Measurement of urinary oxypurinol by high performance liquid chromatography-tandem mass spectrometry

被引:11
|
作者
Stocker, Sophie L. [2 ]
Franklin, Michael E. [1 ]
Anderson, Jacqueline M. [3 ,4 ]
Pillans, Peter I. [1 ]
Williams, Kenneth M. [3 ,4 ]
McLachlan, Andrew J. [2 ,5 ]
Day, Richard O. [3 ,4 ]
Taylor, Paul J. [1 ]
机构
[1] Princess Alexandra Hosp, Dept Clin Pharmacol, Brisbane, Qld 4102, Australia
[2] Univ Sydney, Fac Pharm, Sydney, NSW 2006, Australia
[3] St Vincents Hosp, Dept Clin Pharmacol, Sydney, NSW 2010, Australia
[4] Univ New S Wales, Sydney, NSW 2010, Australia
[5] Concord Hosp, Ctr Educ & Res Ageing, Sydney, NSW, Australia
基金
澳大利亚国家健康与医学研究理事会;
关键词
Oxypurinol; Urine; HPLC; Mass spectrometry; Gout; HUMAN-PLASMA; URIC-ACID; ALLOPURINOL; GOUT; OXIPURINOL; ADHERENCE; PATTERNS; THERAPY; PURINES; FLUIDS;
D O I
10.1016/j.jchromb.2010.07.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Oxypurinol is the active metabolite of allopurinol which is used to treat hyperuricaemia associated with gout. Both oxypurinol and allopurinol inhibit xanthine oxidase which forms uric acid from xanthine and hypoxanthine. Plasma oxypurinol concentrations vary substantially between individuals and the source of this variability remains unclear. The aim of this study was to develop an HPLC-tandem mass spectrometry method to measure oxypurinol in urine to facilitate the study of the renal elimination of oxypurinol in patients with gout. Urine samples (50 mu L) were prepared by dilution with a solution of acetonitrile/methanol/water (95/2/3, v/v; 2 mL) that contained the internal standard (8-methylxanthine; 1.5 mg/L), followed by centrifugation. An aliquot (2 mu L) was injected. Chromatography was performed on an Atlantis HILIC Silica column (31 mu m, 100 mm x 2.1 mm, Waters) at 30 C, using a mobile phase comprised of acetonitrile/methanol/50 mM ammonium acetate in 0.2% formic acid (95/2/3, v/v). Using a flow rate of 0.35 mL/min, the analysis time was 6.0 min. Mass spectrometric detection was by selected reactant monitoring (oxypurinol: m/z 150.8 -> 108.0; internal standard: m/z 164.9 -> 121.8) in negative electrospray ionization mode. Calibration curves were prepared in drug-free urine across the range 10-200 mg/L and fitted using quadratic regression with a weighting factor of 1/x (r(2) > 0.997, n = 7). Quality control samples (20, 80, 150 and 300 mg/L) were used to determine intra-day (n = 5) and inter-day (n = 7) accuracy and imprecision. The inter-day accuracy and imprecision was 96.1-104% and < 11.2%, respectively. Urinary oxypurinol samples were stable when subjected to 3 freeze-thaw cycles and when stored at room temperature for up to 6h. Samples collected from 10 patients, not receiving allopurinol therapy, were screened and showed no significant interferences. The method was suitable for the quantification of oxypurinol in the urine of patients (n = 34) participating in a clinical trial to optimize therapy of gout with allopurinol. (C) 2010 Elsevier BM. All rights reserved.
引用
收藏
页码:2363 / 2368
页数:6
相关论文
共 50 条
  • [1] Determination of allopurinol and oxypurinol in human plasma and urine by liquid chromatography-tandem mass spectrometry
    Liu, Xia
    Ni, Xiao-Jia
    Shang, De-Wei
    Zhang, Ming
    Hu, Jin-Qing
    Qiu, Chang
    Luo, Fu-Tian
    Wen, Yu-Guan
    JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2013, 941 : 10 - 16
  • [2] Residues in Drinks by High Performance Liquid Chromatography-Tandem Mass Spectrometry
    XU Dun-ming
    Zheng Xiang-Hua
    Yang Li-Zhong
    Fang En-Hua
    Chen Lu-Ping
    Lin Li-Yi
    Zhou Yu
    CHINESE JOURNAL OF ANALYTICAL CHEMISTRY, 2012, 40 (02) : 304 - 308
  • [3] Quantitative measurement of porphobilinogen in urine by high performance liquid chromatography-tandem mass spectrometry.
    Ford, RE
    Magera, MJ
    Kloke, K
    Chezick, PA
    Rinaldo, P
    McConnell, JP
    CLINICAL CHEMISTRY, 2001, 47 (06) : A63 - A63
  • [4] Analysis of 18 perfluorinated compounds in river waters: Comparison of high performance liquid chromatography-tandem mass spectrometry, ultra-high-performance liquid chromatography-tandem mass spectrometry and capillary liquid chromatography-mass spectrometry
    Onghena, Matthias
    Moliner-Martinez, Y.
    Pico, Yolanda
    Campins-Falco, P.
    Barcelo, Damia
    JOURNAL OF CHROMATOGRAPHY A, 2012, 1244 : 88 - 97
  • [5] Liquid chromatography-tandem mass spectrometry
    Petrovic, Mira
    Barcelo, Damia
    ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2013, 405 (18) : 5857 - 5858
  • [6] Measurement of cystine in urine by liquid chromatography-tandem mass spectrometry
    Wear, JE
    Keevil, BG
    CLINICAL CHEMISTRY, 2005, 51 (04) : 787 - 789
  • [7] Determination of aflatoxins in cashew by high performance liquid chromatography-tandem mass spectrometry
    Bi Ruifeng
    Fan Zhixian
    Fu Meng
    CHINESE JOURNAL OF CHROMATOGRAPHY, 2011, 29 (12) : 1155 - 1159
  • [8] Determination of chloramphenicol in propolis by high performance liquid chromatography-tandem mass spectrometry
    Zhang Xiaoyan
    Zhang Rui
    Xu Wei
    Huang Juan
    Liu Yan
    Wu Bin
    Chen Lei
    Ding Tao
    Shen Chongyu
    Chen Huilan
    CHINESE JOURNAL OF CHROMATOGRAPHY, 2012, 30 (03) : 314 - 317
  • [9] Determination of catechol in tobacco by high performance liquid chromatography-tandem mass spectrometry
    Ren Zhiqin
    Ai Xiaoyong
    Huang Zhiqiang
    Zhang Yuan
    Wang Zhi
    Zhang Feng
    CHINESE JOURNAL OF CHROMATOGRAPHY, 2015, 33 (05) : 541 - 544
  • [10] Determination of amoxicillin in honey by high performance liquid chromatography-tandem mass spectrometry
    Xu Wei
    Zhang Xiaoyan
    Wu Bin
    Yin Yao
    Yang Wenquan
    CHINESE JOURNAL OF CHROMATOGRAPHY, 2012, 30 (10) : 1089 - 1092