Publication details

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

Authors

ZÍTKA Ondřej KŘÍŽKOVÁ Sona KREJČOVÁ Ludmila HYNEK David GUMULEC Jaromír MASAŘÍK Michal SOCHOR Jiří ADAM Vojtěch HUBÁLEK Jaromír TRNKOVÁ Libuše KIZEK René

Year of publication 2011
Type Article in Periodical
Magazine / Source Electrophoresis
MU Faculty or unit

Faculty of Medicine

Citation
Web http://onlinelibrary.wiley.com/doi/10.1002/elps.201100430/pdf
Doi http://dx.doi.org/10.1002/elps.201100430
Field Biochemistry
Keywords Electrochemistry; ELISA; Magnetic particles; Nanoseparation
Description 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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