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constitutive fluid dynamic equations for modeling blood plasma microchannel  (COMSOL Inc)

 
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    Structured Review

    COMSOL Inc constitutive fluid dynamic equations for modeling blood plasma microchannel
    ( A ) The schematic of the trifurcation <t>microchannel</t> geometry model. ( B ) The meshed geometry of the model includes an inset zoom-in view, which illustrates the triangular-shaped mesh elements with higher density near the channel bifurcation.
    Constitutive Fluid Dynamic Equations For Modeling Blood Plasma Microchannel, supplied by COMSOL Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/models+of+the+microchannels/pmc11852766-112-7-12?v=COMSOL+Inc
    Average 90 stars, based on 1 article reviews
    constitutive fluid dynamic equations for modeling blood plasma microchannel - by Bioz Stars, 2026-07
    90/100 stars

    Images

    1) Product Images from "Intelligent Microfluidics for Plasma Separation: Integrating Computational Fluid Dynamics and Machine Learning for Optimized Microchannel Design"

    Article Title: Intelligent Microfluidics for Plasma Separation: Integrating Computational Fluid Dynamics and Machine Learning for Optimized Microchannel Design

    Journal: Biosensors

    doi: 10.3390/bios15020094

    ( A ) The schematic of the trifurcation microchannel geometry model. ( B ) The meshed geometry of the model includes an inset zoom-in view, which illustrates the triangular-shaped mesh elements with higher density near the channel bifurcation.
    Figure Legend Snippet: ( A ) The schematic of the trifurcation microchannel geometry model. ( B ) The meshed geometry of the model includes an inset zoom-in view, which illustrates the triangular-shaped mesh elements with higher density near the channel bifurcation.

    Techniques Used:

    Comparative study of  microchannel  design optimization for blood plasma separation.
    Figure Legend Snippet: Comparative study of microchannel design optimization for blood plasma separation.

    Techniques Used: Clinical Proteomics, High Throughput Screening Assay, Software



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    ( A ) The schematic of the trifurcation <t>microchannel</t> geometry model. ( B ) The meshed geometry of the model includes an inset zoom-in view, which illustrates the triangular-shaped mesh elements with higher density near the channel bifurcation.
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    Image Search Results


    ( A ) The schematic of the trifurcation microchannel geometry model. ( B ) The meshed geometry of the model includes an inset zoom-in view, which illustrates the triangular-shaped mesh elements with higher density near the channel bifurcation.

    Journal: Biosensors

    Article Title: Intelligent Microfluidics for Plasma Separation: Integrating Computational Fluid Dynamics and Machine Learning for Optimized Microchannel Design

    doi: 10.3390/bios15020094

    Figure Lengend Snippet: ( A ) The schematic of the trifurcation microchannel geometry model. ( B ) The meshed geometry of the model includes an inset zoom-in view, which illustrates the triangular-shaped mesh elements with higher density near the channel bifurcation.

    Article Snippet: These three constitutive fluid dynamic equations for modeling blood plasma microchannel in COMSOL are as follows: The Reynolds number (Re): (2) Re = ρ v D h μ Here, ρ is the density of the blood, v is the inlet velocity provided to the microchannel, Dh is a characteristic length, and μ is the dynamic viscosity of the blood.

    Techniques:

    Comparative study of  microchannel  design optimization for blood plasma separation.

    Journal: Biosensors

    Article Title: Intelligent Microfluidics for Plasma Separation: Integrating Computational Fluid Dynamics and Machine Learning for Optimized Microchannel Design

    doi: 10.3390/bios15020094

    Figure Lengend Snippet: Comparative study of microchannel design optimization for blood plasma separation.

    Article Snippet: These three constitutive fluid dynamic equations for modeling blood plasma microchannel in COMSOL are as follows: The Reynolds number (Re): (2) Re = ρ v D h μ Here, ρ is the density of the blood, v is the inlet velocity provided to the microchannel, Dh is a characteristic length, and μ is the dynamic viscosity of the blood.

    Techniques: Clinical Proteomics, High Throughput Screening Assay, Software

    Working principle of the microfluidic impedance flow cytometer leveraging a virtual constriction microchannel formed by crossflow of conductive sample and insulated sheath fluids with underneath micro-electrodes for impedance measurements, including ( a ) schematic of the microfluidic impedance flow cytometer utilizing virtual constriction microchannel and ( b ) a typcial single-cell pluse and and its formation: as a cell travels through the virtual constriction microchannel between two electrodes, in amplitude, there is a peak due to blockage of electrical lines and then a dip because of expansion of the sample-sheath boundaries due to the traveling cell. As to phase variations, at high frequency domain (e.g., 2.5 MHz), there is a clear dip while at low frequency domain (e.g., 400 kHz), the phase profiles may be affected by the electrical double layer

    Journal: Microsystems & Nanoengineering

    Article Title: Microfluidic impedance flow cytometer leveraging virtual constriction microchannel and its application in leukocyte differential

    doi: 10.1038/s41378-024-00833-y

    Figure Lengend Snippet: Working principle of the microfluidic impedance flow cytometer leveraging a virtual constriction microchannel formed by crossflow of conductive sample and insulated sheath fluids with underneath micro-electrodes for impedance measurements, including ( a ) schematic of the microfluidic impedance flow cytometer utilizing virtual constriction microchannel and ( b ) a typcial single-cell pluse and and its formation: as a cell travels through the virtual constriction microchannel between two electrodes, in amplitude, there is a peak due to blockage of electrical lines and then a dip because of expansion of the sample-sheath boundaries due to the traveling cell. As to phase variations, at high frequency domain (e.g., 2.5 MHz), there is a clear dip while at low frequency domain (e.g., 400 kHz), the phase profiles may be affected by the electrical double layer

    Article Snippet: As to numerical simulation, a 3D simulation model of the virtual constriction microchannel was established using COMSOL Multiphysics 5.5.

    Techniques: Flow Cytometry

    Impedance amplitude and phase profiles of individual ( a ) K562, ( b ) Jurkat, and ( c ) HL-60 traveling through the virtual constriction microchannel with representative microscopic images shown in ( d ) where the expansion of the sample-sheath boundaries due to a traveling cell was noticed

    Journal: Microsystems & Nanoengineering

    Article Title: Microfluidic impedance flow cytometer leveraging virtual constriction microchannel and its application in leukocyte differential

    doi: 10.1038/s41378-024-00833-y

    Figure Lengend Snippet: Impedance amplitude and phase profiles of individual ( a ) K562, ( b ) Jurkat, and ( c ) HL-60 traveling through the virtual constriction microchannel with representative microscopic images shown in ( d ) where the expansion of the sample-sheath boundaries due to a traveling cell was noticed

    Article Snippet: As to numerical simulation, a 3D simulation model of the virtual constriction microchannel was established using COMSOL Multiphysics 5.5.

    Techniques:

    Impedance amplitude and phase profiles of individual ( a ) NEU, ( b ) EOS, ( c ) MON, and ( d ) LYM from Donor 1, Donor 2, and Donor 3 traveling through the virtual constriction microchannel

    Journal: Microsystems & Nanoengineering

    Article Title: Microfluidic impedance flow cytometer leveraging virtual constriction microchannel and its application in leukocyte differential

    doi: 10.1038/s41378-024-00833-y

    Figure Lengend Snippet: Impedance amplitude and phase profiles of individual ( a ) NEU, ( b ) EOS, ( c ) MON, and ( d ) LYM from Donor 1, Donor 2, and Donor 3 traveling through the virtual constriction microchannel

    Article Snippet: As to numerical simulation, a 3D simulation model of the virtual constriction microchannel was established using COMSOL Multiphysics 5.5.

    Techniques:

    Simulated in vitro and in vivo oxygen concentrations in the tissue unit as a function of islet perifusion rate 10 min after introducing glucose (28 mM) in the bulk fluid (a). Surface plots of oxygen concentration gradient across the tissue unit with radial and longitudinal cross‐sections halfway through the unit. The average oxygen concentration at the islet cores farthest from the microchannel (worst‐case scenario) plotted at (b) 160 mmHg and (c) 95 mmHg inlet pO 2 . Simulations at arterial pO 2 levels suggest that at least 100 nl/min/IEQ (***) is required to be within the oxygen threshold of uninhibited maximal insulin production (0.034 mol/m 3 ). See Table for correlation between perifusion rate and islet density loading levels. Statistical significance is expressed as * p < .05 and ** p < .001

    Journal: Bioengineering & Translational Medicine

    Article Title: Characterization of human islet function in a convection‐driven intravascular bioartificial pancreas

    doi: 10.1002/btm2.10444

    Figure Lengend Snippet: Simulated in vitro and in vivo oxygen concentrations in the tissue unit as a function of islet perifusion rate 10 min after introducing glucose (28 mM) in the bulk fluid (a). Surface plots of oxygen concentration gradient across the tissue unit with radial and longitudinal cross‐sections halfway through the unit. The average oxygen concentration at the islet cores farthest from the microchannel (worst‐case scenario) plotted at (b) 160 mmHg and (c) 95 mmHg inlet pO 2 . Simulations at arterial pO 2 levels suggest that at least 100 nl/min/IEQ (***) is required to be within the oxygen threshold of uninhibited maximal insulin production (0.034 mol/m 3 ). See Table for correlation between perifusion rate and islet density loading levels. Statistical significance is expressed as * p < .05 and ** p < .001

    Article Snippet: Single microchannel models of the 2.5%, 10.0%, and 20.0% (v/v) islet densities shown in Figure were created in COMSOL and their outer walls were defined by the symmetry boundary condition.

    Techniques: In Vitro, In Vivo, Concentration Assay