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- Publisher Website: 10.1016/j.bios.2023.115831
- Scopus: eid_2-s2.0-85181395339
- PMID: 38008058
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Article: An integrated and multi-functional droplet-based microfluidic platform for digital DNA amplification
Title | An integrated and multi-functional droplet-based microfluidic platform for digital DNA amplification |
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Authors | |
Keywords | Digital LAMP Digital PCR Droplet Gene mutation Microfluidics |
Issue Date | 15-Feb-2024 |
Publisher | Elsevier |
Citation | Biosensors and Bioelectronics, 2024, v. 246 How to Cite? |
Abstract | Digital DNA amplification is a powerful method for detecting and quantifying rare nucleic acids. In this study, we developed a multi-functional droplet-based platform that integrates the traditional digital DNA amplification workflow into a one-step device. This platform enables efficient droplet generation, transition, and signal detection within a 5-min timeframe, distributing the sample into a uniform array of 4 × 104 droplets (variation <2%) within a chamber. Subsequent in-situ DNA amplification, fluorescence detection, and signal analysis were carried out. To assess the platform's performance, we quantitatively detected the human epidermal growth factor receptor (EGFR) mutation and human papillomavirus (HPV) mutation using digital polymerase chain reaction (dPCR) and digital loop-mediated isothermal amplification (dLAMP), respectively. The fluorescence results exhibited a positive, linear, and statistically significant correlation with target DNA concentrations ranging from 101 to 105 copies/μL, demonstrating the capability and feasibility of the integrated device for dPCR and dLAMP. This platform offers high-throughput droplet generation, eliminates droplet fusion and transition, is user-friendly, reduces costs compared to current methods, and holds potential for thermocycling and isothermal nucleic acid quantification with high sensitivity and accuracy. |
Persistent Identifier | http://hdl.handle.net/10722/348253 |
ISSN | 2023 Impact Factor: 10.7 2023 SCImago Journal Rankings: 2.052 |
DC Field | Value | Language |
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dc.contributor.author | Wang, Yuan | - |
dc.contributor.author | Zhou, Xiaoyu | - |
dc.contributor.author | Yang, Zihan | - |
dc.contributor.author | Xu, Tao | - |
dc.contributor.author | Fu, Huayang | - |
dc.contributor.author | Fong, Chi Chun | - |
dc.contributor.author | Sun, Jiayu | - |
dc.contributor.author | Chin, Y Rebecca | - |
dc.contributor.author | Zhang, Liang | - |
dc.contributor.author | Guan, Xinyuan | - |
dc.contributor.author | Yang, Mengsu | - |
dc.date.accessioned | 2024-10-08T00:31:15Z | - |
dc.date.available | 2024-10-08T00:31:15Z | - |
dc.date.issued | 2024-02-15 | - |
dc.identifier.citation | Biosensors and Bioelectronics, 2024, v. 246 | - |
dc.identifier.issn | 0956-5663 | - |
dc.identifier.uri | http://hdl.handle.net/10722/348253 | - |
dc.description.abstract | <p>Digital DNA amplification is a powerful method for detecting and quantifying rare nucleic acids. In this study, we developed a multi-functional droplet-based platform that integrates the traditional digital DNA amplification workflow into a one-step device. This platform enables efficient droplet generation, transition, and signal detection within a 5-min timeframe, distributing the sample into a uniform array of 4 × 104 droplets (variation <2%) within a chamber. Subsequent in-situ DNA amplification, fluorescence detection, and signal analysis were carried out. To assess the platform's performance, we quantitatively detected the human epidermal growth factor receptor (EGFR) mutation and human papillomavirus (HPV) mutation using digital polymerase chain reaction (dPCR) and digital loop-mediated isothermal amplification (dLAMP), respectively. The fluorescence results exhibited a positive, linear, and statistically significant correlation with target DNA concentrations ranging from 101 to 105 copies/μL, demonstrating the capability and feasibility of the integrated device for dPCR and dLAMP. This platform offers high-throughput droplet generation, eliminates droplet fusion and transition, is user-friendly, reduces costs compared to current methods, and holds potential for thermocycling and isothermal nucleic acid quantification with high sensitivity and accuracy.</p> | - |
dc.language | eng | - |
dc.publisher | Elsevier | - |
dc.relation.ispartof | Biosensors and Bioelectronics | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Digital LAMP | - |
dc.subject | Digital PCR | - |
dc.subject | Droplet | - |
dc.subject | Gene mutation | - |
dc.subject | Microfluidics | - |
dc.title | An integrated and multi-functional droplet-based microfluidic platform for digital DNA amplification | - |
dc.type | Article | - |
dc.identifier.doi | 10.1016/j.bios.2023.115831 | - |
dc.identifier.pmid | 38008058 | - |
dc.identifier.scopus | eid_2-s2.0-85181395339 | - |
dc.identifier.volume | 246 | - |
dc.identifier.eissn | 1873-4235 | - |
dc.identifier.issnl | 0956-5663 | - |