Establishment of a time-resolved fluoroimmunoassay in detection of human epidermal growth factor receptor 2
Jun Kai Fan, Yi Zhang, Ke Wang, Wenwei Sun, Jue Zhang, Bin Zhou, Lixin Fu, Biao Huang, Qin Yang
Abstract
Jun Kai Fan, Yi Zhang, Ke Wang, Wenwei Sun, Jue Zhang, Bin Zhou, Lixin Fu, Biao Huang, Qin Yang
Abstract
Objective To set up a time-resolved fluoroimmunoassay (TRFIA) method for human epidermal growth factor receptor 2 (HER2) detection and to evaluate its performance. Methods Each well of the 96-microwell plate was coated with monoclonal antibody of HER2(H7) and another monoclonal antibody of HER2(E5) was labeled by Eu3+ . The sensitivity, stability, specificity, measurement range and reference value of this method were tested. The correlation between chemiluminescence (CLIA) method and TRFIA method was analyzed. Results The sensitivity of HER2-TRFIA method was 0.214 ng/ml. The measurement range was 0.214-1 000 ng/ml. The mean within-run CV and mean between-run CV were 3.48% and 4.13%, respectively. HER2-TRFIA method had no cross-reaction with HER1 and its reference range was 0-13.20 ng/ml. The correlation coefficient between TRFIA and CLIA was 0.997. The same batch of reagents were found to be stable for more than 6 months at 4 ℃. Conclusions HER2-TRFIA method has high sensitivity, specificity, stability and wide detecting range. It might be suitable for clinical use. Key words: Receptor, epidermal growth factor; Breast neoplasms; Fluoroimmunoassay
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Objective To set up a time-resolved fluoroimmunoassay (TRFIA) method for human epidermal growth factor receptor 2 (HER2) detection and to evaluate its performance. Methods Each well of the 96-microwell plate was coated with monoclonal antibody of HER2(H7) and another monoclonal antibody of HER2(E5) was labeled by Eu3+ . The sensitivity, stability, specificity, measurement range and reference value of this method were tested. The correlation between chemiluminescence (CLIA) method and TRFIA method was analyzed. Results The sensitivity of HER2-TRFIA method was 0.214 ng/ml. The measurement range was 0.214-1 000 ng/ml. The mean within-run CV and mean between-run CV were 3.48% and 4.13%, respectively. HER2-TRFIA method had no cross-reaction with HER1 and its reference range was 0-13.20 ng/ml. The correlation coefficient between TRFIA and CLIA was 0.997. The same batch of reagents were found to be stable for more than 6 months at 4 ℃. Conclusions HER2-TRFIA method has high sensitivity, specificity, stability and wide detecting range. It might be suitable for clinical use. Key words: Receptor, epidermal growth factor; Breast neoplasms; Fluoroimmunoassay
Key concepts: Monoclonal antibody, Chemistry, Chromatography, Epidermal growth factor receptor, Epidermal growth factor, Human Epidermal Growth Factor Receptor 2, Reagent, Coefficient of variation