The CAM cancer xenograft as a model for initial evaluation of MR labelled compounds

Sci Rep. 2017 May 3:7:46690. doi: 10.1038/srep46690.

Abstract

Non-invasive assessment of the biodistribution is of great importance during the development of new pharmaceutical compounds. In this contribution, the applicability of in ovo MRI for monitoring the biodistribution of MR contrast agent-labelled compounds was investigated in mamaria carcinomas xentotransplanted on the chorioallantoic membrane (CAM) exemplarily for Gd-DOTA and cHSA-PEO (2000)16-Gd after systemic injection of the compounds into a chorioallantoic capillary vein. MRI was performed directly prior and 30 min, 3 h, 5 h, 20 h, and 40 h after injection of the compound. The biodistribution of injected compounds could be assessed by MRI in different organs of the chicken embryo as well as in xenotransplanted tumors at all time points. A clearly prolonged enhancement of the tumor substrate could be shown for cHSA-PEO (2000)16-Gd. In conclusion, high-resolution in ovo MR imaging can be used for assessment of the in vivo biodistribution of labelled compounds, thus enabling efficient non-invasive initial testing.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Breast Neoplasms / diagnostic imaging*
  • Breast Neoplasms / metabolism
  • Cell Line, Tumor
  • Chick Embryo
  • Chorioallantoic Membrane / diagnostic imaging*
  • Chorioallantoic Membrane / metabolism
  • Contrast Media / administration & dosage
  • Contrast Media / pharmacokinetics*
  • Female
  • Heterocyclic Compounds / administration & dosage
  • Heterocyclic Compounds / pharmacokinetics*
  • Humans
  • Magnetic Resonance Imaging / methods*
  • Organometallic Compounds / administration & dosage
  • Organometallic Compounds / pharmacokinetics*
  • Time Factors
  • Tissue Distribution
  • Transplantation, Heterologous

Substances

  • Contrast Media
  • Heterocyclic Compounds
  • Organometallic Compounds
  • gadolinium 1,4,7,10-tetraazacyclododecane-N,N',N'',N'''-tetraacetate