College of Chemistry and Chemical Engineering, Central South University, Changsha, 410083, Hunan, China; Key Laboratory of Modern Preparation of Traditional Chinese Medicine Under Ministry of Education, Jiangxi University of Traditional Chinese Medicine, Nanchang 330004, Jiangxi, China.
College of Chemistry and Chemical Engineering, Central South University, Changsha, 410083, Hunan, China.
Biosens Bioelectron. 2022 Jan 15;196:113691. doi: 10.1016/j.bios.2021.113691. Epub 2021 Oct 6.
On-site multiplex enzyme detection is crucial for diagnosis, therapeutics and prognostic. To date, it is still a daunting challenge to develop portable, low-cost, and efficient multi-enzyme detection methods. Herein, a novel sample-in-result-out platform integrating ratiometric fluorescent assays with 3D origami microfluidic paper-based device (μPAD) was developed for simultaneous visual point-of-care testing (POCT) of alkaline phosphatase (ALP) and butyrylcholinesterase (BChE). Cascade catalytic reaction with the same two fluorescent signal indicators was rationally designed to ratiometric fluorescent detection of ALP and BChE: substrate of ALP (pyrophosphate) and product of BChE (thiocholine) can strongly complex with Cu, Cu oxidizes o-phenylenediamine to fluorescent 2,3-diaminophenazine (oxOPD) (emission, 565 nm), oxOPD quenches the fluorescence of carbon dots (CDs, emission at 445 nm) via inner filter effect, thus oxOPD/CDs values are relevant to ALP and BChE activities. Then 3D origami μPAD composing of four layers and two parallel channels was fabricated and simply prepared by one-step plotting with black oil-based marker and specific metal molds. After simple folding and unfolding neighboring layers to sequentially initiate reactions of pre-loaded reagents, fluorescent images on the detection zone can be captured by smartphone and analyzed by red-green-blue software for quantitative analysis. Under optimal conditions, the proposed platform was successfully performed to detect ALP and BChE with activity difference at 3 orders of magnitude in human serum samples without any pretreatment procedures. Excellent selectivity, good precision, favorable linear range, and high accuracy were exhibited. Importantly, the platform opens a promising horizon for high-throughput POCT of multiplex biomarkers.
现场多重酶检测对于诊断、治疗和预后至关重要。迄今为止,开发便携式、低成本、高效率的多酶检测方法仍然是一项艰巨的挑战。在此,我们开发了一种新颖的样本内-结果输出平台,将比率荧光分析与 3D 折纸微流控纸基器件(μPAD)集成在一起,用于同时进行即时护理检测(POCT)碱性磷酸酶(ALP)和丁酰胆碱酯酶(BChE)。通过两个相同的荧光信号指示剂的级联催化反应,合理设计了用于 ALP 和 BChE 的比率荧光检测:ALP 的底物(焦磷酸盐)和 BChE 的产物(硫代胆碱)可以与 Cu 强烈络合,Cu 将邻苯二胺氧化为荧光 2,3-二氨基吩嗪(oxOPD)(发射波长 565nm),oxOPD 通过内滤效应猝灭碳点(CDs,发射波长 445nm)的荧光,因此 oxOPD/CDs 值与 ALP 和 BChE 的活性相关。然后,采用一步绘图法,用黑色油性标记笔和特定的金属模具制作了由四层和两条平行通道组成的 3D 折纸 μPAD。通过简单地折叠和展开相邻层,以顺序启动预加载试剂的反应,可以使用智能手机捕获检测区的荧光图像,并通过红-绿-蓝软件进行分析,实现定量分析。在最佳条件下,该平台成功地用于检测人血清样品中的 ALP 和 BChE,其活性差异达到 3 个数量级,无需任何预处理步骤。该平台表现出出色的选择性、良好的精密度、有利的线性范围和高准确性。重要的是,该平台为高通量 POCT 多重生物标志物开辟了广阔的前景。