Huang Xiaopeng, Li Yuqin, Huang Xiang, Xie Xiaona, Xu Yanping, Chen Yaowen, Gao Wenhua
Department of Chemistry and Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province, Shantou University, Shantou, Guangdong, 515063, China.
Department of Pharmacy, Taishan Medicine College, Taian, Shandong, 271016, China.
Anal Bioanal Chem. 2016 Jan;408(2):619-27. doi: 10.1007/s00216-015-9144-x. Epub 2015 Nov 7.
A novel and environmentally friendly reverse fluorescent immunoassay approach was proposed and utilized for sensing human chorionic gonadotropin (HCG) in human serum by coupling a newly prepared and highly fluorescent glutathione-stabilized silver-gold nano-alloy (GSH-AgAuNAs) with magnetic nanoparticles (MNPs). To construct such a reverse system, fluorescent GSH-AgAuNAs and MNPs were first prepared and bio-functionalized with monoclonal antibodies (Mab-I and Mab-II) toward HCG antigen, respectively. Then, the GSH-AgAuNAs functionalized with Mab-I were incubated with HCG, followed by the addition of MNPs attached to Mab-II. Thereafter, a sandwich-type immunoassay could be constructed for determination of HCG owing to the antibody-antigen recognition between the functionalized GSH-AgAuNAs and MNPs. Afterwards, a magnetic collection was employed. Hence, the amount of GSH-AgAuNAs would be reduced through an immuno-magnetic separation, thus weakening the fluorescent intensity. Different from conventional immunoassay, our work determined the quantitative signal by measuring the decreasing gradient fluorescent intensity. Under optimal conditions, the developed reverse method exhibited a wide linear range of 0.5-600 ng mL(-1) toward HCG with a detection limit of 0.25 ng mL(-1). Additionally, the proposed immunoassay was validated using spiked samples, illustrating a satisfactory result in practical application.
提出了一种新型且环保的反向荧光免疫分析方法,并将其用于检测人血清中的人绒毛膜促性腺激素(HCG),该方法通过将新制备的具有高荧光性的谷胱甘肽稳定化银金纳米合金(GSH-AgAuNAs)与磁性纳米颗粒(MNPs)相结合来实现。为构建这样一个反向系统,首先制备荧光GSH-AgAuNAs和MNPs,并分别用针对HCG抗原的单克隆抗体(Mab-I和Mab-II)进行生物功能化。然后,将用Mab-I功能化的GSH-AgAuNAs与HCG孵育,接着加入连接有Mab-II的MNPs。此后,由于功能化的GSH-AgAuNAs与MNPs之间的抗体-抗原识别作用,可以构建一种夹心型免疫分析法来测定HCG。之后,采用磁性收集。因此,通过免疫磁分离,GSH-AgAuNAs的量会减少,从而减弱荧光强度。与传统免疫分析不同,我们的工作通过测量荧光强度的下降梯度来确定定量信号。在最佳条件下,所开发的反向方法对HCG的线性范围为0.5 - 600 ng mL(-1),检测限为0.25 ng mL(-1)。此外,使用加标样品对所提出的免疫分析法进行了验证,结果表明其在实际应用中令人满意。