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Instrumentation-Free Semiquantitative Immunoanalysis Using a Specially Patterned Lateral Flow Assay Device

机译:使用特殊图案化的横向流动测定装置的无仪器半定量免疫分析

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摘要

In traditional colorimetric lateral flow immunoassay (LFI) using gold nanoparticles (AuNPs) as a probe, additional optical transducers are required to quantify the signal intensity of the test line because it presents as a single red-colored line. In order to eliminate external equipment, the LFI signal should be quantifiable by the naked eye without the involvement of optical instruments. Given this objective, the single line test zone of conventional LFI was converted to several spots that formed herringbone patterns. When the sandwich immunoassay was performed on a newly developed semi-quantitative (SQ)-LFI system using AuNPs as an optical probe, the spots were colorized and the number of colored spots increased proportionally with the analyte concentration. By counting the number of colored spots, the analyte concentration can be easily estimated with the naked eye. To demonstrate the applicability of the SQ-LFI system in practical immunoanalysis, microalbumin, which is a diagnostic marker for renal failure, was analyzed using microalbumin-spiked artificial urine samples. Using the SQ-LFI system, the calibration results for artificial urine-based microalbumin were studied, ranging from 0 to 500 μg/mL, covering the required clinical detection range, and the limit of detection (LOD) value was calculated to be 15.5 μg/mL. Thus, the SQ-LFI system provides an avenue for the realization of an efficient quantification diagnostic device in resource-limited conditions.
机译:在传统的比色横向流动免疫测定(LFI)中使用金纳米颗粒(AUNP)作为探针,需要附加的光学换能器来量化测试线的信号强度,因为它作为单个红色线。为了消除外部设备,LFI信号应通过肉眼来量化,而不会参与光学仪器。鉴于此目的,常规LFI的单线测试区被转换为形成人字形图案的几个斑点。当使用AUNPS作为光学探针的新开发的半定量(SQ)-LFI系统对新开发的半定量(SQ)-LFI系统进行了夹层时,斑点着色,彩色斑点的数量与分析物浓度成比例地增加。通过计算彩色斑点的数量,可以用肉眼容易地估计分析物浓度。为了证明SQ-LFI系统在实际免疫分析中的适用性,使用微蛋白掺入的人造尿液样品分析了作为肾功能衰竭的诊断标志物的微蛋白。使用SQ-LFI系统,研究了人造尿基微蛋白的校准结果,范围为0至500μg/ ml,覆盖所需的临床检测范围,并且检测极限(LOD)值计算为15.5μg / ml。因此,SQ-LFI系统提供了在资源有限条件下实现有效量化诊断装置的途径。

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