Magnetic induction spectroscopy (MIS) as potential non-contact label-free technique for DNA amplification follow-up.

Q3 Biochemistry, Genetics and Molecular Biology
Journal of Electrical Bioimpedance Pub Date : 2026-08-18 eCollection Date: 2026-01-01 DOI:10.2478/joeb-2026-0011
César A González-Díaz, Amelia Laveille, Ulascan Yuce, Franck M André, Lluis M Mir
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引用次数: 0

Abstract

Gene amplification and detection techniques such as polymerase chain reaction (PCR) or quantitative PCR (qPCR) require the use of fluorescent reagents and probes or dyes. Both PCR and qPCR must be performed by trained personnel. The aim of this work was to assess the potential use of magnetic induction spectroscopy (MIS) as a non-contact, label-free and easy-to-use technique to detect gene amplification in final PCR products. We extracted Deoxyribonucleic Acids (DNA) from samples of mouse tissue and processed it for gene amplification through PCR. We considered six different biological samples for the exploration of four genotypes and their corresponding blank controls. In every sample, we carried out MIS measurements in two stages (before and after PCR) in the range of 0.073 to 1.125 MHz and compared the differences. The results indicate a MIS magnitude differential pattern in the range of 500 to 650 kHz, which warrants the potential use of the MIS technique for the development of a fully contactless, label-free biosensor and capable of detecting DNA directly from PCR products.

磁感应光谱(MIS)作为一种潜在的非接触式无标记DNA扩增跟踪技术。
基因扩增和检测技术,如聚合酶链反应(PCR)或定量PCR (qPCR)需要使用荧光试剂和探针或染料。PCR和qPCR都必须由训练有素的人员进行。这项工作的目的是评估磁感应光谱(MIS)作为一种非接触、无标签和易于使用的技术检测最终PCR产物中的基因扩增的潜力。我们从小鼠组织样品中提取脱氧核糖核酸(DNA),并对其进行PCR扩增。我们考虑了六种不同的生物样本来探索四种基因型及其相应的空白对照。在每个样本中,我们在0.073至1.125 MHz范围内分两个阶段(PCR前和PCR后)进行MIS测量,并比较差异。结果表明,在500至650 kHz范围内存在MIS量级差异模式,这保证了MIS技术在开发完全非接触式、无标签生物传感器以及能够直接从PCR产物中检测DNA方面的潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Electrical Bioimpedance
Journal of Electrical Bioimpedance Engineering-Biomedical Engineering
CiteScore
3.00
自引率
0.00%
发文量
8
审稿时长
17 weeks
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