PMID- 23062558 OWN - NLM STAT- MEDLINE DCOM- 20130530 LR - 20151119 IS - 1873-4235 (Electronic) IS - 0956-5663 (Linking) VI - 41 DP - 2013 Mar 15 TI - Multiplexed sandwich immunoassays using flow-injection electrochemiluminescence with designed substrate spatial-resolved technique for detection of tumor markers. PG - 684-90 LID - S0956-5663(12)00650-1 [pii] LID - 10.1016/j.bios.2012.09.044 [doi] AB - Convenient sensor array for simultaneous multi-analyte testing was increasingly needed in clinical diagnosis. A novel electrochemiluminescence (ECL) immunosensor array for the sequential detection of multiple tumor markers was developed by site-selectively immobilizing multiple antigens on different electrodes. Disposable indium tin oxide (ITO) glass array was employed as detection platform. With a sandwich-type immunoassay format, the amount of carbon dots coated silica (SiO(2)@C-dots) labeled antibodies increased with the increment of antigens in the samples. The ECL signal from different immunosensors was collected in turn by a photomultiplier (PMT) with the aid of a home-made potential transformer equiped with a home-made multiplexed-switch. Using carcino embryonic antigen (CEA), prostate specific antigen (PSA) and alpha-fetoprotein (alpha-AFP) as model analytes, the proposed immunoassay exhibited excellent precision and sensitivity. For all three analytes, the relative standard deviations (RSDs) for six times detection were lower than 7.1% and the detection limits were in the range of 0.003-0.006 ng mL(-1). The results for real sample analysis demonstrated that the newly constructed immunosensor array provided a rapid, simple, simultaneous multi-analyte immunoassay with high throughput, cost-effective and sufficiently low detection limits for clinical applications. Importantly, the novel individually addressable immunosensor array for multi-analyte immunoassay by introducing the ECL readout mechanism with the aid of the home-made potential transformer and multiplexed-switch could be a useful supplement to commercial assay methods in clinical chemistry. CI - Copyright (c) 2012. Published by Elsevier B.V. FAU - Zhang, Yan AU - Zhang Y AD - Key Laboratory of Chemical Sensing & Analysis in Universities of Shandong, School of Chemistry and Chemical Engineering, University of Jinan, Jinan 250022, PR China. FAU - Liu, Weiyan AU - Liu W FAU - Ge, Shenguang AU - Ge S FAU - Yan, Mei AU - Yan M FAU - Wang, Shaowei AU - Wang S FAU - Yu, Jinghua AU - Yu J FAU - Li, Nianqiang AU - Li N FAU - Song, Xianrang AU - Song X LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20120928 PL - England TA - Biosens Bioelectron JT - Biosensors & bioelectronics JID - 9001289 RN - 0 (Biomarkers, Tumor) RN - 0 (Neoplasm Proteins) SB - IM MH - Biomarkers, Tumor/*blood MH - Biosensing Techniques/instrumentation MH - Conductometry/*instrumentation MH - Equipment Design MH - Equipment Failure Analysis MH - Flow Injection Analysis/*instrumentation MH - Humans MH - Immunoassay/*instrumentation MH - Luminescent Measurements/*instrumentation MH - Neoplasm Proteins/*blood MH - Neoplasms, Experimental/*blood/diagnosis MH - Reproducibility of Results MH - Sensitivity and Specificity EDAT- 2012/10/16 06:00 MHDA- 2013/06/01 06:00 CRDT- 2012/10/16 06:00 PHST- 2012/07/22 00:00 [received] PHST- 2012/09/09 00:00 [revised] PHST- 2012/09/22 00:00 [accepted] PHST- 2012/10/16 06:00 [entrez] PHST- 2012/10/16 06:00 [pubmed] PHST- 2013/06/01 06:00 [medline] AID - S0956-5663(12)00650-1 [pii] AID - 10.1016/j.bios.2012.09.044 [doi] PST - ppublish SO - Biosens Bioelectron. 2013 Mar 15;41:684-90. doi: 10.1016/j.bios.2012.09.044. Epub 2012 Sep 28.