Development of a Microfluidic Point-of-Care Platform for HPV Detection Based on Helicase-Dependent Amplification.

IF 2.6 4区 医学 Q2 INFECTIOUS DISEASES
Everardo González-González, Elda A Flores-Contreras, Gerardo de Jesús Trujillo-Rodríguez, Mariana Lizbeth Jiménez-Martínez, Iram P Rodríguez-Sánchez, Adriana Ancer-Arellano, Salomon Alvarez-Cuevas, Margarita L Martinez-Fierro, Iván A Marino-Martínez, Idalia Garza-Veloz
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引用次数: 0

Abstract

Human papillomavirus (HPV) is the most prevalent sexually transmitted infection worldwide and a leading cause of cervical cancer, accounting for over 300,000 deaths annually, primarily due to high-risk genotypes HPV-16 and HPV-18. Conventional molecular diagnostic methods, such as polymerase chain reaction (PCR), require expensive instrumentation and well-equipped laboratories, which limits their applicability in low-resource or decentralized settings. To address this challenge, the aim of this study was to develop a prototype point-of-care (POC) diagnostic platform based on helicase-dependent amplification (HDA) integrated into a microfluidic device for the specific detection of HPV-16 and HPV-18. The proposed POC platform comprises a disposable poly (methyl methacrylate) (PMMA) microfluidic device, a portable warming mat for isothermal amplification at 65 °C, and a compact electrophoresis chamber for fluorescence-based visualization using SYBR Safe dye, with an approximate total cost of $320 USD. Platform validation was performed on 33 samples, demonstrating amplification of target sequences in less than 60 min with only 20 µL of reaction volume, a limit of detection (LOD) of 15 copies (cp) per reaction, a sensitivity of 95.52%, and a specificity of 100%. This portable and scalable platform constitutes a cost-effective and reliable tool for the detection of HPV, supporting global health initiatives, including those driven by the World Health Organization (WHO), aimed at eliminating cervical cancer as a public health threat, as it can be implemented in decentralized or resource-limited settings.

基于解旋酶依赖扩增的HPV检测微流控护理点平台的开发。
人类乳头瘤病毒(HPV)是世界上最普遍的性传播感染,也是宫颈癌的主要原因,每年造成30多万人死亡,主要是由于高危基因型HPV-16和HPV-18。传统的分子诊断方法,如聚合酶链反应(PCR),需要昂贵的仪器和设备齐全的实验室,这限制了它们在资源匮乏或分散环境中的适用性。为了解决这一挑战,本研究的目的是开发一个基于解旋酶依赖性扩增(HDA)的原型护理点(POC)诊断平台,该平台集成到一个微流控装置中,用于特异性检测HPV-16和HPV-18。提议的POC平台包括一个一次性聚甲基丙烯酸甲酯(PMMA)微流控装置,一个用于65°C等温扩增的便携式加热垫,以及一个使用SYBR安全染料进行荧光可视化的紧凑电泳室,总成本约为320美元。对33个样品进行了平台验证,结果表明,在不到60分钟的时间内,仅用20µL的反应体积扩增目标序列,每个反应的检出限(LOD)为15拷贝(cp),灵敏度为95.52%,特异性为100%。这种便携式和可扩展的平台是一种具有成本效益和可靠的HPV检测工具,支持全球卫生倡议,包括世界卫生组织(世卫组织)推动的旨在消除作为公共卫生威胁的宫颈癌的倡议,因为它可以在分散或资源有限的环境中实施。
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
Tropical Medicine and Infectious Disease
Tropical Medicine and Infectious Disease Medicine-Public Health, Environmental and Occupational Health
CiteScore
3.90
自引率
10.30%
发文量
353
审稿时长
11 weeks
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