Drug delivery and method having coated microprojections incorporating vasoconstrictors

• US 20080226687A1
• Filed: 05/21/2008
• Published: 09/18/2008
• Est. Priority Date: 09/30/2002
• Status: Abandoned Application

• Current Assignee: ALZA Corporation (Johnson & Johnson)
• Original Assignee: ALZA Corporation (Johnson & Johnson)
• Inventors: Cormier, Michel, Lin, WeiQi, Matriano, James, Young, Wendy
• Application Number:
  US12/154,373
• Publication Number:
  US 20080226687A1
• Time in Patent Office: Days
• US Class Current: 424/422
• CPC Class Codes: A61K 45/06 Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
• CPC Class Codes: A61K 9/0021 Intradermal administration, e.g. through microneedle arrays, needleless injectors mechanical aspects A61M

Abstract

A device and method are provided for percutaneous transdermal delivery of a biologically active agent. The coating formulation containing the biologically active agent and a vasoconstrictor is applied to the skin piercing elements using known coating techniques and then dried. The device is applied to the skin of a living animal, causing the microprojections to pierce the stratum corneum and to deliver an effective dose of the biologically active agent and vasoconstrictor to the animal.

Claims

1. A device for transdermally delivering a biologically active agent, comprising:

a member having a plurality of stratum corneum-piercing microprotrusions; and

a coating disposed on said member, said coating including a biologically active agent and a vasoconstrictor.

2. The device of claim 1, wherein said biologically active agent comprises a vaccine selected from the group consisting of conventional vaccines, recombinant protein vaccines, DNA vaccines and therapeutic cancer vaccines.

3. The device of claim 1, wherein said biologically active agent is selected from the group consisting of ACTH (1-24), calcitonin, desmopressin, LHRH, LHRH analogs, goserelin, leuprolide, parathyroid hormone (PTH), vasopressin, deamino [Val4, D-Arg8] arginine vasopressin, buserlin, triptorelin, interferon alpha, interferon beta, interferon gamma, FSH, EPO, GM-CSF, G-CSF, IL-10, glucagon, growth hormone releasing factor (GRF) and analogs of these agents, including pharmaceutically acceptable salts thereof, and mixtures thereof.

4. The device of claim 1, wherein said vasoconstrictor is selected from the group consisting of amidephrine, cafaminol, cyclopentamine, deoxyepinephrine, epinephrine, felypressin, indanazoline, metizoline, midodrine, naphazoline, nordefrin, octodrine, orinpressin, oxymethazoline, phenylephrine, phenylethanolamine, phenylpropanolamine, propylhexedrine, pseudoephedrine, tetrahydrozoline, tramazoline, tuaminoheptane, tymazoline, vasopressin, xylometazoline and mixtures thereof.

5. The device of claim 4, wherein said vasoconstrictor comprises in the range of 0.1-10.0 wt. % of said coating.

6. The device of claim 1, wherein said coating comprises a dry coating, said dry coating comprising an aqueous solution prior to drying.

7. (canceled)

8. (canceled)

9. A device for transdermally delivering a biologically active agent and a vasoconstrictor, comprising:

a member having a plurality of stratum corneum-piercing microprotrusions; and

a dry coating disposed on at least one of said plurality of stratum corneum-piercing microprotrusions, said coating including a biologically active agent and a vasoconstrictor.

10. The device of claim 9, wherein said biologically active agent comprises a vaccine selected from the group consisting of conventional vaccines, recombinant protein vaccines, DNA vaccines and therapeutic cancer vaccines.

11. The device of claim 9, wherein said biologically active agent is selected from the group consisting of ACTH (1-24), calcitonin, desmopressin, LHRH, LHRH analogs, goserelin, leuprolide, parathyroid hormone (PTH), vasopressin, deamino [Val4, D-Arg8] arginine vasopressin, buserlin, triptorelin, interferon alpha, interferon beta, interferon gamma, FSH, EPO, GM-CSF, G-CSF, IL-10, glucagon, growth hormone releasing factor (GRF) and analogs of these agents, including pharmaceutically acceptable salts thereof and mixtures thereof.

12. The device of claim 9, wherein said vasoconstrictor is selected from the group consisting of amidephrine, cafaminol, cyclopentamine, deoxyepinephrine, epinephrine, felypressin, indanazoline, metizoline, midodrine, naphazoline, nordefrin, octodrine, orinpressin, oxymethazoline, phenylephrine, phenylethanolamine, phenylpropanolamine, propylhexedrine, pseudoephedrine, tetrahydrozoline, tramazoline, tuaminoheptane, tymazoline, vasopressin, xylometazoline and mixtures thereof.

13. The device of claim 12, wherein said vasoconstrictor comprises in the range of 0.1-10.0 wt. % of said coating.

14. The device of claim 9, wherein each of said plurality of stratum corneum-piercing microprotrusions has a length less than approximately 1000 microns.

15. The device of claim 14, wherein each of said plurality of stratum corneum-piercing microprotrusions has a length less than approximately 500 microns.

16. The device of claim 9, wherein each of said plurality of stratum corneum-piercing microprotrusions has a thickness in the range of approximately 5-50 microns.

17. The device of claim 9, wherein said coating has a thickness less than 50 microns.

18. The device of claim 17, wherein said coating thickness is less than 10 microns.

19. The device of claim 9, wherein each of said plurality of stratum corneum-piercing microprotrusions includes in the range of 1 microgram to 1 milligram of said biologically active agent.

20. (canceled)

21. A method of making a device for transdermally delivering a biologically active agent and a vasoconstrictor, the method comprising:

providing a member having a plurality of stratum corneum-piercing microprotrusions, said microprotrusions having a length of less than 1000 microns;

applying an aqueous solution of a biologically active agent and a vasoconstrictor onto the member; and

drying said applied aqueous solution to form a dry agent-containing coating on said member.

22. The method of claim 21, wherein said biologically active agent comprises a vaccine selected from the group consisting of conventional vaccines, recombinant protein vaccines, DNA vaccines and therapeutic cancer vaccines.

23. The method of claim 21, wherein said biologically active agent is selected from the group consisting of ACTH (1-24), calcitonin, desmopressin, LHRH, LHRH analogs, goserelin, leuprolide, parathyroid hormone (PTH), vasopressin, deamino [Val4, D-Arg8] arginine vasopressin, buserlin, triptorelin, interferon alpha, interferon beta, interferon gamma, FSH, EPO, GM-CSF, G-CSF, IL-10, glucagon, growth hormone releasing factor (GRF) and analogs of these agents, and mixtures thereof.

24. The method of claim 21, wherein said vasoconstrictor is selected from the group consisting of amidephrine, cafaminol, cyclopentamine, deoxyepinephrine, epinephrine, felypressin, indanazoline, metizoline, midodrine, naphazoline, nordefrin, octodrine, orinpressin, oxymethazoline, phenylephrine, phenylethanolamine, phenylpropanolamine, propylhexedrine, pseudoephedrine, tetrahydrozoline, tramazoline, tuaminoheptane, tymazoline, vasopressin, xylometazoline and mixtures thereof.

25. The device of claim 24, wherein said vasoconstrictor comprises in the range of 0.1-10.0 wt. % of said coating.

26. The method of claim 21, wherein said coating is applied by dip coating.

27. The method of claim 21, wherein said coating is applied by spray coating.

28. The method of claim 21, wherein said coating is applied by pattern coating.

29. A method of making a device for transdermally delivering a biologically active agent and a vasoconstrictor, the method comprising:

providing a sheet member;

etching a microprojection array on said sheet member to form a plurality of microprojections;

bending said plurality of microprojections whereby said plurality of microprojections project from a plane of said sheet member;

coating at least a first microprojection of said plurality of microprojections with an aqueous solution containing a biological active agent and a vasoconstrictor; and

drying said applied aqueous solution to form a dry agent containing coating on said first microprojection.

30-39. -39. (canceled)