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<Articles><Article><Journal><PublisherName></PublisherName><JournalTitle>DARU Journal of Pharmaceutical Sciences</JournalTitle><Volume>11</Volume><Issue>2</Issue></Journal><ArticleTitle>Solvent-Detergent Treatment of IgM-Enriched Immunoglobulin</ArticleTitle><FirstPage>47</FirstPage><LastPage>51</LastPage><AuthorList><Author><FirstName></FirstName><LastName>Mojgan Pourmokhtar</LastName></Author><Author><FirstName></FirstName><LastName>Rassoul Dinarvand</LastName></Author><Author><FirstName></FirstName><LastName>Kamran Mousavi Hosseini</LastName></Author><Author><FirstName></FirstName><LastName>Houri Rezvan</LastName></Author><Author><FirstName></FirstName><LastName>Mohammad Ali Jalili</LastName></Author></AuthorList><History><PubDate PubStatus="received"><Year>2015</Year><Month>10</Month><Day>06</Day></PubDate></History><Abstract>Viral safety of human plasma products plays a key role in their safe uses. Solvent- detergent (SD) virus-inactivation method has gained widespread popularity in the manufacture of biological products. This treatment which inactivates lipid-enveloped viruses effectively consists of incubation of a plasma protein solution in the presence of a non-volatile organic solvent and a detergent. In this study, IgM-enriched immunoglobulin was incubated at 24 °C for 6 h under slow stirring in the presence of tri(n-butyl) phosphate (0.3% w/w ) as solvent and tween 80 (1% w/w) as detergent. After completion of the inactivation process and removal of the solvent-detergent, the ability of SD-treatment to remove Infectious Bovine Rhinotracheitis (IBR) virus  (a lipid-enveloped virus) and Foot-and-Mouth Disease virus (a non-enveloped virus) were evaluated by "virus spiking studies" using a scaled down process. Reduction factor of 4 log was obtained for the SD-treatment of IgM-enriched immunoglobulin spiked with IBR virus. No virus inactivation was observed in the SD-treated IgM-enriched immunoglobulin, spiked with Foot-and-Mouth Disease virus. It was concluded that treatment of IgM-enriched immunoglobulin with TNBP-TWEEN 80 may be considered as an efficient lipid-enveloped virus inactivation step in the manufacture of this product.</Abstract><web_url>https://daru.tums.ac.ir/index.php/daru/article/view/168</web_url><pdf_url>https://daru.tums.ac.ir/index.php/daru/article/download/168/168</pdf_url></Article></Articles>
