User: Guest  Login
Title:

Chemoselective pre-conjugate radiohalogenation of unprotected mono- and multimeric peptides via oxime formation

Document type:
Article
Author(s):
Poethko, T; Schottelius, M; Thumshirn, G; Herz, M; Haubner, R; Henriksen, G; Kessler, H; Schwaiger, M; Wester, HJ
Abstract:
As part of our ongoing efforts in the development of new F-18-labeled peptides for clinical PET imaging. a new two-step F-18-labeling methodology based on the chemoselective oxime formation between an unprotected aminooxy-functionalized peptide and a F-18-labeled aldehyde was investigated and optimized. 4-[F-18]Fluorobenzaldehyde ([F-18]FB-CHO) was prepared by direct n.c.a. fluorination of 4-formyl-N,N,N-trimethylanilimum triflate and purified by radio-HPLC or a strong-cation-exchance/reverse phase cartridge system. The aminooxyacetic acid (Aoa) modified model peptide LEF-NH2 (Leu-Glu-Phe-NH2) and monomeric, dimeric and tetrameric RGD-containing cyclopeptides were synthesized by solid phase peptide synthesis. Radiochemical yields of N(4-[F-18]fluorobenzylidene)-oxime-formation ([F-18]FBOA) with the Aoa-modified unprotected peptides were investigated. Optimized reaction conditions (60degreesC, 0.5 mM peptide, 15 min, aqueous solution, pH 2.5) resulted in 70%-90% conjugation yields for all unprotected peptides studied. Chemoselectivity was demonstrated in competition experiments with amino acid mixtures. Biodistribution in M21 melanoma bearing mice showed improved tumor uptake and excretion behaviour in the series c(RGDfE)HEG-Dpr-[F-18]FBOA < (c(RGDfE)HEG)(2)K-Dpr-[F-18]FBOA < ((c(RGDfE)HEG)(2)K)(2)K-Dpr-[F-18]FBOA. Two hours p.i. the fraction of intact c(RGDfE)HEG-K-Dpr[F-18]FBOA in blood, liver, kidney and tumor was & GT; 90%, indicating high in vivo stability of the oxime linkage. Initial PET studies with ((c(RGDfE)HEG)(2)-K)(2)-K-Dpr-[(18) F]FBOA showed excellent imaging of M21-melanomas in mice. In conclusion, the new two-step chemoselective F-18-labeling fulfills all requirements for large scale syntheses C of peptides in clinical routine. This methodology is also adaptable to other radioisotopes (e.g. radiohalogenation in General) and will thus offer a broad field of application.
Journal title abbreviation:
Radiochim Acta
Year:
2004
Journal volume:
92
Journal issue:
4-6
Pages contribution:
317-327
Language:
eng
Print-ISSN:
0033-8230
TUM Institution:
Klinik und Poliklinik für Nuklearmedizin
 BibTeX