Vittorio N, Oloff C M, Sellers D R
Anal Biochem. 1984 Sep;141(2):423-8. doi: 10.1016/0003-2697(84)90065-4.
A continuous-flow fluorometric procedure for the determination of 2-deoxy-D-glucose (2DG) is described. The method utilizes Technicon Autoanalyzer equipment and modules, and is based on the acid-catalyzed condensation of 3,5-diaminobenzoic acid with 2DG. The procedure permits analysis of 20 samples/h, is sensitive to concentrations of 2DG as low as 0.2 mg/100 ml, and requires sample volumes of only 0.25 ml. 2DG can be quantitatively measured in serum samples or tissue extracts without requiring deproteinization. Glucose does not interfere with the assay while 2-deoxy-D-ribose develops a fluorescence which is about 15% of that produced by the same amount of 2DG and is additive when both deoxy sugars are present together. The procedure is accurate, reproducible, and fast, and can be run continuously.
本文描述了一种用于测定2-脱氧-D-葡萄糖(2DG)的连续流动荧光法。该方法使用Technicon自动分析仪设备和模块,基于3,5-二氨基苯甲酸与2DG的酸催化缩合反应。该方法每小时可分析20个样品,对低至0.2mg/100ml的2DG浓度敏感,且仅需0.25ml的样品体积。2DG可在血清样品或组织提取物中进行定量测量,无需脱蛋白。葡萄糖不干扰该测定,而2-脱氧-D-核糖产生的荧光约为相同量2DG产生荧光的15%,当两种脱氧糖同时存在时具有加和性。该方法准确、可重复且快速,可连续运行。