Niğde University, Faculty of Science and Arts, Chemistry Department, 51100, Niğde, Turkey.
Talanta. 2011 Oct 15;85(5):2405-10. doi: 10.1016/j.talanta.2011.07.076. Epub 2011 Jul 29.
In the present study, metal binding property of humic acid (HA) was successfully adapted to the ligand-exchange concept, and metal-loaded immobilized humic acid was used as a ligand exchanger stationary phase for separation of some nucleosides. Humic-acid bonded aminopropyl silica (EC-HA-APS) was turned into ligand exchanger forms by loading aqueous solutions of Cu(2+), and Co(2+) to the column (4.6 × 150; as mm) packed with EC-HA-APS. Metal ion solutions were loaded to the column in a stepwise manner where the concentration of metal ion solution being loaded to the column was increased gradually between 5 and 100mM. The progress of metal loading process was monitored via the breakthrough curves propagated stepwise. Ligand-exchange chromatography (LEC) studies were performed on an HPLC system, and chromatographic behaviors of the studied nucleosides (i.e. uridine, Urd; thymidine, Tyd; cytidine, Cyd; adenosine, Ado; and guanosine, Guo) were investigated on Cu(2+) and Co(2+) loaded forms of the EC-HA-APS (Cu-EC-HA-APS and Co-EC-HA-APS). Effect of mobile phase composition, temperature, and the type of metal ion loaded to the column on the retentive behaviors of the compounds was studied, in detail. The studied solutes exhibited mixed-mode RPLC/LEC behavior on the stationary phase. Metal-loaded column (M-EC-HA-APS) was easily regenerated into its original form, EC-HA-APS, with 98 ± 2% metal recoveries, by using aqueous mixture of EDTA+NH(3) at pH=7.5. Thus, the stationary phase exhibited a high flexibility between RPLC and LEC modes. This property, also, made it possible to convert the stationary phase into various ligand exchanger forms by loading different metal ions. Hence, capacity and selectivity of the stationary phase towards the studied species was manipulated easily by loading different metal ions to the stationary phase. Baseline separation for the studied species was achieved on Cu-EC-HA-APS and Co-EC-HA-APS and some differentiations were observed in capacity and selectivity, depending on the type of metal loaded. Thus, being as the first endeavor on usability of immobilized HA as a ligand exchanger stationary phase, the present study is believed to be useful to understand multifunctional character of HA-based solid/stationary phases.
在本研究中,成功地将腐殖酸(HA)的金属结合特性应用于配体交换概念,并且将负载金属的固定化腐殖酸用作分离一些核苷的配体交换固定相。通过将铜(II)和钴(II)的水溶液加载到用 EC-HA-APS 填充的(4.6×150; 毫米)柱中,将氨基丙基键合的腐殖酸硅烷(EC-HA-APS)转化为配体交换形式。金属离子溶液以逐步方式加载到柱上,其中加载到柱上的金属离子溶液的浓度在 5 到 100mM 之间逐渐增加。通过逐步传播的突破曲线监测金属负载过程的进展。在 HPLC 系统上进行配体交换色谱(LEC)研究,并研究了研究核碱基(即尿嘧啶、Urd;胸腺嘧啶、Tyd;胞嘧啶、Cyd;腺嘌呤、Ado 和鸟嘌呤、Guo)在负载铜(II)和钴(II)的 EC-HA-APS 形式(Cu-EC-HA-APS 和 Co-EC-HA-APS)上的色谱行为。详细研究了流动相组成、温度和加载到柱上的金属离子类型对化合物保留行为的影响。研究的溶质在固定相上表现出混合模式 RPLC/LEC 行为。金属负载柱(M-EC-HA-APS)可以通过使用 pH=7.5 的 EDTA+NH(3)的水性混合物容易地再生为其原始形式 EC-HA-APS,金属回收率为 98±2%。因此,固定相在 RPLC 和 LEC 模式之间表现出高度的灵活性。该特性还可以通过加载不同的金属离子将固定相转化为各种配体交换形式。因此,通过将不同的金属离子加载到固定相上,可以轻松地操纵固定相对研究物种的容量和选择性。在 Cu-EC-HA-APS 和 Co-EC-HA-APS 上实现了研究物种的基线分离,并观察到根据负载的金属类型,在容量和选择性方面存在一些差异。因此,作为将固定化 HA 用作配体交换固定相的首次尝试,本研究有望有助于理解基于 HA 的固体/固定相的多功能特性。