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Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light
BACKGROUND: A triple storage (TS) set allows for pathogen inactivation (PI) treatment of triple‐dose apheresis platelet products with amotosalen + UVA. We evaluated the quality and metabolic parameters of platelet concentrates (PCs) pathogen inactivated and stored for 7 days. MATERIALS AND METHODS:...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087429/ https://www.ncbi.nlm.nih.gov/pubmed/36124649 http://dx.doi.org/10.1111/tme.12913 |
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author | Infanti, Laura Pehlic, Vildana Mitrovic, Sandra Holbro, Andreas Andresen, Silke Payrat, Jean‐Marc Lin, Jin‐Sying Buser, Andreas |
author_facet | Infanti, Laura Pehlic, Vildana Mitrovic, Sandra Holbro, Andreas Andresen, Silke Payrat, Jean‐Marc Lin, Jin‐Sying Buser, Andreas |
author_sort | Infanti, Laura |
collection | PubMed |
description | BACKGROUND: A triple storage (TS) set allows for pathogen inactivation (PI) treatment of triple‐dose apheresis platelet products with amotosalen + UVA. We evaluated the quality and metabolic parameters of platelet concentrates (PCs) pathogen inactivated and stored for 7 days. MATERIALS AND METHODS: Twelve triple‐dose products collected with two different apheresis platforms were treated with amotosalen+UVA. Products were split into three single‐dose units. Testing was made pretreatment, after splitting, at days 5 and 7 of storage. RESULTS: Single‐dose PI PCs had a mean platelet content of 2.89 ± 0.35 x 10(11). From baseline to day 7, pH remained stable (7.1 ± 0.1 vs. 7.0 ± 0.1), pO(2) increased (11.3 ± 2.4 vs. 18.3 ± 3.5 kPa) as did LDH (201 ± 119 vs. 324 ± 203 U/L) and lactate (3.6 ± 1.7 vs. 12.1 ± 1.5 mmol/L) (all p < 0.01); pCO(2) decreased (4.1 ± 0.8 vs. 1.5 ± 0.7 mmHg; p < 0.01) and so did bicarbonate (6.6 ± 1.1 vs. 2.5 ± 1.4 mmol/L), glucose (5.6 ± 1.2 vs. 0.4 ± 0.4 mmol/L) and ATP (3.4 ± 0.9 vs. 2.5 ± 1.4 nmol/10(8) platelets) (all p < 0.05). CONCLUSION: Triple‐dose PCs processed with the TS sets fulfilled the quality requirements and displayed metabolic changes of expected extent during 7‐day storage. |
format | Online Article Text |
id | pubmed-10087429 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-100874292023-04-12 Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light Infanti, Laura Pehlic, Vildana Mitrovic, Sandra Holbro, Andreas Andresen, Silke Payrat, Jean‐Marc Lin, Jin‐Sying Buser, Andreas Transfus Med Short Communications BACKGROUND: A triple storage (TS) set allows for pathogen inactivation (PI) treatment of triple‐dose apheresis platelet products with amotosalen + UVA. We evaluated the quality and metabolic parameters of platelet concentrates (PCs) pathogen inactivated and stored for 7 days. MATERIALS AND METHODS: Twelve triple‐dose products collected with two different apheresis platforms were treated with amotosalen+UVA. Products were split into three single‐dose units. Testing was made pretreatment, after splitting, at days 5 and 7 of storage. RESULTS: Single‐dose PI PCs had a mean platelet content of 2.89 ± 0.35 x 10(11). From baseline to day 7, pH remained stable (7.1 ± 0.1 vs. 7.0 ± 0.1), pO(2) increased (11.3 ± 2.4 vs. 18.3 ± 3.5 kPa) as did LDH (201 ± 119 vs. 324 ± 203 U/L) and lactate (3.6 ± 1.7 vs. 12.1 ± 1.5 mmol/L) (all p < 0.01); pCO(2) decreased (4.1 ± 0.8 vs. 1.5 ± 0.7 mmHg; p < 0.01) and so did bicarbonate (6.6 ± 1.1 vs. 2.5 ± 1.4 mmol/L), glucose (5.6 ± 1.2 vs. 0.4 ± 0.4 mmol/L) and ATP (3.4 ± 0.9 vs. 2.5 ± 1.4 nmol/10(8) platelets) (all p < 0.05). CONCLUSION: Triple‐dose PCs processed with the TS sets fulfilled the quality requirements and displayed metabolic changes of expected extent during 7‐day storage. Blackwell Publishing Ltd 2022-09-20 2022-12 /pmc/articles/PMC10087429/ /pubmed/36124649 http://dx.doi.org/10.1111/tme.12913 Text en © 2022 The Authors. Transfusion Medicine published by John Wiley & Sons Ltd on behalf of British Blood Transfusion Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Short Communications Infanti, Laura Pehlic, Vildana Mitrovic, Sandra Holbro, Andreas Andresen, Silke Payrat, Jean‐Marc Lin, Jin‐Sying Buser, Andreas Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light |
title | Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light |
title_full | Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light |
title_fullStr | Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light |
title_full_unstemmed | Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light |
title_short | Pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light |
title_sort | pathogen inactivation treatment of triple‐dose apheresis platelets with amotosalen and ultraviolet a light |
topic | Short Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10087429/ https://www.ncbi.nlm.nih.gov/pubmed/36124649 http://dx.doi.org/10.1111/tme.12913 |
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