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Determination of gouty arthritis' biomarkers in human urine using reversed-phase high-performance liquid chromatography

机译:反相高效液相色谱法测定人尿中的痛风性关节炎生物标志物

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摘要

Creatinine, uric acid, hypoxanthine and xanthine are important diagnostic biomarkers in human urine for gouty arthritis or renal disease diacrisis. A simple method for simultaneous determination of these biomarkers in urine based on reversed-phase high-performance liquid chromatography (RP-HPLC) with ultraviolet (UV) detector was proposed. After pretreatment by dilution, centrifugation and filtration, the biomarkers in urine samples were separated by ODS-BP column by elution with methanol/50 mM NaH2PO4 buffer solution at pH 5.26 (5:95). Good linearity between peak areas and concentrations of standards was obtained for the biomarkers with correlation coefficients in the range of 0.9957-0.9993. The proposed analytical method has satisfactory repeatability (the recovery of data in a range of creatinine, uric acid, hypoxanthine and xanthine was 93.49-97.90%, 95.38-96.45%, 112.46-115.78%and 90.82-97.13%with standard deviation of o5%, respectively) and the limits of detection (LODs, S/N Z 3) for creatinine, uric acid, hypoxanthine, and xanthine were 0.010, 0.025, 0.050 and 0.025 mg/L, respectively. The established method was proved to be simple, accurate, sensitive and reliable for the quantitation of gouty arthritis' biomarkers in human urine samples. The ratio of creatinine to uric acid was found to be a possible factor for assessment of gouty arthritis.
机译:肌酐,尿酸,次黄嘌呤和黄嘌呤是人尿中对于痛风性关节炎或肾脏疾病的重要诊断生物标志物。提出了一种基于紫外(UV)检测器的反相高效液相色谱(RP-HPLC)同时测定尿液中生物标志物的简单方法。通过稀释,离心和过滤进行预处理后,通过ODS-BP色谱柱分离尿液样品中的生物标志物,方法是用甲醇/ 50 mM NaH2PO4缓冲溶液在pH 5.26(5:95)上洗脱。生物标志物的峰面积和标准品浓度之间具有良好的线性关系,相关系数在0.9957-0.9993之间。所提出的分析方法具有令人满意的重复性(在肌酐,尿酸,次黄嘌呤和黄嘌呤范围内的数据回收率分别为93.49-97.90%,95.38-96.45%,112.46-115.78%和90.82-97.13%,标准偏差为o5% ,肌酐,尿酸,次黄嘌呤和黄嘌呤的检出限(LODs,S / NZ 3)分别为0.010、0.025、0.050和0.025 mg / L。实践证明,所建立的方法简便,准确,灵敏,可靠,可用于定量测定人尿液中痛风性关节炎的生物标志物。发现肌酐与尿酸的比例是评估痛风性关节炎的可能因素。

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  • 来源
    《药物分析学报(英文)》 |2014年第002期|153-158|共6页
  • 作者单位

    Beijing Key Laboratory of Microanalysis Methods and Instrumentation, Department of Chemistry, Tsinghua University, Beijing 100084, China;

    Beijing Key Laboratory of Microanalysis Methods and Instrumentation, Department of Chemistry, Tsinghua University, Beijing 100084, China;

    Beijing Key Laboratory of Microanalysis Methods and Instrumentation, Department of Chemistry, Tsinghua University, Beijing 100084, China;

    Beijing Key Laboratory of Microanalysis Methods and Instrumentation, Department of Chemistry, Tsinghua University, Beijing 100084, China;

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  • 入库时间 2022-08-19 03:45:48
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