Juan He, Miao Hu, Lin Yang, Jiacheng Yin, Zixin Zhang, Luying Tu, Yuxin Heng, Long Tang, Juan He, Xiandeng Hou, Xue Jiang
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引用次数: 0
摘要
基于催化银沉积在免疫金标签上的信号放大技术已被用于免疫测定。然而,由于体积庞大、成本高昂、操作复杂,传统仪器在进行床旁检测时往往受到限制。在此,我们设计了一种将毛细管液体电极辉光放电(CLEGD)与光发射光谱(OES)相结合的集成便携式 3D 打印设备,用于在微小样本中灵敏测定癌胚抗原(CEA)。无需额外装置,样品溶液在毛细管力和高压的作用下被自动吸入放电室;分析物中的 Ag(I) 在放电等离子体中被雾化和激发,从而产生波长为 328.1 纳米的 Ag 原子发射线。该系统可检测 101-106 ng mL-1 的 Ag(I),并进一步量化癌胚抗原的浓度。在优化条件下,该紧凑型设备的癌胚抗原检测效果与 ICP-OES 相当,线性范围为 1-500 ng mL-1,检测限低至 0.9 ng mL-1。
Portable Capillary-Microplasma Optical Emission Spectrometer: Gold-Labeled and Silver-Stained Signal Amplification for Carcinoembryonic Antigen Detection
Signal amplification techniques based on catalytic silver deposition on immunogold labels have been used for immunoassays. However, conventional instruments often suffer from limitations in point-of-care testing due to their bulky size, high cost, and complex operation. We herein designed an integrated, portable 3D-printed device by integrating capillary liquid electrode glow discharge (CLEGD) with optical emission spectrometer (OES) for the sensitive determination of carcinoembryonic antigen (CEA) in tiny samples. Without the need for additional devices, the sample solution is automatically drawn into the discharge chamber under the action of capillary force and applied high voltage; Ag(I) in the analyte is atomized and excited in the discharge plasma, resulting in Ag atomic emission lines at 328.1 nm. The system enables the detection of 101–106 ng mL–1 Ag(I) and further quantification of carcinoembryonic antigen concentration. Under optimized conditions, the compact equipment achieves CEA detection comparable to that of ICP-OES, with a linear range of 1–500 ng mL–1 and a limit of detection as low as 0.9 ng mL–1.
期刊介绍:
Analytical Chemistry, a peer-reviewed research journal, focuses on disseminating new and original knowledge across all branches of analytical chemistry. Fundamental articles may explore general principles of chemical measurement science and need not directly address existing or potential analytical methodology. They can be entirely theoretical or report experimental results. Contributions may cover various phases of analytical operations, including sampling, bioanalysis, electrochemistry, mass spectrometry, microscale and nanoscale systems, environmental analysis, separations, spectroscopy, chemical reactions and selectivity, instrumentation, imaging, surface analysis, and data processing. Papers discussing known analytical methods should present a significant, original application of the method, a notable improvement, or results on an important analyte.