Abstract

Hollow fiber liquid-phase microextraction (HF-LPME) offers an efficient alternative to classical techniques for sample preparation and preconcentration. Features include high selectivity, good enrichment factors, and improved possibilities for automation. HP-LPME relies on the extraction of target analytes from aqueous samples into a supported liquid membrane (SLM) sustained in the pores of the wall of a porous hollow fiber, and then into an acceptor phase (that can be aqueous or organic) in the lumen of the hollow fiber. After extraction, the acceptor solution is directly subjected to a chemical analysis. HP-LPME can be performed in either the 2- or 3-phases mode. In the 2-phase mode, the organic solvent is present both in the porous wall and inside the lumen of the hollow fiber. In the 3-phase mode, the acceptor phase can be aqueous and this results in a conventional 3-phase system compatible with HPLC or capillary electrophoresis. Alternatively, the acceptor solution is organic and this represents a 3-phase extraction system with two immiscible organic solvents that is compatible with all common analytical instruments. In HP-LPME methods based on the use of SLMs, the mass transfer occurs by passive diffusion, and high extraction yields as well as efficient extraction kinetics are obtained by applying a pH gradient. In addition, active transport can be performed by using carrier or applying an electrical potential across the SLM. Due to high analyte preconcentration, excellent sample clean-up, and low consumption of organic solvent, HF-LPME has a large application potential in areas such as drug analysis and environmental monitoring. This review focuses on the fundamentals of extraction principles, technical implementations, and future trends in HF-LPME.

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