Evidence map›Paper›PMID 24039964›Full record

ArticlePloS one2013

Biocompatible coating of encapsulated cells using ionotropic gelation.

Friederike Ehrhart, Esther Mettler, Thomas Böse, Matthias Max Weber, Julio Alberto Vásquez, Heiko Zimmermann

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
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

6 authors.

Friederike EhrhartBiophysik und Kryotechnologie, Fraunhofer IBMT, Sankt Ingbert, Germany.
Esther Mettler
Thomas Böse
Matthias Max Weber
Julio Alberto Vásquez
Heiko Zimmermann

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The technique of immunoisolated transplantation has seen in the last twenty years improvements in biocompatibility, long term stability and methods for avoidance of fibrosis in alginate capsules. However, two major problems are not yet solved: living cellular material that is not centered in the capsule is not properly protected from the hosts' immune system and the total transplant volume needs to be reduced. To solve these problems, we present a method for applying fully biocompatible alginate multilayers to a barium-alginate core without the use of polycations. We report on the factors that influence layer formation and stability and can therefore provide data for full adjustability of the additional layer. Although known for yeast and plant cells, this technique has not previously been demonstrated with mammalian cells or ultra-high viscous alginates. Viability of murine insulinoma cells was investigated by live-dead staining and live cell imaging, for murine Langerhans' islets viability and insulin secretion have been measured. No hampering effects of the second alginate layer were found. This multi-layer technique therefore has great potential for clinical and in vitro use and is likely to be central in alginate matrix based immunoisolated cell therapy.

Indexed as

AlginatesAnimalsBariumCell Line, TumorCells, CulturedCells, ImmobilizedCell SurvivalCoated Materials, BiocompatibleGelsGlucuronic AcidHexuronic AcidsIslets of LangerhansMiceRatsRats, WistarAlginatesBariumCoated Materials, BiocompatibleGelsGlucuronic AcidHexuronic Acids

Identifiers

PMID24039964
PMCPMC3767676

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Registered trials

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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.