Department of Applied Chemistry, Graduate School of Engineering, The University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-8656, Japan.
Lab Chip. 2012 Dec 7;12(23):4986-91. doi: 10.1039/c2lc40632b.
We present a novel device employing one million femtoliter droplets immobilized on a substrate for the quantitative detection of extremely low concentrations of biomolecules in a sample. Surface-modified polystyrene beads carrying either zero or a single biomolecule-reporter enzyme complex are efficiently isolated into femtoliter droplets formed on hydrophilic-in-hydrophobic surfaces. Using a conventional micropipette, this is achieved by sequential injection first with an aqueous solution containing beads, and then with fluorinated oil. The concentration of target biomolecules is estimated from the ratio of the number of signal-emitting droplets to the total number of trapped beads (digital counting). The performance of our digital counting device was demonstrated by detecting a streptavidin-β-galactosidase conjugate with a limit of detection (LOD) of 10 zM. The sensitivity of our device was >20-fold higher than that noted in previous studies where a smaller number of reactors (fifty thousand reactors) were used. Such a low LOD was achieved because of the large number of droplets in an array, allowing simultaneous examination of a large number of beads. When combined with bead-based enzyme-linked immunosorbent assay (digital ELISA), the LOD for the detection of prostate specific antigen reached 2 aM. This value, again, was improved over that noted in a previous study, because of the decreased coefficient of variance of the background measurement determined by the Poisson noise. Our digital counting device using one million droplets has great potential as a highly sensitive, portable immunoassay device that could be used to diagnose diseases.
我们提出了一种新颖的装置,该装置采用了固定在基底上的一百万滴毫微微升液滴,用于定量检测样品中极其低浓度的生物分子。表面修饰的聚苯乙烯珠粒,携带零个或单个生物分子报告酶复合物,能够有效地被分离到在亲水-疏水表面形成的毫微微升液滴中。使用常规的微移液器,通过依次注入首先含有珠粒的水溶液,然后注入全氟油来实现这一点。通过比较发射信号的液滴数量与捕获的珠粒总数(数字计数),可以估算出目标生物分子的浓度。我们的数字计数装置的性能通过检测链霉亲和素-β-半乳糖苷酶缀合物来证明,其检测限(LOD)为 10 zM。我们的装置的灵敏度比以前使用较少反应器(五十万个反应器)的研究中报道的灵敏度高 20 多倍。如此低的 LOD 是由于阵列中有大量的液滴,可以同时检查大量的珠粒。当与基于珠粒的酶联免疫吸附测定(数字 ELISA)结合使用时,前列腺特异性抗原的检测下限达到 2 aM。与之前的研究相比,这个值也得到了提高,这是因为泊松噪声确定的背景测量的方差系数降低了。我们的使用一百万滴液滴的数字计数装置具有作为高度敏感、便携式免疫分析装置的巨大潜力,可用于诊断疾病。