Vashist Sandeep Kumar, Marion Schneider E, Lam Edmond, Hrapovic Sabahudin, Luong John H T
1] HSG-IMIT - Institut für Mikro- und Informationstechnik, Georges-Koehler-Allee 103, 79110 Freiburg, Germany [2] Laboratory for MEMS Applications, Department of Microsystems Engineering -IMTEK, University of Freiburg, Georges-Koehler-Allee 103, 79110 Freiburg, Germany.
Sektion Experimentelle Anaesthesiologie, University Hospital Ulm, Albert Einstein Allee 23; 89081 Ulm, Germany.
Sci Rep. 2014 Mar 18;4:4407. doi: 10.1038/srep04407.
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°C 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.
已开发出一种使用一步抗体固定化的改进酶联免疫吸附(ELISA)测定法,用于检测人胎球蛋白A(HFA),它是动脉粥样硬化和肝细胞癌的一种特异性生物标志物。抗HFA通过离子和疏水相互作用与3-氨丙基三乙氧基硅烷(APTES)形成稳定复合物。吸附在微量滴定板上的复合物对HFA的检测范围为4.9 pg mL(-1)至20 ng mL(-1),检测限为7 pg mL(-1)。此外,实现了10 pg mL(-1)的分析灵敏度,比商业夹心ELISA试剂盒的灵敏度提高了51倍。在稀释的人全血和血浆中加标HFA所获得的结果显示出与商业试剂盒相同的精密度。当在4°C下于0.1 M磷酸盐缓冲盐水(PBS,pH 7.4)中储存时,抗HFA包被的微量滴定板在两个月后其功能活性没有显著下降。新的ELISA方法被扩展用于检测C反应蛋白、人白蛋白和人脂质运载蛋白-2,具有出色的分析性能。