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An inkjet printing paper-based immunodevice for fluorescence determination of immunoglobulin G

机译:喷墨印刷纸基免疫装置,用于免疫球蛋白G的荧光测定

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A sequential inkjet printing strategy was utilized on a microfluidic paper-based fluorescence (FL) immunodevice for immunoglobulin G (IgG) detection. Assisted with four cartridges, capture antibodies, antigens, bovine serum albumin (BSA) and detection antibodies were sequentially printed on the paper surface with better reproducibility. For enzyme-linked immunosorbent assay (ELISA), the analysis time with inkjet printing on 10 paper-based devices can be reduced by about 4 min. IgG can be detected with a wide linear range and the detection limit was 0.4 ng mL?1. With the advantages of better repeatability, the size effect of gold nanoparticles (AuNPs) was also investigated using the inkjet printer's nozzle. As a result, particles with a diameter of less than 150 nm can be successfully printed on the paper surface without affecting the detection results. This work will provide a new strategy for time-saving and large-scale sample detection in the field of immunoassay.
机译:在基于微流体纸的荧光(FL)免疫设备上采用顺序喷墨打印策略进行免疫球蛋白G(IgG)检测。在四个墨盒的辅助下,捕获抗体,抗原,牛血清白蛋白(BSA)和检测抗体被依次打印在纸面上,具有更好的重现性。对于酶联免疫吸附测定(ELISA),在10个纸基设备上进行喷墨打印的分析时间可减少约4分钟。 IgG的线性范围很广,检出限为0.4 ng mL?1。由于具有更好的可重复性,还使用喷墨打印机的喷嘴研究了金纳米颗粒(AuNPs)的尺寸效应。结果,直径小于150 nm的颗粒可以成功地打印在纸张表面上,而不会影响检测结果。这项工作将为节省免疫分析领域中的时间和大规模样品提供新的策略。

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