明胶
压实
颗粒
材料科学
剂型
药物输送
纳米颗粒
控制释放
微粒
纳米技术
生物医学工程
化学
色谱法
医学
复合材料
有机化学
生物化学
作者
Nihad Al-hashimi,Nazish Begg,Raid G. Alany,Hany Hassanin,Amr ElShaer
出处
期刊:Pharmaceutics
[Multidisciplinary Digital Publishing Institute]
日期:2018-10-04
卷期号:10 (4): 176-176
被引量:67
标识
DOI:10.3390/pharmaceutics10040176
摘要
Oral modified-release multiparticulate dosage forms, which are also referred to as oral multiple-unit particulate systems, are becoming increasingly popular for oral drug delivery applications. The compaction of polymer-coated multiparticulates into tablets to produce a sustained-release dosage form is preferred over hard gelatin capsules. Moreover, multiparticulate tablets are a promising solution to chronic conditions, patients’ adherence, and swallowing difficulties if incorporated into orodispersible matrices. Nonetheless, the compaction of multiparticulates often damages the functional polymer coat, which results in a rapid release of the drug substance and the subsequent loss of sustained-release properties. This review brings to the forefront key formulation variables that are likely to influence the compaction of coated multiparticulates into sustained-release tablets. It focusses on the tabletting of coated drug-loaded pellets, microparticles, and nanoparticles with a designated section on each. Furthermore, it explores the various approaches that are used to evaluate the compaction behaviour of particulate systems.
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