ArticlePloS one2016
Computational Intelligence Modeling of the Macromolecules Release from PLGA Microspheres-Focus on Feature Selection.
Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed.
- Predicting early and complete drug release from long-acting injectables using explainable machine learning.International journal of pharmaceutics · 2026Article
- Predicting Early and Complete Drug Release from Long-Acting Injectables Using Explainable Machine Learning.ArXiv · 2026Article
- In Vitro liposome release profile prediction using explainable machine learning approaches.PloS one · 2026Article
- Deep learning for property prediction of natural fiber polymer composites.Scientific reports · 2025Article
- Machine learning integrated with in vitro experiments for study of drug release from PLGA nanoparticles.Scientific reports · 2025Article
- Quantification of Microsphere Drug Release by Fluorescence Imaging with the FRET System.Pharmaceutics · 2024Article
- Machine Learning for Predicting Drug Release Behavior of PLGA Microspheres.AMIA ... Annual Symposium proceedings. AMIA Symposium · 2024Article
- Machine learning in accelerating microsphere formulation development.Drug delivery and translational research · 2023Article
- State-of-the-Art Review of Artificial Neural Networks to Predict, Characterize and Optimize Pharmaceutical Formulation.Pharmaceutics · 2022Review
- Deep learning forActa pharmaceutica Sinica. B · 2019Article
- The Next Era: Deep Learning in Pharmaceutical Research.Pharmaceutical research · 2016Review
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Poly-lactide-co-glycolide (PLGA) is a copolymer of lactic and glycolic acid. Drug release from PLGA microspheres depends not only on polymer properties but also on drug type, particle size, morphology of microspheres, release conditions, etc. Selecting a subset of relevant properties for PLGA is a challenging machine learning task as there are over three hundred features to consider. In this work, we formulate the selection of critical attributes for PLGA as a multiobjective optimization problem with the aim of minimizing the error of predicting the dissolution profile while reducing the number of attributes selected. Four bio-inspired optimization algorithms: antlion optimization, binary version of antlion optimization, grey wolf optimization, and social spider optimization are used to select the optimal feature set for predicting the dissolution profile of PLGA. Besides these, LASSO algorithm is also used for comparisons. Selection of crucial variables is performed under the assumption that both predictability and model simplicity are of equal importance to the final result. During the feature selection process, a set of input variables is employed to find minimum generalization error across different predictive models and their settings/architectures. The methodology is evaluated using predictive modeling for which various tools are chosen, such as Cubist, random forests, artificial neural networks (monotonic MLP, deep learning MLP), multivariate adaptive regression splines, classification and regression tree, and hybrid systems of fuzzy logic and evolutionary computations (fugeR). The experimental results are compared with the results reported by Szlȩk. We obtain a normalized root mean square error (NRMSE) of 15.97% versus 15.4%, and the number of selected input features is smaller, nine versus eleven.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.