Affiliation:
1. Hebei Key Laboratory of Smart Sensing and Human‐robot Interactions, School of Mechanical Engineering Hebei University of Technology Tianjin P. R. China
2. State Key Laboratory of Reliability and Intelligence of Electrical Equipment Hebei University of Technology Tianjin P. R. China
3. Department of Electrical Engineering and Computer Science The University of Tennessee Knoxville Tennessee USA
4. Institute of Biophysics, School of Health Sciences and Biomedical Engineering Hebei University of Technology Tianjin P. R. China
Abstract
AbstractMeat adulteration detection is a common concern of consumers. Here, we proposed a multiplex digital polymerase chain reaction method and a low‐cost device for meat adulteration detection. Using a polydimethylsiloxane microfluidic device, polymerase chain reaction reagents could be pump‐free loaded into microchambers (40 × 40 chambers) automatically. Due to the independence of multiplex fluorescence channels, deoxyribonucleic acid templates extracted from different animal species could be distinguished by one test. In this paper, we designed primers and probes for four types of meat (beef, chicken, pork, and duck) and labeled each of the four fluorescent markers (hexachlorocyclohexane [HEX], 6‐carboxyfluorescein [FAM], X‐rhodamine [ROX], and cyanine dyes 5 [CY5]) on the probes. Specific detection and mixed detection experiments were performed on four types of meat, realizing a limit of detection of 3 copies/µL. A mixture of four different species can be detected by four independent fluorescence channels. The quantitative capability of this method is found to meet the requirements of meat adulteration detections. This method has great potential for point‐of‐care testing together with portable microscopy equipment.
Funder
National Natural Science Foundation of China
Subject
Clinical Biochemistry,Biochemistry,Analytical Chemistry
Cited by
4 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献