HYNEK, David, Sona KRIZKOVA, Ludmila KREJCOVA, Jaromír GUMULEC, Markéta RYVOLOVÁ, Natalia CERNEI, Michal MASAŘÍK, Vojtěch ADAM, Libuše TRNKOVÁ, Marie STIBOROVÁ, Tomáš ECKSCHLAGER, Jaromír HUBALEK and René KIZEK. Femtogram Electroanalytical Detection of Prostatic Specific Antigen by Brdicka Reaction. International Journal of Electrochemical Science. 2012, vol. 7, No 3, p. 1749-1766. ISSN 1452-3981.
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Basic information
Original name Femtogram Electroanalytical Detection of Prostatic Specific Antigen by Brdicka Reaction
Authors HYNEK, David (203 Czech Republic), Sona KRIZKOVA (203 Czech Republic), Ludmila KREJCOVA (203 Czech Republic), Jaromír GUMULEC (203 Czech Republic, belonging to the institution), Markéta RYVOLOVÁ (203 Czech Republic), Natalia CERNEI (203 Czech Republic), Michal MASAŘÍK (203 Czech Republic, belonging to the institution), Vojtěch ADAM (203 Czech Republic), Libuše TRNKOVÁ (203 Czech Republic, belonging to the institution), Marie STIBOROVÁ (203 Czech Republic), Tomáš ECKSCHLAGER (203 Czech Republic), Jaromír HUBALEK (203 Czech Republic) and René KIZEK (203 Czech Republic, guarantor).
Edition International Journal of Electrochemical Science, 2012, 1452-3981.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10405 Electrochemistry
Country of publisher Serbia
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 3.729 in 2011
RIV identification code RIV/00216224:14110/12:00059530
Organization unit Faculty of Medicine
UT WoS 000302730300002
Keywords in English prostate specific antigen; electrochemical detection; electrophoresis; voltammetry; adsorptive transfer stripping technique; catalytic signal; protein
Tags International impact
Changed by Changed by: Ing. Mgr. Věra Pospíšilíková, učo 9005. Changed: 16/4/2013 16:35.
Abstract
Prostatic-specific antigen is considered as the best marker for prostate cancer. Due to the importance of PSA for diagnostic purposes it is not surprising that there are tested and optimized various methods for its determination. In spite of such intensive research in the field of electrochemical detection of some by-products connected with concentration of PSA, electrochemical behaviour of PSA has not been studied yet. The aim of this study was to investigate electrochemical catalytic signals of PSA using differential pulse voltammetry Brdicka reaction. The catalytic signals were studied using adsorptive transfer stripping technique as well as directly in the electrochemical cell. Nevertheless, we primarily tested detection of PSA by standard immunoanalysis and by gel and capillary chip electrophoresis to investigate behaviour of this protein in electric field. Both electrophoretic methods showed that the most intensive band of PSA was determined at 37 kDa under reducing conditions and at 26 kDa under non-reducing. Band at 37 kDa corresponds to a reduced, and at 26 kDa to non-reduced PSA. Studying of basic electrochemical behaviour of PSA was primarily carried out using standard electrochemical cell and HMDE as a working electrode. Co(NH3)6Cl3 (1 mM) was used as a supporting electrolyte. Temperature of the electrolyte was maintained at 4 C. The effects of accumulation time and concentration of Co(NH3)6Cl3 as a key component of supporting electrolyte were studied. Time of accumulation of 240 s and 1.00 mM Co(NH3)6Cl3 were found the optimal for detection of PSA in electrochemical cell. Further, we used adsorptive transfer stripping technique coupled with differential pulse voltammetry Brdicka reaction for detection of PSA. Two temperatures of adsorption as 4 C and 20 C and several times of adsorption as 40, 60, 80, 120, 180, 240, 360 and 420 s were tested. Under the optimized conditions (4 C temperature of adsorption and 240 s time of adsorption) calibration curve with the following equation y = 36.865x - 11.949, R2 = 0.9911 within the concentration interval from 1 to 1,500 pg/ml was measured. Detection limit of PSA expressed as 3 S/N was estimated down to 1 fg of PSA in 0.5 microl.
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