Methods and compositions for F-18 labeling of proteins, peptides and other molecules
The present application discloses compositions and methods of synthesis and use of F-18 labeled molecules of use, for example, in PET imaging techniques. The labeled molecules may be peptides or proteins, although other types of molecules may be labeled by the described methods. Preferably, the F-18 may be conjugated to a targeting molecule by formation of a metal complex and binding of the F-18-metal complex to a chelating moiety. Alternatively, the metal may first be conjugated to the chelating group and subsequently the F-18 bound to the metal. In other embodiments, the F-18 labeled moiety may comprise a targetable construct used in combination with a bispecific or multispecific antibody to target F-18 to a disease-associated antigen, such as a tumor-associated antigen. The F-18 labeled targetable construct peptides are stable in serum at 37° C. for a sufficient time to perform PET imaging analysis.
1. A method of F-18 imaging by positron emission tomography (PET) comprising:
a) reacting F-18 with a metal selected from the group consisting of aluminum, gallium, indium, lutetium or thallium to form an F-18 metal complex;
b) attaching the F-18 metal complex to a molecule to form one or more F-18 labeled molecules;
c) administering the F-18 labeled molecules to a subject; and
d) imaging the distribution of the F-18 labeled molecule by PET scanning.
2. The method of claim 1 , wherein the F-18 labeled molecule is administered to the subject without separating the F-18 labeled molecules from unlabeled molecules.
3. The method of claim 1 , further comprising:
e) separating the F-18 labeled molecules from unlabeled molecules to produce purified F-18 labeled molecules before the F-18 labeled molecules are administered to the subject.
4. The method of claim 1 , wherein the imaged distribution of F-18 labeled molecules is indicative of the presence or absence of a disease selected from the group consisting of solid cancers, hematopoietic cancers, autoimmune disease, neurodegenerative disease and cardiovascular disease.
5. The method of claim 4 , wherein the disease is selected from the group consisting of sarcomas, melanomas, gliomas, breast cancer, lung cancer, pancreatic cancer, ovarian cancer, colorectal cancer, prostatic cancer, leukemias, lymphomas, myelomas Alzheimer's disease, myocardial infarction, congestive heart failure, cardiac necrosis, thrombosis, stroke, atherosclerosis, rheumatoid arthritis, lupus erythematosus; and AIDS.
6. The method of claim 1 , wherein the F-18 labeled molecule is used to image receptors.
7. The method of claim 6 wherein the receptors are angiogenesis receptors and the F-18 labeled molecule is Al-18F conjugated RGD-NOTA.
8. The method of claim 1 , wherein the F-18 labeled molecule is used to image tumors.
9. The method of claim 8 , wherein the F-18 labeled molecule is F-18 labeled bombesin.
10. The method of claim 8 , wherein the F-18 labeled molecule is an antibody or fragment thereof, selected from the group consisting of hLL1, hLL2, hImmu31, hPAM4, hRS7, hA1g, hA20, hMN-14, hMu-9, hMN-3, hMN-15 and hL243.
11. The method of claim 1 , wherein the F-18 labeled molecule is F-18 labeled NOTA, C-NETA or lysine-NETA and the F-18 labeled molecule is used to image renal flow.
12. The method of claim 1 , wherein the F-18 labeled molecule comprises antibody or an antibody fragment.
13. The method of claim 1 , where the F-18 labeled molecule is a targetable construct that binds to a bispecific antibody.
14. The method of claim 13 , further comprising:
i) administering a bispecific antibody to a subject, said bispecific antibody having at least one binding site for the targetable construct and at least one binding site for an antigen, wherein the presence of the antigen is indicative of a disease or condition; and
ii) allowing a sufficient amount of time for bispecific antibody that is not bound to the antigen to clear from circulation prior to the administration of the targetable construct.
15. The method of claim 14 , wherein the antigen is a tumor-associated antigen.
16. The method of claim 14 , wherein the antigen is present on a pathogenic organism.
17. The method of claim 16 , wherein the pathogen is a virus, bacterium, fungus, yeast or microorganism.
18. The method of claim 17 , wherein the virus is selected from the group consisting of human immunodeficiency virus (HIV), herpes virus, cytomegalovirus, rabies virus, influenza virus, hepatitis B virus, Sendai virus, feline leukemia virus, Reo virus, polio virus, human serum parvo-like virus, simian virus 40, respiratory syncytial virus, mouse mammary tumor virus, Varicella-Zoster virus, Dengue virus, rubella virus, measles virus, adenovirus, human T-cell leukemia viruses, Epstein-Barr virus, murine leukemia virus, mumps virus, vesicular stomatitis virus, Sindbis virus, lymphocytic choriomeningitis virus, wart virus and blue tongue virus; or the bacterium is selected from the group consisting of Streptococcus agalactiae, Legionella pneumophila, Streptococcus pyogenes, Escherichia coli, Neisseria gonorrhoeae, Neisseria meningitidis, Pneumococcus, Hemophiluis influenzae B, Treponema pallidum, Lyme disease spirochetes, Pseudomonas aeruginosa, Mycobacterium leprae, Brucella abortus, Mycobacterium tuberculosis and Clostridium tetani.
19. The method of claim 15 , wherein the antigen is selected from the group consisting of colon-specific antigen-p (CSAp), carcinoembryonic antigen (CEA), CD4, CDS, CD8, CD14, CD15, CD19, CD 2 O, CD21, CD22, CD23, CD25, CD30, CD45, CD66a-d, CD67, CD74, CD79a, CD80, CD138, HLA-DR, Ia, Ii, MUC1, MUC2, MUC3, MUC4, NCA, EGFR, HER 2/neu receptor, TAG-72, EGP-1, EGP-2, A3, KS-1, Le(y), S100, PSMA, PSA, tenascin, folate receptor, VEGFR, EGFR, PDGFR, FGFR, P1GF, ILGF-1, necrosis antigens, IL-2, IL-6, T101, MAGE, or a combination of these antigens.
20. The method of claim 19 , wherein the bispecific antibody comprises an antibody or fragment thereof selected from the group consisting of hLL1, hLL2, hImmu31, hPAM4, hRS7, hAl9, hA20, hMN-14, hMu-9, hMN-3, hMN-15 and hL243.
21. The method of claim 1 , wherein the molecule is folic acid.
22. The method of claim 1 , wherein the molecule is TA138.