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使用新型亚甲蓝基装置灭活悬浮于新鲜冰冻血浆中的模型病毒。

Inactivation of model viruses suspended in fresh frozen plasma using novel methylene blue based device.

作者信息

Elikaei Ameneh, Sharifi Zohreh, Hosseini Seyed Masoud, Latifi Hamid, Musavi Hosseini Mir Kamaran

机构信息

Department of Microbiology, Faculty of Biological Science ShahidBeheshti University GC,Tehran, Iran.

Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran.

出版信息

Iran J Microbiol. 2014 Feb;6(1):41-5.

Abstract

BACKGROUND AND OBJECTIVE

There is a concern on safety of human Fresh Frozen Plasma (FFP) as it is a source of some medicinal products. The possibility of transmission of blood-borne are reported often due to emerging viruses. There are some Pathogen Reduction Technologies (PRT) to inactivate viruses. Methylene Blue (MB) based method is one of them. The aim of this study was to examine new designated device to inactivate model viruses.

MATERIALS AND METHODS

Four model viruses were used in this study:Vesicular stomatitis virus (VSV), Herpes Simplex Virus I (HSV-1), Bovine Viral DiarrheaVirus(BVDV) and Polio Virus.50% Tissue Culture Infective Dose (TCID 50) and Reed-Muench Methods were used to titer the viruses. MB in two final concentration of 0.1 μM and 1 μM and illumination in about 627nm with red LED (Lamp Emitting Diode) for 15, 30, 45 and 60 minutes were used. Three replicates employed for each experiments.

RESULTS

1μMconcentration of MB showed more effective than 0.1μMin all designed illumination period for inactivation of HSV, VSV and BVDV. This method also demonstrated best results for enveloped model viruses. The most Log reduction for HSV, VSV and BVDV were6.28, 5.54 and 6.22, respectively. For HSV and BVDV inactivation, the best illumination period was 45 minutes.

CONCLUSION

Model viruses showed sensitivity combination of MB and illumination using red LEDs. As results show this device could inactivate model viruses and reduce their titer very close to approved commercial devices, in compare.

摘要

背景与目的

由于人新鲜冰冻血浆(FFP)是某些药品的来源,其安全性备受关注。由于新出现的病毒,血液传播的可能性经常被报道。有一些病原体灭活技术(PRT)可用于灭活病毒。基于亚甲蓝(MB)的方法就是其中之一。本研究的目的是检测新指定的用于灭活模型病毒的装置。

材料与方法

本研究使用了四种模型病毒:水疱性口炎病毒(VSV)、单纯疱疹病毒I型(HSV - 1)、牛病毒性腹泻病毒(BVDV)和脊髓灰质炎病毒。采用50%组织培养感染剂量(TCID50)和里德 - 孟奇方法对病毒进行滴定。使用终浓度为0.1μM和1μM的亚甲蓝,并通过红色发光二极管(LED)在约627nm波长下照射15、30、45和60分钟。每个实验进行三次重复。

结果

在所有设定的照射时间内,1μM浓度的亚甲蓝在灭活HSV、VSV和BVDV方面比0.1μM更有效。该方法对包膜模型病毒也显示出最佳效果。HSV、VSV和BVDV的最大对数减少量分别为6.28、5.54和6.22。对于HSV和BVDV的灭活,最佳照射时间为45分钟。

结论

模型病毒对亚甲蓝和红色LED照射的组合显示出敏感性。结果表明,与已批准的商业装置相比,该装置能够灭活模型病毒并将其滴度降低到非常接近的水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f47/4419045/6ebc67ac8793/IJM-6-41f1.jpg

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