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Covalent immobilisation of antibodies in Teflon-FEP microfluidic devices for sensitive quantification of clinically relevant protein biomarkers

机译:铁氟龙-FEP微流控设备中抗体的共价固定化,可对临床相关蛋白质生物标志物进行敏感定量

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摘要

This study reports for the first time sensitive colorimetric and fluorescence detection of clinically relevant protein biomarkers by sandwich immunoassays using covalent immobilisation of antibodies onto the fluoropolymer surface inside Teflon®-FEP microfluidic devices. Teflon®-FEP has outstanding optical transparency ideal for high-sensitivity colorimetric and fluorescence bioassays, however this thermoplastic is regarded as chemically inert and very hydrophobic. Covalent immobilisation can offer benefits over passive adsorption to plastic surfaces by allowing better control over antibody density, orientation and analyte binding capacity, and so we tested a range of different and novel covalent immobilisation strategies. We first functionalised the inner surface of a 10-bore, 200 µm internal diameter FEP microcapillary film with high-molecular weight polyvinyl alcohol (PVOH) without changing the outstanding optical transparency of the device delivered by the matched refractive index of FEP and water. Glutaraldehyde immobilisation was compared with use of photoactivated linkers and NHS-ester crosslinkers for covalently immobilising capture antibodies onto PVOH. Three clinically relevant sandwich ELISAs were tested, against the cytokine IL-1ß, the myocardial infarct marker cardiac troponin I (cTnI), and the chronic heart failure marker brain natriuretic peptide (BNP). Overall, glutaraldehyde immobilisation was effective for BNP assays, but yielded unacceptable background for IL-1ß and cTnI assays caused by direct binding of biotinylated detection antibody to the modified PVOH surface. We found NHS-ester groups reacted with APTES-treated PVOH coated fluoropolymer. This facilitated a novel method for capture antibody immobilisation onto fluoropolymer devices using a bifunctional NHS-maleimide crosslinker. The density of covalently immobilised capture antibodies achieved using PVOH/APTES/NHS/Maleimide approached levels seen with passive adsorption, and sensitive and quantitative assay performance was achieved using this method. Overall, PVOH coating provided an excellent surface for controlled covalent antibody immobilisation onto Teflon®-FEP for performing high-sensitivity immunoassays.
机译:这项研究首次报道了通过夹心免疫测定法对临床相关蛋白生物标记物进行比色和荧光检测的首次灵敏性检测,方法是将抗体共价固定在Teflon®-FEP微流体装置内部的含氟聚合物表面上。 Teflon®-FEP具有出色的光学透明性,非常适合用于高灵敏度比色法和荧光生物测定,但是这种热塑性塑料被认为是化学惰性的,并且非常疏水。通过更好地控制抗体密度,方向和分析物结合能力,共价固定可提供优于被动吸附到塑料表面的好处,因此我们测试了一系列不同的新颖共价固定策略。我们首先用高分子量聚乙烯醇(PVOH)对内径为200微米的10孔FEP微毛细管膜的内表面进行了功能化处理,而没有改变FEP和水的匹配折射率所带来的出色的光学透明性。将戊二醛固定化与使用光活化接头和NHS-酯交联剂将捕获抗体共价固定在PVOH上进行了比较。针对细胞因子IL-1ß,心肌梗塞标志物心肌肌钙蛋白I(cTnI)和慢性心力衰竭标志物脑钠肽(BNP),测试了三种临床相关的夹心ELISA。总体而言,戊二醛固定对BNP测定有效,但由于生物素化的检测抗体与修饰的PVOH表面直接结合而导致的IL-1ß和cTnI测定产生无法接受的背景。我们发现NHS酯基团与APTES处理的PVOH涂层含氟聚合物反应。这促进了使用双功能NHS-马来酰亚胺交联剂将抗体固定在含氟聚合物装置上的新颖方法。使用PVOH / APTES / NHS /马来酰亚胺获得的共价固定捕获抗体的密度接近被动吸附所见的水平,并且使用此方法可实现灵敏和定量的测定性能。总体而言,PVOH涂层为将共价抗体固定在Teflon®-FEP上提供了出色的表面,可用于进行高灵敏度的免疫分析。

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