低温键合玻璃膜微流控装置用于体外器官芯片细胞培养模型

Kyall J. Pocock, Xiaofang Gao, Chenxi Wang, C. Priest, C. Prestidge, K. Mawatari, T. Kitamori, B. Thierry
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引用次数: 1

摘要

微流体与活体生物系统的整合为“器官芯片”这一激动人心的概念铺平了道路,该概念旨在开发先进的体外模型,复制人体器官的关键特征。玻璃基器件在微流体领域的应用由来已久,但在多层玻璃微器件(如聚合物膜)中集成替代功能元件仍然是一个挑战。为此,我们扩展了先前报道的玻璃器件低温键合方法,使功能性聚碳酸酯多孔膜的集成成为可能。该工艺最初是在专用低温粘接设备(μTAS2001, Bondtech,日本)上开发和优化的,随后适用于更广泛使用的热压花机设备(EVG520HE热压花机,EVG,奥地利)。这种方法的关键方面是使用低温兼容的聚合物膜。与硼硅玻璃键合(650°C)和石英/熔融二氧化硅键合(1050°C)工艺相比,该方法保持了膜的完整性和功能(聚碳酸酯的Tg为150°C)。泄漏测试表明,在长达150小时内,膜没有损坏或完整性丧失,表明具有足够的粘合强度,可以长期进行细胞培养。可行性研究证实,Caco-2细胞在5天内生长出致密和功能单层。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Low-temperature bonded glass-membrane microfluidic device for in vitro organ-on-a-chip cell culture models
The integration of microfluidics with living biological systems has paved the way to the exciting concept of “organson- a-chip”, which aims at the development of advanced in vitro models that replicate the key features of human organs. Glass based devices have long been utilised in the field of microfluidics but the integration of alternative functional elements within multi-layered glass microdevices, such as polymeric membranes, remains a challenge. To this end, we have extended a previously reported approach for the low-temperature bonding of glass devices that enables the integration of a functional polycarbonate porous membrane. The process was initially developed and optimised on specialty low-temperature bonding equipment (μTAS2001, Bondtech, Japan) and subsequently adapted to more widely accessible hot embosser units (EVG520HE Hot Embosser, EVG, Austria). The key aspect of this method is the use of low temperatures compatible with polymeric membranes. Compared to borosilicate glass bonding (650 °C) and quartz/fused silica bonding (1050 °C) processes, this method maintains the integrity and functionality of the membrane (Tg 150 °C for polycarbonate). Leak tests performed showed no damage or loss of integrity of the membrane for up to 150 hours, indicating sufficient bond strength for long term cell culture. A feasibility study confirmed the growth of dense and functional monolayers of Caco-2 cells within 5 days.
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