Highly sensitive and selective lateral flow immunoassay based on magnetic nanoparticles for quantitative detection of carcinoembryonic antigen

被引:60
|
作者
Liu, Fangming [1 ,2 ]
Zhang, Honglian [2 ]
Wu, Zhenhua [2 ]
Dong, Haidao [2 ,4 ]
Zhou, Lin [2 ]
Yang, Dawei [3 ]
Ge, Yuqing [2 ]
Jia, Chunping [2 ]
Liu, Huiying [4 ]
Jin, Qinghui [2 ]
Zhao, Jianlong [2 ]
Zhang, Qiqing [1 ]
Mao, Hongju [2 ]
机构
[1] Fuzhou Univ, Inst Biomed & Pharmaceut Technol, 523 Gongye Rd, Fuzhou 350002, Fujian Province, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Microsyst & Informat Technol, State Key Lab Transducer Technol, Shanghai 200050, Peoples R China
[3] Fudan Univ, Zhongshan Hosp, Dept Pulm Med, Shanghai 200032, Peoples R China
[4] Dalian Med Univ, Sch Stomatol, Dept Oral & Maxillofacial, Dalian 116023, Peoples R China
基金
美国国家科学基金会;
关键词
Lateral-flow immunoassay; Magnetic nanoparticles; Carcinoembryonic antigen; Diagnosis; GOLD NANOPARTICLES; TEST STRIP; CANCER; CYFRA21-1;
D O I
10.1016/j.talanta.2016.08.048
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Carcinoembryonic antigen (CEA) is an important biomarker in cancer diagnosis. Here, we present an efficient, selective lateral-flow immunoassay (LFIA) based on magnetic nanoparticles (MNPs) for in situ sensitive and accurate point-of-care detection of CEA. Signal amplification mechanism involved linking of detection MNPs with signal MNPs through biotin-modified single-stranded DNA (ssDNA) and streptavidin. To verify the effectiveness of this modified LFIA system, the sensitivity and specificity were evaluated. Sensitivity evaluation showed a broad detection range of 0.25-1000 ng/ml for CEA protein by the modified LFIA, and the limit of detection (LOD) of the modified LFIA was 0.25 ng/ml, thus producing significant increase in detection threshold compared with the traditional LFIA. The modified LFIA could selectively recognize CEA in presence of several interfering proteins. In addition, this newly developed assay was applied for quantitative detection of CEA in human serum specimens collected from 10 randomly selected patients. The modified LFIA system detected minimum 0.27 ng/ml of CEA concentration in serum samples. The results were consistent with the clinical data obtained using commercial electrochemiluminescence immunoassay (ECLIA) (p < 0.01). In conclusion, the MNPs based LFIA system not only demonstrated enhanced signal to noise ratio, it also detected CEA with higher sensitivity and selectivity, and thus has great potential to be commercially applied as a sensitive tumor marker filtration system. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:205 / 210
页数:6
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