WO2000027363B1 - Aerosols comprising nanoparticle drugs - Google Patents

Aerosols comprising nanoparticle drugs

Info

Publication number
WO2000027363B1
WO2000027363B1 PCT/US1999/026799 US9926799W WO0027363B1 WO 2000027363 B1 WO2000027363 B1 WO 2000027363B1 US 9926799 W US9926799 W US 9926799W WO 0027363 B1 WO0027363 B1 WO 0027363B1
Authority
WO
WIPO (PCT)
Prior art keywords
drug
aerosol
less
nanoparticulate
therapies
Prior art date
Application number
PCT/US1999/026799
Other languages
French (fr)
Other versions
WO2000027363A1 (en
WO2000027363A9 (en
Inventor
H William Bosch
Kevin D Ostrander
Eugene R Cooper
Original Assignee
Nanosystems
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nanosystems filed Critical Nanosystems
Priority to CA002350074A priority Critical patent/CA2350074C/en
Priority to JP2000580594A priority patent/JP4758548B2/en
Priority to AU13469/00A priority patent/AU1346900A/en
Priority to EP99956981A priority patent/EP1128814B1/en
Priority to DE69943112T priority patent/DE69943112D1/en
Priority to AT99956981T priority patent/ATE493971T1/en
Priority to DK99956981.7T priority patent/DK1128814T3/en
Publication of WO2000027363A1 publication Critical patent/WO2000027363A1/en
Publication of WO2000027363B1 publication Critical patent/WO2000027363B1/en
Publication of WO2000027363A9 publication Critical patent/WO2000027363A9/en

Links

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
    • A61K9/0078—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy for inhalation via a nebulizer such as a jet nebulizer, ultrasonic nebulizer, e.g. in the form of aqueous drug solutions or dispersions
    • 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
    • A61K9/0075—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy for inhalation via a dry powder inhaler [DPI], e.g. comprising micronized drug mixed with lactose carrier particles
    • 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
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
    • A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
    • 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
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/1682—Processes
    • A61K9/1694—Processes resulting in granules or microspheres of the matrix type containing more than 5% of excipient
    • 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
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/19—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles lyophilised, i.e. freeze-dried, solutions or dispersions
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/02—Stomatological preparations, e.g. drugs for caries, aphtae, periodontitis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/08—Bronchodilators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • A61P31/06—Antibacterial agents for tuberculosis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/10—Antimycotics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system

Abstract

The invention discloses aqueous dispersions of nanoparticulate aerosol formulations, dry powder nanoparticulate aerosol formulation, propellant-based aerosol formulations, methods of using the formulations in aerosol delivery devices, and methods of making such formulations. The nanoparticles of the aqueous dispersions or dry powder formulations comprise insoluble drug particles having a surface modifier on the surface thereof.

Claims

AMENDED CLAIMS[received by the International Bureau on 10 May 2000 (10.05.00); original claims 1, 6-11, 18-23, 29-33, 35-37, 39, 40 and 42-44 amended; remaining claims unchanged (9 pages)]
1. An aerosol composition of an aqueous dispersion of nanoparticulate drug particles, wherein:
(a) essentially each droplet of the aerosol comprises at least one nanoparticulate drug particle;
(b) the droplets of the aerosol are less than or equal to about 100 microns in diameter, and
(c) the nanoparticulate drug particles comprise a poorly soluble crystalline drug, have an effective average particle size of less than about 1000 nm, and have a surface modifier adsorbed on the surface thereof.
2. The aerosol composition of claim 1, wherein the drug is selected from the group consisting of proteins, peptide, bronchodilators, corticosteroids, elastase inhibitors, analgesics, anti-fungals, cystic-fibrosis therapies, asthma therapies, emphysema therapies, respiratory distress syndrome therapies, chronic bronchitis therapies, chronic obstructive pulmonary disease therapies, organ-transplant rejection therapies, therapies for tuberculosis and other infections of the luDg, fungal infection therapies, respiratory illness therapies associated with acquired immune deficiency syndrome, an oncology drug, an anti-emetic, an analgesic, and a cardiovascular agent.
3. The aerosol composition of claim 1, wherein the nanoparticulate drug particles have an effective average particle size selected from the group consisting of less than about 400 nm, less than about 300 nm, less than about 250 ran, less than about 100 nm, and less than about 50 n .
4. The aerosol composition of claim 1, wherein the aerosol comprises a concentration of a drug in an amount of from about 0.05 mg/mL up to about 600 mg/mL.
5. The aerosol composition of claim 4, wherein the aerosol comprises a concentration of a drug selected from the group consisting of about 0 mg/mL or more, about
52 100 mg/mL or more, about 200 mg/mL or more, about 400 mg/mL or more, and about 600 mg/mL.
6. The aerosol composition of claim 1, wherein the droplets of the aerosol have a mass median aerodynamic diameter of about 2 to about 10 microns.
7. The aerosol composition of claim 6, wherein the droplets of the aerosol have a mass median aerodynamic diameter of from about 2 to about 6 microns.
8. The aerosol composition of claim 1, wherein the droplets of the aerosol have a mass median aerodynamic diameter of less than about 2 microns.
9. The aerosol composition of claim 1, wherein the droplets of the aerosol have an mass median aerodynamic diameter of about 5 to about 100 microns .
10. The aerosol composition of claim 9, wherein the droplets of the aerosol have an mass median aerodynaniic diameter of about 30 to about 60 microns.
11. A spray-dried powder aerosol composition comprising aggregates of nanoparticulate drug particles, wherein:
(a) the nanoparticulate drug particles comprise a poorly soluble crystalline drug, have an effective average particle size of less than about 1000 nm, and have a surface modifier adsorbed on the surface thereof; and
(b) the aggregates of spray-dried drug particles are less than or equal to about 100 microns in diameter,
12. The aerosol composition of claim 11 further comprising a diluent.
53
13. The aerosol composition of claim 12, wherein essentially every diluent particle comprises at least one embedded nanoparticulate drug particle having a surface modifier adhered to the surface of the drug particle.
14. The aerosol composition of claim 11, wherein the drug is selected from the group consisting of proteins, peptides, bronchodilators, corticosteroids, elastase inhibitors, analgesics, anti-fungals, cystic-fibrosis therapies, asthma therapies, emphysema therapies, respiratory distress syndrome therapies, chronic bronchitis therapies, chronic obstructive pulmonary disease therapies, organ-transplant rejection therapies, therapies for tuberculosis and other infections of the lung, fungal infection therapies, and respiratory illness therapies associated with acquired immune deficiency syndrome, an oncology drug, an anti-emetic, an analgesic, and a cardiovascular agent.
15. The aerosol composition of claim 11 , wherein the nanoparticulate drug particles have an effective average particle size selected from the group consisting of less than about 400 nm, less than about 300 nm, less than about 250 nm, less than about 100 nm, and less than about 50 nm.
16. The aerosol composition of claim 11 , wherein the aerosol comprises a concentration of a drug in an amount of from about 0.05 mg/g up to about 900 mg/g.
17. The aerosol composition of claim 16, wherein the aerosol comprises a concentration of a drug selected from the group consisting of about 10 mg/g or more, about 100 mg/g or more, about 200 mg/g or more, about 400 mg/g or more, about 600 mg/g or more, and about 900 mg/g.
18. The aerosol composition of claim 11 , wherein the aggregates of the nanoparticulate drug particles have a mass median aerodynamic diameter of about 2 to about 10 microns.
19. The aerosol composition of claim 18, wherein the aggregates of the nanoparticulate drug particles have a mass median aerodynamic diameter of about 2 to about 6 microns,
20. The aerosol composition of claim 11, wherein the aggregates of the nanoparticulate drug particles have a mass median aerodynamic diameter of less than about 2 microns.
21. The aerosol composition of claim 11 , wherein the aggregates of the nanoparticulate drug particles have a mass median aerodynamic diameter of about 5 to about 100 μm.
22. The aerosol composition of claim 21, wherein the aggregates of the nanoparticulate drug particles have a mass median aerodynamic diameter of about 30 to about 60 μm.
23. A freeze-dried powder aerosol composition comprising aggregates of nanoparticulate drug particles, wherein:
(a) the aggregates of freeze-dried drug particles are less than or equal to about 100 microns in diameter;
(b) the nanoparticulate drug particles comprise a poorly soluble crystalline drug, have an effective average particle size of less than about 1000 nm, and have a surface modifier adsorbed on the surface thereof.
24. The aerosol composition of claim 23, further comprising a diluent.
25. The aerosol composition of claim 23, wherein the drug is selected from the group consisting of proteins, peptides, bronchodilators, corticosteroids, elastase inhibitors, analgesics, anti-fungals, cystic-fibrosis therapies, asthma therapies, emphysema therapies, respiratory distress syndrome therapies, chronic bronchitis therapies, chronic obstructive
55 pulmonary disease therapies, organ-transplant rejection therapies, therapies for tuberculosis and other infections of the lung, fungal infection therapies, and respiratory illness therapies associated with acquired immune deficiency syndrome, an oncology drug, an anti-emetic, an analgesic, and a cardiovascular agent.
26. The aerosol composition of claim 23, wherein the nanoparticulate drug particles have an effective average particle size selected from the group consisting of less than about 400 nm, less than about 300 nm, less than about 250 nm, less than about 100 nm, and less than about 50 nm.
27. The aerosol composition of claim 23, wherein the aerosol comprises a concentration of a drug in an amount of from about 0.05 mg/g up to about 900 mg/g.
28. The aerosol composition of claim 27, wherein the aerosol comprises a concentration of a drug selected from the group consisting of about 10 mg/g or more, about 100 mg/g or more, about 200 mg/g or more, about 400 mg/g or more, about 600 mg/g or more, and about 900 mg/g.
29. The aerosol composition of claim 23, wherein the aggregates of the nanoparticulate drug particles have a mass median aerodynamic diameter of about 2 to about 10 microns.
30. The aerosol composition of claim 29, wherein the aggregates of the nanoparticulate drug particles have a mass median aerodynamic diameter of about 2 to about 6 microns.
31. The aerosol composition of claim 23, wherein the aggregates of the nanoparticulate drug particles have a mass median aerodynamic diameter of less than about 2 microns.
56
32. The aerosol composition of claim 23, wherein the aggregates of the nanoparticulate drug particles have amass median aerodynamic diameter of about 5 to about 100 μm.
33. The aerosol composition of claim 32, wherein the aggregates of the nanoparticulate drug particles have a mass median aerodynamic diameter of about 30 to about 60 μm.
34. The aerosol composition of claim 23, further comprising spray-dried nanoparticulate drug powder, wherein the drug of the freeze-dried nanoparticulate drug powder is either the same or different from the drug of the spray-dried nanoparticulate drug powder.
35. A dry powder nanoparticulate aerosol composition for use in a propellant-based pMDl comprising:
(a) aggregates of a nanoparticulate poorly soluble crystalline drug, wherein the drug has a surface modifier adsorbed on the surface thereof, and the drug has an effective average particle size of less than about 1000 nm, wherein the aggregates are less than or equal to about 100 microns in diameter, and
(b) a non-aqueous propellant.
36. The aerosol composition of claim 35, wherein the propellant is a non-CFC propellant.
37. A nanoparticulate aerosol composition for use in a propellant-based pMDI comprising!
(a) a nanoparticulate poorly soluble crystalline drug, wherein the drug has a surface modifier adsorbed on the surface thereof, and the drug has an effective average particle size of less than about 1000 nm,
(b) essentially each droplet of the aerosol comprises at least one nanoparticulate
57 drug particle, wherein the droplets of the aerosol generated by the pMDI have a diameter of less than or equal to about 100 microns, and (c) a non-aqueous propellant.
38. The aerosol composition of claim 38, wherein the propellant is a non-CFC propellant.
39. A method of making an aerosol of an aqueous dispersion of nanoparticulate drug particles, wherein said nanoparticulate drug particles comprise a poorly soluble ciystalhne drug, have an effective average particle size of less than about 1000 nm, and have a surface modifier adsorbed on the surface thereof; wherein the method comprises:
(a) providing an aqueous dispersion of said nanoparticulate drug particles; and
(b) nebulizing said dispersion to form an aerosol, wherein essentially each droplet of the aerosol comprises at least one nanoparticulate drug particle and a surface modifier, and wherein the droplets of the aerosol have a diameter of less than or equal to about 100 microns.
40. A method of making a dry powder nanoparticulate drug composition comprising:
(a) forming an aqueous nanoparticulate dispersion of a poorly soluble drug, wherein the dispersion comprises ciystalhne drug particles and a surface modifier adsorbed on the surface thereof, wherein the drug particles have an effective average particle size of less than about 1000 nm; b) spray-drying the nanoparticulate dispersion to form a dry powder of aggregates of the nanoparticulate drug and surface modifier particles, wherein the aggregates have a diameter of less than or equal to about 100 microns.
58
41. The method of claim 40, further comprising adding a diluent to the nanoparticulate dispersion prior to spray-drying, wherein following spray-drying essentially every diluent particle contains at least one embedded drug particle and a surface modifier.
42. A method of making a dry powder nanoparticulate drug aerosol formulation comprising:
(a) milling under non-pressurized conditions a poorly soluble crystalline drug and a surface modifier in a non-aqueous medium having a high boiling point to obtain a nanoparticulate drug composition having an effective average particle size of less than about 1000 nm, and
(b) evaporating the non-aqueous medium to obtain a dry powder of aggregates of drug and surface modifier particles, wherein the aggregates have a diameter of less than or equal to about 100 microns.
43. A method of making a nanoparticulate drug aerosol formulation comprising:
(a) milling under pressurized conditions a poorly soluble crystalline drug and a surface modifier in a non-aqueous medium; and
(b) evaporating the non-aqueous medium to obtain a dry powder of aggregates of drug and surface modifier particles, wherein the aggregates have a diameter of less than or equal to about 100 microns.
44. A method of making a dry powder nanoparticulate drug composition comprising:
(a) forming an aqueous nanoparticulate dispersion of a poorly soluble drug, wherein the dispersion comprises crystalline drug particles and a surface modifier adsorbed on the surface thereof, wherein the drug particles have an effective average particle size of less than about 1000 nm;
(b) freeze-drying the nanoparticulate dispersion to form a dry powder of aggregates of the nanoparticulate drug and surface modifier particles, wherein the aggregates have a diameter of less than or equal to about 100 microns.
59
45. The method of claim 44, further comprising adding a diluent to the nanoparticulate dispersion prior to freeze-drying, wherein following freeze-drying essentially every diluent particle contains at least one embedded drug particle and a surface modifier,
46. A method of administering the aerosol of claim 1 to a patient, wherein the aerosol comprises drug at a concentration of 10 mg/mL or greater, and wherein the patient delivery time for the aerosol administration is about 15 seconds or less.
47. A method of administering the aerosol of claim 11 to a patient, wherein the aerosol comprises drug at a concentration of 10 mg/g or greater, and wherein the patient delivery time for the aerosol administration is about 15 seconds or less.
48. A method of administering the aerosol of claim 23 to a patient, wherein the aerosol comprises drug at a concentration of 10 mg/g or greater, and wherein the patient delivery time for the aerosol administration is about 15 seconds or less.
49. A method of administering the aerosol of claim 35 to a patient, wherein the aerosol comprises drug at a concentration of 10 mg/g or greater, and wherein the patient delivery time for the aerosol administration is about 1 seconds or less.
50. A method of administering the aerosol of claim 37 to a patient, wherein the aerosol comprises drug at a concentration of 10 mg/g or greater, and wherein the patient dehvery time for the aerosol administration is about 15 seconds or less.
60
PCT/US1999/026799 1998-11-12 1999-11-12 Aerosols comprising nanoparticle drugs WO2000027363A1 (en)

Priority Applications (7)

Application Number Priority Date Filing Date Title
CA002350074A CA2350074C (en) 1998-11-12 1999-11-12 Aerosols comprising nanoparticle drugs
JP2000580594A JP4758548B2 (en) 1998-11-12 1999-11-12 Aerosol comprising ultrafine drug
AU13469/00A AU1346900A (en) 1998-11-12 1999-11-12 Aerosols comprising nanoparticle drugs
EP99956981A EP1128814B1 (en) 1998-11-12 1999-11-12 Aerosols comprising nanoparticle drugs
DE69943112T DE69943112D1 (en) 1998-11-12 1999-11-12 AEROSOLS CONTAINING PHARMACEUTICAL NANOPARTICLES
AT99956981T ATE493971T1 (en) 1998-11-12 1999-11-12 AEROSOLS CONTAINING MEDICINAL NANOPARTICLES
DK99956981.7T DK1128814T3 (en) 1998-11-12 1999-11-12 Aerosols comprising nanoparticulate drugs

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US09/190,138 1998-11-12
US09/190,138 US7521068B2 (en) 1998-11-12 1998-11-12 Dry powder aerosols of nanoparticulate drugs

Publications (3)

Publication Number Publication Date
WO2000027363A1 WO2000027363A1 (en) 2000-05-18
WO2000027363B1 true WO2000027363B1 (en) 2000-07-13
WO2000027363A9 WO2000027363A9 (en) 2000-11-30

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ID=22700162

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1999/026799 WO2000027363A1 (en) 1998-11-12 1999-11-12 Aerosols comprising nanoparticle drugs

Country Status (12)

Country Link
US (4) US7521068B2 (en)
EP (2) EP1128814B1 (en)
JP (1) JP4758548B2 (en)
AT (2) ATE493971T1 (en)
AU (1) AU1346900A (en)
CA (1) CA2350074C (en)
CY (2) CY1111344T1 (en)
DE (1) DE69943112D1 (en)
DK (2) DK2263652T3 (en)
ES (2) ES2387749T3 (en)
PT (1) PT2263652E (en)
WO (1) WO2000027363A1 (en)

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US9217129B2 (en) 2007-02-09 2015-12-22 Massachusetts Institute Of Technology Oscillating cell culture bioreactor
US9233072B2 (en) 2008-10-12 2016-01-12 Massachusetts Institute Of Technology Adjuvant incorporation in immunonanotherapeutics
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