利用数字微流体进行多次稀释的片上样品制备

D. Mitra, Sudip Roy, K. Chakrabarty, B. Bhattacharya
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引用次数: 32

摘要

在许多生化方案中,溶液制备是按给定比例混合两种或两种以上流体的预处理步骤。生化样品/试剂的稀释是混合或溶液制备的特殊情况,其中只有两种不同类型的流体,其中一种是缓冲溶液,按所需浓度因子的一定比例混合。在数字微流体生物芯片上实施的生物测定可能需要相同样品/试剂的几个不同的浓度值。在本文中,我们提出了一种方案,该方案可以在最小混合分裂步骤中以可接受的误差范围产生一组不同的目标液滴(浓度值范围在0%到100%之间)。该方法不需要任何中间存储,因为在每一步中,当前液滴仅与样品(浓度为100%)或缓冲液滴(浓度为0%)混合。生成多个目标浓度的问题已在二元德布鲁因图的基础上表述。该技术在混合分裂步骤数和废液滴数方面都优于现有的基于单目标的方法。这反过来又减少了执行时间、电极驱动次数和样品/试剂要求。一个数字微流体平台也可以很容易地设计来实现这种芯片上的样品制备。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
On-Chip Sample Preparation with Multiple Dilutions Using Digital Microfluidics
In many biochemical protocols, solution preparation is a preprocessing step for mixing two or more fluids in a given ratio. Dilution of a biochemical sample/reagent is the special case of mixing or solution preparation where only two different type of fluids, one of which is a buffer solution, are mixed at a certain ratio corresponding to the desired concentration factor. Bioassays implemented on digital micro fluidic biochips may require several different concentration values of the same sample/reagent. In this paper, we present a scheme in which a set of different target droplets (with concentration values ranged between 0% and 100%) can be produced with an acceptable error bound in minimum mix-split steps. The method does not require any intermediate storage since, at each step, the current droplet is mixed only with the sample (with 100% concentration) or with the buffer (with 0% concentration) droplet. The problem of generating multiple target concentrations has been formulated based on a binary de Bruijn graph. The proposed technique outperforms the existing single target based methods in terms of both the number of mix-split steps and the number of waste droplets. This in turn, reduces the execution time, the number of electrode actuations, and sample/reagent requirement. A digital micro fluidic platform can also be easily designed to implement such on-chip sample preparation.
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