US3155574A - Aerosol composition - Google Patents
Aerosol composition Download PDFInfo
- Publication number
- US3155574A US3155574A US197284A US19728462A US3155574A US 3155574 A US3155574 A US 3155574A US 197284 A US197284 A US 197284A US 19728462 A US19728462 A US 19728462A US 3155574 A US3155574 A US 3155574A
- Authority
- US
- United States
- Prior art keywords
- nitroglycerin
- propellant
- composition
- aerosol
- glycol
- 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.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims description 52
- 239000000443 aerosol Substances 0.000 title claims description 22
- SNIOPGDIGTZGOP-UHFFFAOYSA-N Nitroglycerin Chemical compound [O-][N+](=O)OCC(O[N+]([O-])=O)CO[N+]([O-])=O SNIOPGDIGTZGOP-UHFFFAOYSA-N 0.000 claims description 51
- 229960003711 glyceryl trinitrate Drugs 0.000 claims description 51
- 239000000006 Nitroglycerin Substances 0.000 claims description 50
- 239000003380 propellant Substances 0.000 claims description 30
- 239000007788 liquid Substances 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 26
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 16
- 239000003975 dentin desensitizing agent Substances 0.000 description 13
- 231100000252 nontoxic Toxicity 0.000 description 13
- 230000003000 nontoxic effect Effects 0.000 description 13
- 238000000034 method Methods 0.000 description 12
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 10
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 10
- 239000003814 drug Substances 0.000 description 9
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 9
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 9
- 235000019441 ethanol Nutrition 0.000 description 8
- 206010002383 Angina Pectoris Diseases 0.000 description 7
- 229940079593 drug Drugs 0.000 description 6
- 238000002664 inhalation therapy Methods 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- 229940090898 Desensitizer Drugs 0.000 description 5
- 125000004432 carbon atom Chemical group C* 0.000 description 5
- 125000002252 acyl group Chemical group 0.000 description 4
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 4
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 4
- -1 ketoalkyl Chemical group 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 125000002947 alkylene group Chemical group 0.000 description 2
- 210000002565 arteriole Anatomy 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 2
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 2
- 229960003750 ethyl chloride Drugs 0.000 description 2
- 125000003827 glycol group Chemical group 0.000 description 2
- 239000001257 hydrogen Chemical class 0.000 description 2
- 229910052739 hydrogen Chemical class 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000001282 iso-butane Substances 0.000 description 2
- 229920001223 polyethylene glycol Polymers 0.000 description 2
- 229920001451 polypropylene glycol Polymers 0.000 description 2
- 230000001235 sensitizing effect Effects 0.000 description 2
- 230000003381 solubilizing effect Effects 0.000 description 2
- QIVUCLWGARAQIO-OLIXTKCUSA-N (3s)-n-[(3s,5s,6r)-6-methyl-2-oxo-1-(2,2,2-trifluoroethyl)-5-(2,3,6-trifluorophenyl)piperidin-3-yl]-2-oxospiro[1h-pyrrolo[2,3-b]pyridine-3,6'-5,7-dihydrocyclopenta[b]pyridine]-3'-carboxamide Chemical compound C1([C@H]2[C@H](N(C(=O)[C@@H](NC(=O)C=3C=C4C[C@]5(CC4=NC=3)C3=CC=CN=C3NC5=O)C2)CC(F)(F)F)C)=C(F)C=CC(F)=C1F QIVUCLWGARAQIO-OLIXTKCUSA-N 0.000 description 1
- UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 1
- NPNPZTNLOVBDOC-UHFFFAOYSA-N 1,1-difluoroethane Chemical compound CC(F)F NPNPZTNLOVBDOC-UHFFFAOYSA-N 0.000 description 1
- RRQYJINTUHWNHW-UHFFFAOYSA-N 1-ethoxy-2-(2-ethoxyethoxy)ethane Chemical compound CCOCCOCCOCC RRQYJINTUHWNHW-UHFFFAOYSA-N 0.000 description 1
- RHOWRFZABIDWNW-UHFFFAOYSA-N 1-methoxy-2,2,4-trimethylpentane Chemical compound COCC(C)(C)CC(C)C RHOWRFZABIDWNW-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- FPZWZCWUIYYYBU-UHFFFAOYSA-N 2-(2-ethoxyethoxy)ethyl acetate Chemical compound CCOCCOCCOC(C)=O FPZWZCWUIYYYBU-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- BJINVQNEBGOMCR-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethyl acetate Chemical compound COCCOCCOC(C)=O BJINVQNEBGOMCR-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- KNDAEDDIIQYRHY-UHFFFAOYSA-N 2-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-3-(piperazin-1-ylmethyl)pyrazol-1-yl]-1-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C=1C(=NN(C=1)CC(=O)N1CC2=C(CC1)NN=N2)CN1CCNCC1 KNDAEDDIIQYRHY-UHFFFAOYSA-N 0.000 description 1
- AWFYPPSBLUWMFQ-UHFFFAOYSA-N 2-[5-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]-1,3,4-oxadiazol-2-yl]-1-(1,4,6,7-tetrahydropyrazolo[4,3-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)C1=NN=C(O1)CC(=O)N1CC2=C(CC1)NN=C2 AWFYPPSBLUWMFQ-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- HXDLWJWIAHWIKI-UHFFFAOYSA-N 2-hydroxyethyl acetate Chemical compound CC(=O)OCCO HXDLWJWIAHWIKI-UHFFFAOYSA-N 0.000 description 1
- HFGHRUCCKVYFKL-UHFFFAOYSA-N 4-ethoxy-2-piperazin-1-yl-7-pyridin-4-yl-5h-pyrimido[5,4-b]indole Chemical compound C1=C2NC=3C(OCC)=NC(N4CCNCC4)=NC=3C2=CC=C1C1=CC=NC=C1 HFGHRUCCKVYFKL-UHFFFAOYSA-N 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- 208000002193 Pain Diseases 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000004004 anti-anginal agent Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 210000004351 coronary vessel Anatomy 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- UMNKXPULIDJLSU-UHFFFAOYSA-N dichlorofluoromethane Chemical compound FC(Cl)Cl UMNKXPULIDJLSU-UHFFFAOYSA-N 0.000 description 1
- 229940099364 dichlorofluoromethane Drugs 0.000 description 1
- UBPGILLNMDGSDS-UHFFFAOYSA-N diethylene glycol diacetate Chemical compound CC(=O)OCCOCCOC(C)=O UBPGILLNMDGSDS-UHFFFAOYSA-N 0.000 description 1
- 229940019778 diethylene glycol diethyl ether Drugs 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 239000002360 explosive Substances 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 239000003517 fume Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 210000001035 gastrointestinal tract Anatomy 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 238000001990 intravenous administration Methods 0.000 description 1
- 239000003915 liquefied petroleum gas Substances 0.000 description 1
- 210000004185 liver Anatomy 0.000 description 1
- 231100000053 low toxicity Toxicity 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- VOVZXURTCKPRDQ-CQSZACIVSA-N n-[4-[chloro(difluoro)methoxy]phenyl]-6-[(3r)-3-hydroxypyrrolidin-1-yl]-5-(1h-pyrazol-5-yl)pyridine-3-carboxamide Chemical compound C1[C@H](O)CCN1C1=NC=C(C(=O)NC=2C=CC(OC(F)(F)Cl)=CC=2)C=C1C1=CC=NN1 VOVZXURTCKPRDQ-CQSZACIVSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 231100000404 nontoxic agent Toxicity 0.000 description 1
- 230000000803 paradoxical effect Effects 0.000 description 1
- 230000002085 persistent effect Effects 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 1
- 230000002685 pulmonary effect Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- ZUHZGEOKBKGPSW-UHFFFAOYSA-N tetraglyme Chemical compound COCCOCCOCCOCCOC ZUHZGEOKBKGPSW-UHFFFAOYSA-N 0.000 description 1
- 229940124597 therapeutic agent Drugs 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 229940029284 trichlorofluoromethane Drugs 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- KMIOJWCYOHBUJS-HAKPAVFJSA-N vorolanib Chemical compound C1N(C(=O)N(C)C)CC[C@@H]1NC(=O)C1=C(C)NC(\C=C/2C3=CC(F)=CC=C3NC\2=O)=C1C KMIOJWCYOHBUJS-HAKPAVFJSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/007—Pulmonary tract; Aromatherapy
- A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
- A61K9/008—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy comprising drug dissolved or suspended in liquid propellant for inhalation via a pressurized metered dose inhaler [MDI]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
Definitions
- This invention relates to aerosol compositions, and to methods for making and using the same.
- this invention relates to aerosol compositions containing nitroglycerin, to methods of making the same, and to the use of such aerosol compositions in inhalation therapy.
- nitroglycerin in relieving the pain associated with angina pectoris has long been known in the art. Although numerous other medicaments have been prescribed for the treatment of anginal pain, nitroglycerin remains the most effective and medically safest -therapeutic agent in this field.
- nitroglycerin is relatively involatile, and not suitable to administration by direct inhalation of its fumes.
- a solid desensitizing agent e.g., a therapeutically inert substance such as mannitol
- nitroglycerin is of little value because the time required for the drug to be absorbed into the blood stream and carried to the coronary arterioles usually far exceeds the duration of the paroxysm of anginal pain which the drug is intended to relieve, and the drug is rapidly destroyed in the gastro-intestinal tract or is removed by the liver.
- Sublingual administration suffers from similar limitations.
- the speed of action of sublingual administration may be as long as 2 to 3 minutes.
- sublingual administration is erratic, since there is no control over the amount of nitroglycerin eiiectively absorbed by the mucous membranes of the mouth.
- the nitroglycerin present in the uncoated tablets of the prior art is gradually decomposed on exposure to air and the efiicacy of the tablets is reduced with time. This lack of stability of the tablets is not only undesirable from a marketing standpoint, but also contributes to the problem of erratic dosing.
- the present invention concerns methods for treating anginal pain associated with constriction of the coronary arteries with nitroglycerin by inhalation therapy, specifically by inhalation of a nitroglycerin-containing aerosol composition.
- safe, controlled, and speedy administration of nitroglycerin can be effected.
- Inhalation therapy with pulmonary absorption of nitroglycerin into the bloodstream, is comparable in speed to intravenous administration, and insures prompt delivery of the nitroglycerin to the coronary arterioles in about 30 seconds or so.
- the use of metered valves with aerosol packages of the compositions of the invention insures that a controlled dose of the drug is administred.
- the compositions retain their potency and efiicacy at original levels, making the product not only more accurate for dosing purposes, but more desirable from a marketing viewpoint.
- compositions of the present invention comprise 3,155,574 Patented Nov. 3, 1964 from about 30 to about percent by weight of a nontoxic volatile liquefied and/or liquid propellant, preferably from about 65 to about 95 percent, in admixture with about 5 to about 50 percent, preferably about 5 to about 25 percent, by Weight of a non-toxic substance solubilizing a desensitized nitroglycerin component in the propellant, the balance being a stabilized nitroglycerin component in which component about 1 to about 10 percent by weight, preferably about 5 to 10 percent, is the therapeutically active nitroglycerin and the balance is a nontoxic non-volatile liquid desensitizing agent for the nitroglycerin.
- Suitable non-toxic volatile liquid or liquefied propellants are Well known in the aerosol art. These materials are generally fluorinated, chlorinated, or fiuorochlorinated saturated lower aliphatic hydrocarbons, or liquefied petroleurn gases. Suitably halogenated lower alkanes containing 1 to 4 carbon atoms, preferably 1 or 2 carbon atoms, and at least 1 fluorine atom, are often generically referred to as fiuorohydrocarbon propellants, and are commercially available under the trade names Freons, Genetrons, Ucons, etc. These materials include such particularly useful propellants as dichlorodifluoromethane (Freon 12), dichlorotetrafiuoroethane (Freon 114),
- propellants are ethyl chloride, 1,1,l-trichloroethane, butane, isobutane, propane, etc.
- propellants are such as produce a desirable vapor pressure for the composition between about 15 and about 60 pounds per square inch at room temperatures (20-25 0.), preferably between about 35 and about 40 pounds per square inch at these temperatures.
- a combination of propellants particularly suitable for use in the present invention comprises a mixture of about 60 parts by Weight of Freon 12 with 40 parts by weight of Freon 11.
- individual Freons or mixtures of Freons can be employed in the invention in various amounts with the other ingredients mentioned before so that the resulting mixtures show a pressure within the limits recited.
- ethyl alcohol As the non-toxic agent solubilizing the stabilized nitroglycerin component, in the propellants just mentioned, ethyl alcohol has proved to be particularly suitable. This substance promotes the formation of uniform, homogeneous mixtures of the nitroglycerin-containing component with the propellants, and is unobjectionable from a clinical standpoint.
- the alcohol is suitably employed in amounts sufiicient to prevent separation of the nitroglycerin from the propellant but insufficient to reduce the volatility of the final composition below the pressure limits mentioned earlier as desirable in areosol packages.
- the nitroglycerin-containing component which is a mixture of nitroglycerin with one or more non-toxic nonvolatile liquid desensitizing agents, is compounded to contain from 5 to 10 percent by weight of nitroglycerin. If the amount of nitroglycerin is much in excess of the latter figure, the sensitivity of the composition may increase to a point at which the highly safe properties of the present compositions are lost. On the other hand, decreasing the amount of nitroglycerin in the composition merely increases the amount of therapeutically inactive desensitizing agent administered.
- the desensitizing agents are preferably those non-toxic non-volatile liquid compounds having at least 3 carbon atoms and characterized by the structural formula XO(RO),,Y, in which R is alkylene, ketoalkylene or hydroxyalkylene having from 2 to 6 carbon atoms, X and Y may be different and are alkyl, ketoalkyl, hydroxyalkyl,
- acyl, oxy-substituted acyl, and hydrogen and n is an integer from 1 to 10.
- desensitizing substances of this class are the following: propanediol-1,2; diethylene glycol; polypropylene glycol (M.W. 400); diethylene glycol diacetate; polyethylene glycol (M.W. 200); diethyleneglycol butyl ether; glycol monoethyl ether; diethyleneglycol diethyl ether; diacetone alcohol; triethylene glycol; polyethylene glycol (M.W.
- hydroxyethyl acetate diethyleneglycol ethyl ether; dimethoxytetraglycol; trimethylene glycol; glycol diethyl ether; ethoxyethyl acetoxyethyl ether; diethyleneglycol methyl ether; methoxyethyl acetoxyethyl ether; glycol monomethyl ether; bis- (methoxyethyl) formal; bis(methoxyethyl) acetal; 2- methoxymethyl-2,4-dimethylpentane diol-1,5; butanedioi- 1,3; Z-methyl-pentanediol-2,4, and the like.
- propanediol-1,2 has proved particularly suitable for use in the compositions of the invention, not only because of its excellent desensitizing properties, but also because of its extremely low toxicity.
- the glycol is compatible with the propellants commonly used in aerosol compositions, and blends well with the remaining components of the aerosol compositions of the invention with the formation of a homogeneous solution.
- sensitizing agents described above particularly other glycols
- other of the sensitizing agents described above can be used in compounding the compositions of the invention.
- sensitizing agent dispensed in practicing the inhalation therapy of nitroglycerin according to certain methods of the present invention toxicity problems are minimized, and many materials otherwise considered unsuitable for inhalation can be employed.
- a dose of nitroglycerin of between about 0.05 to about 1.0 milligram, preferably 0.1 to 0.4 milligram, as contemplated by the present invention, as little as about 0.45 milligram of the desensitizing agent is inhaled.
- nonvolatile is defined as having vapor pressure characteristics such that evaporation of a mixture of nitroglycerin and the desensitizer in the proportions contemplated herein will not leave a nitroglycerin residue, e.g., the desensitizer has vapor pressure characteristics similar to those of nitroglycerin.
- compositions of the invention are conveniently prepared by dissolving a pharmaceutical grade of nitroglycerin in a suitable liquid desensitizer. This combination is then mixed with a solubilizing agent such as absolute ethyl alcohol. This mixture may then be combined with the propellants and put into containers, or the mixture and propellants may be separately put into containers by conventional cold fill or pressure methods.
- a solubilizing agent such as absolute ethyl alcohol
- the amounts of propellant and active ingredients in the aerosol composition and the quantity of composition delivered by the valve are, relatively, such that a desired predetermined dose of active ingredient is delivered.
- Administration is suitably effected by directing the orifice of the aerosol unit into the mouth and simultaneously inhaling and activating the metered valve.
- Example 1 An aerosol composition suitable for inhalation therapy and having a pressure of 53 p.s.i.g. at 70 F. was prepared by combining 4 weight percent of a combination of propanediol-l,2 and nitroglycerin containing 10 weight percent of nitroglycerin with 10 parts by weight of anhydrous ethyl alcohol, 51.6 parts by weight of dichlorodifluoromethane (Propellant 12), and 34.4 parts of dichloromonofluoromethane (Propellant 11).
- Butanediol-LZ, propanediol-L3 or polypropylene glycol (MFN. about 300) can be substituted for propanediol-1,2 as desensitizers.
- Example 2 A composition having a vapor pressure of 45 p.s.i.g. was prepared from 1.43 parts by Weight of a mixture containing 10 percent nitroglycerin (N6) in propanediol- 1,2 (PG), 10 parts of anhydrous ethanol, 53.13 parts of ropellant 12, and 35.44 parts of Propellant 11.
- Example3 10% NG/PG 10.0 Anhydrous ethanol 25.0 Propellant 12 26.0 Propellant 11 39.0
- Example4 5% NG/PG 10.0 Anhydrous ethanol 25.0 Propellant l2 39.0 Propellant 11 26.0
- Example6 10% NG/PG 10.0 Anhydrous ethanol 35.0 Propellant 12 20.0 Ethyl chloride 35.0
- Example7 10% NG/PG 10.0 Anhydrous ethanol 40.0 Propellant 11 30.0 Isobutane 20.0
- Example8 10% NG/PG 10.0 Anhydrous ethanol 50.0 Propellant 12 30.0 1,1,1-trichloroethane 10.0
- Example9 10% NG/PG 10.0 Anhydrous ethanol 25.0 Propellant l2 8.0 Propellant 11 32.0 Dichlorotctrafluoroethane (Propellant 114) 25.0
- Example 11 10% NG/PG 10.0 Anhydrous ethanol 25.0 1,1-difluoroethane 65.0
- Example 12 10% NG/PG 10.0 Anhydrous ethanol 25.0 l-chloro-l,l-difluoroethane 65.0
- An aerosol composition comprising a liquefied propellant, nitroglycerin and a non-volatile liquid desensitizing agent therefor, and an agent solubiiizing said nitroglycerin in said propellant.
- An aerosol composition comprising a liquefied propellant, ethyl alcohol, nitroglycerin and a non-volatile liquid desensitizing agent therefor of the formula in which R is selected from the group consisting of alkylene, ketoalkylene, and hydroxyalkylene having 2-6 carbon atoms, X and Y are individually selected from the group consisting of alkyl, ketoalkyl, hydroxyalkyl, acyl, oxy-substitutcd acyl, and hydrogen, and n is an integer from 1 to 10.
- composition as in claim 2 wherein said desensitizing agent is a glycol.
- a desensitized nitroglycerin-containing areosol composition comprising about 30-95 percent by weight of a volatile non-toxic liquefied propellant, about 5-50 percent by weight of ethyl alcohol, the balance being a mixture containing about 1-10 percent by weight of nitroglycerin with a non-toxic non-volatile liquid glycol.
- composition as in claim 4 wherein said glycol is propanediol-LZ.
- the method of treating anginal pain by inhalation therapy which comprises inhaling between about 0.05-1.0 milligram of nitroglycerin in an aerosol composition containing the same, said composition comprising a volatile non-toxic liquefied propellant, ethyl alcohol, and nitroglycerin, and a non-toxic non-volatile liquid desensitizing agent therefor.
- non-toxic liquefied propellant is selected from the group consisting of fluorinated and fluorochlorinated saturated lower aliphatic hydrocarbons and said desensitizing agent is a glycol.
- the method of treating anginal pain which comprises inhaling between 0.05-1.0 milligram of nitroglycerin in an aerosol composition containing the same, said composition comprising about 30-95 percent by weight of a volatile non-toxic liquefied propellant selected from the group consisting of liquefied petroleum gases, chlorinated, fluorinated and fluorochlorinated saturated lower aliphatic hydrocarbons, about 5-50 percent by weight of ethyl alcohol, the balance being a mixture containing about 1-10 percent by weight of nitroglycerin with a non-toxic non-volatile glycol.
- a volatile non-toxic liquefied propellant selected from the group consisting of liquefied petroleum gases, chlorinated, fluorinated and fluorochlorinated saturated lower aliphatic hydrocarbons, about 5-50 percent by weight of ethyl alcohol, the balance being a mixture containing about 1-10 percent by weight of nitroglycerin with a non-toxic non-volatile glycol.
- composition has a vapor pressure of about 15-60 pounds per square inch at room temperatures and said propellant is at least one fluorochlorinated saturated lower aliphatic hydrocarbon.
Landscapes
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Epidemiology (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Emergency Medicine (AREA)
- Otolaryngology (AREA)
- Pulmonology (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicinal Preparation (AREA)
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
BE632504D BE632504A (da) | 1962-05-24 | ||
US197284A US3155574A (en) | 1962-05-24 | 1962-05-24 | Aerosol composition |
GB18354/63A GB970027A (en) | 1962-05-24 | 1963-05-09 | Aerosol compositions |
FR934743A FR2735M (fr) | 1962-05-24 | 1963-05-14 | Composition pour aérosols, utilisable pour soulager la douleur accompagnant l'angine de poitrine. |
ES300000A ES300000A3 (es) | 1962-05-24 | 1964-05-19 | Un procedimiento para preparar una composición para aerosoles |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US197284A US3155574A (en) | 1962-05-24 | 1962-05-24 | Aerosol composition |
Publications (1)
Publication Number | Publication Date |
---|---|
US3155574A true US3155574A (en) | 1964-11-03 |
Family
ID=22728762
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US197284A Expired - Lifetime US3155574A (en) | 1962-05-24 | 1962-05-24 | Aerosol composition |
Country Status (5)
Country | Link |
---|---|
US (1) | US3155574A (da) |
BE (1) | BE632504A (da) |
ES (1) | ES300000A3 (da) |
FR (1) | FR2735M (da) |
GB (1) | GB970027A (da) |
Cited By (42)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3445564A (en) * | 1965-01-04 | 1969-05-20 | Ely A Kirschner | Rapidly drying lower aliphatic alcohol-acetone sanitizing composition and method |
US3456052A (en) * | 1965-09-28 | 1969-07-15 | Garrett Lab Inc | Aerosol composition containing butoxymonoether of a polyoxyalkylene glycol |
US4323577A (en) * | 1979-11-13 | 1982-04-06 | Nippon Kayaku Kabushiki Kaisha | Aqueous solution of nitroglycerin |
US4380505A (en) * | 1978-11-11 | 1983-04-19 | Von Treu Ag | Apparatus for producing aerosol product |
US4581225A (en) * | 1984-04-25 | 1986-04-08 | Eli Lilly And Company | Sustained release intranasal formulation and method of use thereof |
US4919919A (en) * | 1987-09-30 | 1990-04-24 | Nippon Kayaku Kabushiki Kaisha | Nitroglycerin spray |
US4976965A (en) * | 1987-04-30 | 1990-12-11 | Kali-Chemie Pharma Gmbh | Coronary affecting medicinal composition |
EP0461505A1 (de) * | 1990-06-13 | 1991-12-18 | Schwarz Pharma Ag | Nitroglycerin-Spray |
DE4026072A1 (de) * | 1990-08-17 | 1992-02-20 | Sanol Arznei Schwarz Gmbh | Nitroglycerinhaltiger, hydrophiler, waessriger pumpspray |
US5370862A (en) * | 1990-06-13 | 1994-12-06 | Schwarz Pharma Ag | Pharmaceutical hydrophilic spray containing nitroglycerin for treating angina |
WO1997038687A1 (en) * | 1996-04-12 | 1997-10-23 | Flemington Pharmaceutical Corporation | Buccal, non-polar spray for nitroglycerin |
US20030077229A1 (en) * | 1997-10-01 | 2003-04-24 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing cardiovascular or renal drugs |
US20030077228A1 (en) * | 1997-10-01 | 2003-04-24 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing drugs for treating endocrine disorders |
US20030077227A1 (en) * | 1997-10-01 | 2003-04-24 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing drugs for treating disorders of the central nervous system |
US20030082107A1 (en) * | 1997-10-01 | 2003-05-01 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing drugs for treating an infectious disease or cancer |
US20030095925A1 (en) * | 1997-10-01 | 2003-05-22 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing drugs for treating metabolic disorders |
US20030095926A1 (en) * | 1997-10-01 | 2003-05-22 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing drugs for treating disorders of the gastrointestinal tract or urinary tract |
US20030095927A1 (en) * | 1997-10-01 | 2003-05-22 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing drugs for treating muscular and skeletal disorders |
US20030190286A1 (en) * | 1997-10-01 | 2003-10-09 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing drugs for treating allergies or asthma |
US6676931B2 (en) | 1997-10-01 | 2004-01-13 | Novadel Pharma Inc. | Buccal, polar and non-polar spray or capsule |
US20040120896A1 (en) * | 1997-10-01 | 2004-06-24 | Novadel Pharma, Inc. | Buccal, polar and non-polar spray or capsule containing drugs for treating pain |
US20040136913A1 (en) * | 1997-10-01 | 2004-07-15 | Dugger Harry A. | Buccal, polar and non-polar spray containing sumatriptan |
US20040136914A1 (en) * | 1997-10-01 | 2004-07-15 | Dugger Harry A. | Buccal, polar and non-polar spray containing ondansetron |
US20040141923A1 (en) * | 1997-10-01 | 2004-07-22 | Dugger Harry A. | Buccal, polar and non-polar spray containing alprazolam |
US20040265239A1 (en) * | 1997-10-01 | 2004-12-30 | Novadel Pharma Inc. | Buccal, polar and non-polar spray containing zolpidem |
US20050002867A1 (en) * | 1997-10-01 | 2005-01-06 | Novadel Pharma Inc. | Buccal, polar and non-polar sprays containing propofol |
US20050163719A1 (en) * | 1997-10-01 | 2005-07-28 | Dugger Harry A.Iii | Buccal, polar and non-polar spray containing diazepam |
US20050180923A1 (en) * | 1997-10-01 | 2005-08-18 | Dugger Harry A.Iii | Buccal, polar and non-polar spray containing testosterone |
US20050281752A1 (en) * | 1997-10-01 | 2005-12-22 | Dugger Harry A Iii | Buccal, polar and non-polar spray or capsule containing drugs for treating disorders of the central nervous system |
US20050287075A1 (en) * | 1997-10-01 | 2005-12-29 | Dugger Harry A Iii | Buccal, polar and non-polar spray or capsule containing drugs for treating pain |
US20070048229A1 (en) * | 1997-10-01 | 2007-03-01 | Novadel Pharma Inc. | Buccal, polar and non-polar spray containing atropine |
WO2007088327A1 (en) * | 2006-02-03 | 2007-08-09 | Futura Medical Developments Limited | Composition for promoting vascular smooth muscle relaxation |
US20070248548A1 (en) * | 2006-04-19 | 2007-10-25 | Blondino Frank E | Stable hydroalcoholic oral spray formulations and methods |
US20080171089A1 (en) * | 2006-12-22 | 2008-07-17 | Blondino Frank E | Stable anti-nausea oral spray formulations and methods |
DE202008007318U1 (de) | 2008-03-14 | 2008-07-31 | G. Pohl-Boskamp Gmbh & Co. Kg | Langzeitstabile pharmazeutische Zubereitung mit dem Wirkstoff Glyceroltrinitrat |
US20080280947A1 (en) * | 2007-05-10 | 2008-11-13 | Blondino Frank E | Anti-insomnia compositions and methods |
WO2012016691A1 (en) | 2010-08-03 | 2012-02-09 | G. Pohl-Boskamp Gmbh & Co. Kg | Use of glyceryl trinitrate for treating traumatic edema |
EP2767163A1 (en) | 2005-02-17 | 2014-08-20 | Abbott Laboratories | Transmucosal administration of drug compositions for treating and preventing disorders in animals |
EP2878310A1 (en) | 2013-11-29 | 2015-06-03 | G. Pohl-Boskamp GmbH & Co. KG | Sprayable aqueous composition comprising glyceryl trinitrate |
US9101592B2 (en) | 2011-02-25 | 2015-08-11 | G. Pohl-Boskamp Gmbh & Co. Kg | Stabilized granules containing glyceryl trinitrate |
US9248099B2 (en) | 2012-05-31 | 2016-02-02 | Desmoid Aktiengesellschaft | Use of stabilized granules containing glyceryl trinitrate for arteriogenesis |
US11166931B2 (en) | 2012-05-31 | 2021-11-09 | G. Pohl-Boskamp Gmbh & Co. Kg | Induction of arteriogenesis with an NO (nitric oxide) donor |
Families Citing this family (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3326089A1 (de) * | 1983-07-20 | 1985-02-07 | Gödecke AG, 1000 Berlin | Zur inhalation bestimmte darreichungsform von calcium-antagonisten |
EP0175671A1 (de) * | 1984-08-23 | 1986-03-26 | Kuhlemann & Co. | Pharmazeutische Zubereitung sowie Verfahren zum Darreichen dieser pharmazeutischen Zubereitung |
HU199678B (en) * | 1988-07-08 | 1990-03-28 | Egyt Gyogyszervegyeszeti Gyar | Process for producing aerosols containing nitroglicerol |
GB9118830D0 (en) * | 1991-09-03 | 1991-10-16 | Minnesota Mining & Mfg | Medical aerosol formulations |
ES2183001T3 (es) | 1995-06-27 | 2003-03-16 | Boehringer Ingelheim Pharma | Nuevo preparado medicamentoso estable para la produccion de aerosoles exentos de gas propulsor. |
US6413496B1 (en) | 1996-12-04 | 2002-07-02 | Biogland Ireland (R&D) Limited | Pharmaceutical compositions and devices for their administration |
US6197280B1 (en) | 1997-09-09 | 2001-03-06 | Bioglan Laboratories Limited | Pharmaceutical compositions and devices for their administration |
GB2592376A (en) * | 2020-02-25 | 2021-09-01 | Aer Beatha Ltd | Canister |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2648698A (en) * | 1949-07-29 | 1953-08-11 | Hercules Powder Co Ltd | Desensitized liquid explosives |
US2868691A (en) * | 1956-03-21 | 1959-01-13 | Riker Laboratories Inc | Self-propelling compositions for inhalation therapy containing a salt of isoproterenol or epinephrine |
US3014844A (en) * | 1957-01-31 | 1961-12-26 | Riker Laboratories Inc | Self-propelling powder dispensing compositions |
-
0
- BE BE632504D patent/BE632504A/xx unknown
-
1962
- 1962-05-24 US US197284A patent/US3155574A/en not_active Expired - Lifetime
-
1963
- 1963-05-09 GB GB18354/63A patent/GB970027A/en not_active Expired
- 1963-05-14 FR FR934743A patent/FR2735M/fr not_active Expired
-
1964
- 1964-05-19 ES ES300000A patent/ES300000A3/es not_active Expired
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2648698A (en) * | 1949-07-29 | 1953-08-11 | Hercules Powder Co Ltd | Desensitized liquid explosives |
US2868691A (en) * | 1956-03-21 | 1959-01-13 | Riker Laboratories Inc | Self-propelling compositions for inhalation therapy containing a salt of isoproterenol or epinephrine |
US3014844A (en) * | 1957-01-31 | 1961-12-26 | Riker Laboratories Inc | Self-propelling powder dispensing compositions |
Cited By (87)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3445564A (en) * | 1965-01-04 | 1969-05-20 | Ely A Kirschner | Rapidly drying lower aliphatic alcohol-acetone sanitizing composition and method |
US3456052A (en) * | 1965-09-28 | 1969-07-15 | Garrett Lab Inc | Aerosol composition containing butoxymonoether of a polyoxyalkylene glycol |
US4380505A (en) * | 1978-11-11 | 1983-04-19 | Von Treu Ag | Apparatus for producing aerosol product |
US4323577A (en) * | 1979-11-13 | 1982-04-06 | Nippon Kayaku Kabushiki Kaisha | Aqueous solution of nitroglycerin |
US4581225A (en) * | 1984-04-25 | 1986-04-08 | Eli Lilly And Company | Sustained release intranasal formulation and method of use thereof |
US4976965A (en) * | 1987-04-30 | 1990-12-11 | Kali-Chemie Pharma Gmbh | Coronary affecting medicinal composition |
US4919919A (en) * | 1987-09-30 | 1990-04-24 | Nippon Kayaku Kabushiki Kaisha | Nitroglycerin spray |
EP0461505A1 (de) * | 1990-06-13 | 1991-12-18 | Schwarz Pharma Ag | Nitroglycerin-Spray |
DE4018919A1 (de) * | 1990-06-13 | 1991-12-19 | Sanol Arznei Schwarz Gmbh | Nitroglycerin-spray |
US5370862A (en) * | 1990-06-13 | 1994-12-06 | Schwarz Pharma Ag | Pharmaceutical hydrophilic spray containing nitroglycerin for treating angina |
DE4026072A1 (de) * | 1990-08-17 | 1992-02-20 | Sanol Arznei Schwarz Gmbh | Nitroglycerinhaltiger, hydrophiler, waessriger pumpspray |
US5744124A (en) * | 1990-08-17 | 1998-04-28 | Schwarz Pharma Ag | Nitroglycerin-containing hydrophilic aqueous pumpable spray composition |
WO1997038687A1 (en) * | 1996-04-12 | 1997-10-23 | Flemington Pharmaceutical Corporation | Buccal, non-polar spray for nitroglycerin |
US20050287075A1 (en) * | 1997-10-01 | 2005-12-29 | Dugger Harry A Iii | Buccal, polar and non-polar spray or capsule containing drugs for treating pain |
US20060216240A1 (en) * | 1997-10-01 | 2006-09-28 | Novadel Pharma Inc. | Buccal, polar and non-polar spray containing zolpidem |
US20030077227A1 (en) * | 1997-10-01 | 2003-04-24 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing drugs for treating disorders of the central nervous system |
US20030082107A1 (en) * | 1997-10-01 | 2003-05-01 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing drugs for treating an infectious disease or cancer |
US20030095925A1 (en) * | 1997-10-01 | 2003-05-22 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing drugs for treating metabolic disorders |
US20030095926A1 (en) * | 1997-10-01 | 2003-05-22 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing drugs for treating disorders of the gastrointestinal tract or urinary tract |
US20030095927A1 (en) * | 1997-10-01 | 2003-05-22 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing drugs for treating muscular and skeletal disorders |
US20030190286A1 (en) * | 1997-10-01 | 2003-10-09 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing drugs for treating allergies or asthma |
US6676931B2 (en) | 1997-10-01 | 2004-01-13 | Novadel Pharma Inc. | Buccal, polar and non-polar spray or capsule |
US20040062716A1 (en) * | 1997-10-01 | 2004-04-01 | Novadel Pharma Inc. | Buccal, polar and non-polar spray of capsule |
US20040120896A1 (en) * | 1997-10-01 | 2004-06-24 | Novadel Pharma, Inc. | Buccal, polar and non-polar spray or capsule containing drugs for treating pain |
US20040136913A1 (en) * | 1997-10-01 | 2004-07-15 | Dugger Harry A. | Buccal, polar and non-polar spray containing sumatriptan |
US20040136914A1 (en) * | 1997-10-01 | 2004-07-15 | Dugger Harry A. | Buccal, polar and non-polar spray containing ondansetron |
US20040141923A1 (en) * | 1997-10-01 | 2004-07-22 | Dugger Harry A. | Buccal, polar and non-polar spray containing alprazolam |
US20040265239A1 (en) * | 1997-10-01 | 2004-12-30 | Novadel Pharma Inc. | Buccal, polar and non-polar spray containing zolpidem |
US20050002867A1 (en) * | 1997-10-01 | 2005-01-06 | Novadel Pharma Inc. | Buccal, polar and non-polar sprays containing propofol |
US20050025712A1 (en) * | 1997-10-01 | 2005-02-03 | Novadel Pharma, Inc. | Buccal, polar and non-polar spray or capsule containing drugs for treating allergies or asthma |
US20050025715A1 (en) * | 1997-10-01 | 2005-02-03 | Novadel Pharma, Inc. | Buccal, polar and non-polar spray or capsule containing drugs for treating endocrine disorders |
US20050025716A1 (en) * | 1997-10-01 | 2005-02-03 | Novadel Pharma, Inc. | Buccal, polar and non-polar spray or capsule containing drugs for treating disorders of the gastrointestinal tract or urinary tract |
US20050025714A1 (en) * | 1997-10-01 | 2005-02-03 | Novadel Pharma, Inc. | Buccal, polar and non-polar spray or capsule containing drugs for treating metabolic disorders |
US20050025713A1 (en) * | 1997-10-01 | 2005-02-03 | Novadel Pharma, Inc. | Buccal, polar and non-polar spray or capsule containing cardiovascular or renal drugs |
US20050025717A1 (en) * | 1997-10-01 | 2005-02-03 | Novadel Pharma, Inc. | Buccal, polar and non-polar spray or capsule containing drugs for treating muscular and skeletal disorders |
US20050142069A1 (en) * | 1997-10-01 | 2005-06-30 | Novadel Pharma, Inc. | Buccal, polar and non-polar spray or capsule containing drugs for treating an infectious disease or cancer |
US20050163719A1 (en) * | 1997-10-01 | 2005-07-28 | Dugger Harry A.Iii | Buccal, polar and non-polar spray containing diazepam |
US20050180923A1 (en) * | 1997-10-01 | 2005-08-18 | Dugger Harry A.Iii | Buccal, polar and non-polar spray containing testosterone |
US6969508B2 (en) | 1997-10-01 | 2005-11-29 | Novadel Pharma, Inc. | Buccal, polar and non-polar spray or capsule containing drugs for treating pain |
US6977070B2 (en) | 1997-10-01 | 2005-12-20 | Novadel Pharma, Inc. | Buccal, polar and non-polar spray or capsule containing drugs for treating disorders of the central nervous system |
US20050281752A1 (en) * | 1997-10-01 | 2005-12-22 | Dugger Harry A Iii | Buccal, polar and non-polar spray or capsule containing drugs for treating disorders of the central nervous system |
US20050281753A1 (en) * | 1997-10-01 | 2005-12-22 | Dugger Harry A Iii | Buccal, polar and non-polar spray or capsule |
US20030077229A1 (en) * | 1997-10-01 | 2003-04-24 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing cardiovascular or renal drugs |
US6998110B2 (en) | 1997-10-01 | 2006-02-14 | Novadel Pharma, Inc. | Buccal, polar and non-polar spray or capsule |
US20060159624A1 (en) * | 1997-10-01 | 2006-07-20 | Dugger Harry A Iii | Buccal, polar and non-polar spray containing zolpidem |
US20060165604A1 (en) * | 1997-10-01 | 2006-07-27 | Dugger Harry A Iii | Buccal, polar and non-polar spray containing sumatriptan |
US20060171896A1 (en) * | 1997-10-01 | 2006-08-03 | Dugger Harry A Iii | Buccal, polar and non-polar spray containing alprazolam |
US20060198790A1 (en) * | 1997-10-01 | 2006-09-07 | Dugger Harry A Iii | Buccal, polar and non-polar spray containing ondansetron |
US20060210484A1 (en) * | 1997-10-01 | 2006-09-21 | Novadel Pharma Inc. | Buccal, polar and non-polar spray containing testosterone |
US20060216241A1 (en) * | 1997-10-01 | 2006-09-28 | Novadel Pharma Inc. | Buccal, polar and non-polar spray containing diazepam |
US20030077228A1 (en) * | 1997-10-01 | 2003-04-24 | Dugger Harry A. | Buccal, polar and non-polar spray or capsule containing drugs for treating endocrine disorders |
US20060222597A1 (en) * | 1997-10-01 | 2006-10-05 | Novadel Pharma Inc. | Buccal, polar and non-polar sprays containing propofol |
US20070048229A1 (en) * | 1997-10-01 | 2007-03-01 | Novadel Pharma Inc. | Buccal, polar and non-polar spray containing atropine |
EP1952802A2 (en) | 1997-10-01 | 2008-08-06 | Novadel Pharma Inc. | Buccal, polar and non-polar spray or capsule |
US9078816B2 (en) | 1997-10-01 | 2015-07-14 | Suda Ltd. | Buccal, polar and non-polar spray containing ondansetron |
US8236285B2 (en) | 1997-10-01 | 2012-08-07 | Novadel Pharma Inc. | Buccal, polar and non-polar spray containing zolpidem |
US20100092403A1 (en) * | 1997-10-01 | 2010-04-15 | Dugger Iii Harry A | Buccal, polar and non-polar spray containing zolpidem |
US20090118170A1 (en) * | 1997-10-01 | 2009-05-07 | Dugger Iii Harry A | Buccal, polar and non-polar spray or capsule |
EP2042161A1 (en) | 1997-10-01 | 2009-04-01 | Novadel Pharma Inc. | Propellant-free spray composition comprising anti-emetic agent |
EP2452675A1 (en) | 2002-08-29 | 2012-05-16 | Novadel Pharma Inc. | Buccal spray containing sildenafil |
EP2277506A1 (en) | 2002-08-29 | 2011-01-26 | Novadel Pharma Inc. | Non-polar buccal spray of a sedative |
EP2283813A1 (en) | 2002-08-29 | 2011-02-16 | Novadel Pharma Inc. | Propellant-free polar buccal spray of a sedative |
EP2283814A1 (en) | 2002-08-29 | 2011-02-16 | Novadel Pharma Inc. | Polar buccal spray of a sedative |
EP2283815A1 (en) | 2002-08-29 | 2011-02-16 | Novadel Pharma Inc. | Propellant-free non polar buccal spray of a sedative |
EP2767163A1 (en) | 2005-02-17 | 2014-08-20 | Abbott Laboratories | Transmucosal administration of drug compositions for treating and preventing disorders in animals |
WO2007088327A1 (en) * | 2006-02-03 | 2007-08-09 | Futura Medical Developments Limited | Composition for promoting vascular smooth muscle relaxation |
US9265721B2 (en) | 2006-02-03 | 2016-02-23 | Futura Medical Developments Limited | Composition for promoting vascular smooth muscle relaxation |
US20070248548A1 (en) * | 2006-04-19 | 2007-10-25 | Blondino Frank E | Stable hydroalcoholic oral spray formulations and methods |
US20080171089A1 (en) * | 2006-12-22 | 2008-07-17 | Blondino Frank E | Stable anti-nausea oral spray formulations and methods |
US20110040266A1 (en) * | 2007-05-10 | 2011-02-17 | Blondino Frank E | Anti-insomnia compositions and methods |
US20080280947A1 (en) * | 2007-05-10 | 2008-11-13 | Blondino Frank E | Anti-insomnia compositions and methods |
DE202008007318U1 (de) | 2008-03-14 | 2008-07-31 | G. Pohl-Boskamp Gmbh & Co. Kg | Langzeitstabile pharmazeutische Zubereitung mit dem Wirkstoff Glyceroltrinitrat |
AU2011287948B2 (en) * | 2010-08-03 | 2014-11-06 | G. Pohl-Boskamp Gmbh & Co. Kg | Use of glyceryl trinitrate for treating traumatic edema |
WO2012016691A1 (en) | 2010-08-03 | 2012-02-09 | G. Pohl-Boskamp Gmbh & Co. Kg | Use of glyceryl trinitrate for treating traumatic edema |
US9693983B2 (en) | 2010-08-03 | 2017-07-04 | G. Pohl-Boskamp Gmbh & Co. Kg | Use of glyceryl trinitrate for treating traumatic edema |
WO2012016690A1 (en) | 2010-08-03 | 2012-02-09 | G. Pohl-Boskamp Gmbh & Co. Kg | Use of glyceryl trinitrate for treating hematomas |
US20130129638A1 (en) * | 2010-08-03 | 2013-05-23 | G. Pohl-Boskamp Gmbh & Co. Kg | Use of Glyceryl Trinitrate for Treating Traumatic Edema |
US9180109B2 (en) * | 2010-08-03 | 2015-11-10 | G. Pohl-Boskamp Gmbh & Co. Kg | Use of glyceryl trinitrate for treating traumatic edema |
EP2990032A1 (en) | 2010-08-03 | 2016-03-02 | G. Pohl-Boskamp GmbH & Co. KG | Use of glyceryl trinitrate for treating traumatic edema |
US9101592B2 (en) | 2011-02-25 | 2015-08-11 | G. Pohl-Boskamp Gmbh & Co. Kg | Stabilized granules containing glyceryl trinitrate |
US9616023B2 (en) | 2011-02-25 | 2017-04-11 | G. Pohl-Boskamp Gmbh & Co. Kg | Stabilized granules containing glyceryl trinitrate |
US9248099B2 (en) | 2012-05-31 | 2016-02-02 | Desmoid Aktiengesellschaft | Use of stabilized granules containing glyceryl trinitrate for arteriogenesis |
US9675552B2 (en) | 2012-05-31 | 2017-06-13 | Desmoid Aktiengesellschaft | Use of stabilized granules containing glyceryl trinitrate for arteriogenesis |
US11166931B2 (en) | 2012-05-31 | 2021-11-09 | G. Pohl-Boskamp Gmbh & Co. Kg | Induction of arteriogenesis with an NO (nitric oxide) donor |
EP2878310A1 (en) | 2013-11-29 | 2015-06-03 | G. Pohl-Boskamp GmbH & Co. KG | Sprayable aqueous composition comprising glyceryl trinitrate |
US10034850B2 (en) | 2013-11-29 | 2018-07-31 | G. Pohl-Boskamp Gmbh & Co. Kg | Sprayable aqueous composition comprising glyceryl trinitrate |
US10987332B2 (en) | 2013-11-29 | 2021-04-27 | G. Pohl-Boskamp Gmbh & Co. Kg | Sprayable aqueous composition comprising glyceryl trinitrate |
Also Published As
Publication number | Publication date |
---|---|
BE632504A (da) | |
GB970027A (en) | 1964-09-16 |
FR2735M (fr) | 1964-08-17 |
ES300000A3 (es) | 1964-11-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US3155574A (en) | Aerosol composition | |
US2868691A (en) | Self-propelling compositions for inhalation therapy containing a salt of isoproterenol or epinephrine | |
CA2411047C (en) | Stable pharmaceutical solution formulations for pressurised metered dose inhalers | |
ES2077971T5 (es) | Formulaciones medicinales en aerosol que comprenden salbutamol. | |
KR100312357B1 (ko) | 안정화된약제의에어로졸용액제제 | |
US3014844A (en) | Self-propelling powder dispensing compositions | |
RU2129424C1 (ru) | Аэрозольная фармацевтическая композиция, способ лечения респираторных заболеваний | |
ES2391563T3 (es) | Formulaciones en suspensión de aerosol con TG 227 ea como agente propulsor | |
EP0918507B2 (en) | Aerosol formulations | |
CA2353959A1 (en) | A medicinal aerosol formulation | |
PT656207E (pt) | Formulacoes de aerossois sem clorofluorocarbonetos | |
RU98118908A (ru) | Баллон для доставки фармацевтического состава, дозирующий ингалятор | |
US5744124A (en) | Nitroglycerin-containing hydrophilic aqueous pumpable spray composition | |
HU214914B (hu) | Gáznyomás alatti csomagolások poli(oxi-etilén)-gliceril-oleátok alkalmazásával és eljárás azok előállítására | |
KR100281626B1 (ko) | 약학조성물및그투여장치 | |
US4041148A (en) | New aerosol propellants for personal products | |
ES2247959T1 (es) | Formulacion medica en aerosol estabilizada en agua. | |
PE20011271A1 (es) | Formulaciones que contienen una droga glucocorticoide para el tratamiento de enfermedades broncopulmonares | |
ES2259915A1 (es) | Nueva formulacion estable de aerosoles en suspension y procedimiento de obtencion. | |
JP2624396B2 (ja) | ニトログリセリンエアゾールスプレー | |
US3039929A (en) | Stable isoproteronol compositions | |
US3608065A (en) | Aerosol composition containing a vasoconstrictor | |
CA3142215A1 (en) | Method for charging a container for use with a medication delivery apparatus, container for such an apparatus and method for treating a patient | |
TH9164B (th) | สูตรผสมยาละอองลอยทางเภสัชซึ่งประกอบด้วยบีโคลเมธาโซนไดโพรพิโอเนท | |
TH13269A (th) | สูตรผสมยาละอองลอยทางเภสัชซึ่งประกอบด้วยบีโคลเมธาโซนไดโพรพิโอเนท |