Literature DB >> 3657186

Design of experiments for the precise estimation of dose-response parameters: the Hill equation.

M Bezeau1, L Endrenyi.   

Abstract

Optimal experimental designs were evaluated for the precise estimation of parameters of the Hill model. The optimally effective designs were obtained by using the criterion of D-optimization. For the Hill model, optimal designs replicate 3 sampling points. These points were shown to be quite sensitive to the behavior of the experimental error. Since an investigator is often uncertain about error conditions in biological studies, a practical approach would use the sampling scheme calculated for an intermediate error condition. Thus, if the behavior of error variances is not known, precise parameters of the Hill model are obtained by choosing concentrations which yield fractional responses (responses divided by their asymptotic, maximum value) of 0.086, 0.581 and 1.0. When experimental constraints limit the maximum attainable concentration and response, all design points are lowered. Appropriate designs can be constructed based on the design which is optimal when constraints result in a maximum attainable fractional response of 0.5. The optimal designs were found to be robust when the parameter values assumed by the investigator did not equal their true values. The estimating efficiencies obtained by using two frequently applied designs were assessed. Uniformly spaced concentrations yielded imprecise parameters. Six-point, geometrically spaced designs gave generally good results. However, their estimating efficiency was generally exceeded by the recommended sampling schemes even in the presence of uncertainty about error conditions. The method exemplified in this paper can be used for other models.

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Year:  1986        PMID: 3657186     DOI: 10.1016/s0022-5193(86)80211-9

Source DB:  PubMed          Journal:  J Theor Biol        ISSN: 0022-5193            Impact factor:   2.691


  7 in total

1.  Optimal experimental design for precise estimation of the parameters of the axial dispersion model of hepatic elimination.

Authors:  C H Chou; L Aarons; M Rowland
Journal:  J Pharmacokinet Biopharm       Date:  1998-10

2.  An example of optimal phase II design for exposure response modelling.

Authors:  Alan Maloney; Marloes Schaddelee; Jan Freijer; Walter Krauwinkel; Marcel van Gelderen; Philippe Jacqmin; Ulrika S H Simonsson
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3.  Optimal design for estimating parameters of the 4-parameter hill model.

Authors:  Leonid A Khinkis; Laurence Levasseur; Hélène Faessel; William R Greco
Journal:  Nonlinearity Biol Toxicol Med       Date:  2003-07

4.  A sulfide:quinone oxidoreductase from Chlorobaculum tepidum displays unusual kinetic properties.

Authors:  Kevin E Shuman; Thomas E Hanson
Journal:  FEMS Microbiol Lett       Date:  2016-04-18       Impact factor: 2.742

5.  Characterization of the interaction constants for the binding of two unlabelled ligands to the sites of a receptor. An experimental strategy.

Authors:  S Swillens; A Gourdin; O Delahaut
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1989-05       Impact factor: 3.000

6.  Quantitative high-throughput screening data analysis: challenges and recent advances.

Authors:  Keith R Shockley
Journal:  Drug Discov Today       Date:  2014-10-23       Impact factor: 7.851

7.  Efficient Optimization of Stimuli for Model-Based Design of Experiments to Resolve Dynamical Uncertainty.

Authors:  Thembi Mdluli; Gregery T Buzzard; Ann E Rundell
Journal:  PLoS Comput Biol       Date:  2015-09-17       Impact factor: 4.475

  7 in total

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