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Título
Building Artificial Neural Networks for the Optimization of Sustained-Release Kinetics of Metronidazole from Colonic Hydrophilic Matrices
Autor(es)
Palabras clave
artificial neural network
computational prediction
in vitro modelling
colonic drug delivery
pharmaceutical formulation
controlled release systems
artificial intelligence
Clasificación UNESCO
1203.04 Inteligencia Artificial
3209 Farmacología
3314 Tecnología Médica
32 Ciencias Médicas
Fecha de publicación
2025-11-10
Editor
MDPI
Citación
Maderuelo, C., Arévalo-Pérez, R., & Lanao, J. M. (2025). Building Artificial Neural Networks for the Optimization of Sustained-Release Kinetics of Metronidazole from Colonic Hydrophilic Matrices. Pharmaceutics, 17(11), 1451. https://doi.org/10.3390/pharmaceutics17111451
Resumen
Introduction: Drug development has traditionally used mathematical models to predict formulation behavior. Objective: Building artificial neural networks for the drug release evaluation of drug delivery systems using sustained-release metronidazole-coated colonic hydrophilic matrices as a model. Methods: The technological factors associated with the biopharmaceutical performance of hydrophilic metronidazole matrices were evaluated using a quality by design approach (QbD). The developed neural network includes variables related to the technological process for producing the matrices. These are related to the materials used, such as the type and viscosity of core polymers, the type of coating agent, or the matrix production process, such as the mixing time of core materials or the percentage of the coating agent. The output variables of the neural network were the percentages of drug released in vitro at 1, 6, 12, and 24 h and the mean dissolution time of the matrix. An iterative quasi-Newton method was used to train the artificial neural network. Results: A neural network with excellent prediction capacity allows selecting the technological variables with the greatest influence on the % of drug dissolved: the type of coating agent used and the percentage of the total weight increase after coating for 1 h and 6 h of drug release and also the viscosity of the HPMC for 12 and 24 h. Conclusions: The optimized neural network demonstrated an excellent predictive capacity for in vitro drug dissolution profiles, allowing the use of this type of methodology based on artificial intelligence methods in the optimization of drug delivery systems.
URI
ISSN
1999-4923
DOI
10.3390/pharmaceutics17111451
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