Article ID Journal Published Year Pages File Type
1213269 Journal of Chromatography B 2011 9 Pages PDF
Abstract

A sensitive and specific ultra performance liquid chromatography–tandem mass spectrometry method for the simultaneous quantification of nicotine, its metabolites cotinine and trans-3′-hydroxycotinine and varenicline in human plasma was developed and validated. Sample preparation was realized by solid phase extraction of the target compounds and of the internal standards (nicotine-d4, cotinine-d3, trans-3′-hydroxycotinine-d3 and CP-533,633, a structural analog of varenicline) from 0.5 mL of plasma, using a mixed-mode cation exchange support. Chromatographic separations were performed on a hydrophilic interaction liquid chromatography column (HILIC BEH 2.1 × 100 mm, 1.7 μm). A gradient program was used, with a 10 mM ammonium formate buffer pH 3/acetonitrile mobile phase at a flow of 0.4 mL/min. The compounds were detected on a triple quadrupole mass spectrometer, operated with an electrospray interface in positive ionization mode and quantification was performed using multiple reaction monitoring. Matrix effects were quantitatively evaluated with success, with coefficients of variation inferior to 8%. The procedure was fully validated according to Food and Drug Administration guidelines and to Société Française des Sciences et Techniques Pharmaceutiques. The concentration range was 2–500 ng/mL for nicotine, 1–1000 ng/mL for cotinine, 2–1000 ng/mL for trans-3′-hydroxycotinine and 1–500 ng/mL for varenicline, according to levels usually measured in plasma. Trueness (86.2–113.6%), repeatability (1.9–12.3%) and intermediate precision (4.4–15.9%) were found to be satisfactory, as well as stability in plasma. The procedure was successfully used to quantify nicotine, its metabolites and varenicline in more than 400 plasma samples from participants in a clinical study on smoking cessation.

► Nicotine, metabolites and varenicline were simultaneously quantified by UPLC–MS/MS. ► Hydrophilic interaction liquid chromatography was used to increase sensitivity. ► The procedure was sensitive and specific, and matrix effects were insignificant. ► Validation led to good results concerning accuracy, precision, trueness, stability. ► The assay was successfully applied to human plasma samples from a clinical study.

Related Topics
Physical Sciences and Engineering Chemistry Analytical Chemistry
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