000 claims description 3
- 150000007524 organic acids Chemical group 0.000 claims description 3
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 claims description 2
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 claims description 2
- 229960004106 citric acid Drugs 0.000 claims description 2
- 239000004744 fabric Substances 0.000 claims description 2
- 239000001630 malic acid Substances 0.000 claims description 2
- 235000011090 malic acid Nutrition 0.000 claims description 2
- 210000004379 membrane Anatomy 0.000 description 60
- 210000004072 lung Anatomy 0.000 description 11
- 239000003380 propellant Substances 0.000 description 7
- 230000009467 reduction Effects 0.000 description 6
- 239000002253 acid Substances 0.000 description 5
- 239000002131 composite material Substances 0.000 description 5
- 238000011161 development Methods 0.000 description 5
- 230000018109 developmental process Effects 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- 239000004480 active ingredient Substances 0.000 description 4
- 239000013543 active substance Substances 0.000 description 4
- -1 alkali metal bicarbonates Chemical class 0.000 description 4
- NDAUXUAQIAJITI-UHFFFAOYSA-N albuterol Chemical compound CC(C)(C)NCC(O)C1=CC=C(O)C(CO)=C1 NDAUXUAQIAJITI-UHFFFAOYSA-N 0.000 description 3
- 210000000621 bronchi Anatomy 0.000 description 3
- 238000009826 distribution Methods 0.000 description 3
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- 239000003814 drug Substances 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000003595 mist Substances 0.000 description 3
- 229960002052 salbutamol Drugs 0.000 description 3
- KWGRBVOPPLSCSI-WPRPVWTQSA-N (-)-ephedrine Chemical compound CN[C@@H](C)[C@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WPRPVWTQSA-N 0.000 description 2
- UWYZHKAOTLEWKK-UHFFFAOYSA-N 1,2,3,4-tetrahydroisoquinoline Chemical compound C1=CC=C2CNCCC2=C1 UWYZHKAOTLEWKK-UHFFFAOYSA-N 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 2
- FXFANIORDKRCCA-UHFFFAOYSA-N Norcotinine Chemical compound N1C(=O)CCC1C1=CC=CN=C1 FXFANIORDKRCCA-UHFFFAOYSA-N 0.000 description 2
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 2
- 238000010521 absorption reaction Methods 0.000 description 2
- ILLGYRJAYAAAEW-QMMMGPOBSA-N abt-418 Chemical compound CN1CCC[C@H]1C1=CC(C)=NO1 ILLGYRJAYAAAEW-QMMMGPOBSA-N 0.000 description 2
- SLRCCWJSBJZJBV-UHFFFAOYSA-N alpha-isosparteine Natural products C1N2CCCCC2C2CN3CCCCC3C1C2 SLRCCWJSBJZJBV-UHFFFAOYSA-N 0.000 description 2
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- 230000036760 body temperature Effects 0.000 description 2
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 2
- DLNKOYKMWOXYQA-IONNQARKSA-N cathine Chemical compound C[C@H](N)[C@@H](O)C1=CC=CC=C1 DLNKOYKMWOXYQA-IONNQARKSA-N 0.000 description 2
- KWGRBVOPPLSCSI-UHFFFAOYSA-N d-ephedrine Natural products CNC(C)C(O)C1=CC=CC=C1 KWGRBVOPPLSCSI-UHFFFAOYSA-N 0.000 description 2
- DLNKOYKMWOXYQA-UHFFFAOYSA-N dl-pseudophenylpropanolamine Natural products CC(N)C(O)C1=CC=CC=C1 DLNKOYKMWOXYQA-UHFFFAOYSA-N 0.000 description 2
- ASUTZQLVASHGKV-JDFRZJQESA-N galanthamine Chemical compound O1C(=C23)C(OC)=CC=C2CN(C)CC[C@]23[C@@H]1C[C@@H](O)C=C2 ASUTZQLVASHGKV-JDFRZJQESA-N 0.000 description 2
- KUBCEEMXQZUPDQ-UHFFFAOYSA-N hordenine Chemical compound CN(C)CCC1=CC=C(O)C=C1 KUBCEEMXQZUPDQ-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 239000008263 liquid aerosol Substances 0.000 description 2
- RHCSKNNOAZULRK-UHFFFAOYSA-N mescaline Chemical compound COC1=CC(CCN)=CC(OC)=C1OC RHCSKNNOAZULRK-UHFFFAOYSA-N 0.000 description 2
- 210000002200 mouth mucosa Anatomy 0.000 description 2
- 210000004400 mucous membrane Anatomy 0.000 description 2
- 210000003800 pharynx Anatomy 0.000 description 2
- AQHHHDLHHXJYJD-UHFFFAOYSA-N propranolol Chemical compound C1=CC=C2C(OCC(O)CNC(C)C)=CC=CC2=C1 AQHHHDLHHXJYJD-UHFFFAOYSA-N 0.000 description 2
- YJYPZLAZNIGNRP-UHFFFAOYSA-N rjr-2429 Chemical compound C1CN2CCC1CC2C1=CC=CN=C1 YJYPZLAZNIGNRP-UHFFFAOYSA-N 0.000 description 2
- 230000000391 smoking effect Effects 0.000 description 2
- SLRCCWJSBJZJBV-AJNGGQMLSA-N sparteine Chemical compound C1N2CCCC[C@H]2[C@@H]2CN3CCCC[C@H]3[C@H]1C2 SLRCCWJSBJZJBV-AJNGGQMLSA-N 0.000 description 2
- 229960001945 sparteine Drugs 0.000 description 2
- APJYDQYYACXCRM-UHFFFAOYSA-N tryptamine Chemical compound C1=CC=C2C(CCN)=CNC2=C1 APJYDQYYACXCRM-UHFFFAOYSA-N 0.000 description 2
- CEMAWMOMDPGJMB-UHFFFAOYSA-N (+-)-Oxprenolol Chemical compound CC(C)NCC(O)COC1=CC=CC=C1OCC=C CEMAWMOMDPGJMB-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
- MXYUKLILVYORSK-UHFFFAOYSA-N (+/-)-allo-lobeline Natural products C1CCC(CC(=O)C=2C=CC=CC=2)N(C)C1CC(O)C1=CC=CC=C1 MXYUKLILVYORSK-UHFFFAOYSA-N 0.000 description 1
- UIKROCXWUNQSPJ-VIFPVBQESA-N (-)-cotinine Chemical compound C1CC(=O)N(C)[C@@H]1C1=CC=CN=C1 UIKROCXWUNQSPJ-VIFPVBQESA-N 0.000 description 1
- MXYUKLILVYORSK-HBMCJLEFSA-N (-)-lobeline Chemical compound C1([C@@H](O)C[C@H]2N([C@H](CCC2)CC(=O)C=2C=CC=CC=2)C)=CC=CC=C1 MXYUKLILVYORSK-HBMCJLEFSA-N 0.000 description 1
- IGLYMJRIWWIQQE-QUOODJBBSA-N (1S,2R)-2-phenylcyclopropan-1-amine (1R,2S)-2-phenylcyclopropan-1-amine Chemical compound N[C@H]1C[C@@H]1C1=CC=CC=C1.N[C@@H]1C[C@H]1C1=CC=CC=C1 IGLYMJRIWWIQQE-QUOODJBBSA-N 0.000 description 1
- KWTSXDURSIMDCE-QMMMGPOBSA-N (S)-amphetamine Chemical compound C[C@H](N)CC1=CC=CC=C1 KWTSXDURSIMDCE-QMMMGPOBSA-N 0.000 description 1
- MTXSIJUGVMTTMU-JTQLQIEISA-N (S)-anabasine Chemical compound N1CCCC[C@H]1C1=CC=CN=C1 MTXSIJUGVMTTMU-JTQLQIEISA-N 0.000 description 1
- RKUNBYITZUJHSG-FXUDXRNXSA-N (S)-atropine Chemical compound C1([C@@H](CO)C(=O)O[C@H]2C[C@H]3CC[C@@H](C2)N3C)=CC=CC=C1 RKUNBYITZUJHSG-FXUDXRNXSA-N 0.000 description 1
- MYKUKUCHPMASKF-VIFPVBQESA-N (S)-nornicotine Chemical compound C1CCN[C@@H]1C1=CC=CN=C1 MYKUKUCHPMASKF-VIFPVBQESA-N 0.000 description 1
- SGTNSNPWRIOYBX-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-{[2-(3,4-dimethoxyphenyl)ethyl](methyl)amino}-2-(propan-2-yl)pentanenitrile Chemical compound C1=C(OC)C(OC)=CC=C1CCN(C)CCCC(C#N)(C(C)C)C1=CC=C(OC)C(OC)=C1 SGTNSNPWRIOYBX-UHFFFAOYSA-N 0.000 description 1
- WAOQONBSWFLFPE-VIFPVBQESA-N 3,5-dichloro-N-[[(2S)-1-ethyl-2-pyrrolidinyl]methyl]-2-hydroxy-6-methoxybenzamide Chemical compound CCN1CCC[C@H]1CNC(=O)C1=C(O)C(Cl)=CC(Cl)=C1OC WAOQONBSWFLFPE-VIFPVBQESA-N 0.000 description 1
- GIKNHHRFLCDOEU-UHFFFAOYSA-N 4-(2-aminopropyl)phenol Chemical compound CC(N)CC1=CC=C(O)C=C1 GIKNHHRFLCDOEU-UHFFFAOYSA-N 0.000 description 1
- XKFPYPQQHFEXRZ-UHFFFAOYSA-N 5-methyl-N'-(phenylmethyl)-3-isoxazolecarbohydrazide Chemical compound O1C(C)=CC(C(=O)NNCC=2C=CC=CC=2)=N1 XKFPYPQQHFEXRZ-UHFFFAOYSA-N 0.000 description 1
- RYENLSMHLCNXJT-CYXFISRXSA-N 7-Hydroxymitragynine Chemical compound C1=CC(OC)=C2[C@@]3(O)CCN4C[C@@H](CC)[C@@H](\C(=C/OC)C(=O)OC)C[C@H]4C3=NC2=C1 RYENLSMHLCNXJT-CYXFISRXSA-N 0.000 description 1
- 229930000680 A04AD01 - Scopolamine Natural products 0.000 description 1
- SOPPBXUYQGUQHE-JTQLQIEISA-N Anatabine Chemical compound C1C=CCN[C@@H]1C1=CC=CN=C1 SOPPBXUYQGUQHE-JTQLQIEISA-N 0.000 description 1
- SOPPBXUYQGUQHE-UHFFFAOYSA-N Anatabine Natural products C1C=CCNC1C1=CC=CN=C1 SOPPBXUYQGUQHE-UHFFFAOYSA-N 0.000 description 1
- 239000005528 B01AC05 - Ticlopidine Substances 0.000 description 1
- 239000004604 Blowing Agent Substances 0.000 description 1
- 229930008564 C01BA04 - Sparteine Natural products 0.000 description 1
- UIKROCXWUNQSPJ-UHFFFAOYSA-N Cotinine Natural products C1CC(=O)N(C)C1C1=CC=CN=C1 UIKROCXWUNQSPJ-UHFFFAOYSA-N 0.000 description 1
- ZZZCUOFIHGPKAK-UHFFFAOYSA-N D-erythro-ascorbic acid Natural products OCC1OC(=O)C(O)=C1O ZZZCUOFIHGPKAK-UHFFFAOYSA-N 0.000 description 1
- NLPRAJRHRHZCQQ-UHFFFAOYSA-N Epibatidine Natural products C1=NC(Cl)=CC=C1C1C(N2)CCC2C1 NLPRAJRHRHZCQQ-UHFFFAOYSA-N 0.000 description 1
- RKUNBYITZUJHSG-UHFFFAOYSA-N Hyosciamin-hydrochlorid Natural products CN1C(C2)CCC1CC2OC(=O)C(CO)C1=CC=CC=C1 RKUNBYITZUJHSG-UHFFFAOYSA-N 0.000 description 1
- STECJAGHUSJQJN-GAUPFVANSA-N Hyoscine Natural products C1([C@H](CO)C(=O)OC2C[C@@H]3N([C@H](C2)[C@@H]2[C@H]3O2)C)=CC=CC=C1 STECJAGHUSJQJN-GAUPFVANSA-N 0.000 description 1
- NYMGNSNKLVNMIA-UHFFFAOYSA-N Iproniazid Chemical compound CC(C)NNC(=O)C1=CC=NC=C1 NYMGNSNKLVNMIA-UHFFFAOYSA-N 0.000 description 1
- JAQUASYNZVUNQP-USXIJHARSA-N Levorphanol Chemical compound C1C2=CC=C(O)C=C2[C@]23CCN(C)[C@H]1[C@@H]2CCCC3 JAQUASYNZVUNQP-USXIJHARSA-N 0.000 description 1
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- LELBFTMXCIIKKX-QVRQZEMUSA-N Mitragynine Chemical compound C1=CC(OC)=C2C(CCN3C[C@H]([C@H](C[C@H]33)\C(=C/OC)C(=O)OC)CC)=C3NC2=C1 LELBFTMXCIIKKX-QVRQZEMUSA-N 0.000 description 1
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- RYENLSMHLCNXJT-UHFFFAOYSA-N Mitragynine hydroxyindolenine Natural products C1=CC(OC)=C2C3(O)CCN4CC(CC)C(C(=COC)C(=O)OC)CC4C3=NC2=C1 RYENLSMHLCNXJT-UHFFFAOYSA-N 0.000 description 1
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- DMULVCHRPCFFGV-UHFFFAOYSA-N N,N-dimethyltryptamine Chemical compound C1=CC=C2C(CCN(C)C)=CNC2=C1 DMULVCHRPCFFGV-UHFFFAOYSA-N 0.000 description 1
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- RMUCZJUITONUFY-UHFFFAOYSA-N Phenelzine Chemical compound NNCCC1=CC=CC=C1 RMUCZJUITONUFY-UHFFFAOYSA-N 0.000 description 1
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- DAHIQPJTGIHDGO-UHFFFAOYSA-N mesembrine Natural products C1=C(OC)C(OC)=CC=C1C1(CCC(=O)C2)C2N(C)CC1 DAHIQPJTGIHDGO-UHFFFAOYSA-N 0.000 description 1
- LMOINURANNBYCM-UHFFFAOYSA-N metaproterenol Chemical compound CC(C)NCC(O)C1=CC(O)=CC(O)=C1 LMOINURANNBYCM-UHFFFAOYSA-N 0.000 description 1
- SVXZBICQLNEMLC-UHFFFAOYSA-N methyl 1-methyl-3,6-dihydro-2h-pyridine-4-carboxylate Chemical compound COC(=O)C1=CCN(C)CC1 SVXZBICQLNEMLC-UHFFFAOYSA-N 0.000 description 1
- 229960002497 nicorandil Drugs 0.000 description 1
- LBHIOVVIQHSOQN-UHFFFAOYSA-N nicorandil Chemical compound [O-][N+](=O)OCCNC(=O)C1=CC=CN=C1 LBHIOVVIQHSOQN-UHFFFAOYSA-N 0.000 description 1
- 239000004745 nonwoven fabric Substances 0.000 description 1
- 229960002657 orciprenaline Drugs 0.000 description 1
- 210000003300 oropharynx Anatomy 0.000 description 1
- 229960004570 oxprenolol Drugs 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 229960000964 phenelzine Drugs 0.000 description 1
- PIJVFDBKTWXHHD-HIFRSBDPSA-N physostigmine Chemical compound C12=CC(OC(=O)NC)=CC=C2N(C)[C@@H]2[C@@]1(C)CCN2C PIJVFDBKTWXHHD-HIFRSBDPSA-N 0.000 description 1
- 229960001697 physostigmine Drugs 0.000 description 1
- MFDFERRIHVXMIY-UHFFFAOYSA-N procaine Chemical compound CCN(CC)CCOC(=O)C1=CC=C(N)C=C1 MFDFERRIHVXMIY-UHFFFAOYSA-N 0.000 description 1
- 229960004919 procaine Drugs 0.000 description 1
- 229960003712 propranolol Drugs 0.000 description 1
- KWGRBVOPPLSCSI-WCBMZHEXSA-N pseudoephedrine Chemical compound CN[C@@H](C)[C@@H](O)C1=CC=CC=C1 KWGRBVOPPLSCSI-WCBMZHEXSA-N 0.000 description 1
- 229960003908 pseudoephedrine Drugs 0.000 description 1
- 238000009613 pulmonary function test Methods 0.000 description 1
- 229960002290 pyridostigmine Drugs 0.000 description 1
- 229950001518 raclopride Drugs 0.000 description 1
- 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
- 229960001634 ritodrine Drugs 0.000 description 1
- STECJAGHUSJQJN-FWXGHANASA-N scopolamine Chemical compound C1([C@@H](CO)C(=O)O[C@H]2C[C@@H]3N([C@H](C2)[C@@H]2[C@H]3O2)C)=CC=CC=C1 STECJAGHUSJQJN-FWXGHANASA-N 0.000 description 1
- 229960002646 scopolamine Drugs 0.000 description 1
- 230000005586 smoking cessation Effects 0.000 description 1
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 1
- 235000017557 sodium bicarbonate Nutrition 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229960001685 tacrine Drugs 0.000 description 1
- YLJREFDVOIBQDA-UHFFFAOYSA-N tacrine Chemical compound C1=CC=C2C(N)=C(CCCC3)C3=NC2=C1 YLJREFDVOIBQDA-UHFFFAOYSA-N 0.000 description 1
- MKTAGSRKQIGEBH-SSDOTTSWSA-N tebanicline Chemical compound C1=NC(Cl)=CC=C1OC[C@@H]1NCC1 MKTAGSRKQIGEBH-SSDOTTSWSA-N 0.000 description 1
- 229960000195 terbutaline Drugs 0.000 description 1
- PHWBOXQYWZNQIN-UHFFFAOYSA-N ticlopidine Chemical compound ClC1=CC=CC=C1CN1CC(C=CS2)=C2CC1 PHWBOXQYWZNQIN-UHFFFAOYSA-N 0.000 description 1
- 229960005001 ticlopidine Drugs 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 229960003741 tranylcypromine Drugs 0.000 description 1
- 229960001722 verapamil Drugs 0.000 description 1
- 235000019154 vitamin C Nutrition 0.000 description 1
- 239000011718 vitamin C Substances 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
- A61M15/009—Inhalators using medicine packages with incorporated spraying means, e.g. aerosol cans
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05B—SPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
- B05B1/00—Nozzles, spray heads or other outlets, with or without auxiliary devices such as valves, heating means
-
- 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
- A61M11/001—Particle size control
- A61M11/003—Particle size control by passing the aerosol trough sieves or filters
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05B—SPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
- B05B15/00—Details of spraying plant or spraying apparatus not otherwise provided for; Accessories
- B05B15/40—Filters located upstream of the spraying outlets
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D83/00—Containers or packages with special means for dispensing contents
- B65D83/14—Containers for dispensing liquid or semi-liquid contents by internal gaseous pressure, i.e. aerosol containers comprising propellant
- B65D83/28—Nozzles, nozzle fittings or accessories specially adapted therefor
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B65—CONVEYING; PACKING; STORING; HANDLING THIN OR FILAMENTARY MATERIAL
- B65D—CONTAINERS FOR STORAGE OR TRANSPORT OF ARTICLES OR MATERIALS, e.g. BAGS, BARRELS, BOTTLES, BOXES, CANS, CARTONS, CRATES, DRUMS, JARS, TANKS, HOPPERS, FORWARDING CONTAINERS; ACCESSORIES, CLOSURES, OR FITTINGS THEREFOR; PACKAGING ELEMENTS; PACKAGES
- B65D83/00—Containers or packages with special means for dispensing contents
- B65D83/14—Containers for dispensing liquid or semi-liquid contents by internal gaseous pressure, i.e. aerosol containers comprising propellant
- B65D83/75—Aerosol containers not provided for in groups B65D83/16 - B65D83/74
- B65D83/754—Aerosol containers not provided for in groups B65D83/16 - B65D83/74 comprising filters in the fluid flow path
-
- 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
- A61M11/02—Sprayers or atomisers specially adapted for therapeutic purposes operated by air or other gas pressure applied to the liquid or other product to be sprayed or atomised
-
- 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
- A61M15/06—Inhaling appliances shaped like cigars, cigarettes or pipes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05B—SPRAYING APPARATUS; ATOMISING APPARATUS; NOZZLES
- B05B1/00—Nozzles, spray heads or other outlets, with or without auxiliary devices such as valves, heating means
- B05B1/14—Nozzles, spray heads or other outlets, with or without auxiliary devices such as valves, heating means with multiple outlet openings; with strainers in or outside the outlet opening
Definitions
- the invention relates to an inhaler, in particular for generating an aerosol. Furthermore, the invention relates to a method for producing an aerosol by means of a
- Metered aerosols are known. These are used, for example, as an asthma spray.
- the inhaler used for this purpose comprises a spray head, over which a particle-containing mist is released. This way you can talk about the
- Particle mist active ingredients through the lungs particularly quickly enter the bloodstream.
- Metered dose inhalers due to their particle size quite quickly, which means that the desired dosage is only achieved if the user agrees to inhalation well on the spray.
- nicotine-containing metered dose inhalers For smoking cessation, especially as a substitute for cigarettes, nicotine-containing metered dose inhalers are known. However, such nicotine-containing metered dose inhalers have so far often not achieved the desired effect. This could be because nicotine is primarily absorbed through the lungs when smoking.
- known inhalers for producing aerosols generally produce particles of at least 5 ⁇ m in size. Such particles are not respirable and do not enter the alveoli. Rather, the particles predominantly settle in the throat and sometimes even in the bronchi. Thus, nicotine can be absorbed by the body, which reduces withdrawal symptoms. However, due to the slower absorption, the user does not experience the kick typical of smoking due to a rapid increase in nicotine in the blood.
- Chamber is sprayed. In this chamber, the Speed of the particles due to the longer
- Metered aerosols usually due to the high pressure with which escape the particles of the spray as well as due to the particle velocity, the temperature of the mist is relatively low, especially well below
- the invention is based on the object to provide an inhaler and a method for producing an aerosol, in which can be easily generate aerosols with improved lung compliance. It is further an object of the invention that
- the invention relates to an inhaler. This is
- Dosage aerosol or an asthma medication includes for this purpose a container with a nicotine-containing solution.
- a propellant is used to generate an aerosol, which produces an aerosol in a nozzle in a manner known per se to a person skilled in the art.
- the inhaler comprises a spray head with a nozzle.
- At least one is in front of the nozzle
- the volume of a fluid channel between the nozzle and the filter membrane is less than half as large, preferably less than a quarter of the volume of a spray of the
- Speed of the particles can be reduced without causing blockages of the filter membrane or the retention of aerosol particles.
- a filter membrane in particular a nonwoven or
- Screen fabric which is in particular made of plastic, can be used.
- the filter membrane preferably has a middle one
- the average pore diameter should be at least 5 times larger such as the mean particle size of the active ingredient contained in the suspension.
- the filter membrane preferably has an open area which is at most five times, more preferably at most twice, and most preferably at most 1.5 times the cross-sectional area which the nozzle has, from which the aerosol flows out. It is particularly preferred that the open area of the
- Filter membrane substantially corresponds to the cross-sectional area of the nozzle.
- the cross-sectional area of the membrane and the open area of the membrane can be achieved depending on the solution or suspension used that a large part of the droplet formation takes place on the filter membrane.
- the open area of the filter membrane is between _5 and 25% of the total area of the filter membrane.
- the open area of the filter membrane can be between 2 and 60%
- a filter membrane with a diameter of 0.5 to 3 mm is preferably used.
- a perforated plate is used as filter membrane, wherein the holes the perforated plate are at least partially inclined so that the spray is divided into individual beams, which meet at a distance from the perforated plate.
- the perforated plate with one or more peripheral rings which are inclined relative to the central axis of the perforated plate in such a way that the divided aerosol is focused, as it were, in front of the inhaler at a distance of a few centimeters. This leads to collisions and turbulences in the area in which particles meet, what the middle
- the trained as a perforated plate filter membrane can also be combined with other layers, in particular nonwoven layers.
- Filter membrane small than the average particle size of an aerosol generated by the nozzle.
- an aerosol is first generated by means of a nozzle, which is accelerated in the direction of the filter membrane or pressed through the filter membrane. Due to the finer pores of the filter membrane, a smaller average particle diameter can be achieved in the aerosol leaving the membrane than by means of the nozzle. So can easily be respirable
- Particles with an average particle size of already 1 ym are already respirable. Depending on the aerosol used, however, it is already inhaled while the aerosol is being inhaled and flows in the direction of the lungs again
- a filter membrane is thus understood in particular to be any structure, in particular planar structure, which has holes which have a diameter which is smaller than the mean particle size of the aerosol, ie in particular pores in the sense of holes with an average diameter of less than 5 ⁇ m.
- the filter membrane may in particular be formed as a nonwoven, which has a three-dimensional open-pored structure.
- a screen mesh is also conceivable. The inventor has also found that in addition to a reduction of the particle size it surprisingly also to a significant reduction in the
- the aerosol cloud generated by the inhaler according to the invention therefore has a higher residence time than is the case with known inhalers.
- particles can be produced which on average have less than half the speed, like the particles that enter the filter membrane.
- the particles Due to the lower speed, the particles are easier to inhale. As a rule, a larger proportion of the particles produced reaches the lungs and the use of the inhaler is simplified for the user in such a way that the spray must be less accurately coordinated with the inhalation.
- the velocity of the aerosol particles, as they exit the nozzle, is typically between 30 and 100 m / s.
- Through the filter membrane is preferably the
- Aersol is actually inhaled in an aerosol cloud and how much of the active substance it contains depending on
- An advantage of the use of a filter membrane is that it can be made very compact and immediate in front of a nozzle, from which an aerosol emerges, can be arranged.
- the distance is the
- Filter membrane in front of the nozzle less than 10 millimeters.
- at least two filter membranes with different are in front of the nozzle
- Diameter arranged.
- first filter membrane in which particles having an average particle size of more than 2 ⁇ m are initially produced.
- the last filter membrane used should have an average pore size of less than 0.5 ym.
- the aerosol is partially pressed by different filter membranes or by a different number of filter membranes. It is by means of this embodiment of the invention
- Spray impulse contain on the one hand a particle fraction, which is respirable and the "Kick" popular with smokers triggers. Another fraction of particles is so large that these predominantly in the bronchi or in the
- Pharynx be resorbed. Over the slow absorption there can be achieved a long-lasting high nicotine level in the blood after generating the kicks, which leads to the fact that the smoker only after a long time the
- respirable is respirable. It has been found that due to the usually not optimal coordination of spraying and inhalation also a part of respirable particles remain in the oropharynx and over there
- the filter membranes can, as provided in a particular embodiment of the invention,
- a filter membrane occupies a smaller surface area than the other
- Filter membrane with smaller, average pore diameter occupies a smaller surface area, this can contain almost any shaped recesses.
- the filter membrane with larger pore diameter is behind this
- One part of the particles thus passes through two filter membranes, whereas against another part of the particles only the filter membrane with a larger pore diameter is created.
- the filter membranes can be used as a layer package
- a filter membrane package which preferably has substantially the contour of a circle, by means of a ring in a housing. This is how a simple and inexpensive way to inhale
- the spray head of the inhaler comprises filter membranes with at least three
- the spray head may also contain four or more superimposed filter membranes.
- at least one filter membrane is connected to a support layer which has a larger pore diameter than the filter membrane.
- the support layer which also acts as a filter membrane
- the thickness of the filter membrane can be reduced, which reduces the flow resistance of the layer package.
- a support layer is used which
- the support layer has at least three times, preferably at least five times the pore diameter of the filter membrane. Furthermore, the support layer preferably has twice, and more preferably at least three times, the thickness of the filter membrane.
- the at least one filter membrane can both be
- a filter membrane is arranged on both sides of the support layer.
- the layer package can for example be clamped edge side, glued or welded, or glued surface or selectively or welded.
- Aerosol is usually between 4 and 10 ym.
- the inhaler is with a nicotine-containing solution at a concentration of 0.3-20 mg / ml, preferably 1 - 10 mg / ml and more preferably 4 to 8 mg / ml filled.
- the inhaler is preferably designed such that a spray contains 0.05 to 0.5 mg, preferably 0.1 to 0.3 mg, of nicotine.
- the inhaler is filled with a solution which contains at least one organic acid, in particular acetylsalicylic acid, ascorbic acid, citric acid and / or malic acid.
- an acid reduces the pH of the solution, in particular the nicotine-containing solution. So it is particularly possible, an aerosol with a pH of less than 7.5; preferably less than 7,
- the acid can serve as a flavoring.
- the acid may also serve as an active ingredient to concurrently the arteries
- the solution used for the inhaler contains an organic or
- the solution preferably contains carbonates and / or bicarbonates. Particularly preferably, the solution contains alkali metal bicarbonates and most preferably sodium bicarbonate.
- the content of bicarbonate is preferably 10 to 50 mg / ml, preferably 25 to 45 mg / ml. This is advantageous because, in an aqueous environment, especially on the oral mucosa, a pH of 6.5 to 7 can be obtained. This pH is beneficial for the uptake of nicotine via the oral mucosa.
- the addition of carbonates can serve as a buffer for the pH, in particular with the simultaneous addition of an acid
- the solution contains ascorbic acid as organic acid.
- a content of ascorbic acid of 20 to 75 mg / ml, preferably 27 to 65 mg / ml and most preferably from 30 to 45 mg / ml has been found to be particularly advantageous.
- a spray thus preferably contains 0.5 to 1.5 mg
- the smoker When ascorbic acid is used, the smoker receives the vitamin C, which is particularly important for smokers, when using the inhaler.
- inhaler according to the invention can also be used for the following exemplified active substances or combinations thereof:
- Bupropion cathine (D-norpseudoephedrine), cathinone ( ⁇ -ketoamphetamine), chlorpheneramine, dibucaine, dimemorphan dimethyltryptamine, diphenhydramine, ephedrine, hordenine,
- Hyoscyamine i35coline, levorphanol, lobeline, mescaline, mesembrine, mitragynine, muscarine, parahydroxyamphetamine, Procaine, pseudoephedrine, pyrilamine, raclopride, ritodrine, scopolamine, sparteine (lupinidine), ticlopidine, 1,2,3,4-tetrahydroisoquinoline, anabasine, anatabine, cotinine,
- the invention further relates to a method for producing an aerosol, wherein an aerosol is generated by means of a nozzle, in which a valve is opened and the aerosol flows out of the nozzle and then passes through a filter membrane.
- the aerosol after the nozzle preferably passes through a fluid channel which leads to the filter membrane and whose volume is so small that a pressure builds up in the fluid channel which at least partially prevents aerosol formation in the fluid channel. A part of the aerosol thus arises only when the still liquid aerosol leaves the filter membrane.
- the invention further relates to a method for producing an aerosol, in particular by means of an inhaler as described above. In this case, an aerosol with an average particle size of more than 3 ym is generated by means of a nozzle, which is separated by at least two filter membranes with different mean
- Pore diameter is pressed, the same as before
- a first fraction having an average particle size of less than 1.5 ⁇ m and another fraction having an average particle size of more than 2 ⁇ m are produced.
- the invention further relates to the use of an inhaler described above for producing an aerosol having at least 2 fractions of particles with different average particle size, wherein
- the average particle size of a fraction differs by at least 0.5, preferably at least 1 ym, from the particle size of the other fraction.
- the particle sizes can, for example, by means of
- Laser interferometry can be determined.
- FIGS. 1 to 17 DESCRIPTION OF THE DRAWINGS The invention will be described below with reference to the drawings, FIGS. 1 to 17, with reference to FIG.
- FIG. 1 shows, schematically illustrated, a sectional view of the spray head of an embodiment of a
- Components such as reservoir, actuators, etc., which are not shown in detail below, as these are known from the prior art, for example of metered dose inhaler containers for asthma.
- the spray head 1 has a housing 2. Via a nozzle 3, an aerosol with a mean particle size of over 4 ym is pumped into a chamber. In the area of the nozzle 3, the chamber 4 has a diameter of a few millimeters and widens in the direction of a membrane packet consisting of the filter membranes 5 to 8. There is the
- the filter membranes 5 to 8 are inserted into the housing 2 and are fixed by the ring 9 inserted in the housing 2. This ring can be clamped, glued or
- a membrane with a mean pore diameter of this embodiment 2 ym In the membrane packet is arranged as a first filter membrane 5, a membrane with a mean pore diameter of this embodiment 2 ym. This extends over the entire diameter. Then follows the membrane 6 with a very small average pore diameters of 0.25 ym. However, this membrane only occupies part of the area of the membrane packet. On the membrane 6 followed by membrane 7 with a middle
- Membrane can pass through more or less unhindered. In the overlap region of the membrane 5 with the membrane 7, that is, at the locations where the membrane 6 is not arranged in the membrane 7, the leaked from the membrane 5 particles pass through the filter membrane 7. On the
- Filter membrane 7 follows the filter membrane 8 with a
- Layer a filter membrane is arranged, which occupies the entire surface area of the membrane packet, since this serves as a support for the other membranes.
- the particles produced by the nozzle 3 can thus be divided into three particle fractions
- a part of the particles passes through the membrane 6 as well as the other membranes that are in contact and have a decreasing diameter.
- the fraction of particles that passes through all the filter membranes has the smallest mean particle diameter.
- Pore diameter can be almost any
- Particle size distribution can be adjusted.
- a further nozzle 10 is provided, via which a propellant is injected into the chamber 4.
- a propellant is injected into the chamber 4.
- this propellant which preferably in a separate
- Container of the inhaler is introduced, 4 pressure is generated in the chamber, which causes the particles generated by the nozzle 3 are pressed through the membrane package.
- Fig. 2 shows the membrane package shown in Fig. 1 in plan view
- the illustration in Fig. 1 is a
- the filter membranes 6 and 7 comprise a circular central part, which is held by webs extending to the ring in which the
- Membrane packages is held extend. Between these webs is the area in which the respective filter membrane is recessed, so that the particles do not pass through the respective filter membrane.
- the first filter membrane 5 after the nozzle which has the shape of a circle, can first be seen in FIG. This has a mean pore diameter of 2 ym.
- Fig. 4 shows the subsequent membrane 6, which has a circular central region, on which webs extend, which can be clamped between ring and housing (shown in Fig. 1).
- Fig. 5 shows the following membrane 7 with an average pore diameter of 0.5 ym. This corresponds in the
- Fig. 6 shows the last membrane 8 of the filter membrane package, which is circular in shape with a mean pore diameter of 1 ym.
- Fig. 7 shows an example calculated
- Membrane package It can be seen that the theoretical particle sizes are between 0.5 and 2.3 ⁇ m and in particular that a large part of the particles has an average particle size of less than 1 ⁇ m.
- Fig. 8 shows a further embodiment of the invention, in which between the filter membranes 12 and 14 a
- Support layer 13 is arranged.
- the support layer 13 serves for the mechanical stabilization of the filter membranes 12 and 14.
- the filter membranes 12 and 14 may therefore be made particularly thin without the risk of tearing exists. As a result, the flow resistance of the sandwich composite thus provided is reduced.
- the support layer 13 is also a filter membrane, which however is thicker and has a substantially larger pore diameter.
- Pore diameters are used with a diameter between 0.5 ym and 5 ym, whereas the support layer has a pore diameter of about 20 ym. Despite its thickness, the support layer therefore provides little resistance to the particles of the aerosol.
- the sandwich composite for example, along the
- the sandwich composite shown in FIG. 8, comprising the filter membrane layers 12 and 14 and the support layer 13, is integrated in the housing 2.
- the sandwich composite of the layers 12, 13 and 14 is clamped by means of the ring 9 in the housing 2.
- the ring 9 comprises at least one bead 15, which engages in a corresponding groove of the housing 2. It is understood that in addition to or alternatively the sandwich composite can also be glued or welded in addition to a clamp connection.
- FIG. 10 shows a further embodiment of the invention, in which a part of the housing with the at least one filter membrane is fastened in a detachable carrier 16.
- FIG. 10 otherwise corresponds to the embodiment of FIG. 9, wherein it can be seen that in particular the attachment of the filter membrane can also be done in other ways.
- the housing 2 in this embodiment comprises a removable carrier 16.
- the lower comprises
- Housing part front side a diameter-tapered section with an external thread.
- the carrier 16 includes an internal thread, so that the two housing parts via the thread 17 are joined together.
- Carrier can also be designed removable in other ways, for example by means of a clamping or
- the carrier 16 may have a structured outer side for better gripping and / or means to remove the carrier 16 by means of a handling tool.
- the carrier 16 is without use of a
- Filter membrane such as when aerosol drops
- Aerosol formation takes place mainly on the flow side behind the filter membrane.
- a housing 2 with a receptacle 19 for a commercial aerosol vial which has a diameter of 0.5 to 2 mm.
- the slightly oblique shot 19 goes into one
- Fluid channel 18 via. At the end of the fluid channel, in which this on a
- Diameter of 3 to 5 mm expands, is fixed by means of the ring 9 designed as a nonwoven filter membrane. This has a mean pore diameter of 10 to 20 ym.
- the volume of the fluid channel 18 is now dimensioned such that the volume of the aerosol of a spray at
- Standard conditions according to SATP is at least five times that.
- the open area of the filter membrane 5 is dimensioned such that it is at most twice as large as the inside diameter of the nozzle (not shown) used in the receptacle 19 of the aerosol vial.
- the filter membrane 5 still has a much larger diameter than the nozzle, since the open area is only about 5 to 15% of the total area.
- Propellant remains in the liquid state and there is an aerosol formation after passing through the filter membrane 5.
- Fig. 12 another embodiment will be explained. This essentially corresponds to the components of FIG. 11.
- Embodiment a perforated plate with inclined channels 21 used. Via the channels 21, the spray is divided into several beams and at some distance in front of the inhaler
- a fleece 23 may be used to provide finer pores in front of the filter membrane 5 formed as a perforated plate 20.
- Both the nonwoven 23 and the perforated plate 20 are fixed by the ring 9.
- Fig. 13 shows how the spray is divided and focused by the perforated plate 20 into a plurality of beams.
- Aerosols which slows down the speed.
- FIGS. 15 and 16 show different ones
- Fig. 15 shows an alternative embodiment of a perforated plate with a central hole, which is exactly perpendicular to
- the perforated plate is arranged and that extend around eight more oblique holes, which focus the split into multiple jets of spray.
- Fig. 16 only four holes are arranged around the central hole, but the diameter of the holes is slightly thicker. Even when using a perforated plate as a filter membrane, the total open area should be a maximum of twice as large as the inner surface of the inner diameter of the nozzle, from which the aerosol emerges.
- Fig. 17 shows two tables of results of one
- Pulmonary function tests in which a subject has taken by inhaler the same amount of the active substance salbutamol, a bronchospasmolytic.
- Table 1 shows the subjects' values using a conventional inhaler comprising only a nozzle but not a membrane.
- Table 2 shows the values of the subject, with a
- Inventive inhaler was used with a membrane which was used as a nonwoven with an average pore size of 15 ym is formed.
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- Anesthesiology (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Veterinary Medicine (AREA)
- Mechanical Engineering (AREA)
- Fluid Mechanics (AREA)
- Physics & Mathematics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Medicinal Preparation (AREA)
Abstract
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102011117612 | 2011-11-04 | ||
| DE102012001526 | 2012-01-27 | ||
| DE102012003930 | 2012-03-01 | ||
| DE102012108090 | 2012-08-31 | ||
| PCT/EP2012/071847 WO2013064690A1 (fr) | 2011-11-04 | 2012-11-05 | Inhalateur et procédé de production d'un aérosol |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP2773409A1 true EP2773409A1 (fr) | 2014-09-10 |
Family
ID=47297121
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP12797738.7A Withdrawn EP2773409A1 (fr) | 2011-11-04 | 2012-11-05 | Inhalateur et procédé de production d'un aérosol |
Country Status (2)
| Country | Link |
|---|---|
| EP (1) | EP2773409A1 (fr) |
| WO (1) | WO2013064690A1 (fr) |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US10034988B2 (en) | 2012-11-28 | 2018-07-31 | Fontem Holdings I B.V. | Methods and devices for compound delivery |
| WO2015042412A1 (fr) | 2013-09-20 | 2015-03-26 | E-Nicotine Technology. Inc. | Dispositifs et procédés de modification de dispositifs de distribution |
| WO2015091346A2 (fr) * | 2013-12-16 | 2015-06-25 | Chv Pharma Gmbh & Co. Kg | Produit succédané de tabac |
| EP3095522A1 (fr) * | 2015-05-20 | 2016-11-23 | Aptar Radolfzell GmbH | Dispositif d'inhalation, kit pour un dispositif d'inhalation et porte-filière associé |
| GB201514620D0 (en) | 2015-08-17 | 2015-09-30 | Landa Labs 2012 Ltd | Air knife |
| DE102015117811A1 (de) * | 2015-10-20 | 2017-04-20 | Chv Pharma Gmbh & Co. Kg | Inhalator sowie wirkstoffhaltige Zubereitung für einen Inhalator |
| EP3275558B1 (fr) * | 2016-07-27 | 2019-03-20 | Aptar Radolfzell GmbH | Ensemble de pulverisation et distributeur comprenant un tel ensemble de pulverisation et tete distributrice pour un tel distributeur |
| CN107350617B (zh) * | 2017-08-14 | 2023-10-20 | 上海华瑞气雾剂有限公司 | 一种用于吸入器的钢丝网焊接工艺及其装置 |
| EP3717134B1 (fr) * | 2017-12-01 | 2023-08-02 | Aptar France SAS | Tête de distribution de produit fluide |
| DE102019109079B4 (de) * | 2018-07-03 | 2020-06-04 | MO GmbH & Co. KG | Aerosol-Dispersionseinrichtung |
| DE102019109080A1 (de) * | 2018-07-03 | 2020-01-09 | MO GmbH & Co. KG | Aerosol-Dispersionseinrichtung |
| PH12022553135A1 (en) | 2020-05-19 | 2024-03-04 | Cybin Irl Ltd | Deuterated tryptamine derivatives and methods of use |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4706663A (en) * | 1986-04-25 | 1987-11-17 | Makiej Paul A | Particle catcher for inhalation devices |
| SG45171A1 (en) * | 1990-03-21 | 1998-01-16 | Boehringer Ingelheim Int | Atomising devices and methods |
| US6196218B1 (en) * | 1999-02-24 | 2001-03-06 | Ponwell Enterprises Ltd | Piezo inhaler |
| US6626171B2 (en) * | 2000-05-12 | 2003-09-30 | Iep Pharmaceutical Devices Inc. | Powder/liquid metering valve |
| ES2321468B1 (es) * | 2007-08-28 | 2010-07-07 | Jorge Fernandez Pernia | Vaporizador de esencias portatil. |
| US8495998B2 (en) * | 2009-06-17 | 2013-07-30 | British American Tobacco (Investments) Limited | Inhaler |
| GB201001760D0 (en) * | 2010-02-03 | 2010-03-24 | Bacon Raymond J | Dipenser |
-
2012
- 2012-11-05 EP EP12797738.7A patent/EP2773409A1/fr not_active Withdrawn
- 2012-11-05 WO PCT/EP2012/071847 patent/WO2013064690A1/fr not_active Ceased
Non-Patent Citations (2)
| Title |
|---|
| None * |
| See also references of WO2013064690A1 * |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2013064690A1 (fr) | 2013-05-10 |
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