Polyaniline-polycaprolactone electrospun nanofibrous mat: new polymeric support with anion exchange characteristic for immobilizing liquid membrane in efficient on-chip electromembrane extraction of polar acidic drugs.

The potential of application of an electrospun nanofiber sheet as new polymeric support for immobilizing the liquid membrane, instead of a common commercial polypropylene sheet, in on-chip electromembrane extraction (EME) of some acidic polar drugs followed by HPLC with ultraviolet detection is presented. The nanofiber sheet was prepared by electrospinning a mixture of polycaprolactone and polyaniline. The successful synthesis of the electrospun nanofiber sheet was confirmed by field emission-scanning electron microscopy, energy-dispersive X-ray spectroscopy, elemental mapping, and atomic force microscopy. Several parameters affecting the efficiency of the microextraction method, including pHs of the donor and acceptor phases, applied voltage, sample flow rate, phosphate content of the acceptor phase, and sample volume, were investigated and optimized. After optimization, the linearity range of 0.5–250.0 µg L−1 and detection limits of 0.2–1.0 µg L−1 were obtained for the analytes. The extraction recovery values and preconcentration factors were 10.7–55.3% and 16–83, respectively. The presence of polyaniline in the composition of the nanofibers significantly improved the extraction efficiency of the polar acidic drugs due to providing the possibility of various interactions with the target analytes such as hydrogen bonding, π-stacking, and anion exchange. The obtained results demonstrate the excellent efficiency of the synthesized electrospun nanofibrous mat as a novel support membrane for immobilizing 1-octanol and as an interactive substrate for electromembrane extraction of acidic polar drugs. Eventually, the proposed on-chip EME method exhibits acceptable precision (relative standard deviations less than 9.7% (n = 3)) and good accuracy (86–112%) for determining the target analytes in the plasma samples. [ABSTRACT FROM AUTHOR]