Department of Bioengineering, Center for Bioactive Materials and Tissue Engineering, University of Pennsylvania, Philadelphia, PA 19104, USA.
J Mater Sci Mater Med. 2013 Jan;24(1):137-46. doi: 10.1007/s10856-012-4783-3. Epub 2012 Oct 10.
Conventional sol-gel processing requires several distinct steps involving hydrolysis, condensation and drying to obtain a highly porous, glassy solid material. With the goal of achieving controlled release of small molecules, herein we focus on the acceleration of the condensation and drying steps by casting the hydrolyzed sol on a large open surface to achieve a denser 100 % silica xerogel structure. Thus, cast xerogel with a more limited porosity was prepared. The effect of synthesis parameters during sol-gel synthesis on the release kinetics of bupivacaine, vancomycin and cephalexin was investigated. The release kinetics fitted well with the Higuchi model, suggesting a diffusional release mechanism. Combining the release and nanostructure data, the formation mechanism of cast xerogel is described. Without introducing additional precursors or additives into sol-gel systems, sol-gel casting is an easy technique that further expands the applicability of sol-gel materials as excellent carriers for the controlled release of a variety of drugs.
传统的溶胶-凝胶工艺需要经过水解、缩合和干燥等几个不同的步骤,才能得到高度多孔的玻璃态固体材料。为了实现小分子的控制释放,我们专注于通过将水解后的溶胶浇铸在大的开放表面上来加速缩合和干燥步骤,以获得更致密的 100%二氧化硅气凝胶结构。因此,制备了具有更有限孔隙率的浇铸气凝胶。研究了溶胶-凝胶合成过程中的合成参数对布比卡因、万古霉素和头孢氨苄释放动力学的影响。释放动力学很好地符合 Higuchi 模型,表明是扩散释放机制。结合释放和纳米结构数据,描述了浇铸气凝胶的形成机制。在溶胶-凝胶体系中不引入额外的前体或添加剂的情况下,溶胶-凝胶浇铸是一种简单的技术,进一步扩展了溶胶-凝胶材料作为各种药物控制释放的优良载体的适用性。