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Bio-templated bioactive glass particles with hierarchical macro-nano porous structure and drug delivery capability

机译:具有分层宏观纳米多孔结构和药物递送能力的生物模板化生物活性玻璃颗粒

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摘要

Hierarchically porous bioactive glass particles (BGPs) were synthesized by a facile sol-gel process using pollen grains as the templates. The synthesized pollen-templated bioactive glass particles (PBGPs) exhibited dual macro-nano porous structure. The macro pores (similar to 1 mu m) were inherited from the template of pollen grains while the nano pores (similar to 9.5 nm) were induced by the intrinsic mechanism of the sol-gel process. PBGPs possessed a high specific surface area (111.4 m(2)/g) and pore volume (0.35 cm(3)/g). Hydroxyapatite (HA) formation on PBGPs was detected within 3 days after immersion in simulated body fluid (SBF). Due to their larger specific surface area and pore volume, PBGPs could be loaded with more tetracycline hydrochloride (TCH) than non-templated BGPs and conventional melt-derived 45S5 BGPs. In addition, PBGPs exhibited a low initial burst release (within 10% of the loaded amount) within 18 h and a sustained release with a two-stage release pattern for up to 6 days in phosphate buffered saline (PBS). The antibacterial assay confirmed that the TCH-loaded PBGPs could release TCH within 5 days, and the released TCH could reach the minimum inhibitory concentration (MIC) against Escherichia coli. MTT assay indicated that PBGPs showed non-cytotoxic effects toward human hepatocellular carcinoma (Hep G2) cells after co-culture for up to 72 h in vitro. These results showed that the biocompatible hierarchically macro-nano porous PBGPs are potential for bone regeneration and local drug delivery applications. (c) 2015 Elsevier B.V. All rights reserved.
机译:通过使用花粉晶体作为模板,通过容易溶胶 - 凝胶工艺合成分层多孔生物活性玻璃颗粒(BGP)。合成的花粉模板化生物活性玻璃颗粒(PBGPS)表现出双宏纳米多孔结构。宏观孔(类似于1μm)从花粉颗粒的模板继承,同时通过溶胶 - 凝胶法的固有机理诱导纳米孔(类似于9.5nm)。 PBGP具有高比表面积(111.4m(2)/ g)和孔体积(0.35cm(3)/ g)。在模拟体液(SBF)浸泡后3天内检测在PBGP上的羟基磷灰石(HA)形成。由于其较大的表面积和孔体积,PBGP可以与非模板BGP和常规熔体衍生的45s5bGP一起加载更多的四环素盐酸盐(TCH)。此外,PBGP在18小时内表现出低初始爆发(在负载量的10%以内),并且在磷酸盐缓冲盐水(PBS)中具有高达6天的两级释放模式的持续释放。抗菌测定证实,TCH负载的PBGP可以在5天内释放TCH,并且释放的TCH可以达到对大肠杆菌的最小抑制浓度(MIC)。 MTT测定表明,PBGP在共同培养到体外高达72小时后对人肝细胞癌(HEP G2)细胞的非细胞毒性作用显示出非细胞毒性作用。这些结果表明,生物相容性的分层宏观纳米多孔PBGP是骨再生和局部药物递送应用的潜力。 (c)2015 Elsevier B.v.保留所有权利。

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