Evidence map›Paper›PMID 30332824›Full record

ArticleBioengineering (Basel, Switzerland)2018

A Standardized Collagen-Based Scaffold Improves Human Hepatocyte Shipment and Allows Metabolic Studies over 10 Days.

Marc Ruoß, Victor Häussling, Frank Schügner, Leon H H Olde Damink, Serene M L Lee, Liming Ge, Sabrina Ehnert, Andreas K Nussler

Open access · goldAbstract read
In one paragraph

Article in Bioengineering (Basel, Switzerland), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.2field-weighted citation impact, top 10% of its field
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

22 citing papers in PubMed, 44 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Marc RuoßDepartment of Traumatology, Siegfried Weller Institute, Eberhard Karls University, 72076 Tübingen, Germany. m.ruoss@hotmail.de.ORCID 0000-0002-0193-4425
Victor HäusslingDepartment of Traumatology, Siegfried Weller Institute, Eberhard Karls University, 72076 Tübingen, Germany. victor.haeussling@hotmail.de.
Frank SchügnerMatricel GmbH, 52134 Herzogenrath, Germany. schuegner@matricel.de.
Leon H H Olde DaminkMatricel GmbH, 52134 Herzogenrath, Germany. olde_damink@matricel.de.
Serene M L LeeHepacult GmbH, 82152 Martinsried/Planegg, Germany. Serene.Lee@med.uni-muenchen.de.
Liming GeHepacult GmbH, 82152 Martinsried/Planegg, Germany. liming.ge@hepacult.de.
Sabrina EhnertDepartment of Traumatology, Siegfried Weller Institute, Eberhard Karls University, 72076 Tübingen, Germany. sabrina.ehnert@gmail.com.
Andreas K NusslerDepartment of Traumatology, Siegfried Weller Institute, Eberhard Karls University, 72076 Tübingen, Germany. andreas.nuessler@gmail.com.ORCID 0000-0002-6666-6791
LMU Klinikum · DE

Funding

Deutsche Forschungsgemeinschaft and Open Access Publishing Fund of University of Tübingen -Federal Ministry for Economic Affairs and Energy, Germany ZIM program (AZ: ZF4301401CS6, ZF4301001CS6, ZF4301101CS6)
6 · The paper itself

Abstract

Due to pronounced species differences, hepatotoxicity of new drugs often cannot be detected in animal studies. Alternatively, human hepatocytes could be used, but there are some limitations. The cells are not always available on demand or in sufficient amounts, so far there has been only limited success to allow the transport of freshly isolated hepatocytes without massive loss of function or their cultivation for a long time. Since it is well accepted that the cultivation of hepatocytes in 3D is related to an improved function, we here tested the Optimaix-3D Scaffold from Matricel for the transport and cultivation of hepatocytes. After characterization of the scaffold, we shipped cells on the scaffold and/or cultivated them over 10 days. With the evaluation of hepatocyte functions such as urea production, albumin synthesis, and CYP activity, we showed that the metabolic activity of the cells on the scaffold remained nearly constant over the culture time whereas a significant decrease in metabolic activity occurred in 2D cultures. In addition, we demonstrated that significantly fewer cells were lost during transport. In summary, the collagen-based scaffold allows the transport and cultivation of hepatocytes without loss of function over 10 days.

Indexed as

cells shipmentdrug-induced hepatotoxicitynatural collagen scaffoldspre-clinical drug testing

Identifiers

PMID30332824
PMCPMC6316810
OpenAlexW2895781269

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.