Le The Son, He Sizun, Takahashi Mari, Enomoto Yasushi, Matsumura Yasufumi, Maenosono Shinya
School of Materials Science, Japan Advanced Institute of Science and Technology, 1-1 Asahidai, Nomi, Ishikawa 923-1292, Japan.
New Materials Development Center, Research & Development Division, Nippon Steel Chemical & Material Co., Ltd., 1-Tsukiji, Kisarazu, Chiba 292-0835, Japan.
Langmuir. 2021 Jun 1;37(21):6566-6577. doi: 10.1021/acs.langmuir.1c00905. Epub 2021 May 19.
For lateral flow immunoassay (LFIA), it is an important challenge to enhance the detection sensitivity to the same level as polymerase chain reaction or enzyme-linked immunosorbent assay to make LFIA pervasive in the field of on-site environmental analysis. We recently demonstrated that the LFIA sensitivity is dramatically enhanced by using Pt-nanoparticle-latex nanocomposite beads (Pt-P2VPs) as probes for the detection of the influenza A (H1N1) antigen compared with using conventional Au colloids as probes. Here, to further enhance the LFIA sensitivity using Pt-P2VPs, superparamagnetic iron oxide nanoparticles (SPIONs) were chemically conjugated to Pt-P2VPs (Pt-P2VP@SPION) to give them magnetic separation capability (enrichment and/or purification). To investigate the effect of magnetic enrichment on the LFIA sensitivity in a sandwich format, the C-reactive protein (CRP) was chosen as a model analyte and anti-CRP antibody (CRPAb)-conjugated Pt-P2VP@SPION (Pt-P2VP@SPION-CRPAb) beads were used as probes. The visual limit of detection (LOD) of LFIA was successfully lowered by increasing the magnetic enrichment factor φ. The minimum LOD under the present experimental conditions was 0.08 ng/mL for φ = 40, which is 26-fold lower than that of the standard Au-nanoparticle-based LFIA. In theory, the LOD can be unlimitedly decreased by just increasing φ. However, the times required for both the antigen-antibody binding reaction and magnetic separation dramatically increase with φ. We also propose solutions to overcome this drawback.
对于侧向流动免疫分析(LFIA)而言,要将检测灵敏度提高到与聚合酶链反应或酶联免疫吸附测定相同的水平,从而使LFIA在现场环境分析领域得到广泛应用,是一项重大挑战。我们最近证明,与使用传统金胶体作为探针相比,使用铂纳米颗粒-乳胶纳米复合珠(Pt-P2VPs)作为检测甲型流感(H1N1)抗原的探针,可显著提高LFIA的灵敏度。在此,为了使用Pt-P2VPs进一步提高LFIA的灵敏度,将超顺磁性氧化铁纳米颗粒(SPIONs)化学偶联到Pt-P2VPs(Pt-P2VP@SPION)上,赋予它们磁分离能力(富集和/或纯化)。为了研究磁富集对夹心式LFIA灵敏度的影响,选择C反应蛋白(CRP)作为模型分析物,并使用抗CRP抗体(CRPAb)偶联的Pt-P2VP@SPION(Pt-P2VP@SPION-CRPAb)珠作为探针。通过增加磁富集因子φ,成功降低了LFIA的目视检测限(LOD)。在当前实验条件下,当φ = 40时,最低LOD为0.08 ng/mL,比基于标准金纳米颗粒的LFIA低26倍。理论上,仅通过增加φ,LOD就可以无限降低。然而,抗原-抗体结合反应和磁分离所需的时间都随着φ的增加而显著增加。我们还提出了克服这一缺点的解决方案。