Beer N Reginald, Hindson Benjamin J, Wheeler Elizabeth K, Hall Sara B, Rose Klint A, Kennedy Ian M, Colston Bill W
Lawrence Livermore National Laboratory, 7000 East Avenue, Livermore, California 94551, USA.
Anal Chem. 2007 Nov 15;79(22):8471-5. doi: 10.1021/ac701809w. Epub 2007 Oct 11.
The first lab-on-chip system for picoliter droplet generation and PCR amplification with real-time fluorescence detection has performed PCR in isolated droplets at volumes 106 smaller than commercial real-time PCR instruments. The system utilized a shearing T-junction in a silicon device to generate a stream of monodisperse picoliter droplets that were isolated from the microfluidic channel walls and each other by the oil-phase carrier. An off-chip valving system stopped the droplets on-chip, allowing them to be thermally cycled through the PCR protocol without droplet motion. With this system, a 10-pL droplet, encapsulating less than one copy of viral genomic DNA through Poisson statistics, showed real-time PCR amplification curves with a cycle threshold of approximately 18, 20 cycles earlier than commercial instruments. This combination of the established real-time PCR assay with digital microfluidics is ideal for isolating single-copy nucleic acids in a complex environment.
首个用于皮升液滴生成及采用实时荧光检测进行PCR扩增的芯片实验室系统,已在隔离的液滴中进行了PCR,其体积比商用实时PCR仪器小106倍。该系统利用硅器件中的剪切T型结来生成单分散皮升液滴流,这些液滴通过油相载体与微流控通道壁及彼此隔离开。芯片外阀门系统使液滴在芯片上停止,使其能够在不发生液滴移动的情况下通过PCR流程进行热循环。使用该系统时,一个10皮升的液滴,通过泊松统计法封装少于一份病毒基因组DNA,显示出实时PCR扩增曲线,其循环阈值约为18,比商用仪器早20个循环。将成熟的实时PCR检测与数字微流控相结合,非常适合在复杂环境中分离单拷贝核酸。