4.3 Article

Development of alginate-based hydrogels for blood vessel engineering

期刊

BIOMATERIALS ADVANCES
卷 134, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.msec.2021.112588

关键词

Tissue-engineered vascular graft; Natural polymers; Barium ions; Freestanding tubular hydrogels; Sacrificial mould

资金

  1. Portuguese Foundation for Science and Technology (FCT) [PTDC/BTM-SAL/28882/2017]
  2. NORTE 2020 Structured Project [Norte2020, NORTE01-0145-FEDER-000021]
  3. Fundação para a Ciência e a Tecnologia [PTDC/BTM-SAL/28882/2017] Funding Source: FCT

向作者/读者索取更多资源

Vascular diseases are a leading cause of death worldwide. This study explores tissue engineering-based solutions for the treatment of vascular diseases by developing freestanding vascular substitutes with tunable properties in terms of size, shape, and wall thickness.
Vascular diseases arc among the primary causes of death worldwide. In serious conditions, replacement of the damaged vessel is required. Autologous grafts arc preferred, but their limited availability and difficulty of the harvesting procedures favour synthetic alternatives use. however, as synthetic grafts may present significant drawbacks, tissue engineering-based solutions arc proposed. Herein, tubular hydrogels of alginate combined with collagen type I and/or silk fibroin were prepared by ionotropic gelation using gelatin hydrogel sacrificial moulds loaded with calcium ions (Ca-2(+)). The time of exposure of alginate solutions to Ca2+-loaded gelatin was used to control the wall thickness of the hydrogels (0.47 +/- 0.10 mm-1.41 +/- 0.21 mm). A second crosslinking step with barium chloride prevented their degradation for a 14 day period and improved mechanical properties by two-fold. Protein leaching tests showed that collagen type I, unlike silk fibroin, was strongly incorporated in the hydrogels. The presence of silk fibroin in the alginate matrix, containing or not collagen, did not significantly improve hydrogels' properties. Conversely, hydrogels enriched only with collagen were able to better support EA.hy926 and MRG5 cells growth and characteristic phenotype. These results suggest that a two-step crosslinking procedure combined with the use of collagen type I allow for producing freestanding vascular substitutes with tuneable properties in terms of size, shape and wall thickness.

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