CdZnTeS quantum dots based electrochemiluminescent image immunoanalysis

被引:50
作者
Liang, Xiu-Li [1 ]
Bao, Ning [2 ]
Luo, Xiliang [3 ]
Ding, Shou-Nian [1 ]
机构
[1] Southeast Univ, Sch Chem & Chem Engn, Jiangsu Prov Hitech Key Lab Biomed Res, Nanjing 211189, Jiangsu, Peoples R China
[2] Nantong Univ, Sch Publ Hlth, Nantong 226019, Jiangsu, Peoples R China
[3] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Minist Educ, Key Lab Sensor Anal Tumor Marker, Qingdao 266042, Peoples R China
基金
中国国家自然科学基金;
关键词
CdZnTeS QDs; Immunosensors; Electrochemiluminescent image analysis; Alpha-fetoprotein; Cancer antigen 125; MAGNETIC SEPARABLE CARRIERS; ELECTROGENERATED CHEMILUMINESCENCE; SIGNAL AMPLIFICATION; ANODIC ELECTROCHEMILUMINESCENCE; ELECTROCHEMICAL IMMUNOASSAY; GOLD NANOPARTICLES; IMMUNOSENSOR; PHOTOLUMINESCENCE; NANOCOMPOSITES; NANOCRYSTALS;
D O I
10.1016/j.bios.2018.06.006
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this work, quaternary CdZnTeS quantum dots (QDs) with a particularly strong electrochemiluminescence (ECL) were synthesized as ECL signal labels. The strong ECL signals can be obtained at both cathode and anode with the ECL efficiencies of 19.78% and 1.62%, respectively. The sandwich-structured ECL immunosensors for the detection of alpha-fetoprotein (AFP) and cancer antigen 125 (CA125) were accomplished with direct ECL image analysis. Under optimal conditions, the QDs-based ECL image immunoanalysis possessed good linearity from 0.5 ng/mL to 20 ng/mL for AFP and from 20 U/mL to 500 U/mL for CA125 with the detection limit of 0.1 ng/mL and 6 U/mL, respectively (S/N = 3), and the lower detection limit obtained by photomultiplier tube were 0.1 fg/mL for AFP and 0.03 mU/mL for CA125 with the wide dynamic range from 0.5 fg/mL to 20 ng/mL and from 0.1 mU/mL to 500 U/mL, respectively (S/N = 3). Furthermore, the ECL immunoanalysis was evaluated with commercial enzyme-linked immunosorbent assay in human serum samples. The good results indicated that CdZnTeS QDs-based ECL biosensor has great potential for fast biomedical screening and multi assays in clinical diagnosis.
引用
收藏
页码:145 / 152
页数:8
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