An Ultra-Rapid Biosensory Point-of-Care (POC) Assay for Prostate-Specific Antigen (PSA) Detection in Human Serum.
Sophie S MavrikouGeorgia MoschopoulouAthanasios ZafeirakisKonstantina KalogeropoulouGeorgios GiannakosAthanasios SkevisSpyridon KintziosPublished in: Sensors (Basel, Switzerland) (2018)
Prostate-specific antigen (PSA) is the established routine screening tool for the detection of early-stage prostate cancer. Given the laboratory-centric nature of the process, the development of a portable, ultra rapid high-throughput system for PSA screening is highly desirable. In this study, an advancedpoint-of-care system for PSA detection in human serum was developed based on a cellular biosensor where the cell membrane was modified by electroinserting a specific antibody against PSA. Thirty nine human serum samples were used for validation of this biosensory system for PSA detection. Samples were analyzed in parallel with a standard immunoradiometric assay (IRMA) and an established electrochemical immunoassay was used for comparison purposes. They were classified in three different PSA concentration ranges (0, <4 and ≥4 ng/mL). Cells membrane-engineered with 0.25 μg/mL anti-PSA antibody demonstrated a statistically lower response against the upper (≥4 ng/mL) PSA concentration range. In addition, the cell-based biosensor performed better than the immunosensor in terms of sensitivity and resolution against positive samples containing <4 ng/mL PSA. In spite of its preliminary, proof-of-concept stage of development, the cell-based biosensor could be used as aninitiative for the development of a fast, low-cost, and high-throughput POC screening system for PSA.
Keyphrases
- prostate cancer
- radical prostatectomy
- label free
- high throughput
- loop mediated isothermal amplification
- sensitive detection
- early stage
- gold nanoparticles
- single cell
- low cost
- healthcare
- real time pcr
- cell therapy
- induced apoptosis
- signaling pathway
- radiation therapy
- mesenchymal stem cells
- oxidative stress
- bone marrow
- single molecule
- neoadjuvant chemotherapy
- tandem mass spectrometry