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Published on: January 31, 2018
Oral Modified Release Multiple-Unit Particulate Systems: Compressed Pellets, Microparticles and Nanoparticles
Nihad Al-Hashimi1, Nazish Begg2, Raid G Alany3
1Drug Discovery, Delivery and Patient Care (DDDPC), School of Life Sciences, Pharmacy and Chemistry, Kingston University, Kingston upon Thames, Surrey KT1 2EE, UK. k1406374@kingston.ac.uk.
Compacting polymer-coated multiparticulates into tablets can damage the drug release coat, compromising sustained-release properties. This review examines formulation factors affecting coated multiparticulates during tabletting for improved oral drug delivery.
Area of Science:
- Pharmaceutical Technology
- Drug Delivery Systems
- Materials Science
Background:
- Oral modified-release multiparticulate dosage forms (oral multiple-unit particulate systems) are gaining traction for drug delivery.
- Tablets formed by compacting polymer-coated multiparticulates offer advantages over capsules for sustained drug release.
- These systems can address challenges in chronic conditions, patient adherence, and swallowing difficulties.
Purpose of the Study:
- To review key formulation variables influencing the compaction of coated multiparticulates into sustained-release tablets.
- To focus on the tabletting of coated drug-loaded pellets, microparticles, and nanoparticles.
- To explore methods for evaluating the compaction behavior of particulate systems.
Main Methods:
- Literature review of formulation variables affecting coated multiparticulates during tabletting.
- Analysis of compaction effects on drug-loaded pellets, microparticles, and nanoparticles.
- Examination of techniques for assessing particulate system compaction behavior.
Main Results:
- Compaction of multiparticulates can damage polymer coats, leading to premature drug release and loss of sustained-release characteristics.
- Specific formulation variables significantly impact the integrity of coated multiparticulates during tabletting.
- Various evaluation methods exist to assess the compaction behavior of these systems.
Conclusions:
- Understanding and controlling formulation variables are crucial to prevent coat damage during the compaction of multiparticulates into sustained-release tablets.
- Optimized tabletting processes are necessary to maintain the integrity of coated multiparticulates for effective oral drug delivery.
- Further research into compaction behavior evaluation is needed for advanced multiparticulate tablet design.
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