Solvent bar microextraction of emerging pollutants from drain water samples
The efficiency of a
given microextraction technique depends on both thermodynamic and kinetic
aspects. The distribution constant defines the maximum extractable analyte
whereas the kinetic establishes the rate at which this distribution takes
place. Among the kinetic factors, the efficient diffusion of the target analytes from the bulk sample solution to
the acceptor phase is a key aspect. This diffusion can be easily enhanced
by an efficient stirring of the sample or the acceptor phase during the
extraction.
Solvent bar
microextraction (SBME), which was firstly presented by Jiang and Lee in 2004,
(1) enhances the diffusion of the analytes through an efficient stirring of the
acceptor phase. SBME uses a solvent immobilized in the lumen and pores
of a polypropylene hollow fiber as extracting phase. Both ends of the hollow
fiber are sealed and the resulting solvent bar is introduced in the sample
where it moves free and randomly. After the extraction, the solvent bar is
recovered and the extractant is finally analyzed by an appropriate instrumental
technique.
Guo and Lee, in a
recent article published in Journal of Chromatography A, have proposed a SBME procedure
for the extraction of six residual pharmaceuticals (naproxen, ibuprofen,
ketoprofen, propanolol, diclofenac and alprenolol) from drain water, being the
analytes finally determined by gas chromatography/mass spectrometry (GC/MS).(2)
Taking into account the polarity of the analytes, which is a shortcoming for
GC/MS analysis, a derivatization step is required. Derivatization and extraction are performed at the same time by adding the derivatizing reagent to the
extraction solvent. The SBME procedure provides better results than classic
hollow-fiber liquid phase microextraction using the same extraction solvent,
due to the enhanced contact with the sample. Moreover, SBME provides comparable results to
those obtained by solid phase microextraction, although the SBME is faster (20 vs
60 min) and it avoids carry-over as a new solvent bar is used in each new
extraction.
In the referenced article (2), the
readers will find the optimization of the extraction procedure, the analytical characterization
of the proposed method and a critical comparison with its main counterparts.
References
(1)Solvent Bar
Microextraction. Link to the article
(2)One step solvent bar
microextraction and derivatization followed by gas chromatography–mass
spectrometry for the determination of pharmaceutically active compounds in
drain water samples. Link to the article
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