Evaluation of Perfluorohexyloctane/Polydimethylsiloxane for Pancreas Preservation for Clinical Islet Isolation and Transplantation

被引:3
|
作者
Stahle, Magnus [1 ]
Foss, Aksel [2 ]
Gustafsson, Bengt [3 ]
Lempinen, Marko [4 ]
Lundgren, Torbjorn [5 ]
Rafael, Ehab [6 ]
Tufveson, Gunnar [7 ]
Theisinger, Bastian [8 ]
Brandhorst, Daniel [1 ]
Korsgren, Olle [1 ]
Friberg, Andrew [1 ]
机构
[1] Uppsala Univ, Dept Immunol Genet & Pathol, Uppsala, Sweden
[2] Radiumhosp Med Ctr, Rikshosp, Dept Transplantat Surg, Oslo, Norway
[3] Univ Hosp, Dept Transplantat, Gothenburg, Sweden
[4] Univ Helsinki, Surg Hosp, Div Transplantat, Helsinki, Finland
[5] Karolinska Inst, CLINTEC, Div Transplantat Surg, Stockholm, Sweden
[6] Univ Hosp, Dept Nephrol & Transplantat, Malmo, Sweden
[7] Univ Uppsala Hosp, Div Transplantat Surg, Dept Surg Sci, Uppsala, Sweden
[8] Novaliq GmbH, Heidelberg, Germany
基金
美国国家卫生研究院; 瑞典研究理事会;
关键词
Islet isolation; Pancreas preservation; Clinical islet transplantation; Perfluorohydrocarbons; Oxygenation; Hypoxia; TYPE-1; DIABETES-MELLITUS; 2-LAYER METHOD; SINGLE-DONOR; STORAGE; PERFLUOROCARBON; OUTCOMES; SYSTEM;
D O I
10.3727/096368916X691709
中图分类号
Q813 [细胞工程];
学科分类号
摘要
This study aimed to evaluate a 50:50 mix of perfluorohexyloctane/polydimethylsiloxane 5 (F6H8S5) preservation of pancreases in a clinical setting compared with standard solutions for 1) cold ischemia time (CIT) <10 h and 2) an extended CIT >20 h. Procured clinical-grade pancreases were shipped in either F6H8S5 or in standard preservation solutions, that is, University of Wisconsin (UW) or Custodiol. F6H5S5 was preoxygenated for at least 15 min. Included clinical-grade pancreases were procured in UW or Custodiol. Upon arrival at the islet isolation laboratory, the duodenum was removed followed by rough trimming while F6H8S5 was oxygenated for 15-20 min. Trimmed pancreases were immersed into oxygenated F6H8S5 and stored at 4 C overnight followed by subsequent islet isolation. Pancreas preservation using F6H8S5 proved as effective as UW and Custadiol when used within CIT up to 10 h, in terms of both isolation outcome and islet functionality. Preservation in F6H8S5 of pancreases with extended CIT gave results similar to controls with CIT <10 h for both isolated islet functionality and isolation outcome. This study of clinically obtained pancreases indicates a clear benefit of using F6H8S5 on pancreases with extended CIT as it seems to allow extended cold ischemic time without affecting islet function and islet numbers.
引用
收藏
页码:2269 / 2276
页数:8
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