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Drug interaction: focusing on response surface models

Anesthesiologists have been aware of the importance of optimal drug combination long ago and performed many investigations about the combined use of anesthetic agents. There are 3 classes of drug interaction: additive, synergistic, and antagonistic. These definitions of drug interaction suggest that...

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Autor principal: Lee, Soo-il
Formato: Texto
Lenguaje:English
Publicado: The Korean Society of Anesthesiologists 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2881515/
https://www.ncbi.nlm.nih.gov/pubmed/20532049
http://dx.doi.org/10.4097/kjae.2010.58.5.421
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author Lee, Soo-il
author_facet Lee, Soo-il
author_sort Lee, Soo-il
collection PubMed
description Anesthesiologists have been aware of the importance of optimal drug combination long ago and performed many investigations about the combined use of anesthetic agents. There are 3 classes of drug interaction: additive, synergistic, and antagonistic. These definitions of drug interaction suggest that a zero interaction model should exist to be used as a reference in classifying the interaction of drug combinations. The Loewe additivity has been used as a universal reference model for classifying drug interaction. Most anesthetic drugs follow the sigmoid E(max) model (Hill equation); this model will be used for modeling response surface. Among lots of models for drug interaction in the anesthetic area, the Greco model, Machado model, Plummer model, Carter model, Minto model, Fidler model, and Kong model are adequate to be applied to the data of anesthetic drug interaction. A model with a single interaction parameter does not accept an inconsistency in the classes of drug interactions. To solve this problem, some researchers proposed parametric models which have a polynomial interaction function to capture synergy, additivity, and antagonism scattered all over the surface of drug combinations. Inference about truth must be based on an optimal approximating model. Akaike information criterion (AIC) is the most popular approach to choosing the best model among the aforementioned models. Whatever the good qualities of a chosen model, it is uncertain whether the chosen model is the best model. A more robust inference can be extracted from averaging several models that are considered relevant.
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spelling pubmed-28815152010-06-08 Drug interaction: focusing on response surface models Lee, Soo-il Korean J Anesthesiol Review Article Anesthesiologists have been aware of the importance of optimal drug combination long ago and performed many investigations about the combined use of anesthetic agents. There are 3 classes of drug interaction: additive, synergistic, and antagonistic. These definitions of drug interaction suggest that a zero interaction model should exist to be used as a reference in classifying the interaction of drug combinations. The Loewe additivity has been used as a universal reference model for classifying drug interaction. Most anesthetic drugs follow the sigmoid E(max) model (Hill equation); this model will be used for modeling response surface. Among lots of models for drug interaction in the anesthetic area, the Greco model, Machado model, Plummer model, Carter model, Minto model, Fidler model, and Kong model are adequate to be applied to the data of anesthetic drug interaction. A model with a single interaction parameter does not accept an inconsistency in the classes of drug interactions. To solve this problem, some researchers proposed parametric models which have a polynomial interaction function to capture synergy, additivity, and antagonism scattered all over the surface of drug combinations. Inference about truth must be based on an optimal approximating model. Akaike information criterion (AIC) is the most popular approach to choosing the best model among the aforementioned models. Whatever the good qualities of a chosen model, it is uncertain whether the chosen model is the best model. A more robust inference can be extracted from averaging several models that are considered relevant. The Korean Society of Anesthesiologists 2010-05 2010-05-29 /pmc/articles/PMC2881515/ /pubmed/20532049 http://dx.doi.org/10.4097/kjae.2010.58.5.421 Text en Copyright © The Korean Society of Anesthesiologists, 2010 http://creativecommons.org/licenses/by-nc/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Lee, Soo-il
Drug interaction: focusing on response surface models
title Drug interaction: focusing on response surface models
title_full Drug interaction: focusing on response surface models
title_fullStr Drug interaction: focusing on response surface models
title_full_unstemmed Drug interaction: focusing on response surface models
title_short Drug interaction: focusing on response surface models
title_sort drug interaction: focusing on response surface models
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2881515/
https://www.ncbi.nlm.nih.gov/pubmed/20532049
http://dx.doi.org/10.4097/kjae.2010.58.5.421
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