Evidence map›Paper›PMID 41736386›Full record

ArticleJournal of separation science2026

Enabling Large-Volume Injections in Hydrophilic Interaction Chromatography of Oligonucleotides Through In-Line Mixing.

Joshka Verduin, Luca Tutiš, Antonia Kritsima, Andrea F G Gargano, Govert W Somsen

Abstract read
In one paragraph

Article in Journal of separation science, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Joshka VerduinDepartment of Chemistry and Pharmaceutical Sciences, Division of BioAnalytical Chemistry, Amsterdam Institute of Molecular and Life Sciences (AIMMS), Vrije Universiteit Amsterdam, Amsterdam, Netherlands.ORCID https://orcid.org/0000-0002-5862-6036
Luca TutišDepartment of Chemistry and Pharmaceutical Sciences, Division of BioAnalytical Chemistry, Amsterdam Institute of Molecular and Life Sciences (AIMMS), Vrije Universiteit Amsterdam, Amsterdam, Netherlands.ORCID https://orcid.org/0009-0001-1348-7183
Antonia KritsimaCentre for Analytical Sciences Amsterdam (CASA), Amsterdam, Netherlands.ORCID https://orcid.org/0009-0001-9955-1958
Andrea F G GarganoCentre for Analytical Sciences Amsterdam (CASA), Amsterdam, Netherlands.ORCID https://orcid.org/0000-0003-3361-7341
Govert W SomsenDepartment of Chemistry and Pharmaceutical Sciences, Division of BioAnalytical Chemistry, Amsterdam Institute of Molecular and Life Sciences (AIMMS), Vrije Universiteit Amsterdam, Amsterdam, Netherlands.ORCID https://orcid.org/0000-0003-4200-2015

Funding

NWO ENPPS.TA.019.001NWO KICH1.ST01.20.041
6 · The paper itself

Abstract

Hydrophilic interaction chromatography (HILIC) is an attractive separation mode for the analysis of therapeutic oligonucleotides (ONs). ONs are very polar compounds that are commonly dissolved in highly aqueous media, whereas HILIC eluents often comprise a high percentage of organic solvent. This solvent mismatch can cause breakthrough and peak splitting. In this study, we investigated the effects of the sample solvent composition and injection volume on the HILIC separation of nucleobases and ONs, and to what extent an in-line mixer between injector and column can mitigate breakthrough and peak splitting. Using isocratic HILIC with nucleobases as medium-polar, less-retentive test compounds, we illustrated that an injection solvent of 90% water results in peak broadening, which deteriorates with increasing injection volume, leading to serious peak deformations and asymmetries. Here, in-line mixing did not improve peak shapes, as the mixer volume adds to band broadening and the homogenization of the injection solvent with the HILIC eluent does not lead to on-column focusing conditions. When analyzing an ON mixture (15/16/17-mer) dissolved in a weak solvent (30% water) by gradient HILIC, injection volumes could be increased up to 20 µL (5.7% of the column volume) without losing separation performance. However, when the ON mixture was dissolved in 100% water, injection volumes above 2 µL caused severe peak distortion and extensive analyte breakthrough in gradient HILIC. When injecting the ONs in 100% water with a 100-µL in-line mixer, no analyte breakthrough and peak splitting were observed for injection volumes up to 40 µL, while maintaining baseline separation of the ONs. The usefulness of in-line mixing in HILIC was demonstrated by the analysis of a pharmaceutical antisense ON (ASO). Large-volume injection of this ON in 100% water allowed for the separation and detection of the main compound and adjacent minor impurities, without breakthrough or severe peak distortion.

Indexed as

OligonucleotidesChromatography, LiquidHydrophobic and Hydrophilic InteractionsSolventsOligonucleotidesSolventsaqueous injectionHILICmixersnucleobasestherapeutic oligonucleotides

Identifiers

PMID41736386
PMCPMC12932959

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.