Ghost cells as a two-phase blood analog fluid-high-volume and high-concentration production.

fluorescent hemolysis detection locally resolved thrombosis detection particle image velocimetry resealed ghost cells translucent two‐phase blood analog fluid

Journal

Artificial organs
ISSN: 1525-1594
Titre abrégé: Artif Organs
Pays: United States
ID NLM: 7802778

Informations de publication

Date de publication:
27 Aug 2024
Historique:
revised: 12 07 2024
received: 24 04 2024
accepted: 07 08 2024
medline: 27 8 2024
pubmed: 27 8 2024
entrez: 27 8 2024
Statut: aheadofprint

Résumé

Hemolysis in mechanical circulatory support systems is currently determined quantitatively. To also locally resolve hemolysis, we are developing a fluorescent hemolysis detection method. This requires a translucent two-phase blood analog fluid combined with particle image velocimetry, an optical flow field measurement. The blood analog fluid is composed of red blood cell surrogates. However, producing surrogates in sufficient volume is a challenge. We therefore present a high-volume and high-concentration production for our surrogates: ghost cells, hemoglobin-depleted erythrocytes. In the ghost cell production, the hemoglobin is removed by a repeated controlled osmolar lysis. We have varied the solution mixture, centrifugation time, and centrifugation force in order to increase production efficiency. The production is characterized by measurements of output volume, hematocrit, transparency, and rheology of the blood analog fluid. The volume of produced ghost cells was significantly increased, and reproducibility was improved. An average production of 389 mL of ghost cells were achieved per day. Those ghost cells diluted in plasma have a rheology similar to blood while being permeable to light. The volume of ghost cells produced is sufficient for optical measurements as particle image velocimetry in mechanical circulatory support systems. This makes further work on experimental measurements for a locally resolved hemolysis detection possible.

Sections du résumé

BACKGROUND BACKGROUND
Hemolysis in mechanical circulatory support systems is currently determined quantitatively. To also locally resolve hemolysis, we are developing a fluorescent hemolysis detection method. This requires a translucent two-phase blood analog fluid combined with particle image velocimetry, an optical flow field measurement. The blood analog fluid is composed of red blood cell surrogates. However, producing surrogates in sufficient volume is a challenge. We therefore present a high-volume and high-concentration production for our surrogates: ghost cells, hemoglobin-depleted erythrocytes.
METHODS METHODS
In the ghost cell production, the hemoglobin is removed by a repeated controlled osmolar lysis. We have varied the solution mixture, centrifugation time, and centrifugation force in order to increase production efficiency. The production is characterized by measurements of output volume, hematocrit, transparency, and rheology of the blood analog fluid.
RESULTS RESULTS
The volume of produced ghost cells was significantly increased, and reproducibility was improved. An average production of 389 mL of ghost cells were achieved per day. Those ghost cells diluted in plasma have a rheology similar to blood while being permeable to light.
CONCLUSION CONCLUSIONS
The volume of ghost cells produced is sufficient for optical measurements as particle image velocimetry in mechanical circulatory support systems. This makes further work on experimental measurements for a locally resolved hemolysis detection possible.

Identifiants

pubmed: 39189702
doi: 10.1111/aor.14846
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : Deutsche Forschungsgemeinschaft
ID : STE 1680/12-2

Informations de copyright

© 2024 The Author(s). Artificial Organs published by International Center for Artificial Organ and Transplantation (ICAOT) and Wiley Periodicals LLC.

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Auteurs

Benjamin J Schürmann (BJ)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, University Hospital RWTH Aachen University, Aachen, Germany.

Pia Creutz (P)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, University Hospital RWTH Aachen University, Aachen, Germany.

Thomas Schmitz-Rode (T)

Institute of Applied Medical Engineering, University Hospital RWTH Aachen University, Aachen, Germany.

Ulrich Steinseifer (U)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, University Hospital RWTH Aachen University, Aachen, Germany.

Johanna C Clauser (JC)

Department of Cardiovascular Engineering, Institute of Applied Medical Engineering, University Hospital RWTH Aachen University, Aachen, Germany.

Classifications MeSH