Khalil O S, Hanna C F, Huff D, Zurek T F, Murphy B, Pepe C, Genger K
Diagnostics Division, Abbott Laboratories, Abbott Park, IL 60064.
Clin Chem. 1991 Sep;37(9):1612-7.
We describe a reaction tray for a heterogeneous chemiluminescence (CL) immunoassay having the following features: separate sample incubation and signal detection wells; a design that allows for noncontact transfer of the reaction mixture from incubation wells to detection wells; surface features to mate with a detector and create a light-tight seal for CL detection; and self-contained means for liquid removal. The reaction mixture is transferred by injecting a wash solution from a group of nozzles into the incubation well. Quantitative transfer of microparticles (transfer efficiencies greater than 95% and CV less than 5%) is achieved by injecting two 300-microL pulses of transfer solution at a rate of 2.1 m/s. The performance of the tray and method of transfer is tested by determining the precision of CL signal for a sample containing a concentration of anti-hepatitis B core antigen (anti-HBc) or hepatitis B surface antigen (HBsAg) close to the cutoff value for the assay.
我们描述了一种用于异相化学发光(CL)免疫分析的反应盘,其具有以下特征:独立的样品孵育和信号检测孔;一种允许反应混合物从孵育孔非接触转移至检测孔的设计;与检测器配合并为CL检测创建不透光密封的表面特征;以及独立的液体去除装置。通过从一组喷嘴向孵育孔中注入洗涤溶液来转移反应混合物。通过以2.1 m/s的速率注入两个300 μL的转移溶液脉冲,实现了微粒的定量转移(转移效率大于95%且CV小于5%)。通过测定含有接近该分析临界值浓度的抗乙型肝炎核心抗原(抗-HBc)或乙型肝炎表面抗原(HBsAg)的样品的CL信号精度,来测试反应盘的性能和转移方法。