利用分裂树在微电极点阵数字微流控生物芯片上制备样品时尽量减少反应物和废物

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引用次数: 0

摘要

摘要 围绕 "片上实验室(LoC)"的生物检测需要多种浓度(或稀释)因子,以满足特定样品浓度的要求。遗憾的是,它们大多具有非定位性和不可保护性,需要占用大量空间,购买成本高昂。数字几何技术可为数字微流控生物芯片(DMFB)生成任意梯度曲线。基于微电极点阵(MEDA)结构的下一代 DMFB 已被提出,该结构可通过通道分配和层叠混合来产生和分散液滴。该领域的前期工作必须解决反应物和废物最小化以及同时制备多目标浓度样品的问题。本文首次提出了在 MEDA 上实现多目标浓度反应物和废物最小化的分裂-液滴共享算法。所提出的算法不仅最大限度地减少了试剂消耗,还通过同时制备目标浓度样品减少了废液滴的数量。为了支持所提出的方法,我们展示了一系列指数梯度的实验结果,证明了该方法的有效性和高效性。与之前的工作相比,所提出的算法最多可减少 24.8% 的样品用量,平均减少 50% 的废液滴。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reactant and Waste Minimization during Sample Preparation on Micro-Electrode-Dot-Array Digital Microfluidic Biochips using Splitting Trees

Abstract

Biological assays around “lab-on-a-chip (LoC)” are required in multiple concentration (or dilution) factors, satisfying specific sample concentrations. Unfortunately, most of them suffer from non-locality and are non-protectable, requiring a large footprint and high purchase cost. A digital geometric technique can generate arbitrary gradient profiles for digital microfluidic biochips (DMFBs). A next- generation DMFB has been proposed based on the microelectrode-dot-array (MEDA) architectures are shown to produce and disperse droplets by channel dispensing and lamination mixing. Prior work in this area must address the problem of reactant and waste minimization and concurrent sample preparation for multiple target concentrations. This paper proposes the first splitting-droplet sharing algorithm for reactant and waste minimization of multiple target concentrations on MEDAs. The proposed algorithm not only minimizes the consumption of reagents but also reduces the number of waste droplets by preparing the target concentrations concurrently. Experimental results on a sequence of exponential gradients are presented in support of the proposed method and demonstrate its effectiveness and efficiency. Compared to prior work, the proposed algorithm can achieve up to a 24.8% reduction in sample usage and reach an average of 50% reduction in waste droplets.

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