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Sensitive determination of free benzophenone-3 in human urine samples based on an ionic liquid as extractant phase in
Lorena Vidal1, Alberto Chisvert, Antonio Canals
1Departamento de Química Analítica, Nutrición y Bromatología, Facultad de Ciencias, Universidad de Alicante, P.O. Box 99, E-03080 Alicante, Spain.
Abstract:
Benzophenone-3 (BZ3), one of the compounds most commonly used as UV filter in cosmetic products, can be absorbed through the skin into the human body, since it can be found at trace levels in urine from users of cosmetic products that contain BZ3. Moreover, different undesirable effects have been attributed to this compound. Thus, sensitive analytical methods to monitor urinary excretion of this compound should be developed. This paper presents a selective and sensitive methodology for BZ3 determination at ultratrace levels in human urine samples. The methodology is based on a novel microextraction technique, known as single-drop microextraction (SDME). An ionic liquid (IL) has been used as extractant phase instead of an organic solvent. After the microextraction process, the extractant phase was injected into a liquid chromatography system. The variables of interest in the SDME process were optimized using a multivariate optimization approach. A Plackett-Burman design for screening and a circumscribed central composite design for optimizing the significant variables were applied. Ionic strength, extraction time, stirring speed, pH, ionic liquid type, drop volume and sample volume were the variables studied. The optimum experimental conditions found were: sodium chloride concentration, 13% (w/v); extraction time, 25 min; stirring speed, 900 rpm; pH, 2; ionic liquid type, 1-hexyl-3-methylimidazolium hexafluorophosphate ([C(6)MIM][PF(6)]); drop volume, 5 microL; and sample volume, 10 mL. The proposed method requires a standard addition calibration approach, and it has been successfully employed to determine free BZ3 in urine samples coming from human volunteers who applied a sunscreen cosmetic containing this UV filter. The limit of detection was in the order of 1.3 ng mL(-1) and repeatability of the method, expressed as relative standard deviation, was 6% (n=8).
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