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使用可操作的微丝进行瞬态微流控分隔,用于生化分析、细胞培养和芯片上器官。

Transient microfluidic compartmentalization using actionable microfilaments for biochemical assays, cell culture and organs-on-chip.

机构信息

Laboratoire Physico Chimie Curie, Institut Curie, PSL Research University, CNRS UMR168, 75005, Paris, France.

Institut Curie, Centre de Recherche, PSL Research University, 75005, Paris, France and ART group, Inserm U830, 75248 Paris, France.

出版信息

Lab Chip. 2016 Nov 29;16(24):4691-4701. doi: 10.1039/c6lc01143h.

Abstract

We report here a simple yet robust transient compartmentalization system for microfluidic platforms. Cylindrical microfilaments made of commercially available fishing lines are embedded in a microfluidic chamber and employed as removable walls, dividing the chamber into several compartments. These partitions allow tight sealing for hours, and can be removed at any time by longitudinal sliding with minimal hydrodynamic perturbation. This allows the easy implementation of various functions, previously impossible or requiring more complex instrumentation. In this study, we demonstrate the applications of our strategy, firstly to trigger chemical diffusion, then to make surface co-coating or cell co-culture on a two-dimensional substrate, and finally to form multiple cell-laden hydrogel compartments for three-dimensional cell co-culture in a microfluidic device. This technology provides easy and low-cost solutions, without the use of pneumatic valves or external equipment, for constructing well-controlled microenvironments for biochemical and cellular assays.

摘要

我们在此报告了一种简单而强大的微流控平台瞬态隔室化系统。由市售钓鱼线制成的圆柱形微丝嵌入微流控室中,并用作可移动壁,将腔室分隔成几个隔室。这些隔室可实现数小时的紧密密封,并且可以通过最小的流体动力干扰进行纵向滑动随时移除。这使得各种功能的实现变得简单,这些功能以前是不可能的,或者需要更复杂的仪器。在这项研究中,我们展示了我们的策略的应用,首先是触发化学扩散,然后是在二维基底上进行表面共涂层或细胞共培养,最后是在微流控装置中形成多个含有细胞的水凝胶隔室以进行三维细胞共培养。该技术提供了简单且低成本的解决方案,无需使用气动阀或外部设备,即可构建用于生化和细胞分析的良好控制的微环境。

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