Yin Juxin, Zou Zheyu, Hu Zhenming, Zhang Shan, Zhang Fengping, Wang Ben, Lv Shaowu, Mu Ying
Research Centre for Analytical Instrumentation, Institute of Cyber-Systems and Control, State Key Laboratory of Industrial Control Technology, Zhejiang University, Hangzhou, Zhejiang Province 310058, P. R. China.
HeZe Municipal hospital, HeZe 274000, China.
Lab Chip. 2020 Mar 3;20(5):979-986. doi: 10.1039/c9lc01143a.
Point-of-care (POC) testing offers rapid diagnostic results. However, the quantification of current methods is performed using standard curves and external references, and not direct and absolute quantification. This paper describes an integrated multiplex digital recombinase polymerase amplification (ImdRPA) microfluidic chip which combines DNA extraction, multiplex digital RPA and fluorescence detection together in one chip, creating a "sample-in-multiplex-digital-answer-out" system. Multi-layer soft lithography technology was used, with polydimethylsiloxane (PDMS) as the chip material and a glass slide as the substrate. This microfluidic chip has a six-layer structure and screw microvalve control function. The sample preparation for the chip involved magnetic bead-based nucleic acid extraction, which was completed within 15 min without any instrument dependence. The dRPA region was divided into 4 regions (3 positive detection areas and 1 negative control area) and included a total of 12 800 chambers, with each chamber being able to contain a volume of 2.7 nL. The screw valve allowed for the reaction components of each specific goal to be pre-embedded in different regions of the chambers. The reagents were passively driven into the dRPA region using vacuum-based self-priming introduction. Furthermore, we successfully demonstrated that the chip can simultaneously detect three species of pathogenic bacteria within 45 min and give digital quantitative results without the need to establish a standard curve in contaminated milk. Moreover, the detection limit of this ImdRPA microfluidic chip was found to be 10 bacterial cells for each kind of pathogen. These characteristics enhance its applicability for rapid detection of foodborne bacteria at the point-of-care (POC). We envision that the further development of this integrated chip will lead to rapid, multiplex and accurate detection of foodborne bacteria in a feasible manner.
即时检测(POC)可提供快速诊断结果。然而,当前方法的定量是使用标准曲线和外部参考进行的,而非直接和绝对定量。本文描述了一种集成式多重数字重组酶聚合酶扩增(ImdRPA)微流控芯片,该芯片将DNA提取、多重数字RPA和荧光检测整合在一个芯片中,创建了一个“样本进-多重数字出”系统。采用多层软光刻技术,以聚二甲基硅氧烷(PDMS)为芯片材料,玻璃载玻片为基底。该微流控芯片具有六层结构和螺旋微阀控制功能。芯片的样品制备涉及基于磁珠的核酸提取,无需任何仪器,15分钟内即可完成。dRPA区域分为4个区域(3个阳性检测区域和1个阴性对照区域),共有12800个反应室,每个反应室可容纳2.7 nL的体积。螺旋阀可将每个特定目标的反应组分预先嵌入反应室的不同区域。试剂通过基于真空的自吸引入被动驱动到dRPA区域。此外,我们成功证明该芯片能够在45分钟内同时检测出污染牛奶中的三种病原菌,并给出数字定量结果,无需建立标准曲线。而且,这种ImdRPA微流控芯片对每种病原菌的检测限为10个细菌细胞。这些特性增强了其在即时检测(POC)中快速检测食源细菌的适用性。我们设想,这种集成芯片的进一步发展将以可行的方式实现对食源细菌的快速、多重和准确检测。