Zhang Kaixiang, Kang Dong-Ku, Ali M Monsur, Liu Linan, Labanieh Louai, Lu Mengrou, Riazifar Hamidreza, Nguyen Thi N, Zell Jason A, Digman Michelle A, Gratton Enrico, Li Jinghong, Zhao Weian
Department of Chemistry, Beijing Key Laboratory for Analytical Methods and Instrumentation, Tsinghua University, Beijing, 100084, China.
Lab Chip. 2015 Nov 7;15(21):4217-26. doi: 10.1039/c5lc00650c. Epub 2015 Sep 21.
Quantification of miRNAs in blood can be potentially used for early disease detection, surveillance monitoring and drug response evaluation. However, quantitative and robust measurement of miRNAs in blood is still a major challenge in large part due to their low concentration and complicated sample preparation processes typically required in conventional assays. Here, we present the 'Integrated Comprehensive Droplet Digital Detection' (IC 3D) system where the plasma sample containing target miRNAs is encapsulated into microdroplets, enzymatically amplified and digitally counted using a novel, high-throughput 3D particle counter. Using Let-7a as a target, we demonstrate that IC 3D can specifically quantify target miRNA directly from blood plasma at extremely low concentrations ranging from 10s to 10 000 copies per mL in ≤3 hours without the need for sample processing such as RNA extraction. Using this new tool, we demonstrate that target miRNA content in colon cancer patient blood is significantly higher than that in healthy donor samples. Our IC 3D system has the potential to introduce a new paradigm for rapid, sensitive and specific detection of low-abundance biomarkers in biological samples with minimal sample processing.
血液中微小RNA(miRNA)的定量分析可潜在地用于疾病早期检测、监测以及药物反应评估。然而,血液中miRNA的定量和可靠测量仍是一项重大挑战,很大程度上是因为其浓度低,且传统检测方法通常需要复杂的样本制备过程。在此,我们展示了“集成式综合液滴数字检测”(IC 3D)系统,其中含有目标miRNA的血浆样本被封装入微滴中,通过酶促扩增,并使用新型高通量3D粒子计数器进行数字计数。以Let-7a作为目标,我们证明IC 3D能够在≤3小时内直接从血浆中特异性地定量极低浓度(每毫升10至10000拷贝)的目标miRNA,而无需进行诸如RNA提取等样本处理。使用这一新工具,我们证明结肠癌患者血液中的目标miRNA含量显著高于健康供体样本。我们的IC 3D系统有潜力为在最少样本处理情况下快速、灵敏且特异地检测生物样本中低丰度生物标志物引入一种新范例。