Stolle D, Rick W
J Clin Chem Clin Biochem. 1976 May;14(5):239-44. doi: 10.1515/cclm.1976.14.1-12.239.
An improved method for the determination of creatine kinase activity (EC 2.7.3.2) is described. For the reactivation of creatine kinase serum is first preincubated in the test solution in the presence of dithioerythritol. Then the enzymatic reaction is started by adding creatine phosphate. By optimizing the concentrations in the test solution and by altering the measurement procedure using dithioerythritol as reactivator, the assay is made more sensitive, and a far higher enzyme activity in serum is measured in comparison with other recommended tests. The reaction rate is linear for ten minutes up to 700 U/l. An increase in activity by enzyme dilution was not observed. In this study a sensitivity of detection of 0.9 U/l was achieved. This would be especially advantageous in the detection of the isoenzymes of creatine kinase after chromatography. Within-run precision was 1.2% (CV), day-to-day precision was 2.0% (CV). The test solution is stable for at least 24 hours.
本文描述了一种改进的肌酸激酶活性(EC 2.7.3.2)测定方法。为使肌酸激酶重新激活,首先将血清在含有二硫苏糖醇的测试溶液中进行预孵育。然后通过添加磷酸肌酸启动酶促反应。通过优化测试溶液中的浓度以及改变使用二硫苏糖醇作为重新激活剂的测量程序,该测定方法变得更加灵敏,与其他推荐测试相比,测得的血清酶活性要高得多。反应速率在长达700 U/l的情况下十分钟内呈线性。未观察到酶稀释导致的活性增加。在本研究中,检测灵敏度达到了0.9 U/l。这在色谱分离后肌酸激酶同工酶的检测中尤其有利。批内精密度为1.2%(CV),日间精密度为2.0%(CV)。测试溶液至少稳定24小时。