Ciper Mesut, Bodmeier Roland
College of Pharmacy, Freie Universität Berlin, Kelchstr. 31, 12169 Berlin, Germany.
Int J Pharm. 2005 Oct 13;303(1-2):62-71. doi: 10.1016/j.ijpharm.2005.07.004.
The objective of this study was to prepare novel capsule-based fast disintegrating dosage forms for the oral cavity (Fastcaps). First, cast films were prepared from various additive-containing gelatin solutions and evaluated with respect to disintegration time and mechanical properties in order to identify suitable formulations for the capsule preparation. The disintegration time of films decreased with decreasing bloom strength and could be further decreased by the addition of sugars or PEGs. Fast disintegrating capsules were successfully prepared by a dipping process, whereby parameters such as the viscosity and temperature of the dipping solution and the dipping velocity of the steel pins were optimized. The required viscosity range of the dipping solution for Fastcap manufacturing was 500-600 cP. The addition of the hydrophilic additives (xylitol, sorbitol or PEG 1500) did not significantly affect the viscosity and gelation temperature of the dipping solution. The in vitro disintegration of Fastcaps (30-45 s) was twice as rapid as the one of regular hard gelatin capsules. In vivo, Fastcaps disintegrated rapidly (9-13 s) and their content was spread throughout the oral cavity within seconds. Lactose and/or microcrystalline cellulose were suitable fillers for Fastcaps. The mechanical properties of Fastcaps were similar to commercially available gelatin capsules, which assures good processability and handling.
本研究的目的是制备用于口腔的新型胶囊型快速崩解剂型(速溶胶囊)。首先,由含各种添加剂的明胶溶液制备铸膜,并就崩解时间和机械性能进行评估,以便确定适合制备胶囊的配方。膜的崩解时间随勃氏强度降低而缩短,添加糖类或聚乙二醇可进一步缩短崩解时间。通过浸渍工艺成功制备了快速崩解胶囊,对浸渍溶液的粘度、温度以及钢针的浸渍速度等参数进行了优化。制备速溶胶囊所需浸渍溶液的粘度范围为500 - 600厘泊。添加亲水性添加剂(木糖醇、山梨醇或聚乙二醇1500)对浸渍溶液的粘度和凝胶化温度没有显著影响。速溶胶囊的体外崩解时间(30 - 45秒)是普通硬明胶胶囊的两倍。在体内,速溶胶囊崩解迅速(9 - 13秒),其内容物在数秒内遍布口腔。乳糖和/或微晶纤维素是速溶胶囊的合适填充剂。速溶胶囊的机械性能与市售明胶胶囊相似,确保了良好的加工性能和操作便利性。