Viraraghavan S, Blass K G
Department of Chemistry, University of Regina, Saskatchewan, Canada.
J Clin Chem Clin Biochem. 1990 Feb;28(2):95-105. doi: 10.1515/cclm.1990.28.2.95.
The reactivity of glucose in aqueous alkaline picrate was investigated by spectrophotometry and polarography at 25 degrees C in 0.51 mol/l sodium hydroxide. Thin-layer chromatography and infrared spectroscopy studies have conclusively identified the presence of picramic acid in 5:1 and 10:1 glucose picrate test solutions incubated at 25 degrees C. The polarographic data of an alkaline picrate blank with a concentration of 0.284 mmol/l, show three well-defined nitro group reduction waves with approximate half-wave potentials of -0.62 V, -0.78 V, and -0.93 V and a fourth broad wave appearing near -1.31 V versus a saturated calomel electrode. The addition of glucose to alkaline picrate resulted in a decreased diffusion current for reduction waves 1-3, with little change in reduction wave 4. The reactivity of test solutions containing glucose:picrate in 1:1, 2:1, 5:1 and 10:1 molar ratios was investigated at varied time intervals between 10 and 180 minutes. The absorption spectra of a 10:1 glucose:picrate solution shifted from 356 nm to 375 nm and a broad tailing shoulder absorbance formed in the 450-600 nm region. An orange coloured minor product, separated by thin-layer chromatography, was observed to fluoresce. The maximum excitation and emission wavelengths were 318 nm and 545 nm, respectively. A major, red-coloured product was isolated and identified as picramic acid by infrared spectroscopy. For 10:1 glucose:picrate test solutions incubated at 25 degrees C, picramic acid formed within 10 minutes. Within the first minute, the colour was observed to change from yellow to orange and then to red.
通过分光光度法和极谱法,在25℃、0.51mol/L氢氧化钠溶液中研究了葡萄糖在碱性苦味酸盐水溶液中的反应活性。薄层色谱和红外光谱研究已确凿证实,在25℃下孵育的5:1和10:1葡萄糖苦味酸盐测试溶液中存在苦味酸。浓度为0.284mmol/L的碱性苦味酸盐空白溶液的极谱数据显示,有三个明确的硝基还原波,其半波电位约为-0.62V、-0.78V和-0.93V,相对于饱和甘汞电极,在-1.31V附近出现第四个宽波。向碱性苦味酸盐中添加葡萄糖会导致还原波1-3的扩散电流降低,而还原波4变化不大。研究了在10至180分钟的不同时间间隔内,葡萄糖与苦味酸盐摩尔比为1:1、2:1、5:1和10:1的测试溶液的反应活性。10:1葡萄糖:苦味酸盐溶液的吸收光谱从356nm移至375nm,并在450-600nm区域形成一个宽的拖尾肩峰吸收。通过薄层色谱分离出一种橙色次要产物,观察到其发出荧光。最大激发波长和发射波长分别为318nm和545nm。分离出一种主要的红色产物,并通过红外光谱鉴定为苦味酸。对于在25℃下孵育的10:1葡萄糖:苦味酸盐测试溶液,苦味酸在10分钟内形成。在第一分钟内,观察到颜色从黄色变为橙色,然后变为红色。