A review on integrated machine learning and deep learning driven artificial intelligence models for pharmacokinetics and toxicokinetics predictions, and their application

Обзор интегрированных моделей искусственного интеллекта на основе машинного и глубокого обучения для прогнозирования фармакокинетики и токсикокинетики и их применения
Isha Taneja, M. Malarvannan, S. Monohar, Sanskruti Sitaram Kate, Swati Jaiswal, Bhupesh Pratap, Prakash Chandra Rathi, Shikha Thakur, David Paul, Muhammad Wahajuddin
2026-01-22

ADMET property predictiondrug discoveryhybrid artificial intelligencepharmacokinetics predictionstoxicokinetics predictions
The development of artificial intelligence (AI) tools and technology has made AI-driven drug discovery a more prominent field. We are firmly in the AI era, with hybrid designs that eventually comprise deep learning (DL) and conventional machine learning (ML). Although traditional models can predict ADMET (Absorption, Distribution, Metabolism, Excretion, and Toxicity) properties, they remain relatively unsuccessful, and improving the accuracy of predictions remains challenging. Recently, several researchers have developed a hybrid learning model that successfully addresses these problems and improves prediction accuracy. The systematic tendencies facing AI-powered transformation from conventional DL and ML to hybrid learning AI models are examined in this review. Compared with traditional ML and DL, hybrid AI models have increased efficiency by reducing drug development time and costs, and improved success rates. In this context, the ongoing development of new ADMET software based on hybrid AI and multimodeling techniques can enhance the accuracy of pharmacokinetic-pharmacodynamic predictions, improve ADMET endpoint predictions, and expedite the drug discovery of new chemical entities. Moreover, this review covers the future of AI in pharmaceutical sciences and ADMET predictions, including AI-driven prediction models that range from basic ML/DL to newly developed hybrid models, evaluation parameters, and their applications in ADMET property prediction. SIGNIFICANCE STATEMENT: The article covers the compilation of ongoing research in the development of ADMET (Absorption, Distribution, Metabolism, Excretion, and Toxicity) software based on hybrid artificial intelligence and multimodeling techniques, which may increase the accuracy of pharmacokinetic-pharmacodynamic predictions, improve ADMET endpoint predictions, and accelerate drug discovery.
1
Compared with traditional machine-learning and deep-learning approaches, hybrid AI models are reported to improve efficiency, reduce drug-development time and costs, and increase success rates.
2
Despite progress, accurate ADMET prediction remains challenging, motivating continued development and evaluation of integrated AI models.
3
Hybrid AI and multimodeling software may improve pharmacokinetic–pharmacodynamic and ADMET endpoint predictions, thereby accelerating discovery of new chemical entities.
4
Hybrid AI models combining conventional machine learning and deep learning are increasingly developed to address limited accuracy in traditional ADMET prediction models.
5
The review synthesizes AI approaches for pharmacokinetic and toxicokinetic prediction, covering model types, evaluation parameters, applications, and the transition toward hybrid architectures.

AI-driven hybrid machine learning and deep learning models for pharmacokinetic, toxicokinetic, and ADMET prediction in drug discovery

Prediction accuracy, efficiency, and application of ADMET and pharmacokinetic–pharmacodynamic endpoints using integrated hybrid AI and multimodeling approaches

Publication Details
Publication Date
2026-01-22
Journal
Publisher
ISSN
Cited by
7
Access Type
Author Information
Authors
Isha Taneja
M. Malarvannan
S. Monohar
Sanskruti Sitaram Kate
Swati Jaiswal
Bhupesh Pratap
Prakash Chandra Rathi
Shikha Thakur
David Paul
Muhammad Wahajuddin
Explore further
Open the scid.ai AI chat with a ready-made request: it will find papers on a similar topic and help build a literature review.
Find similar papers in the chat
Make a presentation
100%