Nanoparticle labelling-based magnetic immunoassay on chip combined with electrothermal vaporization - inductively coupled plasma mass spectrometry for the determination of carcinoembryonic antigen in human serum

被引:41
作者
Chen, Beibei [1 ]
Hu, Bin [1 ]
Jiang, Ping [1 ]
He, Man [1 ]
Peng, Hanyong [1 ]
Zhang, Xing [1 ]
机构
[1] Wuhan Univ, Dept Chem, Minist Educ, Key Lab Analyt Chem Biol & Med, Wuhan 430072, Peoples R China
关键词
ELECTROCHEMICAL DETECTION; OPTICAL SPECTROSCOPY; MARKER; CANCER; TAGS;
D O I
10.1039/c1an15387k
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A sensitive and selective on chip magnetic immunoassay method, based on a sandwich-type immunoreaction with PbS nanoparticle (NPs) labels in combination with electrothermal vaporization-inductively coupled plasma mass spectrometry (ETV-ICP-MS), was proposed for the determination of carcinoembryonic antigen (CEA). We designed and fabricated a microfluidic chip for magnetic immunoassay, and the prepared iminodiacetic acid modified silica coated magnetic nanoparticles (IDA-SCMNPs) were packed into the central microchannel to form a solid phase column by self-assembly under the magnetic field. After completion of the immunoreaction involving a primary antibody, CEA and a secondary antibody labeled with PbS NPs on a magnetic solid phase packed-column, ETV-ICP-MS was used to determine the concentration of Pb that was released from the captured PbS NPs using an acid-dissolution step. The concentrations of CEA can be correlated with that of Pb. The established method demonstrated a limit of detection of 0.058 mu g L-1 for CEA, with a relative standard deviation (RSD) of 6.7% (c = 10 mu g L-1, n = 7). A linearity ranging from 0.2 mu g L-1 to 50 mu g L-1 and a 2-fold enrichment factor (from 60 mu L sample solution to 30 mu L eluent) were achieved. The proposed method was further validated by analyzing CEA in human serum. The results were in good agreement with those obtained by chemiluminescent immunoassay, which is currently used as a clinical method. Overall, this method offers the advantages of high speed, high sensitivity, high selectivity, low sample/reagents consumption, high integrity and versatility. Moreover, it can be easily applied to other biological and medical assays.
引用
收藏
页码:3934 / 3942
页数:9
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