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Determination of the oxidative stress biomarker urinary 8-hydroxy-2'-deoxyguanosine by automated on-line in-tube solid-phase microextraction coupled with liquid chromatography-tandem mass spectrometry.

Abstract

A simple and sensitive method for the determination of 8-hydroxy-2'-deoxyguanosine (8-OHdG), a marker of oxidative DNA damage in human urine, was developed using automated on-line in-tube solid-phase microextraction (SPME) coupled with stable isotope-dilution liquid chromatography-tandem mass spectrometry (LC-MS/MS). Creatinine was also analyzed simultaneously to normalize urine volume by the in-tube SPME LC-MS/MS method, and 8-OHdG and creatinine were separated within 3 min using a Zorbax Eclipse XDB-C8 column. Electrospray MS/MS for these compounds was performed on an API 4000 triple quadruple mass spectrometer in the positive ion mode by multiple reaction monitoring. The optimum in-tube SPME conditions were 20 draw/eject cycles of 40 μL of sample at a flow rate of 200 μL/min using a Carboxen 1006 PLOT capillary column as an extraction device. The extracted compounds were easily desorbed from the capillary by passage of the mobile phase, and no carryover was observed. The calibration curve for 8-OHdG using its stable isotope-labeled internal standard was linear in the range of 0.05-10 ng/mL, and the detection limit was 8.3 pg/mL. The intra-day and inter-day precision (relative standard deviations) were below 3.1% and 9.6% (n=5), respectively. This method was applied successfully to the analysis of urine samples without any other pretreatment and interference peaks, with good recovery rates above 91% in spiked urine samples. The limits of quantification of 8-OHdG and creatinine in 0.1 mL urine samples were about 0.32 and 0.69 ng/mL (S/N=10), respectively. This method was utilized to assess the effects of smoking, green tea drinking and alcohol drinking on the urinary excretion of 8-OHdG.

Authors+Show Affiliations

School of Pharmacy, Shujitsu University, Nishigawara, Okayama 703-8516, Japan. Electronic address: hkataoka@shujitsu.ac.jp.School of Pharmacy, Shujitsu University, Nishigawara, Okayama 703-8516, Japan.School of Pharmacy, Shujitsu University, Nishigawara, Okayama 703-8516, Japan.School of Pharmacy, Shujitsu University, Nishigawara, Okayama 703-8516, Japan.

Pub Type(s)

Evaluation Study
Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

26349944

Citation

Kataoka, Hiroyuki, et al. "Determination of the Oxidative Stress Biomarker Urinary 8-hydroxy-2'-deoxyguanosine By Automated On-line In-tube Solid-phase Microextraction Coupled With Liquid Chromatography-tandem Mass Spectrometry." Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, vol. 1019, 2016, pp. 140-6.
Kataoka H, Mizuno K, Oda E, et al. Determination of the oxidative stress biomarker urinary 8-hydroxy-2'-deoxyguanosine by automated on-line in-tube solid-phase microextraction coupled with liquid chromatography-tandem mass spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci. 2016;1019:140-6.
Kataoka, H., Mizuno, K., Oda, E., & Saito, A. (2016). Determination of the oxidative stress biomarker urinary 8-hydroxy-2'-deoxyguanosine by automated on-line in-tube solid-phase microextraction coupled with liquid chromatography-tandem mass spectrometry. Journal of Chromatography. B, Analytical Technologies in the Biomedical and Life Sciences, 1019, 140-6. https://doi.org/10.1016/j.jchromb.2015.08.028
Kataoka H, et al. Determination of the Oxidative Stress Biomarker Urinary 8-hydroxy-2'-deoxyguanosine By Automated On-line In-tube Solid-phase Microextraction Coupled With Liquid Chromatography-tandem Mass Spectrometry. J Chromatogr B Analyt Technol Biomed Life Sci. 2016 Apr 15;1019:140-6. PubMed PMID: 26349944.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Determination of the oxidative stress biomarker urinary 8-hydroxy-2'-deoxyguanosine by automated on-line in-tube solid-phase microextraction coupled with liquid chromatography-tandem mass spectrometry. AU - Kataoka,Hiroyuki, AU - Mizuno,Keisuke, AU - Oda,Eri, AU - Saito,Akihiro, Y1 - 2015/09/05/ PY - 2015/05/30/received PY - 2015/08/18/revised PY - 2015/08/20/accepted PY - 2015/9/10/entrez PY - 2015/9/10/pubmed PY - 2016/12/15/medline KW - 8-Hydroxy-2′-deoxyguanosine KW - In-tube solid-phase microextraction KW - Liquid chromatography–tandem mass spectrometry KW - Oxidative stress biomarker SP - 140 EP - 6 JF - Journal of chromatography. B, Analytical technologies in the biomedical and life sciences JO - J Chromatogr B Analyt Technol Biomed Life Sci VL - 1019 N2 - A simple and sensitive method for the determination of 8-hydroxy-2'-deoxyguanosine (8-OHdG), a marker of oxidative DNA damage in human urine, was developed using automated on-line in-tube solid-phase microextraction (SPME) coupled with stable isotope-dilution liquid chromatography-tandem mass spectrometry (LC-MS/MS). Creatinine was also analyzed simultaneously to normalize urine volume by the in-tube SPME LC-MS/MS method, and 8-OHdG and creatinine were separated within 3 min using a Zorbax Eclipse XDB-C8 column. Electrospray MS/MS for these compounds was performed on an API 4000 triple quadruple mass spectrometer in the positive ion mode by multiple reaction monitoring. The optimum in-tube SPME conditions were 20 draw/eject cycles of 40 μL of sample at a flow rate of 200 μL/min using a Carboxen 1006 PLOT capillary column as an extraction device. The extracted compounds were easily desorbed from the capillary by passage of the mobile phase, and no carryover was observed. The calibration curve for 8-OHdG using its stable isotope-labeled internal standard was linear in the range of 0.05-10 ng/mL, and the detection limit was 8.3 pg/mL. The intra-day and inter-day precision (relative standard deviations) were below 3.1% and 9.6% (n=5), respectively. This method was applied successfully to the analysis of urine samples without any other pretreatment and interference peaks, with good recovery rates above 91% in spiked urine samples. The limits of quantification of 8-OHdG and creatinine in 0.1 mL urine samples were about 0.32 and 0.69 ng/mL (S/N=10), respectively. This method was utilized to assess the effects of smoking, green tea drinking and alcohol drinking on the urinary excretion of 8-OHdG. SN - 1873-376X UR - https://www.unboundmedicine.com/medline/citation/26349944/Determination_of_the_oxidative_stress_biomarker_urinary_8_hydroxy_2'_deoxyguanosine_by_automated_on_line_in_tube_solid_phase_microextraction_coupled_with_liquid_chromatography_tandem_mass_spectrometry_ DB - PRIME DP - Unbound Medicine ER -