TY - JOUR
T1 - An integrated microfluidic platform for rapid detection and subtyping of influenza viruses from clinical samples
AU - Tai, Chien Hsuan
AU - Tsai, Yi Che
AU - Wang, Chih Hung
AU - Ho, Tzong Shiann
AU - Chang, Chih Peng
AU - Lee, Gwo Bin
N1 - Funding Information:
Acknowledgments The authors would like to thank the National Science Council in Taiwan for financial support (NSC101-2120-M-007-014). Partial financial support from the Towards a World-Class University Project is also greatly appreciated.
PY - 2014/3
Y1 - 2014/3
N2 - This study reports on the development of an integrated microfluidic system that performs sample pretreatment, nucleic acid amplification, and optical detection for molecular diagnosis of influenza viruses. The entire analysis protocol including virus lysis, extraction of ribonucleic acid, reverse transcription, polymerase chain reaction, and optical detection was successfully performed using the microfluidic system, which automatically performed the rapid diagnosis and subtyping of the influenza viruses. Signals obtained from an optical detection module could accurately differentiate influenza A/H1 (infA/H1), influenza A/H3 (infA/H3), influenza B (infB), and positive and negative control samples. More importantly, the entire process could be integrated and performed automatically with less human intervention. The experimental results demonstrated that this developed microfluidic system can successfully distinguish between infA/H1, infA/H3, and infB within 60 min. Furthermore, oral swabs from 92 patients were successfully tested using the developed microfluidic system. Thus, it may be a promising tool for rapid detection of novel and seasonal influenza strains in the near future.
AB - This study reports on the development of an integrated microfluidic system that performs sample pretreatment, nucleic acid amplification, and optical detection for molecular diagnosis of influenza viruses. The entire analysis protocol including virus lysis, extraction of ribonucleic acid, reverse transcription, polymerase chain reaction, and optical detection was successfully performed using the microfluidic system, which automatically performed the rapid diagnosis and subtyping of the influenza viruses. Signals obtained from an optical detection module could accurately differentiate influenza A/H1 (infA/H1), influenza A/H3 (infA/H3), influenza B (infB), and positive and negative control samples. More importantly, the entire process could be integrated and performed automatically with less human intervention. The experimental results demonstrated that this developed microfluidic system can successfully distinguish between infA/H1, infA/H3, and infB within 60 min. Furthermore, oral swabs from 92 patients were successfully tested using the developed microfluidic system. Thus, it may be a promising tool for rapid detection of novel and seasonal influenza strains in the near future.
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U2 - 10.1007/s10404-013-1249-y
DO - 10.1007/s10404-013-1249-y
M3 - Article
AN - SCOPUS:84896404026
SN - 1613-4982
VL - 16
SP - 501
EP - 512
JO - Microfluidics and Nanofluidics
JF - Microfluidics and Nanofluidics
IS - 3
ER -