부산대학교 도서관

Background and Objectives: Due to increasing concerns about possible endocrine‐disrupting properties, the use of the plasticizer di(2‐ethylhexyl) phthalate (DEHP) will be banned in future blood storage. Di(2‐ethylhexyl) terephthalate (DEHT) provides sufficient red blood cell (RBC) quality during conventional blood bank storage. It is important that a new plasticizer also maintains acceptable quality during exposure to high cell stress, such as irradiation, which is commonly used to prevent graft‐versus‐host disease. Materials and Methods: A total of 59 RBC units were collected and processed in polyvinyl chloride (PVC)‐DEHT or PVC‐DEHP blood bags combined with either saline‐adenine‐glucose‐mannitol (SAGM) or phosphate‐adenine‐glucose‐guanosine‐saline‐mannitol (PAGGSM) additive solution. All units were X‐ray irradiated on day 2 post‐collection. Sampling for assessment of parameters of storage lesion was performed on day 2 pre‐irradiation and day 14 and 28 post‐irradiation. Results: Though irradiation increased cell stress, DEHT/PAGGSM and current common European preference DEHP/SAGM were equally affected up to 14 days post‐irradiation for all measured parameters. At day 28, haemolysis and microvesicle count were slightly increased in DEHT, whereas extracellular potassium ions, glucose, lactate, pH, mean corpuscular volume and microvesicle phosphatidylserine remained unaffected by plasticizer choice throughout storage. No individual unit exceeded 0.8% haemolysis, not even in DEHT/SAGM, the combination overall most affected by irradiation. Of the four combinations, membrane stability was least impacted in DEHP/PAGGSM. Conclusion: We demonstrate that DEHT is a suitable plasticizer for storage of RBCs after X‐ray irradiation cell stress. This strengthens the option of DEHT as a viable non‐phthalate substitute for DEHP. [ABSTRACT FROM AUTHOR]