Portable and integrated microfluidic flow control system using off-the-shelf components towards organs-on-chip applications

IF 3 4区 医学 Q3 ENGINEERING, BIOMEDICAL
Haoyu Zhu, Gürhan Özkayar, Joost Lötters, Marcel Tichem, Murali Krishna Ghatkesar
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引用次数: 2

Abstract

Organ-on-a-chip (OoC) devices require the precise control of various media. This is mostly done using several fluid control components, which are much larger than the typical OoC device and connected through fluidic tubing, i.e., the fluidic system is not integrated, which inhibits the system’s portability. Here, we explore the limits of fluidic system integration using off-the-shelf fluidic control components. A flow control configuration is proposed that uses a vacuum to generate a fluctuation-free flow and minimizes the number of components used in the system. 3D printing is used to fabricate a custom-designed platform box for mounting the chosen smallest footprint components. It provides flexibility in arranging the various components to create experiment-specific systems. A demonstrator system is realized for lung-on-a-chip experiments. The 3D-printed platform box is 290 mm long, 240 mm wide and 37 mm tall. After integrating all the components, it weighs 4.8 kg. The system comprises of a switch valve, flow and pressure controllers, and a vacuum pump to control the diverse media flows. The system generates liquid flow rates ranging from 1.5 \(\upmu\)Lmin\(^{-1}\) to 68 \(\upmu\)Lmin\(^{-1}\) in the cell chambers, and a cyclic vacuum of 280 mbar below atmospheric pressure with 0.5 Hz frequency in the side channels to induce mechanical strain on the cells-substrate. The components are modular for easy exchange. The battery operated platform box can be mounted on either upright or inverted microscopes and fits in a standard incubator. Overall, it is shown that a compact integrated and portable fluidic system for OoC experiments can be constructed using off-the-shelf components. For further down-scaling, the fluidic control components, like the pump, switch valves, and flow controllers, require significant miniaturization while having a wide flow rate range with high resolution.

Abstract Image

便携式和集成的微流控系统使用现成的组件对器官芯片上的应用
器官芯片(OoC)设备需要对各种介质进行精确控制。这主要是使用几个流体控制组件来完成的,这些流体控制组件比典型的OoC设备大得多,并且通过流体管连接,即流体系统没有集成,这限制了系统的可移植性。在这里,我们探讨了使用现成的流体控制组件的流体系统集成的局限性。提出了一种利用真空产生无波动流动并使系统中使用的元件数量最小化的流量控制配置。3D打印用于制造定制设计的平台盒,用于安装选定的最小占地组件。它可以灵活地安排各种组件来创建特定于实验的系统。实现了肺部片上实验的演示系统。3d打印平台箱体长290毫米,宽240毫米,高37毫米。在整合所有部件后,它的重量为4.8公斤。该系统包括一个开关阀,流量和压力控制器,以及一个真空泵来控制各种介质的流量。该系统在细胞腔中产生的液体流速范围为1.5 \(\upmu\) Lmin \(^{-1}\)至68 \(\upmu\) Lmin \(^{-1}\),并且在侧通道中产生低于大气压280毫巴的循环真空,频率为0.5 Hz,以诱导细胞-衬底的机械应变。组件是模块化的,便于交换。电池操作的平台箱可以安装在直立或倒置的显微镜上,并适合于标准的培养箱。总体而言,研究表明,使用现成的组件可以构建一个紧凑的集成便携式流体系统用于OoC实验。为了进一步缩小规模,流体控制组件,如泵,开关阀和流量控制器,需要显着小型化,同时具有高分辨率的宽流量范围。
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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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