Watanabe N, Kamei S, Ohkubo A, Yamanaka M, Ohsawa S, Makino K, Tokuda K
Clin Chem. 1986 Aug;32(8):1551-4.
In this new method for determining urinary protein, the reaction is complete within 10 min at 37 degrees C. This method is applicable to automated as well as manual measurements. Protein concentration and absorbance at 600 nm are linearly related throughout a wide range of concentrations, 10 to 16 000 mg/L. However, the chromogenicity of the gamma-globulins in this method is 70% of that of albumin, as estimated from results by a biuret method. Within-run CVs were less than 3.3%; the day-to-day CV was 2.9%. Errors due to interfering components in urine are less than 2%. The normal range for urinary protein as measured by this method was from 28 to 141 mg/day. Results by this method (y) and by a trichloroacetic acid-biuret method (x) correlated well (n = 80, r = 0.995; y = 0.99x - 2.9).
在这种测定尿蛋白的新方法中,反应在37℃下10分钟内完成。该方法适用于自动测量和手动测量。在10至16000mg/L的广泛浓度范围内,蛋白质浓度与600nm处的吸光度呈线性相关。然而,根据双缩脲法的结果估计,该方法中γ-球蛋白的显色性是白蛋白的70%。批内变异系数小于3.3%;日间变异系数为2.9%。尿液中干扰成分引起的误差小于2%。用该方法测定的尿蛋白正常范围为28至141mg/天。该方法的结果(y)与三氯乙酸-双缩脲法的结果(x)相关性良好(n = 80,r = 0.995;y = 0.99x - 2.9)。