Research Center for Analytical Instrumentation, Institute of Cyber-Systems and Control, State Key Laboratory of Industrial Control Technology, Zhejiang University, Hangzhou, PR China.
Lab Chip. 2012 Nov 21;12(22):4755-63. doi: 10.1039/c2lc40774d.
Digital nucleic acid amplification provides unprecedented opportunities for absolute nucleic acid quantification by counting of single molecules. This technique is useful for molecular genetic analysis in cancer, stem cell, bacterial, non-invasive prenatal diagnosis in which many biologists are interested. This paper describes a self-priming compartmentalization (SPC) microfluidic chip platform for performing digital loop-mediated amplification (LAMP). The energy for the pumping is pre-stored in the degassed bulk PDMS by exploiting the high gas solubility of PDMS; therefore, no additional structures other than channels and reservoirs are required. The sample and oil are sequentially sucked into the channels, and the pressure difference of gas dissolved in PDMS allows sample self-compartmentalization without the need for further chip manipulation such as with pneumatic microvalves and control systems, and so on. The SPC digital LAMP chip can be used like a 384-well plate, so, the world-to-chip fluidic interconnections are avoided. The microfluidic chip contains 4 separate panels, each panel contains 1200 independent 6 nL chambers and can be used to detect 4 samples simultaneously. Digital LAMP on the microfluidic chip was tested quantitatively by using β-actin DNA from humans. The self-priming compartmentalization behavior is roughly predictable using a two-dimensional model. The uniformity of compartmentalization was analyzed by fluorescent intensity and fraction of volume. The results showed that the feasibility and flexibility of the microfluidic chip platform for amplifying single nucleic acid molecules in different chambers made by diluting and distributing sample solutions. The SPC chip has the potential to meet the requirements of a general laboratory: power-free, valve-free, operating at isothermal temperature, inexpensive, sensitive, economizing labour time and reagents. The disposable analytical devices with appropriate air-tight packaging should be useful for point-of-care, and enabling it to become one of the common tools for biology research, especially, in point-of-care testing.
数字核酸扩增通过对单分子进行计数,为绝对核酸定量提供了前所未有的机会。这项技术在癌症、干细胞、细菌的分子遗传学分析中非常有用,也常用于非侵入性产前诊断,许多生物学家都对这些领域感兴趣。本文描述了一种用于进行数字环介导扩增(LAMP)的自引发分隔(SPC)微流控芯片平台。通过利用 PDMS 的高气溶性,在脱气的 PDMS 本体中预先储存泵送能量;因此,不需要通道和储液器以外的其他结构。样品和油依次被吸入通道,PDMS 中溶解的气体的压力差允许样品自我分隔,而无需进一步的芯片操作,如气动微阀和控制系统等。SPC 数字 LAMP 芯片可以像 384 孔板一样使用,因此避免了世界与芯片之间的流体连接。微流控芯片包含 4 个独立的面板,每个面板包含 1200 个独立的 6 nL 腔室,可以同时检测 4 个样本。通过使用来自人类的β-肌动蛋白 DNA,在微流控芯片上对数字 LAMP 进行了定量测试。使用二维模型可以大致预测自引发分隔行为。通过荧光强度和体积分数分析了分隔的均匀性。结果表明,通过稀释和分配样品溶液,可以在不同腔室中实现对单个核酸分子进行扩增的微流控芯片平台的可行性和灵活性。SPC 芯片具有满足一般实验室要求的潜力:无电源、无阀、在等温温度下运行、成本低廉、灵敏、节省劳动时间和试剂。具有适当密封包装的一次性分析装置应该对即时护理有用,并使其成为生物学研究的常用工具之一,特别是在即时护理测试中。