Meka Venkata Srikanth, Murthy Kolapalli Venkata Ramana
School of Pharmacy, International Medical University, No. 126, Jalan Jalil Perkasa 19, Bukit Jalil, 57000, Kuala Lumpur, Malaysia.
Curr Drug Deliv. 2016;13(6):971-81. doi: 10.2174/1567201812666151009115756.
A central composite design was applied to design a novel gastric floating drug delivery system comprising propranolol HCl in Terminalia catappa gum and to evaluate the buoyancy, in vitro drug release behavior, and pharmacokinetic parameters. All formulations exhibited good buoyancy properties in vitro reflected by floating lag time of 1-110 sec, total floating time of 9-16 h and prolonged release behaviour (upto 12 h). Statistically optimised formulation (PBGRso) was orally administered to human volunteers under both fasted and fed conditions to evaluate gastric floating behavior under different food conditions by X-ray evaluation. In vivo studies of optimised formulations revealed that the gastric residence time of floating tablets was enhanced in the fed but not in the fasted state. Pharmacokinetic studies of the optimised Terminalia catappa formulation and a commercial product (Ciplar LA 80) carried out on healthy human volunteers showed a significant improvement in the bioavailability (132%) of propranolol HCl released from from the experimental Terminalia catappa formulations compared with Ciplar LA 80.
采用中心复合设计法设计了一种新型胃漂浮药物递送系统,该系统由盐酸普萘洛尔和榄仁树胶组成,并对其浮力、体外药物释放行为和药代动力学参数进行了评估。所有制剂在体外均表现出良好的漂浮性能,漂浮滞后时间为1 - 110秒,总漂浮时间为9 - 16小时,且具有缓释行为(长达12小时)。通过X射线评估,将经统计优化的制剂(PBGRso)在禁食和进食条件下口服给人类志愿者,以评估不同食物条件下的胃漂浮行为。优化制剂的体内研究表明,漂浮片在进食状态下的胃滞留时间延长,但在禁食状态下未延长。对健康人类志愿者进行的优化榄仁树胶制剂和市售产品(西普拉 LA 80)的药代动力学研究表明,与西普拉 LA 80相比,从实验性榄仁树胶制剂中释放的盐酸普萘洛尔的生物利用度有显著提高(132%)。