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Improvement in the Reproducibility of a Paper-based Analytical Device (PAD) Using Stable Covalent Binding between Proteins and Cellulose Paper

机译:利用蛋白质和纤维素纸之间的稳定共价结合提高纸质分析装置(PAD)的可重复性

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摘要

Paper-based analytical devices (PADs) have been widely used in many fields because they are affordable and portable. For reproducible quantitative analysis, it is crucial to strongly immobilize proteins on PADs. Conventional techniques for immobilizing proteins on PADs are based on physical adsorption, but proteins can be easily removed by weak physical forces. Therefore, it is difficult to ensure the reproducibility of the analytical results of PADs using physical adsorption. To overcome this limitation, in this study, we showed a method of covalent binding of proteins to cellulose paper. This method consists of three steps, which include periodate oxidation of paper, the formation of a Schiff base, and reductive amination. We identified aldehyde and imine groups formed on paper using FT-IR analysis. This covalent bonding approach enhanced the binding force and binding capacity of proteins. We confirmed the activity of an immobilized antibody through a sandwich immunoassay. We expect that this immobilization method will contribute to the commercialization of PADs with high reproducibility and sensitivity.
机译:纸质分析设备(PAD)由于价格合理且便携,已在许多领域得到广泛使用。对于可重复的定量分析,至关重要的是将蛋白质牢固地固定在PAD上。将蛋白质固定在PAD上的常规技术是基于物理吸附的,但是可以通过弱物理力轻松去除蛋白质。因此,难以确保使用物理吸附的PAD分析结果的可重复性。为了克服这个限制,在这项研究中,我们展示了一种蛋白质与纤维素纸共价结合的方法。该方法包括三个步骤,包括纸的高碘酸盐氧化,席夫碱的形成和还原胺化。我们使用FT-IR分析鉴定了在纸上形成的醛基和亚胺基。这种共价键合方法增强了蛋白质的结合力和结合能力。我们通过三明治免疫测定法确认了固定化抗体的活性。我们希望这种固定化方法将有助于具有高重现性和敏感性的PAD的商业化。

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