P. Wadhwani College of Pharmacy, Yavatmal, Maharashtra, 445001, India.
J Control Release. 2010 Oct 1;147(1):2-16. doi: 10.1016/j.jconrel.2010.05.014. Epub 2010 May 19.
Oral modified-release multiple-unit dosage forms have always been more effective therapeutic alternative to conventional or immediate release single-unit dosage forms. With regards to the final dosage form, the multiparticulates are usually formulated into single-unit dosage forms such as filling them into hard gelatin capsules or compressing them into tablets. There are many relevant articles and literature available on the preparation of pellets and coating technology. However, only few research articles discuss the issue of compaction of pellets into tablets. This review provides an update on this research area and discusses the phenomena and mechanisms involved during compaction of multiparticulate system and material and/or process-related parameters influencing tableting of multiparticulates to produce multiple-unit pellet system (MUPS) or pellet-containing tablets, which are expected to disintegrate rapidly into individual pellets and provide drug release profile similar to that obtained from uncoated pellets.
口服控释多单位剂型一直是比传统或即释单单位剂型更有效的治疗选择。就最终剂型而言,多颗粒剂通常被制成单单位剂型,例如将其填充到硬胶囊中或压制成片剂。关于制备微丸和包衣技术,有许多相关的文章和文献。然而,只有少数研究文章讨论了将微丸压制成片剂的问题。本综述提供了该研究领域的最新信息,并讨论了多颗粒系统压缩过程中涉及的现象和机制,以及影响多颗粒剂压制成多单位微丸系统(MUPS)或含微丸片剂的物料和/或工艺相关参数,以期迅速崩解成单个微丸,并提供类似于未包衣微丸获得的药物释放特征。