Selectivity limits of and opportunities for ion pair chromatographic separation of oligonucleotides.


Journal

Journal of chromatography. A
ISSN: 1873-3778
Titre abrégé: J Chromatogr A
Pays: Netherlands
ID NLM: 9318488

Informations de publication

Date de publication:
16 Aug 2021
Historique:
received: 21 12 2020
revised: 12 05 2021
accepted: 15 05 2021
pubmed: 9 6 2021
medline: 22 7 2021
entrez: 8 6 2021
Statut: ppublish

Résumé

Here it was investigated how oligonucleotide retention and selectivity factors are affected by electrostatic and non-electrostatic interactions in ion pair chromatography. A framework was derived describing how selectivity depends on the electrostatic potential generated by the ion-pair reagent concentration, co-solvent volume fraction, charge difference between the analytes, and temperature. Isocratic experiments verified that, in separation problems concerning oligonucleotides of different charges, selectivity increases with increasing surface potential and analyte charge difference and with decreasing co-solvent volume fraction and temperature. For analytes of the same charge, for example, diastereomers of phosphorothioated oligonucleotides, selectivity can be increased by decreasing the co-solvent volume fraction or the temperature and has only a minor dependency on the ion-pairing reagent concentration. An important observation is that oligonucleotide retention is driven predominantly by electrostatic interaction generated by the adsorption of the ion-pairing reagent. We therefore compared classical gradient elution in which the co-solvent volume fraction increases over time versus gradient elution with a constant co-solvent volume fraction but with decreasing ion-pair reagent concentration over time. Both modes decrease the electrostatic potential. Oligonucleotide selectivity was found to increase with decreasing ion-pairing reagent concentration. The two elution modes were finally applied to two different model antisense oligonucleotide separation problems, and it was shown that the ion-pair reagent gradient increases the selectivity of non-charge-based separation problems while maintaining charge-difference-based selectivity.

Identifiants

pubmed: 34102400
pii: S0021-9673(21)00393-9
doi: 10.1016/j.chroma.2021.462269
pii:
doi:

Substances chimiques

Indicators and Reagents 0
Oligonucleotides 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

462269

Informations de copyright

Copyright © 2021. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Martin Enmark (M)

Department of Engineering and Chemical Sciences, Karlstad University, SE-651 88 Karlstad, Sweden.

Said Harun (S)

Advanced Drug Delivery, Pharmaceutical Sciences, BioPharmaceuticals R&D, AstraZeneca,Gothenburg, 431 83, Mölndal, Sweden.

Jörgen Samuelsson (J)

Department of Engineering and Chemical Sciences, Karlstad University, SE-651 88 Karlstad, Sweden. Electronic address: Jorgen.Samuelsson@kau.se.

Eivor Örnskov (E)

Advanced Drug Delivery, Pharmaceutical Sciences, BioPharmaceuticals R&D, AstraZeneca,Gothenburg, 431 83, Mölndal, Sweden.

Linda Thunberg (L)

Early Chemical Development, Pharmaceutical Sciences, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, 431 83, Mölndal, Sweden.

Anders Dahlén (A)

Oligonucleotide Discovery, Discovery Sciences, BioPharmaceuticals R&D, AstraZeneca, Gothenburg, 431 83, Mölndal, Sweden.

Torgny Fornstedt (T)

Department of Engineering and Chemical Sciences, Karlstad University, SE-651 88 Karlstad, Sweden. Electronic address: Torgny.Fornstedt@kau.se.

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Classifications MeSH