Bioactive effects of silica nanoparticles on bone cells are size, surface, and composition dependent.

Bioactive effects of silica nanoparticles on bone cells are size, surface, and composition dependent.
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DOI:
10.1016/j.actbio.2018.10.018
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发表时间:
2018-12
期刊:
影响因子:
9.7
通讯作者:
Beck, George R., Jr.
Beck, George R., Jr.
中科院分区:
工程技术1区
文献类型:
--
作者:
Ha, Shin-Woo;Viggeswarapu, Manjula;Habib, Mark M.;Beck, George R., Jr.

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Silica based nanoparticles have been demonstrated to have intrinsic biologic activity towards the skeleton and to function by promoting the differentiation of bone forming osteoblasts while inhibiting the differentiation of bone resorbing osteoclasts. The excitement surrounding nanomedicine in part revolves around the almost unlimited possibilities for varying the physicochemical properties including size, composition, and surface charge. To date few studies have attempted to manipulate these characteristics in concert to optimize a complex biologic outcome. Towards this end, spherical silica nanoparticles of various sizes (50–450 nm), of different surface properties (OH, CO2H, NR4+, mNH2), and of different composition (silica, gold, and polystyrene) were synthesized and evaluated for biological activity toward skeletal cells. Osteoblast activity was most influenced by composition and size variables, whereas osteoclasts were most affected by surface property variation. The study also establishes nanoparticle mediated suppression of Nfatc1, a key transcriptional regulator for osteoclast differentiation, identifying a novel mechanism of action. Collectively, the study highlights how during the design of bioactive nanoparticles, it is vital to consider not only the myriad of physical properties that can be manipulated, but also that the characteristics of the target cell plays an equally integral role in determining biological outcome.
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