Journal
ANALYTICA CHIMICA ACTA
Volume 902, Issue -, Pages 115-122Publisher
ELSEVIER
DOI: 10.1016/j.aca.2015.11.013
Keywords
Boronate affinity adsorbents; High capacity; Reversible addition-fragmentation chain; transfer polymerization; Enrichment; Ribonucleosides
Categories
Funding
- National Natural Science Foundation in China [21575114, 20705028, 21275115]
- Research Project on Social Development by the Science and Technology Department of Shaanxi Province [2013K13-02-10]
- Open Project of State Key Laboratory of Supramolecular Structure and Materials [SKLSSM201133]
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Boronate affinity adsorption is uniquely selective for cis-diol-containing molecules. The preparation and application of boronate affinity materials has attracted much attention in recent years. In this work, a high capacity boronate affinity adsorbent was prepared by surface -initiated reversible addition fragmentation chain transfer polymerization (SI-RAFT). Commercial aminated poly(glycidyl methacrylate) (PGMA) rnicrospheres were modified with the chain transfer agent (CTA) S-1-dodecyl-S-(alpha,alpha-dimethyl-alpha-acetic acid)trithiocarbonate (DDATC). Boronate-affinity adsorbents were then prepared via SI-RAFT polymerization employing 3-acrylamidophenylboronic acid (AAPBA) as the monomer. The Fourier transform infrared spectroscopy (FT-IR), nitrogen adsorption and desorption measurements have proven the successful grafting of AAPBA on PGMA microspheres surface. The boronate affinity adsorbents thus prepared possess much higher adsorption capacity (99.2 mu mol/g of adenosine) and both faster adsorption and desorption speed towards ribonucleosides, the adsorption and desorption could be completed in 2 min. The high selectivity of the adsorbents to ribonucleosicies was verified in the presence of a large excess of deoxynucleosides. The boronate affinity adsorbents were then employed for sample pretreatment before HPLC analysis of ribonucleosides in serum. The ribonucleosides were effectively enriched by boronate affinity dispersive solid-phase extraction (BA-DSPE), with high mass recoveries and good precision. The simultaneous determination of uridine and guanosine in calf serutn was achieved by utilizing the standard addition method, their contents were determined to be 170 +/- 11.6 ng/mL and 39.6 +/- 4.4 ng/mL respectively. The results proved that the prepared boronate affinity materials could be applied for sample pretreatment of cis-diol containing molecules in biological samples. (C) 2015 Elsevier B.V. All rights reserved.
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