Evidence map›Paper›PMID 42449032›Full record

ArticlePharmaceutical research2026

Raman Spectroscopy for Characterizing Monoclonal Antibody Reduction: A Process Analytical Technology Approach for Antibody-Drug Conjugation Process Development.

David Pople, Zhenshu Wang, Anton Kozyryev, Bhumit Patel, Emmanuel Appiah-Amponsah, Hanzhou Feng

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Article in Pharmaceutical research, 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

6 authors.

David PopleCenter for Advanced Biotechnology and Medicine, Rutgers University, Piscataway, NJ, USA.
Zhenshu WangBiologic Process Research & Development, Merck & Co., Inc, Rahway, NJ, USA.
Anton KozyryevAnalytical Research & Development, Merck & Co., Inc, Rahway, NJ, USA.
Bhumit PatelAnalytical Research & Development, Merck & Co., Inc, Rahway, NJ, USA.
Emmanuel Appiah-AmponsahAnalytical Research & Development, Merck & Co., Inc, Rahway, NJ, USA.
Hanzhou FengAnalytical Research & Development, Merck & Co., Inc, Rahway, NJ, USA. Hanzhou.feng@merck.com.ORCID http://orcid.org/0000-0002-0822-2965

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundControlled disulfide bond reduction is critical in antibody-drug conjugate (ADC) manufacturing, enabling site-specific conjugation and desired drug-to-antibody ratios. Current characterization relies on time-consuming offline capillary electrophoresis, creating bottlenecks in process development where multiple conditions must be rapidly screened. This study evaluates Raman spectroscopy as a process analytical technology (PAT) to elucidate reduction kinetics and accelerate optimization for ADC development.

methodsA Design of Experiments approach investigated TCEP-mediated reduction of an IgG1 antibody under varying TCEP/mAb ratios (5-15) and pH conditions (5.5-7.5). Raman spectra were collected throughout reduction reactions. Principal component analysis (PCA) characterized reduction kinetics, while partial least squares (PLS) regression quantified fragment formation against non-reduced capillary electrophoresis sodium dodecyl sulfate (nrCE-SDS) measurements.

resultsPCA effectively captured reduction kinetics, with PC1 trajectories correlating strongly with heavy chain (HC) formation measured by nrCE-SDS. The analysis revealed pH-dependent TCEP saturation effects: higher pH showed convergent kinetics at elevated ratios while lower pH maintained ratio-dependent rates. PLS models successfully predicted HC formation, demonstrating potential for endpoint detection despite the interchain disulfide bonds representing only ~ 0.2% of total protein mass.

conclusionsRaman spectroscopy with chemometric analysis provides valuable insights for ADC process development. PCA enables rapid screening of reduction conditions without nrCE-SDS confirmation, reducing analytical burden during early development. Unlike offline nrCE-SDS, Raman offers potential for real-time online PAT implementation. Future work focusing on narrower operating ranges could enhance model performance for manufacturing applications.

Indexed as

Antibodies, MonoclonalImmunoconjugatesSpectrum Analysis, RamanDisulfidesElectrophoresis, CapillaryHydrogen-Ion ConcentrationImmunoglobulin GKineticsLeast-Squares AnalysisOxidation-ReductionPrincipal Component AnalysisAntibodies, MonoclonalDisulfidesImmunoconjugatesImmunoglobulin Gantibody drug conjugatechemometricsdisulfide reductionprocess analytical technologyraman spectroscopy

Identifiers

PMID42449032

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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.