材料科学
胶体金
免疫分析
介孔二氧化硅
荧光
纳米颗粒
检出限
单克隆抗体
纳米技术
抗原
生物传感器
量子点
抗体
介孔材料
色谱法
化学
生物化学
催化作用
生物
物理
免疫学
量子力学
遗传学
作者
Shiyi Tao,Xiaomin Zhao,Dongping Bao,Xuecheng Liu,Wei Zhang,Liying Zhao,Yujiao Tang,Hongbin Wu,Huayue Ye,Yili Yang,Dawei Deng
标识
DOI:10.1021/acsami.3c03434
摘要
The extensive research into developing novel strategies for detecting respiratory syndrome coronavirus 2 (SARS-CoV-2) antigens in clinical specimens, especially the sensitive point-of-care testing method, is still urgently needed to reach rapid screening of viral infections. Herein, a new lateral flow immunoassay (LFIA) platform was reported for the detection of SARS-CoV-2 spike-S1 protein antigens, in which four sensitive and specific SARS-CoV-2 mouse monoclonal antibodies (MmAbs) were tailored by using quantum dot (QD)-loaded dendritic mesoporous silica nanoparticles modified further for achieving the -COOH group surface coating (named Q/S-COOH nanospheres). Importantly, compact QD adsorption was achieved in mesoporous channels of silica nanoparticles on account of highly accessible central-radial pores and electrostatic interactions, leading to significant signal amplification. As such, a limit of detection for SARS-CoV-2 spike-S1 testing was found to be 0.03 ng/mL, which is lower compared with those of AuNPs-LFIA (traditional colloidal gold nanoparticles, Au NPs) and enzyme-linked immunosorbent assay methods. These results show that optimizing the affinity of antibody and the intensity of fluorescent nanospheres simultaneously is of great significance to improve the sensitivity of LFIA.
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