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10.1038/s41598-017-01584-9

http://scihub22266oqcxt.onion/10.1038/s41598-017-01584-9
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suck abstract from ncbi


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pmid28490729
      Sci+Rep 2017 ; 7 (1 ): 1689
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  • A comparative multi-parametric in vitro model identifies the power of test conditions to predict the fibrotic tendency of a biomaterial #MMPMID28490729
  • Jannasch M ; Gaetzner S ; Weigel T ; Walles H ; Schmitz T ; Hansmann J
  • Sci Rep 2017[May]; 7 (1 ): 1689 PMID28490729 show ga
  • Despite growing effort to advance materials towards a low fibrotic progression, all implants elicit adverse tissue responses. Pre-clinical biomaterial assessment relies on animals testing, which can be complemented by in vitro tests to address the Russell and Burch's 3R aspect of reducing animal burden. However, a poor correlation between in vitro and in vivo biomaterial assessments confirms a need for suitable in vitro biomaterial tests. The aim of the study was to identify a test setting, which is predictive and might be time- and cost-efficient. We demonstrated how sensitive in vitro biomaterial assessment based on human primary macrophages depends on test conditions. Moreover, possible clinical scenarios such as lipopolysaccharide contamination, contact to autologous blood plasma, and presence of IL-4 in an immune niche influence the outcome of a biomaterial ranking. Nevertheless, by using glass, titanium, polytetrafluorethylene, silicone, and polyethylene representing a specific material-induced fibrotic response and by comparison to literature data, we were able to identify a test condition that provides a high correlation to state-of-the-art in vivo studies. Most important, biomaterial ranking obtained under native plasma test conditions showed a high predictive accuracy compared to in vivo assessments, strengthening a biomimetic three-dimensional in vitro test platform.
  • |*Models, Biological [MESH]
  • |Biocompatible Materials/*adverse effects [MESH]
  • |Cell Differentiation/drug effects [MESH]
  • |Cell Shape/drug effects [MESH]
  • |Cell Survival/drug effects [MESH]
  • |Cytokines/metabolism [MESH]
  • |Fibrosis [MESH]
  • |Humans [MESH]
  • |Inflammation Mediators/metabolism [MESH]
  • |Macrophages/drug effects/pathology [MESH]
  • |Phenotype [MESH]


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