Song S-W, Hidajat K, Kawi S
Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, Singapore 119260.
Langmuir. 2005 Oct 11;21(21):9568-75. doi: 10.1021/la051167e.
Mesoporous SBA-15 materials were functionalized with amine groups through postsynthesis and one-pot synthesis, and the resulting functionalized materials were investigated as matrixes for controlled drug delivery. The materials were characterized by FTIR, N(2) adsorption/desorption analysis, zeta potential measurement, XRD, XPS, and TEM. Ibuprofen (IBU) and bovine serum albumin (BSA) were selected as model drugs and loaded onto the unmodified and functionalized SBA-15. It was revealed that the adsorption capacities and release behaviors of these model drugs were highly dependent on the different surface properties of SBA-15 materials. The release rate of IBU from SBA-15 functionalized by postsynthesis is found to be effectively controlled as compared to that from pure SBA-15 and SBA-15 functionalized by one-pot synthesis due to the ionic interaction between carboxyl groups in IBU and amine groups on the surface of SBA-15. However, SBA-15 functionalized by one-pot synthesis is found to be more favorable for the adsorption and release of BSA due to the balance of electrostatic interaction and hydrophilic interaction between BSA and the functionalized SBA-15 matrix.
介孔SBA - 15材料通过后合成法和一锅合成法用胺基进行功能化,所得功能化材料作为可控药物递送的基质进行了研究。通过傅里叶变换红外光谱(FTIR)、N₂吸附/脱附分析、zeta电位测量、X射线衍射(XRD)、X射线光电子能谱(XPS)和透射电子显微镜(TEM)对材料进行了表征。选择布洛芬(IBU)和牛血清白蛋白(BSA)作为模型药物,并负载到未改性和功能化的SBA - 15上。结果表明,这些模型药物的吸附容量和释放行为高度依赖于SBA - 15材料不同的表面性质。由于IBU中的羧基与SBA - 15表面的胺基之间的离子相互作用,与纯SBA - 15和通过一锅合成法功能化的SBA - 15相比,后合成法功能化的SBA - 15中IBU的释放速率得到有效控制。然而,由于BSA与功能化的SBA - 15基质之间静电相互作用和亲水相互作用的平衡,发现通过一锅合成法功能化的SBA - 15对BSA的吸附和释放更有利。