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基于抗体偶联金纳米粒子和光纤局域表面等离子体共振的三明治免疫分析的高性能生物传感器。

High-performance biosensor using a sandwich assay via antibody-conjugated gold nanoparticles and fiber-optic localized surface plasmon resonance.

机构信息

Department of Electronics and Electrical Engineering, Dankook University, Yongin, 16890, Republic of Korea.

Department of Electronics and Electrical Engineering, Dankook University, Yongin, 16890, Republic of Korea.

出版信息

Anal Chim Acta. 2022 Jun 22;1213:339960. doi: 10.1016/j.aca.2022.339960. Epub 2022 May 20.

DOI:10.1016/j.aca.2022.339960
PMID:35641064
Abstract

For real-time and high-sensitivity analysis of low-concentration targets, a sandwich immunoassay using second antibody-second gold nanoparticle (2nd Ab-2nd AuNP) conjugates was combined with fiber-optic localized surface plasmon resonance (FO LSPR). An FO LSPR format was constructed by immobilizing AuNPs on a fiber-optic cross-section for compactness, portability, and ease of handling. In addition, it was combined with a microfluidic system to ensure reproducibility and reliability of measurements. A detection limit of 97.6 fg/mL (148 aM) was obtained for thyroglobulin (Tg) without a sandwich assay. The detection limit was enhanced by approximately 15 times (6.6 fg/mL, 10 aM) when a sandwich strategy was performed with a 2nd Ab-2nd AuNP signal amplifier to further improve the responsivity. Additionally, the good selectivity of the proposed method was confirmed against the unpaired antigen. To evaluate its practical applicability in the field, an FO LSPR biosensor boosted with a sandwich assay using antibody-functionalized AuNPs was applied to detect Tg contained in patient serum, and the results were compared and verified with those of a commercial radioimmunoassay kit. Based on the above results, the signal-enhancing immunoassay with FO LSPR will contribute to the development of optical biosensors for early diagnosis and preventive applications.

摘要

为了实时、高灵敏度地分析低浓度靶标,我们将基于二抗-二金纳米粒子(2nd Ab-2nd AuNP)偶联物的三明治免疫测定法与光纤局域表面等离子体共振(FO LSPR)相结合。通过将 AuNPs 固定在光纤横截面上,构建了紧凑、便携且易于操作的 FO LSPR 格式。此外,还将其与微流控系统相结合,以确保测量的重现性和可靠性。对于甲状腺球蛋白(Tg),无需三明治测定即可获得 97.6 fg/mL(148 aM)的检测限。通过使用 2nd Ab-2nd AuNP 信号放大器进行三明治策略,检测限提高了约 15 倍(6.6 fg/mL,10 aM),从而进一步提高了响应性。此外,还通过与未配对的抗原进行对比,验证了该方法具有良好的选择性。为了评估其在实际应用中的可行性,我们使用抗体功能化 AuNPs 增强的三明治免疫测定法,对患者血清中的 Tg 进行了检测,并将结果与商业放射免疫试剂盒的结果进行了比较和验证。基于上述结果,基于 FO LSPR 的信号增强免疫测定法将有助于开发用于早期诊断和预防应用的光学生物传感器。

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