Digital Microfluidics for Isothermal Nucleic Acid Amplification: Exploring Sensing Methodologies
Autor(a) principal: | |
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Data de Publicação: | 2023 |
Idioma: | eng |
Título da fonte: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
Texto Completo: | http://hdl.handle.net/10362/162097 |
Resumo: | Digital Microfluidics (DMF) has recently emerged as a promising candidate for nucleic acid amplification for molecular diagnostics, by virtue of its precise control over unit droplets without the need of any propulsion devices, ease of integration with chemical/biological reac-tions and multiplex assay capabilities. Nevertheless, current scientific research is still far from accomplishing the full potential of the technique, so new, innovative nanotechnology/biotech-nology hybrid approaches are necessary. As such, the purpose of this work is to contribute for the paradigm shift of nucleic acid amplification from central laboratories to point-of-care (POC) by designing and fabricating DMF devices compatible with isothermal nucleic acid amplifica-tion (loop-mediated isothermal amplification - LAMP). For biological validation of the devices, detection of cancer biomarker c-Myc is performed, and further real-time amplification moni-toring is attempted through several methodologies, namely fluorescence, impedance and elec-trochemical measurements. The DMF devices produced herein enable optimal temperature control, crucial for LAMP reactions, and further allow for a novel methodology of reagent mix-ing, based on dual actuation with back-and-forth motion and actuation frequency tuning. Such innovations lead to successful amplification of 0.5 ng/μL or 90 pg of c-Myc in one hour, in line with the range reported in the literature, and further monitoring of the LAMP reaction profile by microscopy-based fluorescence measurements. Impedimetric and electrochemical method-ologies did not meet the tight criteria required for biomarker detection, yet the developments achieved herein open the path for other applications. Lastly, the dielectric layer (key element of a DMF device) was optimized to assure long reactions (up to two hours) without device degradation. |
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Digital Microfluidics for Isothermal Nucleic Acid Amplification: Exploring Sensing MethodologiesDigital microfluidicsloop-mediated isothermal amplificationreal-time nucleic acid amplification monitoringDomínio/Área Científica::Engenharia e Tecnologia::NanotecnologiaDigital Microfluidics (DMF) has recently emerged as a promising candidate for nucleic acid amplification for molecular diagnostics, by virtue of its precise control over unit droplets without the need of any propulsion devices, ease of integration with chemical/biological reac-tions and multiplex assay capabilities. Nevertheless, current scientific research is still far from accomplishing the full potential of the technique, so new, innovative nanotechnology/biotech-nology hybrid approaches are necessary. As such, the purpose of this work is to contribute for the paradigm shift of nucleic acid amplification from central laboratories to point-of-care (POC) by designing and fabricating DMF devices compatible with isothermal nucleic acid amplifica-tion (loop-mediated isothermal amplification - LAMP). For biological validation of the devices, detection of cancer biomarker c-Myc is performed, and further real-time amplification moni-toring is attempted through several methodologies, namely fluorescence, impedance and elec-trochemical measurements. The DMF devices produced herein enable optimal temperature control, crucial for LAMP reactions, and further allow for a novel methodology of reagent mix-ing, based on dual actuation with back-and-forth motion and actuation frequency tuning. Such innovations lead to successful amplification of 0.5 ng/μL or 90 pg of c-Myc in one hour, in line with the range reported in the literature, and further monitoring of the LAMP reaction profile by microscopy-based fluorescence measurements. Impedimetric and electrochemical method-ologies did not meet the tight criteria required for biomarker detection, yet the developments achieved herein open the path for other applications. Lastly, the dielectric layer (key element of a DMF device) was optimized to assure long reactions (up to two hours) without device degradation.A microfluídica digital (MFD) surgiu como uma tecnologia promissora para amplificação de ácidos nucleicos em diagnóstico molecular, permitindo controlo sobre gotas unitárias sem necessidade de dispositivos de propulsão, facilidade de integração com reações químicas/bi-ológicas e capacidade de realização de ensaios simultâneos. Contudo, a investigação científica atual ainda está longe de atingir o máximo potencial da técnica, pelo que são necessárias abordagens novas, inovadoras e híbridas de nanotecnologia e biotecnologia. Como tal, o pro-pósito deste trabalho é contribuir para a mudança de paradigma da amplificação de ácidos nucleicos de laboratórios centralizados para ponto-de-atendimento (PDA) através do desenho e fabricação de dispositivos de MFD compatíveis com amplificação isotérmica de ácidos nu-cleicos (loop-mediated istothermal amplification - LAMP). Para validação biológica dos dispo-sitivos, será detetado o biomarcador de cancro c-Myc, e testada a monitorização da amplifica-ção em tempo real através de várias metodologias, nomeadamente medidas de fluorescência, impedância ou medidas eletroquímicas. Os dispositivos MFD produzidos permitem um con-trolo ótimo da temperatura, crucial para reações LAMP, e introduzem uma metodologia para mistura de reagentes, com movimentos em vaivém e ajuste da frequência de atuação. Tais inovações conduziram à amplificação de 0.5 ng/μL ou 90 pg de c-Myc em uma hora, em linha com o intervalo relatado na literatura, permitindo ainda monitorização do perfil da reação LAMP através de medidas de fluorescência mediadas por microscopia. As metodologias impe-dimétricas e eletroquímicas não cumpriram os exigentes critérios requeridos para deteção de biomarcadores, no entanto, os desenvolvimentos alcançados abrem caminho para outras apli-cações. Por último, a camada dielétrica (elemento-chave de um dispositivo MFD) foi otimizada para assegurar reações mais longas (até duas horas) sem degradação do dispositivo.Martins, RodrigoBaptista, PedroIgreja, RuiRUNCoelho, Beatriz Jorge2024-01-10T15:29:30Z20232023-01-01T00:00:00Zdoctoral thesisinfo:eu-repo/semantics/publishedVersionapplication/pdfhttp://hdl.handle.net/10362/162097enginfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2024-05-22T18:17:14Zoai:run.unl.pt:10362/162097Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-28T17:47:51.831861Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
dc.title.none.fl_str_mv |
Digital Microfluidics for Isothermal Nucleic Acid Amplification: Exploring Sensing Methodologies |
title |
Digital Microfluidics for Isothermal Nucleic Acid Amplification: Exploring Sensing Methodologies |
spellingShingle |
Digital Microfluidics for Isothermal Nucleic Acid Amplification: Exploring Sensing Methodologies Coelho, Beatriz Jorge Digital microfluidics loop-mediated isothermal amplification real-time nucleic acid amplification monitoring Domínio/Área Científica::Engenharia e Tecnologia::Nanotecnologia |
title_short |
Digital Microfluidics for Isothermal Nucleic Acid Amplification: Exploring Sensing Methodologies |
title_full |
Digital Microfluidics for Isothermal Nucleic Acid Amplification: Exploring Sensing Methodologies |
title_fullStr |
Digital Microfluidics for Isothermal Nucleic Acid Amplification: Exploring Sensing Methodologies |
title_full_unstemmed |
Digital Microfluidics for Isothermal Nucleic Acid Amplification: Exploring Sensing Methodologies |
title_sort |
Digital Microfluidics for Isothermal Nucleic Acid Amplification: Exploring Sensing Methodologies |
author |
Coelho, Beatriz Jorge |
author_facet |
Coelho, Beatriz Jorge |
author_role |
author |
dc.contributor.none.fl_str_mv |
Martins, Rodrigo Baptista, Pedro Igreja, Rui RUN |
dc.contributor.author.fl_str_mv |
Coelho, Beatriz Jorge |
dc.subject.por.fl_str_mv |
Digital microfluidics loop-mediated isothermal amplification real-time nucleic acid amplification monitoring Domínio/Área Científica::Engenharia e Tecnologia::Nanotecnologia |
topic |
Digital microfluidics loop-mediated isothermal amplification real-time nucleic acid amplification monitoring Domínio/Área Científica::Engenharia e Tecnologia::Nanotecnologia |
description |
Digital Microfluidics (DMF) has recently emerged as a promising candidate for nucleic acid amplification for molecular diagnostics, by virtue of its precise control over unit droplets without the need of any propulsion devices, ease of integration with chemical/biological reac-tions and multiplex assay capabilities. Nevertheless, current scientific research is still far from accomplishing the full potential of the technique, so new, innovative nanotechnology/biotech-nology hybrid approaches are necessary. As such, the purpose of this work is to contribute for the paradigm shift of nucleic acid amplification from central laboratories to point-of-care (POC) by designing and fabricating DMF devices compatible with isothermal nucleic acid amplifica-tion (loop-mediated isothermal amplification - LAMP). For biological validation of the devices, detection of cancer biomarker c-Myc is performed, and further real-time amplification moni-toring is attempted through several methodologies, namely fluorescence, impedance and elec-trochemical measurements. The DMF devices produced herein enable optimal temperature control, crucial for LAMP reactions, and further allow for a novel methodology of reagent mix-ing, based on dual actuation with back-and-forth motion and actuation frequency tuning. Such innovations lead to successful amplification of 0.5 ng/μL or 90 pg of c-Myc in one hour, in line with the range reported in the literature, and further monitoring of the LAMP reaction profile by microscopy-based fluorescence measurements. Impedimetric and electrochemical method-ologies did not meet the tight criteria required for biomarker detection, yet the developments achieved herein open the path for other applications. Lastly, the dielectric layer (key element of a DMF device) was optimized to assure long reactions (up to two hours) without device degradation. |
publishDate |
2023 |
dc.date.none.fl_str_mv |
2023 2023-01-01T00:00:00Z 2024-01-10T15:29:30Z |
dc.type.driver.fl_str_mv |
doctoral thesis |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10362/162097 |
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eng |
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