Borota R, Popov J, Krajnović J
Medicinski fakultet, Institut za patolosku fiziologiju, Novi Sad.
Med Pregl. 1990;43(7-8):317-22.
On the basis of our long-term experience, presented are the current clinically useful methods for determining erythropoietin, the granulocytopoiesis growth factor and thrombocytopoietin with the results in their use. Facts are shown, concerning the long-used method of determining erythropoietin through the use of the biological test on polycythemic mice. In our conditions, mice treated with physiological solution (negative controls) have a Fe-59 incorporation below 0.5% of the given dose, while 0.2 units of the international erythropoietin standard (positive control) increases that incorporation to 3.0%. Also presented, are results of determining erythropoietin by means of the newest immunometric method which has shown exceptional features: the whole procedure, including necessary rinsings, lasts about six hours, and it is possible, in the course of one work day, to all at once precisely determine the erythropoietin concentration in 80 samples of human serum. This fact, as well as the outstanding sensitivity of the method which is about 2 mJ/ml (that is 50 times the sensitivity of the biological test) has as a result, the wide introduction of erythropoietin determination in the clinical use of today and the definition of its clinical importance. The measurement range of the method is from 2-200 J/L which can be extended further by specimen dilution. It is especially important that duplicate measurements at one point of the curve almost coincide, which indicates great method precision. The lowest measured concentration in our series amounted to 0 J/L and the greatest to greater than 250 J/L. Elevated values were found in 17 of the 114 serums.(ABSTRACT TRUNCATED AT 250 WORDS)
基于我们的长期经验,本文介绍了目前临床上用于测定促红细胞生成素、粒细胞生成生长因子和血小板生成素的实用方法及其应用结果。文中展示了关于长期使用的通过对红细胞增多症小鼠进行生物测试来测定促红细胞生成素的方法的相关事实。在我们的实验条件下,用生理盐水处理的小鼠(阴性对照)的铁 - 59掺入量低于给定剂量的0.5%,而0.2单位的国际促红细胞生成素标准品(阳性对照)可使该掺入量增加至3.0%。还介绍了采用最新免疫测定法测定促红细胞生成素的结果,该方法具有显著特点:整个过程,包括必要的冲洗,持续约6小时,并且在一个工作日内可以一次性精确测定80份人血清样本中的促红细胞生成素浓度。这一事实以及该方法约2 mJ/ml的出色灵敏度(即生物测试灵敏度的50倍),使得促红细胞生成素测定在当今临床应用中得到广泛采用,并明确了其临床重要性。该方法的测量范围为2 - 200 J/L,可通过样本稀释进一步扩展。特别重要的是,曲线上某一点的重复测量值几乎重合,这表明该方法具有很高的精密度。我们系列中测得的最低浓度为0 J/L,最高浓度大于250 J/L。在114份血清中的17份中发现了升高值。(摘要截短为250字)