Preparation of gelatin hydrogel sponges incorporating bioactive glasses capable for the controlled release of fibroblast growth factor-2

被引:9
作者
Washio, Ayako [1 ]
Teshima, Hiroki [2 ]
Yokota, Kazuyoshi [2 ]
Kitamura, Chiaki [1 ]
Tabata, Yasuhiko [3 ]
机构
[1] Kyushu Dent Univ, Dept Oral Funct, Div Endodont & Restorat Dent, Kitakyushu, Fukuoka, Japan
[2] Nippon Shika Yakuhin Co Ltd, Res & Dev Dept, Shimonoseki, Yamaguchi, Japan
[3] Kyoto Univ, Inst Frontier Life & Med Sci, Dept Regenerat Sci & Engn, Lab Biomat, Kyoto, Japan
关键词
bioactive glass; fibroblast growth factor-2; gelatin hydrogel; hydroxyapatite; scaffold; COLLAGEN SPONGE; DENTIN DEFECTS; PULP CELLS; IN-VITRO; BONE; ANGIOGENESIS; SCAFFOLDS; BIOGLASS(R); BIOCERAMICS; SURFACE;
D O I
10.1080/09205063.2018.1544474
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Gelatin hydrogel sponges incorporating bioactive glasses (Gel-BG) were fabricated. We evaluated the characteristics of Gel-BG as scaffolds from the perspective of their mechanical properties and the formation of hydroxyapatite by the incorporation of bioactive glasses (BG). In addition, the Gel-BG degradation and the profile of fibroblast growth factor-2 (FGF-2) release from the Gel-BG were examined. Every Gel-BG showed an interconnected pore structure with the pore size range of 180-200 mu m. The compression modulus of sponges incorporating BG increased. The time profiles of degradation for the 72-h crosslinked gelatin hydrogel sponges incorporating 10 wt% BG (Gel-BG(10)) and 50 wt% BG (Gel-BG(50)) were analogous to that of the 24-h crosslinked gelatin hydrogel sponge without BG (Gel-BG(0)). In measuring the release of FGF-2 from Gel-BG, the Gel-BG(10) and Gel-BG(50) showed almost analogous 100% cumulative release within 28 days in vivo. Additionally, a bioactivity evaluation showed that the presence of gelatin does not affect the in vitro bioactivity of Gel-BG. These sponges showed mechanical and chemical functionality as scaffolds, featuring both the controlled release of FGF-2 and the induction of hydroxyapatite crystallization.
引用
收藏
页码:49 / 63
页数:15
相关论文
共 56 条
[1]   Bioceramics for drug delivery [J].
Arcos, Daniel ;
Vallet-Regi, Maria .
ACTA MATERIALIA, 2013, 61 (03) :890-911
[2]   Mechanical properties of highly porous PDLLA/Bioglass® composite foams as scaffolds for bone tissue engineering [J].
Blaker, JJ ;
Maquet, V ;
Jérôme, R ;
Boccaccini, AR ;
Nazhat, SN .
ACTA BIOMATERIALIA, 2005, 1 (06) :643-652
[3]   Bioactive composite materials for tissue engineering scaffolds [J].
Boccaccini, AR ;
Blaker, JJ .
EXPERT REVIEW OF MEDICAL DEVICES, 2005, 2 (03) :303-317
[4]   Can bioactivity be tested in vitro with SBF solution? [J].
Bohner, Marc ;
Lemaitre, Jacques .
BIOMATERIALS, 2009, 30 (12) :2175-2179
[5]   Manipulating angiogenesis in medicine [J].
Carmeliet, P .
JOURNAL OF INTERNAL MEDICINE, 2004, 255 (05) :538-561
[6]  
Chen GP, 2000, J BIOMED MATER RES, V51, P273, DOI 10.1002/(SICI)1097-4636(200008)51:2<273::AID-JBM16>3.0.CO
[7]  
2-O
[8]   Collagen release kinetics of surface functionalized 4555 Bioglass®-based porous scaffolds [J].
Chen, Q. Z. ;
Ahmed, I. ;
Knowles, J. C. ;
Nazhat, S. N. ;
Boccaccini, A. R. ;
Rezwan, K. .
JOURNAL OF BIOMEDICAL MATERIALS RESEARCH PART A, 2008, 86A (04) :987-995
[9]  
DUCHEYNE P, 1987, J BIOMED MATER RES-A, V21, P219
[10]   Effects of GDNF-Loaded Injectable Gelatin-Based Hydrogels on Endogenous Neural Progenitor Cell Migration [J].
Fon, Deniece ;
Al-Abboodi, Aswan ;
Chan, Peggy P. Y. ;
Zhou, Kun ;
Crack, Peter ;
Finkelstein, David I. ;
Forsythe, John S. .
ADVANCED HEALTHCARE MATERIALS, 2014, 3 (05) :761-774