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基于同步光引发逐步聚合和开环聚合制备的聚并五苯-g-聚(ε-己内酯)用于 SARS-CoV-2 检测的荧光生物测定法。

Fluorescent bioassay for SARS-CoV-2 detection using polypyrene-g-poly(ε-caprolactone) prepared by simultaneous photoinduced step-growth and ring-opening polymerizations.

机构信息

Department of Chemistry, Istanbul Technical University, 34469, Maslak, Istanbul, Turkey.

Department of Biochemistry, Faculty of Science, Ege University, 35100, Bornova, Izmir, Turkey.

出版信息

Mikrochim Acta. 2022 Apr 26;189(5):202. doi: 10.1007/s00604-022-05244-2.

Abstract

The construction of a rapid and easy immunofluorescence bioassay for SARS-CoV-2 detection is described. We report for the first time a novel one-pot synthetic approach for simultaneous photoinduced step-growth polymerization of pyrene (Py) and ring-opening polymerization of ε-caprolactone (PCL) to produce a graft fluorescent copolymer PPy-g-PCL that was conjugated to SARS-CoV-2-specific antibodies using EDC/NHS chemistry. The synthesis steps and conjugation products were fully characterized using standard spectral analysis. Next, the PPy-g-PCL was used for the construction of a dot-blot assay which was calibrated for applications to human nasopharyngeal samples. The analytical features of the proposed sensor showed a detection range of 6.03-8.7 LOG viral copy mL (Ct Scores: 8-25), the limit of detection (LOD), and quantification (LOQ) of 1.84 and 6.16 LOG viral copy mL, respectively. The repeatability and reproducibility of the platform had a coefficient of variation (CV) ranging between 1.2 and 5.9%. The fluorescence-based dot-blot assay was tested with human samples. Significant differences were observed between the fluorescence intensity of the negative and positive samples, with an overall correct response of 93.33%. The assay demonstrated a high correlation with RT-PCR data. This strategy opens new insights into simplified synthesis procedures of the reporter molecules and their high potential sensing and diagnosis applications.

摘要

本文描述了一种用于 SARS-CoV-2 检测的快速简便免疫荧光生物测定法的构建。我们首次报道了一种新颖的一锅法,用于同时进行芘(Py)的光诱导逐步聚合和ε-己内酯(PCL)的开环聚合,以产生接枝荧光共聚物 PPy-g-PCL,然后使用 EDC/NHS 化学将 SARS-CoV-2 特异性抗体连接到该共聚物上。使用标准光谱分析对合成步骤和缀合产物进行了充分的表征。接下来,将 PPy-g-PCL 用于点印迹测定的构建,该测定已针对人鼻咽样本进行了校准。所提出的传感器的分析特征显示出 6.03-8.7 LOG 病毒拷贝 mL 的检测范围(Ct 分数:8-25),检测限(LOD)和定量限(LOQ)分别为 1.84 和 6.16 LOG 病毒拷贝 mL。该平台的重复性和重现性的变异系数(CV)在 1.2 到 5.9%之间。该荧光斑点印迹测定法已用人样本进行了测试。在阴性和阳性样本之间观察到荧光强度存在显着差异,总体正确响应率为 93.33%。该测定法与 RT-PCR 数据具有高度相关性。该策略为简化报告分子的合成程序以及它们在传感和诊断方面的高潜在应用提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7119/9042169/d67ec80e713d/604_2022_5244_Fig1_HTML.jpg

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