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大学医院实验室治疗药物监测模式分析。CEDIA检测法的适用性和性能。

Analyses of the pattern of therapeutic drug monitoring in a university hospital laboratory. Suitability and performance of the CEDIA assays.

作者信息

Hänseler E, Bigler S, Wad N

机构信息

Institute for Clinical Chemistry, University Hospital Zurich, Switzerland.

出版信息

Wien Klin Wochenschr Suppl. 1992;191:23-6.

PMID:1509748
Abstract

New homogeneous enzyme immunoassays (CEDIA assays) for therapeutic drug monitoring were evaluated on Boehringer Mannheim/Hitachi 704. A fluorescence polarization immunoassay and HPLC were chosen as comparison methods. A good correlation of patient data was observed for both methods (slopes 1.033-1.167). Imprecision within-run and between-day as well as the recovery in control samples of an external quality control survey were excellent and comparable to the routine method. In order to optimize the use of the CEDIA assays also for parameters which are less frequently requested, a parameter-setting for the batch-analyzer COBAS Fara was worked out. Performance of the CEDIA assays on random access analyzers is discussed with regard to the background of a laboratory for clinical chemistry in a University Hospital.

摘要

在勃林格殷格翰/日立704仪器上对用于治疗药物监测的新型均相酶免疫分析(CEDIA分析)进行了评估。选择荧光偏振免疫分析和高效液相色谱法作为比较方法。两种方法的患者数据相关性良好(斜率为1.033 - 1.167)。外部质量控制调查中对照样品的批内精密度、批间精密度以及回收率都非常好,与常规方法相当。为了优化CEDIA分析对较少检测参数的应用,制定了用于批量分析仪COBAS Fara的参数设置。结合大学医院临床化学实验室的背景,讨论了CEDIA分析在随机存取分析仪上的性能。

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