Original Article
Journal of Exposure Analysis and Environmental Epidemiology (1999) 9, 181–191. 10.1038/sj.jea.7500018
Evaluation of solid phase microextraction for the analysis of hydrophilic compounds
JODY A SHOEMAKER1, JEAN W MUNCH1 and THOMAS D BEHYMER1
1U.S. Environmental Protection Agency, National Exposure Research Laboratory, 26 West Martin Luther King Drive, Cincinnati, Ohio
Correspondence: Jody A. Shoemaker, U.S. EPA/NERL, MS 564, 26 W. Martin Luther King Drive, Cincinnati, OH 45268. Tel.: (513)569-7298. E-mail: shoemaker.jody@epa.gov
Accepted 14 September 1998.
Abstract
Two commercially available solid phase microextraction (SPME) fibers, polyacrylate and carboxen/polydimethylsiloxane (PDMS), were evaluated for their ability to extract hydrophilic compounds from drinking water. Conditions, such as desorption time, desorption temperature, sample temperature, sample stirring, methanol concentration in the sample, and ionic strength of the sample, were optimized for 12 hydrophilic compounds (e.g., amines and alcohols) with both fibers. Accuracy, precision, and method detection limits (MDLs) were determined for the target analytes with both fibers. In general, both fibers exhibited excellent accuracy and precision in the range of 91–110% and 1.0–13%, respectively. The carboxen/PDMS fiber extracted these hydrophilic compounds from water with 10 to 100 times lower MDLs (0.10 to 15
g/l) than the polyacrylate fiber (1.5 to 80
g/l). The MDLs of the carboxen/PDMS fiber demonstrate that SPME is a feasible approach for extracting hydrophilic compounds from drinking water.
Keywords:
disinfection by-products, drinking water, gas chromatography/mass spectrometry, solid phase microextraction.
