Ankireddy Seshadri Reddy, Kim Jongsung
J Nanosci Nanotechnol. 2015 Oct;15(10):7918-21. doi: 10.1166/jnn.2015.11218.
The development of chip-based, quantum dot (QD)-bead-DNA conjugate probes for hybridization detection is a prime research focus in the field of microfluidics. QD-Bead-DNA probe-based hybridization detection methods are often called "bead-based assays," and their success is substantially influenced by the dispensing and manipulation capabilities of microfluidic technology. Met was identified as a prognostic marker in different cancers including lung, renal, liver, head and neck, stomach, and breast. In this report, the cancer causing Met gene was detected with QDs attached to polystyrene microbeads. We constructed a microfluidic platform using a flexible PDMS polymer. The chip consists of two channels, with two inlets and two outlets. The two channels were integrated with QD-bead-DNA probes for simultaneous detection of wild type target DNA and mutant DNA, containing three nucleotide changes compared to the wild type sequence. The fluorescence quenching ability of QDs within the channels of microfluidic chips were compared for both DNAs.
用于杂交检测的基于芯片的量子点(QD)-微珠-DNA共轭探针的开发是微流控领域的主要研究重点。基于QD-微珠-DNA探针的杂交检测方法通常被称为“基于微珠的检测”,其成功很大程度上受到微流控技术的分配和操作能力的影响。Met被确定为包括肺癌、肾癌、肝癌、头颈癌、胃癌和乳腺癌在内的不同癌症的预后标志物。在本报告中,使用附着在聚苯乙烯微珠上的量子点检测致癌的Met基因。我们使用柔性聚二甲基硅氧烷(PDMS)聚合物构建了一个微流控平台。该芯片由两个通道组成,有两个入口和两个出口。这两个通道与QD-微珠-DNA探针集成在一起,用于同时检测野生型靶DNA和突变DNA,与野生型序列相比,突变DNA包含三个核苷酸变化。比较了微流控芯片通道内两种DNA的量子点荧光猝灭能力。