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在艾姆斯自动分析仪上进行的地高辛干片免疫测定法。

A dry-strip immunometric assay for digoxin on the Ames Seralyzer.

作者信息

Iosefsohn M, Soldin S J, Hicks J M

机构信息

Department of Laboratory Medicine, Children's National Medical Center, Washington, D.C. 20010.

出版信息

Ther Drug Monit. 1990 Mar;12(2):201-5. doi: 10.1097/00007691-199003000-00016.

DOI:10.1097/00007691-199003000-00016
PMID:2315978
Abstract

We evaluated the Ames Seralyzer III with a new reagent and drystrip test for assay of digoxin. Assay precision was acceptable in the therapeutic range. Within-run imprecision (coefficient of variation, n = 20) was 7% at 0.9 ng/ml (1.2 nM) and 3.5% at 1.9 ng/ml (2.4 nM); run-to-run imprecision was 7.6% at 0.8 ng/ml (1.0 nM) and 5.7% at 2.1 ng/ml (2.7 nM). The method is very reproducible and is linear between 0.5 and 4.3 ng/ml (0.6-5.5 nM). The assay performed well with patient samples, with Abbott TDx used as the reference procedure. Bilirubin up to 16 mg/dl (273 microM) and hemoglobin up to 11 g/l do not cause interference. Digoxin-like immunoreactive factors cause minimal interference. Some digoxin metabolites such as monodigitoxoside, bis-digitoxoside, and digoxigenin cross-react with the digoxin antibody. Patients on spironolactone have falsely increased digoxin values. The new digoxin assay is easy to perform and uses 30 microliters serum; the result can be reported in 15-20 min.

摘要

我们使用一种新试剂和干条试验对Ames Seralyzer III进行了评估,以测定地高辛。在治疗范围内,测定精密度可接受。批内不精密度(变异系数,n = 20)在0.9 ng/ml(1.2 nM)时为7%,在1.9 ng/ml(2.4 nM)时为3.5%;批间不精密度在0.8 ng/ml(1.0 nM)时为7.6%,在2.1 ng/ml(2.7 nM)时为5.7%。该方法具有很高的重现性,在0.5至4.3 ng/ml(0.6 - 5.5 nM)之间呈线性。以雅培TDx作为参考方法,该检测方法对患者样本检测效果良好。胆红素高达16 mg/dl(273 microM)和血红蛋白高达11 g/l时不会产生干扰。地高辛样免疫反应因子产生的干扰最小。一些地高辛代谢物,如单洋地黄毒苷、双洋地黄毒苷和洋地黄毒苷元,会与地高辛抗体发生交叉反应。使用螺内酯的患者地高辛值会假性升高。这种新的地高辛检测方法操作简便,只需30微升血清;结果可在15 - 20分钟内报告。

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