Claims for Patent: 6,624,141

Summary for Patent: 6,624,141

Title:	Protamine fragment compositions and methods of use
Abstract:	Provided are bioactive, low-toxicity protamine fragments, compositions, combinations, kits and methods of using these components in a variety of embodiments, including neutralizing heparin and reducing post-operative bleeding. Improved protamine fragment-insulin solutions and methods for treating diabetes are also provided.
Inventor(s):	Yang; Victor C. (Ann Arbor, MI), Byun; Youngro (Kwangsan-Ku Kwangju, KR)
Assignee:	The Regents of The University of Michigan (Ann Arbor, MI)
Application Number:	09/700,967
Patent Claims:	1. A purified protamine that is bioactive, that has a molecular weight of between about 400 and about 2500 Daltons and that has reduced immunoresponsiveness or toxicity compared to native protamine. 2. The protamine of claim 1, wherein said bioactive protamine is a salmine protamine. 3. The protamine of claim 1, wherein said bioactive protamine is a clupeine protamine. 4. The protamine of claim 1, wherein said bioactive protamine has a molecular weight of between about 400 and about 2000 Daltons. 5. The protamine of claim 4, wherein said bioactive protamine has a molecular weight of between about 450 and about 1500 Daltons. 6. The protamine of claim 5, wherein said bioactive protamine has a molecular weight of between about 500 and about 1350 Daltons. 7. The protamine of claim 6, wherein said bioactive protamine has a molecular weight of between about 1100 and about 1300 Daltons. 8. The protamine of claim 7, wherein said bioactive protamine has a molecular weight of about 1200 Daltons. 9. A composition comprising at least a first purified bioactive protamine in accordance with claim 1. 10. The composition of claim 9, wherein said composition comprises at least a first and at least a second purified bioactive protamine. 11. The composition of claim 10, wherein said composition comprises a plurality of purified bioactive protamines. 12. The composition of claim 9, further comprising at least one additional biologically active agent. 13. The composition of claim 12, further comprising at least one additional coagulant. 14. The composition of claim 12, further comprising at least a first therapeutic protein or polypeptide. 15. The composition of claim 14, further comprising insulin. 16. The composition of claim 15, further comprising recombinant insulin. 17. The composition of claim 15, further comprising human insulin. 18. The composition of claim 9, wherein said composition is a pharmaceutical composition. 19. The composition of claim 18, wherein said pharmaceutical composition is formulated for injection. 20. The protamine of claim 4, wherein said bioactive protamine has a molecular weight of between about 1000 and about 2000 Daltons. 21. The protamine of claim 20, wherein said bioactive protamine has a molecular weight of about 1300 Daltons. 22. The protamine of claim 20, wherein said bioactive protamine has a molecular weight of about 1400 Daltons. 23. The protamine of claim 20, wherein said bioactive protamine has a molecular weight of about 1500 Daltons. 24. The protamine of claim 20, wherein said bioactive protamine has a molecular weight of about 1600 Daltons. 25. The protamine of claim 20, wherein said bioactive protamine has a molecular weight of about 1700 Daltons. 26. The protamine of claim 20, wherein said bioactive protamine has a molecular weight of about 1800 Daltons. 27. The protamine of claim 20, wherein said bioactive protamine has a molecular weight of about 1900 Daltons. 28. The protamine of claim 20, wherein said bioactive protamine has a molecular weight of about 2000 Daltons. 29. A method of preparing at least a first bioactive protamine, that has a low molecular weight and that has reduced immunoresponsiveness or toxicity compared to native protamine, comprising contacting a native protamine composition with at least a first proteolytic composition comprising an amount of at least a first proteolytic enzyme effective to produce said at least a first bioactive protamine. 30. The method of claim 29, wherein said at least a first proteolytic composition comprises at least a first thermolysin enzyme. 31. The method of claim 29, wherein said at least a first proteolytic composition comprises at least a first ficin enzyme. 32. The method of claim 29, wherein said at least a first proteolytic composition comprises at least a first collagenase enzyme. 33. The method of claim 29, wherein said at least a first proteolytic composition comprises at least a first kallikrein enzyme. 34. The method of claim 29, wherein said at least a first proteolytic composition comprises at least a first proline-specific endopeptidase enzyme. 35. The method of claim 29, wherein said at least a first proteolytic composition comprises at least a first and at least a second proteolytic enzyme. 36. The method of claim 29, wherein said at least a first proteolytic enzyme is removed after said at least a first bioactive protamine is produced. 37. The method of claim 29, wherein at least a first and a second bioactive protamine is produced. 38. The method of claim 29, wherein a plurality of bioactive protamines are produced. 39. The method of claim 29, wherein the at least a first bioactive protamine produced has a molecular weight of between about 450 Daltons and about 1350 Daltons. 40. The method of claim 29, further comprising formulating the at least a first bioactive protamine produced in a pharmaceutically acceptable composition. 41. The method of claim 29, wherein the at least a first bioactive protamine produced has a molecular weight of between about 2000 Daltons. 42. The method of claim 41, wherein the at least a first bioactive protamine produced has a molecular weight of about 1300 Daltons. 43. The method of claim 41, wherein the at least a first bioactive protamine produced has a molecular weight of about 1400 Daltons. 44. The method of claim 41, wherein the at least a first bioactive protamine produced has a molecular weight of about 1500 Daltons. 45. The method of claim 41, wherein the at least a first bioactive protamine produced has a molecular weight of about 1600 Daltons. 46. The method of claim 41, wherein the at least a first bioactive protamine produced has a molecular weight of about 1700 Daltons. 47. The method of claim 41, wherein the at least a first bioactive protamine produced has a molecular weight of about 1800 Daltons. 48. The method of claim 41, wherein the at least a first bioactive protamine produced has a molecular weight of about 1900 Daltons. 49. The method of claim 41, wherein the at least a first bioactive protamine produced has a molecular weight of about 2000 Daltons. 50. A purified, bioactive protamine that has a molecular weight of between 400 and 2500 Daltons and that has reduced immunoresponsiveness or toxicity compared to native protamine; wherein said bioactive protamine binds to and neutralizes heparin or low molecular weight heparin, forms a complex with insulin or .alpha.-interferon or prolongs the adsorption of insulin. 51. The protamine of claim 50, wherein said bioactive protamine has a molecular weight of between 400 and 2000 Daltons. 52. The protamine of claim 51, wherein said bioactive protamine has a molecular weight of between 450 and 1500 Daltons. 53. The protamine of claim 52, wherein said bioactive protamine has a molecular weight of between 500 and 1350 Daltons. 54. The protamine of claim 53, wherein said bioactive protamine has a molecular weight of between 1100 and 1300 Daltons. 55. The protamine of claim 50, wherein said bioactive protamine has a molecular weight of between 1000 and 2000 Daltons. 56. The protamine of claim 55, wherein said bioactive protamine has a molecular weight of about 1300 Daltons. 57. The protamine of claim 55, wherein said bioactive protamine has a molecular weight of about 1400 Daltons. 58. The protamine of claim 55, wherein said bioactive protamine has a molecular weight of about 1500 Daltons. 59. The protamine of claim 55, wherein said bioactive protamine has a molecular weight of about 1600 Daltons. 60. The protamine of claim 55, wherein said bioactive protamine has a molecular weight of about 1700 Daltons. 61. The protamine of claim 55, wherein said bioactive protamine has a molecular weight of about 1800 Daltons. 62. The protamine of claim 55, wherein said bioactive protamine has a molecular weight of about 1900 Daltons. 63. The protamine of claim 55, wherein said bioactive protamine has a molecular weight of about 2000 Daltons. 64. A purified, bioactive protamine that has a molecular weight of between 400 and 2000 Daltons and that has reduced immunoresponsiveness or toxicity compared to native protamine; wherein said bioactive protamine binds to and neutralizes heparin or low molecular weight heparin or prolongs the adsorption of insulin. 65. A purified, bioactive protamine that has a molecular weight of between 400 and 2000 Daltons, that retains heparin binding and neutralization activity and that has reduced immunoresponsiveness or toxicity compared to native protamine. 66. The protamine of claim 65, wherein said bioactive protamine has a molecular weight of between 450 and 1500 Daltons. 67. The protamine of claim 66, wherein said bioactive protamine has a molecular weight of between 500 and about 1350 Daltons. 68. The protamine of claim 67, wherein said bioactive protamine has a molecular weight of between 1100 and 1300 Daltons. 69. The protamine of claim 65, wherein said bioactive protamine has a molecular weight of between 1000 and 2000 Daltons. 70. The protamine of claim 69, wherein said bioactive protamine has a molecular weight of about 1300 Daltons. 71. The protamine of claim 69, wherein said bioactive protamine has a molecular weight of about 1400 Daltons. 72. The protamine of claim 69, wherein said bioactive protamine has a molecular weight of about 1500 Daltons. 73. The protamine of claim 69, wherein said bioactive protamine has a molecular weight of about 1600 Daltons. 74. The protamine of claim 69, wherein said bioactive protamine has a molecular weight of about 1700 Daltons. 75. The protamine of claim 69, wherein said bioactive protamine has a molecular weight of about 1800 Daltons. 76. The protamine of claim 69, wherein said bioactive protamine has a molecular weight of about 1900 Daltons. 77. The protamine of claim 69, wherein said bioactive protamine has a molecular weight of about 2000 Daltons. 78. A kit comprising at least a first container that comprises at least a first purified bioactive protamine in accordance with claim 1. 79. The kit of claim 78, further comprising at least one additional anticoagulant. 80. The kit of claim 79, wherein said at least one anticoagulant is heparin or low molecular weight heparin. 81. A purified, bioactive protamine that has a molecular weight of between 1000 and 2000 Daltons, that retains heparin binding and neutralization activity and that has reduced immunoresponsiveness or toxicity compared to native protamine. 82. The protamine of claim 81, wherein said bioactive protamine has a molecular weight of about 1300 Daltons. 83. The protamine of claim 81, wherein said bioactive protamine has a molecular weight of about 1400 Daltons. 84. The protamine of claim 81, wherein said bioactive protamine has a molecular weight of about 1500 Daltons. 85. The protamine of claim 81, wherein said bioactive protamine has a molecular weight of about 1600 Daltons. 86. The protamine of claim 81, wherein said bioactive protamine has a molecular weight of about 1700 Daltons. 87. The protamine of claim 81, wherein said bioactive protamine has a molecular weight of about 1800 Daltons. 88. The protamine of claim 81, wherein said bioactive protamine has a molecular weight of about 1900 Daltons. 89. The protamine of claim 81, wherein said bioactive protamine has a molecular weight of about 2000 Daltons.

Details for Patent 6,624,141

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Smith & Nephew, Inc.	SANTYL	collagenase	Ointment	101995	06/04/1965		2019-03-17