[Conditional optimization and methodological evaluation of liquid protein microarray in detecting cystatin C].

Chaoqun Sun, Jiangping Niu, Jiyong Yin, Junsheng Huo, Jing Sun, Jian Huang, Tiantong Li, Yuhe Liu, Ailing Liu
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Abstract

Objective: To optimize the detection conditions and evaluate of cystatin C(CysC) by liquid protein microarray.

Methods: CysC was detected by double antibody sandwich method using liquid protein microarray. On the basis of determining the optimal concentration combination of captured antibody and detected antibody, the detection conditions were optimized by determining the biological detection limit and lower detection limit, drawing the S-shaped curve and judging the linear range, and establishing the standard curve and regression equation. Methodsologically evaluate the accuracy, precision, reportable range and analytical specificity of the detection method.

Results: The optimal concentration combinations of CycC trapping-detection antibodies were 26.6 μg/mL-1∶800. The lower limits of detection and biologic limits of detection of the CysC were 0.037 and 0.237 ng/mL, respectively. Regression equation were as followes: y=-3.315x~2+283.04x+160.89, R~2=0.9921. The relative bias of CysC which was detected on the liquid protein microarry was 5.81%. The dilution recovery and recovery were 70.35%-84.91%(n=3)and 79.94%-122.41%(n=3)respectively. The correlation coefficient of method ology comparison experiment was r=0.616, P<0.05, and there was no significant difference between the two method(t=0.948, P=0.358); The within-run precision range from 3.54% to 4.03%(n=10); The between-run precision range from 12.07% to 15.05%(D=5, n=3); The reportable range was 0.26-3784.04 ng/mL. The analysis of interference test result showed that the both concentrations of hemoglobin(160.00, 71.11 g/L) had interference to the result of CysC detected on the chip.

Conclusion: This study completed the optimization of conditions and methodological evaluation of liquid protein microarray in detecting CysC.

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液体蛋白芯片检测胱抑素C的条件优化及方法学评价[j]。
目的:优化液体蛋白芯片检测胱抑素C(cystatin C, CysC)的检测条件并对其进行评价。方法:采用液体蛋白芯片双抗体夹心法检测CysC。在确定捕获抗体与检测抗体最佳浓度组合的基础上,通过确定生物检出限和下检出限,绘制s型曲线并判断线性范围,建立标准曲线和回归方程,对检测条件进行优化。方法学评价检测方法的准确性、精密度、报告范围和分析特异性。结果:CycC捕集检测抗体的最佳浓度组合为26.6 μg/mL-1∶800。CysC的检测下限为0.037 ng/mL,生物学下限为0.237 ng/mL。回归方程为:y=-3.315x~2+283.04x+160.89, R~2=0.9921。液体蛋白微阵列检测CysC的相对偏倚为5.81%。稀释回收率为70.35% ~ 84.91%(n=3),回收率为79.94% ~ 122.41%(n=3)。方法学比较实验相关系数r=0.616, P<0.05,两种方法间差异无统计学意义(t=0.948, P=0.358);运行精度范围为3.54% ~ 4.03%(n=10);运行间精密度范围为12.07% ~ 15.05%(D=5, n=3);报告范围为0.26 ~ 3784.04 ng/mL。干扰测试结果分析表明,两种血红蛋白浓度(160.00、71.11 g/L)对芯片上检测的CysC结果均有干扰。结论:本研究完成了液体蛋白芯片检测CysC的条件优化和方法学评价。
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