INTERCEPT Pathogen Reduction in Platelet Concentrates, in Contrast to Gamma Irradiation, Induces the Formation of


Journal

Biomolecules
ISSN: 2218-273X
Titre abrégé: Biomolecules
Pays: Switzerland
ID NLM: 101596414

Informations de publication

Date de publication:
07 09 2022
Historique:
received: 03 08 2022
revised: 01 09 2022
accepted: 05 09 2022
entrez: 23 9 2022
pubmed: 24 9 2022
medline: 28 9 2022
Statut: epublish

Résumé

Pathogen inactivation techniques for blood products have been implemented to optimize clinically safe blood components supply. The INTERCEPT system uses amotosalen together with ultraviolet light wavelength A (UVA) irradiation. Irradiation-induced inactivation of nucleic acids may actually be accompanied by modifications of chemically reactive polyunsaturated fatty acids known to be important mediators of platelet functions. Thus, here, we investigated eicosanoids and the related fatty acids released upon treatment and during storage of platelet concentrates for 7 days, complemented by the analysis of functional and metabolic consequences of these treatments. Metabolic and functional issues like glucose consumption, lactate formation, platelet aggregation, and clot firmness hardly differed between the two treatment groups. In contrast to gamma irradiation, here, we demonstrated that INTERCEPT treatment immediately caused new formation of

Identifiants

pubmed: 36139096
pii: biom12091258
doi: 10.3390/biom12091258
pmc: PMC9496540
pii:
doi:

Substances chimiques

Arachidonic Acids 0
Hydroxyeicosatetraenoic Acids 0
Lactates 0
Nucleic Acids 0
Sulfhydryl Compounds 0
Arachidonic Acid 27YG812J1I
12-Hydroxy-5,8,10,14-eicosatetraenoic Acid 59985-28-3
Arachidonate 12-Lipoxygenase EC 1.13.11.31
Glucose IY9XDZ35W2

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Gerda C Leitner (GC)

Department of Blood Group Serology and Transfusion Medicine, Medical University of Vienna, 1090 Vienna, Austria.

Gerhard Hagn (G)

Department of Analytical Chemistry, Faculty of Chemistry, University of Vienna, 1090 Vienna, Austria.

Laura Niederstaetter (L)

Department of Analytical Chemistry, Faculty of Chemistry, University of Vienna, 1090 Vienna, Austria.

Andrea Bileck (A)

Department of Analytical Chemistry, Faculty of Chemistry, University of Vienna, 1090 Vienna, Austria.
Joint Metabolome Facility, Faculty of Chemistry, University of Vienna, 1090 Vienna, Austria.

Kerstin Plessl-Walder (K)

Division of Biomedical Science, University of Applied Sciences, FH Campus Wien, 1100 Vienna, Austria.

Michaela Horvath (M)

Department of Blood Group Serology and Transfusion Medicine, Medical University of Vienna, 1090 Vienna, Austria.

Vera Kolovratova (V)

Department of Blood Group Serology and Transfusion Medicine, Medical University of Vienna, 1090 Vienna, Austria.

Andreas Tanzmann (A)

Department of Blood Group Serology and Transfusion Medicine, Medical University of Vienna, 1090 Vienna, Austria.

Alexander Tolios (A)

Department of Blood Group Serology and Transfusion Medicine, Medical University of Vienna, 1090 Vienna, Austria.

Werner Rabitsch (W)

Internal Medicine 1, Stem Cell Transplantation Unit, Medical University of Vienna, 1090 Vienna, Austria.

Philipp Wohlfarth (P)

Internal Medicine 1, Stem Cell Transplantation Unit, Medical University of Vienna, 1090 Vienna, Austria.

Christopher Gerner (C)

Department of Analytical Chemistry, Faculty of Chemistry, University of Vienna, 1090 Vienna, Austria.
Joint Metabolome Facility, Faculty of Chemistry, University of Vienna, 1090 Vienna, Austria.

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Classifications MeSH