Evidence map›Paper›PMID 38634379›Full record

ArticleBioanalysis2024

Observations from a decade of oligonucleotide bioanalysis by LC-MS.

Matthew Ewles, Aaron R Ledvina, Brendan Powers, C Eric Thomas

Abstract read
In one paragraph

Article in Bioanalysis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Article
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

4 authors.

Matthew EwlesLabcorp Early Development Laboratories Limited; Otley Road, Harrogate; North Yorkshire, HG3 1PY, UK.
Aaron R LedvinaLabcorp Early Development Laboratories, Inc.; 3301 Kinsman Blvd., Madison, WI 53704, USA.
Brendan PowersLabcorp Early Development Laboratories, Inc.; 3301 Kinsman Blvd., Madison, WI 53704, USA.
C Eric ThomasLabcorp Central Laboratory Services Limited Partnership; 8211 SciCor Drive, Indianapolis, IN 46214, USA.ORCID 0009-0005-3498-5471

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is a growing need for efficient bioanalysis of oligonucleotide therapeutics. This broad class of molecules presents numerous challenges relative to traditional small molecule therapeutics. Methodologies including ligand-binding assays or polymerase chain reaction may be fit-for-purpose in many instances, but liquid chromatography coupled to mass spectrometry (LC-MS) often delivers the best balance of sensitivity and selectivity. Over the last decade, we have engaged with many such molecules and derived insights into challenges and solutions. Herein, we provide four case studies illustrating challenges we have encountered. These issues include low or variable analyte recovery, poor resolution from related species, chromatographic abnormalities or challenging sensitivity. We present a summary of considerations, based on these experiences, to assist others working in the area.

Indexed as

Mass SpectrometryOligonucleotidesChromatography, LiquidHumansLiquid Chromatography-Mass SpectrometryOligonucleotidesbioanalysischromatographicHRMSLC-MSoligonucleotideperspectivesiRNAtriple quadrupole

Identifiers

PMID38634379
PMCPMC11352704

What OpenQuestion holds

Textmetadata
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.