Evaluation of chromosomal aberrations induced by 188Re-dendrimer nanosystem on B16f1 melanoma cells

Int J Radiat Biol. 2018 Jul;94(7):664-670. doi: 10.1080/09553002.2018.1478161. Epub 2018 Jun 19.

Abstract

Purpose: To study the rhenium-188 labeling of polyamidoamine (PAMAM) generation 4 (G4) dendrimer and its evaluation on biodistribution and chromosomal aberrations in melanoma cells induced by ionizing radiation as potential treatment agent.

Materials and methods: Dendrimers were first conjugated with Suc-HYNIC (succinimidyl 6-hydrazinopyridine-3-carboxylic acid hydrochloride). Dendrimer-HYNIC was then incubated with 188ReO4-. Biodistribution was performed administrating 188Re-dendrimer to normal (NM) or melanoma-bearing mice (MBM). Chromosome aberration test was conducted in order to measure treatment capacity of 188Re-dendrimer in melanoma cells.

Results: Radiolabeling yield of dendrimer was approx. 70%. Biodistribution studies in NM showed blood clearance with hepatic and renal depuration. MBM showed a similar pattern of biodistribution with tumor uptake of 6% of injected dose. Aberrant metaphases quantified in control cells were 7%, increasing to 29.5% in cells treated with 15μCi (0.555 MBq) of 188Re-dendrimer for 24 h.

Conclusions: 188Re-dendrimer can produce double-stranded breaks in DNA induced by ionizing radiation in melanoma cells in vitro.

Keywords: 188Re; Dendrimer; anti-tumor therapy; chromosomal aberrations; melanoma.

MeSH terms

  • Animals
  • Cell Line, Tumor
  • Chromosome Aberrations / radiation effects*
  • DNA Breaks, Double-Stranded
  • Dendrimers / chemistry*
  • Isotope Labeling
  • Melanoma, Experimental / genetics
  • Melanoma, Experimental / pathology
  • Melanoma, Experimental / radiotherapy*
  • Mice
  • Mice, Inbred C57BL
  • Radioisotopes / pharmacokinetics
  • Radioisotopes / toxicity*
  • Rhenium / pharmacokinetics
  • Rhenium / toxicity*
  • Tissue Distribution

Substances

  • Dendrimers
  • Radioisotopes
  • Rhenium-188
  • Rhenium