On-line molecularly imprinted solid-phase extraction for the selective spectrophotometric determination of nicotine in the urine of smokers

• Published in: Analytica chimica acta 2009-03, Vol.635 (1), p.102-107
• Main Authors: Figueiredo, Eduardo Costa, de Oliveira, Daniela Mayra, de Siqueira, Maria Elisa Pereira Bastos, Arruda, Marco Aurélio Zezzi
• Format: Article
• Language: English
• Subjects: Buffers; Calibration; Humans; Hydrogen-Ion Concentration; Molecularly imprinted polymers; Nicotine; Nicotine - urine; Reproducibility of Results; Sensitivity and Specificity; Smoking - urine; Solid-phase extraction; Spectrophotometry; Spectrophotometry - methods; Temperature; Urine
• ISSN: 0003-2670; 1873-4324
• DOI: 10.1016/j.aca.2008.12.045

This work describes an on-line molecularly imprinted solid-phase extraction (MISPE) method for spectrophotometric determination of nicotine in urine samples of smokers. This method is based on manganese (VII) to manganese (VI) reduction in an alkaline medium, promoted by nicotine. Two wash solutions (1:4 (v/v) acetonitrile:sodium hydroxide – pH 11.4, and nitric acid – pH 2.5) were employed to circumvent interferences. Aqueous solutions containing nicotine plus different possible concomitants (cotinine, anabasine, norcotinine and caffeine) were tested individually. The analytical calibration curve was prepared in urine samples collected from non-smokers and spiked with nicotine standard from 1.1 to 60 μmol L −1 ( r 2 > 0.998). The limit of quantification and the analytical frequency were 1.1 μmol L −1 and 11 h −1, respectively. The precision, evaluated using 3, 10 and 30 μmol L −1 nicotine in urine, was 10, 10 and 4% (intra-day precision) and 12, 13 and 5% (inter-day precision), respectively. Accuracy was checked through high performance liquid chromatography and the results did not present significant differences at the 95% confidence level according to the Student's t-test.