Key Laboratory for the Chemistry and Molecular Engineering of Medicinal Resources (Ministry of Education of China), College of Chemistry and Chemical Engineering of Guangxi Normal University, Guilin 541004, China.
Talanta. 2012 Apr 15;92:72-7. doi: 10.1016/j.talanta.2012.01.051. Epub 2012 Feb 2.
A multicolor quantum dot (QD)-based nanosensor for multiplex detection of two tumor markers in a homogeneous format based on fluorescence polarization immunoassay was proposed. QDs520 and QDs620 were labeled alpha-fetoprotein(α-AFP) and carcinoembryonic antigen (CEA), respectively. After separated and purified by ultrafiltration, they were used in fluorescence polarization immunoassay for the simultaneous detection of human serum alpha-fetoprotein and carcinoembryonic antigen. Under the optimal conditions, the multi-analyte immunosensor had a wide linear range (from 0.5 ng mL(-1) to 500 ng mL(-1)) for both two tumor markers and good correlation (0.996 for α-AFP and 0.993 for CEA). The detection limits (LOD) were 0.36 ng mL(-1) for CEA and 0.28 ng mL(-1) for α-AFP (S/N=3). The carcinoembryonic antigen and fetoprotein in clinical serum samples were simultaneously detected. The results from 28 serum samples had a good agreement with enzyme-linked immunosorbent assay (ELISA). The relative standard deviation and the recovery suggested that the precision and the accuracy of this analytical method were satisfactory. This strategy with high sensitivity, good specificity, easy procedures and short analysis time shows great promise for clinical diagnoses and basic discovery. The application of QDs with longer fluorescence lifetime and small fluorescence polarization can be used for the determination of high molecular-weight substances which cannot be analyzed using dye fluorescence polarization immunoassay.
基于荧光偏振免疫分析,提出了一种基于多色量子点(QD)的纳米传感器,用于均相格式中两种肿瘤标志物的多重检测。QD520 和 QD620 分别标记甲胎蛋白(α-AFP)和癌胚抗原(CEA)。经过超滤分离和纯化后,它们被用于荧光偏振免疫分析,用于同时检测人血清中的甲胎蛋白和癌胚抗原。在最佳条件下,多分析物免疫传感器对两种肿瘤标志物均具有宽线性范围(从 0.5 ng mL(-1)到 500 ng mL(-1)),并且相关性良好(α-AFP 为 0.996,CEA 为 0.993)。CEA 的检测限(LOD)为 0.36 ng mL(-1),α-AFP 的检测限为 0.28 ng mL(-1)(S/N=3)。同时检测了临床血清样本中的癌胚抗原和胎蛋白。28 个血清样本的结果与酶联免疫吸附测定(ELISA)具有良好的一致性。相对标准偏差和回收率表明该分析方法具有令人满意的精密度和准确性。该策略具有灵敏度高、特异性好、操作简单、分析时间短等优点,有望用于临床诊断和基础发现。具有较长荧光寿命和小荧光偏振的量子点的应用可用于分析无法用染料荧光偏振免疫分析分析的高分子量物质的测定。