• DocumentCode
    2499220
  • Title

    Application of Polyvinyl Alcohol (PVA) Macro-Encapsulated Islets in Islet Transplantation

  • Author

    Qi, Zhi ; Qi, Meirigeng ; Sakata, Naoaki ; Yamamoto, Chizuru ; Yanai, Goichi ; Ikenoue, Etsuko ; Wu, Qian ; Hiura, Akihito ; Sumi, Shoichiro

  • Author_Institution
    Dept. of Organ Reconstruction, Kyoto Univ., Kyoto, Japan
  • fYear
    2009
  • fDate
    11-13 June 2009
  • Firstpage
    1
  • Lastpage
    3
  • Abstract
    Background: Islet transplantation has shown great success in the treatment of type 1 diabetes. However, it still has two major problems to overcome, namely donor shortage and the side effects of immunosuppression. Encapsulated islets have emerged as a potential option on islet transplantation because it can, at least partly, overcome these two problems. Methods: After making PVA macro-encapsulated islets, recovery rate, insulin content, insulin secretion test, and morphological changes in culture with/without fresh human plasma were evaluated in vitro. PVA macro-encapsulated rat islets were transplanted into the peritoneal cavity of STZ-diabetic mice and rats. We observed blood glucose, body weight, survival rate, blood urea nitrogen (BUN), creatinine (Cr), and performed histological assessment in vivo. Results: After 14-day culture, the encapsulated islets, maintained a normal morphology and better insulin secretion in response to high glucose. Addition of fresh human plasma into the culture medium destroyed free islets in 48 hours but did not affect the morphology and insulin content of PVA macro-encapsulated islets. After transplantation to diabetic mice and rats, encapsulated islets decreased blood glucose levels, prevented weight loss and improved the survival rate in comparison to the negative control groups. The BUN and Cr levels were also decreased significantly after 1 week in the PVA group with amelioration of ketosis. Conclusions: PVA macro-encapsulated islets can protect islets against discordant immunorejection, and ameliorate hyperglycemia, ketosis and diabetic renal dysfunction in STZ induced diabetic mice and rats.
  • Keywords
    biomedical materials; blood; diseases; encapsulation; patient treatment; polymers; sugar; STZ-diabetic mice; STZ-diabetic rats; ameliorate hyperglycemia; blood glucose; blood urea nitrogen; body weight; creatinine; diabetic renal dysfunction; fresh human plasma; insulin content; insulin secretion test; islet transplantation; ketosis; peritoneal cavity; polyvinyl alcohol macroencapsulated islets; survival rate; time 48 h to 14 day; type 1 diabetes; Blood; Diabetes; Fluids and secretions; Humans; Immune system; Insulin; Mice; Plasmas; Rats; Sugar;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    Bioinformatics and Biomedical Engineering , 2009. ICBBE 2009. 3rd International Conference on
  • Conference_Location
    Beijing
  • Print_ISBN
    978-1-4244-2901-1
  • Electronic_ISBN
    978-1-4244-2902-8
  • Type

    conf

  • DOI
    10.1109/ICBBE.2009.5162392
  • Filename
    5162392