Microfluidic tool based on the antibodymodified paramagnetic particles for detection of 8-hydroxy-20-deoxyguanosine in urine of prostate cancer patients

Varování

Publikace nespadá pod Ekonomicko-správní fakultu, ale pod Lékařskou fakultu. Oficiální stránka publikace je na webu muni.cz.
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ZÍTKA Ondřej KŘÍŽKOVÁ Sona KREJČOVÁ Ludmila HYNEK David GUMULEC Jaromír MASAŘÍK Michal SOCHOR Jiří ADAM Vojtěch HUBÁLEK Jaromír TRNKOVÁ Libuše KIZEK René

Rok publikování 2011
Druh Článek v odborném periodiku
Časopis / Zdroj Electrophoresis
Fakulta / Pracoviště MU

Lékařská fakulta

Citace
www http://onlinelibrary.wiley.com/doi/10.1002/elps.201100430/pdf
Doi http://dx.doi.org/10.1002/elps.201100430
Obor Biochemie
Klíčová slova Electrochemistry; ELISA; Magnetic particles; Nanoseparation
Popis Guanosine derivatives are important for diagnosis of oxidative DNA damage including 8-hydroxy-20-deoxyguanosine (8-OHdG) as one of the most abundant products of DNA oxidation. This compound is commonly determined in urine, which makes 8-OHdG a good non-invasive marker of oxidation stress. In this study, we optimized and tested the isolation of 8-OHdG from biological matrix by using paramagnetic particles with an antibody-modified surface. 8-OHdG was determined using 1-naphthol generated by alkaline phosphatase conjugated with the secondary antibody. 1-Naphthol was determined by stopped flow injection analysis (SFIA) with electrochemical detector using a glassy carbon working electrode and by stationary electrochemical detection using linear sweep voltammetry. A special modular electrochemical SFIA system which needs only 10 mL of sample including working buffer for one analysis was completely designed and successfully verified. The recoveries in different matrices and analyte concentration were estimated. Detection limit (3 S/N) was estimated as 5 pg/mL of 8-OHdG. This method promises to be very easily modified to microfluidic systems as ‘‘lab on valve’’. The optimized method had sufficient selectivity and thus could be used for determination of 8-OHDG in human urine and therefore for estimation of oxidative DNA damage as a result of oxidation stress in prostate cancer patients.
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