4.5 Article

Generation of genipin cross-linked fibrin-agarose hydrogel tissue-like models for tissue engineering applications

期刊

BIOMEDICAL MATERIALS
卷 13, 期 2, 页码 -

出版社

IOP PUBLISHING LTD
DOI: 10.1088/1748-605X/aa9ad2

关键词

tissue engineering; nanostructuration technique; genipin cross-linking; fibrin-agarose; hydrogels; cell-biomaterial interactions; rheology

资金

  1. Plan Nacionalde Investigacion Cientifica, Desarrollo e innovacion Tecnologica (I+D+I) del Ministerio de Economia y Competitividad, Espana (Institutos de Salud Carlos III) [FIS PI14/1343]
  2. FEDER, European Union
  3. Fundacion Progreso y Salud, Junta de Andalucia, Espana [SAS PI-400-2016]

向作者/读者索取更多资源

The generation of biomimetic and biocompatible artificial tissues is the basic research objective for tissue engineering (TE). In this sense, the biofabrication of scaffolds that resemble the tissues' extracellular matrix is an essential aim in this field. Uncompressed and nanostructured fibrin-agarose hydrogels (FAH and NFAH, respectively) have emerged as promising scaffolds in TE, but their structure and biomechanical properties must be improved in order to broaden their TE applications. Here, we generated and characterized novel membrane-like models with increased structural and biomechanical properties based on the chemical cross-linking of FAH and NFAH with genipin (GP at 0.1%, 0.25%, 0.5% and 0.75%). Furthermore, the scaffolds were subjected to rheological (G, G', G '' modulus), ultrastructural and ex vivo biocompatibility analyses. Results showed that all GP concentrations increased the stiffness (G) and especially the elasticity (G') of FAH and NFAH. Ultrastructural analyses demonstrated that GP and nanostructuration of FAH allowed us to control the porosity of FAH. In addition, biological studies revealed that higher concentration of GP (0.75%) started to compromise the cell function and viability. Finally, this study demonstrated the possibility to generate natural and biocompatible FAH and NFAH with improved structural and biomechanical properties by using 0.1%-0.5% of GP. However, further in vivo studies are needed in order to demonstrate the biocompatibility, biodegradability and regeneration capability of these cross-linked scaffolds.

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