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ToxSci Advance Access originally published online on September 14, 2005
Toxicological Sciences 2005 88(2):467-476; doi:10.1093/toxsci/kfi320
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© The Author 2005. Published by Oxford University Press on behalf of the Society of Toxicology. All rights reserved. For Permissions, please email: journals.permissions@oxfordjournals.org

D-Optimal Experimental Designs to Test for Departure from Additivity in a Fixed-Ratio Mixture Ray

Todd Coffey*, Chris Gennings*,1, Jane Ellen Simmons{dagger} and David W. Herr{dagger}

* Department of Biostatistics, Virginia Commonwealth University, Richmond, Virginia 23298; {dagger} National Health and Environmental Effects Research Laboratory, ORD, U.S. Environmental Protection Agency, Research Triangle Park, North Carolina 27711

Received May 17, 2005; accepted September 7, 2005

Traditional factorial designs for evaluating interactions among chemicals in a mixture may be prohibitive when the number of chemicals is large. Using a mixture of chemicals with a fixed ratio (mixture ray) results in an economical design that allows estimation of additivity or nonadditive interaction for a mixture of interest. This methodology is extended easily to a mixture with a large number of chemicals. Optimal experimental conditions can be chosen that result in increased power to detect departures from additivity. Although these designs are used widely for linear models, optimal designs for nonlinear threshold models are less well known. In the present work, the use of D-optimal designs is demonstrated for nonlinear threshold models applied to a fixed-ratio mixture ray. For a fixed sample size, this design criterion selects the experimental doses and number of subjects per dose level that result in minimum variance of the model parameters and thus increased power to detect departures from additivity. An optimal design is illustrated for a 2:1 ratio (chlorpyrifos:carbaryl) mixture experiment. For this example, and in general, the optimal designs for the nonlinear threshold model depend on prior specification of the slope and dose threshold parameters. Use of a D-optimal criterion produces experimental designs with increased power, whereas standard nonoptimal designs with equally spaced dose groups may result in low power if the active range or threshold is missed.

Key Words: additivity; nonadditivity; nonlinear threshold models; optimal designs.


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