Wung W E, Howell S B
Clin Chem. 1980 Nov;26(12):1704-8.
A reversed-phase "high-pressure" liquid-chromatographic method is described for simultaneous analysis for 5-fluorouracil, uridine, hypoxanthine, xanthine, uric acid, allopurinol, and oxipurinol. Separation was optimal with phosphate buffer (50 mmol/L, pH 4.60) as eluent. A simple acid extraction procedure yielded quantitative recoveries and permitted adequate separation for interfering peaks. Compounds were identified by their retention times, absorbance ratios, co-elution with standards, and enzymatic shifts. With a computerized integrator we quantitated these compounds in widely varying concentrations with a single injection. The limit of sensitivity was 0.1 mumol/L for the compounds studied. This method was applied to determine mean values for those compounds in normal human plasma. They are (in mumol/L): uric acid 276 (SD 55), hypoxanthine 0.46 (SD 0.21), xanthine 0.40 (SD 0.27), and uridine 4.50 (SD 1.70). Erythrocytes and platelets can continue to release hypoxanthine and xanthine into plasma or serum after a blood specimen has been drawn. We believe this explains the higher values previously reported for hypoxanthine and xanthine in serum.
本文描述了一种反相“高压”液相色谱法,用于同时分析5-氟尿嘧啶、尿苷、次黄嘌呤、黄嘌呤、尿酸、别嘌呤醇和氧嘌呤醇。以磷酸盐缓冲液(50 mmol/L,pH 4.60)作为洗脱剂时分离效果最佳。一个简单的酸提取程序可实现定量回收,并能充分分离干扰峰。通过保留时间、吸光度比、与标准品共洗脱以及酶促变化来鉴定化合物。使用计算机积分仪,单次进样即可对这些浓度差异很大的化合物进行定量分析。所研究化合物的检测限为0.1 μmol/L。该方法用于测定正常人血浆中这些化合物的平均值。其值(以μmol/L计)分别为:尿酸276(标准差55)、次黄嘌呤0.46(标准差0.21)、黄嘌呤0.40(标准差0.27)和尿苷4.50(标准差1.70)。采血后,红细胞和血小板可继续向血浆或血清中释放次黄嘌呤和黄嘌呤。我们认为这解释了先前报道的血清中次黄嘌呤和黄嘌呤含量较高的原因。