M. Zhou et al., DETERMINATION OF METSULFURON METHYL AND ITS 2 METABOLITES IN CROPS BYLIQUID-CHROMATOGRAPHY WITH ULTRAVIOLET DETECTION, Journal of AOAC International, 77(6), 1994, pp. 1654-1659
Metsulfuron methyl, its hydroxy metabolite (A1), and its glucose conju
gate metabolite (A) were determined in several crops by liquid chromat
ography (LC) using a simple extraction and cleanup scheme. After the p
arent and 2 major metabolites were extracted from crops with methanol,
metabolite A was enzymatically hydrolyzed to metabolite A1 with beta-
glucosidase. The treated extracts were cleaned up chromatographically,
and then metsulfuron methyl and metabolite A1 were quantitatively det
ermined by reversed-phase LC with UV detection at 254 nm. Recovery of
metsulfuron methyl and its 2 metabolites was 90 +/- 6% over a range of
0.005 to 0.4 ppm from fortified samples of brown grain, wheat, barley
, sugarcane stalk, and oat straw. Method detection limits (MDLs) were
0.005 ppm for metsulfuron methyl, 0.006 ppm for metabolite A, and 0.00
3 ppm for metabolite Al in such crops as brown grain, wheat, barley, a
nd sugarcane, and 0.01 ppm far metsulfuron methyl, 0.015 ppm for metab
olite A, and 0.01 ppm for metabolite A1 in oat straw. The MDLs were es
timated on the basis of a signal-to-noise ratio of 5 within a confiden
ce interval of 95%. The method has potential application for the analy
ses of these analytes in other crops and feeds and may be applicable t
o other sulfonylurea herbicides.