AI-integrated microfluidics for drug screening: From single cell to organ-on-a-chip

Drug discovery remains a protracted and capital-intensive process, primarily hindered by inefficiencies in drug screening. Microfluidic technology provides a promising approach for in vitro drug screening, enabling physiologically relevant, high-throughput, and cost-effective analysis by mimicking key aspects of cellular microenvironments. The synergistic integration of artificial intelligence (AI) with microfluidics constitutes a pivotal advancement in biomedical analysis. The convergence of the two facilitates automated data analysis, complex pattern recognition, and intelligent experimental control, thereby accelerating drug screening and contributing to enhanced precision. This review systematically presents the latest advancements in AI-assisted microfluidic drug screening, organized by increasing biological complexity: from single-cell analysis (1D), multicellular arrays (2D), and spheroids (3D), to sophisticated Organ-on-a-chip (OoC, 3D+) platforms. We detail how AI algorithms promote screening throughput, sensitivity, and physiological relevance at each scale. Furthermore, we critically discuss the prevailing challenges, including those related to data, model robustness, interpretability, and system integration. Finally, we outline future directions, highlighting the potential of AI-enhanced microfluidics to further advance precision drug discovery and biomedical research. We believe this timely review will offer a useful reference for researchers working in the interdisciplinary field of AI, microfluidics, and pharmacology. AI-assisted microfluidic platforms enable drug screening across hierarchical biological complexity, from 1D single cells and 2D multicellular arrays to 3D spheroids and Organ-on-a-chip (3D+) models.

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Publication Details

Journal
Acta Pharmaceutica Sinica B
Published
2026-01-08
DOI
https://doi.org/10.1016/j.apsb.2026.01.001
Citations
1
Primary Topic
3D Printing in Biomedical Research
Type
article
Field-Weighted Citation Impact
21.28
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article

AI-integrated microfluidics for drug screening: From single cell to organ-on-a-chip

Zinuo Shen, Yutao Li, Na Du, Ying Li et al.
1 citations
Acta Pharmaceutica Sinica B
3D Printing in Biomedical Research
21.28
article

AI-integrated microfluidics for drug screening: From single cell to organ-on-a-chip

Zinuo Shen, Yutao Li, Na Du, Ying Li, Shibo Cheng, Yanwei Jia, Hongyun Yin, Zheyu Li, Shiying Wang, Jie Zhou
article en
1 citations

Abstract

Drug discovery remains a protracted and capital-intensive process, primarily hindered by inefficiencies in drug screening. Microfluidic technology provides a promising approach for in vitro drug screening, enabling physiologically relevant, high-throughput, and cost-effective analysis by mimicking key aspects of cellular microenvironments. The synergistic integration of artificial intelligence (AI) with microfluidics constitutes a pivotal advancement in biomedical analysis. The convergence of the two facilitates automated data analysis, complex pattern recognition, and intelligent experimental control, thereby accelerating drug screening and contributing to enhanced precision. This review systematically presents the latest advancements in AI-assisted microfluidic drug screening, organized by increasing biological complexity: from single-cell analysis (1D), multicellular arrays (2D), and spheroids (3D), to sophisticated Organ-on-a-chip (OoC, 3D+) platforms. We detail how AI algorithms promote screening throughput, sensitivity, and physiological relevance at each scale. Furthermore, we critically discuss the prevailing challenges, including those related to data, model robustness, interpretability, and system integration. Finally, we outline future directions, highlighting the potential of AI-enhanced microfluidics to further advance precision drug discovery and biomedical research. We believe this timely review will offer a useful reference for researchers working in the interdisciplinary field of AI, microfluidics, and pharmacology. AI-assisted microfluidic platforms enable drug screening across hierarchical biological complexity, from 1D single cells and 2D multicellular arrays to 3D spheroids and Organ-on-a-chip (3D+) models.

Acta Pharmaceutica Sinica BVol. 16(3)
University of Macau (MO), Hubei University of Chinese Medicine (CN), Hubei Provincial Hospital of Traditional Chinese Medicine (CN)
Openalex Percentile: Top 3%
3D Printing in Biomedical Research
21.28
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