Evidence map›Paper›PMID 41814779›Full record

ArticleElectrophoresis2026

Improvement of Peak Integration in Capillary Electrophoresis: Reference Data Set No. 1.

Marlon Krompholz, Timothy Blanc, Huixin Lu, Patricia Christensen, Frédéric Ginot, Gábor Járvás, Trang D Nguyen, Ashley Prout, Timothy Riehlman, Brian Wei and 5 more

Abstract read
In one paragraph

Article in Electrophoresis, 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

15 authors.

Marlon KrompholzInstitute of Medicinal and Pharmaceutical Chemistry, Technische Universität Braunschweig, Braunschweig, Germany.
Timothy BlancBiopharm Control Strategy, LLC., Branchburg, New Jersey, USA.
Huixin LuCentre for Oncology, Radiopharmaceuticals and Research, Health Canada, Health Products and Food Branch, Biologic and Radiopharmaceutical Drugs Directorate, Ottawa, Ontario, Canada.
Patricia ChristensenVaccines Analytical Research and Development, Merck & Co., Inc., West Point, Pennsylvania, USA.
Frédéric GinotADELIS SAS, Labège, France.
Gábor JárvásResearch Institute of Biomolecular and Chemical Engineering, University of Pannonia, Veszprem, Hungary.
Trang D NguyenEli Lilly and Company, Indianapolis, Indiana, USA.
Ashley ProutVaccines Analytical Research and Development, Merck & Co., Inc., West Point, Pennsylvania, USA.
Timothy RiehlmanRegeneron Pharmaceuticals, Rensselaer, New York, USA.
Brian WeiBioProcess Analytics, Sanofi, Framingham, Massachusetts, USA.
Andrei Hutanuten23 health, Basel, Switzerland.
Steffen Kiessigten23 health, Basel, Switzerland.
Knut BaumannInstitute of Medicinal and Pharmaceutical Chemistry, Technische Universität Braunschweig, Braunschweig, Germany.
Cari E Sänger-van de GriendInstitute of Medicinal and Pharmaceutical Chemistry, Technische Universität Braunschweig, Braunschweig, Germany.
Hermann WätzigInstitute of Medicinal and Pharmaceutical Chemistry, Technische Universität Braunschweig, Braunschweig, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Capillary electrophoresis (CE) often provides superior separation of macromolecules such as monoclonal antibodies (mAbs), a major biopharmaceutical class, compared with liquid chromatography. However, electropherograms frequently exhibit complex baselines and peak shapes that are not reliably handled by integration algorithms designed for chromatographic data, and manual integration is often required. Many concepts have been proposed to improve peak integration, ranging from incremental algorithmic refinements and signal-to-noise (S/N)-based approaches to artificial intelligence (AI)-driven strategies, but objective performance comparisons are not possible without shared reference data sets and agreed peak limits. To address this gap, we initiated a multinational collaboration involving industrial and academic laboratories to create a comprehensive reference data set for CE peak integration. A total of 227 challenging and practically relevant electropherograms were collected from diverse applications, converted to a standardized format, and independently integrated by multiple experts. Using dedicated software tools and a structured consensus process, mutually accepted reference integration limits were established for each data set. These reference electropherograms, together with the underlying integration rules, are now made available to the scientific community. Analysis of the reference data set identified general principles for reliable peak integration, including the importance of standardized zoom levels and consistent handling of small peaks near the noise level. The data set provides a common foundation for benchmarking commercial chromatography data systems (CDS) and for developing and validating new algorithmic and AI-based integration methods. We expect this work to speed up the development of practical, automated integration strategies for CE and that these core concepts can be applied to other separation techniques.

Indexed as

Electrophoresis, CapillaryAlgorithmsAntibodies, MonoclonalReference StandardsSignal-To-Noise RatioSoftwareAntibodies, Monoclonal

Identifiers

PMID41814779
PMCPMC13084974

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Registered trials

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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.