| Literature DB >> 29908158 |
Somayeh Mohammadi1, Abdollah Salimi2, Somayeh Hamd-Ghadareh1, Fardin Fathi3, Farzad Soleimani3.
Abstract
We proposed a FRET immunosensing for detection of CA15-3 tumor marker by highly biospecific interactions between CA 15-3 antigen and the corresponding antibody and aptamer. In this sandwich type immunoassay, CA15-3 antibody-functionalized carbon dots and AuNPs labeled PAMAM-Dendrimer/aptamer were used as donor/acceptor, respectively. When CA 15-3 Ag was added to homogenous immunoassay, the strong complex interaction between CA15-3 Ab-CA15-3 Ag- aptamer caused in more coming closer carbon dot and AuNPs and more decreasing fluorescence signal. The decreased fluorescence intensity was linear at three ranges including in concentration range 1.1 μUmL-1 to 16 μU mL-1 with regression of R2 = 0.9879, at the concentration range 16 μU mL-1 to 0.163 mU mL-1 with regression of R2 = 0.9944 and at the concentration range 0.163 mU mL-1 to 5.0 mU mL-1 with regression of R2 = 0.9805. The detection limit of the FRET immunoassay was 0.9 μU mL-1. This assay revealed good sensitivity and specificity with MDA-MB-231 breast cancer cells concentrations from 1000 to 40000 cells/mL with correlation coefficient of 0.9955 and detection limit of 300 cells/mL (3 cells in 10 μL of injected sample). In addition, this FRET immunosensing is applicable in diluted human serum. The recovery values were in the range of 95.86-96.97% for CA 15-3 Ag in spiked serum sample with RSD lower than 7.3%. The proposed immunoassay could be a valid model for establishing other immunoassays for detection of different cancer tumor markers with relevant antigens and antibodies.Entities:
Keywords: Aptamer; AuNPs; Breast cancer cells; CA 15-3 immunoassay; Cancer diagnosis; Carbon dot; Fluorescence resonance energy transfer; PAMAM-Dendrimer
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Year: 2018 PMID: 29908158 DOI: 10.1016/j.ab.2018.06.008
Source DB: PubMed Journal: Anal Biochem ISSN: 0003-2697 Impact factor: 3.365