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用铕纳米颗粒提高侧向流动分析法的灵敏度以准确定量人免疫球蛋白G

Enhancing the Sensitivity of Lateral Flow Assay with Europium Nanoparticles for Accurate Human IgG Quantification.

作者信息

Natarajan Satheesh, Priye Aashish

机构信息

Healthcare Technology Innovation Center, Indian Institute of Technology, Chennai 600113, India.

Department of Chemical and Environmental Engineering, University of Cincinnati, Cincinnati, OH 45221, USA.

出版信息

Micromachines (Basel). 2023 Oct 27;14(11):1993. doi: 10.3390/mi14111993.

Abstract

Accurate quantification of immunoglobulin G (IgG) levels is vital for understanding immune status and diagnosing various medical conditions. Lateral flow assays (LFAs) offer rapid and convenient diagnostic tools, but their sensitivity has been a limitation. Our research introduces a refined method incorporating europium nanoparticles, enhancing both sensitivity and accuracy of LFAs in human IgG measurement. Utilizing a unique sandwich format, carboxylate-modified polystyrene Eu (III) chelate microparticles (CM-EUs) acted as the primary reporters. The concentrations of both detection and capture antibodies on the strip were optimized to bolster the LFA's quantitative performance. The subsequent calibration curve between the IgG concentration and the measured intensity ratio () established the linearity and analytical sensitivity of our method with a high correlation coefficient (r = 0.99) and an impressively low limit of detection (LoD = 0.04 ng/mL). Our precision assessment, segmented into intra-assay and inter-assay evaluations, showcases the method's consistency and reproducibility. The LFA assay's stability was established by demonstrating its resistance to degradation and affirming its potential for extended storage without a dip in performance. The study's findings underscore the potential of this method to contribute to diagnostic medicine and improve patient care.

摘要

准确量化免疫球蛋白G(IgG)水平对于了解免疫状态和诊断各种疾病至关重要。侧向流动分析(LFA)提供了快速便捷的诊断工具,但其灵敏度一直是个限制因素。我们的研究引入了一种结合铕纳米颗粒的改进方法,提高了LFA在检测人IgG时的灵敏度和准确性。采用独特的夹心形式,羧基修饰的聚苯乙烯铕(III)螯合微粒(CM-EUs)作为主要报告分子。对试纸上检测抗体和捕获抗体的浓度进行了优化,以增强LFA的定量性能。随后在IgG浓度与测量强度比()之间建立的校准曲线确定了我们方法的线性和分析灵敏度,相关系数高(r = 0.99),检测限极低(LoD = 0.04 ng/mL)。我们的精密度评估分为批内和批间评估,展示了该方法的一致性和可重复性。通过证明LFA检测对降解的抗性并确认其在性能不下降的情况下可长期保存的潜力,确定了该检测方法的稳定性。该研究结果强调了这种方法在诊断医学中做出贡献并改善患者护理的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fd93/10673117/66628f795ff3/micromachines-14-01993-g001.jpg

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