一种可广泛使用的、先进的大规模微流控芯片气道的开发。

IF 3.7 3区 医学 Q2 ENGINEERING, BIOMEDICAL Bioengineering Pub Date : 2025-02-13 DOI:10.3390/bioengineering12020182
Brady Rae, Gwenda F Vasse, Jalal Mosayebi, Maarten van den Berge, Simon D Pouwels, Irene H Heijink
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引用次数: 0

摘要

片上微流体是先进的体外模型,它比静态2D模型更接近模拟肺组织的原生3D环境,以研究导致肺部疾病的复杂肺结构和多因素过程。当前的微流体系统可以限制从单个微通道中提取的生物样品的数量,如RNA,蛋白质和上清。在这里,我们描述了一种新开发的大规模片上气道模型,该模型采用比当前可用系统更宽的细胞培养表面积。这使得样品的收集量与传统细胞培养系统相当,使该设备适用于利用这些静态系统(RNA分离,ELISA等)的任何工作流程。通过我们的构建方法,这个更大的培养区域可以更容易地处理,具有广泛暴露的潜力,以及收集少量样品(例如挥发物或线粒体RNA)。该模型由两个大的聚二甲基硅氧烷(PDMS)细胞培养室组成,在独立的介质或空气流动下,由半透聚乙烯(PET)细胞培养膜(厚23 μm,孔径0.4 μm)隔开。每个腔室携带5 × 18 mm, 90 mm2(带有锥形腔室入口的92 mm2)表面积,可容纳多达1-2 × 104个贴壁结构肺细胞,可用于不同肺细胞类型的密切接触共培养研究,包括气道上皮细胞,成纤维细胞,平滑肌细胞和内皮细胞。芯片的平行双室设计允许上皮细胞在气液界面(ALI)培养,并在生物流速下分化成致密、多层、假分层上皮。这种微流体气道芯片通过提供易于复制,易于调节和具有成本效益的大规模流体3D气道细胞培养平台来推进该领域。
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Development of a Widely Accessible, Advanced Large-Scale Microfluidic Airway-on-Chip.

On-chip microfluidics are advanced in vitro models that simulate lung tissue's native 3D environment more closely than static 2D models to investigate the complex lung architecture and multifactorial processes that lead to pulmonary disease. Current microfluidic systems can be restrictive in the quantities of biological sample that can be retrieved from a single micro-channel, such as RNA, protein, and supernatant. Here, we describe a newly developed large-scale airway-on-chip model that employs a surface area for a cell culture wider than that in currently available systems. This enables the collection of samples comparable in volume to traditional cell culture systems, making the device applicable to any workflow utilizing these static systems (RNA isolation, ELISA, etc.). With our construction method, this larger culture area allows for easier handling, the potential for a wide range of exposures, as well as the collection of low-quantity samples (e.g., volatiles or mitochondrial RNA). The model consists of two large polydimethylsiloxane (PDMS) cell culture chambers under an independent flow of medium or air, separated by a semi-permeable polyethylene (PET) cell culture membrane (23 μm thick, 0.4 μm pore size). Each chamber carries a 5 × 18 mm, 90 mm2 (92 mm2 with tapered chamber inlets) surface area that can contain up to 1-2 × 104 adherent structural lung cells and can be utilized for close contact co-culture studies of different lung cell types, including airway epithelial cells, fibroblasts, smooth muscle cells, and endothelial cells. The parallel bi-chambered design of the chip allows for epithelial cells to be cultured at the air-liquid interface (ALI) and differentiation into a dense, multi-layered, pseudostratified epithelium under biological flow rates. This millifluidic airway-on-chip advances the field by providing a readily reproducible, easily adjustable, and cost-effective large-scale fluidic 3D airway cell culture platform.

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来源期刊
Bioengineering
Bioengineering Chemical Engineering-Bioengineering
CiteScore
4.00
自引率
8.70%
发文量
661
期刊介绍: Aims Bioengineering (ISSN 2306-5354) provides an advanced forum for the science and technology of bioengineering. It publishes original research papers, comprehensive reviews, communications and case reports. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. All aspects of bioengineering are welcomed from theoretical concepts to education and applications. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. There are, in addition, four key features of this Journal: ● We are introducing a new concept in scientific and technical publications “The Translational Case Report in Bioengineering”. It is a descriptive explanatory analysis of a transformative or translational event. Understanding that the goal of bioengineering scholarship is to advance towards a transformative or clinical solution to an identified transformative/clinical need, the translational case report is used to explore causation in order to find underlying principles that may guide other similar transformative/translational undertakings. ● Manuscripts regarding research proposals and research ideas will be particularly welcomed. ● Electronic files and software regarding the full details of the calculation and experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material. ● We also accept manuscripts communicating to a broader audience with regard to research projects financed with public funds. Scope ● Bionics and biological cybernetics: implantology; bio–abio interfaces ● Bioelectronics: wearable electronics; implantable electronics; “more than Moore” electronics; bioelectronics devices ● Bioprocess and biosystems engineering and applications: bioprocess design; biocatalysis; bioseparation and bioreactors; bioinformatics; bioenergy; etc. ● Biomolecular, cellular and tissue engineering and applications: tissue engineering; chromosome engineering; embryo engineering; cellular, molecular and synthetic biology; metabolic engineering; bio-nanotechnology; micro/nano technologies; genetic engineering; transgenic technology ● Biomedical engineering and applications: biomechatronics; biomedical electronics; biomechanics; biomaterials; biomimetics; biomedical diagnostics; biomedical therapy; biomedical devices; sensors and circuits; biomedical imaging and medical information systems; implants and regenerative medicine; neurotechnology; clinical engineering; rehabilitation engineering ● Biochemical engineering and applications: metabolic pathway engineering; modeling and simulation ● Translational bioengineering
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