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用于预测竞争性酶联免疫吸附测定检测限和定量范围的模拟模型。

Simulation model for predicting limit of detection and range of quantitation of competitive enzyme-linked immunosorbent assay.

作者信息

Choi Dong Hwan, Katakura Yoshio, Matsuda Rieko, Hayashi Yuzuru, Ninomiya Kazuaki, Shioya Suteaki

机构信息

Department of Biotechnology, Graduate School of Engineering, Osaka University, Suita, Osaka, Japan.

出版信息

J Biosci Bioeng. 2007 May;103(5):427-31. doi: 10.1263/jbb.103.427.

Abstract

The limit of detection (LOD) and range of quantitation (ROQ) of competitive enzyme-linked immunosorbent assay (ELISA) were determined from a model describing the calibration curve and precision profile of the assay. The calibration curve is given by solving the differential equations describing the change in the concentrations of an antigen-antibody complex and an enzyme-conjugated antigen-antibody complex by a Runge-Kutta method. The precision profile is described in terms of possible error sources such as the pipetting volumes of the analyte, enzyme-conjugated antigen, antibody and substrate solutions, calibration curve and inherent absorbances between the wells in an ELISA plate. An appropriate concentration of the enzyme-conjugated antigen that balances a low detection limit and sufficient color development was found to be in a narrow range, which is consistent with the empirical rule. The optimum conditions for competitive ELISA using an antibody with a kinetic property can be designed from our model.

摘要

通过描述竞争性酶联免疫吸附测定(ELISA)校准曲线和精密度曲线的模型,确定了该测定方法的检测限(LOD)和定量范围(ROQ)。校准曲线通过用龙格 - 库塔方法求解描述抗原 - 抗体复合物和酶联抗原 - 抗体复合物浓度变化的微分方程得到。精密度曲线根据可能的误差来源进行描述,如分析物、酶联抗原、抗体和底物溶液的移液体积、校准曲线以及ELISA板孔间的固有吸光度。发现能平衡低检测限和足够显色的酶联抗原的合适浓度处于狭窄范围内,这与经验法则一致。利用我们的模型可以设计使用具有动力学特性抗体的竞争性ELISA的最佳条件。

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