CPC A61K 51/082 (2013.01) [A61K 9/51 (2013.01); A61K 47/6893 (2017.08); A61K 51/1027 (2013.01); C07D 255/02 (2013.01); C07D 257/02 (2013.01); C07K 7/06 (2013.01); C07K 7/64 (2013.01); C07K 16/30 (2013.01); G01N 33/5008 (2013.01); G01N 33/60 (2013.01); C07K 2319/00 (2013.01)] | 12 Claims |
1. A composition comprising:
a. a first targeting probe comprising:
i) an antibody or fragment thereof targeting a first cancer antigen, and
ii) a first bioorthogonal ligation moiety; and
b. a second targeting probe comprising:
i) a peptide targeting a second cancer antigen,
ii) a second bioorthogonal ligation moiety, and
iii) a detectable label;
wherein the antibody of fragment thereof is selected from the group consisting of cetuximab, pertuzumab, trastuzumab, bevacizumab, mAb 8G7, 1116NS19-9, CP-870,893, atezolizumab, UMB2, etaracizumab, and E398P
wherein the peptide is selected from the group consisting of LLP2A, AE105, BBN(7-14), tyr(3)-octreotate, DAPTA, T140, CPCR4-2, RGD, cyclo(RGDyK), and PTP;
wherein the first bioorthogonal ligation moiety is selected from the group consisting of trans-cyclooctene, cyclooctyne, alkyne, alkene, photo-DIBO, cyclopropenone, oxa-dibenzocyclooctyne, and dibenzocyclooctyne, and the second bioorthogonal ligation moiety is selected from the group consisting of tetrazine, azide, tetrazole, and photo-tetrazole.
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