Analysis of terbumeton and its major metabolites by SPE and DAD-HPLC in soil bulk water

被引:2
|
作者
Conrad, A.
Couderchet, M.
Biagianti-Risbourg, S.
机构
[1] Univ Reims, Lab Ecotoxicol, Unite Rech Vignes & Vins Champagne, F-51687 Reims 02, France
[2] Univ Reims, Lab Plantes Pesticides & Dev Durable, Unite Rech Vignes & Vins Champagne, F-51687 Reims, France
关键词
column liquid chromatography; solid-phase extraction; diode array detection; soil bulk water; s-triazine herbicides;
D O I
10.1365/s10337-006-0132-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A rapid and inexpensive method for simultaneous quantification of terbumeton (TER), and its major potential metabolites (TED; terbumeton-desethyl, TOH; terbumeton-2-hydroxy and TID; terbumeton-deisopropyl) in soil bulk water (SBW) samples is proposed. The analytical method involves extraction-concentration from SBW samples using a graphitized carbon black (GCB) cartridge followed by their separation-detection by reversed-phase high-performance liquid chromatography analysis using a C-18 column and a diode array detector. A mobile phase of acetonitrile-0.005 mol L-1 phosphate buffer (pH 7.0) (35:65, v/v) at a flow rate of 0.8 mL min(-1) in isocratic elution mode has been used. After optimization of the extraction and separation conditions, this method can be used for the simultaneous determination of investigated compounds in the range of the international limits of 0.1 mu g L-1. For TER the detection limit was 0.009 mu g L-1 and it was 0.100, 0.550, and 0.480 mu g L-1 for TED, TOH, and TID, respectively. The recoveries of TER, TED, TOH, and TID from SBW samples, measured at three levels of concentration range, were found to be between 48.0 and 102.0%. The intra-day precision measured by relative standard deviation (RSD) was always lower than 9.0%.
引用
收藏
页码:155 / 161
页数:7
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