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基于竞争荧光免疫分析平台,定制不同尺寸的量子点纳米珠,用于灵敏和定量检测。

Tailored different sizes of quantum dot nanobeads for sensitive and quantitative detection based on the competition fluorescence-linked immunosorbent assay platform.

机构信息

Key Lab for Special Functional Materials of Ministry of Education, and School of Materials, Henan University, Kaifeng, 475004, China.

Key Lab for Special Functional Materials of Ministry of Education, and School of Materials, Henan University, Kaifeng, 475004, China.

出版信息

Talanta. 2024 Aug 15;276:126296. doi: 10.1016/j.talanta.2024.126296. Epub 2024 May 21.

DOI:10.1016/j.talanta.2024.126296
PMID:38795648
Abstract

Highly stable and multicolor photoluminescent (PL) quantum dots (QDs) have attracted widespread attention as ideal probe materials in the field of in vitro diagnostics (IVD), especially the fluorescence-linked immunosorbent assay (FLISA), due to their advantages of high-throughput, high stability, and high sensitivity. However, the size of QDs as fluorescent probes have significant effects on antigen-antibody performance. Therefore, it is critical to design suitable QDs for obtain excellent quantitative detection-based biosensors. In this paper, we prepared different sizes of aqueous QDs (30 nm, 116 nm, 219 nm, and 320 nm) as fluorescent probes to optimize the competitive FLISA platform. The SARS-CoV-2 neutralizing antibody (NTAB) assay was used as an example, and it was found that the size of the QDs has a significant impact on the antigen-antibody binding efficiency and detection sensitivity in competitive FLISA platform. The results showed that these QD nanobeads (QBs, ∼219 nm) could be used as a labeled probe for competitive FLISA, with half-maximal inhibitory concentration (IC50) of 1.34 ng/mL and limit of detection (LOD) of 0.21 pg/mL for NTAB detection. More importantly, the results showed good specificity and accuracy, and the QB probe was able to efficiently bind NTAB without interference from other substances in the serum. Given the above advantages, the nanoprobe material (∼200 nm) offers considerable potential as a competitive FLISA platform in the field of IVD.

摘要

高稳定性和多色光致发光(PL)量子点(QD)由于其高通量、高稳定性和高灵敏度等优点,作为体外诊断(IVD)领域中理想的探针材料,特别是荧光酶联免疫吸附测定(FLISA),引起了广泛关注。然而,QD 作为荧光探针的尺寸对抗原-抗体性能有显著影响。因此,设计合适的 QD 以获得基于优异定量检测的生物传感器至关重要。在本文中,我们制备了不同尺寸的水性 QD(30nm、116nm、219nm 和 320nm)作为荧光探针,以优化竞争性 FLISA 平台。以 SARS-CoV-2 中和抗体(NTAB)测定为例,结果发现 QD 的尺寸对竞争性 FLISA 平台中的抗原-抗体结合效率和检测灵敏度有显著影响。结果表明,这些 QD 纳米珠(QDbs,219nm)可作为竞争性 FLISA 的标记探针,用于 NTAB 检测的半抑制浓度(IC50)为 1.34ng/mL,检测限(LOD)为 0.21pg/mL。更重要的是,结果显示出良好的特异性和准确性,QDbs 探针能够有效地与 NTAB 结合,而不受血清中其他物质的干扰。鉴于上述优势,该纳米探针材料(200nm)在 IVD 领域作为竞争性 FLISA 平台具有相当大的潜力。

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