Compartmentalized organ-on-a-chip structure for spatiotemporal control of oxygen microenvironments

IF 3 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Kaisa Tornberg, Hannu Välimäki, Silmu Valaskivi, Antti-Juhana Mäki, Matias Jokinen, Joose Kreutzer, Pasi Kallio
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引用次数: 2

Abstract

Hypoxia is a condition where tissue oxygen levels fall below normal levels. In locally induced hypoxia due to blood vessel blockage, oxygen delivery becomes compromised. The site where blood flow is diminished the most forms a zero-oxygen core, and different oxygenation zones form around this core with varying oxygen concentrations. Naturally, these differing oxygen microenvironments drive cells to respond according to their oxygenation status. To study these cellular processes in laboratory settings, the cellular gas microenvironments should be controlled rapidly and precisely. In this study, we propose an organ-on-a-chip device that provides control over the oxygen environments in three separate compartments as well as the possibility of rapidly changing the corresponding oxygen concentrations. The proposed device includes a microfluidic channel structure with three separate arrays of narrow microchannels that guide gas mixtures with desired oxygen concentrations to diffuse through a thin gas-permeable membrane into cell culture areas. The proposed microfluidic channel structure is characterized using a 2D ratiometric oxygen imaging system, and the measurements confirm that the oxygen concentrations at the cell culture surface can be modulated in a few minutes. The structure is capable of creating hypoxic oxygen tension, and distinct oxygen environments can be generated simultaneously in the three compartments. By combining the microfluidic channel structure with an open-well coculture device, multicellular cultures can be established together with compartmentalized oxygen environment modulation. We demonstrate that the proposed compartmentalized organ-on-a-chip structure is suitable for cell culture.

Abstract Image

用于氧微环境时空控制的分区器官芯片结构
缺氧是组织含氧量低于正常水平的一种情况。在血管阻塞引起的局部缺氧中,氧气输送受到损害。血流减少最多的部位形成零氧核心,不同的氧合区在这个核心周围形成不同的氧浓度。自然地,这些不同的氧微环境驱动细胞根据它们的氧合状态做出反应。为了在实验室环境中研究这些细胞过程,细胞气体微环境必须得到快速而精确的控制。在这项研究中,我们提出了一种器官芯片装置,该装置可以控制三个独立隔间中的氧气环境,并可以快速改变相应的氧气浓度。所提出的装置包括一个微流控通道结构,该结构具有三个独立的窄微通道阵列,其引导具有所需氧浓度的气体混合物通过薄的透气膜扩散到细胞培养区域。采用二维比例氧成像系统对所提出的微流控通道结构进行了表征,测量结果证实,细胞培养表面的氧浓度可以在几分钟内调节。该结构能够产生低氧张力,并且可以在三个隔间中同时产生不同的氧气环境。通过将微流控通道结构与开孔共培养装置相结合,可以建立多细胞培养并进行区隔氧环境调节。我们证明了所提出的区隔化器官芯片结构适用于细胞培养。
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来源期刊
Biomedical Microdevices
Biomedical Microdevices 工程技术-工程:生物医学
CiteScore
6.90
自引率
3.60%
发文量
32
审稿时长
6 months
期刊介绍: Biomedical Microdevices: BioMEMS and Biomedical Nanotechnology is an interdisciplinary periodical devoted to all aspects of research in the medical diagnostic and therapeutic applications of Micro-Electro-Mechanical Systems (BioMEMS) and nanotechnology for medicine and biology. General subjects of interest include the design, characterization, testing, modeling and clinical validation of microfabricated systems, and their integration on-chip and in larger functional units. The specific interests of the Journal include systems for neural stimulation and recording, bioseparation technologies such as nanofilters and electrophoretic equipment, miniaturized analytic and DNA identification systems, biosensors, and micro/nanotechnologies for cell and tissue research, tissue engineering, cell transplantation, and the controlled release of drugs and biological molecules. Contributions reporting on fundamental and applied investigations of the material science, biochemistry, and physics of biomedical microdevices and nanotechnology are encouraged. A non-exhaustive list of fields of interest includes: nanoparticle synthesis, characterization, and validation of therapeutic or imaging efficacy in animal models; biocompatibility; biochemical modification of microfabricated devices, with reference to non-specific protein adsorption, and the active immobilization and patterning of proteins on micro/nanofabricated surfaces; the dynamics of fluids in micro-and-nano-fabricated channels; the electromechanical and structural response of micro/nanofabricated systems; the interactions of microdevices with cells and tissues, including biocompatibility and biodegradation studies; variations in the characteristics of the systems as a function of the micro/nanofabrication parameters.
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