Patel Kapil D, Singh Rajendra K, Mahapatra Chinmaya, Lee Eun-Jung, Kim Hae-Won
J Biomed Nanotechnol. 2016 Oct;12(10):1876-89. doi: 10.1166/jbn.2016.2301.
Coatings of metallic implants facilitate a new bioactive interface that favors osteogenic responses and bone formation. Providing a therapeutic capacity to the coatings, involving with a sustainable and controllable delivery of drug molecules, significantly improves the bone regenerative potential. Here we design a novel nanocomposite coating, made of mesoporous silica-shelled hydroxyapatite (MS-HA) nanoparticles and chitosan (Chi), incorporating osteogenic drug dexamethasone phosphate (Dex(P)) within the MS-HA, by the process of an electrophoretic deposition (EPD). MS-HA, produced by a sol–gel reaction of silica onto an HA nanorod, exhibited mono-dispersed core–shell nanoparticles with a size of ∼40 nm and a shell thickness of ∼25 nm. The highly mesoporous structure enabled an effective loading of Dex(P) onto the nanocarriers, showing a loading capacity as high as 15% by weight. The Dex(P) loaded MS-HA were homogenized with Chi in acidic ethanol/water to allow for the EPD process. Nanocomposite coatings were produced well, forming thicknesses a few micrometers largely tunable with EPD parameters and exhibiting MS-HA nanoparticles evenly distributed within Chi matrix. While Dex(P) release from the bare MS-HA nanocarrier was very abrupt, showing a complete release within 24 h, the Dex(P) release from the nanocomposite coatings profiled a highly sustainable pattern over a month. Rat mesenchymal stem cells cultured on the Dex(P)-releasing coatings were substantially stimulated to an osteoblastic lineage, presenting enhanced alkaline phosphate activity and higher levels of osteogenic genes, with respect to coatings free of Dex(P). An indirect culture test also confirmed the long-term release effects of Dex(P) from the coatings over 4 weeks. The currently-developed nanocomposite EPD coatings, with a capacity to load osteogenic drug at large quantity and to deliver for a long-term period, are considered as a promising therapeutic coating platform for metallic bone implants.
金属植入物的涂层有助于形成新的生物活性界面,有利于成骨反应和骨形成。赋予涂层治疗能力,即实现药物分子的可持续和可控递送,可显著提高骨再生潜力。在此,我们设计了一种新型纳米复合涂层,由介孔二氧化硅包覆的羟基磷灰石(MS-HA)纳米颗粒和壳聚糖(Chi)制成,通过电泳沉积(EPD)工艺将成骨药物磷酸地塞米松(Dex(P))掺入MS-HA中。MS-HA是通过二氧化硅在HA纳米棒上的溶胶-凝胶反应制备的,呈现出尺寸约为40nm、壳厚度约为25nm的单分散核壳纳米颗粒。高度介孔结构使Dex(P)能够有效负载到纳米载体上,负载量高达15%(重量)。将负载Dex(P)的MS-HA与Chi在酸性乙醇/水中均匀混合,以进行EPD工艺。纳米复合涂层制备良好,形成的厚度可达几微米,可通过EPD参数进行很大程度的调节,并且MS-HA纳米颗粒均匀分布在Chi基质中。虽然裸露的MS-HA纳米载体中Dex(P)的释放非常突然,在24小时内完全释放,但纳米复合涂层中Dex(P)的释放在一个月内呈现出高度可持续的模式。在释放Dex(P)的涂层上培养的大鼠间充质干细胞被显著刺激向成骨细胞谱系分化,相对于不含Dex(P)的涂层,其碱性磷酸酶活性增强,成骨基因水平更高。间接培养试验也证实了Dex(P)从涂层中长达4周的长期释放效果。目前开发的纳米复合EPD涂层具有大量负载成骨药物并长期递送的能力,被认为是金属骨植入物的一个有前景的治疗涂层平台。