Kumar Natish, Kumari Monika, Chander Devtulya, Dogra Sandeep, Chaubey Asha, Arun Ravi Kumar
Department of Chemical Engineering, Indian Institute of Technology, Jammu 181221, India.
Fermentation and Microbial Biotechnology Division, CSIR-Indian Institute of Integrative Medicine, Canal Road, Jammu 180001, India.
Biomicrofluidics. 2024 Dec 4;18(6):064104. doi: 10.1063/5.0211812. eCollection 2024 Dec.
Accurate detection of pathogenic nucleic acids is crucial for early diagnosis, effective treatment, and containment of infectious diseases. It facilitates the timely identification of pathogens, aids in monitoring disease outbreaks, and helps prevent the spread of infections within healthcare settings and communities. We developed a multi-layered, paper-based microfluidic and miniaturized electrophoresis system for rapid nucleic acid extraction, separation, amplification, and detection, designed for resource-limited settings. Constructed from acrylic, transparency film, pressure-sensitive adhesion, and Whatman paper using a CO laser, the setup simplifies traditional methods and eliminates the need for complex equipment. DNA extraction and purification are achieved using Zweifach-Fung bifurcation and Fahraeus effect principles, with detection via a hydrogel-assisted colorimetric isothermal reverse transcriptase-loop-mediated isothermal amplification technique. The system accurately identified the SARS-CoV-2 N-gene and β-actin human gene, validated by a compact electrophoresis setup. In clinical validation with 12 patient specimens, the system demonstrated a positive predictive agreement of 83.0% and a negative predictive agreement of 100%. The system achieves a limit of detection of 1 copy/l and can potentially transform nucleic acid detection assays in healthcare settings. This study addresses key challenges in nucleic acid detection, such as ensuring sample quality and quantity, reducing reliance on sophisticated equipment, preventing contamination, simplifying procedures, and providing rapid and accurate diagnostics for emerging pathogens.
准确检测病原核酸对于传染病的早期诊断、有效治疗和控制至关重要。它有助于及时识别病原体,辅助监测疾病爆发,并有助于防止感染在医疗机构和社区内传播。我们开发了一种多层纸质微流控和小型化电泳系统,用于快速核酸提取、分离、扩增和检测,专为资源有限的环境设计。该装置由丙烯酸、透明薄膜、压敏粘合剂和Whatman纸使用CO激光构建而成,简化了传统方法,无需复杂设备。利用 Zweifach-Fung 分叉和法厄斯效应原理实现DNA提取和纯化,通过水凝胶辅助比色等温逆转录环介导等温扩增技术进行检测。该系统准确识别了 SARS-CoV-2 N 基因和人类β-肌动蛋白基因,并通过紧凑型电泳装置进行了验证。在对12份患者标本的临床验证中,该系统的阳性预测一致性为83.0%,阴性预测一致性为100%。该系统实现了1拷贝/微升的检测限,有可能改变医疗机构中的核酸检测方法。本研究解决了核酸检测中的关键挑战,如确保样本质量和数量、减少对复杂设备的依赖、防止污染、简化程序以及为新兴病原体提供快速准确的诊断。