Bretaudiere J P, Phung H T, Bailly M
Clin Chem. 1976 Oct;22(10):1614-7.
A direct enzymatic micromethod (sample volume, 3mul) has been adapted to the centrifugal analyzer (ENI-GEMSAEC) for measurement of urea in plasma and urine. The method is based on urease (urea amidohydrolase, EC3.5.1.5)/glutamate dehydrogenase [l-glutamate:NAD(P)+oxidoreductase (deaminating), EC1.41.3] coupled reactions, and uses a two-point fixed-time (t(1)=20s,t(2)=50s)kinetic scheme for monitoring the rate of comsumption of NADH at 340 nm. Sensitivity and precision of the method are excellent,and results compare well with those from a commonly used continuous-flow method.
一种直接酶促微量法(样本体积为3微升)已被适配到离心分析仪(ENI-GEMSAEC)上,用于测定血浆和尿液中的尿素。该方法基于脲酶(尿素酰胺水解酶,EC3.5.1.5)/谷氨酸脱氢酶 [L-谷氨酸:NAD(P)+氧化还原酶(脱氨基),EC1.41.3] 的偶联反应,并采用两点固定时间(t(1)=20秒,t(2)=50秒)动力学方案来监测340纳米处NADH的消耗速率。该方法的灵敏度和精密度极佳,结果与常用的连续流动法所得结果相当。