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Scalable Fabrication of Stretchable, Dual Channel, Microfluidic Organ Chips
Published on: October 20, 2018
Sensor-Integrated Organ-on-a-Chip Platforms: Advances in Drug Evaluation and Disease Modeling
Zhaofeng Huang1, Yaohui Zhang2, Feiyang Li1
1Engineering Research Center of Optical Instrument and System, The Ministry of Education, Shanghai Engineering Research Center of Environmental Biosafety Instruments and Equipment, Shanghai Key Laboratory of Modern Optical System, University of Shanghai for Science and Technology, Shanghai200093, P. R. China.
Abstract:
Organ-on-a-chip (OoC) platforms have made remarkable progress in simulating the physiological complexity of human tissues, and provide advanced in vitro models for drug development. These platforms offer superior physiological relevance over conventional cell culture and animal models and thus enhance preclinical drug testing. However, a key challenge is how to align the dynamics of these systems with analytical methods. The wide use of static endpoint assays can restrict the depth of obtainable mechanistic data, and often capture correlative results rather than the basic kinetic processes of a drug effect. This review probes into the premise that functional combination of sensors for real-time non-terminal detection is a critical trend for strengthening the analytical capability of OoC technology. Herein, this perspective is illustrated by systematically examining recent applications in drug toxicity evaluation and disease modeling. The discussion highlights how the focus of sensor-integrated platforms is shifting from physiological endpoint replication to dynamic mechanistic inquiry. These systems enable the continuous detection of key cellular and environmental indices, and thus provide high-resolution temporal data and a more detailed view of pharmacological responses. Finally, the current technological landscape, remaining challenges, and future outlook are summarized, positing that a further integration of sensing technologies is the key to exposing the full potential of OoCs for mechanistic and predictive drug assessment.

