Acoustofluidic Plasmapheresis System Designed for Ultralow Blood Volume Applications
- Amal Nath 1, Sara Marie Larsson 2,3, Andreas Lenshof 1, Wei Qiu 1, Thierry Baasch 1, Linda Nilsson 3, Thomas Thymann 4, Stanislava Pankratova 4, Magnus Gram 3,5,6, David Ley 3, Thomas Laurell 1
- Amal Nath 1, Sara Marie Larsson 2,3, Andreas Lenshof 1
- 1Department of Biomedical Engineering, Lund University, Lund SE-223 63, Sweden.
- 2Clinical Chemistry, Hospitals of Halland, Varberg SE-432 37, Sweden.
- 3Department of Clinical Sciences Lund, Pediatrics, Lund University, Lund SE-221 84, Sweden.
- 4Comparative Pediatrics, Section for Biomedicine, Department of Veterinary and Animal Sciences, University of Copenhagen, Frederiksberg DK-1870, Denmark.
- 5Department of Neonatology, Skåne University Hospital, Lund SE-222 42, Sweden.
- 6Department of Biomedical Science, Faculty of Health and Society, Biofilms-Research Center for Biointerfaces, Malmö University, Malmö SE-205 06, Sweden.
- 0Department of Biomedical Engineering, Lund University, Lund SE-223 63, Sweden.
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View abstract on PubMed
Summary
This summary is machine-generated.This study introduces an acoustofluidic plasmapheresis system for neonates, achieving high-purity plasma separation from minimal blood volumes. The innovative device supports critical care by enabling continuous, closed-loop plasma generation for infants.
Area Of Science
- Biomedical Engineering
- Microfluidics
- Acoustics
Background
- Neonatal intensive care requires precise management of extremely low blood volumes.
- Existing plasma separation methods often demand larger sample volumes, posing risks for neonates.
- There is a need for efficient, in-line plasma separation systems suitable for point-of-care neonatal applications.
Purpose Of The Study
- To develop and validate an integrated acoustofluidic plasmapheresis system for ultralow blood volume applications, specifically in neonatal care.
- To enable continuous, closed-loop plasma separation with minimal sample loss for neonates.
- To achieve high plasma purity and throughput while maintaining system robustness.
Main Methods
- Integration of a two-stage acoustophoresis chip with microperistaltic pumps and PDMS-based flow pulsation dampeners.
- Acoustic separation of whole blood into cell-free plasma and a returnable cell fraction.
- Validation of plasma quality through hemolysis and residual cellular content quantification.
- Testing system robustness across a range of hematocrit levels (up to 50%).
Main Results
- The system achieved a plasma generation rate of 27.5 μL/min with approximately 100% cell removal.
- Demonstrated superior plasma purity, throughput, and minimal sample volume compared to previous microfluidic approaches.
- Validated plasma quality and system robustness, performing effectively at hematocrit levels relevant to neonates.
- Achieved the fastest generation of clinical-quality undiluted plasma with the lowest blood volume requirement.
Conclusions
- The developed acoustofluidic plasmapheresis system is highly suitable for point-of-care integration in neonatal intensive care units.
- It offers a significant advancement for managing ultralow blood volumes in neonatal patients.
- The system provides a safe, efficient, and effective solution for plasma separation in critical neonatal care settings.
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