Chengdu Institute of Biology, Chinese Academy of Sciences, No. 93 South Keyuan Road, Gaoxin Distinct, Chengdu, 610041, PR China; University of Chinese Academy of Sciences, Beijing, 100049, PR China.
Chengdu Institute of Biology, Chinese Academy of Sciences, No. 93 South Keyuan Road, Gaoxin Distinct, Chengdu, 610041, PR China.
Anal Chim Acta. 2019 Aug 13;1065:64-70. doi: 10.1016/j.aca.2019.02.046. Epub 2019 Mar 3.
In most cases, three-dimensional paper-based microfluidic analytical devices (3D-μPADs) were fabricated manually by stacking or folding methods. For the first time, digital light processing stereolithography (DLP-SLA) 3D printing technology was adopted to automatically make 3D-μPADs. In the fabrication process, a printing pause was set between two layers to allow paper to be placed in the resin tank. The resin on the fresh paper spontaneously bonded to the former cured paper layer during curing, thus realizing the automatic bonding and alignment between different layers of paper and avoiding the human participation and errors as in stacking and folding methods. There was a gap between two vertical aligned flow paths, therefore the liquid did not flow spontaneously from the upper layer to the lower layer. Most of the fluid flow in 3D-μPADs was spontaneous or manually activated, which was not conducive to complex assays that require different regents to be delivered sequentially. Herein, we used an electric field or airflow to trigger the fluid flow and demonstrated the flow controllability by a proof-of-concept colorimetric assay. The limits of detection of glucose and albumin were 0.8 mM and 3.5 μM, respectively, which were sufficient for clinical requirements. Given the characteristic of flow controllability, we believe that the proposed 3D-μPADs have great potential to make paper-based complex assays automated and programmable.
在大多数情况下,三维纸质微流控分析器件(3D-μPADs)是通过堆叠或折叠方法手动制造的。首次采用数字光处理立体光刻(DLP-SLA)3D 打印技术自动制作 3D-μPADs。在制造过程中,在两层之间设置打印暂停,以便将纸张放入树脂槽中。新纸上的树脂在固化过程中会自发地与前一层已固化的纸张层结合,从而实现不同纸张层之间的自动粘结和对准,避免了堆叠和折叠方法中需要人工参与和出错的问题。两个垂直对齐的流道之间存在间隙,因此液体不会自发地从上层流到下层。3D-μPADs 中的大部分流体流动是自发的或手动激活的,这不利于需要顺序输送不同试剂的复杂分析。在此,我们使用电场或气流来触发流体流动,并通过概念验证比色分析证明了其流动可控性。葡萄糖和白蛋白的检测限分别为 0.8mM 和 3.5μM,足以满足临床需求。鉴于其流动可控性的特点,我们相信所提出的 3D-μPADs 具有使基于纸张的复杂分析自动化和可编程化的巨大潜力。