Method and device for controlling drug pharmacokinetics

• US 10,322,272 B2
• Filed: 11/02/2015
• Issued: 06/18/2019
• Est. Priority Date: 05/06/2002
• Status: Active Grant

• Current Assignee: Becton, Dickinson & Co
• Original Assignee: Becton, Dickinson & Co
• Inventors: Pettis, Ronald J., Harvey, Noel G., Ginsberg, Barry
• Primary Examiner(s): Lee, Brandy S
• Application Number:
  US14/929,945
• Publication Number:
  US 20160051807A1
• Time in Patent Office: 1,324 Days
• CPC Class Codes: A61M 2037/0023 Drug applicators using microneedles
• CPC Class Codes: A61M 2037/0061 Methods for using microneedles
• CPC Class Codes: A61M 37/0015 by using microneedles
• CPC Class Codes: A61M 5/3291 Shafts with additional lateral openings

Abstract

Methods and devices for administration of substances into at least two compartments of skin for systemic absorption and improved pharmacokinetics, based on biphasic or bimodel kinetic profiling.

Claims

1. An injection device for delivering a therapeutic substance to a subject comprising:

a reservoir having at least a pre-selected volume of the therapeutic substance; and

a fluid conduit in fluid communication to the reservoir and sized to deliver the pre-selected volume of the substance within or beneath the skin solely into a first compartment, said first compartment having a volume capacity,

wherein the pre-selected volume of the reservoir is selected such that it is greater than said volume capacity of the first compartment, whereby when the volume of the therapeutic substance that is delivered to the first compartment exceeds the volume capacity of the first compartment, the therapeutic substance flows into a second compartment, and

wherein said first and second compartments afford therapeutic substance differing pharmacokinetics, which enhance the effectiveness of the therapeutic substance in terms of a resultant composite pharmacokinetics compared to delivery to a single compartment.

2. The device of claim 1, wherein the fluid conduit is at least one needle or cannula.

3. The device of claim 2, wherein the at least one needle is a single needle or cannula and is adapted to be inserted into the first compartment.

4. The device of claim 2, wherein the at least one needle is multiple needles or needle arrays and are adapted to be inserted into the first compartment.

5. The device of claim 2, wherein the at least one needle or cannula is 300 μ

m to 5 mm long.

6. The device of claim 5, wherein the at least one needle or cannula is 500 μ

m to 1 mm long.

7. The device of claim 2, wherein the at least one needle or cannula has an outlet placed at a depth of 250 μ

m to 2 mm when it is inserted into the first compartment.

8. The device of claim 7, wherein the outlet is at a depth of 750 μ

m to 1.5 mm when the at least one needle or cannula is inserted.

9. The device of claim 8, wherein the outlet has an exposed height of 0 to 1 mm.

10. The device of claim 9, wherein the outlet has an exposed height of 0 to 300 μ

m.

11. The device of claim 1, wherein the fluid conduit is selected from the group consisting of microneedles, catheter needles, and injection needles.

12. The device of claim 1, further comprising means for controlling the delivery rate of the substance to the first compartment.

13. The device of claim 12, wherein said delivery rate is controlled pursuant to an algorithm having logic components which include physiologic models, rules based models or moving average methods, therapy pharmacokinetic models, monitoring signal processing algorithms, predictive control models, or combinations thereof.

14. The device of claim 1, wherein the first compartment is the intradermal compartment and second compartment is the subcutaneous tissue compartment.

15. The device of claim 14, wherein delivery to the first and second compartments is by at least one needle that is adapted to target the interface of the intradermal and subcutaneous compartments.

16. The device of claim 1, wherein a portion of said therapeutic substance is absorbed more rapidly into an intradermal tissue space, and the remaining portion is absorbed less rapidly into a subcutaneous tissue space.

17. The device of claim 1, wherein the enhanced effectiveness is a decrease in T_max.

18. The device of claim 1, herein the enhanced effectiveness is an increase in C_max.

19. The device of claim 1, wherein the enhanced effectiveness is a decrease in T_lag.

20. The device of claim 1, wherein the enhanced effectiveness is enhanced absorption rate.

21. The device of claim 1, wherein the enhanced effectiveness is improved bioavailability.

22. An injection device for delivering a therapeutic substance to a subject comprising:

a reservoir to contain the therapeutic substance; and

at least two needles in fluid communication to the reservoir and sized to deliver the substance within or beneath the skin into at least two different compartments,

wherein only one of the compartments is the intradermal compartment, and

wherein said compartments afford substance differing pharmacokinetics, which enhance the effectiveness of the substance in terms of a resultant composite pharmacokinetics compared to delivery to a single compartment.

23. The device of claim 22, wherein the at least two needles have different lengths.

24. The device of claim 23, wherein at least one of the needles is 300 μ

m to 5 mm long.

25. The device of claim 24, wherein at least one of the needles is 500 μ

m to 1 mm long.

26. The device of claim 23, wherein at least one of the needles has an outlet placed at a depth of 250 μ

m to 2 mm when it is inserted into the intradermal compartment.

27. The device of claim 26, wherein the outlet is at a depth of 750 μ

m to 1.5 mm when the at least one of the needles is inserted.

28. The device of claim 27, wherein the outlet has an exposed height of 0 to 1 mm.

29. The device of claim 28, wherein the outlet has an exposed height of 0 to 300 μ

m.

30. The device of claim 22, further comprising means for controlling the delivery rate or volume delivered of the substance to the intradermal compartment.

31. The device of claim 22, wherein the multiple compartments are intradermal and subcutaneous tissue compartments.

32. The device of claim 22, wherein the enhanced effectiveness is a decrease in T_max.

33. The device of claim 22, wherein the enhanced effectiveness is an increase in C_max.

34. The device of claim 22, wherein the enhanced effectiveness is a decrease in T_lag.

35. The device of claim 22, wherein the enhanced effectiveness is enhanced absorption rate.

36. The device of claim 22, wherein the enhanced effectiveness is improved bioavailability.