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A lab-on-a-chip for preconcentration of bacteria and nucleic acid extraction

机译:用于细菌预富集和核酸提取的芯片实验室

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To improve detection sensitivity, molecular diagnostics require preconcentration of low concentrated samples followed by rapid nucleic acid extraction. This is usually achieved by multiple centrifugation, lysis and purification steps, for instance, using chemical reagents, spin columns or magnetic beads. These require extensive infrastructure as well as time consuming manual handling steps and are thus not suitable for point of care testing (POCT). To overcome these challenges, we developed a microfluidic chip combining free-flow electrophoretic (FFE) preconcentration (1 ml down to 5 μl) and thermoelectric lysis of bacteria as well as purification of nucleic acids by gel-electrophoresis. The integration of these techniques in a single chip is unique and enables fast, easy and space-saving sample pretreatment without the need for laboratory facilities, making it ideal for the integration into small POCT devices. A preconcentration efficiency of nearly 100% and a lysis/gel-electrophoresis efficiency of about 65% were achieved for the detection of E. coli . The genetic material was analyzed by RT-qPCR targeting the superfolder Green Fluorescent Protein (sfGFP) transcripts to quantify mRNA recovery and qPCR to determine DNA background.
机译:为了提高检测灵敏度,分子诊断需要对低浓度样品进行预浓缩,然后进行快速核酸提取。这通常通过多个离心,裂解和纯化步骤来实现,例如,使用化学试剂,旋转柱或磁珠。这些要求大量的基础结构以及费时的手动处理步骤,因此不适合进行即时检验(POCT)。为了克服这些挑战,我们开发了一种微流控芯片,该芯片结合了自由流动电泳(FFE)预浓缩(1 ml至5μl)和细菌的热电裂解以及通过凝胶电泳纯化核酸的能力。这些技术在单个芯片中的集成是独特的,无需实验室设施即可进行快速,轻松和节省空间的样品预处理,使其非常适合集成到小型POCT器件中。对于大肠杆菌的检测,实现了近100%的预浓缩效率和约65%的裂解/凝胶电泳效率。通过靶向超文件夹绿色荧光蛋白(sfGFP)转录本的RT-qPCR分析遗传物质,以定量mRNA回收,并通过qPCR确定DNA背景。

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