Biotin derivatives carrying two chelating DOTA units. Synthesis, in vitro evaluation of biotinidases resistance, avidin binding, and radiolabeling tests

Alessandro Pratesi, Francesca Bucelli, Ilaria Mori, Marco Chinol, Antonio Verdoliva, Giovanni Paganelli, Vincenzo Rivieccio, Lucia Gariboldi, Mauro Ginanneschi

Research output: Contribution to journalArticle

Abstract

The synthesis of four biotin derivatives carrying two DOTA moieties for each ligand (BisDOTA set) is reported, for increasing radiation/dose ratio and improving efficiency in the pretargeted avidin-biotin radioimmunotherapy. The biotin-containing scaffold of two BisDOTAwas similar to the mono-DOTA derivative previously described. Then the scaffold was elongated by trifunctionalized spacers of different length and conjugated with one of the COOH groups of two DOTA. Two others were prepared starting from a on-resin lysine residue. The lysine R-NH2 was bonded to biotin, and then spacers were appended to the ε-NH2 and conjugated with two DOTA molecules. One compound contained a p-aminobenzoic acid spacer, which ensured higher head-to-tail distance and increased rigidity of the chain. These last two compounds had a very high ability to bond avidin and were labeled with 90Y at high specific activity. All the compounds were resistant to the action of serum biotinidases.

Original languageEnglish
Pages (from-to)432-440
Number of pages9
JournalJournal of Medicinal Chemistry
Volume53
Issue number1
DOIs
Publication statusPublished - 2010

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ASJC Scopus subject areas

  • Molecular Medicine
  • Drug Discovery

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