Department of Chemistry, University of Hull, Cottingham Road, Hull, UK HU6 7RX.
Lab Chip. 2011 Feb 7;11(3):443-8. doi: 10.1039/c0lc00346h. Epub 2010 Nov 12.
Integrated DNA extraction and amplification have been carried out in a microfluidic device using electro-osmotic pumping (EOP) for fluidic control. All the necessary reagents for performing both DNA extraction and polymerase chain reaction (PCR) amplification were pre-loaded into the microfluidic device following encapsulation in agarose gel. Buccal cells were collected using OmniSwabs [Whatman™, UK] and manually added to a chaotropic binding/lysis solution pre-loaded into the microfluidic device. The released DNA was then adsorbed onto a silica monolith contained within the DNA extraction chamber and the microfluidic device sealed using polymer electrodes. The washing and elution steps for DNA extraction were carried out using EOP, resulting in transfer of the eluted DNA into the PCR chamber. Thermal cycling, achieved using a Peltier element, resulted in amplification of the Amelogenin locus as confirmed using conventional capillary gel electrophoresis. It was demonstrated that the PCR reagents could be stored in the microfluidic device for at least 8 weeks at 4 °C with no significant loss of activity. Such methodology lends itself to the production of 'ready-to-use' microfluidic devices containing all the necessary reagents for sample processing, with many obvious applications in forensics and clinical medicine.
已经在使用电渗流(EOP)进行流体控制的微流控设备中进行了 DNA 提取和扩增的集成。在使用琼脂糖凝胶进行封装后,将进行 DNA 提取和聚合酶链反应(PCR)扩增所需的所有试剂预先加载到微流控设备中。使用 OmniSwabs [Whatman™,英国]收集口腔细胞,并手动将其添加到预先加载到微流控设备中的变性结合/裂解溶液中。释放的 DNA 随后被吸附到 DNA 提取室中的二氧化硅整体上,并且使用聚合物电极密封微流控设备。使用 EOP 进行 DNA 提取的洗涤和洗脱步骤,导致洗脱的 DNA转移到 PCR 室中。使用珀耳帖元件(Peltier element)实现热循环,从而扩增 amelogenin 基因座,这通过常规毛细管凝胶电泳得到证实。已经证明,PCR 试剂可以在 4°C 下至少在微流控设备中储存 8 周而不会显着失去活性。这种方法非常适合生产“即用型”微流控设备,其中包含用于样品处理的所有必要试剂,在法医学和临床医学中有许多明显的应用。