Department of Physical Chemistry, Medical University of Gdańsk, Hallera 107, 80-416, Gdańsk, Poland.
Bernal Institute and Department of Chemical Sciences, Pharmaceutical Powder Engineering, University of Limerick, Limerick, Ireland.
AAPS PharmSciTech. 2018 Dec 20;20(1):17. doi: 10.1208/s12249-018-1243-5.
Here, we report an inorganic hexagonally ordered mesoporous fibre-like carrier made of silica as an effective drug delivery system with mineralisation potential. Fibre-like SBA-15 has been modified by employing a simple surface activation (rehydroxylation) procedure. The surface-rehydroxylated fibre-like SBA-15 (SBA-15-R) was used to investigate the possible mechanism of hydroxyapatite (HA) nucleation and deposition onto silica's surface after immersion in simulated body fluid (SBF). Amorphous calcium phosphate, Ca-deficient HA and bone-like HA deposits were observed on SBA-15-R surface consecutively after 7, 14 and 21 days of immersion in SBF. Accordingly, our low-angle XRD, STEM and N adsorption/desorption results indicated that deposited ions were mostly located at the silica's surface and could modify the size of the mesopores. The SBA-15-R was studied in vitro as the potential bioactive drug delivery system using doxorubicin (DOX) as a model water-soluble and anticancer drug. The adsorbed DOX molecules were mostly located at the pore walls and pore openings, likely together with the silanol groups. The DOX release was diffusion-controlled and relatively slower in SBF (pH = 7.4) than in phosphate-buffered solution (pH = 5.0), most probably due to both the stronger electrostatic interactions occurring between the DOX and the SBA-15-R and the simultaneous deposition of calcium and phosphates ions from SBF.
在这里,我们报道了一种由二氧化硅制成的无机六边形有序介孔纤维状载体,作为一种具有矿化潜力的有效药物输送系统。纤维状 SBA-15 通过采用简单的表面活化(再羟化)程序进行改性。表面再羟化的纤维状 SBA-15(SBA-15-R)用于研究在浸入模拟体液(SBF)后羟基磷灰石(HA)在二氧化硅表面成核和沉积的可能机制。在 SBF 中浸泡 7、14 和 21 天后,观察到 SBA-15-R 表面上依次出现无定形磷酸钙、缺钙 HA 和骨样 HA 沉积物。相应地,我们的低角度 XRD、STEM 和 N 吸附/解吸结果表明,沉积的离子主要位于二氧化硅表面,并且可以改变介孔的大小。SBA-15-R 作为潜在的生物活性药物输送系统,使用阿霉素(DOX)作为模型水溶性和抗癌药物进行了体外研究。吸附的 DOX 分子主要位于孔壁和孔口处,可能与硅醇基团一起。DOX 的释放是扩散控制的,在 SBF(pH = 7.4)中比在磷酸盐缓冲溶液(pH = 5.0)中更慢,这很可能是由于 DOX 和 SBA-15-R 之间发生的更强静电相互作用以及来自 SBF 的钙和磷酸盐离子的同时沉积所致。