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One-step antibody immobilization-based rapid and highly-sensitive sandwich ELISA procedure for potential in vitro diagnostics

机译:基于一步抗体固定化的快速高灵敏度三明治ELISA程序,可用于潜在的体外诊断

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摘要

An improved enzyme-linked immunosorbent (ELISA) assay using one-step antibody immobilization has been developed for the detection of human fetuin A (HFA), a specific biomarker for atherosclerosis and hepatocellular carcinoma. The anti-HFA formed a stable complex with 3-aminopropyltriethoxysilane (APTES) by ionic and hydrophobic interactions. The complex adsorbed on microtiter plates exhibited a detection range of 4.9 pg mL-1 to 20 ng mL-1 HFA, with a limit of detection of 7 pg mL-1. Furthermore, an analytical sensitivity of 10 pg mL-1 was achieved, representing a 51-fold increase in sensitivity over the commercial sandwich ELISA kit. The results obtained for HFA spiked in diluted human whole blood and plasma showed the same precision as the commercial kit. When stored at 4\ub0C in 0.1 M phosphate-buffered saline (PBS, pH 7.4), the anti-HFA bound microtiter plates displayed no significant decrease in their functional activity after two months. The new ELISA procedure was extended for the detection of C-reactive protein, human albumin and human lipocalin-2 with excellent analytical performance.
机译:已开发出一种使用一步抗体固定化的改进的酶联免疫吸附(ELISA)分析方法,用于检测人胎球蛋白A(HFA),后者是动脉粥样硬化和肝细胞癌的一种特殊生物标记。抗-HFA通过离子和疏水作用与3-氨丙基三乙氧基硅烷(APTES)形成稳定的络合物。吸附在微量滴定板上的复合物的检测范围为4.9 pg mL-1至20 ng mL-1 HFA,检测限为7 pg mL-1。此外,达到了10 pg mL-1的分析灵敏度,这表明其灵敏度比市售夹心ELISA试剂盒高51倍。在稀释的人全血和血浆中加标HFA的结果显示出与市售试剂盒相同的精度。当在4 UbC中储存在0.1 M磷酸盐缓冲液(PBS,pH 7.4)中时,抗-HFA结合的微量滴定板在两个月后未显示其功能活性显着降低。新的ELISA程序已扩展到检测C反应蛋白,人白蛋白和人lipocalin-2,具有出色的分析性能。

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