On the existence conditions of interaction indices in response surface models

Response-surface models (RSMs) are widely used to characterize the combined effects of two agents and to classify their interaction as additivity, synergy, or antagonism. In this context, an interaction index is frequently used as a quantitative measure. However, estimation of the interaction index outside feasible ranges may result in complex-valued or biologically implausible predictions in certain regions of the input domain, thereby limiting the validity of the model. This paper introduces a feasibility analysis framework that distinguishes between isobole-level feasibility (i.e. the existence of well-defined isoboles at a given effect level) and global feasibility (i.e. well-posedness across the entire domain). The analysis explicitly characterizes the singular sets that arise when feasibility conditions are violated, thereby explaining when and how models fail. The approach is demonstrated on three canonical models, i.e. Greco, Minto, and Finney, and supported by numerical illustrations, offering practical guidance for systematic and robust parameter selection in drug combination studies, toxicology, and process engineering.

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Publication Details

Journal
Journal of Pharmacokinetics and Pharmacodynamics
Published
2026-03-02
DOI
https://doi.org/10.1007/s10928-026-10026-x
Primary Topic
Stochastic processes and statistical mechanics
Type
article
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article

On the existence conditions of interaction indices in response surface models

Clara M. Ionescu, Erhan Yumuk
Journal of Pharmacokinetics and Pharmacodynamics
Stochastic processes and statistical mechanics
article

On the existence conditions of interaction indices in response surface models

Clara M. Ionescu, Erhan Yumuk
article en

Abstract

Response-surface models (RSMs) are widely used to characterize the combined effects of two agents and to classify their interaction as additivity, synergy, or antagonism. In this context, an interaction index is frequently used as a quantitative measure. However, estimation of the interaction index outside feasible ranges may result in complex-valued or biologically implausible predictions in certain regions of the input domain, thereby limiting the validity of the model. This paper introduces a feasibility analysis framework that distinguishes between isobole-level feasibility (i.e. the existence of well-defined isoboles at a given effect level) and global feasibility (i.e. well-posedness across the entire domain). The analysis explicitly characterizes the singular sets that arise when feasibility conditions are violated, thereby explaining when and how models fail. The approach is demonstrated on three canonical models, i.e. Greco, Minto, and Finney, and supported by numerical illustrations, offering practical guidance for systematic and robust parameter selection in drug combination studies, toxicology, and process engineering.

Journal of Pharmacokinetics and PharmacodynamicsVol. 53(2)
Ghent University (BE), Flanders Make (Belgium) (BE), Dynamic Systems (United States) (US), Istanbul Technical University (TR)
Climate action
Openalex Percentile: Top 33%
Stochastic processes and statistical mechanics
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