Tanaka Nobuo, Kimura Hiroshi, Tokuda Daisuke, Hosoya Ken, Ikegami Tohru, Ishizuka Norio, Minakuchi Hiroyoshi, Nakanishi Kazuki, Shintani Yukihiro, Furuno Masahiro, Cabrera Karin
Department of Polymer Science and Engineering, Kyoto Institute of Technology, Matsugasaki, Sakyo-ku, Kyoto 606-8585, Japan.
Anal Chem. 2004 Mar 1;76(5):1273-81. doi: 10.1021/ac034925j.
Simple and comprehensive two-dimensional (2D)-HPLC was studied in a reversed-phase mode using monolithic silica columns for second-dimension (2nd-D) separation. Every fraction from the first column, 15 cm long (4.6-mm i.d.), packed with fluoroalkylsilyl-bonded (FR) silica particles, was subjected to the separation in the 2nd-D using one or two octadecylsilylated (C(18)) monolithic silica columns (4.6-mm i.d., 3 cm). Monolithic silica columns in the 2nd-D were eluted at a flow rate of up to 10 mL/min with separation time of 30 s that meets the fractionation every 15-30 s at the first dimension (1st-D) operated at a flow rate of 0.4-0.8 mL/min. Three cases were studied. (1) In the simplest scheme of 2D-HPLC, effluent of the 1st-D was directly loaded into an injector loop of 2nd-D HPLC for 28 s, and 2 s was allowed for injection. (2) Two six-port valves each having a sample loop were used to hold the effluent of the 1st-D alternately for 30 s for one 2nd-D column to effect comprehensive 2D-HPLC without the loss of 1st-D effluent. (3) Two monolithic silica columns were used for 2nd-D by using a switching valve and two sets of 2nd-D chromatographs separating each fraction of the 1st-D effluent with the two 2nd-D columns alternately. In this case, two columns of the same stationary phase (C(18)) or different phases, C(18) and (pentabromobenzyloxy)propylsilyl-bonded (PBB), could be employed at the 2nd-D, although the latter needed two complementary runs. The systems produced peak capacity of approximately 1000 in approximately 60 min in cases 1 and 2 and in approximately 30 min in case 3. The three stationary phases, FR, C(18), and PBB, showed widely different selectivity from each other, making 2D separations possible. The simple and comprehensive 2D-HPLC utilizes the stability and high efficiency at high linear velocities of monolithic silica columns.
采用整体硅胶柱进行二维(2D)分离的反相模式研究了简单且全面的二维高效液相色谱法。第一根柱子长15厘米(内径4.6毫米),填充有氟代烷基硅烷键合(FR)硅胶颗粒,其每一个馏分都使用一根或两根十八烷基硅烷化(C(18))整体硅胶柱(内径4.6毫米,长3厘米)在第二维进行分离。第二维的整体硅胶柱以高达10毫升/分钟的流速洗脱,分离时间为30秒,这满足了在流速为0.4 - 0.8毫升/分钟的第一维(1st - D)每15 - 30秒进行一次馏分收集的要求。研究了三种情况。(1)在二维高效液相色谱最简单的方案中,第一维的流出物直接装入二维高效液相色谱的进样环28秒,留出2秒用于进样。(2)使用两个各带有一个样品环的六通阀交替保留第一维的流出物30秒,以便在一根二维柱上实现全面的二维高效液相色谱,而不会损失第一维的流出物。(3)通过一个切换阀和两套二维色谱仪,使用两根整体硅胶柱进行第二维分离,两根二维柱交替分离第一维流出物的各个馏分。在这种情况下,第二维可以使用两根相同固定相(C(18))的柱子,也可以使用不同相的柱子,即C(18)和五溴苄氧基丙基硅烷键合(PBB)的柱子,不过后者需要进行两次互补运行。在情况1和2中,该系统在大约60分钟内产生约1000的峰容量,在情况3中约30分钟内产生约1000的峰容量。三种固定相,FR、C(十八烷基硅烷)和PBB,彼此之间表现出广泛不同的选择性,使得二维分离成为可能。简单且全面的二维高效液相色谱法利用了整体硅胶柱在高线速度下的稳定性和高效性。