Chromatographic characterisation of aptamer-modified poly(EDMA-co-GMA) monolithic disk format for protein binding and separation

Caleb Acquah, Michael K. Danquah*, Yi Wei Chan, Charles K.S. Moy, Clarence M. Ongkudon, Sie Yon Lau

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)

Abstract

The introduction of aptameric ligands onto disk-monolithic adsorbent, representing a unique strategy for convective isolation of target molecules with high specificity and selectivity, is investigated for the first time. Experimental results showed that the disk monolith possessed a good permeability of 1.67 ± 0.05 × 10–14 m2 (RSD = 3.2%). The aptameric ligand density for the aptamer-modified disk monolith was 480 pmol/uL. Chromatographic analysis of the aptamer disk-monolith efficiency showed an optimum linear velocity of 126 cm/min (≈0.25 mL/min) at room temperatures 25 ± 2°C. The theoretical number of plates corresponding to the optimum linear velocity was 128.2 with an height equivalent to the theoretical plate of 0.022 mm. The disk aptamer-immobilised monolithic system demonstrated good selectivity and isolation of thrombin from non-targets.

Original languageEnglish
Pages (from-to)2100-2111
Number of pages12
JournalSeparation Science and Technology (Philadelphia)
Volume53
Issue number13
DOIs
Publication statusPublished - 2 Sept 2018

Keywords

  • Disk monoliths
  • affinity binding
  • aptamer
  • liquid chromatography
  • protein separation

Fingerprint

Dive into the research topics of 'Chromatographic characterisation of aptamer-modified poly(EDMA-co-GMA) monolithic disk format for protein binding and separation'. Together they form a unique fingerprint.

Cite this