Occlusive biomedical devices, punctum plugs, and methods of use thereof

• US 20050197614A1
• Filed: 03/04/2005
• Published: 09/08/2005
• Est. Priority Date: 03/04/2004
• Status: Abandoned Application

• Current Assignee: Claria Corporation
• Original Assignee: Claria Corporation
• Inventors: Flowers, Cedric, Pritchard, Wilson, Prescott, Tony, Mendius, Rick, Hallam, Clive
• Application Number:
  US11/071,985
• Publication Number:
  US 20050197614A1
• Time in Patent Office: Days
• US Class Current: 604/8
• CPC Class Codes: A61F 2210/0061 swellable
• CPC Class Codes: A61F 9/00772 Apparatus for restoration of tear ducts

Abstract

Certain embodiments include a punctum plug for blocking flow of lacrimal fluid in an eye, the plug having an introducible portion comprising a dehydrated material hydratable by physiological saline to swell from a first diameter to a second diameter that is at least 50% greater than the first diameter, wherein the portion is swellable by the lacrimal fluid to occlude the punctal opening to block the flow of the lacrimal fluid through the punctal opening, wherein the dehydratable material degrades in less than about seven days in the punctal opening of the patient. Certain embodiments include a device for occluding a nasolacrimal passage, the device comprising an introducible portion made with an anisotropically swellable material. Some embodiments are punctum plugs made with a polysaccharide in the group consisting of gellan, welan, S-88, S-198 and rhamsan gum.

Claims

1. A punctum plug for blocking flow of lacrimal fluid in an eye comprising:

an introducible portion of the plug sized for introduction into a punctal opening of the eye, the portion comprising a dehydrated material hydratable by physiological saline to swell from a first diameter to a second diameter that is at least 50% greater than the first diameter, wherein the portion is swellable by the lacrimal fluid to occlude the punctal opening to block the flow of the lacrimal fluid through the punctal opening, wherein the dehydratable material degrades in less than about seven days in the punctal opening of the patient.

2. The plug of claim 1, wherein the second diameter is at least twice the first diameter.

3. The plug of claim 1, wherein the introducible portion is a shaft.

4. The plug of claim 1, wherein the shaft further comprises a ridge or a collapsible portion.

5. The plug of claim 4, wherein the shaft is connected to a head formed substantially as a dome.

6. The plug of claim 1, wherein the dehydrated material is partially dehydrated prior to introduction into the punctal opening of the eye.

7. The plug of claim 1, further comprising a member that is sized to remain outside the punctal opening of the eye.

8. The plug of claim 1, wherein the dehydrated material comprises a polysaccharide.

9. The plug of claim 8, wherein the dehydrated material comprises a member of the group consisting of gellan, welan, S-88, S-198, and a rhamsan gum.

10. The plug of claim 1, wherein the dehydrated material comprises a member of the group consisting of alginate, curdlan, carboxymethylcellulose, crosscarmellose, poly(acrylic acid), xanthan, carrageenan, carboxymethyl chitosan, hydroxypropyl carboxymethyl cellulose, pectin, gum Arabic, karaya gum, psyllium seed gum, carboxymethyl guar, and mesquite gum.

11. The plug of claim 1, wherein the plug comprises a therapeutic agent for release from the plug after contact with the lacrimal fluid.

12. The plug of claim 1, wherein the plug comprises a preservative agent, an antimicrobial agent, an agent that is both a preservative and an antimicrobial, or a combination thereof.

13. The plug of claim 1, wherein the plug comprises silver.

14. The plug of claim 1, wherein the plug is comprised of anionic polymers crosslinked by an insoluble metal salt.

15. A method of occluding a punctal opening of an eye comprising:

introducing an introducible portion of a punctum plug into the punctal opening of the eye, the introducible portion comprising a dehydrated material hydratable by physiological saline to swell from a first diameter to a second diameter that is at least 50% greater than the first diameter, wherein the portion is swellable by the lacrimal fluid to occlude the punctal opening to block the flow of the lacrimal fluid.

16. The method of claim 15, further comprising inserting said introducible portion through the punctal opening until a head of the punctum plug is positioned outside and adjacent to the punctal opening.

17. The method of claim 15, wherein the second diameter is at least twice the first diameter.

18. The method of claim 15, wherein the dehydrated material is partially dehydrated prior to introduction into the punctal opening of the eye.

19. The method of claim 15, wherein the dehydrated material comprises a polysaccharide.

20. The method of claim 19, wherein the dehydrated material comprises a member of the group consisting of gellan, welan, S-88, S-198, and a rhamsan gum.

21. The method of claim 15, wherein the plug further comprises a therapeutic agent for release from the plug after contact with the lacrimal fluid.

22. The method of claim 15, wherein the plug comprises a preservative agent, an antimicrobial agent, an agent that is both a preservative and an antimicrobial, or a combination thereof.

23. The method of claim 15, wherein the plug comprises silver.

24. The method of claim 15, wherein the plug is comprised of anionic polymers crosslinked by an insoluble metal salt.

25. A device for occluding a nasolacrimal passage, the device comprising an introducible portion that is introducible into the nasolacrimal passage to at least partially block movement of a fluid through the passage, wherein the introducible portion comprises an anisotropically swellable material that anisotropically swells in vitro in a physiological saline solution when not subjected to constraining forces.

26. The device of claim 25, wherein the anisotropically swellable material comprises a volume, a first length and a second length perpendicular to the first length, wherein exposure to physiological fluid causes the volume to increase, the first length to undergo a first percentage increase and the second length to undergo a second percentage increase that is less than the first percentage increase for the first length.

28. The device of claim 26, wherein the second percentage increase is less than 0%.

29. The device of claim 26, wherein the first length is structured to swell against a wall of the nasolacrimal passage when disposed in the nasolacrimal passage.

30. The device of claim 25, wherein the device further comprises a shaft and a head at a proximal end of the shaft, with the shaft comprising the introducible portion.

31. The device of claim 25, wherein the anisotropically swellable material comprises polymers processed into an arrangement of polymers that are substantially parallel to each other.

32. The device of claim 25, wherein the anisotropically swellable material comprises a polysaccharide.

33. The device of claim 32, further comprising copper or iron associated with the polysaccharide.

34. The device of claim 25, wherein the anisotropically swellable material comprises at least one polysaccharide chosen from the group consisting of gellan, welan, S-88, S-198, and a rhamsan gum.

35. The device of claim 25, wherein the anisotropically swellable material comprises an acidic polysaccharide or salt thereof depolymerized to lower the molecular weight of the acidic polysaccharide.

36. The device of claim 25, further comprising a degradable portion.

37. The device of claim 25, further comprising a therapeutic agent.

38. The device of claim 25, wherein the plug further comprises a preservative agent, an antimicrobial agent, an agent that is both a preservative and an antimicrobial, or a combination thereof.

39. The device of claim 25 further comprises a metal and the plug is degradable by metal-catalyzed oxidation using an oxidation agent.

40. The device of claim 25, wherein the device comprises silver.

41. The device of claim 25, wherein the device comprises borate.

42. The device of claim 25, wherein the introducible portion is comprised of anionic polymers crosslinked by an insoluble metal salt.

27. The device of clam 26, wherein the first percentage increase is at least 100%.

43. A method of occluding a nasolacrimal passage, the method comprising introducing an occlusive device into the passage, wherein the device comprises an introducible portion that is introducible into the passage to at least partially block movement of a fluid through the passage, wherein the introducible portion comprises an anisotropically swellable material that anisotropically swells in vitro in a physiological saline solution when not subjected to constraining forces.

44. The method of claim 43, further comprising using the device to treat at least one eye in a patient having at least one condition chosen from the group consisting of dry eye, seasonal allergy, and trauma caused by surgical correction.

45. A method of making a nasolacrimal occlusive device that includes a polymeric material made of polymers, the method comprising:

aligning the polymers of the polymeric material in a predominantly parallel orientation relative to each other.

46. The method of claim 45, wherein aligning the polymers comprises at least one technique chosen from the group consisting of spin coating, spray coating, stretching, unidirectional freezing, extrusion from liquid crystalline solution, ordered convection, and stretching plus drying of an extrusion.

47. The method of claim 45, wherein aligning the polymers comprises stretching the material.

49. The method of claim 45, wherein the polymeric material comprises at least one member of the group consisting of gellan gum and its salts, carboxymethylcellulose and its salts and alginic acid and its salts.

50. The method of claim 45, wherein aligning the polymers comprises acidification of anionic polymers before dissolution in an organic solvent.

51. The method of claim 45, wherein the device comprises silver or borate.

52. The method of claim 45, wherein the introducible portion is comprised of anionic polymers crosslinked by an insoluble metal salt.

48. The method of 47, further comprising soaking the polymeric material in a fluid comprising mineral acids, organic acids or salts of monovalent cations before stretching the polymeric material.

53. A device for occluding a nasolacrimal passage, the device comprising:

an introducible portion that is introducible into the nasolacrimal passage having a structure to at least partially block movement of a fluid through the passage, wherein at least a part of the introducible portion comprises at least one polysaccharide in the group consisting of gellan, welan, S-88, S-198 and rhamsan gum.

54. The device of claim 53, wherein the device further comprises a shaft and a head at a proximal end of the shaft, with the shaft comprising the introducible portion.

55. The device of claim 53, wherein the polysaccharide comprises an acidic polysaccharide or salts thereof depolymerized to lower the molecular weight of the acidic polysaccharide.

56. The device of claim 53, further comprising copper or iron associated with the polysaccharide.

57. The device of claim 53, wherein the polysaccharide comprises polymers processed into an arrangement of polymers that are substantially parallel to each other.

58. The device of claim 53, further comprising a therapeutic agent.

59. The device of claim 53, further comprising a preservative agent, an antimicrobial agent, an agent that is both a preservative and an antimicrobial, or a combination thereof.

60. The device of claim 53, further comprising a borate ester.

61. The device of claim 53, wherein the device is essentially completely degradable in less than about 7 days in vitro in a physiological saline solution kept at 37°

C.

62. The device of claim 61, wherein the introducible portion is the entire device.

63. The device of claim 53, wherein the device comprises silver.

64. The device of claim 53, wherein the introducible portion is comprised of anionic polymers crosslinked by an insoluble metal salt.

65. A method of occluding a punctal opening of an eye comprising:

introducing an introducible portion of a punctum plug into the punctal opening of the eye, the introducible portion comprising wherein at least a part of the introducible portion comprises at least one polysaccharide in the group consisting of gellan, welan, S-88, S-198 and rhamsan gum.

66. The method of claim 65, wherein the device further comprises a shaft and a head at a proximal end of the shaft, with the shaft comprising the introducible portion.

67. The method of claim 65, wherein the polysaccharide comprises an acidic polysaccharide or salt thereof depolymerized to lower the molecular weight of the acidic polysaccharide.

68. The method of claim 65, further comprising copper or iron associated with the polysaccharide.

69. The method of claim 65, wherein the polysaccharide comprises polymers processed into an arrangement of polymers that are substantially parallel to each other.

70. The method of claim 65, with the plug further comprising a therapeutic agent.

71. The method of claim 65, wherein the plug further comprises a preservative agent, an antimicrobial agent, an agent that is both a preservative and an antimicrobial, or a combination thereof.

72. The method of claim 65, wherein the plug further comprises a metal and the plug is degradable by metal-catalyzed oxidation using an oxidation agent.

73. The method of claim 65, further comprising shrinking the plug by exposure to hypertonic solutions.

74. The method of claim 65, wherein the plug further comprises borate.

75. The method of claim 65, wherein the device is essentially completely degradable in less than about 7 days in vitro in a physiological saline solution kept at 37°

C.

76. The method of claim 65, wherein the introducible portion is the entire device.

77. The method of claim 65, further comprising using the device for treatment of at least one eye in a patient having at least one condition chosen from the group consisting of dry eye, seasonal allergy, and trauma caused by surgical correction.

78. The method of claim 65, wherein the device comprises silver.

79. The method of claim 65, wherein the introducible portion is comprised of anionic polymers crosslinked by an insoluble metal salt.