Ha Seung-Mo, Cho Woong, Ahn Yoomin, Hwang Seung Yong
Department of Mechanical Engineering, Graduate School, Hanyang University, Seoul 133-791, Korea.
J Nanosci Nanotechnol. 2011 May;11(5):4250-3. doi: 10.1166/jnn.2011.3640.
In this paper, we describe the design and fabrication of a microfluidic device for cell lysis and DNA purification, and the results of device tests using a real sample of buccal cells. Cell lysis was thermally executed for two minutes at 80 degrees C in a serpentine type microreactor (20 microL) using an Au microheater with a microsensor. The DNA was then mixed with other residual products and purified by a new filtration process involving micropillars and 50-80 microm microbeads. The entire process of sample loading, cell lysis, DNA purification, and sample extraction was successfully completed in the microchip within five minutes. Sample preparation within the microchip was verified by performing a SY158 gene PCR analysis and gel electrophoresis on the products obtained from the chip. The new purification method enhanced DNA purity from 0.93 to 1.62 after purification.
在本文中,我们描述了一种用于细胞裂解和DNA纯化的微流控装置的设计与制造,以及使用口腔细胞真实样本进行的装置测试结果。在一个蛇形微反应器(20微升)中,使用带有微传感器的金微加热器,于80摄氏度下热执行细胞裂解两分钟。然后将DNA与其他残留产物混合,并通过一种涉及微柱和50 - 80微米微珠的新过滤工艺进行纯化。样品加载、细胞裂解、DNA纯化和样品提取的整个过程在微芯片内五分钟内成功完成。通过对从芯片获得的产物进行SY158基因PCR分析和凝胶电泳,验证了微芯片内的样品制备。新的纯化方法使纯化后的DNA纯度从0.93提高到了1.62。