0492495 - ÚOCHB 2019 RIV NL eng J - Journal Article
Chaloupková, Z. - Balzerová, A. - Bařinková, J. - Medříková, Z. - Šácha, Pavel - Beneš, P. - Ranc, V. - Konvalinka, J. - Zbořil, R.
Label-free determination of prostate specific membrane antigen in human whole blood at nanomolar levels by magnetically assisted surface enhanced Raman spectroscopy.
Analytica Chimica Acta. Roč. 997, Jan 2 (2018), s. 44-51. ISSN 0003-2670. E-ISSN 1873-4324
R&D Projects: GA MŠMT LO1302; GA MŠMT(CZ) LO1304; GA ČR(CZ) GA16-02938S
Institutional support: RVO:61388963
Keywords : Raman spectroscopy * nanocomposites * prostate cancer * GCPII * MA-SERS
OECD category: Biochemistry and molecular biology
Impact factor: 5.256, year: 2018

Prostate cancer is one of the most common cancers among men and can in its later stages cause serious medical problems. Due to the limited suitability of current diagnostic biochemical markers, new biomarkers for the detection of prostate cancer are highly sought after. An ideal biomarker should serve as a reliable prognostic marker, be applicable for early diagnosis, and be applicable for monitoring of therapeutic response. One potential candidate is glutamate carboxypeptidase II (GCPII), also known as prostate specific membrane antigen (PSMA), which has a promising role for direct imaging. GCPII is considerably over-expressed on cancerous prostatic epithelial cells, its analysis typically follows radiological or spectrophotometric principles. Its role as a biomarker present in blood has been recently investigated and potential correlation between a concentration of GCPII and prostate cancer has been proposed. The wider inclusion of GCPII detection in clinical praxis limits mainly the time and cost per analysis. Here, we present a novel analytical nanosensor applicable to quantification of GCPII in human whole blood consisted of Fe3O4@Ag magnetic nanocomposite surface-functionalized by an artificial antibody (low-molecular-weight GCPII synthetic inhibitor). The nanocomposite allows a simple magnetic isolation of GCPII using external magnetic force and its consecutive determination by magnetically assisted surface enhanced Raman spectroscopy (MA-SERS) with a limit of detection 6 pmol. L-1. This method enables a rapid determination of picomolar concentrations of GCPII in whole human blood of healthy individuals using a standard addition method without a complicated sample pre-treatment.
Permanent Link: http://hdl.handle.net/11104/0286008