2012Journal of Liquid Chromatography & Related TechnologiesRequires access

A MICELLAR LIQUID CHROMATOGRAPHIC METHOD FOR THE DETERMINATION OF CARBARYL AND 1-NAPHTHOL IN BIOLOGICAL SAMPLES

Josep Esteve‐Romero, Sergio Marco-Peiró, Maria Rambla-Alegre, Abhi̧lasha Durgbanshi, Devasish Bose, Sandeep K. Mourya

Open publisher page 10 citations

Abstract

Micellar liquid chromatography (MLC) is a useful technique for the determination of compounds in biological samples. Here, a sensitive procedure has been developed for the determination of carbaryl, a phenyl-N-methylcarbamate, and its main metabolite, 1-naphthol, using a C18 column (150 mm × 4.6 mm) and fluorescence detection. After performing optimization studies with an interpretative strategy, the selected mobile phase was sodium dodecyl sulfate (SDS) 0.15 M – 6% (v/v) pentanol - NaH2PO4 0.01 M buffered at pH 3. The validation studies include linearity (r2 > 0.9999), limits of detection and quantification, (0.0325 and 0.1 µM for carbaryl; 0.125 and 0.350 µM for 1-naphthol, respectively), intra- and inter-day precisions below 4%, and robustness parameters below 5%, all of which are adequate for the quantification of these two compounds in urine and serum samples to be directly injected into the chromatographic system.

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What this paper is about

Micellar liquid chromatography (MLC) is a useful technique for the determination of compounds in biological samples. Here, a sensitive procedure has been developed for the determination of carbaryl, a phenyl-N-methylcarbamate, and its main metabolite, 1-naphthol, using a C18 column (150 mm × 4.6 mm) and fluorescence detection. After performing optimization studies with an interpretative strategy, the selected mobile phase was sodium dodecyl sulfate (SDS) 0.15 M – 6% (v/v) pentanol - NaH2PO4 0.01 M buffered at pH 3. The validation studies include linearity (r2 > 0.9999), limits of detection and quantification, (0.0325 and 0.1 µM for carbaryl; 0.125 and 0.350 µM for 1-naphthol, respectively), intra- and inter-day precisions below 4%, and robustness parameters below 5%, all of which are adequate for the quantification of these two compounds in urine and serum samples to be directly injected into the chromatographic system.

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Available abstract

Micellar liquid chromatography (MLC) is a useful technique for the determination of compounds in biological samples. Here, a sensitive procedure has been developed for the determination of carbaryl, a phenyl-N-methylcarbamate, and its main metabolite, 1-naphthol, using a C18 column (150 mm × 4.6 mm) and fluorescence detection. After performing optimization studies with an interpretative strategy, the selected mobile phase was sodium dodecyl sulfate (SDS) 0.15 M – 6% (v/v) pentanol - NaH2PO4 0.01 M buffered at pH 3. The validation studies include linearity (r2 > 0.9999), limits of detection and quantification, (0.0325 and 0.1 µM for carbaryl; 0.125 and 0.350 µM for 1-naphthol, respectively), intra- and inter-day precisions below 4%, and robustness parameters below 5%, all of which are adequate for the quantification of these two compounds in urine and serum samples to be directly injected into the chromatographic system.

Key concepts: Chemistry, Chromatography, Carbaryl, Micellar liquid chromatography, 1-Naphthol, Metabolite, Sodium dodecyl sulfate, Detection limit

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