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Electrophysiology chip on a microfluidic platform

Electrophysiology chip on a microfluidic platform
微流控平台上的电生理芯片
批准号:
BB/H013369/1
负责人:
Jonathan Cooper
金额:
$62.34万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2011
资助国家:
英国
项目状态:
已结题
起止时间:
2011 至 --

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中文摘要
翻译
心脏的活动可以被简化为一组大肌肉,它们的同步收缩将血液吸入腔室并再次将其排出。肌肉收缩的时机对其正常运作至关重要。一种测试心脏活动的方法被称为“贴片夹紧”,这种方法可以测量细胞的电活动。这是一项技术上困难且耗时的技术,通常需要熟练的科学家来完成,我们相信我们可以通过制造新仪器来解决这个问题。该项目旨在创建一个芯片实验室,在芯片上实现高功能测量,收集单个细胞的机械收缩和电活动的信息。这些芯片要么对细胞收缩的程度进行一般测量,要么对细胞收缩时的电压和电流流动进行更具体的测量,或者同时对两者进行测量。该项目将提供一种易于使用的仪器,可以快速、低成本地测量心脏或肌肉细胞的机械和电活动,从而使科学界受益。该平台的性质将使我们不仅可以使用该芯片检查细胞内信号,还可以检查细胞间信号。为了证明该芯片在其他电活性细胞类型中使用的更通用的性质,我们还将研究在我们的芯片系统中使用原发平滑肌以及人类胚胎干细胞(hESC)衍生的心肌细胞和平滑肌。
英文摘要
The action of the heart can be simplified by considering it as a set of large muscles, whose synchronised contractions draws blood in the chambers and forces it out again. This timing of the muscle's contractions are crucial to its correct functioning. One method for testing the activity of the heart is known as 'patch clamping', in which it is possible to measure the electrical activity of the cell. This is a technically difficult, time consuming technique which often needs to be performed by skilled scientists, and which we believe we can address by making new instruments. The project aims to create a Lab-on-a-Chip, where highly functional measurements, which collect information on both the mechanical contraction and the electrical activity of the single cell, will be implemented on such chips. These chips will either make general measurements of how well the cell contractsor more specific measurements on the flow of voltages and currents as the cell contracts, or both, at the same time. The project will benefit the scientific community by providing an easy to use instrument, that can quickly, and at low cost, measure both the mechanical and the electrical activity of the heart or muscle cell. The nature of the platform will be such that we can not only use the chip to examine intracellular signalling, but also inter-cellular signalling, between cells. In order to demonstrate the more generic nature of the chip for use with other electrically active cell types, we will also investigate the use of primary smooth muscle as well as human embryonic stem cells (hESC) derived cardiomyocytes and smooth muscle in our chip systems.
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