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Characterizing Antibody-Microsphere Conjugates for Fluorescence-Based Lateral Flow Immunoassays

机译:用于荧光基侧流动免疫测定抗体微球缀合物的特征

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Fluorescence- based lateral flow immunoassays (LFIAs) remain relatively unexplored compared to colorimetric LFIAs for point-of-care (PoC) disease diagnosis and health monitoring. For fluorescence-based LFIAs, a major challenge includes the auto-fluorescence of the nitrocellulose and nonspecific binding of fluorescent polystyrene microspheres. In this paper, we aim to characterize antibody-microsphere conjugates in a fluorescence-based serological assay on nitrocellulose. Factors such as coating concentration and quantity of microspheres were considered and their impacts on nonspecific binding and signal-to-noise ratio are discussed. Finally, we use the determined conditions for the antibody-microsphere conjugates to demonstrate the sensitivity of a proof-of-concept assay detecting antibodies to Epstein-Barr Nuclear Antigen-1 in pooled human plasma samples. A titration of the seropositive plasma samples demonstrated a titer approaching 1:1,000 using only 30 μL of diluted sample and a sample-to-result time of less than one hour.
机译:与比色LFIAS相比,基于荧光的横向流动免疫测定(LFIAS)仍然是未探测的,以进行COLLICETRIC LFIAS,用于治疗点(POC)疾病诊断和健康监测。对于基于荧光的LFIAS,主要挑战包括硝酸纤维素的自荧光和荧光聚苯乙烯微球的非特异性结合。在本文中,我们的目标是在硝酸纤维素上的荧光血液测定中表征抗体微球缀合物。考虑了涂层浓度和微球的涂层浓度和量等因素,并讨论了对非特异性结合和信噪比的影响。最后,我们使用确定的抗体微球缀合物的病症来证明概念证据测定检测抗体对汇集的人血浆样品中的Epstein-Barr核抗原-1的敏感性。血清阳性等离子体样品的滴定证明了使用仅30μl稀释的样品和较小一小时的样品与结果时间接近1:1,000的滴度。

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