Rammeloo T, van Haard P M, Beunis M H
Clin Chem. 1982 Jan;28(1):145-9.
Serum pancreatic isoamylase activity was measured by a method involving inhibition of salivary isoamylase and by a well-known agarose electrophoretic method, modified by us. We saw changes in electrophoretic patterns of pancreatic isoamylase fractions after storage of serum samples for three weeks at 4-8 degrees C, but with the inhibition method no alterations in activities were found. Within-assay and between-assay imprecisions of both methods were about the same. Serum pancreatic amylase activities as measured by the inhibition method exceeded by about 10% those obtained by the electrophoretic method. The inhibition method seems to be a reasonable candidate for routine application, whereas the electrophoretic method is still time-consuming and requires special skill to perform. Some suggestions are given for improving the calibration of the inhibition method recommended by the manufacturer.
血清胰淀粉酶活性采用一种抑制唾液淀粉酶的方法以及我们改良的一种知名琼脂糖电泳法进行测定。我们发现血清样本在4 - 8摄氏度下储存三周后,胰淀粉酶组分的电泳图谱发生了变化,但采用抑制法未发现活性有改变。两种方法的批内和批间不精密度大致相同。通过抑制法测得的血清胰淀粉酶活性比电泳法测得的约高10%。抑制法似乎是常规应用的合理选择,而电泳法仍然耗时且需要特殊技能来操作。针对改进制造商推荐的抑制法的校准给出了一些建议。