Inhaled hypertonic saline delivered by a heated nasal cannula

• US 9,408,988 B2
• Filed: 10/07/2013
• Issued: 08/09/2016
• Est. Priority Date: 10/10/2007
• Status: Active Grant

• Current Assignee: Parion Sciences, Inc.
• Original Assignee: Parion Sciences, Inc.
• Inventors: Boucher, Richard C., Johnson, Michael Ross
• Primary Examiner(s): Wax, Robert A
• Assistant Examiner(s): MERCIER, MELISSA S
• Application Number:
  US14/047,281
• Publication Number:
  US 20140096765A1
• Time in Patent Office: 1,037 Days
• Field of Search: None
• US Class Current: 1/1
• CPC Class Codes: A61M 11/001 Particle size control
• CPC Class Codes: A61M 11/02 operated by air or other gas pressure applied to the liquid or other product to be sprayed or atomised sprayers for horticulture A01G, A01H; killing insects A01M; air humidifying by nozzles F24F6/14, F24F6/18; cooling by spraying F28B, F28C
• CPC Class Codes: A61M 15/08 Inhaling devices inserted into the nose
• CPC Class Codes: A61M 16/0666 Nasal cannulas or tubing devices for improving normal breathing through the nose A61F5/08; nose filters A62B23/06; outside holding devices A61M25/02
• CPC Class Codes: A61M 16/0875 Connecting tubes
• CPC Class Codes: A61M 16/1075 by influencing the temperature A61M16/1045 takes precedence
• CPC Class Codes: A61M 16/1095 in the connecting tubes
• CPC Class Codes: A61M 16/14 by mixing different fluids, one of them being in a liquid phase
• CPC Class Codes: A61M 16/18 Vaporising devices for anaesthetic preparations
• CPC Class Codes: A61M 2202/0488 Surfactant, e.g. for the lung
• CPC Class Codes: A61P 11/02 Nasal agents, e.g. decongestants

Abstract

The invention described herein is directed to method of treating chronic obstructive pulmonary disease, comprising administering an effective amount of an osmolyte by at least one nasal cannula to a subject in need thereof. Also provided is a nasal cannula system for delivering an osmolyte, comprising a nebulizer and tubing having two ends, where the first end of the tubing is connected to the nebulizer and the second end of the tubing is tapered to fit in the nostril of a subject.

Claims

1. An apparatus, comprising:

a nasal cannula assembly configured to receive at a first end portion a flow of aerosolized medicament, the nasal cannula assembly configured to convey from the first end portion to a second end portion the flow of aerosolized medicament to deliver the flow of aerosolized medicament transnasally to a subject, the nasal cannula assembly configured to limit accumulation of liquid droplets from the flow of aerosolized medicament.

2. The apparatus of claim 1, wherein the aerosolized medicament is an aerosolized osmolyte.

3. The apparatus of claim 1, wherein the aerosolized medicament is hypertonic saline.

4. The apparatus of claim 1, further comprising:

an aerosol preparation mechanism, the aerosol preparation mechanism configured to produce the aerosolized medicament including respirable particles having a particle size of 1-5 microns MMD.

5. The apparatus of claim 1, wherein the nasal cannula assembly is configured to deliver the aerosolized medicament to the subject over a period of at least 80 minutes.

6. The apparatus of claim 1, wherein the nasal cannula assembly is configured to deliver the aerosolized medicament to the subject over a period of at least 80 minutes, the aerosolized medicament having a particle size of 1-5 microns MMD.

7. The apparatus of claim 1, further comprising:

a heater configured to heat at least a portion of the nasal cannula assembly such that condensation of the aerosolized medicament in the nasal cannula assembly is limited.

8. The apparatus of claim 1, wherein an inner surface of the nasal cannula assembly includes a coating formulated to minimize accumulation of the aerosolized medicament.

9. The apparatus of claim 1, wherein a length from the first end portion of the nasal cannula assembly to the second end portion of the nasal cannula assembly is at least two meters.

10. The apparatus of claim 1, wherein at least a portion of the nasal cannula assembly has an inner diameter of less than five millimeters.

11. The apparatus of claim 1, wherein a delivery portion of the second end portion of the nasal cannula assembly is tapered such that it can engage at least one nostril of the subject.

12. The apparatus of claim 1, further comprising:

an aerosol preparation mechanism configured to receive a flow of air at a first port and produce the flow of aerosolized medicament, the aerosol preparation mechanism configured to convey, from a second port and to the first end portion of the nasal cannula assembly, the flow of aerosolized medicament.

13. The apparatus of claim 1, further comprising:

an aerosol preparation mechanism configured to receive a flow of air at a first port, the aerosol preparation mechanism configured to convey over a period of at least 80 minutes, from a second port and to the first end portion of the nasal cannula assembly, the flow of aerosolized medicament.

14. An apparatus, comprising:

a nasal cannula assembly having a tube portion and a face piece portion, the tube portion configured to be coupled to an aerosol preparation mechanism, the face piece portion configured to be coupled to a nostril of a subject,

the nasal cannula assembly configured to receive, at the tube portion and from the aerosol preparation mechanism, an aerosolized osmolyte, the nasal cannula assembly configured to convey, over a period of at least eighty minutes and via the face piece portion, the aerosolized osmolyte to the nostril of the subject, the nasal cannula assembly configured to limit accumulation of liquid droplets therein.

15. The apparatus of claim 14, further comprising:

a heater configured to heat at least a portion of the nasal cannula assembly such that condensation of the aerosolized osmoltye in the nasal cannula assembly is limited.

16. The apparatus of claim 14, further comprising:

the aerosol preparation mechanism, the aerosol preparation mechanism configured to produce the aerosolized osmolyte including respirable particles having a particle size of 1-5 microns MMD.

17. The apparatus of claim 14, wherein a portion of the face piece portion is tapered such that it can engage the nostril of the subject.

18. The apparatus of claim 14, wherein an inner surface of the nasal cannula assembly includes a coating formulated to minimize accumulation of the aerosolized osmolyte.

19. The apparatus of claim 14, wherein the nasal cannula assembly is configured to convey the aerosolized osmolyte over a period of at least about 8 hours.

20. The apparatus of claim 14, further comprising:

a container containing the aerosolized osmolyte, the aerosolized osmolyte formulated to treat chronic obstructive pulmonary disease.

21. An apparatus, comprising:

a nasal cannula assembly having a tube portion and a face piece portion, the tube portion configured to be operably coupled to an aerosol preparation mechanism, the face piece portion configured to be removably coupled to a nostril of a subject,

the nasal cannula assembly configured to receive, at the tube portion and from the aerosol preparation mechanism, a flow of aerosolized osmolyte including respirable particles having a particle size of 1-5 microns MMD, the nasal cannula assembly configured to convey, via the face piece portion, the aerosolized osmolyte to the notstril of the subject, the nasal cannula assembly configured to limit accumulation of the aerosolized osmolyte therein.

22. The apparatus of claim 21, further comprising:

the aerosol preparation mechanism, the aerosol preparation mechanism configured to produce the aerosolized osmolyte.

23. The apparatus of claim 21, further comprising:

a heater configured to heat at least a portion of the nasal cannula assembly such that condensation of the aerosolized osmolyte in the nasal cannula assembly is limited.

24. The apparatus of claim 21, wherein the nasal cannula assembly is configured to convey the aerosolized osmolyte over a period of at least about 8 hours.

25. The apparatus of claim 21, further comprising:

the aerosol preparation mechanism, the aerosol preparation mechanism configured to receive a flow of air at a first port and produce the flow of aerosolized osmolyte, the aerosol preparation mechanism configured to convey, from a second port and to a first end of the tube portion of the nasal cannula assembly, the flow of aerosolized osmolyte.