Mixed-acidic cation-exchange material for the separation of underivatized amino acids

Mixed-acidic cation-exchange (MCX) columns with both strongly (SCX) and weakly (WCX) acidic functional groups were developed for the separation of standard amino acids. The resins were prepared by carboxylation of highly crosslinked monodisperse poly(styrene-divinylbenzene) copolymer particles with performic acid and subsequent sulfonation with sulfuric acid. The degree of functionalization was varied independently for each processing step and controlled by measuring pH dependent retention of the obtained resins. A series of mixed-acidic resins with different SCX/WCX-ratios was chromatographically characterized by variation of formic acid and acetonitrile concentration in the aqueous eluent. The overall cation-exchange capacity was varied from 33 to 68 mu mol/mL. The comparison with two commercial columns (Metrohm Metrosep C6, WCX and Hamilton PRP X-200, SCX) revealed the additive character of the different functional group properties within MCX columns and a unique selectivity which can be adjusted by both eluent composition and SCX/WCX-ratio of the resin. The retention window between neutral and basic amino acids was altered by varying the amount of sulfonic acid groups attached to the polymer. Orthogonality plots demonstrated constant selectivity for neutral amino acids. Correlating the retention data with log P data demonstrated the influence of non-ionic hydrophobic and pi-pi-interactions for the separation of amino acids on PS/DVB-based cation-exchangers. An isocratic IC-ESI-MS method was developed to separate and quantitate 20 underivatized standard amino acids within 30 min. Limits of detection were between 4 and 64 nmol L-1 and a high linearity of calibration curves was obtained for all analytes. The method was validated by comparing a certified reference standard with external calibration data. (C) 2021 Elsevier B.V. All rights reserved.

Automated summary

Mixed-acidic cation-exchange (MCX) columns with adjustable selectivity were developed for the separation and quantitation of standard amino acids. The resins were prepared by carboxylation and sulfonation of crosslinked polymer particles, and the functionalization was controlled by measuring pH dependent retention. The method allowed fast analysis of 20 underivatized amino acids within 30 minutes.