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Assessment of dengue virus inactivation in random donor platelets using amotosalen and ultraviolet A illumination
OBJECTIVES: The study objective was evaluation of amotosalen and ultraviolet A (UVA) illumination-based inactivation of dengue virus (DENV) in blood platelets. MATERIALS AND METHODS: Whole blood was collected from healthy donors and platelet concentrates were prepared at a tertiary care hospital in...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9528557/ https://www.ncbi.nlm.nih.gov/pubmed/36199414 http://dx.doi.org/10.4103/ajts.AJTS_108_19 |
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author | Kumar, Ankit Tiwari, Aseem Kumar Kumar, Satendra Biswas, Ashutosh Singh, Gurpreet Chatterjee, Kabita Chakroborty, Sourit Sunil, Sujatha |
author_facet | Kumar, Ankit Tiwari, Aseem Kumar Kumar, Satendra Biswas, Ashutosh Singh, Gurpreet Chatterjee, Kabita Chakroborty, Sourit Sunil, Sujatha |
author_sort | Kumar, Ankit |
collection | PubMed |
description | OBJECTIVES: The study objective was evaluation of amotosalen and ultraviolet A (UVA) illumination-based inactivation of dengue virus (DENV) in blood platelets. MATERIALS AND METHODS: Whole blood was collected from healthy donors and platelet concentrates were prepared at a tertiary care hospital in Gurugram, India. Platelet units collected from five blood group matched individuals were pooled and spiked with DENV. The spiked platelet units were subjected to amotosalen treatment followed by UVA illumination, to evaluate the efficiency of this method for viral inactivation. The treated platelet units were evaluated for the presence of infectious DENV. Amotosalen levels were quantified in the treated samples using high-performance liquid chromatography. RESULTS: The presence of replicating DENV was not observed in spiked platelet units treated with amotosalen and UVA illumination, whereas untreated units contained actively replicating DENV. Amotosalen levels were found to be in the permissible range after photochemical inactivation. CONCLUSIONS: Amotosalen/UVA pathogen inactivation treatment showed efficient inactivation of DENV in platelet components. Therefore, it seems to be a promising method for mitigating the risk of dengue transmission through transfusion of potentially contaminated platelet components in dengue-endemic countries such as India. |
format | Online Article Text |
id | pubmed-9528557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-95285572022-10-04 Assessment of dengue virus inactivation in random donor platelets using amotosalen and ultraviolet A illumination Kumar, Ankit Tiwari, Aseem Kumar Kumar, Satendra Biswas, Ashutosh Singh, Gurpreet Chatterjee, Kabita Chakroborty, Sourit Sunil, Sujatha Asian J Transfus Sci Original Article OBJECTIVES: The study objective was evaluation of amotosalen and ultraviolet A (UVA) illumination-based inactivation of dengue virus (DENV) in blood platelets. MATERIALS AND METHODS: Whole blood was collected from healthy donors and platelet concentrates were prepared at a tertiary care hospital in Gurugram, India. Platelet units collected from five blood group matched individuals were pooled and spiked with DENV. The spiked platelet units were subjected to amotosalen treatment followed by UVA illumination, to evaluate the efficiency of this method for viral inactivation. The treated platelet units were evaluated for the presence of infectious DENV. Amotosalen levels were quantified in the treated samples using high-performance liquid chromatography. RESULTS: The presence of replicating DENV was not observed in spiked platelet units treated with amotosalen and UVA illumination, whereas untreated units contained actively replicating DENV. Amotosalen levels were found to be in the permissible range after photochemical inactivation. CONCLUSIONS: Amotosalen/UVA pathogen inactivation treatment showed efficient inactivation of DENV in platelet components. Therefore, it seems to be a promising method for mitigating the risk of dengue transmission through transfusion of potentially contaminated platelet components in dengue-endemic countries such as India. Wolters Kluwer - Medknow 2022 2022-05-26 /pmc/articles/PMC9528557/ /pubmed/36199414 http://dx.doi.org/10.4103/ajts.AJTS_108_19 Text en Copyright: © 2022 Asian Journal of Transfusion Science https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Original Article Kumar, Ankit Tiwari, Aseem Kumar Kumar, Satendra Biswas, Ashutosh Singh, Gurpreet Chatterjee, Kabita Chakroborty, Sourit Sunil, Sujatha Assessment of dengue virus inactivation in random donor platelets using amotosalen and ultraviolet A illumination |
title | Assessment of dengue virus inactivation in random donor platelets using amotosalen and ultraviolet A illumination |
title_full | Assessment of dengue virus inactivation in random donor platelets using amotosalen and ultraviolet A illumination |
title_fullStr | Assessment of dengue virus inactivation in random donor platelets using amotosalen and ultraviolet A illumination |
title_full_unstemmed | Assessment of dengue virus inactivation in random donor platelets using amotosalen and ultraviolet A illumination |
title_short | Assessment of dengue virus inactivation in random donor platelets using amotosalen and ultraviolet A illumination |
title_sort | assessment of dengue virus inactivation in random donor platelets using amotosalen and ultraviolet a illumination |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9528557/ https://www.ncbi.nlm.nih.gov/pubmed/36199414 http://dx.doi.org/10.4103/ajts.AJTS_108_19 |
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