首页> 外文期刊>Journal of biomedical materials research. Part B, Applied biomaterials. >Concentration-dependent effects of alendronate and pamidronate functionalized gold nanoparticles on osteoclast and osteoblast viability
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Concentration-dependent effects of alendronate and pamidronate functionalized gold nanoparticles on osteoclast and osteoblast viability

机译:Alendronate和Pamidronate官能化金纳米颗粒对骨酸和成骨细胞活力的浓度依赖性作用

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Severe osteoporotic diseases, such as Paget's disease, Osteogenesis Imperfecta, and Legg Calve Perthes disease, lack treatments that address the pathobiology of the diseases, as well as, long-term and prospective studies. Bisphosphonates, which are known to dramatically hinder the viability of osteoclast cells, along with gold nanoparticles (GNP) are a potential theranostic for osteoporotic diseases. We evaluated GNP functionalized with two different bisphosphonates, namely, alendronate and pamidronate. RANKL differentiated murine pre-osteoclasts (Raw 264.7) and murine osteoblasts (7F2) were treated with varying concentrations ranging from 0.1-5 mu M of free and GNP bound bisphosphonates. GNPs with an average size of approximate to 15 nm were functionalized with alendronate and pamidronate through surface modification by self-assembly. MTT viability assay results show no changes in viability of the osteoclasts when treated with free bisphosphonates in the range of 1-5 mu M, but significant decrease on treatment with functionalized GNP at concentrations above the range of 0.1-1 mu M depending on the bisphosphonate. Osteoblast cell viability is maintained at all but the highest concentrations used. Qualitative and quantitative characterization by Western Blot for RANKL expression in the osteoblast cell line shows that expression is largely maintained. These results provide a basis for methods that use bisphosphonate functionalized GNP in the treatment of osteoporotic bone diseases. (c) 2015 Wiley Periodicals, Inc. J Biomed Mater Res Part B: Appl Biomater, 105B: 21-29, 2017.
机译:严重的骨质疏松疾病,如Paget疾病,骨肉骨质植物缺陷和腿部腐败疾病,缺乏解决疾病病病病毒学的治疗,以及长期和前瞻性研究。已知的双膦酸盐显着地阻碍破骨细胞细胞的活力以及金纳米颗粒(GNP)是骨质疏松疾病的潜在治疗症。我们评估了用两种不同的双膦酸盐,即醛膦酸酯和氨基磺酸酯官能化的GNP。 RANKL分化的鼠前骨质蛋白酶(RAW 264.7)和鼠成骨细胞(7F2)用不同浓度的自由和GNP结合双膦酸盐的不同浓度处理。通过自组装的表面改性,用Alynetronate和Pamidronate官能化平均尺寸的GNP,通过自组装的表面改性来官能化。 MTT活力测定结果显示在1-5μm的游离双膦酸盐的游离双膦酸盐处理时没有变化,但在1-5μm的范围内,但根据双膦酸盐,在0.1-1μm的浓度下用官能化GNP处理显着降低。骨细胞细胞活力完全保持,但使用的最高浓度。蛋白质细胞系中蛋白质印迹的定性和定量表征表明,成骨细胞系中的表达表明,表达在很大程度上保持。这些结果为使用双膦酸酯官能化GNP治疗骨质疏松骨病的方法提供了基础。 (c)2015年Wiley期刊,Inc。J生物密制Res B部分:苹果生物摩特,105B:21-29,2017。

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