Jarausch J, Cano Y, Hammer E, Hafner G, Kaspar P, Malandain H, Pokieser L, Wieland H, Willems D, Windisch M
Boehringer Mannheim GmbH, Federal Republic of Germany.
Wien Klin Wochenschr Suppl. 1992;191:73-6.
We evaluated a CEDIA assay for the determination of digitoxin in serum on random access analyzers. The multicenter evaluation included studies on the analytical range, calibration stability and reproducibility of the new assay. Moreover, recovery in controls, transferability of results obtained in different laboratories, comparability with routine methods, and the effect of various interfering factors have been analyzed. Summarized the analytical performance was comparable to that of routine methods. The CEDIA Digitoxin assay represents an attractive alternative to established digitoxin immunoassays because it can be performed on random access analyzers, thus permitting the simultaneous determination of digitoxin and other serum analytes without sample splitting.
我们评估了一种用于在随机存取分析仪上测定血清中洋地黄毒苷的CEDIA检测法。多中心评估包括对新检测法的分析范围、校准稳定性和重现性的研究。此外,还分析了对照品中的回收率、不同实验室所得结果的可转移性、与常规方法的可比性以及各种干扰因素的影响。总体而言,该检测法的分析性能与常规方法相当。CEDIA洋地黄毒苷检测法是现有洋地黄毒苷免疫检测法的一种有吸引力的替代方法,因为它可在随机存取分析仪上进行,从而无需分样即可同时测定洋地黄毒苷和其他血清分析物。