Frontiers in Bioengineering and Biotechnology (Jun 2025)

Acellular porcine placental membranes as a novel biomaterial for tissue repair applications

  • Gustavo Henrique Doná Rodrigues Almeida,
  • Luan Stefani Lima,
  • Mariana Sversut Gibbin,
  • Beatriz Lopomo,
  • Rafael Oliveira Bergamo,
  • Raquel Souza da Silva,
  • Giovanna Vitória Consani Santos,
  • Bruna Gomes Silva,
  • Isabela Paulillo D’Onofrio,
  • Henrique dos Santos,
  • Lediane Pedroso Silva,
  • Tais da Silva,
  • Henrique Lança Fuzeti,
  • Bianca Fuzeti Candian,
  • Thais Naomi Gonçalves Nesiyama,
  • João Victor Damin,
  • Claudio Guilherme de Assis Oliveira,
  • Lucas Paulo Jacinto Saavedra,
  • Guilherme Henrique Gonçalves de Almeida,
  • Douglas Lopes de Almeida,
  • Jaqueline de Carvalho Rinaldi,
  • Francielle Sato,
  • Mauro Luciano Baesso,
  • Luzmarina Hernandes,
  • Flávio Vieira Meirelles,
  • Rose Eli Grassi Rici,
  • Durvanei Augusto Maria,
  • Paulo Cezar de Freitas Mathias,
  • Ana Claudia Oliveira Carreira,
  • Ana Claudia Oliveira Carreira

DOI
https://doi.org/10.3389/fbioe.2025.1606615
Journal volume & issue
Vol. 13

Abstract

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Biological dressings derived from the extracellular matrix (ECM) of human placental tissues have proven effective in treating complex skin wounds and other anatomical sites, offering potential for new therapeutic applications. However, the use of human tissues is limited by ethical and biosafety concerns, restricting large-scale production. To address this, biomaterials from placentas of livestock animals offer a cost-effective, accessible alternative without harming animal welfare. Given pigs’ large-scale production, short gestation periods, and abundant material availability, this study aimed to produce, characterize, and validate acellular biomembranes derived from decellularized porcine allantochorion for tissue repair. Placental fragments from Duroc sows were decellularized using a protocol involving immersion and orbital shaking in 0.1% SDS and 0.5% Triton X-100, followed by low-frequency ultrasonication. Accelularity was confirmed by total genomic DNA quantification and H&E and DAPI staining for nuclear visualization. Membrane structure and composition were analyzed using histological, immunohistochemical methods, and scanning electron microscopy. Spectroscopic analyses detected physicochemical changes in placental ECM, and biomechanical testing assessed membrane strength and stiffness. Biological functionality was validated through in vitro cell viability and adhesion assays with canine endothelial progenitor cells and L929 murine fibroblasts. In vivo biocompatibility was tested by subcutaneously implanting the biomaterial in rats for histopathological evaluation. Results showed efficient decellularization, with preserved ECM structure. The scaffolds were cytocompatible, supporting cell adhesion and high viability. In vivo testing revealed no immune rejection, confirming biocompatibility and biodegradability. In conclusion, acellular porcine placental biomembranes have the necessary characteristics to be explored as scaffolds for tissue engineering and novel repair therapies.

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