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The Effects of Ultraviolet Light and Riboflavin on Inactivation of Viruses and the Quality of Platelet Concentrates at Laboratory Scale

BACKGROUND: This study investigated the effects of Riboflavin (RB) combined with different doses of UV on Platelet Concentrate (PC) which was infected by three models of virus. Platelet quality after treatment was also assessed. METHODS: Three models of virus used in this study were Vesicular Stomat...

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Autores principales: Mirshafiee, Hamideh, Sharifi, Zohreh, Hosseini, Syed Masoud, Yari, Fatemeh, Nikbakht, Hamed, Latifi, Hamid
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Avicenna Research Institute 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4483315/
https://www.ncbi.nlm.nih.gov/pubmed/26140182
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author Mirshafiee, Hamideh
Sharifi, Zohreh
Hosseini, Syed Masoud
Yari, Fatemeh
Nikbakht, Hamed
Latifi, Hamid
author_facet Mirshafiee, Hamideh
Sharifi, Zohreh
Hosseini, Syed Masoud
Yari, Fatemeh
Nikbakht, Hamed
Latifi, Hamid
author_sort Mirshafiee, Hamideh
collection PubMed
description BACKGROUND: This study investigated the effects of Riboflavin (RB) combined with different doses of UV on Platelet Concentrate (PC) which was infected by three models of virus. Platelet quality after treatment was also assessed. METHODS: Three models of virus used in this study were Vesicular Stomatitis Virus (VSV), Herpes Simplex Virus (HSV), and Polio virus, which were added to PC. After photochemical treatment with RB and UV light, residual viral infectivity was titrated using 50% Tissue Culture Infective Dose (TCID(50))/ml. This treatment was done with concentration of 50 μM of RB and different doses of UV light (0.24, 0.48, 0.97, 1.29 J/cm(2)). Platelet quality was assessed by measuring pH, Lactate Dehydrogenase (LDH), MTT assay and cell count after treatments and during 4 days of storage against control groups. RESULTS: Concentration of 50 μM RB with combination of 1.29 J/cm(2) dose of UV resulted in the highest titer reduction of VSV (4 log (10)) and HSV (4.26 log(10)) and lowest titer reduction of Polio virus (2.6 log(10)). No significant difference was observed between different doses in comparison with control groups. In all treatment groups, the storage stability of platelets in PC was in the acceptable range in comparison with control group. CONCLUSION: This study indicated that RB/UV treatment was a promising pathogen reduction technique in PC and had limited effects on platelet quality. However, further optimization of this method is necessary to deal with blood-borne viruses like non-enveloped viruses.
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spelling pubmed-44833152015-07-02 The Effects of Ultraviolet Light and Riboflavin on Inactivation of Viruses and the Quality of Platelet Concentrates at Laboratory Scale Mirshafiee, Hamideh Sharifi, Zohreh Hosseini, Syed Masoud Yari, Fatemeh Nikbakht, Hamed Latifi, Hamid Avicenna J Med Biotechnol Original Article BACKGROUND: This study investigated the effects of Riboflavin (RB) combined with different doses of UV on Platelet Concentrate (PC) which was infected by three models of virus. Platelet quality after treatment was also assessed. METHODS: Three models of virus used in this study were Vesicular Stomatitis Virus (VSV), Herpes Simplex Virus (HSV), and Polio virus, which were added to PC. After photochemical treatment with RB and UV light, residual viral infectivity was titrated using 50% Tissue Culture Infective Dose (TCID(50))/ml. This treatment was done with concentration of 50 μM of RB and different doses of UV light (0.24, 0.48, 0.97, 1.29 J/cm(2)). Platelet quality was assessed by measuring pH, Lactate Dehydrogenase (LDH), MTT assay and cell count after treatments and during 4 days of storage against control groups. RESULTS: Concentration of 50 μM RB with combination of 1.29 J/cm(2) dose of UV resulted in the highest titer reduction of VSV (4 log (10)) and HSV (4.26 log(10)) and lowest titer reduction of Polio virus (2.6 log(10)). No significant difference was observed between different doses in comparison with control groups. In all treatment groups, the storage stability of platelets in PC was in the acceptable range in comparison with control group. CONCLUSION: This study indicated that RB/UV treatment was a promising pathogen reduction technique in PC and had limited effects on platelet quality. However, further optimization of this method is necessary to deal with blood-borne viruses like non-enveloped viruses. Avicenna Research Institute 2015 2015-04 /pmc/articles/PMC4483315/ /pubmed/26140182 Text en Copyright© 2015 Avicenna Research Institute This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly.
spellingShingle Original Article
Mirshafiee, Hamideh
Sharifi, Zohreh
Hosseini, Syed Masoud
Yari, Fatemeh
Nikbakht, Hamed
Latifi, Hamid
The Effects of Ultraviolet Light and Riboflavin on Inactivation of Viruses and the Quality of Platelet Concentrates at Laboratory Scale
title The Effects of Ultraviolet Light and Riboflavin on Inactivation of Viruses and the Quality of Platelet Concentrates at Laboratory Scale
title_full The Effects of Ultraviolet Light and Riboflavin on Inactivation of Viruses and the Quality of Platelet Concentrates at Laboratory Scale
title_fullStr The Effects of Ultraviolet Light and Riboflavin on Inactivation of Viruses and the Quality of Platelet Concentrates at Laboratory Scale
title_full_unstemmed The Effects of Ultraviolet Light and Riboflavin on Inactivation of Viruses and the Quality of Platelet Concentrates at Laboratory Scale
title_short The Effects of Ultraviolet Light and Riboflavin on Inactivation of Viruses and the Quality of Platelet Concentrates at Laboratory Scale
title_sort effects of ultraviolet light and riboflavin on inactivation of viruses and the quality of platelet concentrates at laboratory scale
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4483315/
https://www.ncbi.nlm.nih.gov/pubmed/26140182
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