Mahmoudi Tohid, Shirdel Behnaz, Mansoori Behzad, Baradaran Behzad
Immunology Research Center Tabriz University of Medical Sciences Tabriz Iran.
Student Research Committee Tabriz University of Medical Sciences Tabriz Iran.
Anal Sci Adv. 2020 Jun 23;1(3):161-172. doi: 10.1002/ansa.202000023. eCollection 2020 Oct.
In this work, we presented the development of cost-effective dual sensitivity enhancement in gold nanoparticle-based lateral flow test strip for detection of carcinoembryonic antigen. On the one hand, we employed protein G as a host matrix for oriented immobilization of antibodies within the nitrocellulose membrane. On the other hand, we utilized gold enhancement approach to visualize the final signals effectively. Primary examinations revealed that the smaller sized nanoparticles have greater signal enhancement compared to bigger ones. So, mono-dispersed gold nanoparticles with average diameters of 11.40 ± 1.40 nm were utilized as tags. The measurement of fluorescent intensity of FITC-tagged secondary antibody attached to the polyclonal antibody, in the presence/absence of protein G as a host matrix on microplate wells, showed the successful oriented immobilization of antibodies via the host matrix. The FESEM images confirmed the attachment and growth of nanoparticles within the porous nitrocellulose membrane, after gold enhancement. Finally, under the optimized conditions, the developed strip could quantify the standard values of target within 2-50 ng/mL range with a limit of detection of 0.35 ng/mL. This strategy enabled the reduction of antibody consumption from a conventional amount of 0.6 µg/strip down to 0.012 µg/strip. The serum samples containing carcinoembryonic antigen were also successfully analyzed by the developed strip with a visual detection limit of 10 ng/mL, which confirms favorable characteristics of the developed test strip for point-of-care applications.
在这项工作中,我们展示了用于检测癌胚抗原的基于金纳米颗粒的侧向流动测试条中具有成本效益的双灵敏度增强技术的发展。一方面,我们使用蛋白G作为宿主基质,将抗体定向固定在硝酸纤维素膜内。另一方面,我们采用金增强方法有效地可视化最终信号。初步检查表明,与较大尺寸的纳米颗粒相比,较小尺寸的纳米颗粒具有更大的信号增强。因此,使用平均直径为11.40±1.40 nm的单分散金纳米颗粒作为标记物。在微孔板孔中存在/不存在作为宿主基质的蛋白G的情况下,对附着于多克隆抗体的FITC标记二抗的荧光强度进行测量,结果表明通过宿主基质成功地定向固定了抗体。场发射扫描电子显微镜(FESEM)图像证实了金增强后纳米颗粒在多孔硝酸纤维素膜内的附着和生长。最后,在优化条件下,所开发的测试条能够在2 - 50 ng/mL范围内定量目标物的标准值,检测限为0.35 ng/mL。该策略使抗体消耗量从传统的每条0.6 μg降低至每条0.012 μg。所开发的测试条还成功分析了含有癌胚抗原的血清样本,视觉检测限为10 ng/mL,这证实了所开发的测试条在即时检测应用中的良好特性。