A systematic implementation of padlock probing-based rolling circle amplification in an integrated microfluidic device for quantitative biomolecular analyses

IF 6 2区 化学 Q1 CHEMISTRY, ANALYTICAL Analytica Chimica Acta Pub Date : 2025-05-15 Epub Date: 2025-02-23 DOI:10.1016/j.aca.2025.343834
Catarina R.F. Caneira , Rafaela R. Rosa , Virginia Chu , Mats Nilsson , Narayanan Madaboosi , Ruben R.G. Soares , João P. Conde
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Abstract

Background

Pathogen detection in primary care is crucial not only to identify viruses like SARS-CoV-2 but also for antibiotic-resistant bacteria. While microfluidic devices enable point-of-care diagnostics, they often lack sufficient sensitivity. On-chip isothermal amplification techniques, such as padlock probing-based rolling circle amplification (PLP-RCA), can enhance specificity and sensitivity while keeping device complexity low. However, integrating PLP-RCA on-chip requires precise optimization of enzyme concentrations, flow conditions, and target capture to achieve its full potential.

Results

This study demonstrates a microfluidic RCA assay using porous agarose microbeads as a solid-phase capture, packed inside a microfluidic device. Various target capture strategies were systematically compared and quantitatively investigated, progressing from single-stranded synthetic DNA oligonucleotides to double-stranded Staphylococcus aureus genomic DNA. The best strategy for double-stranded Staphylococcus aureus genomic DNA used a primer bound to the beads that capture the PLP and the target genomic DNA. The system integrates an amorphous-hydrogenated silicon (a-Si:H) thin film p-i-n photodiode and a high-pass interference filter, enabling on-chip fluorescence signal acquisition of amplicons. This integration allows for a fully functional PLP-RCA assay on-chip, along with the added merits of device portability and compatibility with clinical demands.

Significance and novelty

This study systematically evaluates single- and double-stranded target capture for on-chip PLP-RCA assays. It demonstrates the successful integration of microfluidics with a solid-phase capture medium and fluorescence detection system. The findings highlight the potential of this platform for developing sensitive, portable pathogen detection devices suited for clinical applications.”

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基于挂锁探针的滚动圆放大在集成微流控装置中的系统实现,用于定量生物分子分析
初级保健中的病原体检测不仅对识别SARS-CoV-2等病毒至关重要,而且对耐抗生素细菌也至关重要。虽然微流控装置可以实现即时诊断,但它们往往缺乏足够的灵敏度。片上等温扩增技术,如基于挂锁探针的滚动圆扩增(PLP-RCA),可以提高特异性和灵敏度,同时保持较低的器件复杂性。然而,将PLP-RCA集成到芯片上需要精确优化酶浓度、流动条件和目标捕获,以充分发挥其潜力。本研究展示了一种微流控RCA分析,使用多孔琼脂糖微珠作为固相捕获,包装在微流控装置内。从单链合成DNA寡核苷酸到双链金黄色葡萄球菌基因组DNA,系统比较和定量研究了各种靶标捕获策略。获取双链金黄色葡萄球菌基因组DNA的最佳策略是使用与捕获PLP和目标基因组DNA的珠子结合的引物。该系统集成了一个非晶氢化硅(a- si:H)薄膜p-i-n光电二极管和一个高通干涉滤波器,实现了片上荧光信号采集的放大。这种集成允许在片上进行全功能的PLP-RCA分析,以及设备可移植性和与临床需求的兼容性的附加优点。本研究系统地评估了单链和双链靶捕获在片上PLP-RCA分析中的应用。它证明了微流体与固相捕获介质和荧光检测系统的成功集成。这些发现突出了这个平台在开发适合临床应用的敏感、便携式病原体检测设备方面的潜力。”
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来源期刊
Analytica Chimica Acta
Analytica Chimica Acta 化学-分析化学
CiteScore
10.40
自引率
6.50%
发文量
1081
审稿时长
38 days
期刊介绍: Analytica Chimica Acta has an open access mirror journal Analytica Chimica Acta: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review. Analytica Chimica Acta provides a forum for the rapid publication of original research, and critical, comprehensive reviews dealing with all aspects of fundamental and applied modern analytical chemistry. The journal welcomes the submission of research papers which report studies concerning the development of new and significant analytical methodologies. In determining the suitability of submitted articles for publication, particular scrutiny will be placed on the degree of novelty and impact of the research and the extent to which it adds to the existing body of knowledge in analytical chemistry.
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