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Article: Hand-Powered Microfluidics for Parallel Droplet Digital Loop-Mediated Isothermal Amplification Assays

TitleHand-Powered Microfluidics for Parallel Droplet Digital Loop-Mediated Isothermal Amplification Assays
Authors
Keywordscompartmentalization
droplet digital loop-mediated isothermal amplification
droplet generation
droplet microfluidics
multi-sample detection
nucleic acid quantification
pathogen detection
Issue Date27-Aug-2021
PublisherAmerican Chemical Society
Citation
ACS Sensors, 2021, v. 6, n. 8, p. 2868-2874 How to Cite?
Abstract

Droplet digital loop-mediated isothermal amplification (ddLAMP) is an important assay for pathogen detection due to its high accuracy, specificity, and ability to quantify nucleic acids. However, performing ddLAMP requires expensive instrumentation and the need for highly trained personnel with expertise in microfluidics. To make ddLAMP more accessible, a ddLAMP assay is developed, featuring significantly decreased operational difficulty and instrumentation requirements. The proposed assay consists of three simplified steps: (1) droplet generation step, in which a LAMP mixture can be emulsified just by manually pulling a syringe connected to a microfluidic device. In this step, for the first time, we verify that highly monodispersed droplets can be generated with unstable flow rates or pressures, allowing untrained personnel to operate the microfluidic device and perform ddLAMP assay; (2) heating step, in which the droplets are isothermally heated in a water bath, which can be found in most laboratories; and (3) result analysis step, in which the ddLAMP result can be determined using only a fluorescence microscopy and an open-source analyzing software. Throughout the process, no droplet microfluidic expertise or equipment is required. More importantly, the proposed system enables multiple samples to be processed simultaneously with a detection limit of 10 copies/μL. The test is simple and intuitive to operate in most laboratories for multi-sample detection, significantly enhancing the accessibility and detection throughput of the ddLAMP technique.


Persistent Identifierhttp://hdl.handle.net/10722/344821
ISSN
2023 Impact Factor: 8.2
2023 SCImago Journal Rankings: 1.701

 

DC FieldValueLanguage
dc.contributor.authorYuan, Hao-
dc.contributor.authorTian, Jingxuan-
dc.contributor.authorChao, Youchuang-
dc.contributor.authorChien, Yuh Shiuan-
dc.contributor.authorLuo, Ren Hao-
dc.contributor.authorGuo, Jun Yu-
dc.contributor.authorLi, Shanshan-
dc.contributor.authorChou, Yi Ju-
dc.contributor.authorShum, Ho Cheung-
dc.contributor.authorChen, Chien Fu-
dc.date.accessioned2024-08-12T04:07:38Z-
dc.date.available2024-08-12T04:07:38Z-
dc.date.issued2021-08-27-
dc.identifier.citationACS Sensors, 2021, v. 6, n. 8, p. 2868-2874-
dc.identifier.issn2379-3694-
dc.identifier.urihttp://hdl.handle.net/10722/344821-
dc.description.abstract<p>Droplet digital loop-mediated isothermal amplification (ddLAMP) is an important assay for pathogen detection due to its high accuracy, specificity, and ability to quantify nucleic acids. However, performing ddLAMP requires expensive instrumentation and the need for highly trained personnel with expertise in microfluidics. To make ddLAMP more accessible, a ddLAMP assay is developed, featuring significantly decreased operational difficulty and instrumentation requirements. The proposed assay consists of three simplified steps: (1) droplet generation step, in which a LAMP mixture can be emulsified just by manually pulling a syringe connected to a microfluidic device. In this step, for the first time, we verify that highly monodispersed droplets can be generated with unstable flow rates or pressures, allowing untrained personnel to operate the microfluidic device and perform ddLAMP assay; (2) heating step, in which the droplets are isothermally heated in a water bath, which can be found in most laboratories; and (3) result analysis step, in which the ddLAMP result can be determined using only a fluorescence microscopy and an open-source analyzing software. Throughout the process, no droplet microfluidic expertise or equipment is required. More importantly, the proposed system enables multiple samples to be processed simultaneously with a detection limit of 10 copies/μL. The test is simple and intuitive to operate in most laboratories for multi-sample detection, significantly enhancing the accessibility and detection throughput of the ddLAMP technique.</p>-
dc.languageeng-
dc.publisherAmerican Chemical Society-
dc.relation.ispartofACS Sensors-
dc.subjectcompartmentalization-
dc.subjectdroplet digital loop-mediated isothermal amplification-
dc.subjectdroplet generation-
dc.subjectdroplet microfluidics-
dc.subjectmulti-sample detection-
dc.subjectnucleic acid quantification-
dc.subjectpathogen detection-
dc.titleHand-Powered Microfluidics for Parallel Droplet Digital Loop-Mediated Isothermal Amplification Assays-
dc.typeArticle-
dc.identifier.doi10.1021/acssensors.1c00184-
dc.identifier.pmid34156242-
dc.identifier.scopuseid_2-s2.0-85110260067-
dc.identifier.volume6-
dc.identifier.issue8-
dc.identifier.spage2868-
dc.identifier.epage2874-
dc.identifier.eissn2379-3694-
dc.identifier.issnl2379-3694-

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