Department of Biomedical Engineering, School of Geosciences and Info-Physics, Central South University, Changsha 410083, China.
J Pharm Biomed Anal. 2011 Dec 15;56(5):1035-40. doi: 10.1016/j.jpba.2011.08.008. Epub 2011 Aug 10.
A barcode semiquantitative lateral flow immunochromatographic strip for prostate acid phosphatase (PAP) was developed, in which the monoclonal antibody specific for PAP was labeled to gold nanoparticle and another monoclonal antibody was immobilized on nitrocellulose membrane in the barcode fashion respectively. Based on the stepwise capture of analyte, the system expresses the concentration of PAP in nanogram range as four distinct ladder bars in 30 min, therefore, which could be detected directly by naked eye or image analyzer. Serum PAP from 65 patients was detected with this method and compared with enzyme linked immunosorbent assay (ELISA). There is a good agreement between the methods. Its easily readable result, and also its simplicity and low cost offers an alternative for testing PAP. By incorporating with different specific antibody, the assay can be further extended to detect a variety of analytes with clinical importance.
我们开发了一种用于前列腺酸性磷酸酶(PAP)的条码半定量侧向流动免疫层析条,其中针对 PAP 的单克隆抗体被标记到金纳米颗粒上,另一个单克隆抗体以条码的方式固定在硝酸纤维素膜上。基于分析物的逐步捕获,该系统在 30 分钟内将 PAP 的浓度以四个不同的梯级条表示,因此可以通过肉眼或图像分析仪直接检测。用该方法检测了 65 例患者的血清 PAP,并与酶联免疫吸附测定(ELISA)进行了比较。两种方法之间有良好的一致性。该方法的结果易于读取,且简单、成本低,为 PAP 的检测提供了一种替代方法。通过结合不同的特异性抗体,该测定方法可以进一步扩展到检测具有临床意义的多种分析物。