Guo Xiaoxuan, Wang Zhiqiang, Wu Jin, Yiu Yun-Mui, Hu Yongfeng, Zhu Ying-Jie, Sham Tsun-Kong
†Department of Chemistry, University of Western Ontario, London, Ontario N6A 5B7, Canada.
‡Shanghai Institute of Ceramics, Chinese Academy of Sciences, Shanghai 200050, China.
J Phys Chem B. 2015 Aug 6;119(31):10052-9. doi: 10.1021/acs.jpcb.5b04115. Epub 2015 Jul 23.
Mesoporous spheres of calcium silicate hydrate (MS-CSH) have been prepared by an ultrasonic method. Following an earlier work in which we have revealed the interactions between ibuprofen (IBU) and CSH carriers with different morphologies by X-ray absorption near edge structures (XANES) analysis. In the present investigation, two new drug molecules, alendronate sodium (ALN) and gentamicin sulfate (GS), were incorporated into MS-CSH, and their drug loading capacities (DLCs) were measured using thermogravimetric analysis to establish the relationship between drug-carrier interactions and DLCs. The XANES spectra clearly indicate that acidic functional groups of the drug molecules linked to the active sites (Ca-OH and Si-OH groups) of MS-CSH on the surface by electrostatic interactions. In addition, it is found that the stoichiometric ratio of Ca(2+) ions of CSH carriers and the functional groups of drug molecules may significantly influence the DLCs.
通过超声法制备了水合硅酸钙介孔球(MS-CSH)。此前我们通过X射线吸收近边结构(XANES)分析揭示了布洛芬(IBU)与不同形态的CSH载体之间的相互作用。在本研究中,将两种新的药物分子阿仑膦酸钠(ALN)和硫酸庆大霉素(GS)掺入MS-CSH中,并使用热重分析测量它们的载药量(DLC),以建立药物-载体相互作用与DLC之间的关系。XANES光谱清楚地表明,药物分子的酸性官能团通过静电相互作用与MS-CSH表面的活性位点(Ca-OH和Si-OH基团)相连。此外,发现CSH载体的Ca(2+)离子与药物分子的官能团的化学计量比可能会显著影响DLC。