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通过多步溶胀聚合方法制备的用于(-)-表没食子儿茶素没食子酸酯、表儿茶素没食子酸酯和没食子儿茶素没食子酸酯的尺寸均匀的分子印迹聚合物。

Uniformly-sized, molecularly imprinted polymers for (-)-epigallocatechin gallate, -epicatechin gallate and -gallocatechin gallate by multi-step swelling and polymerization method.

作者信息

Haginaka Jun, Tabo Hiromi, Ichitani Masaki, Takihara Takanobu, Sugimoto Akio, Sambe Haruyo

机构信息

Faculty of Pharmaceutical Sciences, Mukogawa Women's University, Nishinomiya, Japan.

出版信息

J Chromatogr A. 2007 Jul 13;1156(1-2):45-50. doi: 10.1016/j.chroma.2006.10.026. Epub 2006 Oct 27.

DOI:10.1016/j.chroma.2006.10.026
PMID:17070533
Abstract

Uniformly-sized, molecularly imprinted polymers (MIPs) for (-)-epigallocatechin gallate (EGCg), -epicatechin gallate (ECg) and -gallocatechin gallate (GCg) were prepared by a multi-step swelling and polymerization method using 2-vinylpyridine as a functional monomer, ethylene glycol dimethacrylate as a cross-linker and cyclohexanol as a porogen. Molecular recognition abilities of the obtained MIPs were evaluated in liquid chromatography using a mixture of ethanol and water, or ethanol as the eluent. Each MIP gave the highest molecular recognition ability for the respective template molecule. In addition, (-)-EGCg and -ECg had the same configuration (2R,3R) at positions 2 and 3, and therefore resulting in high cross reactivity each other. However, (-)-GCg, which has different configuration at position 2 with (-)-EGCg and -ECg, showed low cross reactivity with them. On the other hand, those MIPs showed no molecular recognition against (-)-epigallocatechin and -epicatechin, which have no gallate group at position 3. These results indicate that the MIPs prepared can recognize configuration at position 2 and a gallate group at position 3. Furthermore, the MIP for (-)-GCg could be successfully used for isolating (-)-EGCg and -ECg from green tea extract.

摘要

采用多步溶胀聚合法,以2-乙烯基吡啶为功能单体、乙二醇二甲基丙烯酸酯为交联剂、环己醇为致孔剂,制备了尺寸均匀的用于(-)-表没食子儿茶素没食子酸酯(EGCg)、表儿茶素没食子酸酯(ECg)和没食子儿茶素没食子酸酯(GCg)的分子印迹聚合物(MIPs)。使用乙醇和水的混合物或乙醇作为洗脱剂,通过液相色谱法评估所得MIPs的分子识别能力。每种MIP对各自的模板分子具有最高的分子识别能力。此外,(-)-EGCg和-ECg在2位和3位具有相同的构型(2R,3R),因此彼此之间具有较高的交叉反应性。然而,(-)-GCg在2位的构型与(-)-EGCg和-ECg不同,与它们的交叉反应性较低。另一方面,那些MIPs对3位没有没食子酸基团的(-)-表没食子儿茶素和表儿茶素没有分子识别能力。这些结果表明,所制备的MIPs可以识别2位的构型和3位的没食子酸基团。此外,(-)-GCg的MIP可以成功用于从绿茶提取物中分离(-)-EGCg和-ECg。

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