PET imaging of infection with a HYNIC-conjugated LTB4 antagonist labeled with F-18 via hydrazone formation
DOI 10.1016/j.nucmedbio.2007.04.012, PII S096980510700128X
Rennen HJ, Laverman P, van Eerd JE, Oyen WJ, Corstens FH, Boerman OC. PET imaging of infection with a HYNIC-conjugated LTB4 antagonist labeled with F-18 via hydrazone formation. Nucl Med Biol. 2007;34:691-695. (Pubitemid 47248281)
18F-labeled tracer suitable for routine clinical imaging of sst receptor-expressing tumors using positron emission tomography
DOI 10.1158/1078-0432.CCR-03-0359
Schottelius M, Poethko T, Herz M, et al. First 18F-labeled tracer suitable for routine clinical imaging of sst receptor-expressing tumors using positron emission tomography. Clin Cancer Res. 2004;10:3593-3606. (Pubitemid 38697592)
Influence of different spacers on the biological profile of a DOTA-somatostatin analogue
DOI 10.1021/bc0601673
Antunes P, Ginj M, Walter MA, Chen J, Reubi JC, Maecke HR. Influence of different spacers on the biological profile of a DOTA-somatostatin analogue. Bioconjug Chem. 2007;18:84-92. (Pubitemid 46145997)
18F]fluoropropionyl-(D)phe1)-octreotide, a potential radiopharmaceutical for quantitative somatostatin receptor imaging with PET: Synthesis, radiolabeling, in vitro validation and biodistribution in mice
18F] fluoropropionyl-(D)phe1)-octreotide, a potential radiopharmaceutical for quantitative somatostatin receptor imaging with PET: synthesis, radiolabeling, in vitro validation and biodistribution in mice. Nucl Med Biol. 1994;21:819-825.