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Mesoporous bioactive glasses for the combined application of osteosarcoma treatment and bone regeneration

机译:介孔生物活性玻璃结合骨肉瘤治疗和骨再生的应用

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摘要

In this study, mesoporous bioactive glass (MBG) sub-micro particles were prepared through sol-gel synthesis and possessed a uniform and spherical structure with particle size of 302 +/- 43 nm, a pore size of 4 nm and a high surface area of 354 m(2) g(-1). Alendronate (AL) is often used for the treatment of bone associated diseases, in particular osteosarcoma. However, due to the low bioavailability and high toxicity at increased doses, local and sustained release would be an ideal approach to AL delivery. Here, MBGs and aminated MBGs (AMBG) were applied as carriers for AL loading. High encapsulation efficiency of 75% and 85% and loading efficiency of 60% and 63%, for MBG and AMBG, respectively, was achieved. The release profile of AL from AMBG showed a better sustained and controlled release mechanism compared to MBG. In vitro results demonstrated the non-cytotoxic nature of both MBG and AMBG following exposure to MG63 osteoblast like cell line. AL release from MBG and AMBG, even at lower concentration, provoked decreased MG63 proliferation. The osteogenic potential of MBG and AMBG following exposure to dental pulp stem cells was evaluated using alizarin red assay.
机译:本研究通过溶胶-凝胶合成法制备了介孔生物活性玻璃(MBG)亚微米颗粒,具有均匀球形的结构,粒径为302 +/- 43 nm,孔径为4 nm,表面积较大。 354 m(2)g(-1)。阿仑膦酸盐(AL)通常用于治疗骨相关疾病,特别是骨肉瘤。然而,由于剂量增加时生物利用度低和毒性高,局部和持续释放将是AL递送的理想方法。在这里,MBG和胺化MBG(AMBG)被用作AL装载的载体。对于MBG和AMBG,分别实现了75%和85%的高封装效率以及60%和63%的加载效率。与MBG相比,AL从AMBG的释放曲线显示出更好的持续控制释放机制。体外结果表明,暴露于MG63成骨细胞样细胞系后,MBG和AMBG均具有非细胞毒性。即使在较低浓度下,MBG和AMBG中的AL释放也导致MG63增殖减少。使用茜素红试验评估了暴露于牙髓干细胞后MBG和AMBG的成骨潜力。

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