Evidence map›Paper›PMID 42653172›Full record

ArticleInternational journal of molecular sciences2026

Condition-Specific LC Retention Time Prediction: Feature-Selected QSRR Versus Pretrained Graph Isomorphism Network Transfer Learning.

Roman Szucs, Emília Sýkorová, Iveta Boháčová, Ilaria Neri, Lucy M Morgan, Merisa Moriarty, Melissa Hanna-Brown

Abstract read
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Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Roman SzucsDepartment of Analytical Chemistry, Faculty of Natural Sciences, Comenius University Bratislava, Ilkovičova 6, SK-84215 Bratislava, Slovakia.ORCID 0000-0003-0011-0317
Emília SýkorováDepartment of Analytical Chemistry, Faculty of Natural Sciences, Comenius University Bratislava, Ilkovičova 6, SK-84215 Bratislava, Slovakia.ORCID 0009-0005-9152-4698
Iveta BoháčováDepartment of Analytical Chemistry, Faculty of Natural Sciences, Comenius University Bratislava, Ilkovičova 6, SK-84215 Bratislava, Slovakia.
Ilaria NeriSchool of Chemistry, University College Cork, College Road, T12 YN60 Cork, Ireland.
Lucy M MorganPfizer Worldwide Research, Development and Medical, Sandwich CT13 9NJ, UK.ORCID 0000-0002-6432-3760
Merisa MoriartyPfizer Worldwide Research, Development and Medical, Ringaskiddy, P43 X336 Cork, Ireland.
Melissa Hanna-BrownSchool of Chemistry, University College Cork, College Road, T12 YN60 Cork, Ireland.ORCID 0009-0001-8228-3440

Funding

Slovak Research and Development Agency APVV-24-0242
6 · The paper itself

Abstract

Condition-specific liquid chromatographic retention time prediction remains challenging because retention depends on both molecular structure and experimental conditions. This study compared feature-selected quantitative structure-retention relationship (FS-QSRR) models with pretrained graph isomorphism network (GIN) transfer learning for three reversed-phase LC datasets measured under acidic, neutral, and basic conditions. Mordred descriptor-based QSRR models were developed using leakage-safe preprocessing, nested cross-validation, and feature selection. The selected FS-QSRR workflow for each dataset was then compared with pretrained GIN transfer learning using identical 100 repeated random 80/20 train-test splits. Feature selection substantially reduced descriptor dimensionality but did not consistently improve predictive accuracy over the best baseline descriptor models. Under matched validation, GIN transfer learning gave lower RMSE for all three datasets, decreasing error from 0.816 to 0.613 min under acidic conditions, from 0.868 to 0.665 min under neutral conditions, and from 1.019 to 0.876 min under basic conditions. The corresponding RMSE reductions were 24.8%, 23.4%, and 14.0%, respectively. Matched prediction error analysis showed that GIN particularly reduced the frequency and magnitude of large errors, although the improvement was more modest under basic conditions. Descriptor frequency analysis revealed condition-dependent contributions from lipophilicity, ionization-related, electronic, and topological descriptor groups. These findings support pretrained GIN transfer learning as the stronger predictive approach, while FS-QSRR remains valuable for model simplification and chemical interpretation.

Indexed as

Chromatography, Reverse-PhaseQuantitative Structure-Activity RelationshipChromatography, Liquiddeep learningfeature selectiongraph isomorphism networkmolecular graphsMordred descriptorsquantitative structure–retention relationshipsretention time predictionreversed-phase liquid chromatographytransfer learning

Identifiers

PMID42653172
PMCPMC13513519

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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.