资源受限的数字微流控生物芯片需求驱动的多靶点样品制备

Sudip Poddar, Sukanta Bhattacharjee, Shao-Yun Fang, Tsung-Yi Ho, B. B. Bhattacharya
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引用次数: 1

摘要

微流控芯片实验室为在微小芯片上实现各种生化实验室方案的自动化提供了有前途的技术。样品制备(Sample preparation, SP)是任何生化实验的重要组成部分,其目的是对样品或多种试剂按一定比例进行稀释。该领域的一个主要目标是制备具有不同浓度因子的给定流体的稀释剂,每种稀释剂都具有一定的体积,这被称为需求驱动的多目标(DDMT)生成问题。带有微流控生物芯片的SP需要对流体体积的混合分裂步骤进行适当的排序,并且需要存储单元来节省中间流体,同时产生所需的目标比率。SP的性能取决于底层混合算法和片上存储的可用性,而后者通常受到物理设计期间施加的约束的限制。由于DDMT涉及多个目标比率,因此在存储限制下解决它变得更加困难。此外,从SP精度的角度来看,减少混合分裂步骤是可取的,因为每一个这样的步骤都是体积分裂误差的潜在来源。在本文中,我们提出了一种存储感知的DDMT算法,该算法减少了数字微流控芯片实验室的混合分裂操作次数。我们还介绍了生物芯片的布局和它们的分配技术。仿真结果表明,与现有的多目标SP算法相比,该方法具有明显的优越性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Demand-Driven Multi-Target Sample Preparation on Resource-Constrained Digital Microfluidic Biochips
Microfluidic lab-on-chips offer promising technology for the automation of various biochemical laboratory protocols on a minuscule chip. Sample preparation (SP) is an essential part of any biochemical experiments, which aims to produce dilution of a sample or a mixture of multiple reagents in a certain ratio. One major objective in this area is to prepare dilutions of a given fluid with different concentration factors, each with certain volume, which is referred to as the demand-driven multiple-target (DDMT) generation problem. SP with microfluidic biochips requires proper sequencing of mix-split steps on fluid volumes and needs storage units to save intermediate fluids while producing the desired target ratio. The performance of SP depends on the underlying mixing algorithm and the availability of on-chip storage, and the latter is often limited by the constraints imposed during physical design. Since DDMT involves several target ratios, solving it under storage constraints becomes even harder. Furthermore, reduction of mix-split steps is desirable from the viewpoint of accuracy of SP, as every such step is a potential source of volumetric split error. In this article, we propose a storage-aware DDMT algorithm that reduces the number of mix-split operations on a digital microfluidic lab-on-chip. We also present the layout of the biochip with -storage cells and their allocation technique for . Simulation results reveal the superiority of the proposed method compared to the state-of-the-art multi-target SP algorithms.
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