A cyclen-based tetraphosphinate chelator for the preparation of radiolabeled tetrameric bioconjugates

Jakub Šimeček, Petr Hermann, Jana Havlíčková, Eberhardt Herdtweck, Tobias G. Kapp, Nils Engelbogen, Horst Kessler, Hans Jürgen Wester, Johannes Notni

Research output: Contribution to journalArticlepeer-review

34 Scopus citations

Abstract

The cyclen-based tetraphosphinate chelator 1,4,7,10-tetraazacyclododecane- 1,4,7,10-tetrakis[methylene(2-carboxyethyl)phosphinic acid] (DOTPI) comprises four additional carboxylic acid moieties for bioconjugation. The thermodynamic stability constants (logKML) of metal complexes, as determined by potentiometry, were 23.11 for CuII, 20.0 for LuIII, 19.6 for YIII, and 21.0 for GdIII. DOTPI was functionalized with four cyclo(Arg-Gly-Asp-D-Phe-Lys) (RGD) peptides through polyethylene glycol (PEG4) linkers. The resulting tetrameric conjugate DOTPI(RGD)4 was radiolabeled with 177Lu and 64Cu and showed improved labeling efficiency compared with 1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid (DOTA). The labeled compounds were fully stable in transchelation challenges against trisodium diethylenetriaminepentaacetate (DTPA) and disodium ethylenediaminetetraacetic acid (ETDA), in phosphate buffered saline (PBS), and human plasma. Integrin αvβ3 affinities of the non-radioactive Lu III and CuII complexes of DOTPI(RGD)4 were 18 times higher (both IC50 about 70 picomolar) than that of the c(RGDfK) peptide (IC50=1.3 nanomolar). Facile access to tetrameric conjugates and the possibility of radiolabeling with therapeutic and diagnostic radionuclides render DOTPI suitable for application in peptide receptor radionuclide imaging (PRRI) and therapy (PRRT).

Original languageEnglish
Pages (from-to)7748-7757
Number of pages10
JournalChemistry - A European Journal
Volume19
Issue number24
DOIs
StatePublished - 10 Jun 2013

Keywords

  • bioconjugates
  • ligands
  • nuclear imaging
  • peptides
  • phosphinic acid
  • radiopharmaceuticals

Fingerprint

Dive into the research topics of 'A cyclen-based tetraphosphinate chelator for the preparation of radiolabeled tetrameric bioconjugates'. Together they form a unique fingerprint.

Cite this