Department of Molecular Medicine, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran; Research Center for Pharmaceutical Nanotechnology, Biomedicine Institute, Tabriz University of Medical Sciences, Tabriz, Iran.
Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Biosens Bioelectron. 2018 Dec 30;122:8-15. doi: 10.1016/j.bios.2018.08.047. Epub 2018 Aug 23.
An early on-time detection of breast cancer can effectively affect the outcome of the treatment. Here, we developed an ultrasensitive, simple and reliable immunosensor to detect the lowest alteration of CA 15-3, the standard biomarker of breast cancer patients. The proposed immunosensor was achieved by modification of gold electrode by streptavidin to immobilize the biotinylated anti-CA 15-3 monoclonal antibody (mAb). Bovine serum albumin was used to prevent nonspecific binding. To improve the sensitivity of modified immunosensor, the sandwich signal enhancer consisting of streptavidin-coated magnetic beads conjugated with biotinylated horseradish peroxidase (HRP) and anti-CA 15-3 biotinylated mAb was applied. The electrochemical measurements were obtained in the presence of hydroquinone as a redox agent and HO as the activating agent of HRP. Under optimized condition and using square wave voltammetry, the lower limit of quantification was obtained as 15 × 10 U/mL and the linear CA 15-3 concentration range was 50-15 × 10 U/mL. While showing significant stability, the immunosensor displayed an excellent sensitivity and specificity for the detection of CA 15-3 even in the human serum as compared to the enzyme-linked immunosorbent assay (ELISA) as a gold standard method. Based on our findings, the engineered immunosensor is proposed as a robust diagnostic tool for the clinical determination of CA 15-3 and other cancer biomarkers.
早期发现乳腺癌可以有效影响治疗结果。在这里,我们开发了一种超灵敏、简单且可靠的免疫传感器,用于检测乳腺癌患者的标准生物标志物 CA 15-3 的最低变化。该免疫传感器通过在金电极上修饰链霉亲和素来固定生物素化的抗 CA 15-3 单克隆抗体 (mAb) 来实现。牛血清白蛋白 (BSA) 用于防止非特异性结合。为了提高修饰后的免疫传感器的灵敏度,应用了由链霉亲和素包被的磁性珠与生物素化辣根过氧化物酶 (HRP) 和抗 CA 15-3 生物素化 mAb 组成的三明治信号增强剂。在存在氢醌作为氧化还原试剂和 HO 作为 HRP 激活剂的情况下进行电化学测量。在优化条件下,使用方波伏安法,获得的定量下限为 15×10 U/mL,CA 15-3 的线性浓度范围为 50-15×10 U/mL。与酶联免疫吸附测定 (ELISA) 作为金标准方法相比,该免疫传感器在人血清中显示出优异的稳定性、灵敏度和特异性,可用于 CA 15-3 的检测。基于我们的发现,所设计的免疫传感器可作为用于临床测定 CA 15-3 和其他癌症生物标志物的强大诊断工具。