<p>Simultaneous Detection of VEGF and CEA by Time-Resolved Chemiluminescence Enzyme-Linked Aptamer Assay</p>

癌胚抗原 适体 校准曲线 检出限 化学发光 色谱法 血管内皮生长因子 生物标志物 线性范围 化学 血管内皮生长因子受体 癌症 分子生物学 医学 癌症研究 生物 内科学 生物化学
作者
Jin Man,Jiajia Dong,Yilin Wang,Leiliang He,Songcheng Yu,Fei Yu,Jia Wang,Yongmei Tian,Lie Liu,Runping Han,Hongchao Guo,Yongjun Wu,Lingbo Qu
出处
期刊:International Journal of Nanomedicine [Dove Medical Press]
卷期号:Volume 15: 9975-9985 被引量:13
标识
DOI:10.2147/ijn.s286317
摘要

Background: As two important tumor markers, vascular endothelial growth factor (VEGF) and carcinoembryonic antigen (CEA) have a great value for clinical application in the early diagnosis of cancer. Due to the complex composition of biological samples, the results from combined detection of CEA and VEGF are often taken as a comprehensive indicator in order to make an accurate judgment on a disease. However, most of the current methods can only be used to detect the content of one biomarker. Therefore, it is necessary to explore a simple, rapid, low-cost, and highly sensitive method for the simultaneous detection of CEA and VEGF. Methods: Based on specific aptamers and magnetic separation, a time-resolved chemiluminescence enzyme-linked aptamer assay was developed for the simultaneous detections of CEA and VEGF in serum samples. Results: Under the optimal conditions, the linear range of the calibration curve for VEGF was from 0.5 to 80 ng mL − 1 , and the limit of detection was 0.1 ng mL − 1 . The linear range of the calibration curve for CEA was 0.5 to 160 ng mL − 1 , and the limit of detection was 0.1 ng mL − 1 . The established method was applied to detect VEGF and CEA in serum samples. The results were consistent with those of commercial kits. Conclusion: The method has high sensitivity and can quickly obtain accurate results, which could greatly improve the measurement efficiency, reduce the cost, and also reduce the volume of sample consumed. It can be seen that the method established in this study has important application value and broad application prospect in clinical diagnosis. Keywords: chemiluminescence assay, simultaneous detection, vascular endothelial growth factor, time-resolved, carcinoembryonic antigen
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