Microfluidic organ chip of fluid–solid dynamic curved interface

Author:

Su Haoran1,Ma Tianxiang1ORCID,Liu Xiao1ORCID,Wang Li1ORCID,Shu Fangjun2ORCID,Liang Zhuqing1ORCID,Zhang Dongrui1ORCID,Zhang Xing1ORCID,Li Kexin1ORCID,Wang Min3ORCID,Xin Chen4ORCID,Zhang Yu5ORCID,Zhang Jing1ORCID,Du Yao6ORCID,Fan Yubo17ORCID

Affiliation:

1. Key Laboratory of Biomechanics and Mechanobiology (Beihang University), Ministry of Education, Beijing Advanced Innovation Center for Biomedical Engineering, School of Biological Science and Medical Engineering, Beihang University 1 , Beijing 100083, China

2. Department of Mechanical and Aerospace Engineering, New Mexico State University 2 , Las Cruces, New Mexico 88003, USA

3. Department of Gynecology and Obstetrics, Strategic Support Force Medical Center 3 , Beijing 100101, China

4. Glaucoma Department, Beijing Tongren Eye Center, Beijing Tongren Hospital, Capital Medical University 4 , Beijing 100730, China

5. State Industrial Base for Stem Cell Engineering Products 5 , Tianjin, 300384, China

6. School of Automation Science and Electrical Engineering, Beihang University 6 , Beijing 100083, China

7. School of Engineering Medicine, Beihang University 7 , Beijing 100083, China

Abstract

Dynamic curved interfaces are fundamental and ubiquitous structures in biological systems. However, replicating the structure and function associated with these interfaces for mechanobiology and drug screening is challenging. Here, we develop a dynamic curvature-enabled microfluidic organ chip of two fluid–solid dynamic curved interfaces. One interface effectively integrates adjustable biomechanics, and the other controls drug release with open microfluidics. The fluid–solid interface sensed by the cells can modulate the residual stress, stiffness, strain of the solid phase, and the flow shear stress of the fluid phase. Using the chip, we investigate the mechanotransductive responses of endothelial and epithelial cells, including Piezo1, Ca2+, and YAP, and reveal that the response of the endothelium to combined dynamic cyclic strain and flow shear stress is different from separate stimulation and also disparate from the epithelium. Furthermore, direct and high-efficiency drug release to cells is realized by constructing the other fluid–solid interface on the back side of cells, where drugs are encapsulated within cross-linked alginate hydrogel in the open microfluidic channel. Then, we replicate object-specific and location-specific biomechanical environments within carotid bifurcation and prove the effectiveness of drug delivery. Our design exemplifies dynamic curved biological interfaces with controlled mechanical environments and holds potential for patient-specific medicine.

Funder

National Natural Science Foundation of China

the Fundamental Research Funds for the General Universities

the 111 Project

Publisher

AIP Publishing

Subject

General Physics and Astronomy

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