Abstract
Nonlinear mixed effect model is the most used technique when developing a pharmacokinetic population model (PopPK), the characterization of a drug disposition into the body and taking decisions related to the dose adjustments. The covariate model is used to establish a relationship between the model parameters and the characteristics of the patients, and it helps to explain sources of variability in the PopPK. A known problem in the development of a covariate model is to decide which covariates should or should not be included in the model. In this work, a genetic algorithm (GA) was used to decide which covariates contribute in a major degree prediction of the variability in a PopPK model.
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Acknowledgments
We thank to Instituto Politécnico Nacional (IPN), to the Comisión de Fomento y Apoyo Académico del IPN (COFAA), and the Mexican National Council of Science and Technology (CONACYT) for supporting our research activities.
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Montiel, O., Cornejo, J.M., Sepúlveda, C., Sepúlveda, R. (2015). Obtaining Pharmacokinetic Population Models Using a Genetic Algorithm Approach. In: Melin, P., Castillo, O., Kacprzyk, J. (eds) Design of Intelligent Systems Based on Fuzzy Logic, Neural Networks and Nature-Inspired Optimization. Studies in Computational Intelligence, vol 601. Springer, Cham. https://doi.org/10.1007/978-3-319-17747-2_24
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DOI: https://doi.org/10.1007/978-3-319-17747-2_24
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