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Development of amperometric immunosensors for protein biomarkers using single wall carbon nanotube forest and electrochemical detection of enzyme labels.

机译:使用单壁碳纳米管森林和酶标记物的电化学检测技术开发用于蛋白质生物标记物的安培免疫传感器。

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摘要

Single-walled carbon nanotube forest based electrochemical immunosensors for rapid, cost-effective, selective and highly sensitive detection of proteins and cancer biomarker proteins in various matrix including human serum and tumor tissue have been developed. The immunosensor has strong potential of being applied in large scale clinical disease screening and point-of-care diagnostics.; The first generation of such immunosensors was developed by conjugating capture antibodies to the carboxylated ends of vertically aligned arrays of single-wall carbon nanotubes (SWNT forests) on pyrolytic graphite (PG) surfaces. Using amperometric detection of enzyme horseradish peroxidase (HRP) labels on the tracer antibodies in a sandwich immunoassay format, as low as 75 pmol mL-1 human serum albumin (HSA) was reproducibly detected.; The sensitivity of this detection method was significantly improved in the second generation immunosensor with the use of water soluble mediator hydroquinone (HQ) to improve electron transfer between the HRP labels and electrode. Detection limits 0.01 pmol mL-1 Prostate Specific Antigen (PSA) was achieved. The DL is similar to clinical ELISA kit, but the sensor developed herein only requires 10 times less patient sample. An excellent match between the detection of PSA in patient samples using the methods developed and clinical ELISA kit was also observed.; A tremendous improvement was accomplished with the third generation immunosensors, which utilize covalent loading of multiple enzyme (HRP) labels and anti-PSA antibodies to the side wall of highly functionalized MWCNTs. Multiple enzyme labels per binding event great increased signal and lowered the detection limit. A detection limit of 0.1 fmol mL-1 PSA in merely 10 muL of undiluted serum was achieved. The mass detection limit of this method is only 40 fg, ∼100 times lower than all commercially available techniques. Using this method, PSA in as low as 1000 tumor cells from patients was reproducibly detected.; Also described in this thesis is the much enhanced catalytic response to H2O2 resulted from highly efficient wiring of enzymes (Mb and HRP) to electrode by using ultra-thin conductive sulfonated polyaniline (SPANI) underlayer, which behaved like molecular wires and significantly improved the efficiency of electron transfer.
机译:已经开发出基于单壁碳纳米管森林的电化学免疫传感器,用于快速,经济高效,选择性和高度灵敏地检测包括人血清和肿瘤组织在内的各种基质中的蛋白质和癌症生物标志物蛋白质。该免疫传感器具有用于大规模临床疾病筛查和即时诊断的强大潜力。通过将捕获抗体与热解石墨(PG)表面上垂直排列的单壁碳纳米管(SWNT森林)的垂直排列阵列的羧化末端缀合来开发这种免疫传感器的第一代产品。使用夹心免疫分析法对示踪抗体上的辣根过氧化物酶(HRP)标记进行安培检测,可重复检测出低至75 pmol mL-1的人血清白蛋白(HSA)。通过使用水溶性介体对苯二酚(HQ)改善HRP标签和电极之间的电子转移,在第二代免疫传感器中此检测方法的灵敏度得到了显着提高。检测限达到0.01 pmol mL-1前列腺特异性抗原(PSA)。 DL与临床ELISA试剂盒相似,但本文开发的传感器仅需要少10倍的患者样品。使用开发的方法和临床ELISA试剂盒对患者样品中PSA的检测也非常匹配。第三代免疫传感器实现了巨大的进步,该传感器利用多种酶(HRP)标签和抗PSA抗体对高功能化MWCNT侧壁的共价加载。每个结合事件使用多个酶标记物可大大提高信号强度并降低检测限。仅10μL未稀释血清就达到了0.1 fmol mL-1 PSA的检出限。该方法的质量检测限仅为40 fg,比所有市售技术低约100倍。使用这种方法,可重复检测出患者中低至1000个肿瘤细胞中的PSA。本文还描述了通过使用超薄导电磺化聚苯胺(SPANI)底层高效地将酶(Mb和HRP)连接到电极而导致的对H2O2的大大增强的催化反应,其行为类似于分子导线,大大提高了效率电子转移。

著录项

  • 作者

    Yu, Xin.;

  • 作者单位

    University of Connecticut.;

  • 授予单位 University of Connecticut.;
  • 学科 Chemistry Analytical.
  • 学位 Ph.D.
  • 年度 2006
  • 页码 164 p.
  • 总页数 164
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学;
  • 关键词

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