Rapid Homogeneous Fluorescent Enzyme-Linked Immunosorbent Assay (ELISA) for N-Terminal Brain Natriuretic Peptide (NT-proBNP) Combining Magnetic Probes and Ampliflu Red

被引:0
|
作者
Yang, Haixia [1 ]
Lai, Xiangde [1 ]
Jiang, Chenglong [1 ]
Zhao, Xuan [1 ]
Pang, Huajie [1 ]
Li, Dongxia [1 ]
Gao, Zhijun [1 ]
Qiao, Bin [1 ]
Han, Feng [2 ]
Tian, Jia [3 ]
机构
[1] Hainan Med Univ, Affiliated Hosp 2, Sch Trop Med, Dept Clin Lab, 3 Xueyuan Rd, Haikou, Hainan, Peoples R China
[2] Hainan Med Univ, Dept Clin Lab, Affiliated Hosp 1, 31 Longhua Rd, Haikou, Hainan, Peoples R China
[3] Hainan Med Univ, Hainan Gen Hosp, Hainan Affiliated Hosp, Intens Med Unit, 19 Xiuhua Rd, Haikou, Hainan, Peoples R China
基金
中国国家自然科学基金;
关键词
Ampliflu Red; fluorescent enzyme-linked immunosorbent assay (ELISA); N-terminal brain natriuretic peptide (NT-proBNP); serum analysis; BETA-CASEIN; IMMUNOASSAY; IMMUNOSENSOR;
D O I
10.1080/00032719.2024.2348087
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Heart failure (HF) is the leading cause of death from cardiovascular disease, and early diagnosis using serum markers holds extraordinary significance for the treatment of patients. N-terminal brain natriuretic peptide (NT-proBNP) is the gold standard for HF diagnosis. Herein, a novel, rapid, sensitive, and immune-sensing strategy for NT-proBNP is reported employing an enzyme-linked immunosorbent assay (ELISA) that combines the use of magnetic biological probes and the fluorogenic substrate Ampliflu Red. Functionalized immunomagnetic nanoparticles with large surface areas provide an abundant reaction platform and reduce the analysis time due to their superparamagnetic properties. Ampliflu Red is catalyzed by horseradish peroxidase (HRP) using hydrogen peroxide (H2O2) to produce strong fluorescence and a low background. The reported method achieved a good detection limit of 2.73 ng mL-1 and a wide linear range from 3.13 to 100 ng mL-1. The analysis time was less than 1 h, which is superior to that of traditional ELISA (3-4 h). In addition, the recoveries of spiked human serum were satisfactory, indicating that the proposed strategy has potential applications for the rapid determination of NT-proBNP and other biomarkers in clinical settings.
引用
收藏
页码:1011 / 1021
页数:11
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