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用于微流控纸基分析装置核酸检测的工程纳米颗粒

Engineered Nanoparticles for μPAD Nucleic Acid Detection.

作者信息

Morgan R Luc, Zehnder Lillian J, Jenkin Madeline A, Alonso Erika, Haunz Sasha, Bevil Abby, Scott Daniel F

机构信息

Department of Chemistry, Centre College, Danville, Kentucky 40422, United States.

出版信息

ACS Omega. 2025 May 13;10(20):20268-20276. doi: 10.1021/acsomega.4c11390. eCollection 2025 May 27.

Abstract

Point-of-care (POC) diagnostics can provide early disease detection and continued monitoring for millions of people, domestically and internationally, who do not have access to essential support services. POC diagnostics can improve care and treatment decisions by shortening the time from analysis to diagnosis. Current POC diagnostic systems are limited by the availability of analyte options, nonspecific responses, the need for trained personnel, specialized instrumentation, and expensive biological components. Herein is presented a novel approach to develop POC diagnostics based on iron oxide@gold, core@shell, nanoparticles (FeO@Au's). The particles were engineered to release signaling compounds in the presence of the target analytes and built on a paper-based microfluidic (μPAD) platform to allow for inexpensive production and high portability. As a proof-of-concept, an assay for the oligonucleotide target sequence of survivin was developed. The nanoparticles were designed to release a signal in the presence of survivin DNA, which was quantified via a fluorescence signal on the μPAD platforms. The system showed selective response for the targeted survivin sequence, and detection was achieved with buffer, artificial saliva, artificial urine, and human serum matrices.

摘要

即时检测(POC)诊断能够为国内外数百万无法获得基本支持服务的人群提供疾病早期检测和持续监测。POC诊断可通过缩短从分析到诊断的时间来改善护理和治疗决策。当前的POC诊断系统受到分析物选择的可用性、非特异性反应、对训练有素的人员的需求、专用仪器以及昂贵的生物组件的限制。本文介绍了一种基于氧化铁@金核壳纳米颗粒(FeO@Au)开发POC诊断的新方法。这些颗粒经过设计,可在目标分析物存在时释放信号化合物,并构建在基于纸的微流控(μPAD)平台上,以实现低成本生产和高便携性。作为概念验证,开发了一种针对生存素寡核苷酸靶序列的检测方法。这些纳米颗粒被设计为在生存素DNA存在时释放信号,该信号通过μPAD平台上的荧光信号进行定量。该系统对靶向的生存素序列表现出选择性响应,并且在缓冲液、人工唾液、人工尿液和人血清基质中均实现了检测。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e48/12120606/866e3703ce84/ao4c11390_0001.jpg

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