Pharmacognosy and Pharmaceutical Chemistry Department, College of Pharmacy, Taibah University, Medina 30001, Saudi Arabia; Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Assiut University, Assiut 71526, Egypt.
Department of Pharmaceutical Analytical Chemistry, Faculty of Pharmacy, Assiut University, Assiut 71526, Egypt.
Talanta. 2019 Jul 1;199:347-354. doi: 10.1016/j.talanta.2019.02.082. Epub 2019 Feb 23.
If strong cation exchange chromatography (SCX) is combined with ion-pair chromatography, then the solute could be retained selectively with the power of mixed separation modes. This combination is termed selectivity enhanced strong cation exchange chromatography (SE-SCX). Macroporous polystyrene-divinylbenzene (PS/DVB) resin with sulfonate coating that conveys ion exchange and reversed phase characteristics was employed. Sodium dodecyl sulfate (SDS) was utilized as a selectivity modifier and an ion-pair reagent. This separation strategy is exploited for a challenging simultaneous separation of peptide variants having similar isoelectric points (pIs) and comparable retention behaviour. Insulin variants were used as a model in this study. The selective separation of insulin and five structurally-related analogues namely; ASPART, LISPRO, GLULISIN, GLARGIN, and DETEMIR was conducted using gradient elution mode. Three eluents were used for the separation of the target compounds. Eluent A was a mixture of acetonitrile and 10 mmol L SDSat ratio (1:1) and was kept at 20% through the run. Eluent B was 20 mmol L KHPO adjusted at pH = 4.0 and eluent C was eluent B plus 1 mol L NaCl that was increased linearly till 80% at 20 min. It was found that the retention of the tested variants can be modeled mainly by electrostatic interaction that might be hydrophobically-assisted. The developed method was validated in accordance with ICH guidelines and was appropriate for the intended purposes. Finally, this study introduces SE-SCX as a new selective separation strategy for peptides and proteins that may open the door for novel mixed mode perspectives in protein analysis.
如果将强阳离子交换色谱(SCX)与离子对色谱法结合使用,那么溶质可以通过混合分离模式选择性保留。这种组合被称为选择性增强强阳离子交换色谱(SE-SCX)。采用带有磺酸涂层的大孔聚苯乙烯-二乙烯基苯(PS/DVB)树脂,具有离子交换和反相特性。十二烷基硫酸钠(SDS)用作选择性修饰剂和离子对试剂。这种分离策略被用于具有相似等电点(pI)和可比保留行为的肽变体的挑战性同时分离。在这项研究中,胰岛素变体被用作模型。使用梯度洗脱模式对胰岛素和五种结构相关类似物(即 ASPART、LISPRO、GLULISIN、GLARGIN 和 DETEMIR)进行选择性分离。三种洗脱液用于分离目标化合物。洗脱液 A 是乙腈和 10mmol/L SDS 的混合物,比例为 1:1,并在整个运行过程中保持在 20%。洗脱液 B 是 20mmol/L KHPO,pH 值为 4.0,洗脱液 C 是洗脱液 B 加上 1mol/L NaCl,线性增加至 20 分钟时达到 80%。结果表明,测试变体的保留主要可以通过静电相互作用来建模,这种相互作用可能是疏水性辅助的。该方法按照 ICH 指南进行了验证,适用于预期目的。最后,本研究介绍了 SE-SCX 作为一种新的肽和蛋白质选择性分离策略,可能为蛋白质分析开辟新的混合模式视角。