Determination of diuretics in human urine by hollow fiber-based liquid–liquid–liquid microextraction coupled to high performance liquid chromatographyThis paper is part of an Analystthemed issue highlighting Chinese science, with guest editor Mengsu (Michael) Yang.

In competition sports, a diuretic is a substance widely prohibited by the World Anti-Doping Agency (WADA). In this paper, a sensitive, rapid and convenient analytical method for the determination of acidic [furosemide (FUROS) and bumetanide (BUMET)] and basic [triamterene (TRIAM)] diuretics in human urine was developed by hollow fiber-based liquid–liquid–liquid microextraction (LLLME) coupled with HPLC-UV. The LLLME conditions, such as the organic extraction solvent, the acidity and basicity of the donor- and acceptor-phases, stirring speed, extraction time and ionic strength, were studied in detail. Under the optimum conditions, the linear ranges of furosemide, bumetanide and triamterene were 1.2–250, 5.0–250 and 5.0–500 ng mL−1, respectively. The detection limits were 0.5 ng mL−1for furosemide, 1.2 ng mL−1for bumetanide and 2.0 ng mL−1for triamterene. The LLLME obtained a great improvement of the detection limits for all the analytes considered here, to the ng mL−1level, which almost reaches the level of the LC–MS method. This new LLLME method provided very high enrichments: 117-fold for furosemide, 175-fold for bumetanide and 68-fold for triamterene. Since the hollow fiber membrane was sealed, it could be used for extracting the diuretics directly from ‘dirty’ human urine samples without any clean-up procedures. With LLLME–HPLC, the corresponding recoveries ranged from 79.2 to 109% with the RSDs not exceeding 5.5% for the three diuretics in the spiked urine samples. The method was successfully applied to analyse the amounts of the three diuretics in real urine samples of volunteers after oral drug-taking. This new method proves to be sensitive and reliable and thus renders a very suitable means for the determination of trace diuretics in human urine based on the common HPLC instrument. [ABSTRACT FROM AUTHOR]