Generating Microdroplet Array on Photonic Pseudo-paper for Absolute Quantification of Nucleic Acids
Source abstract
Abstract
Here, we propose a new platform for digital nucleic acid assay based on a microdroplet array. The hydrophilic-superhydrophobic property of the pseudopaper photonic nitrocellulose substrate is employed to divide an aqueous sample containing the target nucleic acid into hundreds of microdroplets for loop-mediated isothermal amplification (LAMP). The LAMP reaction leads to the production of fluorescent calcein. By counting the number of microdroplets that are fluorescent, the target nucleic acid (i.e., Staphylococcus aureus DNA) with the copy number ranging from 1 to 1000 can be absolutely quantified without using sophisticated microfluidic devices. The effect of fluorescence enhancement attributed to the photonic nitrocellulose can effectively amplify the detection signal and reduce the amplification time. Thus, we believe that the proposed platform for digital nucleic acid assay based on the microdroplet array is promising for rapid and cost-effective bioanalytical applications.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Biosensors and Analytical Detection · Innovative Microfluidic and Catalytic Techniques Innovation · Electrowetting and Microfluidic Technologies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
State Key Laboratory of Bioelectronics, School of Biological Science and Medical Engineering, Southeast University, Nanjing 210096, China
Funding
Ministry of Education of the People's Republic of China · Ministry of Science and Technology of the People's Republic of China · Government of Jiangsu Province · Central Committee of the Communist Party of China · State Key Laboratory of Bioelectronics, Southeast University
References (40)
Show source-provided references
1. 10.1021/ac103230c10.1021/ac103230c ↗
2. 10.1186/1471-2164-10-11610.1186/1471-2164-10-116 ↗
3. 10.1073/pnas.070576510410.1073/pnas.0705765104 ↗
4. 10.1126/science.113137010.1126/science.1131370 ↗
5. 10.1373/clinchem.2013.20635910.1373/clinchem.2013.206359 ↗
6. 10.1016/j.bios.2017.05.02110.1016/j.bios.2017.05.021 ↗
7. 10.1021/acsnano.5b0733810.1021/acsnano.5b07338 ↗
8. 10.1038/nmeth.263310.1038/nmeth.2633 ↗
9. 10.1021/acs.analchem.7b0003110.1021/acs.analchem.7b00031 ↗
10. 10.1039/c2lc21247a10.1039/c2lc21247a ↗
11. 10.1021/ac900403z10.1021/ac900403z ↗
12. 10.1093/nar/gkq107410.1093/nar/gkq1074 ↗
13. 10.1039/c2lc40774d10.1039/c2lc40774d ↗
14. 10.1021/acs.analchem.7b0404010.1021/acs.analchem.7b04040 ↗
15. 10.1039/c004521g10.1039/c004521g ↗
16. 10.1039/c1lc20561g10.1039/c1lc20561g ↗
17. 10.1021/ac202028g10.1021/ac202028g ↗
18. 10.1021/acs.analchem.7b0327910.1021/acs.analchem.7b03279 ↗
19. 10.1039/c2lc21147e10.1039/c2lc21147e ↗
20. 10.1177/247263031770568010.1177/2472630317705680 ↗
21. 10.1002/anie.20120046010.1002/anie.201200460 ↗
22. 10.1039/C1LC20582J10.1039/C1LC20582J ↗
23. 10.1016/j.jcis.2010.06.03610.1016/j.jcis.2010.06.036 ↗
24. 10.1039/b806706f10.1039/b806706f ↗
25. 10.1002/adma.20150211510.1002/adma.201502115 ↗
26. 10.1002/adma.20160235010.1002/adma.201602350 ↗
27. 10.1002/adhm.20160051810.1002/adhm.201600518 ↗
28. 10.1021/am509177s10.1021/am509177s ↗
29. 10.1002/adfm.20180044810.1002/adfm.201800448 ↗
30. 10.1002/adfm.20130078010.1002/adfm.201300780 ↗
31. 10.1002/adma.20140370910.1002/adma.201403709 ↗
32. 10.1002/adma.20160024710.1002/adma.201600247 ↗
33. 10.1002/adma.20080233910.1002/adma.200802339 ↗
34. 10.1002/anie.20140068610.1002/anie.201400686 ↗
35. 10.1002/anie.20170475210.1002/anie.201704752 ↗
36. 10.1002/smll.20140364010.1002/smll.201403640 ↗
37. 10.1038/nprot.2008.5710.1038/nprot.2008.57 ↗
38. 10.1016/j.ijmultiphaseflow.2010.08.00510.1016/j.ijmultiphaseflow.2010.08.005 ↗
39. 10.1039/c2lc40100b10.1039/c2lc40100b ↗
40. 10.1021/ac500208w10.1021/ac500208w ↗