DHR is a cell-
permeable fluorogenic probe that is used as an indicator of intracellular peroxynitrite formation.
1 It is oxidized by peroxynitrite to the highly fluorescent product rhodamine
in vitro. Neither nitric oxide, superoxide, nor hydrogen peroxide alone appear to oxidize DHR.
1 Formation of rhodamine can be monitored by fluorescence spectroscopy using excitation and emission wavelengths of 500 and 536 nm, respectively, or by absorbance spectroscopy at 500 nm (ε = 78,800 M
−1cm
−1).
2,3,1 DHR has been used to investigate reactive oxygen intermediates produced by endothelial cells, eosinophils, and reactive microglia.
4,5,6