Department of Chemistry, University of Western Ontario, London, Ontario N6A 5B7, Canada.
Nanoscale. 2015 Apr 21;7(15):6767-73. doi: 10.1039/c4nr07471h.
Imaging is one of the most direct and ideal ways to track drug loading distributions in drug carriers on the molecular level, which will facilitate the optimization of drug carriers and drug loading capacities. Herein, we report the mapping of an individual mesoporous calcium silicate hydrate (CSH) microsphere before and after the loading of ibuprofen (IBU) and the interactions between drug carriers and drug molecules simultaneously by scanning transmission X-ray microscopy (STXM). Nanoscaled X-ray absorption near edge structure (XANES) spectroscopy clearly indicates that IBU is bonded to calcium and silicate sites via carboxylic acid groups. More importantly, STXM has been successfully used to determine the absolute thickness of IBU, revealing its distribution in the CSH microsphere.
成像技术是在分子水平上追踪药物载体中药物负载分布最直接、最理想的方法之一,这将有助于优化药物载体和药物负载能力。在此,我们通过扫描透射 X 射线显微镜(STXM)报告了布洛芬(IBU)负载前后单个介孔硅酸钙水合物(CSH)微球的映射以及药物载体和药物分子之间的相互作用。纳米级 X 射线吸收近边结构(XANES)光谱清楚地表明,IBU 通过羧酸基团与钙和硅酸盐位点结合。更重要的是,已经成功地使用 STXM 来确定 IBU 的绝对厚度,揭示了其在 CSH 微球中的分布。