Department of Materials Science, School of Science and Technology, NOVA University of Lisbon and CEMOP/UNINOVA, Campus de Caparica, 2829-516 Caparica, Portugal.
UCIBIO, I4HB, Life Sciences Department, School of Science and Technology, NOVA University of Lisbon, Campus de Caparica, 2829-516 Caparica, Portugal.
Biosensors (Basel). 2022 Mar 28;12(4):201. doi: 10.3390/bios12040201.
We introduce a digital microfluidics (DMF) platform specifically designed to perform a loop-mediated isothermal amplification (LAMP) of DNA and applied it to a real-time amplification to monitor a cancer biomarker, (associated to 40% of all human tumors), using fluorescence microscopy. We demonstrate the full manipulation of the sample and reagents on the DMF platform, resulting in the successful amplification of 90 pg of the target DNA (0.5 ng/µL) in less than one hour. Furthermore, we test the efficiency of an innovative mixing strategy in DMF by employing two mixing methodologies onto the DMF droplets-low frequency AC (alternating current) actuation as well as back-and-forth droplet motion-which allows for improved fluorescence readouts. Fluorophore bleaching effects are minimized through on-chip sample partitioning by DMF processes and sequential droplet irradiation. Finally, LAMP reactions require only 2 µL volume droplets, which represents a 10-fold volume reduction in comparison to benchtop LAMP.
我们介绍了一种专门设计用于进行 DNA 环介导等温扩增 (LAMP) 的数字微流控 (DMF) 平台,并将其应用于实时扩增,以荧光显微镜监测癌症生物标志物(与所有人类肿瘤的 40%相关)。我们展示了在 DMF 平台上对样品和试剂的完全操作,成功地在不到一个小时的时间内扩增了 90 pg 的目标 DNA(0.5 ng/µL)。此外,我们通过在 DMF 液滴中采用两种混合方法——低频交流电(交流)致动以及液滴来回运动——来测试 DMF 中创新混合策略的效率,这使得荧光读出得到了改善。通过 DMF 工艺和顺序液滴照射实现的芯片上样品分区,最大限度地减少了荧光染料的漂白效应。最后,LAMP 反应仅需要 2 µL 体积的液滴,与台式 LAMP 相比,体积减少了 10 倍。