Luk'ianchuk I I, Gotsuliak L E
Ukr Biokhim Zh (1978). 1978 Sep-Oct;50(5):655-8.
A simple method is suggested for accelerated determination of carboanhydrase activity (in 0.01 ml of blood or other biological liquid for 3.0--4.0 min). The method is based on the ability of erythrocytes carboanhydrase to induce specifically carbonic acid gas hydration accompanied by formation of carbonic acid. The latter changes the medium reaction from alkaline (pH9,0) to slightly acid (pH 6.0). The reaction end is fixed by an acid-alkaline indicator (or automatically) according to the time of the solution color changes. A simple design is developed for the device to obtain the substrate which removes the factors affecting negatively the reaction course; the optimal concentration of reagents are selected and a new indicator-buffer mixture having no inhibitatory effect on the carboanhydrase activity is used.
本文提出了一种加速测定碳酸酐酶活性的简单方法(在0.01毫升血液或其他生物液体中进行3.0 - 4.0分钟)。该方法基于红细胞碳酸酐酶特异性诱导碳酸气体水合形成碳酸的能力。后者使介质反应从碱性(pH9.0)变为微酸性(pH6.0)。反应终点通过酸碱指示剂(或自动)根据溶液颜色变化的时间来确定。开发了一种简单的装置设计以获得底物,该底物消除了对反应过程产生负面影响的因素;选择了试剂的最佳浓度,并使用了对碳酸酐酶活性无抑制作用的新型指示剂 - 缓冲液混合物。