Cyclodextrin modified gold nanoparticles-based open-tubular capillary electrochromatographic separations of polyaromatic hydrocarbons

Abstract

In this study, spherical gold nanoparticles (GNPs) of 14.7 nm diameter, prepared by citrate reduction of a gold(III) salt and characterized by UV–Vis absorption spectrometry and transmission electron microscopy, were modified by a covalent attachment of 6I-O-(3-mercaptopropyl)β-cyclodextrin (β-CD-SH) or per-6-deoxy-per-6-mercapto-β-cyclodextrin (β-CD-SH7). Subsequently, via three alternative approaches, β-CD-modified GNPs were immobilized onto the inner wall of the fused-silica (FS) capillaries and applied as special stationary phases for open-tubular capillary electrochromatography (OT-CEC). The first immobilization procedure was based on pre-derivatization of a FS capillary with (3-mercaptopropyl)trimethoxysilane (MPTMS) followed by subsequent reactions with GNPs and β-CD-SH or β-CD-SH7. The other two preparation protocols took advantage of sol–gel approach gaining a significant increase in the interaction surface for solutes. In both instances, the sol–gel created 3D structure was further covalently modified with GNPs. Serving that purpose, either β-CD-SH7 modified GNPs were used for the immobilization into the sol–gel matrix (“one-step sol–gel technique”) or native GNPs were immobilized first into the sol–gel matrix and subsequently modified with β-CD-SH7 (“two-step sol–gel technique”). The separation performance of CD-GNPs modified FS capillaries was tested by OT-CEC in reversed-phase mode applied to separation of a model mixture of five polyaromatic hydrocarbons. The highest separation efficiencies were obtained with the capillaries prepared by two-step sol–gel technique. However, with respect to the relatively low reproducibility of this method, the first of the above preparation procedures, i.e., a simple pre-derivatization of the FS capillary with MPTMS ensued with β-CD-SH7-GNPs immobilization seems to be more feasible approach providing decent separation efficiency.