Microfabricated surgical device

• US 20020188310A1
• Filed: 06/08/2001
• Published: 12/12/2002
• Est. Priority Date: 06/08/2001
• Status: Abandoned Application

• Current Assignee: Regents of the University of California (University of California)
• Original Assignee: Regents of the University of California (University of California)
• Inventors: Seward, Kirk Partick, Pisano, Albert P., Stupar, Philip Anthony
• Application Number:
  US09/877,653
• Publication Number:
  US 20020188310A1
• Time in Patent Office: Days
• US Class Current: 606/185
• CPC Class Codes: A61B 17/205 Vaccinating by means of needles or other puncturing devices
• CPC Class Codes: A61B 17/34 Trocars; Puncturing needles pointed biopsy instruments A61B10/0233; devices for piercing the ear-lobes A44C7/001; seals or hemostasis valves A61M39/06
• CPC Class Codes: A61B 2017/00345 Micromachines, nanomachines, microsystems

Abstract

This invention relates to microfabricated surgical devices made of a conformally coated polymer.

Claims

1. A microfabricated surgical device comprising:

an end portion and a body portion made of a conformally coated polymer.

2. The microfabricated surgical device of claim 1 wherein the polymer is Parylene.

3. The microfabricated surgical device of claim 1 wherein the polymer is deposited by gas vapor deposition.

4. The microfabricated surgical device of claim 1 wherein the polymer is selected from the group consisting of Parylene N, Parylene C, Parylene D, polystyrene, or Teflon®

.

5. The microfabricated surgical device of claim 1 wherein at least the end portion includes a metallic outer surface.

6. The microfabricated surgical device of claim 5 wherein the metallic outer surface is made of a metal selected for the group consisting of aluminum, gold, nickel, tungsten, zirconium, palladium, platinum, titanium, or alloys thereof.

7. The microfabricated surgical device of claim 1 wherein the end portion includes a reinforced section.

8. The microfabricated surgical device of claim 7 wherein the body portion includes a reinforced section.

9. The microfabricated device of claim 1 wherein a catheter is joined to the device opposite the end portion.

10. A microfabricated surgical device comprising:

a tip and a shaft made of a conformal layer of a polymer, wherein at least a portion of the shaft is hollow.

11. The microfabricated device of claim 10 wherein the polymer is Parylene.

12. The microfabricated device of claim 11 wherein the Parylene is deposited by gas vapor deposition.

13. The microfabricated device of claim 10 wherein the polymer is selected from the group consisting of Parylene N, Parylene C, Parylene D, polystyrene, or Teflon®

.

14. The microfabricated device of claim 10 wherein at least the tip includes a metallic outer surface.

15. The microfabricated device of claim 14 wherein the metallic outer surface is made of a metal selected for the group consisting of aluminum, gold, nickel, tungsten, zirconium, palladium, platinum, titanium, or alloys thereof.

16. The microfabricated device of claim 10 wherein the tip includes a reinforced section.

17. The microfabricated device of claim 16 wherein the shaft includes a reinforced section.

18. The microfabricated device of claim 10 wherein a catheter is joined to the device opposite the tip.

19. The microfabricated device of claim 10 wherein an interior cross-sectional dimension of the shaft is between about 10 and 100 microns.

20. The microfabricated device of claim 10 wherein an exterior cross-sectional dimension of the shaft is between about 50 and 250 microns.

21. The microfabricated device of claim 10 having a length of between about 250 microns and five millimeters.

22. A microfabricated needle comprising a tip and a shaft each including a conformal polymer layer.

23. The microfabricated needle of claim 22 wherein the polymer is selected from the group consisting of Parylene N, Parylene C, Parylene D, polystyrene, or Teflon®

.

24. The microfabricated needle of claim 22 wherein at least the tip includes a metallic outer surface.

25. The microfabricated needle of claim 22 wherein the tip includes a reinforced section.

26. The microfabricated needle of claim 25 wherein the shaft includes a reinforced section.

27. The microfabricated needle of claim 22 wherein a channel is formed through at least a portion of the shaft, and further including a fluid entry port formed at a first end of the channel and a fluid exit port formed at a second end of the channel.

28. The microfabricated needle of claim 27 wherein the first end of the channel is in fluid communication with a catheter.

29. The microfabricated needle of claim 22 wherein an interior cross-sectional dimension of the shaft is between about 10 to 100 microns, an exterior cross-sectional dimension of the shaft is between about 50 to 250 microns, and the microfabricated needle has a length of between about 250 microns and five millimeters.

30. A method of making a microfabricated surgical device comprising:

defining features of the device in a surface of a first substrate;

joining a second substrate to the surface of the first substrate to define a mold cavity;

conformally depositing a polymer in the mold cavity to form the device; and

removing the device from the mold cavity.

31. The method of claim 30 where the first and second substrates are each made of material selected from the group consisting of silicon, glass or a polymer.

32. The method of claim 30 wherein the polymer being deposited is either Parylene, polystyrene or Teflon®

.

33. The method of claim 30 wherein the polymer is deposited by gas vapor deposition.

34. The method of claim 30 wherein the features of a plurality of devices are formed in the surface of the first substrate.

36. The method of claim 35 where the first and second substrates are each made of a material selected from the group consisting of silicon, glass or a polymer.

37. The method of claim 35 wherein the polymer is Parylene.

38. The method of claim 37 wherein the Parylene is deposited by gas vapor deposition.

39. The method of claim 35 wherein the sacrificial release layer is either an electroplated photoresist, a polymer, a metal, a semiconductor material, an oxide, or a microsoap.

35. A method of making a microfabricated surgical device comprising:

defining features of the device in a surface of a first substrate;

forming a sacrificial release layer on the surface of the first substrate;

joining a second substrate to the first substrate to define a mold cavity;

forming a conformal layer of a polymer in the mold cavity; and

removing the sacrificial release layer to release the device form the mold cavity.

40. A method of making a microfabricated surgical device comprising:

providing a substrate having a thickness approximately equal to a thickness of the device;

defining features of the device by forming a mold from the substrate;

forming a conformal layer of a polymer on the mold; and

removing at least a portion the mold such that the device includes a hollow portion.

41. A method for making a microfabricated surgical device comprising:

providing a substrate having a thickness approximately equal to a thickness of the device;

defining features of the device by etching through the substrate to form a mold;

forming a conformal layer of a polymer on the mold; and

etching the mold such that the device includes a hollow portion.

42. The method of claim 41 wherein the mold is etched such that the device includes a hollow shaft and a tip portion including the substrate material.

43. The method of claim 41 wherein the mold is etched such that the device has a hollow base, and shaft and tip portions including the substrate material.

44. The method of claim 41 wherein the substrate being provided is selected from the group consisting of silicon, metal, glass or a polymer.

45. The method of claim 41 wherein the conformal layer is formed by gas vapor deposition of Parylene.

47. The method of claim 46 where the first and second substrates are each made of a material selected from the group consisting of silicon, glass or a polymer.

48. The method of claim 46 wherein the polymer is either Parylene, polystyrene or Teflon®

.

49. The method of claim 46 wherein the polymer is deposited by gas vapor deposition.

50. The method of claim 46 wherein the features of a plurality microneedles are formed in the surface of the first substrate.

51. The method of claim 46 wherein the metallic layer is formed by sputtering.

52. The process of claim 46 wherein the metal for the metallic layer being formed is selected from the group consisting of aluminum, gold, nickel, tungsten, zirconium, palladium, platinum, titanium, or alloys thereof.

53. The process of claim 46 wherein the first and second sacrificial layers being coated are each an electroplated photoresist.

54. The process of claim 46 wherein the second sacrificial layer is patterned such that the metallic layer, after the etching step, will remain only at a tip portion of the microneedle.

46. A process for making a microneedle comprising:

defining features of the microneedle in a surface of a first substrate;

coating the surface of the first substrate with a first sacrificial layer;

forming a metallic layer on the first sacrificial layer;

coating the metallic layer with a second sacrificial layer and patterning the second sacrificial layer;

joining a second substrate to the first substrate to define a mold cavity;

conformally depositing a polymer layer in the mold cavity to form the microneedle; and

etching the first and second sacrificial layers to remove the microneedle from the mold.

55. A method of making a microfabricated surgical device comprising:

defining features of the device in a surface of a first substrate;

forming a sacrificial release layer on the surface of the first substrate;

depositing a silicon nitride layer on the sacrificial release layer;

joining a second substrate to the first substrate to define a mold cavity;

forming a conformal layer of a polymer in the mold cavity; and

removing the sacrificial release layer to release the device form the mold cavity.