The Key Laboratory of Life-Organic Analysis, College of Chemistry and Chemical Engineering, Qufu Normal University, Qufu, Shandong 273165, PR China.
Leadernano Tech. L.L.C., Jining, Shandong 272000, PR China.
Biosens Bioelectron. 2015 Sep 15;71:200-206. doi: 10.1016/j.bios.2015.04.008. Epub 2015 Apr 8.
A novel colorimetric immunoassay was designed for the sensitive detection of carbohydrate antigen 125 (CA125). The success of this immunoassay relies on the use of hollow polydopamine-gold nanoparticles (PDA-Au) for signal amplification to achieve sensitive nonenzymatic colorimetric detection. In particular, PDA-Au was used as a stable and sensitive label and aminated-Fe3O4 magnetic nanoparticles (Fe3O4 NPs) were employed to immobilize capture antibody (Ab1) and acted as a separable immunosensing probe. PDA-Au exhibited high catalytic performance towards p-nitrophenol reduction and thus resulted in significant color change and UV/vis signal variations. The immunoassay was performed based on sandwich protocol. As compared to pure Au nanoparticles, the signal amplification and sensitivity of PDA-Au-based assay was significantly improved. For instance, the dynamic range of the developed colorimetric immunoassay for CA125 was 0.1-100 U/mL with a detection limit of 0.1 U/mL at S/N=3. In addition, this immunoassay was also tested for the analysis of clinical serum samples, which demonstrated its potential for practical diagnostic applications.
一种用于灵敏检测糖类抗原 125(CA125)的新型比色免疫分析方法被设计出来。该免疫分析的成功依赖于使用中空聚多巴胺-金纳米粒子(PDA-Au)进行信号放大,以实现灵敏的非酶比色检测。具体来说,PDA-Au 被用作稳定且灵敏的标记物,而氨基化的 Fe3O4 磁性纳米粒子(Fe3O4 NPs)则用于固定捕获抗体(Ab1),并作为可分离的免疫传感探针。PDA-Au 对 p-硝基苯酚的还原具有很高的催化性能,因此导致了明显的颜色变化和紫外/可见信号变化。免疫分析是基于三明治检测原理进行的。与纯 Au 纳米粒子相比,基于 PDA-Au 的检测方法的信号放大和灵敏度得到了显著提高。例如,所开发的 CA125 比色免疫分析的检测范围为 0.1-100 U/mL,检测限为 0.1 U/mL(S/N=3)。此外,该免疫分析还用于临床血清样本的分析,证明了其在实际诊断应用中的潜力。