微流控
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灵敏度(控制系统)
材料科学
分子诊断学
纳米技术
计算机科学
电子工程
生物信息学
化学
色谱法
生物
医学
工程类
护理部
免疫学
作者
Filip Staniszewski,Alexandra Schilder,Lidiya Osinkina,Maximilian Westenthanner,N.A. Kataeva,Barbara Posch,Yasmin Gillitschka,Kilian Stoecker,Kim Silberreis,Sabrina Coen,Angela Cannas,Giulia Matusali,Christina Schmidleithner,Joachim Stehr,Federico Buersgens,Johannes R. Peham
标识
DOI:10.1016/j.bios.2024.116626
摘要
In the past, vast research has been conducted on biosensors and point-of-care (PoC) diagnostics. Despite rapid advances especially during the SARS-CoV-2 pandemic in this research field a low-cost molecular biosensor exhibiting the user-friendliness of a rapid antigen test, and also the sensitivity and specificity of a PCR test, has not been developed yet. To this end we developed a novel microfluidics based and handheld PoC device, that facilitates viral detection at PCR sensitivity and specificity in less than 40 min, including 15 min sample preparation. This was attained by incorporation of pulse controlled amplification (PCA), a method which uses short electrical pulses to rapidly increase the temperature of a small fraction of the sample volume. In this work, we present a low-cost PCA device with a microfluidic consumable intended for the use in a decentralized or home-setting. We used finite element analysis (FEA) simulations to display the fundamental principle and highlight the critical parameter dependency of PCA, such as pulse length and resistor shape. Furthermore, we integrated a simple and fast workflow for sample preparation and evaluated the limit of detection (LoD) for SARS-CoV-2 viral RNA, which is 0.88 copies/μL (=44 copies/reaction), and thus, comparable to conventional RT-qPCR. Additionally, target specificity of the device was validated. Our device and PCA approach enables cost-effective, rapid and mobile molecular diagnostics while remaining highly sensitive and specific.
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