PLESKAČOVÁ, Anna, Stanislav BREJCHA, Lukáš PÁCAL, Kateřina KAŇKOVÁ and Josef TOMANDL. Simultaneous Determination of Uric Acid, Xanthine and Hypoxanthine in Human Plasma and Serum by HPLC–UV: Uric Acid Metabolism Tracking. Chromatographia. Heidelberg: Springer, 2017, vol. 80, No 4, p. 529-536. ISSN 0009-5893. Available from: https://dx.doi.org/10.1007/s10337-016-3208-8.
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Basic information
Original name Simultaneous Determination of Uric Acid, Xanthine and Hypoxanthine in Human Plasma and Serum by HPLC–UV: Uric Acid Metabolism Tracking
Authors PLESKAČOVÁ, Anna (203 Czech Republic, belonging to the institution), Stanislav BREJCHA (203 Czech Republic, belonging to the institution), Lukáš PÁCAL (203 Czech Republic, belonging to the institution), Kateřina KAŇKOVÁ (203 Czech Republic, belonging to the institution) and Josef TOMANDL (203 Czech Republic, guarantor, belonging to the institution).
Edition Chromatographia, Heidelberg, Springer, 2017, 0009-5893.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 10608 Biochemistry and molecular biology
Country of publisher Germany
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 1.401
RIV identification code RIV/00216224:14110/17:00095624
Organization unit Faculty of Medicine
Doi http://dx.doi.org/10.1007/s10337-016-3208-8
UT WoS 000399024500003
Keywords in English HPLC; Uric; acid; Xanthine; Hypoxanthine; Plasma; Serum
Tags EL OK
Tags International impact, Reviewed
Changed by Changed by: Soňa Böhmová, učo 232884. Changed: 21/3/2018 16:34.
Abstract
A simple reversed phase HPLC method with UV detection in isocratic conditions was developed and validated for the simultaneous determination of hypoxanthine, xanthine and uric acid levels in human plasma and serum. One analysis run takes 6.5 min including a short organic mobile phase gradient for column regeneration. Concentrations of uric acid, xanthine and hypoxanthine in plasma and serum samples were highly comparable. However, hypoxanthine levels were increased in serum compared to plasma samples due to a prolonged time between serum and blood elements separation. The method was validated for linearity, precision, accuracy, sensitivity and robustness in a similar manner to that for pharmacokinetic data and it is appropriate for physiological and pathophysiological levels of all analytes. The stability of stock standard solutions was verified using spectrophotometric analysis in different conditions. The method is simple and robust with a good precision for the measurement of hypoxanthine, xanthine and uric acid in human plasma and serum.
Links
MUNI/A/1056/2015, interní kód MUName: Příspěvek chemických a biochemických metodik ke studiu molekulární podstaty vybraných patologických stavů a onemocnění (Acronym: bichepat)
Investor: Masaryk University, Category A
NV16-28040A, research and development projectName: Dlouhodobé dopady gestačního diabetes mellitus pro metabolické zdraví žen časně postpartum: význam nových diagnostických kritérií
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