Methods for circumventing the problem of free radial reduction associated with the use of stable nitroxide free radicals as contrast agents for magnetic reasonance imaging

• US 4,863,717 A
• Filed: 11/10/1986
• Issued: 09/05/1989
• Est. Priority Date: 11/10/1986
• Status: Expired due to Fees

• Current Assignee: Oregon State University (Oregon University System)
• Original Assignee: University of Oregon
• Inventors: Keana, John F. W.
• Primary Examiner(s): Warden, Robert J.
• Assistant Examiner(s): NOT, DEFINED
• Application Number:
  US06/928,943
• Time in Patent Office: 1,030 Days
• Field of Search: 424/9, 128/653, 128/654, 436/173, 436/803, 436/806, 564/300, 548/542, 514/645, 514/408, 530/391
• US Class Current: 424/9.321
• CPC Class Codes: A61K 49/1812 liposomes, polymersomes, e.g. immunoliposomes
• CPC Class Codes: A61K 49/20 containing free radicals , e.g. trityl radical for overhauser
• CPC Class Codes: C07C 291/04 containing amino-oxide bonds
• CPC Class Codes: Y10S 436/803 Stabe free radicals, e.g. spin immunoassay
• CPC Class Codes: Y10S 436/806 Electrical property or magnetic property
• CPC Class Codes: Y10T 436/24 Nuclear magnetic resonance, electron spin resonance or other spin effects or mass spectrometry

Abstract

Nitroxide contrast agents for MRI have a long useful life and can be administered in low concentration doses. Such agents include nitroxide-doped liposomes that encapsulate an oxidant and large molecules having surfaces covered with persistent nitroxide free radicals.

Claims

1. In an MRI contrast agent which is a liposome having a bound spin label that is subject to reduction, and thus loss of contrast enhancement capability when in a reducing environment, the improvement wherein the liposome incorporates oxidizing means for oxidizing and thereby restoring spin labels that have been reduced.

2. The contrast agent of claim 1 wherein the oxidizing means comprises an amount of an oxidant substance encapsulated within a compartment defined by the liposome.

3. A contrast agent of claim 1 in which an antibody, carbohydrate, or other cell recognition targeting agent is attached to the liposome to provide specific targeting.

4. An MRI contrast agent, the agent comprising:

a liposome having a bilayer shaped to define a compartment;

multiple nitroxides incorporated into the bilayer; and

an oxidant substance inside the compartment.

5. The contrast agent of claim 4 wherein the oxidant substance comprises K₃ Fe(CN)₆.

6. A contrast agent of claim 4 in which an antibody, carbohydrate, or other cell recognition targeting agent is attached to the liposome to provide specific targeting.

7. A diagnostic preparation comprising the MRI contrast agent of claim 4 in a biocompatible carrier liquid.

8. A method for enhancing the magnetic resonance image of a target tissue, the method comprising providing, in the target tissue, an MRI contrast agent according to claim 4.

9. An MRI contrast agent comprising a molecule or assembly of molecules, the molecule or assembly having at least ten nitroxide groups positioned to contact surrounding bulk water and effect magnetic relaxation.

10. A contrast agent of claim 9 in which an antibody, carbohydrate, or other cell recognition targeting agent is attached to the molecule to provide specific targeting.

11. The contrast agent of claim 9 comprising a nitroxide doped liposome.

12. The contrast agent of claim 11 comprising a liposome formed from amphipathic molecules, substantially all such molecules having at least one nitroxide group.

13. The contrast agent of claim 11 comprising a liposome formed from amphipathic molecules having at least two nitroxide groups.

14. The contrast agent of claim 11 comprising a liposome formed from amphipathic molecules having three nitroxide groups.

15. The contrast agent of claim 11 wherein the liposome is made up of amphipathic molecules of which the long chains are polymerizable such that, after polymerization of the chains, rapid take-up of the liposome by the liver and spleen is inhibited.

16. The contrast agent of claim 9 comprising a liposome formed from multiple chain amphiphatic molecules attached to a polar group, each chain having a nitroxide group sufficiently near the polar group that the nitroxide can contact bulk water.

17. The contrast agent of claim 16 wherein at least one of the amphipathic molecules have more than two chains.

18. The contrast agent of claim 16 wherein the polar group has at least one nitroxide group.

19. The contrast agent of claim 16 comprising a liposome formed from cations of the formula:

##STR24## wherein R is an alkyl or aromatic group with or without hetero atoms present and with or without a nitroxide.

20. The contrast agent of claim 19 wherin R is --CH₃ or ##STR25##

21. The contrast agent of claim 9 comprising a nitroxide-doped, linear or branched polymer of a molecular weight not more than about 10,000.

22. The contrast agent of claim 21 comprising an arborol of the formula:

##STR26## wherein R is an acyl nitroxide, phosphoryl nitroxide or aromatic nitroxide.

23. A diagnostic preparation comprising the MRI contrast agent of claim 9 in a biocompatible carrier liquid.

24. A method for enhancing the magnetic resonance image of a target tissue, the method comprising providing, in a target tissue, an MRI contrast agent comprising a molecule or assembly of molecules, the molecule or assembly having at least ten nitroxide groups positioned to contact surrounding bulk water and effect magnetic relaxtion, the agent being provided in an amount sufficient to enhance the magnetic resonance image of the target tissue.

25. The method of claim 24 in which an antibody, carbohydrate, or other cell recognition targeting agent is attached to the molecule to provide specific targeting.

26. The method of claim 24 wherein the contrast agent comprises a nitroxide doped liposome.

27. The method of claim 26 wherein the contrast agent comprises a liposome formed from amphipathic molecules, substantially all of such molecules having at least one nitroxide group.

28. The method of claim 26 wherein the contrast agent comprises a liposome formed from amphipathic molecules having at least two nitroxide groups.

29. The method of claim 26 wherein the contrast agent comprises a liposome formed from amphipathic molecules having three nitroxide groups.

30. The method of claim 26 wherein the contrast agent comprises a liposome made up of amphipathic molecules of which the long chains are polymerizable such that, after polymerization of the chains, rapid take-up of the liposome by the liver and spleen is inhibited.

31. The method of claim 26 wherein the contrast agent comprises a liposome formed from multiple double chain amphipathic molecules attached to a polar group, each chain having a nitroxide group sufficiently near the polar group that the nitroxide can contact bulk water.

32. The method of claim 31 wherein at least some of the amphipathic molecules have more than two chains.

33. The method of claim 31 wherein the polar group has at least one nitroxide group.

34. The method of claim 31 wherein the contrast agent comprises a liposome formed from cations of the formula:

##STR27## wherein R is an alkyl or aromatic group with or without hetero atoms present and with or without a nitroxide.

35. The method of claim 34 wherein R is --CH₃ or ##STR28##

36. The method of claim 24 wherein the contrast agent comprises a nitroxide-doped, linear or branched polymer of a molecular weight not more than about 10,000.

37. The method of claim 36 wherein the contrast agent comprises an arborol of the formula ##STR29## wherein R is an acyl nitroxide, phosphoryl nitroxide or aromatic nitroxide.

38. The method of claim 36 wherein the arborol is bound to a liposome.

39. The method of claim 38 in which an antibody, carbohydrate, or other cell recognition targeting agent is attached to the liposome to provide specific targeting.

40. A salt of the cation:

##STR30## wherein R is an alkyl or aromatic group with or without hetero atoms present and with or without a nitroxide.

41. The salt of claim 40 wherein R is --CH₃ or ##STR31##

42. A salt of claim 40 wherein the anion is a halide.

43. A liposome formed from a salt of claim 40.

44. An arborol of the formula:

##STR32## wherein R is an acyl nitroxide, phosphoryl nitroxide or aromatic nitroxide.