Education Ministry Key Laboratory on Luminescence and Real-Time Analysis, College of Chemistry and Chemical Engineering, Southwest University, Chongqing 400715, PR China.
Anal Chim Acta. 2012 Oct 9;746:70-6. doi: 10.1016/j.aca.2012.08.018. Epub 2012 Aug 24.
In this work, a sandwich-type electrochemical immunosensor for simultaneous sensitive detection of prostate specific antigen (PSA) and free prostate specific antigen (fPSA) is fabricated. Gold nanoparticles (AuNPs) modified Prussian blue and nickel hexacyanoferrates nanoparticles were firstly prepared, respectively, and then decorated onion-like mesoporous graphene sheets (denoted as Au@PBNPs/O-GS and Au@NiNPs/O-GS) as distinguishable signal tags to label different detection antibodies. Subsequently, streptavidin and biotinylated alkaline phosphatase (bio-AP) were employed to block the possible remaining active sites. With the employment of the as prepared nanohybrids, the dual catalysis amplification can be achieved by catalysis of the ascorbic acid 2-phosphate to in situ produce AA in the presence of bio-AP, and then AA was further catalyzed by Au@PBNPs/O-GS and Au@NiNPs/O-GS nanohybrids, respectively, to obtain the higher signal responses. The experiment results show that the linear range of the proposed immunosensor for simultaneous determination of fPSA is from 0.02 to 10 ng mL(-1) with a detection limit of 6.7 pg mL(-1) and PSA is from 0.01 to 50 ng mL(-1) with a detection limit of 3.4 pg mL(-1) (S/N=3). Importantly, the proposed method offers promise for rapid, simple and cost-effective analysis of biological samples.
在这项工作中,制备了一种夹心型电化学免疫传感器,用于同时灵敏检测前列腺特异性抗原 (PSA) 和游离前列腺特异性抗原 (fPSA)。首先分别制备了金纳米粒子 (AuNPs) 修饰的普鲁士蓝和镍六氰合铁酸盐纳米粒子,然后将洋葱状介孔石墨烯片 (表示为 Au@PBNPs/O-GS 和 Au@NiNPs/O-GS) 作为可区分的信号标记物来标记不同的检测抗体。随后,链霉亲和素和生物素化碱性磷酸酶 (bio-AP) 被用来阻止可能残留的活性位点。利用所制备的纳米杂化物,可以通过生物素化碱性磷酸酶存在下催化抗坏血酸 2-磷酸原位生成 AA 来实现双重催化放大,然后 AA 分别被 Au@PBNPs/O-GS 和 Au@NiNPs/O-GS 纳米杂化物进一步催化,从而获得更高的信号响应。实验结果表明,所提出的用于同时测定 fPSA 的免疫传感器的线性范围为 0.02 至 10 ng mL(-1),检测限为 6.7 pg mL(-1),PSA 的线性范围为 0.01 至 50 ng mL(-1),检测限为 3.4 pg mL(-1) (S/N=3)。重要的是,该方法有望用于生物样品的快速、简单和经济有效的分析。