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Controlled release of basic fibroblast growth factor from a peptide biomaterial for bone regeneration
Author(s) -
Weikang Zhao,
Yuling Li,
Ao Zhou,
Xiaojun Chen,
Kai Li,
Sinan Chen,
博人 高橋,
Dianming Jiang
Publication year - 2020
Publication title -
royal society open science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.84
H-Index - 51
ISSN - 2054-5703
DOI - 10.1098/rsos.191830
Subject(s) - self healing hydrogels , self assembling peptide , in vivo , mesenchymal stem cell , materials science , biophysics , adhesion , biomedical engineering , biomaterial , chemistry , in vitro , microbiology and biotechnology , basic fibroblast growth factor , regeneration (biology) , alkaline phosphatase , cell adhesion , nanotechnology , growth factor , biochemistry , biology , polymer chemistry , medicine , receptor , composite material , enzyme
Self-assembled peptide scaffolds based on D-RADA16 are an important matrix for controlled drug release and three-dimensional cell culture. In this work, D-RADA16 peptide hydrogels were coated on artificial bone composed of nano-hydroxyapatite/polyamide 66 (nHA/PA66) to obtain a porous drug-releasing structure for treating bone defects. The developed materials were characterized via transmission electron microscopy and scanning electron microscopy. The proliferation and adhesion of bone mesenchymal stem cells (BMSCs) were examined by confocal laser microscopy and CCK-8 experiments. The osteogenic ability of the porous materials towards bone BMSCs was examined in vitro by staining with Alizarin Red S and alkaline phosphatase, and bioactivity was evaluated in vivo . The results revealed that nHA/PA66/D-RADA16/bFGF reduces the degradation rate of D-RADA16 hydrogels and prolongs sustained release of bFGF, which would promote BMSCs proliferation, adhesion and osteogenesis in vitro and bone repair in vivo . Thus, it deserves more attention and is worthy of further research.

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