Sharafeldin Mohamed, Bishop Gregory W, Bhakta Snehasis, El-Sawy Abdelhamid, Suib Steven L, Rusling James F
Department of Chemistry (U-3060), University of Connecticut, 55 North Eagleville Road, Storrs, CT 06269, USA; Analytical Chemistry Department, Faculty of Pharmacy, Zagazig University, Zakazik, Sharkia, Egypt.
Department of Chemistry (U-3060), University of Connecticut, 55 North Eagleville Road, Storrs, CT 06269, USA.
Biosens Bioelectron. 2017 May 15;91:359-366. doi: 10.1016/j.bios.2016.12.052. Epub 2016 Dec 27.
Ultrasensitive mediator-free electrochemical detection for biomarker proteins was achieved at low cost using a novel composite of FeO nanoparticles loaded onto graphene oxide (GO) nano-sheets (FeO@GO). This paramagnetic FeO@GO composite (1µm size range) was decorated with antibodies against prostate specific antigen (PSA) and prostate specific membrane antigen (PSMA), and then used to first capture these biomarkers and then deliver them to an 8-sensor detection chamber of a microfluidic immunoarray. Screen-printed carbon sensors coated with electrochemically reduced graphene oxide (ERGO) and a second set of antibodies selectively capture the biomarker-laden FeO@GO particles, which subsequently catalyze hydrogen peroxide reduction to detect PSA and PSMA. Accuracy was confirmed by good correlation between patient serum assays and enzyme-linked immuno-sorbent assays (ELISA). Excellent detection limits (LOD) of 15 fg/mL for PSA and 4.8 fg/mL for PSMA were achieved in serum. The LOD for PSA was 1000-fold better than the only previous report of PSA detection using FeO. Dynamic ranges were easily tunable for concentration ranges encountered in serum samples by adjusting the FeO@GO Concentration. Reagent cost was only $0.85 for a single 2-protein assay.
使用负载在氧化石墨烯(GO)纳米片上的FeO纳米颗粒的新型复合材料(FeO@GO),以低成本实现了对生物标志物蛋白质的超灵敏无介质电化学检测。这种顺磁性FeO@GO复合材料(尺寸范围为1µm)用抗前列腺特异性抗原(PSA)和前列腺特异性膜抗原(PSMA)的抗体进行修饰,然后首先用于捕获这些生物标志物,然后将它们输送到微流控免疫阵列的8传感器检测室。涂有电化学还原氧化石墨烯(ERGO)和第二组抗体的丝网印刷碳传感器选择性地捕获负载生物标志物的FeO@GO颗粒,这些颗粒随后催化过氧化氢还原以检测PSA和PSMA。通过患者血清检测与酶联免疫吸附测定(ELISA)之间的良好相关性证实了准确性。在血清中实现了PSA的出色检测限(LOD)为15 fg/mL,PSMA的检测限为4.8 fg/mL。PSA的LOD比之前仅有的一篇使用FeO检测PSA的报告好1000倍。通过调整FeO@GO浓度,血清样品中遇到的浓度范围的动态范围易于调节。单次双蛋白检测的试剂成本仅为0.85美元。