2021
Determination of 8-hydroxy-2 '-deoxyguanosine in urine with "linear" mode sparked graphite screen-printed electrodes
TRACHIOTI, Maria G., Jan HRBÁČ a Mamas I. PRODROMIDISZákladní údaje
Originální název
Determination of 8-hydroxy-2 '-deoxyguanosine in urine with "linear" mode sparked graphite screen-printed electrodes
Autoři
TRACHIOTI, Maria G. (300 Řecko), Jan HRBÁČ (203 Česká republika, domácí) a Mamas I. PRODROMIDIS (300 Řecko, garant)
Vydání
Electrochimica Acta, Elsevier, 2021, 0013-4686
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
10405 Electrochemistry
Stát vydavatele
Nizozemské království
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 7.336
Kód RIV
RIV/00216224:14310/21:00122813
Organizační jednotka
Přírodovědecká fakulta
UT WoS
000711318400001
Klíčová slova anglicky
8−hydroxy−2ˊ−deoxyguanosineUrine biomarkersElectrode modification; Screen-printed electrode; Sparking discharge; DNA oxidative damage
Štítky
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 1. 12. 2021 17:35, Mgr. Marie Šípková, DiS.
Anotace
V originále
The development of sensors for diagnostic purposes is of immense importance. Despite the number of proposed sensors showing attractive detection capabilities, the widespread use of these sensors is mainly hindered by selectivity issues and the elaborate tailoring of the sensing surface that eventually increases both the cost of the final sensor and the individual analysis cost. Herein, we report on the development of an advanced sensor for 8−hydroxy−2ˊ−deoxyguanosine (8−OHdG), an important biomarker for DNA oxidative damage. The sensor was developed on a low-cost graphite screen-printed electrode (SPE) by employing for the first time, an extremely fast SPE-to-graphite “linear” mode sparking process that enables the uniform modification of the whole electrode surface in less than 20 s. Graphite-sparked SPEs exhibited a linear relationship with the concentration of 8−OHdG over the range 2–50 nM, while the limit of detection (3σ) was 0.35 nM. The sensors showed a notable resistance to interference by 1000-fold excess of dopamine and ascorbic acid, and 100-fold excess of uric acid. A simple treatment of the samples, based on uricase, that eliminates the interference caused by uric acid under real-world conditions (>1000-fold excess) was optimized and proposed. The method was successfully applied to the determination of 8−OHdG in synthetic urine samples. Recovery was 95%.