Bacterial Cellulose: Long-Term Biocompatibility Studies

被引:103
|
作者
Pertile, Renata A. N. [1 ]
Moreira, Susana [1 ]
Gil da Costa, Rui M. [2 ]
Correia, Alexandra [3 ]
Guardao, Luisa [2 ]
Gartner, Fatima [2 ,4 ]
Vilanova, Manuel [2 ]
Gama, Miguel [1 ]
机构
[1] Univ Minho, IBB, P-4710057 Braga, Portugal
[2] Univ Porto, ICBAS, P-4099003 Oporto, Portugal
[3] Univ Minho, Ctr Biol Mol & Ambiental, CMBA, Dept Biol, P-4710057 Braga, Portugal
[4] Univ Porto, Inst Mol Pathol & Immunol, IPATIMUP, P-4200465 Oporto, Portugal
关键词
Bacterial cellulose; in vivo biocompatibility; nanofibres; tissue engineering; CARBON NANOTUBES; IN-VITRO; MECHANICAL-PROPERTIES; BIOLOGICAL BEHAVIOR; MICROBIAL CELLULOSE; TISSUE; NANOFIBERS; CELLS; VIVO; GENOTOXICITY;
D O I
10.1163/092050611X581516
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The bacterial cellulose (BC) secreted by Gluconacetobacter xylinus is a network of pure cellulose nanofibres which has high crystallinity, wettability and mechanical strength. These characteristics make BC an excellent material for tissue-engineering constructs, noteworthy for artificial vascular grafts. In this work, the in vivo biocompatibility of BC membranes produced by two G. xylinus strains was analyzed through histological analysis of long-term subcutaneous implants in the mice. The BC implants caused a mild and benign inflammatory reaction that decreased along time and did not elicit a foreign body reaction. A tendency to calcify over time, which may be related to the porosity of the BC implants, was observed, especially among the less porous BC-1 implants. In addition, the potential toxicity of BC nanofibres - obtained by chemical-mechanical treatment of BC membranes - subcutaneously implanted in mice was analysed through bone marrow flow cytometry and histological analyses. At 2 and 4 months post-implantation, the nanofibres implants were found to accumulate intracellularly, in subcutaneous foamy macrophages aggregates. Moreover, no differences were observed between the controls and implanted animals in thymocyte populations and in B lymphocyte precursors and myeloid cells in the bone marrow. (C) Koninklijke Brill NV, Leiden, 2011
引用
收藏
页码:1339 / 1354
页数:16
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