• Media type: E-Article
  • Title: Synthesis of a new HYNIC-DAPI derivative for labelling with ⁹⁹ᵐTechnetium and its in vitro evaluation in an FRTL5 cell line
  • Contributor: Ferl, Sandra [Author]; Wunderlich, Gerd [Author]; Smits, René [Author]; Hoepping, Alexander [Author]; Naumann, Anne [Author]; Kotzerke, Jörg [Author]
  • Published: London: Royal Society of Chemistry, [2020]
  • Published in: MedChemComm ; 6,5 (2015), Seite 887-897
  • Language: English
  • DOI: 10.1039/c4md00574k
  • Keywords: Biokonjugation ; Fluorochrom ; bioconjugation ; Zellkompartimente ; Fluoreszenzfarbstoff ; cell compartments ; DNA-bindende Einheiten ; DNA-binding moieties ; fluorescent dye
  • Origination:
  • Footnote:
  • Description: 4′,6-Diamidine-2-phenylindole (DAPI) is a common fluorochrome that is able to bind to deoxyribonucleic acid (DNA) with distinct, sequence-dependent enhancement of fluorescence. This work presents the synthesis of a new multifunctional compound that includes the fluorescent dye as a ⁹⁹ᵐTechnetium (⁹⁹ᵐTc) carrier. A new technique for the bioconjugation of DAPI with 6-hydrazinonicotinic acid (HYNIC) through an amide linkage was developed. The radiolabelling was performed with HYNIC as a chelator and N-IJ2-hydroxy-1,1-bisIJhydroxymethyl)ethyl)glycine (tricine) as a coligand. Furthermore, experimental evidence showed that ⁹⁹ᵐTc complexes with DAPI as DNA-binding moieties are detectable in living Fischer rat thyroid follicular cell line 5 (FRTL5) and their nuclei. The investigations indicated further that the new HYNIC-DAPI derivative is able to interact with double-stranded DNA. This establishes the possibility of locating ⁹⁹ᵐTc in close proximity to biological structures of living cells, of which especially the genetic information-carrying cell compartments are at the centre of interest. In this context, further investigations are related to the radiotoxic effects of DNA-bound ⁹⁹ᵐTc-HYNIC-DAPI derivatives and dosimetric calculations.
  • Access State: Open Access
  • Rights information: In Copyright