Improved Method of Molecular Imprinting of Cyclodextrin on Silica-gel Surface for the Preparation of Stable Stationary HPLC Phase |
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Authors: | TAKAHIKO MATSUI TOMO OSAWA KAZUMI SHIRASAKA MAMI KATAYAMA TAKAYUKI HISHIYA HIROYUKI ASANUMA MAKOTO KOMIYAMA |
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Affiliation: | (1) Research Center for Advanced Science and Technology, The University of Tokyo, Komaba, Meguro-ku, 153-8904 Tokyo, Japan;(2) Precursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency (JST), Kawaguchi, 332-0012 Saitama, Japan;(3) Present address: Department of Molecular Design and Engineering, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa-ku, 464-8603 Nagoya, Japan |
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Abstract: | By using N-(3-triethoxysilyl)propylacrylamide (TPAAm), vinyl groups were introduced onto the surface of silica-gel. On the surface of this silica-gel, β-CyD was molecularly imprinted by using a redox initiator, and the composite was used as stationary phase of high performance liquid chromatography (HPLC). The pump pressure was sufficiently low and did not increase even after continuous elution for 24 h. In order to prepare still more stable columns, a new polymerization process was developed. There, the redox initiator was first mixed with the surface-modified silica-gel and then vinylated β-CyD, crosslinker, and the template were added. This modification promoted the immobilization of β-CyD copolymer to the silica-gel, resulting in still lower pump pressure. Concurrently, the imprinting efficiency was increased in comparison with previous method where the redox initiator was directly added to the mixture of the β-CyD–template complex, crosslinker, and surface-modified silica-gel. The molecularly imprinted β-CyD column, prepared by this new method, efficiently discriminated the enantiomers of N-benzyloxycarbonyltyrosine. |
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Keywords: | amino acid cyclodextrin immobilization HPLC molecular imprinting stationary phase |
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