A RAPID HPLC METHOD FOR THE QUANTIFICATION OF GSH AND GSSG IN OCULAR LENS

Purpose. To develop a rapid and accurate method for the quantification of reduced glutathione (GSH) and oxidized glutathione (GSSG) using mi cro-quantities of ocular lens. Methods. The epithelium, cortex and nuc leus of the lens were separated and also the whole lens was homogenize d in 3% metaphosphoric acid. The homogenate was ultrafiltered by centr ifugation at 10,000 g in an Amicon microconcentrator, molecular weight cut off 3,000 g. The method does not require prior derivatization of the glutathiones. The filtrate was analyzed on a Mircosorb-MV by a hig h performance liquid chromatography (HPLC) column using an isocratic s olvent system (3% methanol and 10 mM potassium phosphate, pH 3.0) and detection at 200 nm. Results. The GSH and GSSG were eluted from the HP LC column at retention times 5 and 10 min, respectively. The detection limit was 10 pmoles applied to the column. The recovery of GSH and GS SG added to the tissue samples was 97-100%. Conclusions. A fast and se nsitive HPLC-method for the quantification of picomole quantities of G SH and GS SG in ocular lens, which does not require prior derivatizati on, has been developed.