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https://hdl.handle.net/10316/5133
Título: | Development of an HPLC method with electrochemical detection of femtomoles of 8-oxo-7,8-dihydroguanine and 8-oxo-7,8-dihydro-2'-deoxyguanosine in the presence of uric acid | Autor: | Rebelo, Isabel A. Piedade, José António P. Brett, Ana Maria Oliveira |
Palavras-chave: | DNA damage; Oxidative stress; 8-oxoGua; 8-oxodGuo; 8-oxo-7,8-Dihydroguanine; 8-oxo-7,8-Dihydro-2'-deoxyguanosine; Biomarker; Uric acid; HPLC-ECD | Data: | 2004 | Citação: | Talanta. 63:2 (2004) 323-331 | Resumo: | A selective method based on high performance liquid chromatography with electrochemical detection (HPLC-ECD) was developed to enable simultaneous detection of 8-oxo-7,8-dihydroguanine (8-oxoGua) and 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodGuo), products of DNA oxidative damage, in the presence of uric acid (UA), a strong interferent in their electrochemical detection. The method developed consists of HPLC isocratic elution with amperometric detection on a glassy carbon electrode, enabling a detection limit for 8-oxoGua and 8-oxodGuo lower than 1 nM in standard mixtures. Detection of low concentrations up to 25 nM of 8-oxoGua and 8-oxodGuo in the presence of UA in a 104-fold higher concentration was achieved after one-step solid phase extraction (SPE). The method was tested with urine samples and it was possible to detect and quantify the presence of 8-oxoGua, and to confirm that UA was eliminated after uricase degradation and SPE. The LOD found in urine samples was about 80 nM, a value higher than in standard mixtures, due to the increase of background current in the urine matrix. The results presented here contribute to the development of a methodological approach to simultaneous determination of 8-oxoGua and 8-oxodGuo in urine samples. | URI: | https://hdl.handle.net/10316/5133 | DOI: | 10.1016/j.talanta.2003.10.051 | Direitos: | openAccess |
Aparece nas coleções: | FCTUC Química - Artigos em Revistas Internacionais |
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filebfd6ac1aa9664e19b3b39237359038ba.pdf | 165.58 kB | Adobe PDF | Ver/Abrir |
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