Watanabe Yuta, Ikegami Tohru, Horie Kanta, Hara Takeshi, Jaafar Jafariah, Tanaka Nobuo
Department of Biomolecular Engineering, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan.
J Chromatogr A. 2009 Oct 30;1216(44):7394-401. doi: 10.1016/j.chroma.2009.07.012. Epub 2009 Jul 14.
Anion-exchange (AEX) columns were prepared by on-column polymerization of acrylates and methacrylates containing tertiary amino or quaternary ammonium groups on monolithic silica in a fused silica capillary modified with anchor groups. The columns provided a plate height (H) of less than 10 microm at optimum linear velocity (u) with keeping their high permeability (K=9-12 x 10(-14) m2). Among seven kinds of AEX columns, a monolithic silica column modified with poly(2-hydroxy-3-(4-methylpiperazin-1-yl)propyl methacrylates) (HMPMA) showed larger retentions and better selectivities for nucleotides and inorganic anions than the others. The HMPMA column of 410 mm length produced 42,000-55,000 theoretical plates (N) at a linear velocity of 0.97 mm/s with a backpressure of 3.8 MPa. The same column could be employed for a fast separation of inorganic anions in 1.8 min at a linear velocity of 5.3 mm/s with a backpressure of 20 MPa. In terms of van Deemter plot and separation impedance, the HMPMA column showed higher performance than a conventional particle-packed AEX column. The HMPMA column showed good recovery of a protein, trypsin inhibitor, and it was applied to the separation of proteins and tryptic digest of bovine serum albumin (BSA) in a gradient elution, to provide better separation compared to a conventional particle-packed AEX column.
阴离子交换(AEX)柱是通过在经锚定基团修饰的熔融石英毛细管中的整体硅胶上,使含有叔氨基或季铵基团的丙烯酸酯和甲基丙烯酸酯进行柱上聚合制备而成。这些柱子在最佳线性流速(u)下提供的板高(H)小于10微米,同时保持其高渗透性(K = 9 - 12×10⁻¹⁴ m²)。在七种AEX柱中,用聚(2 - 羟基 - 3 - (4 - 甲基哌嗪 - 1 - 基)丙基甲基丙烯酸酯)(HMPMA)修饰的整体硅胶柱对核苷酸和无机阴离子的保留能力更强,选择性也优于其他柱子。长度为410毫米的HMPMA柱在0.97毫米/秒的线性流速和3.8兆帕的背压下产生42,000 - 55,000理论塔板数(N)。同一根柱子可在5.3毫米/秒的线性流速和20兆帕的背压下于1.8分钟内快速分离无机阴离子。就范德姆特曲线和分离阻抗而言,HMPMA柱表现出比传统颗粒填充AEX柱更高的性能。HMPMA柱对蛋白质胰蛋白酶抑制剂具有良好的回收率,并应用于梯度洗脱中蛋白质和牛血清白蛋白(BSA)胰蛋白酶消化产物的分离,与传统颗粒填充AEX柱相比,分离效果更好。