Polyparameter Linear Free Energy Models for Polyacrylate Fiber−Water Partition Coefficients to Evaluate the Efficiency of Solid-Phase Microextraction

Abstract

The fiber-water partition coefficient, K(fw), is decisive for performance of solid-phase microextraction (SPME) techniques in organic chemical analyses. In this study, polyacrylate (PA)-coated fiber was evaluated for its K(fw) values toward diverse neutral organic compounds. Literature K(fw) data were thoroughly evaluated, and additional K(fw) values for 69 compounds were measured in phosphate-buffered saline (PBS) solution at 37 °C. These K(fw) data, spanning over 6 orders of magnitude, were used to construct polyparameter linear free energy relationship (PP-LFER) models. The PP-LFER models fit well to the data with a standard deviation of 0.15-0.23 log units. Additional experiments indicated that the differences in temperature (25 vs 37 °C), electrolyte concentrations (pure water vs PBS), and conditioning methods (heat vs methanol) had only minor influences (<0.3 log units) on K(fw). Using the established PP-LFERs, the SPME extraction efficiency of PA coating toward compounds of differing polarity was evaluated in comparison to poly(dimethylsiloxane) (PDMS) coating. PA exhibited higher extraction capacities for H-bond donor compounds (e.g., phenols, anilines, amides, and many drugs and pesticides) with the estimated K(fw) values being 1-4 log units higher than those of PDMS. Also, PA was shown to be more efficient than PDMS for hydrophobic aromatic compounds.