4.7 Article

Effect of Fibrin Concentration on the In Vitro Production of Dermo-Epidermal Equivalents

期刊

出版社

MDPI
DOI: 10.3390/ijms22136746

关键词

fibrin hydrogels; plasma-derived fibrin hydrogel; bilayered in vitro skin substitutes; organotypic skin cultures; platelet-poor plasma (PPP); skin tissue engineering

资金

  1. Programa de Actividades de I+D entre Grupos de Investigacion de la Comunidad de Madrid, Biopieltec-CM [S2018/BAA-4480]
  2. Programa Estatal de I+D+i Orientada a los Retos de la Sociedad [RTI2018-101627-B-I00]
  3. Programa de Apoyo a la Realizacion de Proyectos Interdisciplinares de I+D para Jovenes Investigadores de la Universidad Carlos III de Madrid (project: BIOMASKIN)
  4. Catedra Fundacion Ramon Areces

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This study demonstrates that increasing fibrin concentration can significantly improve mechanical properties and matrix stability, thereby promoting the development of in vitro skin cultures. These new systems will provide better in vitro skin models for testing drugs, cosmetics, and chemicals, and can even be used for personalized skin diagnosis and determining the most effective treatment.
Human plasma-derived bilayered skin substitutes were successfully used by our group to produce human-based in vitro skin models for toxicity, cosmetic, and pharmaceutical testing. However, mechanical weakness, which causes the plasma-derived fibrin matrices to contract significantly, led us to attempt to improve their stability. In this work, we studied whether an increase in fibrin concentration from 1.2 to 2.4 mg/mL (which is the useful fibrinogen concentration range that can be obtained from plasma) improves the matrix and, hence, the performance of the in vitro skin cultures. The results show that this increase in fibrin concentration indeed affected the mechanical properties by doubling the elastic moduli and the maximum load. A structural analysis indicated a decreased porosity for the 2.4 mg/mL hydrogels, which can help explain this mechanical behavior. The contraction was clearly reduced for the 2.4 mg/mL matrices, which also allowed for the growth and proliferation of primary fibroblasts and keratinocytes, although at a somewhat reduced rate compared to the 1.2 mg/mL gels. Finally, both concentrations of fibrin gave rise to organotypic skin cultures with a fully differentiated epidermis, although their lifespans were longer (25-35%) in cultures with more concentrated matrices, which improves their usefulness. These systems will allow the generation of much better in vitro skin models for the testing of drugs, cosmetics and chemicals, or even to personalized skin for the diagnosis or determination of the most effective treatment possible.

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