Non-invasive monitoring of cytotoxicity based on kinetic changes of cellular autofluorescence

Toxicol In Vitro. 2011 Dec;25(8):2088-94. doi: 10.1016/j.tiv.2011.09.008. Epub 2011 Sep 19.

Abstract

A quantitative, non-destructive cellular autofluorescence based in vitro imaging assay has been developed and applied to study the cytotoxicity of Sodium Lauryl Sulfate (SLS) and HgCl2 on Balb/c 3T3 cells. A phenomenological double logistic model was proposed to quantify and relate the observed kinetic changes of fluorescence to the toxic potency of chemical compounds. This work forms the basis for cellular autofluorescence measurements in in vitro toxicity screening assays.

MeSH terms

  • Animals
  • BALB 3T3 Cells
  • Biological Assay
  • Cell Survival
  • Flavin-Adenine Dinucleotide / metabolism*
  • Fluorescence
  • Kinetics
  • Mercuric Chloride / toxicity*
  • Mice
  • NAD / metabolism*
  • Sodium Dodecyl Sulfate / toxicity*
  • Surface-Active Agents / toxicity*
  • Toxicity Tests / methods*

Substances

  • Surface-Active Agents
  • NAD
  • Flavin-Adenine Dinucleotide
  • Sodium Dodecyl Sulfate
  • Mercuric Chloride