Optically-active nanoparticles for use in therapeutic and diagnostic methods

• US 6,530,944 B2
• Filed: 02/08/2001
• Issued: 03/11/2003
• Est. Priority Date: 02/08/2000
• Status: Expired due to Term

• Current Assignee: Rice University
• Original Assignee: Rice University
• Inventors: Hirsch, Leon R., Halas, Nancy J., West, Jennifer L.
• Primary Examiner(s): GIBSON, ROY DEAN
• Application Number:
  US09/779,677
• Publication Number:
  US 20020103517A1
• Time in Patent Office: 761 Days
• Field of Search: 607/88, 607/89, 607/92, 607/94, 607/103, 604/20, 606/2, 606/10, 606/14, 606/15, 606/33, 424/497, 424/490, 428/403
• US Class Current: 607/88
• CPC Class Codes: A61K 41/0042 Photocleavage of drugs in vivo, e.g. cleavage of photolabile linkers in vivo by UV radiation for releasing the pharmacologically-active agent from the administered agent; photothrombosis or photoocclusion
• CPC Class Codes: A61K 41/0052 Thermotherapy; Hyperthermia; Magnetic induction; Induction heating therapy

Abstract

This invention is generally in the field of improved methods for the localized delivery of heat and the localized imaging of biological materials. The delivery may be in vitro or in vivo and is useful for the localized treatment of cancer, inflammation or other disorders involving overproliferation of tissue. The method is also useful for diagnostic imaging. The method involves localized induction of hyperthermia in a cell or tissue by delivering nanoparticles to said cell or tissue and exposing the nanoparticles to an excitation source under conditions wherein they emit heat.

Claims

1. A method for inducing localized hyperthermia in a cell or tissue comprising the steps of delivering nanoparticles to said cell or tissue and exposing said nanoparticles to infrared radiation under conditions wherein said nanoparticles emit heat upon exposure to said infrared radiation.

2. The method of claim 1 wherein the nanoparticles are nanoshells wherein the core material is dielectric or semiconducting and the shell material is conducting.

3. The method of claim 2 wherein the nanoparticles are nanoshells and have a silica core and the shell is metal.

4. The method of claim 1 wherein the nanoparticles are comprised of silica doped with rare earth emitters.

5. The method of claim 1 wherein the nanoparticles are nanoshells and have a core comprised of gold sulfide and a shell comprised of gold.

6. The method of claim 1 wherein the infrared radiation is of wavelengths from 800 nm to 1300 nm or from 1600 nm to 1850 nm.

7. The method of claim 1 wherein said nanoparticles absorb said radiation.

8. The method of claim 1 further comprising the step of coupling molecules to the nanoparticles wherein said molecules specifically bind to the cell or tissue.

9. The method of claim 8 wherein the binding is by the formation of an antigen-antibody complex.

10. The method of claim 8 wherein the binding is by the formation of a ligand-receptor complex.

11. The method of claim 8 wherein said molecules are coupled to the nanoparticles by a polymer tethering chain.

12. The method of claim 1 wherein said cell is a cancer cell.

13. A method for inducing localized hyperthermia in a cell or tissue comprising the steps of delivering nanoshells to said cell or tissue and exposing said nanoshells to radiation selected from the group consisting of ultrasound, magnetic fields, and electric fields under conditions wherein said nanoshells emit heat upon exposure to said radiation.

14. A method for inducing localized hyperthermia in a cell or tissue comprising the steps of administering nanoshells to an animal and exposing said nanoshells to electromagnetic radiation under conditions wherein said nanoshells emit heat upon exposure to said electromagnetic radiation.

15. The method of claim 14 wherein said animal is human.

16. The method of claim 14 further comprising the step of coupling molecules to the nanoshells wherein said molecules specifically bind to the cell or tissue.

17. The method of claim 16 wherein the binding is by the formation of an antigen-antibody complex.

18. The method of claim 16 wherein the binding is by the formation of a ligand-receptor complex.

19. The method of claim 16 wherein said coupling molecules are antibodies, fragments of antibodies, ligands for specific receptors or proteins binding specifically to the cell or tissue.

20. The method of claim 16 wherein said molecules are coupled to the nanoshells by a polymer tethering chain.

21. The method of claim 20 wherein said polymer tethering chain is a difunctional polyethylene glycol derivative.

22. The method of claim 14 wherein said cells or tissue are cancerous.

23. The method of claim 14 wherein said electromagnetic radiation is selected from the group consisting of ultraviolet, visible, infrared and any combination thereof.

24. The method of claim 23 wherein said electromagnetic radiation is infrared radiation.

25. The method of claim 24 wherein said infrared electromagnetic radiation is between 800 nm and 1300 nm.

26. The method of claim 24 wherein said infrared electromagnetic radiation is between 1600 nm and 1850 nm.

27. The method of claim 24 further comprising the step of coupling molecules to the nanoshells wherein said molecules specifically bind to the cell or tissue.

28. The method of claim 27 wherein the binding is by the formation of an antigen-antibody complex.

29. The method of claim 27 wherein the binding is by the formation of a ligand-receptor complex.

30. The method of claim 27 wherein said coupling molecules are antibodies, fragments of antibodies, ligands for specific receptors or proteins binding specifically to the cell or tissue.

31. The method of claim 27 wherein said molecules are coupled to the nanoshells by a polymer tethering chain.

32. The method of claim 31 wherein said polymer tethering chain is a difunctional polyethylene glycol derivative.

33. The method of claim 14 wherein said nanoshells are encapsulated in a liposome.

34. A method for inducing localized hyperthermia in a cell or tissue comprising the steps of delivering nanoshells to cell or tissue and exposing said nanoshells to radiation selected from the group consisting of ultraviolet, visible, or infrared and any combination thereof under conditions wherein said nanoshells emit heat upon exposure to said radiation.

35. The method of claim 34 further comprising the step of coupling molecules to the nanoshells wherein said molecules specifically bind to the cell or tissue.

36. The method of claim 35 wherein the binding is by the formation of an antigen-antibody complex.

37. The method of claim 35 wherein the binding is by the formation of a ligand-receptor complex.

38. The method of claim 35 wherein said coupling molecules are antibodies, fragments of antibodies, ligands for specific receptors or proteins binding specifically to the cell or tissue.

39. The method of claim 35 wherein said molecules are coupled to the nanoshells by a polymer tethering chain.

40. The method of claim 39 wherein said polymer tethering chain is a difunctional polyethylene glycol derivative.

41. The method of claim 34 wherein said cells or tissue are cancerous.

42. The method of claim 34 wherein said radiation is infrared radiation.

43. The method of claim 42 wherein said infrared radiation is between 800 nm and 1300 nm.

44. The method of claim 42 wherein said infrared radiation is between 1600 nm and 1850 nm.

45. A method for inducing localized hyperthermia in non-cellular non-tissue material comprising the steps of delivering nanoshells to said non-cellular, non-tissue material and exposing said nanoshells to radiation selected from the group consisting of ultraviolet, visible, or infrared and any combination thereof under conditions wherein said nanoshells emit heat upon exposure to said radiation.

46. The method of claim 45 wherein said non-cellular non-tissue material is plaque.

47. A method for denaturing proteins comprising the step of inducing localized hyperthermia comprising the steps of delivering nanoshells to said proteins and exposing said nanoshells to a source of electromagnetic radiation under conditions wherein said nanoshells emit heat upon exposure to said electromagnetic radiation.

48. A method for diagnostic imaging of cell or tissue comprising delivering nanoparticles to the cell or tissue and exposing said nanoparticles to electromagnetic radiation under conditions wherein said nanoparticles illuminate the cell or tissue.

49. The method of claim 48 wherein said electromagnetic radiation is selected from the group consisting of ultraviolet, visible, and infrared radiation.

50. The method of claim 49 wherein said nanoparticles absorb or scatter said radiation.

51. The method of claim 49 wherein said electromagnetic radiation is infrared radiation.

52. The method of claim 48 wherein said nanoparticles act as contrast agents with respect to said radiation.

53. The method of claim 48 wherein the nanoparticles have a core and a shell wherein the core is a dielectric or is semiconducting and the shell is conducting.

54. The method of claim 53 wherein the nanoparticles have a silica core and the conducting shell is metal.

55. The method of claim 53 wherein the nanoparticles have a core comprised of gold sulfide and a shell comprised of gold.

56. The method of claim 48 wherein the nanoparticles are comprised of silica doped with rare earth emitters.

57. The method of claim 56 wherein the rare earth emitter is Pr⁺³, Er⁺³, or Nd⁺³.

58. The method of claim 48 wherein said nanoparticle absorbs, fluoresces, or scatters said radiation.

59. The method of claim 48 further comprising the step of coupling molecules to the nanoparticles wherein said molecules specifically bind to the cell or tissue.

60. The method of claim 59 wherein the binding is by the formation of an antigen-antibody complex.

61. A method for diagnostic imaging of cell or tissue comprising the steps of delivering nanoparticles comprising silica doped with rare earth emitters to the cell or tissue and exposing said nanoparticles to ultraviolet, visible, or infrared radiation, or any combination thereof under conditions wherein said nanoparticles illuminate the cell or tissue.

62. A method for diagnostic imaging of cell or tissue comprising the steps of delivering nanoparticles to the cell or tissue and exposing said nanoparticles to radiation selected from the group consisting of ultrasound, magnetic fields, and electric fields.

63. A method for diagnostic imaging of non-cellular non-tissue material comprising the steps of delivering nanoparticles to the non-cellular non-tissue material and exposing said nanoparticles to radiation selected from the group consisting of ultrasound and electric fields.

64. The method of claim 63 wherein said non-cellular non-tissue material is plaque.

65. A method diagnostic imaging of cell or tissue comprising the steps of administering nanoparticles to an animal and exposing said nanoparticles to electromagnetic radiation wherein said nanoparticles illuminate the cell or tissue of said animal.

66. The method of claim 65 wherein said animal is human.

67. A method diagnostic imaging of non-cellular non-tissue material comprising the steps of administering nanoparticles to an animal and exposing said nanoparticles to electromagnetic radiation wherein said nanoparticles illuminate non-cellular non-tissue material of said animal.

68. The method of claim 67 wherein said animal is human.