4.3 Article

Bioactive glass-biopolymers-gold nanoparticle based composites for tissue engineering applications

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ELSEVIER
DOI: 10.1016/j.msec.2021.112006

关键词

Alginate; Pullulan; Silicate glasses; Gold nanoparticles

资金

  1. Ministry of Research and Innovation, CNCS -UEFISCDI, within PNCDI III [PN-III-P1-1.1-TE-2016-1324]
  2. Janos Bolyai Research Scholarship of the Hungarian Academy of Sciences [BO/00066/19/7]
  3. MTA Domus [3031/28/2019/HTMT]

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The study developed novel biomaterials by incorporating bioactive glass with gold nanoparticles into alginate-pullulan polymers, showcasing excellent biocompatibility and angiogenesis potential in tissue engineering. In vitro and in vivo evaluations demonstrated the superior bioactivity and biocompatibility of the composites, highlighting their promising applications in future soft tissue and bone engineering endeavors.
Biomaterials based on bioactive glass with gold nanoparticle composites have many applications in tissue engineering due to their tissue regeneration and angiogenesis capacities. The objectives of the study were to develop new composites using bioactive glass with gold nanospheres (BGAuSP) and gold nanocages (BGAuIND), individually introduced in alginate-pullulan (Alg-Pll) polymer, to evaluate their biocompatibility potential, and to compare the obtained results with those achieved when ll-tricalcium phosphate-hydroxyapatite (llTCP/HA) replaced the BG. The novel composites underwent structural and morphological characterization followed by in vitro viability testing on fibroblast and osteoblast cell lines. Additionally, the biomaterials were subcutaneously implanted in Sprague Dawley rats, for in vivo biocompatibility assessment during 3 separate time frames (14, 30 and 60 days). The biological effects were evaluated by histopathology and immunohistochemistry. The physical characterization revealed the cross-linking between polymers and glasses/ceramics and demonstrated a suitable thermal stability for sterilization processes. The in vitro assays demonstrated adequate form, pore size of composites ranging from few micrometers up to 100 ?m, while the self-assembled apatite layer formed after simulated body fluid immersion confirmed the composites? bioactivity. Viability assays have highlighted optimal cellular proliferation and in vitro biocompatibility for all tested composites. Furthermore, based on the in vivo subcutaneous analyses the polymer composites with BGAuNP have shown excellent biocompatibility at 14, 30 and 60 days, exhibiting marked angiogenesis while, tissue proliferation was confirmed by high number of Vimentin positive cells, in comparison with the polymer composite that contains llTCP/HA, which induced an inflammatory response represented by a foreign body reaction. The obtained results suggest promising, innovative, and biocompatible composites with bioactive properties for future soft tissue and bone engineering endeavours.

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