A Microneedle-Microplate Platform to Detect Biomarkers in the Skin

R. Dixon, W. Lau, K. W. Ng
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Abstract

This research aimed to integrate an established signalquantification technique with immunocapture microneedle arrays (MNAs) to improvebiomarker-based disease diagnostics in the skin. In this miniaturized sandwichenzyme-linked immunosorbent assay (ELISA) platform, the capture antibody wasimmobilised onto the surface of microneedles which, when inserted superficiallyinto porcine skin, captured endogenous porcine immunoglobulin G (IgG) intradermally.Signal development was achieved by incubating the microneedles ino-phenylenediamine (OPD) solution in a 384-well microplate and measuring theabsorbance in a microplate spectrophotometer at 450 nm. This technique allowsfor rapid biomarker detection with high-throughput processing. Immunocapture microneedledevices such as these can be easily adapted for targeting different biomarkersor multiplexed leaving plenty of scope for future work and assay optimisation. 
检测皮肤生物标志物的微针-微孔板平台
本研究旨在将已建立的信号量化技术与免疫捕获微针阵列(MNAs)相结合,以改善基于生物标志物的皮肤疾病诊断。在这个小型的三明治酶联免疫吸附试验(ELISA)平台中,捕获的抗体被固定在微针的表面上,当微针插入猪皮肤表面时,在皮内捕获内源性猪免疫球蛋白G (IgG)。信号发展是通过在384孔微孔板中培养微针到苯二胺(OPD)溶液中,并在微孔板分光光度计450 nm处测量吸光度来实现的。该技术允许高通量处理的快速生物标志物检测。像这样的免疫捕获微针设备可以很容易地适应不同的生物标志物,为未来的工作和分析优化留下了充足的空间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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