Evidence map›Paper›PMID 41493991›Full record

ArticleAnalytical chemistry2026

Acoustofluidic Plasmapheresis System Designed for Ultralow Blood Volume Applications.

Amal Nath, Sara Marie Larsson, Andreas Lenshof, Wei Qiu, Thierry Baasch, Linda Nilsson, Thomas Thymann, Stanislava Pankratova, Magnus Gram, David Ley and 1 more

Abstract read
In one paragraph

Article in Analytical chemistry, 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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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

11 authors.

Amal NathDepartment of Biomedical Engineering, Lund University, Lund SE-223 63, Sweden.ORCID 0000-0002-2508-1455
Sara Marie LarssonClinical Chemistry, Hospitals of Halland, Varberg SE-432 37, Sweden.
Andreas LenshofDepartment of Biomedical Engineering, Lund University, Lund SE-223 63, Sweden.
Wei QiuDepartment of Biomedical Engineering, Lund University, Lund SE-223 63, Sweden.ORCID 0000-0003-3032-4172
Thierry BaaschDepartment of Biomedical Engineering, Lund University, Lund SE-223 63, Sweden.
Linda NilssonDepartment of Clinical Sciences Lund, Pediatrics, Lund University, Lund SE-221 84, Sweden.
Thomas ThymannComparative Pediatrics, Section for Biomedicine, Department of Veterinary and Animal Sciences, University of Copenhagen, Frederiksberg DK-1870, Denmark.
Stanislava PankratovaComparative Pediatrics, Section for Biomedicine, Department of Veterinary and Animal Sciences, University of Copenhagen, Frederiksberg DK-1870, Denmark.ORCID 0000-0002-5406-5163
Magnus GramDepartment of Clinical Sciences Lund, Pediatrics, Lund University, Lund SE-221 84, Sweden.
David LeyDepartment of Clinical Sciences Lund, Pediatrics, Lund University, Lund SE-221 84, Sweden.
Thomas LaurellDepartment of Biomedical Engineering, Lund University, Lund SE-223 63, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We present an integrated acoustofluidic plasmapheresis system designed for ultralow blood volume applications, such as neonatal care, enabling in-line sampling and plasma separation from whole blood. The system combines a two-stage acoustophoresis chip with microperistaltic pumps and PDMS-based flow pulsation dampeners to ensure continuous, stable operation. The input whole blood is acoustically separated into a cell-free plasma fraction and a returnable cell fraction, enabling closed-loop operation for neonates who have a circulating blood volume as low as 50 mL. The system achieves a plasma generation rate of 27.5 μL/min with ∼100% cell removal, outperforming previous microfluidic plasma separation approaches in terms of purity, throughput, and minimal sample volume. Plasma quality was validated by quantifying hemolysis and residual cellular content, while system robustness was demonstrated across hematocrit levels up to 50%, which is close to the average upper hematocrit value in neonates. Compared to previous microfluidic techniques, our system achieves the fastest generation of clinical quality undiluted plasma with the lowest required blood volume, making it highly suitable for point-of-care integration in neonatal intensive care units.

Indexed as

AcousticsBlood VolumeLab-On-A-Chip DevicesMicrofluidic Analytical TechniquesPlasmapheresisEquipment DesignHumansInfant, Newborn

Identifiers

PMID41493991
PMCPMC12824985

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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.