IP Library Granted Patent US 8,524,279
Granted Patent B2
US 8,524,279 · App. 10/284,960 · Granted Sep 3, 2013

Spray drying methods and related compositions

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Quick Facts
Patent No.
US 8,524,279
App. No.
10/284,960
Granted
Sep 3, 2013
Kind
B2
Abstract

A method and apparatus are provided for atomizing a liquid under dispersal conditions suitable for spray drying at a commercial plant scale. In one embodiment, a liquid atomizer has a structural body adapted for connection with a spray dryer and a plurality of atomizing nozzles. Each of the atomizing nozzles includes a liquid nozzle adapted to disperse a supply of liquid and a gas nozzle adapted to disperse a supply of gas. In another embodiment, a process for producing a powder blend of at least two target substances in a single processing step is provided.

Claims (38)

1. A method for making a powder pharmaceutical for pulmonary administration, the method comprising:

providing a feedstock containing an active agent in a liquid vehicle, wherein the active agent comprises one or more of an antibiotic, an anti-inflammatory agent, and a bronchodilator;

providing a multi-nozzle atomizer comprising a housing supporting a central gas nozzle and a plurality of atomization nozzles around the central gas nozzle, wherein each atomization nozzle comprises a liquid nozzle and a gas nozzle that is configured as a cap surrounding the liquid nozzle, and wherein the central gas nozzle is not associated with a liquid nozzle;

atomizing the feedstock from the multi-nozzle atomizer to produce a droplet spray, wherein the feedstock is fed through the housing to the liquid nozzles in each of the atomization nozzles; and

flowing the droplet spray in a heated gas stream to evaporate the liquid vehicle of the feedstock and produce a powder of dry particulates comprising the active agent, wherein the dry particulates have an average particle size of less than 5 microns.

2. The method of claim 1 , wherein the total dissolved or suspended solids content in the feedstock is within a range from 0.5% to 10% by weight.

3. The method of claim 1 , wherein a throughput of the feedstock is at least 500 mL/min.

4. The method of claim 1 , wherein the powder comprises an ultrafine dry powder for pulmonary administration.

5. The method of claim 1 , wherein the dry particulates have a rugosity of greater than 2.0.

6. The method of claim 1 , wherein the dry particulates have a substantially smooth surface.

7. The method of claim 1 , wherein the feedstock further comprises at least one excipient.

8. The method of claim 1 , wherein the multi-nozzle atomizer comprises at least three atomization nozzles.

9. The method of claim 1 , wherein the multi-nozzle atomizer comprises at least four atomization nozzles.

10. The method of claim 1 , wherein the multi-nozzle atomizer comprises at least five atomization nozzles.

11. The method of claim 1 , wherein the multi-nozzle atomizer comprises an atomizer centerline, and wherein each of the plurality of atomization nozzles is disposed at an angle away from the atomizer centerline.

12. The method of claim 11 , wherein the angle away from the atomizer centerline ranges from 10° to 40°.

13. The method of claim 11 , wherein the central gas nozzle has an axis substantially along the atomizer centerline.

14. The method of claim 1 , wherein the feedstock is from a single source.

15. A method for making a powder pharmaceutical for pulmonary administration, the method, comprising:

providing a feedstock containing an active agent in a liquid vehicle, wherein the active agent comprises an antibiotic, wherein the antibiotic comprises one or more of ciprofloxacin, tobramycin, clarithromycin, gentamicin, and azithromycin;

providing a multi-nozzle atomizer comprising a plurality of atomization nozzles, wherein each atomization nozzle comprises a liquid nozzle and a gas nozzle;

atomizing the feedstock from the multi-nozzle atomizer to produce a droplet spray, wherein the feedstock is from a single source and is fed to the liquid nozzles in each of the atomization nozzles; and

flowing the droplet spray in a heated gas stream to evaporate the liquid vehicle of the feedstock and produce a powder of dry particulates comprising the active agent, wherein the dry particulates have an average particle size of less than 5 microns.

16. The method of claim 15 wherein the multi-nozzle atomizer comprises a housing supporting a central gas nozzle and a plurality of atomization nozzles around the central gas nozzle.

17. The method of claim 15 , wherein the total dissolved or suspended solids content in the feedstock is within a range from 0.5% to 10% by weight.

18. The method of claim 15 , wherein a throughput of the feedstock is at least 500 mL/min.

19. The method of claim 15 , wherein the dry particulates have a rugosity of greater than 2.0.

20. A method for making a powder pharmaceutical for pulmonary administration, the method comprising:

providing a feedstock containing an active agent in a liquid vehicle;

providing a multi-nozzle atomizer comprising a housing supporting a central gas nozzle and a plurality of atomization nozzles around the central gas nozzle, wherein each atomization nozzle comprises a liquid nozzle and a gas nozzle that is configured as a cap surrounding the liquid nozzle, and wherein the central gas nozzle is not associated with a liquid nozzle, wherein each of the plurality of atomization nozzles is disposed at an angle away from the atomizer centerline that ranges from 10° to 40°;

atomizing the feedstock from the multi-nozzle atomizer to produce a droplet spray, wherein the feedstock is fed through the housing to the liquid nozzles in each of the atomization nozzles; and

flowing the droplet spray in a heated gas stream to evaporate the liquid vehicle of the feedstock and produce a powder of dry particulates comprising the active agent, wherein the dry particulates have an average particle size of less than 5 microns.

21. The method of claim 20 , wherein a throughput of the feedstock is at least 500 mL/min.

22. The method of claim 20 , wherein the feedstock is from a single source.

23. The method of claim 20 , wherein the dry particulates have a rugosity of greater than 2.0.

24. The method of claim 20 , wherein the multi-nozzle atomizer comprises at least three atomization nozzles.

25. The method of claim 20 , wherein the multi-nozzle atomizer comprises at least four atomization nozzles.

26. The method of claim 20 , wherein the multi-nozzle atomizer comprises at least five atomization nozzles.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 12, 2011
From: NOVARTIS PHARMA AG
To: NOVARTIS AG
Reel/Frame 027047/0344 →
ASSIGNMENT OF PATENT RIGHTS Recorded Jan 7, 2009
From: NEKTAR THERAPEUTICS
To: NOVARTIS PHARMA AG
Reel/Frame 022071/0001 →
CHANGE OF NAME Recorded Feb 25, 2003
From: INHALE THERAPEUTIC SYSTEMS, INC.
To: NEKTAR THERAPEUTICS
Reel/Frame 013525/0753 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 31, 2002
From: SNYDER, HERMAN E.; VOSBERT, MICHAEL J.; VARGA, CHRISTOPHER M.
To: INHALE THERAPEUTIC SYSTEMS, INC.
Reel/Frame 013460/0194 →