Finite element analysis of microfluidic device for Escherichia coli separation from blood-cells for early diagnosis of sepsis
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F46747885%3A24210%2F25%3A00013740" target="_blank" >RIV/46747885:24210/25:00013740 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/46747885:24620/25:00013740
Výsledek na webu
<a href="https://www.sciencedirect.com/science/article/pii/S2590123025026271?pes=vor&utm_source=scopus&getft_integrator=scopus" target="_blank" >https://www.sciencedirect.com/science/article/pii/S2590123025026271?pes=vor&utm_source=scopus&getft_integrator=scopus</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.rineng.2025.106558" target="_blank" >10.1016/j.rineng.2025.106558</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Finite element analysis of microfluidic device for Escherichia coli separation from blood-cells for early diagnosis of sepsis
Popis výsledku v původním jazyce
Blood cell separation and infectious microorganism detection were investigated using COMSOL Multiphysics (R) 5.3a simulation software for finite element analysis (FEA). FEA was used as a preliminary study to optimize physical prototypes and experiments using related numerical techniques. The separation of white blood cells (WBCs) from other particles in the blood sample was achieved through solid-phase microextraction, which relies on size-based separation, whereas the detection of infectious microorganisms was based on their electrical properties. Both these separation and detection methods can be implemented on a microfluidic device with simple processes. The FEA studies demonstrate an efficient microfluidic channel design for optimized flow, enabling blood cell separation through microchannel width manipulation and the detection of infectious microorganisms via applied dielectrophoretic force. The simulation results indicated that a flow rate of 0.05 mL/ min at 3 MHz yields a high recovery efficiency of 85 %, with separation accomplished in below 10 min. Furthermore, fluorescence-based cell counting confirmed a WBC count of 2.0 x 109/L in the designated counting channel, aligning well with the simulation results. The findings proved that early diagnosis of sepsis is effectively possible through rapid WBC analysis and identification of specific infectious microorganisms using a microfluidic device, enabling timely point-of-care treatment without side effects.
Název v anglickém jazyce
Finite element analysis of microfluidic device for Escherichia coli separation from blood-cells for early diagnosis of sepsis
Popis výsledku anglicky
Blood cell separation and infectious microorganism detection were investigated using COMSOL Multiphysics (R) 5.3a simulation software for finite element analysis (FEA). FEA was used as a preliminary study to optimize physical prototypes and experiments using related numerical techniques. The separation of white blood cells (WBCs) from other particles in the blood sample was achieved through solid-phase microextraction, which relies on size-based separation, whereas the detection of infectious microorganisms was based on their electrical properties. Both these separation and detection methods can be implemented on a microfluidic device with simple processes. The FEA studies demonstrate an efficient microfluidic channel design for optimized flow, enabling blood cell separation through microchannel width manipulation and the detection of infectious microorganisms via applied dielectrophoretic force. The simulation results indicated that a flow rate of 0.05 mL/ min at 3 MHz yields a high recovery efficiency of 85 %, with separation accomplished in below 10 min. Furthermore, fluorescence-based cell counting confirmed a WBC count of 2.0 x 109/L in the designated counting channel, aligning well with the simulation results. The findings proved that early diagnosis of sepsis is effectively possible through rapid WBC analysis and identification of specific infectious microorganisms using a microfluidic device, enabling timely point-of-care treatment without side effects.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
21100 - Other engineering and technologies
Návaznosti výsledku
Projekt
<a href="/cs/project/EF16_025%2F0007293" target="_blank" >EF16_025/0007293: Modulární platforma pro autonomní podvozky specializovaných elektrovozidel pro dopravu nákladu a zařízení</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
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
Results in Engineering>
ISSN
2590-1230
e-ISSN
—
Svazek periodika
27
Číslo periodika v rámci svazku
SEP
Stát vydavatele periodika
NL - Nizozemsko
Počet stran výsledku
11
Strana od-do
—
Kód UT WoS článku
001544957000001
EID výsledku v databázi Scopus
2-s2.0-105012267348