Evidence map›Paper›PMID 42371528›Full record

ArticleBioImpacts : BI2026

Computational analysis on design and optimization of low-frequency dielectrophoretic microfluidic lab on a chip for

Saeed Saedy, Navid Alaei-Sheini, Shahrzad Ajabi, Karim Ansari-Asl

Abstract read
In one paragraph

Article in BioImpacts : BI, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Saeed SaedyFaculty of Engineering, Shahid Chamran University of Ahvaz, Ahvaz, Iran.ORCID https://orcid.org/0000-0002-9381-7794
Navid Alaei-SheiniFaculty of Engineering, Shahid Chamran University of Ahvaz, Ahvaz, Iran.ORCID https://orcid.org/0000-0002-6029-8203
Shahrzad AjabiFaculty of Engineering, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
Karim Ansari-AslFaculty of Engineering, Shahid Chamran University of Ahvaz, Ahvaz, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Bloodstream infections (BSIs) caused by Methods: A dual-channel microfluidic separation device was developed with independently operated pathways. The primary channel (2000×198 μm) integrated ten crown-shaped microelectrodes, while the secondary channel (1540×80 μm) incorporated eight microelectrodes. The primary channel isolated both target strains directly from whole blood; the secondary channel enabled further separation between standard Gram-positive MRSA and MSSA. Finite element modeling was performed using COMSOL Multiphysics, which integrated the Electric Currents, Creeping Flow, and Particle Tracing modules. Separation efficiency was evaluated across varying voltages, electrode geometries, and sample-to-buffer flow rate ratios at 1 Hz. Dielectric properties from published data were used to calculate the Clausius-Mossotti (CM) factor for predicting DEP behavior. Results: In the primary channel, nearly 100% separation efficiency and purity were achieved for isolating MRSA and MSSA from red blood cells (RBCs), white blood cells (WBCs), and platelets (PLTs) at 24-28 Vpp and a sample-to-buffer flow rate ratio of 1:2. The secondary channel successfully differentiated MSSA from MRSA at 42-46 Vpp and a 1:5 flow rate ratio, exploiting their distinct membrane characteristics. Crown-shaped electrodes outperformed rectangular designs by generating higher electric field gradients, thereby enhancing separation performance. Conclusion: The dual-channel LOC system enables high-efficiency, label-free separation and identification of MRSA and MSSA directly from whole blood using low-frequency negative DEP (nDEP). The optimized configuration supports rapid pathogen detection, offering substantial advantages over conventional diagnostic platforms.

Indexed as

DielectrophoresisLab on a chipMicrofluidicsMRSAMSSA

Identifiers

PMID42371528
PMCPMC13310248

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.