Evidence map›Paper›PMID 28835662›Full record

ArticleScientific reports2017

Pancreatic islet macroencapsulation using microwell porous membranes.

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

Abstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed.

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  18. In vitro degradation profiles and in vivo biomaterial-tissue interactions of microwell array delivery devices.Journal of biomedical materials research. Part B, Applied biomaterials · 2021
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Katarzyna SkrzypekBioartificial organs, Biomaterials Science and Technology department, MIRA Institute of Biomedical Technology and Technical Medicine, University of Twente, Enschede, The Netherlands.
Milou Groot NibbelinkDevelopmental BioEngineering, MIRA Institute of Biomedical Technology and Technical Medicine, University of Twente, Enschede, The Netherlands.
Jéré van LenteDevelopmental BioEngineering, MIRA Institute of Biomedical Technology and Technical Medicine, University of Twente, Enschede, The Netherlands.ORCID 0000-0001-5896-9269
Mijke BuitingaDepartment of Radiology and Nuclear Medicine, Radboud University Medical Center, Nijmegen, The Netherlands.
Marten A EngelseNephrology, Leiden University Medical Center, Leiden, The Netherlands.
Eelco J P de KoningNephrology, Leiden University Medical Center, Leiden, The Netherlands.
Marcel KarperienDevelopmental BioEngineering, MIRA Institute of Biomedical Technology and Technical Medicine, University of Twente, Enschede, The Netherlands.
Aart van ApeldoornDevelopmental BioEngineering, MIRA Institute of Biomedical Technology and Technical Medicine, University of Twente, Enschede, The Netherlands.
Dimitrios StamatialisBioartificial organs, Biomaterials Science and Technology department, MIRA Institute of Biomedical Technology and Technical Medicine, University of Twente, Enschede, The Netherlands. d.stamatialis@utwente.nl.ORCID 0000-0002-2298-2442

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Biocompatible MaterialsIslets of LangerhansMembranesAnimalsBiological TransportCell LineCell SurvivalDiabetes Mellitus, Type 1GlucoseHumansInsulinIslets of Langerhans TransplantationMicePermeabilityPorosityTissue Culture TechniquesBiocompatible MaterialsGlucoseInsulin

Identifiers

PMID28835662
PMCPMC5569024

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.