Laboratory of Macromolecular Chemistry and Paper Chemistry (MAP), Department of Chemistry, Technische Universität Darmstadt, 64287 Darmstadt, Germany.
Laboratory of Chemistry and Physics of Interfaces, Institute for Microsystems Technology, Technical Faculty, University of Freiburg, 79110 Freiburg, Germany.
Sensors (Basel). 2021 Sep 23;21(19):6348. doi: 10.3390/s21196348.
Microfluidic paper combines pump-free water transport at low cost with a high degree of sustainability, as well as good availability of the paper-forming cellulosic material, thus making it an attractive candidate for point-of-care (POC) analytics and diagnostics. Although a number of interesting demonstrators for such paper devices have been reported to date, a number of challenges still exist, which limit a successful transfer into marketable applications. A strong limitation in this respect is the (unspecific) adsorption of protein analytes to the paper fibers during the lateral flow assay. This interaction may significantly reduce the amount of analyte that reaches the detection zone of the microfluidic paper-based analytical device (µPAD), thereby reducing its overall sensitivity. Here, we introduce a novel approach on reducing the nonspecific adsorption of proteins to lab-made paper sheets for the use in µPADs. To this, cotton linter fibers in lab-formed additive-free paper sheets are modified with a surrounding thin hydrogel layer generated from photo-crosslinked, benzophenone functionalized copolymers based on poly-(oligo-ethylene glycol methacrylate) (POEGMA) and poly-dimethyl acrylamide (PDMAA). This, as we show in tests similar to lateral flow assays, significantly reduces unspecific binding of model proteins. Furthermore, by evaporating the transport fluid during the microfluidic run at the end of the paper strip through local heating, model proteins can almost quantitatively be accumulated in that zone. The possibility of complete, almost quantitative protein transport in a µPAD opens up new opportunities to significantly improve the signal-to-noise (S/N) ratio of paper-based lateral flow assays.
微流控纸结合了低成本的无泵水输送、高度可持续性,以及纸浆纤维素材料的良好可用性,因此成为即时检测(POC)分析和诊断的有吸引力的候选者。尽管迄今为止已经有许多有趣的纸基设备演示,但仍存在一些挑战,限制了其成功转化为商业应用。在这方面的一个主要限制是蛋白质分析物在侧向流动分析过程中(非特异性地)吸附到纸纤维上。这种相互作用可能会显著减少到达微流控纸基分析装置(µPAD)检测区的分析物数量,从而降低其整体灵敏度。在这里,我们引入了一种新的方法,用于减少蛋白质在实验室制造的纸张上的非特异性吸附,以用于µPAD。为此,我们用周围的薄水凝胶层对实验室形成的无添加剂纸页中的棉绒纤维进行改性,该水凝胶层是由光交联的、含苯甲酮官能团的共聚物形成的,该共聚物基于聚(聚乙二醇甲基丙烯酸酯)(POEGMA)和聚二甲基丙烯酰胺(PDMAA)。正如我们在类似侧向流动分析的测试中所展示的,这显著减少了模型蛋白质的非特异性结合。此外,通过在纸条末端的微流运行过程中蒸发运输流体并通过局部加热,可以几乎定量地将模型蛋白质累积在该区域。在 µPAD 中实现完全、几乎定量的蛋白质输送的可能性为显著提高基于纸张的侧向流动分析的信号噪声比(S/N)开辟了新的机会。