Automatic dispenser for respiratory delivery device and method
US-2024058555-A1 · Feb 22, 2024 · US
US9084722B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9084722-B2 |
| Application number | US-200913132708-A |
| Country | US |
| Kind code | B2 |
| Filing date | Dec 4, 2009 |
| Priority date | Dec 5, 2008 |
| Publication date | Jul 21, 2015 |
| Grant date | Jul 21, 2015 |
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Provided herein are methods of preventing, lessening or treating pulmonary fibrosis in a subject. The methods comprise delivering an amount of a powdered extracellular matrix (ECM)-derived material to the respiratory system of the subject effective to prevent, lessen or treat pulmonary fibrosis in a subject. Also provided is an apparatus for delivering the powdered ECM-derived material to a subject.
Opening claim text (preview).
We claim: 1. A method of reducing interstitial lung disease in a subject in need thereof, comprising: administering via the subject's airway a composition comprising a devitalized, decellularized layer of extracellular matrix material that is delaminated from one or more layers of a devitalized epithelial tissue in an amount effective to reduce interstitial lung disease in the subject. 2. The method of claim 1 , in which the airway delivery system is a metered dose inhaler. 3. The method of claim 1 , in which the airway delivery system is a metered-dose inhaler and the composition comprises a propellant. 4. The method of claim 1 , in which the composition is a dry powder. 5. The method of claim 4 , in which the powdered composition has a maximum particle size of 250 μM. 6. The method of claim 4 , in which the powdered composition has a maximum particle size of 75 μM. 7. The method of claim 1 , in which the composition is a liquid. 8. The method of claim 1 , wherein the interstitial lung disease is associated with silicosis; asbestosis; berylliosis; hypersensitivity pneumonitis; drug induced interstitial lung disease, connective tissue disease, systemic sclerosis, dermatomyositis, systemic lupus erythematosus, rheumatoid arthritis; infection, atypical pneumonia, pneumocystis pneumonia (PCP), tuberculosis; idiopathic interstitial lung disease, sarcoidosis, idiopathic pulmonary fibrosis, Hamman-Rich syndrome, a malignancy, or lymphangitic carcinomatosis. 9. The method of claim 1 , wherein between 10 μg and 1000 mg of the composition is delivered to the subject. 10. The method of claim 1 , in which the composition comprises epithelial basement membrane. 11. The method of claim 1 , in which the composition comprises tunica propria. 12. The method of claim 11 , in which the composition further comprises submucosa. 13. The method of claim 1 , in which the composition is administered to a subject prior to or after chemotherapy or radiotherapy. 14. The method of claim 1 , in which the composition is administered to a subject exposed to a chemical agent. 15. The method of claim 1 , in which the composition is solubilized. 16. The method of claim 1 , wherein the administering of the composition to the subject's airway is prior to, during or after exposure to a fibrosis-inducing event. 17. The method of claim 1 , wherein the administering of the composition to the subject's airway is prior to, during or after exposure to chemotherapy.
Sprayers or atomisers specially adapted for therapeutic purposes (in general B05B; {aerosol containers B65D83/14}) · CPC title
for inhalation via a dry powder inhaler [DPI], e.g. comprising micronized drug mixed with lactose carrier particles · CPC title
Tracheal tubes (catheters in general A61M25/00) · CPC title
comprising drug dissolved or suspended in liquid propellant for inhalation via a pressurized metered dose inhaler [MDI] · CPC title
for inhalation via a nebulizer such as a jet nebulizer, ultrasonic nebulizer, e.g. in the form of aqueous drug solutions or dispersions · CPC title
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