Alginate- and gelatin-based bioactive photocross-linkable hybrid materials for bone tissue engineering

被引:61
作者
Lewandowska-Lancucka, Joanna [1 ]
Mystek, Katarzyna [1 ]
Mignon, Am [2 ]
Van Vlierberghe, Sandra [2 ,3 ]
Latkiewicz, Anna [4 ]
Nowakowska, Maria [1 ]
机构
[1] Jagiellonian Univ, Fac Chem, Ingardena 3, PL-30060 Krakow, Poland
[2] Univ Ghent, Dept Organ & Macromol Chem, Krijgslaan 281,Bldg S-4 Bis, BE-9000 Ghent, Belgium
[3] Vrije Univ Brussel, Brussels Photon Team, Pl Laan 2, BE-1050 Brussels, Belgium
[4] Jagiellonian Univ, Inst Geol Sci, Lab Field Emiss Scanning Elect Microscopy & Micro, Oleandry 2A, PL-30060 Krakow, Poland
关键词
Alginate; Gelatin; Hydrogels; Silica; Tissue engineering; MECHANICAL-PROPERTIES; HYDROGELS; SCAFFOLDS; SPECTROSCOPY; COLLAGEN; GROWTH;
D O I
10.1016/j.carbpol.2016.11.051
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The paper presents the synthesis, the physico-chemical and the biological properties of novel hybrid materials prepared from photo-crosslinked gelatin/alginate-based hydrogels and silica particles exhibiting potential for the regeneration of bone tissue. Both alginate and gelatin were functionalized with methacrylate and methacrylamide moieties, respectively to render them photo-crosslinkable. Submicron silica particles of two sizes were dispersed within three types of polymeric sols including alginate, gelatin, and gelatin/alginate blends, which were subsequently photo-crosslinked. The swelling ratio, the gel fraction and the mechanical properties of the hybrid materials developed were examined and compared to these determined for reference hydrogel matrices. The in vitro cell culture studies have shown that the prepared materials exhibited biocompatibility as they supported both MEFs and MG-63 mitochondrial activity. Finally, the in vitro experiments performed under simulated body fluid conditions have revealed that due to inclusion of silica particles into the biopolymeric hydrogel matrices the mineralization was successfully induced. (C) 2016 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1714 / 1722
页数:9
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