Hinds J A, Pincombe C F, Kanowski R K, Day S A, Sanderson J C, Duffy P
Clin Chem. 1984 Jul;30(7):1174-8.
We describe a ligand displacement immunoassay for measurement of theophylline in serum or plasma and show it to be clinically useful. A conjugate of theophylline-specific antiserum covalently bound to micro-crystalline cellulose and a beta-galactosidase-labeled theophylline derivative is prepared as a lyophilized reagent. Sample is added to the conjugate and, after 5-min incubation at room temperature, the bound and displaced enzyme-ligand are separated by brief centrifugation. The enzyme activity of the displaced enzyme-ligand is measured on a spectrophotometer or centrifugal analyzer. Linear calibration curves are obtained with appropriate sample dilution, allowing generation of the standard curve with a saline zero reference and a single calibrator. Performance of the assay compares favorably with that of other theophylline assays; comparison studies with use of 145 clinical specimens gave a coefficient of correlation with EMIT of 0.97.
我们描述了一种用于测定血清或血浆中茶碱的配体置换免疫测定法,并证明其在临床上有用。将与微晶纤维素共价结合的茶碱特异性抗血清与β-半乳糖苷酶标记的茶碱衍生物的缀合物制备成冻干试剂。将样品加入到缀合物中,在室温下孵育5分钟后,通过短暂离心分离结合的和置换的酶-配体。用分光光度计或离心分析仪测量置换的酶-配体的酶活性。通过适当的样品稀释获得线性校准曲线,允许用生理盐水零对照和单一校准物生成标准曲线。该测定法的性能与其他茶碱测定法相比具有优势;使用145份临床标本进行的比较研究得出与EMIT的相关系数为0.97。