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Plasmonic ELISA for the ultrasensitive detection of disease biomarkers with the naked eye

机译:等离子酶联免疫吸附法用于肉眼超灵敏检测疾病生物标志物

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摘要

In resource-constrained countries, affordable methodologies for the detection of disease biomarkers at ultralow concentrations can potentially improve the standard of living1, 2. However, current strategies for ultrasensitive detection often require sophisticated instruments that may not be available in laboratories with fewer resources3, 4, 5, 6, 7, 8, 9, 10, 11. Here, we circumvent this problem by introducing a signal generation mechanism for biosensing that enables the detection of a few molecules of analyte with the naked eye. The enzyme label of an enzyme-linked immunosorbent assay (ELISA) controls the growth of gold nanoparticles and generates coloured solutions with distinct tonality when the analyte is present. Prostate specific antigen (PSA) and HIV-1 capsid antigen p24 were detected in whole serum at the ultralow concentration of 1 × 10−18 g ml−1. p24 was also detected with the naked eye in the sera of HIV-infected patients showing viral loads undetectable by a gold standard nucleic acid-based test
机译:在资源有限的国家,负担得起的超低浓度疾病生物标志物检测方法可潜在地改善生活水平1、2。但是,当前的超灵敏检测策略通常需要精密的仪器,而这些仪器可能在资源较少的实验室中无法使用3、4。 ,5、6、7、8、9、10、11。在这里,我们通过引入一种用于生物传感的信号发生机制来规避此问题,该机制可以用肉眼检测少量分析物分子。酶联免疫吸附测定(ELISA)的酶标记物控制金纳米颗粒的生长,并在存在分析物时产生具有不同色调的有色溶液。在全血清中以1×10-18 g ml-1的超低浓度检测到前列腺特异性抗原(PSA)和HIV-1衣壳抗原p24。还用肉眼在HIV感染患者的血清中检测到p24,显示出基于金标准核酸测试无法检测到的病毒载量

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