Influence of Albumin on Sorption Kinetics in Solid-Phase Microextraction:  Consequences for Chemical Analyses and Uptake Processes

• Published in: Analytical chemistry (Washington) Vol. 79; no. 18; pp. 6941 - 6948
• Main Authors: Kramer, Nynke I, van Eijkeren, Jan C. H, Hermens, Joop L. M
• Format: Journal Article
• Language: English
• Published: Washington, DC American Chemical Society 15.09.2007
• Subjects: Absorption; Albumins - chemistry; Analytical chemistry; Animals; Cattle; Chemistry; Chromatographic methods and physical methods associated with chromatography; Exact sciences and technology; Extraction processes; Kinetics; Models, Chemical; Other chromatographic methods; Phase transitions; Proteins; Pyrenes - chemistry; Reaction kinetics; Serum Albumin, Bovine - chemistry; Solid Phase Microextraction; Solids; Sorption; Cell culture; Chemical analysis; Experimental data; Microanalysis; Albumin; HPLC chromatography; Serum albumin; Chemical enrichment; Thickness; Solid phase microextraction; Sorption; Biological compound; Pyrene; Environment; Chemical uptake; Diffusion
• ISSN: 0003-2700; 1520-6882
• DOI: 10.1021/ac070574n

Because of its simplicity, solid-phase microextraction (SPME) is an increasingly popular technique to use in experiments measuring freely dissolved concentrations of compounds in biological and environmental samples. However, a number of studies have shown that sorption kinetics of compounds in such SPME systems is dependent on the presence of a binding matrix. This affects the interpretability of nonequilibrium SPME data. In this study, this phenomenon was investigated by measuring the rate of depletion of pyrene from a “loaded” poly(dimethylsiloxane) fiber into surrounding cell culture medium containing different concentrations of bovine serum albumin (BSA). The rate of depletion was found to steadily increase with increasing concentrations of BSA. It was postulated that BSA facilitated the transport of pyrene through the medium. This phenomenon was modeled by considering diffusion of BSA-bound pyrene in addition to diffusion of unbound pyrene in the aqueous boundary layer (BL) around the fiber. The model closely fit the experimental data and illustrated that diffusion in the BL was rate limiting because the analyte's affinity for the fiber was high and the BL thickness significant. The concentration of binding matrix and the analyte's affinity for the matrix further determined the extent to which BSA-facilitated transport contributed to the kinetics of the system.