VTT Technical Research Centre of Finland, Oulu, Finland.
PLoS One. 2013 Jul 18;8(7):e68918. doi: 10.1371/journal.pone.0068918. Print 2013.
This paper describes a method for the patterned immobilization of capture antibodies into a microfluidic platform fabricated by roll-to-roll (R2R) hot embossing on poly (methyl methacrylate) (PMMA). Covalent attachment of antibodies was achieved by two sequential inkjet printing steps. First, a polyethyleneimine (PEI) layer was deposited onto oxygen plasma activated PMMA foil and further cross-linked with glutaraldehyde (GA) to provide an amine-reactive aldehyde surface (PEI-GA). This step was followed by a second deposition of antibody by overprinting on the PEI-GA patterned PMMA foil. The PEI polymer ink was first formulated to ensure stable drop formation in inkjet printing and the printed films were characterized using atomic force microscopy (AFM) and X-ray photoelectron spectroscopy (XPS). Anti-CRP antibody was patterned on PMMA foil by the developed method and bonded permanently with R2R hot embossed PMMA microchannels by solvent bonding lamination. The functionality of the immobilized antibody inside the microfluidic channel was evaluated by fluorescence-based sandwich immunoassay for detection of C-reactive protein (CRP). The antibody-antigen assay exhibited a good level of linearity over the range of 10 ng/ml to 500 ng/ml (R(2) = 0.991) with a calculated detection limit of 5.2 ng/ml. The developed patterning method is straightforward, rapid and provides a versatile approach for creating multiple protein patterns in a single microfluidic channel for multiplexed immunoassays.
本文介绍了一种将捕获抗体固定在通过卷对卷(R2R)热压印在聚甲基丙烯酸甲酯(PMMA)上制造的微流控平台中的图案化方法。抗体的共价附着通过两个连续的喷墨打印步骤实现。首先,将聚乙烯亚胺(PEI)层沉积在氧等离子体激活的 PMMA 箔上,并进一步用戊二醛(GA)交联,以提供胺反应性醛表面(PEI-GA)。然后,通过在 PEI-GA 图案化的 PMMA 箔上打印来进行第二次抗体沉积。首先配制 PEI 聚合物墨水以确保在喷墨打印中形成稳定的液滴,并用原子力显微镜(AFM)和 X 射线光电子能谱(XPS)对打印膜进行表征。通过开发的方法在 PMMA 箔上对 CRP 抗体进行图案化,并通过溶剂键合层压将其与 R2R 热压印 PMMA 微通道永久键合。通过荧光夹心免疫测定法评估固定在微流道内的抗体的功能,以检测 C-反应蛋白(CRP)。抗体-抗原测定在 10 ng/ml 至 500 ng/ml 的范围内表现出良好的线性度(R2 = 0.991),计算出的检测限为 5.2 ng/ml。开发的图案化方法简单、快速,为在单个微流道中创建多个蛋白质图案以进行多重免疫分析提供了一种通用方法。