# A Portable Dual-Mode Microfluidic Device Integrating RT-qPCR and RT-LAMP for Rapid Nucleic Acid Detection in Point-of-Care Testing

**Authors:** Baihui Zhang, Xiao Li, Mengjie Huang, Maojie Jiang, Leilei Du, Peng Yin, Xuan Fang, Xiangyu Jiang, Feihu Qi, Yanna Lin, Fuqiang Ma

PMC · DOI: 10.3390/bios16010051 · Biosensors · 2026-01-08

## TL;DR

A portable microfluidic device combines RT-qPCR and RT-LAMP for fast and accurate nucleic acid detection in point-of-care settings.

## Contribution

A dual-mode microfluidic platform integrating RT-qPCR and RT-LAMP with Tesla-valve flow control for rapid, portable nucleic acid detection.

## Key findings

- The device achieves a detection limit of 2.0 copies μL−1 for RT-PCR and 2.95 copies μL−1 for RT-LAMP.
- RT-LAMP assay time is reduced to 42 minutes, significantly faster than traditional methods.
- The system maintains quantitative accuracy comparable to commercial qPCR instruments despite miniaturization.

## Abstract

Point-of-care testing (POCT) has emerged as a vital diagnostic approach in emergency medicine, primary care, and resource-limited environments because of its convenience, affordability, and capacity to provide immediate results. Here, we present a multifunctional portable nucleic acid detection platform integrating reverse transcription polymerase chain reaction (RT-qPCR) and reverse transcription loop-mediated isothermal amplification (RT-LAMP) within a unified microfluidic device. The system leverages Tesla-valve-based passive flow control to enhance reaction efficiency and operational simplicity. A four-channel optical detection unit allows for multiplex fluorescence quantification (CY5, FAM, VIC, ROX) and has high sensitivity and reproducibility for RT-LAMP. The compact design reduces the overall size by approximately 90% compared with conventional qPCR instruments. For RT-PCR, the system achieves a detection limit of 2.0 copies μL−1 and improves analytical efficiency by 27%. For RT-LAMP, the detection limit reaches 2.95 copies μL−1 with a 14% enhancement in analytical efficiency. Compared with commercial qPCR instruments, the device maintains equivalent quantitative accuracy despite significant miniaturization, ensuring reliable performance in decentralized testing. Furthermore, the total RT-LAMP assay time is reduced from more than two hours to 42 min, enabling truly rapid molecular diagnostics. This dual-mode platform offers a flexible, scalable strategy for bridging laboratory-grade molecular assays with real-time POCT applications, supporting early disease detection and epidemic surveillance.

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12839313/full.md

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12839313/full.md

## References

42 references — full list in the complete paper: https://tomesphere.com/paper/PMC12839313/full.md

---
Source: https://tomesphere.com/paper/PMC12839313