Haginaka Jun, Tabo Hiromi, Ichitani Masaki, Takihara Takanobu, Sugimoto Akio, Sambe Haruyo
Faculty of Pharmaceutical Sciences, Mukogawa Women's University, Nishinomiya, Japan.
J Chromatogr A. 2007 Jul 13;1156(1-2):45-50. doi: 10.1016/j.chroma.2006.10.026. Epub 2006 Oct 27.
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.
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。