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Semiautomated quantification of the fibrous tissue response to complex three-dimensional filamentous scaffolds using digital image analysis.
Barsch, Friedrich; Mamilos, Andreas; Babel, Maximilian; Wagner, Willi L; Winther, Hinrich B; Schmitt, Volker H; Hierlemann, Helmut; Teufel, Andreas; Brochhausen, Christoph.
Afiliação
  • Barsch F; Institute for Exercise and Occupational Medicine, Faculty of Medicine, Medical Center, University of Freiburg, Freiburg, Germany.
  • Mamilos A; Institute of Pathology, University Regensburg, Regensburg, Germany.
  • Babel M; Institute of Pathology, University Regensburg, Regensburg, Germany.
  • Wagner WL; Institute of Pathology, University Regensburg, Regensburg, Germany.
  • Winther HB; Central Biobank Regensburg, University Regensburg and University Hospital Regensburg, Regensburg, Germany.
  • Schmitt VH; Department of Diagnostic and Interventional Radiology, University Hospital Heidelberg, Heidelberg, Germany.
  • Hierlemann H; Translational Lung Research Centre Heidelberg (TLRC), German Lung Research Centre (DZL), Heidelberg, Germany.
  • Teufel A; Institute for Diagnostic and Interventional Radiology, Hannover Medical School, Hannover, Germany.
  • Brochhausen C; Department of Cardiology, Cardiology I, University Medical Center Mainz, Johannes Gutenberg-University of Mainz, Mainz, Germany.
J Biomed Mater Res A ; 110(2): 353-364, 2022 02.
Article em En | MEDLINE | ID: mdl-34390322
ABSTRACT
Fibrosis represents a relevant response to the implantation of biomaterials, which occurs not only at the tissue-material interface (fibrotic encapsulation) but also within the void fraction of complex three-dimensional (3D) biomaterial constructions (fibrotic ingrowth). Usual evaluation of the biocompatibility mostly depicts fibrosis at the interface of the biomaterial using semiquantitative scores. Here, the relations between encapsulation and infiltrating fibrotic growth are poorly represented. Virtual pathology and digital image analysis provide new strategies to assess fibrosis in a more differentiated way. In this study, we adopted a method previously used to quantify fibrosis in visceral organs to the quantification of fibrosis to 3D biomaterials. In a proof-of-concept study, we transferred the "Collagen Proportionate Area" (CPA) analysis from hepatology to the field of biomaterials. As one task of an experimental animal study, we used CPA analysis to quantify the fibrotic ingrowth into a filamentous scaffold after subcutaneous implantation. We were able to demonstrate that the application of the CPA analysis is well suited as an additional fibrosis evaluation strategy for new biomaterial constructions. The CPA method can contribute to a better understanding of the fibrotic interactions between 3D scaffolds and the host tissue responses.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Materiais Biocompatíveis / Colágeno Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Revista: J Biomed Mater Res A Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Materiais Biocompatíveis / Colágeno Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Revista: J Biomed Mater Res A Ano de publicação: 2022 Tipo de documento: Article