Evidence map›Paper›PMID 42334899›Full record

ArticleAnalytical chemistry2026

Lévy Formulation of the Stochastic Theory of Chromatography and Extension to Phase-Type Markov Renewal Process.

Arash Mirzahosseini, Annamária Sepsey, Gergő Tóth, Attila Felinger

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Article in Analytical chemistry, 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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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Arash MirzahosseiniDepartment of Pharmaceutical Chemistry, Semmelweis University, Budapest H-1092, Hungary.ORCID 0000-0002-3281-8435
Annamária SepseyInstitute of Bioanalysis, Medical School, University of Pécs, Pécs H-7624, Hungary.
Gergő TóthDepartment of Pharmaceutical Chemistry, Semmelweis University, Budapest H-1092, Hungary.
Attila FelingerInstitute of Bioanalysis, Medical School, University of Pécs, Pécs H-7624, Hungary.ORCID 0000-0001-7130-1968

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The stochastic theory of chromatography describes solute migration as the cumulative result of random retention events superimposed on convective transport and axial dispersion. Classical Poisson-based formulations offer analytical transparency but are limited in their ability to represent heterogeneous, multistep, or multipathway adsorption kinetics increasingly revealed by single-molecule measurements. Here, we reformulate stochastic chromatography within a Lévy-Khintchine characteristic function framework and extend the underlying event structure to phase-type Markov renewal processes, including Erlang and hyper-Erlang waiting-time distributions. This representation preserves analytical tractability through matrix-exponential evaluation while enabling flexible descriptions of heterogeneous adsorption-desorption pathways. We further develop an extended classical characteristic function Fourier inversion method that operates directly in the first-passage domain and incorporates multisite log-normal sojourn heterogeneity, γ distributed stationary residence times, and inverse-Gaussian treatment of mobile-phase dispersion. Application to experimental DNA chromatograms demonstrates accurate reconstruction of peak position, width, asymmetry, and tailing behavior. A hybrid Markov renewal Monte Carlo simulator was also introduced as a mechanistic first-passage benchmark. Identifiability analysis indicated that effective sojourn times and transport parameters are robustly constrained, whereas several microscopic kinetic constants remain structurally nonidentifiable from single chromatograms alone. Overall, the proposed Lévy and Fourier-inversion framework links ensemble chromatographic peak shapes with microscopic adsorption statistics and provides a practical analytical route for modeling heterogeneous stationary phases, biomolecular separations, and single-molecule-informed chromatographic method development.

Identifiers

PMID42334899
PMCPMC13347699

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