Sensing System Research Center, National Institute of Advanced Industrial Science and Technology (AIST), Central 5, 1-1-1 Higashi, Tsukuba, Ibaraki, 305-8565, Japan.
Mikrochim Acta. 2023 Jun 1;190(6):247. doi: 10.1007/s00604-023-05827-7.
Droplet digital PCR (ddPCR) is accurate in nucleic acid quantification owing to its linearity and high sensitivity. Amplification of nucleic acid in droplets, however, is limited by the stability of droplets against thermal cycling. While the use of fluorinated oil or supplementation of surfactant could improve the stability of droplets, this process has also greatly increased the cost of ddPCR and limited post-PCR analysis. Here, we report a novel method known as gel capsule-based digital PCR (gc-dPCR) which includes a method to prepare hydrogel capsules encapsulating the PCR reaction mix, conducting PCR reaction, and readout by either quantitative PCR (qPCR) system or fluorescence microplate reader. We have compared the developed method to vortex ddPCR. Our approach results in higher fluorescence intensity compared to ddPCR suggesting higher sensitivity of the system. As hydrogel capsules are more stable than droplets in fluorinated oil throughout thermal cycling, all partitions can be quantified, thus preventing loss of information from low-concentration samples. The new approach should extend to all droplet-based PCR methods. It has greatly improved ddPCR by increasing droplets stability and sensitivity, and reducing the cost of ddPCR, which help to remove the barrier of ddPCR in settings with limited resources.
微滴式数字 PCR(ddPCR)因其线性和高灵敏度而在核酸定量方面非常准确。然而,在微滴中扩增核酸受到微滴对热循环稳定性的限制。虽然使用氟化油或添加表面活性剂可以提高微滴的稳定性,但这一过程也大大增加了 ddPCR 的成本,并限制了 PCR 后的分析。在这里,我们报告了一种称为凝胶胶囊数字 PCR(gc-dPCR)的新方法,该方法包括制备包封 PCR 反应混合物的水凝胶胶囊、进行 PCR 反应以及通过定量 PCR(qPCR)系统或荧光微孔板读数仪进行读取的方法。我们已经将开发的方法与涡旋 ddPCR 进行了比较。与 ddPCR 相比,我们的方法产生了更高的荧光强度,表明该系统具有更高的灵敏度。由于水凝胶胶囊在整个热循环中比氟化油中的微滴更稳定,因此可以对所有分区进行定量,从而防止来自低浓度样品的信息丢失。这种新方法应该可以扩展到所有基于微滴的 PCR 方法。它通过提高 ddPCR 的稳定性和灵敏度,降低 ddPCR 的成本,极大地改进了 ddPCR,有助于消除资源有限环境中 ddPCR 的障碍。