Dept. of Chemical and Biological Engineering, Chalmers University of Technology, SE-412 96, Gothenburg, Sweden.
Int J Pharm. 2010 Nov 30;401(1-2):60-7. doi: 10.1016/j.ijpharm.2010.09.017. Epub 2010 Sep 29.
The release of a model drug substance, methylparaben, was studied in matrix tablets composed of hydroxypropyl methylcellulose (HPMC) batches of the USP 2208 grade that had different chemical compositions. It was found that chemically heterogeneous HPMC batches with longer sections of low substituted regions and lower hydroxypropoxy content facilitated the formation of reversible gel structures at a temperature as low as 37°C. Most importantly, these structures were shown to affect the release of the drug from matrix tablets, where the drug release decreased with increased heterogeneity and a difference in T80 values of 7h was observed between the compositions. This could be explained by the much lower erosion rate of the heterogeneous HPMC batches, which decreased the drug release rate and also released the drug with a more diffusion based release mechanism compared to the less heterogeneous batches. It can therefore be concluded that the drug release from matrix tablets is very sensitive to variations in the chemical heterogeneity of HPMC.
对由不同化学组成的 USP2208 级羟丙甲纤维素(HPMC)批次组成的基质片剂中模型药物释放的研究表明,具有更长低取代区和较低羟丙氧基含量的化学不均匀 HPMC 批次在低至 37°C 的温度下有利于形成可逆凝胶结构。最重要的是,这些结构被证明会影响药物从基质片剂中的释放,其中药物释放随着不均匀性的增加而降低,并且在组成之间观察到 T80 值相差 7 小时。这可以通过化学不均匀 HPMC 批次的侵蚀率低得多来解释,这降低了药物的释放速率,并与较不均匀的批次相比,以更基于扩散的释放机制释放药物。因此,可以得出结论,药物从基质片剂中的释放对 HPMC 的化学不均匀性的变化非常敏感。