Method for radiolabeling antibodies with yttrium-90
View Patent ↗Methods and kits for radiolabeling proteins, peptides and ligands with radiolytic isotopes, particularly yttrium-90, are disclosed, whereby sufficient purity, specific activity and binding affinity are achieved such that the radiolabeled protein may be directly administered to a patient without further column purification. Such kits and methods will be particularly useful in bringing radioimmunotherapy to the hospital and outpatient setting for the treatment of cancer.
1. A method for radiolabeling a chelator-conjugated antibody or antibody fragment with a therapeutic radioisotope for administration to a patient comprising
(i) mixing the chelator-conjugated antibody or antibody fragment with a solution comprising the therapeutic radioisotope or salt thereof; and
(ii) incubating the mixture for a time between about 2 and 10 minutes under amiable conditions such that a radiolabeled antibody or antibody fragment is produced having sufficient radioincorporation, immunoreactivity of at least 50% and a specific activity of about 5 mCi/mg to about 20 mCi/mg, without further purification of the radiolabeled antibody or antibody fragment from unincorporated radioisotope.
2. The method of claim 1 , wherein said chelator is a bifunctional chelator selected from the group consisting of MX-DTPA, phenyl-DTPA, benzyl-DTPA, CHX-DTPA, DOTA, and derivatives thereof.
3. The method of claim 1 , wherein the antibody fragment is selected from the group consisting of Fab, F(ab′) 2 , and Fv fragments.
4. The method of claim 1 , wherein step (ii) comprises incubating the mixture at a temperature in the range of from about 25° C. to about 43° C.
5. The method of claim 1 , wherein a level of radioincorporation of greater than 95% is achieved.
6. The method of claim 1 , wherein said therapeutic radioisotope is 90Y.
7. The method of claim 6 , wherein the pH of the mixture of chelator-conjugated antibody or antibody fragment and solution comprising the therapeutic radioisotope or salt thereof that is produced in step (i) is in the range of about 3 to about 6.
8. The method of claim 7 , wherein the pH is adjusted with a sodium acetate solution.
9. The method of claim 6 , wherein the specific activity of the radiolabeled antibody or antibody fragment is 10 mCi/mg to about 20 mCi/mg.
10. The method of claim 6 , wherein the radiolabeled antibody or antibody fragment produced in step (ii) has at least 70% immunoreactivity.
11. The method of claim 6 , wherein said 90Y-labeled antibody or antibody fragment having sufficient radioincorporation, and a specific activity of about 5 mCi/mg to about 20 mCi/mg, such that it may be administered directly to the patient without further purification of the radiolabeled antibody or antibody fragment from unincorporated radioisotope, is produced by an incubation time of between about 2 and ten minutes.
12. The method of claim 11 wherein said 90Y-labeled antibody or antibody fragment is produced by an incubation time of between about 2 and less than about eight minutes.
13. The method of claim 6 , wherein the antibody or antibody fragment binds specifically to CD20.
14. The method of claim 13 , wherein the antibody is 2B8.
15. The method of claim 14 , wherein the chelator is MX-DTPA.
16. The method of claim 15 , wherein a level of radioincorporation greater than 96% is achieved.
17. The method of claim 1 , further comprising diluting the radiolabeled antibody or antibody fragment to an appropriate concentration in formulation buffer for administration to a human patient without further purification of the radiolabeled antibody or antibody fragment from unincorporated radiolabel.
18. The method of claim 17 , wherein the mixture is incubated for a time of about 2 to about 5 minutes.
19. The method of claim 1 , further comprising diluting the radiolabeled antibody or antibody fragment to an appropriate concentration in formulation buffer for administration to a human patient without further purification of the radiolabeled antibody or antibody fragment from unincorporated radiolabel.
20. The method of claim 19 , wherein the formulation buffer comprises a radioprotectant and an unconjugated chelator.
21. The method of claim 20 , wherein the radioprotectant is selected from the group consisting of human serum albumin (HSA), ascorbate, ascorbic acid, and a free radical scavenger selected from the group consisting of phenol, sulfites, glutathione, cysteine, gentisic acid, nicotinic acid, ascorbyl palmitate, HOP(:O)H 2 , glycerol, sodium formaldehyde sulfoxylate, Na 2 S 2 O 5 , Na 2 S 2 O 3 , and SO 2 .
22. The method of claim 20 , wherein the unconjugated chelator is DTPA or EDTA.
23. A method for radiolabeling a MX-DTPA-conjugated antibody or antibody fragment with 90 Y for administration to a patient comprising
(i) mixing the MX-DTPA-conjugated antibody or MX-DTPA-conjugated antibody fragment with a solution comprising 90 Y or salt thereof; and
(ii) incubating the mixture for a time between about 2 and 10 minutes under amiable conditions such that a 90 Y-labeled antibody or antibody fragment is produced having sufficient radioincorporation, immunoreactivity of at least 50% and a specific activity of about 5 mCi/mg to about 20 mCi/mg, without further purification of the 90 Y-labeled antibody or antibody fragment from unincorporated 90 Y.
24. The method of claim 23 , wherein a level of radioincorporation greater than 96% is achieved.
25. The method of claim 23 , wherein the antibody or antibody fragment binds specifically to CD20.
26. The method of claim 23 , further comprising diluting the 90Y-labeled antibody or antibody fragment to an appropriate concentration in formulation buffer for administration to a human patient without further purification of the 90Y-labeled antibody or antibody fragment from unincorporated 90Y.
27. The method of claim 26 , wherein the mixture is incubated for a time of about 2 to about 5 minutes.
28. The method of claim 26 , wherein the radioprotectant is selected from the group consisting of human serum albumin (HSA), ascorbate, ascorbic acid, phenol, sulfites, glutathione, cysteine, gentisic acid, nicotinic acid, ascorbyl palmitate, HOP(:O)H 2 , glycerol, sodium formaldehyde sulfoxylate, Na 2 S 2 0 5 , Na 2 S 2 0 3 and SO 2 .
29. The method of claim 28 , wherein the formulation buffer further comprises an unconjugated chelator selected from the group consisting of DTPA and EDTA.