<HashMap><database>biostudies-literature</database><scores/><additional><submitter>van der Meer PF</submitter><funding>NIDDK NIH HHS</funding><pagination>7-16</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12926800</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>121(1)</volume><pubmed_abstract>The application of technologies to inactivate pathogens in pooled plasma products is nowadays the standard. The number of blood centres applying these technologies to platelet concentrates is steadily increasing. However, pathogen inactivation (PI) of red cell concentrates and whole blood (WB) is challenging, as the haemoglobin-containing red cells quench light, and therefore require a different approach. Three technologies are currently under active development: S-303 (Intercept), UV-C (Theraflex) and riboflavin/UV (Mirasol). The S-303 technology is used for PI of red cell concentrates and has seen significant technical and clinical development in the last decade. Using this technology, red cell both ATP and haemolysis levels conform to objective requirements. For the UV-C technology, onl</pubmed_abstract><journal>Vox sanguinis</journal><pubmed_title>Pathogen inactivation of red cell concentrates and whole blood: I. History, technologies and in vitro product preservation studies.</pubmed_title><pmcid>PMC12926800</pmcid><funding_grant_id>R01 DK124115</funding_grant_id><pubmed_authors>Klei TRL</pubmed_authors><pubmed_authors>van der Meer PF</pubmed_authors><pubmed_authors>Cancelas JA</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pathogen inactivation of red cell concentrates and whole blood: I. History, technologies and in vitro product preservation studies.</name><description>The application of technologies to inactivate pathogens in pooled plasma products is nowadays the standard. The number of blood centres applying these technologies to platelet concentrates is steadily increasing. However, pathogen inactivation (PI) of red cell concentrates and whole blood (WB) is challenging, as the haemoglobin-containing red cells quench light, and therefore require a different approach. Three technologies are currently under active development: S-303 (Intercept), UV-C (Theraflex) and riboflavin/UV (Mirasol). The S-303 technology is used for PI of red cell concentrates and has seen significant technical and clinical development in the last decade. Using this technology, red cell both ATP and haemolysis levels conform to objective requirements. For the UV-C technology, onl</description><dates><release>2026-01-01T00:00:00Z</release><publication>2026 Jan</publication><modification>2026-07-16T18:32:36.616Z</modification><creation>2026-07-11T03:07:57.973Z</creation></dates><accession>S-EPMC12926800</accession><cross_references><pubmed>41152674</pubmed><doi>10.1111/vox.70133</doi></cross_references></HashMap>