| Literature DB >> 19995680 |
N A Mufti1, A C Erickson, A K North, D Hanson, L Sawyer, L M Corash, L Lin.
Abstract
A pathogen inactivation (PI) process has been developed using the frangible anchor linker effector (FRALE) compound S-303. A series of experiments were performed in whole blood (WB) to measure the level of viral and bacterial inactivation. The results showed that 0.2mM S-303 and 2mM glutathione (GSH) inactivated >6.5 logs of HIV, >5.7 logs of Bluetongue virus, >7.0 logs of Yersinia enterocolitica, 4.2 logs of Serratia marcescens, and 7.5 logs of Staphylococcus epidermidis. Recent development for S-303 is focused on optimization of the PI process for red blood cell concentrates (RBC). A series of studies in RBC showed that 0.2mM S-303 and 20mM GSH inactivated approximately 5 logs or greater of Y. enterocolitica, E. coli, S. marcescens, S. aureus, HIV, bovine viral diarrhoea virus, bluetongue virus and human adenovirus 5. In both applications of the S-303 process, in vitro parameters of RBC function and physiology were retained compared to conventional RBC. Results from these studies indicate that S-303 can be applicable for PI of RBC and WB. Copyright 2009 The International Association for Biologicals. All rights reserved.Entities:
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Year: 2009 PMID: 19995680 DOI: 10.1016/j.biologicals.2009.10.019
Source DB: PubMed Journal: Biologicals ISSN: 1045-1056 Impact factor: 1.856