采用微接触印迹表面等离子体共振生物传感器快速实时检测降钙素原。
Rapid real-time detection of procalcitonin using a microcontact imprinted surface plasmon resonance biosensor.
机构信息
Hacettepe University, Faculty of Science, Department of Chemistry, Ankara, Turkey.
出版信息
Analyst. 2013 Nov 7;138(21):6422-8. doi: 10.1039/c3an00958k.
Procalcitonin (PCT) is a promising biomarker for identification of the origin and severity of sepsis, which is a deadly body infection. In this work, we report the preparation of a surface plasmon resonance (SPR) biosensor which utilizes a molecular imprinted polymer surface for rapid and reliable detection of PCT. The molecular imprinted surface was prepared using a microcontact imprinting technique, in which PCT molecules were first immobilized onto a glass support and brought into contact with a solution of 2-hydroxyethyl methacrylate (HEMA) and ethylene glycol dimethacrylate (EGDMA) on a SPR sensor, then the polymerization process was performed. After removal of the PCT molecules, specific molecular recognition sites were obtained, where PCT molecules can selectively rebind, only at the surface of the polymer matrix. PCT detection studies were carried out using PCT solutions in phosphate buffer and simulated blood plasma (SBP) at different concentrations. The SPR biosensor can detect very low concentrations (9.9 ng mL(-1)) of PCT within approximately 1 h, in both phosphate buffer and SBP. High selectivity of the biosensor against PCT was also demonstrated in the presence of several competitive proteins such as human serum albumin, myoglobin and cytochrome c.
降钙素原(PCT)是一种有前途的生物标志物,可用于识别脓毒症的起源和严重程度,脓毒症是一种致命的全身感染。在这项工作中,我们报告了一种表面等离子体共振(SPR)生物传感器的制备,该传感器利用分子印迹聚合物表面快速可靠地检测 PCT。分子印迹表面是通过微接触印迹技术制备的,首先将 PCT 分子固定在玻璃载体上,然后将其与 SPR 传感器上的 2-羟乙基甲基丙烯酸酯(HEMA)和乙二醇二甲基丙烯酸酯(EGDMA)溶液接触,然后进行聚合过程。除去 PCT 分子后,获得了特异性的分子识别位点,其中 PCT 分子可以选择性地重新结合,仅在聚合物基质的表面上。使用磷酸盐缓冲液和模拟血浆(SBP)中的不同浓度的 PCT 溶液进行了 PCT 检测研究。SPR 生物传感器可以在磷酸盐缓冲液和 SBP 中检测到非常低浓度(9.9ngmL(-1))的 PCT,大约需要 1 小时。该生物传感器对 PCT 具有很高的选择性,即使在存在几种竞争蛋白(如人血清白蛋白、肌红蛋白和细胞色素 c)的情况下也是如此。