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Updated: Jun 6, 2026

Amplification of Escherichia coli in a Continuous-Flow-PCR Microfluidic Chip and Its Detection with a Capillary Electrophoresis System
Published on: November 21, 2023
Simultaneous multiple enantioseparation with a one-pot imprinted microfluidic channel by microchip capillary
Ping Qu1, Jianping Lei, Jin Sheng
1Key Laboratory of Analytical Chemistry for Life Science (Ministry of Education of China), Department of Chemistry, Nanjing University, Nanjing, 210093, China.
Abstract:
A multi-template imprinted microchannel was prepared by a one-pot in situ imprinting process. The imprinted microchannel led to a novel chip-based strategy for simultaneous multiple enantioseparation. The one-pot imprinting process formed a multi-template imprinted porous thin layer (about 2 μm) on the inner wall of the capillary, which was characterized by scanning electron microscopy, infrared spectroscopy, and solid-state UV-vis spectroscopy. By fixing the imprinted capillary to a support substrate composed of poly(dimethylsiloxane) on a glass slide, a multi-analyte microchip was thus conveniently constructed. Using L-tyrosine (L-Tyr) and L-tryptophan (L-Trp) as the template molecules, two pairs of enantiomers were simultaneously baseline separated in a 6 cm separation channel within 120 s under the optimized preparation and electrochromatographic conditions. The separation showed excellent efficiency. The linear ranges for amperometric detection of four analytes using a carbon fiber microdisk electrode at +1.2 V (vs. Ag/AgCl) were from 20 to 500 μM for racemic Tyr and Trp. This multi-template imprinting strategy could be expanded for simultaneous separation and detection of additional pairs of enantiomers within a short analytical time. It could open up a promising avenue for high-throughput screening of chiral compounds.
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