Nair Renuka, Vemuri Murti, Agrawala Praful, Kim Soo-il
Sanofi-Aventis Pharmaceuticals, Mailstop-BWE103B, Rt. 202-206, Bridgewater, NJ 08807, USA.
AAPS PharmSciTech. 2004 Oct 1;5(4):e57. doi: 10.1208/pt050457.
The purpose of this study was to determine the factors that influence fill weight and weight variability of capsules produced on the In-Cap and to assess any differences in terms of capsule defects between gelatin and HPMC (Quali-V) shells. The In-Cap is an automatic tamping type capsule-filling machine and the low output of approximately 3000 capsules/hour makes it ideal for early formulation development and phase I/IIa clinical supplies manufacture. Four commonly used excipients (Avicel PH101, Avicel PH302, A-Tab, and Prosolv HD90) and a poorly flowing drug blend were encapsulated at various pin settings and powder bed heights. The average fill weight and coefficient of weight variation were determined. The percentage of defective capsules formed during encapsulation was calculated. Results of the study showed that pin setting was critical for controlling the fill weight and the weight variation. The order of pin setting with pin 1 (closer to the powder chute) set to a relatively higher position and pin 4 (before ejection) set to a lower position was found to give higher fill weights with relatively lower weight variability. The powder bed height influenced the fill weight for poorly flowing powders. The capsule machine speed did not appear to significantly influence the fill weight. The fill weight and weight variation were found to depend on the flow property of the material. A large percentage of defective capsules was obtained using HPMC shell size #00. Some of the commonly observed defects included split caps and improperly closed filled capsules. In general, appropriate selection of pin settings and bed height can reduce the weight variability seen, especially with poorly flowing high-dose formulations.
本研究的目的是确定影响In-Cap胶囊填充重量和重量变异性的因素,并评估明胶和羟丙甲纤维素(Quali-V)胶囊壳在胶囊缺陷方面的差异。In-Cap是一台自动夯实式胶囊填充机,其约3000粒胶囊/小时的低产量使其非常适合早期配方开发和I/IIa期临床供应生产。将四种常用辅料(微晶纤维素PH101、微晶纤维素PH302、A-Tab和Prosolv HD90)以及一种流动性差的药物混合物在不同的针设置和粉床高度下进行胶囊填充。测定平均填充重量和重量变异系数。计算封装过程中形成的缺陷胶囊百分比。研究结果表明,针设置对于控制填充重量和重量变异至关重要。发现将靠近粉槽的针1设置在相对较高的位置,将出料前的针4设置在较低的位置,这样的针设置顺序能得到较高的填充重量和相对较低的重量变异性。粉床高度会影响流动性差的粉末的填充重量。胶囊机速度似乎对填充重量没有显著影响。发现填充重量和重量变异取决于物料的流动特性。使用00号羟丙甲纤维素胶囊壳时获得了很大比例的缺陷胶囊。一些常见的缺陷包括胶囊裂开和填充胶囊封口不当。一般来说,适当选择针设置和粉床高度可以减少观察到的重量变异性,尤其是对于流动性差的高剂量制剂。