Pancreatic islet macroencapsulation using microwell porous membranes

Abstract Allogeneic islet transplantation into the liver in combination with immune suppressive drug therapy is widely regarded as a potential cure for type 1 diabetes. However, the intrahepatic system is suboptimal as the concentration of drugs and nutrients there is higher compared to pancreas, wh...

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Autores principales: Katarzyna Skrzypek, Milou Groot Nibbelink, Jéré van Lente, Mijke Buitinga, Marten A. Engelse, Eelco J. P. de Koning, Marcel Karperien, Aart van Apeldoorn, Dimitrios Stamatialis
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Publicado: Nature Portfolio 2017
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Acceso en línea:https://doaj.org/article/98a2240eb1094834a9e554ca7f3d85d2
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spelling oai:doaj.org-article:98a2240eb1094834a9e554ca7f3d85d22021-12-02T12:32:55ZPancreatic islet macroencapsulation using microwell porous membranes10.1038/s41598-017-09647-72045-2322https://doaj.org/article/98a2240eb1094834a9e554ca7f3d85d22017-08-01T00:00:00Zhttps://doi.org/10.1038/s41598-017-09647-7https://doaj.org/toc/2045-2322Abstract Allogeneic islet transplantation into the liver in combination with immune suppressive drug therapy is widely regarded as a potential cure for type 1 diabetes. However, the intrahepatic system is suboptimal as the concentration of drugs and nutrients there is higher compared to pancreas, which negatively affects islet function. Islet encapsulation within semipermeable membranes is a promising strategy that allows for the islet transplantation outside the suboptimal liver portal system and provides environment, where islets can perform their endocrine function. In this study, we develop a macroencapsulation device based on thin microwell membranes. The islets are seeded in separate microwells to avoid aggregation, whereas the membrane porosity is tailored to achieve sufficient transport of nutrients, glucose and insulin. The non-degradable, microwell membranes are composed of poly (ether sulfone)/polyvinylpyrrolidone and manufactured via phase separation micro molding. Our results show that the device prevents aggregation and preserves the islet’s native morphology. Moreover, the encapsulated islets maintain their glucose responsiveness and function after 7 days of culture (stimulation index above 2 for high glucose stimulation), demonstrating the potential of this novel device for islet transplantation.Katarzyna SkrzypekMilou Groot NibbelinkJéré van LenteMijke BuitingaMarten A. EngelseEelco J. P. de KoningMarcel KarperienAart van ApeldoornDimitrios StamatialisNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 7, Iss 1, Pp 1-12 (2017)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Katarzyna Skrzypek
Milou Groot Nibbelink
Jéré van Lente
Mijke Buitinga
Marten A. Engelse
Eelco J. P. de Koning
Marcel Karperien
Aart van Apeldoorn
Dimitrios Stamatialis
Pancreatic islet macroencapsulation using microwell porous membranes
description Abstract Allogeneic islet transplantation into the liver in combination with immune suppressive drug therapy is widely regarded as a potential cure for type 1 diabetes. However, the intrahepatic system is suboptimal as the concentration of drugs and nutrients there is higher compared to pancreas, which negatively affects islet function. Islet encapsulation within semipermeable membranes is a promising strategy that allows for the islet transplantation outside the suboptimal liver portal system and provides environment, where islets can perform their endocrine function. In this study, we develop a macroencapsulation device based on thin microwell membranes. The islets are seeded in separate microwells to avoid aggregation, whereas the membrane porosity is tailored to achieve sufficient transport of nutrients, glucose and insulin. The non-degradable, microwell membranes are composed of poly (ether sulfone)/polyvinylpyrrolidone and manufactured via phase separation micro molding. Our results show that the device prevents aggregation and preserves the islet’s native morphology. Moreover, the encapsulated islets maintain their glucose responsiveness and function after 7 days of culture (stimulation index above 2 for high glucose stimulation), demonstrating the potential of this novel device for islet transplantation.
format article
author Katarzyna Skrzypek
Milou Groot Nibbelink
Jéré van Lente
Mijke Buitinga
Marten A. Engelse
Eelco J. P. de Koning
Marcel Karperien
Aart van Apeldoorn
Dimitrios Stamatialis
author_facet Katarzyna Skrzypek
Milou Groot Nibbelink
Jéré van Lente
Mijke Buitinga
Marten A. Engelse
Eelco J. P. de Koning
Marcel Karperien
Aart van Apeldoorn
Dimitrios Stamatialis
author_sort Katarzyna Skrzypek
title Pancreatic islet macroencapsulation using microwell porous membranes
title_short Pancreatic islet macroencapsulation using microwell porous membranes
title_full Pancreatic islet macroencapsulation using microwell porous membranes
title_fullStr Pancreatic islet macroencapsulation using microwell porous membranes
title_full_unstemmed Pancreatic islet macroencapsulation using microwell porous membranes
title_sort pancreatic islet macroencapsulation using microwell porous membranes
publisher Nature Portfolio
publishDate 2017
url https://doaj.org/article/98a2240eb1094834a9e554ca7f3d85d2
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AT milougrootnibbelink pancreaticisletmacroencapsulationusingmicrowellporousmembranes
AT jerevanlente pancreaticisletmacroencapsulationusingmicrowellporousmembranes
AT mijkebuitinga pancreaticisletmacroencapsulationusingmicrowellporousmembranes
AT martenaengelse pancreaticisletmacroencapsulationusingmicrowellporousmembranes
AT eelcojpdekoning pancreaticisletmacroencapsulationusingmicrowellporousmembranes
AT marcelkarperien pancreaticisletmacroencapsulationusingmicrowellporousmembranes
AT aartvanapeldoorn pancreaticisletmacroencapsulationusingmicrowellporousmembranes
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