Highly sensitive and selective hyphenated technique (molecularly imprinted polymer solid-phase microextraction–molecularly imprinted polymer sensor) for ultra trace analysis of aspartic acid enantiomers

The present work is related to combination of molecularly imprinted solid-phase microextraction and complementary molecularly imprinted polymer-sensor. The molecularly imprinted polymer grafted on titanium dioxide modified silica fiber was used for microextraction, while the same polymer immobilized on multiwalled carbon nanotubes/titanium dioxide modified pencil graphite electrode served as a detection tool. In both cases, the surface initiated polymerization was found to be advantageous to obtain a nanometer thin imprinted film. The modified silica fiber exhibited high adsorption capacity and enantioselective diffusion of aspartic acid isomers into respective molecular cavities. This combination enabled double preconcentrations of d- and l-aspartic acid that helped sensing both isomers in real samples, without any cross-selectivity and matrix complications. Taking into account 6 × 104-fold dilution of serum and 2 × 103-fold dilution of cerebrospinal fluid required by the proposed method, the limit of detection for l-aspartic acid is 0.031 ng m L−1. Also, taking into account 50-fold dilution required by the proposed method, the limit of detection for d-aspartic acid is 0.031 ng m L−1 in cerebrospinal fluid.

► Adopted ‘surface initiated grafting from polymerization’ for making MIP-SPME fiber. ► New combination approach (MIP-SPME–MIP-sensor) used for stringent detection of asp enantiomers. ► LOD realized 0.031 ng m L−1 for d- and l-asp in CSF and serum. ► Minimum volumes of sample volume (1.0 mL) and eluent (100.0 μL) required.