Programmable‐Modulated Ultrasonic Transducer Array for Contactless Detection of Viral RNAs

Author:

Luo Yong12,Zhou Mengyun1,Wang Lirong2,Fan Chuan2,Xu Tailin1ORCID,Zhang Xueji1

Affiliation:

1. School of Biomedical Engineering, Medical School Shenzhen University Shenzhen Guangdong 518060 P. R. China

2. Beijing Key Laboratory for Bioengineering and Sensing Technology University of Science and Technology Beijing Beijing 100083 P. R. China

Abstract

AbstractThe current polymerase chain reactions‐based nucleic acid tests for large‐scale infectious disease diagnosis are always lab‐dependent and generate large amounts of highly infectious plastic waste. Direct non‐linear acoustic driven of microdroplets provide an ideal platform for contactless spatial and temporal manipulation of liquid samples. Here, a strategy to programmable‐manipulate microdroplets using potential pressure well for contactless trace detection is conceptualized and designed. On such contactless modulation platform, up to seventy‐two piezoelectric transducers are precisely self‐focusing single‐axis arranged and controlled, which can generate dynamic pressure nodes for effectively contact‐free manipulating microdroplets without vessel contamination. In addition, the patterned microdroplet array can act as contactless microreactor and allow multiple trace samples (1–5 µL) biochemical analysis, and the ultrasonic vortex can also accelerate non‐equilibrium chemical reactions such as recombinase polymerase amplification (RPA). The results of fluorescence detection indicated that such programmable modulated microdroplet achieved contactless trace nucleic acid detection with a sensitivity of 0.21 copy µL−1 in only 6–14 min, which is 30.3–43.3% shorter than the conventional RPA approach. Such a programmable containerless microdroplet platform can be used for toxic, hazardous, or infectious samples sensing, opening up new avenues for developing future fully automated detection systems.

Publisher

Wiley

Subject

General Materials Science,General Chemistry

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