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Inactivation of model viruses and bacteria in human fresh frozen plasma using riboflavin and long wave ultraviolet rays

BACKGROUND AND OBJECTIVES: Pathogen reduction technologies are among methods to eliminate transfusion transmitted infections. Mirasol method using riboflavin in combination with ultraviolet rays is one of them. The aims of this study were to investigate the effectiveness of Mirasol method to inactiv...

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Autores principales: Elikaei, Ameneh, Hosseini, Seyed Masoud, Sharifi, Zohreh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534005/
https://www.ncbi.nlm.nih.gov/pubmed/28775824
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author Elikaei, Ameneh
Hosseini, Seyed Masoud
Sharifi, Zohreh
author_facet Elikaei, Ameneh
Hosseini, Seyed Masoud
Sharifi, Zohreh
author_sort Elikaei, Ameneh
collection PubMed
description BACKGROUND AND OBJECTIVES: Pathogen reduction technologies are among methods to eliminate transfusion transmitted infections. Mirasol method using riboflavin in combination with ultraviolet rays is one of them. The aims of this study were to investigate the effectiveness of Mirasol method to inactivate some model pathogens as well as examination of the sensitivity of plasma proteins after treatment. MATERIALS AND METHODS: Riboflavin in 50μM concentration and ultraviolet (365 nm) in three different energy doses (3.6, 7.2, and 10.8 j/cm(2)) were employed to inactivate model pathogens. Four standard viruses were used in this study including Vesicular Stomatitis Virus (VSV), Herpes Simplex Virus1 (HSV-1), Bovine Viral Diarrhea Virus (BVDV) and Polio Virus. 50% Tissue Culture Infectious Dose (TCID(50)) and Reed–Muench Methods were used to estimate viruses’ titers. E. coli and Staphylococcus aureus were used as bacterial models. Four plasma proteins including factor V, VIII, fibrinogen and antithromin were used to determine their sensitivity to pathogen inactivation treatment. RESULTS: The most pathogen reduction titre was determined for 15 minutes irradiation period equal to 10.8 J/cm(2) that is corresponding to Log 6.10 for BVDV, Log 6.09 for HSV-1, Log 6.62 for VSV and Log 3.36 for Polio. Bacterial reduction titer was Log 6.94 for E. coli and Log 7.00 for S. aureus. Indicator proteins for plasma activity were determined to be 75% for factor V, 88% for factor VIII, 52% for fibrinogen and 94% for antithrombin. CONCLUSION: Results showed that the employed method can inactivate most of the pathogens in fresh frozen plasma. The acceptable activities of selected plasma proteins remained after treatment.
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spelling pubmed-55340052017-08-03 Inactivation of model viruses and bacteria in human fresh frozen plasma using riboflavin and long wave ultraviolet rays Elikaei, Ameneh Hosseini, Seyed Masoud Sharifi, Zohreh Iran J Microbiol Original Article BACKGROUND AND OBJECTIVES: Pathogen reduction technologies are among methods to eliminate transfusion transmitted infections. Mirasol method using riboflavin in combination with ultraviolet rays is one of them. The aims of this study were to investigate the effectiveness of Mirasol method to inactivate some model pathogens as well as examination of the sensitivity of plasma proteins after treatment. MATERIALS AND METHODS: Riboflavin in 50μM concentration and ultraviolet (365 nm) in three different energy doses (3.6, 7.2, and 10.8 j/cm(2)) were employed to inactivate model pathogens. Four standard viruses were used in this study including Vesicular Stomatitis Virus (VSV), Herpes Simplex Virus1 (HSV-1), Bovine Viral Diarrhea Virus (BVDV) and Polio Virus. 50% Tissue Culture Infectious Dose (TCID(50)) and Reed–Muench Methods were used to estimate viruses’ titers. E. coli and Staphylococcus aureus were used as bacterial models. Four plasma proteins including factor V, VIII, fibrinogen and antithromin were used to determine their sensitivity to pathogen inactivation treatment. RESULTS: The most pathogen reduction titre was determined for 15 minutes irradiation period equal to 10.8 J/cm(2) that is corresponding to Log 6.10 for BVDV, Log 6.09 for HSV-1, Log 6.62 for VSV and Log 3.36 for Polio. Bacterial reduction titer was Log 6.94 for E. coli and Log 7.00 for S. aureus. Indicator proteins for plasma activity were determined to be 75% for factor V, 88% for factor VIII, 52% for fibrinogen and 94% for antithrombin. CONCLUSION: Results showed that the employed method can inactivate most of the pathogens in fresh frozen plasma. The acceptable activities of selected plasma proteins remained after treatment. Tehran University of Medical Sciences 2017-02 /pmc/articles/PMC5534005/ /pubmed/28775824 Text en Copyright© 2017 Iranian Neuroscience Society http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Elikaei, Ameneh
Hosseini, Seyed Masoud
Sharifi, Zohreh
Inactivation of model viruses and bacteria in human fresh frozen plasma using riboflavin and long wave ultraviolet rays
title Inactivation of model viruses and bacteria in human fresh frozen plasma using riboflavin and long wave ultraviolet rays
title_full Inactivation of model viruses and bacteria in human fresh frozen plasma using riboflavin and long wave ultraviolet rays
title_fullStr Inactivation of model viruses and bacteria in human fresh frozen plasma using riboflavin and long wave ultraviolet rays
title_full_unstemmed Inactivation of model viruses and bacteria in human fresh frozen plasma using riboflavin and long wave ultraviolet rays
title_short Inactivation of model viruses and bacteria in human fresh frozen plasma using riboflavin and long wave ultraviolet rays
title_sort inactivation of model viruses and bacteria in human fresh frozen plasma using riboflavin and long wave ultraviolet rays
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5534005/
https://www.ncbi.nlm.nih.gov/pubmed/28775824
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