Multiple Dilution Sample Preparation Using Digital Microfluidic Biochips

Sukanta Bhattacharjee, A. Banerjee, B. Bhattacharya
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引用次数: 14

Abstract

Digital microfluidic (DMF) biochips offer a versatile platform for implementing several laboratory based biochemical protocols. These tiny chips can electrically control the dynamics of nanoliter volume of discrete fluid droplets on an electrode array with desired actuation patterns. One important step in biochemical sample preparation is dilution, where the objective is to prepare a fluid with a desired concentration factor. Bioassays implemented on DMF biochips may require several different concentration values of the same sample. In this paper, we propose a scheme in which a set of different target droplets (target concentration values ranged between 0% and 100%) can be produced using 0% concentration (buffer solution) and 100% concentration (sample/reagent), with an error bounded above by 1/2^(n+1) where concentration values are rounded-off by an n-bit binary fraction. Simulation results show that significant amount of savings in the number of mix-split steps and waste droplets can be achieved in comparison with the repeated use of existing single target based methods for generating multiple concentration factors.
利用数字微流控生物芯片制备多重稀释样品
数字微流控(DMF)生物芯片提供了一个通用的平台来实现几个基于实验室的生化协议。这些微小的芯片可以用电控制纳米升体积的离散液滴在电极阵列上的动力学,并具有所需的驱动模式。生化样品制备中的一个重要步骤是稀释,其目的是制备具有所需浓度因子的液体。在DMF生物芯片上实施的生物测定可能需要同一样品的几个不同的浓度值。在本文中,我们提出了一种方案,在该方案中,可以使用0%浓度(缓冲溶液)和100%浓度(样品/试剂)产生一组不同的目标液滴(目标浓度值范围在0%到100%之间),误差上限为1/2^(n+1),其中浓度值由n位二进制分数四舍五入。仿真结果表明,与重复使用现有的基于单一目标的多浓度因子生成方法相比,可以显著节省混合分裂步骤和浪费液滴的数量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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