Self-mineralizing Ca-enriched methacrylated gellan gum beads for bone tissue engineering

被引:56
作者
Vieira, Silvia [1 ,2 ]
Morais, Alain da Silva [1 ,2 ]
Garet, Elina [3 ,4 ]
Silva-Correia, Joana [1 ,2 ,5 ]
Reis, Rui L. [1 ,2 ,5 ]
Gonzalez-Fernandez, Africa [3 ,4 ]
Miguel Oliveira, J. [1 ,2 ,5 ]
机构
[1] Univ Minho, 3Bs Res Grp, I3Bs Res Inst Biomat Biodegradables & Biomimet, European Inst Excellence Tissue Engn & Regenerat, AvePk,Parque Ciencia & Tecnol, P-4805017 Barco, Guimaraes, Portugal
[2] ICVS 3Bs PT Govt Associate Lab, Braga, Portugal
[3] Ctr Singular Invest Galicia, Ctr Invest Biomed CINBIO, Immunol, Univ Campus, Vigo 36310, Pontevedra, Spain
[4] Galicia Sur Hlth Res Inst IIS GS, Univ Campus, Vigo 36310, Pontevedra, Spain
[5] Univ Minho, Discoveries Ctr Regenerat & Precis Med, AvePk, P-4805017 Barco, Guimaraes, Portugal
关键词
Methacrylated gellan gum; Hydrogels; Mineralization; Bioactivity; Drug delivery; Bone tissue engineering; OSTEOGENIC DIFFERENTIATION; IN-VITRO; STEM-CELLS; HYDROGELS; DEXAMETHASONE; BIOMATERIALS; REPAIR; BIOCOMPATIBILITY; INFLAMMATION; REGENERATION;
D O I
10.1016/j.actbio.2019.01.053
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
In this study, methacrylated gellan-gum (GG-MA) heteropolysaccharide is proposed as a hydrogel for drug delivery and bone tissue engineering applications. Calcium-enriched beads obtained from the crosslinking of 1% (w/v) GG-MA solutions with 0.1 M CaCl2 were investigated, considering their intrinsic capacity to promote self-mineralization by ion binding and deposition. Indeed, when immersed in a physiological environment, the Ca-enriched beads promoted the development of a bone-like apatite layer, as confirmed by EDS and XRD chemical analysis. Additionally, the mild production process is compatible with drugs incorporation and release. After encapsulation, Dextran with different molecular weights as well as Dexamethasone 21-phosphate were efficiently released to the surrounding environment. The engineered system was also evaluated considering its biocompatibility, by means of qualitative determination of total complement activation, macrophage proliferation, cytokine release and in vitro cell culture. These experiments showed that the developed hydrogels may not stimulate a disproportionate pro-inflammatory reaction once transplanted. At last, when implanted subcutaneously in CD1 male mice up to 8 weeks, the beads were completely calcified, and no inflammatory reaction was observed. Summing up, these results show that calcium-enriched GG-MA hydrogel beads hold great potential as news tools for bone tissue regeneration and local drug delivery applications. Statement of Significance This work describes a low-cost and straightforward strategy to prepare bioactive methacrylated gellan gum (GG-MA) hydrogels, which can be used as drug delivery systems. GG-MA is a highly anionic polymer, that can be crosslinked with divalent ions, as calcium. Taking advantage of this feature, it was possible to prepare Ca-enriched GG-MA hydrogel beads. These beads display a bioactive behavior, since they promote apatite deposition when placed in physiological conditions. Studies on the immune response suggest that the developed beads do not trigger severe immune responses. Importantly, the mild processing method render these beads compliant with drug delivery strategies, paving the way for the application of dual-functional materials on bone tissue engineering. (C) 2019 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:74 / 85
页数:12
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