Hassan C M, Stewart J E, Peppas N A
Biomaterials and Drug Delivery Laboratories, School of Chemical Engineering, Purdue University, West Lafayette, IN 47907-1283, USA.
Eur J Pharm Biopharm. 2000 Mar;49(2):161-5. doi: 10.1016/s0939-6411(99)00056-9.
The incorporation of a model protein, bovine serum albumin (BSA), into poly(vinyl alcohol) (PVA) hydrogel films during the freezing and thawing process and its subsequent release behavior were investigated. The effect of the number of freezing and thawing cycles as well as the stability of BSA were examined. BSA release profiles were not significantly different from gels prepared after 3 or 5 cycles. However, the rate and overall amount of PVA dissolution were considerably higher for gels prepared after 3 cycles. These observations were then applied to the development of novel, freeze/thawed PVA laminates. Laminates containing gel layers prepared after 3 or 5 cycles were successfully prepared with good stability over a 6 month swelling period. These structures, containing distinct layers of very specific properties, could be used to achieve zero-order release behavior.
研究了在冻融过程中将模型蛋白牛血清白蛋白(BSA)掺入聚乙烯醇(PVA)水凝胶薄膜及其随后的释放行为。考察了冻融循环次数以及BSA稳定性的影响。BSA的释放曲线与3次或5次循环后制备的凝胶无显著差异。然而,3次循环后制备的凝胶的PVA溶解速率和总量要高得多。然后将这些观察结果应用于新型冻融PVA层压板的开发。成功制备了含有3次或5次循环后制备的凝胶层的层压板,在6个月的溶胀期内具有良好的稳定性。这些具有非常特殊性质的不同层结构可用于实现零级释放行为。