McConville Jason T, Ross Alistair C, Chambers Alan R, Smith Geoff, Florence Alastair J, Stevens Howard N E
Department of Pharmaceutical Sciences, University of Strathclyde, Glasgow, UK.
Eur J Pharm Biopharm. 2004 May;57(3):541-9. doi: 10.1016/j.ejpb.2004.01.004.
The purpose of this study was to investigate the variability in the performance of a pulsatile capsule delivery system induced by wet granulation of an erodible HPMC tablet, used to seal the contents within an insoluble capsule body. Erodible tablets containing HPMC and lactose were prepared by direct compression (DC) and wet granulation (WG) techniques and used to seal the model drug propranolol inside an insoluble capsule body. Dissolution testing of capsules was performed. Physical characterisation of the tablets and powder blends used to form the tablets was undertaken using a range of experimental techniques. The wet granulations were also examined using the novel technique of microwave dielectric analysis (MDA). WG tablets eroded slower and produced longer lag-times than those prepared by DC, the greatest difference was observed with low concentrations of HPMC. No anomalous physical characteristics were detected with either the tablets or powder blends. MDA indicated water-dipole relaxation times of 2.9, 5.4 and 7.7x10(-8)ms for 15, 24 and 30% HPMC concentrations, respectively, confirming that less free water was available for chain disentanglement at high concentrations. In conclusion, at low HPMC concentrations water mobility is at its greatest during the granulation process, such formulations are therefore more sensitive to processing techniques. Microwave dielectric analysis can be used to predict the degree of polymer spreading in an aqueous system, by determination of the water-dipole relaxation time.
本研究的目的是调查由可蚀性羟丙基甲基纤维素(HPMC)片剂湿法制粒引起的脉动胶囊给药系统性能的变异性,该片剂用于密封不溶性胶囊体内的内容物。通过直接压片(DC)和湿法制粒(WG)技术制备含HPMC和乳糖的可蚀性片剂,并用于将模型药物普萘洛尔密封在不溶性胶囊体内。进行了胶囊的溶出度测试。使用一系列实验技术对用于制备片剂的片剂和粉末混合物进行了物理表征。还使用微波介电分析(MDA)新技术对湿法制粒进行了检查。与DC制备的片剂相比,WG片剂的侵蚀速度较慢,滞后时间更长,在低浓度HPMC时观察到最大差异。片剂或粉末混合物均未检测到异常物理特性。MDA表明,对于15%、24%和30%的HPMC浓度,水偶极弛豫时间分别为2.9、5.4和7.7×10(-8)毫秒,证实高浓度下可用于链解缠结的自由水较少。总之,在低HPMC浓度下,制粒过程中水的流动性最大,因此此类制剂对加工技术更敏感。通过测定水偶极弛豫时间,微波介电分析可用于预测聚合物在水性体系中的铺展程度。