Wang J, Tauchi Y, Deguchi Y, Morimoto K, Tabata Y, Ikada Y
Department of Pharmaceutics, Hokkaido College of Pharmacy, Otaru-city, Japan.
Drug Deliv. 2000 Oct-Dec;7(4):237-43. doi: 10.1080/107175400455173.
Gastric mucoadhesive drug delivery systems are very promising for eradication of Helicobacter pylori (H. pylori), a spiral bacterium that resides in the gastric mucus layer and at the mucus-epithelial cell interface. New positively charged biodegradable microspheres were prepared using aminated gelatin by surfactant-free emulsification in olive oil, followed by a cross-linking reaction with glutaraldehyde. The amino group contents of the modified gelatin and the microspheres were determined using a 2,4,6-trinitrobenzenesulfonic acid method. With the increase of glutaraldehyde concentration, the amino group content of the microspheres decreased accordingly. The influence of glutaraldehyde concentration, cross-linking reaction time, drug-loading patterns, and type of release media on the in vitro release characteristics of amoxicillin from the microspheres was investigated. Amoxicillin release rate from the modified gelatin microspheres was significantly reduced compared with that from gelatin microspheres. Furthermore, the release was decreased with the increase of glutaraldehyde concentration and/or cross-linking time. On the other hand, a faster release was observed in a lower pH release medium and/or using a lower pH solution for amoxicillin loading. The gastric mucoadhesive properties of the microspheres were evaluated using RITC-labeled microspheres in an isolated rat stomach. The gastric mucoadhesion of the modified gelatin microspheres was markedly improved compared with that of gelatin microspheres. The modified gelatin microsphere proves to be a possible candidate delivery system for the effective eradication of H. pylori.
胃黏膜黏附给药系统在根除幽门螺杆菌方面极具前景,幽门螺杆菌是一种螺旋状细菌,存在于胃黏液层以及黏液 - 上皮细胞界面。采用胺化明胶通过在橄榄油中无表面活性剂乳化法制备新型带正电荷的可生物降解微球,随后与戊二醛进行交联反应。使用2,4,6 - 三硝基苯磺酸法测定改性明胶和微球的氨基含量。随着戊二醛浓度的增加,微球的氨基含量相应降低。研究了戊二醛浓度、交联反应时间、载药方式以及释放介质类型对阿莫西林从微球中体外释放特性的影响。与明胶微球相比,改性明胶微球中阿莫西林的释放速率显著降低。此外,随着戊二醛浓度和/或交联时间的增加,释放量减少。另一方面,在较低pH值的释放介质中以及/或者使用较低pH值的溶液进行阿莫西林载药时,观察到释放速度更快。使用异硫氰酸罗丹明标记的微球在离体大鼠胃中评估微球的胃黏膜黏附特性。与明胶微球相比,改性明胶微球的胃黏膜黏附性显著提高。改性明胶微球被证明是有效根除幽门螺杆菌的一种可能的候选给药系统。