Hodgkinson A J, Landon J, Smith D S, Sidki A M
Ther Drug Monit. 1986;8(2):236-40. doi: 10.1097/00007691-198606000-00021.
A polarization fluoroimmunoassay for theophylline was developed employing fluorescein-labeled drug and antiserum precombined in a single reagent. Assay was performed simply by addition of sample to an aliquot of the single reagent, incubation, and determination of fluorescence polarization. Because of the relatively rapid dissociation kinetics of the labeled drug from antibody binding, added unlabeled theophylline caused displacement within a practical time period. The precision, accuracy, and specificity of the simplified single-reagent assay were similar to those obtained by a conventional immunoassay procedure using the same reagents. Results for the assay of patients' serum specimens correlated well with those by an established enzymoimmunoassay.
开发了一种用于茶碱的偏振荧光免疫测定法,该方法使用在单一试剂中预先结合的荧光素标记药物和抗血清。通过将样品添加到单一试剂的等分试样中、孵育并测定荧光偏振来进行测定。由于标记药物与抗体结合的解离动力学相对较快,添加的未标记茶碱在实际时间段内引起置换。简化的单一试剂测定法的精密度、准确度和特异性与使用相同试剂的传统免疫测定程序所获得的结果相似。患者血清标本的测定结果与既定的酶免疫测定法的结果相关性良好。