2010Analytical LettersRequires access

Simultaneous Determination of Theobromine, Paraxanthine, Theophylline, and Caffeine in Urine by Reversed-Phase High-Performance Liquid Chromatography with Diode Array UV Detection

Ebru Büyüktuncel

Open publisher page 12 citations

Abstract

A reversed-phase high performance liquid chromatographic method was improved for the simultaneous determination of theobromine, paraxanthine, theophylline, and caffeine in urine. The method includes a liquid-liquid extraction at alkaline pH with ethylacetate. The 7-(2,3-dihidroxypropyl) theophylline was used as an internal standard (ISTD). The separation was achieved on a C18 column using 14:86 methanol:buffer (25 mM KH2PO4 adjusted to pH 4 with ortho-phosphoric acid) solution as mobile phase under isocratic conditions at a flow rate 1 mL min−1. An ultraviolet absorption at 274 nm was monitored. In these conditions, the LOD was 0.03 μg mL−1 for theobromine, 0.02 μg mL−1 for paraxanthine, 0.04 μg mL−1 for theophylline, and 0.08 μg mL−1 for caffeine. The method has been applied to urine samples.

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A reversed-phase high performance liquid chromatographic method was improved for the simultaneous determination of theobromine, paraxanthine, theophylline, and caffeine in urine. The method includes a liquid-liquid extraction at alkaline pH with ethylacetate. The 7-(2,3-dihidroxypropyl) theophylline was used as an internal standard (ISTD). The separation was achieved on a C18 column using 14:86 methanol:buffer (25 mM KH2PO4 adjusted to pH 4 with ortho-phosphoric acid) solution as mobile phase under isocratic conditions at a flow rate 1 mL min−1. An ultraviolet absorption at 274 nm was monitored. In these conditions, the LOD was 0.03 μg mL−1 for theobromine, 0.02 μg mL−1 for paraxanthine, 0.04 μg mL−1 for theophylline, and 0.08 μg mL−1 for caffeine. The method has been applied to urine samples.

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Available abstract

A reversed-phase high performance liquid chromatographic method was improved for the simultaneous determination of theobromine, paraxanthine, theophylline, and caffeine in urine. The method includes a liquid-liquid extraction at alkaline pH with ethylacetate. The 7-(2,3-dihidroxypropyl) theophylline was used as an internal standard (ISTD). The separation was achieved on a C18 column using 14:86 methanol:buffer (25 mM KH2PO4 adjusted to pH 4 with ortho-phosphoric acid) solution as mobile phase under isocratic conditions at a flow rate 1 mL min−1. An ultraviolet absorption at 274 nm was monitored. In these conditions, the LOD was 0.03 μg mL−1 for theobromine, 0.02 μg mL−1 for paraxanthine, 0.04 μg mL−1 for theophylline, and 0.08 μg mL−1 for caffeine. The method has been applied to urine samples.

Key concepts: Theobromine, Chemistry, Theophylline, Chromatography, Paraxanthine, Caffeine, High-performance liquid chromatography, Urine

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Simultaneous Determination of Theobromine, Paraxanthine, Theophylline, and Caffeine in Urine by Reversed-Phase High-Performance Liquid Chromatography with Diode Array UV Detection — Research Paper | ScholarLens