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Low-power microfluidic RT-LAMP system with real-time fluorescence detection for portable nucleic acid testing

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216305%3A26220%2F26%3A0200011" target="_blank" >RIV/00216305:26220/26:0200011 - isvavai.cz</a>

  • Výsledek na webu

    <a href="https://link.springer.com/article/10.1007/s00604-025-07680-2" target="_blank" >https://link.springer.com/article/10.1007/s00604-025-07680-2</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00604-025-07680-2" target="_blank" >10.1007/s00604-025-07680-2</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Low-power microfluidic RT-LAMP system with real-time fluorescence detection for portable nucleic acid testing

  • Popis výsledku v původním jazyce

    A microfluidic reverse transcription loop-mediated isothermal amplification (RT-LAMP) platform is presented featuring integrated real-time fluorescence detection and optimized thermal control. Magnetic bead-based RNA extraction was paired with a thermally insulated reaction chip operated under vacuum to suppress heat loss. Additional energy-saving strategies, including reduced wire cross-section and low-emissivity surface treatment, reduced total power consumption from (2.00 +/- 0.08) W to (0.29 +/- 0.01) W, corresponding to an 85.5 % reduction. Amplification was completed within 20 min, and positive fluorescence signals were detected in less than 11 min. Although LAMP reagents remain more expensive than those used in PCR, the substantial energy savings and system simplification demonstrated here support practical battery-powered operation. The RT-LAMP chemistry used in this system matched a previously validated configuration, which achieved a limit of detection of 256 RNA copies and a signal slope of (- 1.70 +/- 0.20) dec.min(-)1. These parameters remained consistent under the current setup, as power consumption did not influence detection sensitivity provided the reaction temperature was maintained. The platform enables low-power, real-time nucleic acid detection suited for decentralized diagnostics, forensic screening, and environmental monitoring.

  • Název v anglickém jazyce

    Low-power microfluidic RT-LAMP system with real-time fluorescence detection for portable nucleic acid testing

  • Popis výsledku anglicky

    A microfluidic reverse transcription loop-mediated isothermal amplification (RT-LAMP) platform is presented featuring integrated real-time fluorescence detection and optimized thermal control. Magnetic bead-based RNA extraction was paired with a thermally insulated reaction chip operated under vacuum to suppress heat loss. Additional energy-saving strategies, including reduced wire cross-section and low-emissivity surface treatment, reduced total power consumption from (2.00 +/- 0.08) W to (0.29 +/- 0.01) W, corresponding to an 85.5 % reduction. Amplification was completed within 20 min, and positive fluorescence signals were detected in less than 11 min. Although LAMP reagents remain more expensive than those used in PCR, the substantial energy savings and system simplification demonstrated here support practical battery-powered operation. The RT-LAMP chemistry used in this system matched a previously validated configuration, which achieved a limit of detection of 256 RNA copies and a signal slope of (- 1.70 +/- 0.20) dec.min(-)1. These parameters remained consistent under the current setup, as power consumption did not influence detection sensitivity provided the reaction temperature was maintained. The platform enables low-power, real-time nucleic acid detection suited for decentralized diagnostics, forensic screening, and environmental monitoring.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    10406 - Analytical chemistry

Návaznosti výsledku

  • Projekt

    <a href="/cs/project/TN02000017" target="_blank" >TN02000017: Národní Centrum Biotechnologií ve Veterinární Medicíně</a><br>

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach

Ostatní

  • Rok uplatnění

    2025

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    MICROCHIMICA ACTA

  • ISSN

    0026-3672

  • e-ISSN

    1436-5073

  • Svazek periodika

    1

  • Číslo periodika v rámci svazku

    193

  • Stát vydavatele periodika

    AT - Rakouská republika

  • Počet stran výsledku

    12

  • Strana od-do

  • Kód UT WoS článku

    001644808100001

  • EID výsledku v databázi Scopus