Arzoglou P, Goudoula C, Tsantili P, Lessinger J M, Férard G, Mignot V, Samyn N, Demeester J, Lauwers A, Brettschneider H
Department of Chemistry, Aristotle University of Thessaloniki, Greece.
Eur J Clin Chem Clin Biochem. 1994 Oct;32(10):773-7. doi: 10.1515/cclm.1994.32.10.773.
Following the selection of the most appropriate method for emulsification and the optimization of the reaction medium, interlaboratory studies were conducted to check the effect of preparing substrates and measuring the catalytic concentration of lipase at different sites as well as the effect of transport on emulsion. The determinations of lipase activity in an abnormal chemistry control against emulsions prepared by two laboratories (and used by both laboratories) and, also, against five separate emulsions prepared by one laboratory (and used by five different laboratories) resulted in average enzyme activity values (2234 +/- 125 and 2263 +/- 204 U/l respectively) which are not statistically different. Standard preparations of lipase, control sera and reference materials can therefore be titrated according to the procedure followed by at least two laboratories for at least 3 days against two separate emulsions.
在选择了最合适的乳化方法并优化反应介质之后,开展了实验室间研究,以检查在不同地点制备底物和测量脂肪酶催化浓度的影响以及运输对乳液的影响。在针对由两个实验室制备(且两个实验室均使用)的乳液以及针对由一个实验室制备(并由五个不同实验室使用)的五种单独乳液的异常化学对照中测定脂肪酶活性,得到的平均酶活性值(分别为2234±125和2263±204 U/l)在统计学上无差异。因此,脂肪酶的标准制剂、对照血清和参考物质可以按照至少两个实验室遵循的程序,针对两种单独的乳液滴定至少3天。