Steinmann L, Caslavska J, Thormann W
Department of Clinical Pharmacology, University of Bern, Switzerland.
Electrophoresis. 1995 Oct;16(10):1912-6. doi: 10.1002/elps.11501601315.
This paper presents principle and first results of a novel competitive binding immunoassay for monitoring of theophylline in human serum. The assay is based upon short time incubation of a mixture of antiserum, containing the antibody raised against theophylline, fluorescein labelled theophylline (tracer) and serum prior to injection of a few nanoliter of this mixture onto a fused-silica capillary for subsequent separation and analysis of free tracer and the antibody-tracer-complex by micellar electrokinetic capillary chromatography with laser induced fluorescence detection. Quantitation based upon multi-level calibration using the height of the peak produced by the free tracer is shown to provide theophylline serum levels which are in agreement with those obtained by a commercial fluorescence polarization immunoassay and with those determined by micellar elektrokinetic capillary chromatography with direct serum injection and on-column UV absorption detection.
本文介绍了一种用于监测人血清中茶碱的新型竞争性结合免疫分析方法的原理及初步结果。该分析方法基于在将几纳升含有抗血清(其中含有针对茶碱产生的抗体)、荧光素标记的茶碱(示踪剂)和血清的混合物注入熔融石英毛细管之前,先对其进行短时间孵育,随后通过胶束电动毛细管色谱法结合激光诱导荧光检测,对游离示踪剂和抗体 - 示踪剂复合物进行分离和分析。结果表明,基于使用游离示踪剂产生的峰高进行多级校准的定量方法,所得到的茶碱血清水平与通过商业荧光偏振免疫分析获得的结果以及通过直接注入血清并采用柱上紫外吸收检测的胶束电动毛细管色谱法测定的结果一致。