A rapid, instrument-free, sample-to-result nucleic acid amplification test
Autor: | Sujatha Kumar, Lisa Lafleur, Joshua D. Bishop, Xiaohong Zhang, Enos Kline, Peter Kauffman, Barry R. Lutz, Nicolaas M. J. Vermeulen, Ryan Gallagher, Paul Yager, Bhushan J. Toley, Joshua R. Buser, Paula D. Ladd, Noah Scarr, Samantha A. Byrnes, Erin K. Heiniger, Walt Mahoney, Yevgeniy S. Belousov, Maxwell Wheeler |
---|---|
Rok vydání: | 2016 |
Předmět: |
Methicillin-Resistant Staphylococcus aureus
Paper Time Factors Chromatography Sample (material) 010401 analytical chemistry Sample processing Biomedical Engineering Loop-mediated isothermal amplification Bioengineering Equipment Design 02 engineering and technology General Chemistry Nose Biology 021001 nanoscience & nanotechnology 01 natural sciences Biochemistry Molecular biology 0104 chemical sciences Nucleic acid Humans Nucleic Acid Amplification Tests 0210 nano-technology Nucleic Acid Amplification Techniques |
Zdroj: | Lab on a Chip. 16:3777-3787 |
ISSN: | 1473-0189 1473-0197 |
Popis: | The prototype demonstrated here is the first fully integrated sample-to-result diagnostic platform for performing nucleic acid amplification tests that requires no permanent instrument or manual sample processing. The multiplexable autonomous disposable nucleic acid amplification test (MAD NAAT) is based on two-dimensional paper networks, which enable sensitive chemical detection normally reserved for laboratories to be carried out anywhere by untrained users. All reagents are stored dry in the disposable test device and are rehydrated by stored buffer. The paper network is physically multiplexed to allow independent isothermal amplification of multiple targets; each amplification reaction is also chemically multiplexed with an internal amplification control. The total test time is less than one hour. The MAD NAAT prototype was used to characterize a set of human nasal swab specimens pre-screened for methicillin-resistant Staphylococcus aureus (MRSA) bacteria. With qPCR as the quantitative reference method, the lowest input copy number in the range where the MAD NAAT prototype consistently detected MRSA in these specimens was ∼5 × 10(3) genomic copies (∼600 genomic copies per biplexed amplification reaction). |
Databáze: | OpenAIRE |
Externí odkaz: |