Evidence map›Paper›PMID 28768512›Full record

ArticleTheoretical biology & medical modelling2017

Theory of synergistic effects: Hill-type response surfaces as 'null-interaction' models for mixtures.

Michael Schindler

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Article in Theoretical biology & medical modelling, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

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15citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

15 citing papers in PubMed.

  1. Article
  2. Preventing Preterm Birth: The Search for Tocolytic Synergism.Reproductive sciences (Thousand Oaks, Calif.) · 2025
    Review
  3. Article
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  12. Review
  13. Article
  14. Charting the Fragmented Landscape of Drug Synergy.Trends in pharmacological sciences · 2020
    Review
  15. Article
4 · The record

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5 · Who and what money

Authors and funding

1 author.

Michael SchindlerInstitute of Theoretical Chemistry, Ruhr-University Bochum, Universitätsstr., Bochum, Germany. Michael.Schindler@rub.de.ORCID 0000-0002-5141-636X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe classification of effects caused by mixtures of agents as synergistic, antagonistic or additive depends critically on the reference model of 'null interaction'. Two main approaches are currently in use, the Additive Dose (ADM) or concentration addition (CA) and the Multiplicative Survival (MSM) or independent action (IA) models. We compare several response surface models to a newly developed Hill response surface, obtained by solving a logistic partial differential equation (PDE). Assuming that a mixture of chemicals with individual Hill-type dose-response curves can be described by an n-dimensional logistic function, Hill's differential equation for pure agents is replaced by a PDE for mixtures whose solution provides Hill surfaces as 'null-interaction' models and relies neither on Bliss independence or Loewe additivity nor uses Chou's unified general theory.

methodsAn n-dimensional logistic PDE decribing the Hill-type response of n-component mixtures is solved. Appropriate boundary conditions ensure the correct asymptotic behaviour. Mathematica 11 (Wolfram, Mathematica Version 11.0, 2016) is used for the mathematics and graphics presented in this article.

resultsThe Hill response surface ansatz can be applied to mixtures of compounds with arbitrary Hill parameters. Restrictions which are required when deriving analytical expressions for response surfaces from other principles, are unnecessary. Many approaches based on Loewe additivity turn out be special cases of the Hill approach whose increased flexibility permits a better description of 'null-effect' responses. Missing sham-compliance of Bliss IA, known as Colby's model in agrochemistry, leads to incompatibility with the Hill surface ansatz. Examples of binary and ternary mixtures illustrate the differences between the approaches. For Hill-slopes close to one and doses below the half-maximum effect doses MSM (Colby, Bliss, Finney, Abbott) predicts synergistic effects where the Hill model indicates 'null-interaction'. These differences increase considerably with increasing steepness of the individual dose-response curves.

conclusionThe Hill response surface ansatz contains the Loewe additivity concept as a special case and is incompatible with Bliss independent action. Hence, when synergistic effects are claimed, those dose combinations deserve special attention where the differences between independent action approaches and Hill estimations are large.

Indexed as

Drug SynergismModels, BiologicalDioxinsPyrethrinsDioxinsPyrethrinsBliss independenceColby’s formulaHill response surfaceLoewe additivitySynergistic effects

Identifiers

PMID28768512
PMCPMC5541435

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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.