Klausner Eytan A, Lavy Eran, Stepensky David, Friedman Michael, Hoffman Amnon
Department of Pharmaceutics, School of Pharmacy, Faculty of Medicine, The Hebrew University of Jerusalem, Israel.
Pharm Res. 2002 Oct;19(10):1516-23. doi: 10.1023/a:1020412817716.
[corrected] The purpose of this study was to design novel gastroretentive dosage forms (GRDFs) based on unfolding multilayer polymeric films, to investigate the mechanism of their gastroretentivity in dogs, and to assess the effect of compounding a narrow absorption window drug in a GRDF on the drug's absorption properties.
Dosage forms (DFs) with different dimensions and mechanical properties were administered to beagle dogs with acidic buffer (pH = 1.5), whose gastric retention time (GRT) was then determined by X-ray pictures. Concurrent administration of radiopaque markers was used to assess the effect of the GRDF and/or acidic buffer on GRT. The absorption of riboflavin from a prototype GRDF was compared with a nongastroretentive controlled-release DF and to an oral solution of the drug.
Large DFs (> or = 2.5 x 2.5 cm) containing rigid frame had prolonged GRT (>4 h). Administration of 400 mL of acidic buffer (or water) prolonged GRT whereas the GRDF did not cause additional prolongation. The extended absorption phase (>48 h) of riboflavin administered in a GRDF led to 4-fold increased bioavailability.
The combination of large dimensions with rigidity produce gastroretentivity that can be used to improve absorption properties of a model of narrow absorption window drugs in the gastrointestinal tract.
本研究的目的是基于展开式多层聚合物膜设计新型胃滞留剂型(GRDFs),研究其在犬体内胃滞留的机制,并评估在GRDF中加入窄吸收窗药物对药物吸收特性的影响。
将具有不同尺寸和机械性能的剂型(DFs)给予装有酸性缓冲液(pH = 1.5)的比格犬,然后通过X射线照片确定其胃滞留时间(GRT)。同时给予不透射线标记物以评估GRDF和/或酸性缓冲液对GRT的影响。将原型GRDF中核黄素的吸收与非胃滞留控释DF以及该药物的口服溶液进行比较。
含有刚性框架的大型DFs(≥2.5×2.5 cm)具有延长的GRT(>4小时)。给予400 mL酸性缓冲液(或水)可延长GRT,而GRDF不会导致进一步延长。在GRDF中给予核黄素的延长吸收期(>48小时)导致生物利用度提高4倍。
大尺寸与刚性的结合产生胃滞留性,可用于改善胃肠道中窄吸收窗药物模型的吸收特性。