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      • Sugars
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      • Glycols
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      • Povidones
      • Propylene Glycol
      • Other Petrochemical Excipients
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      • Fatty Alcohols
      • Glycerin
      • Mineral Stearates
      • Pharmaceutical Oils
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Startseite » News » Cushion-coated pellets for tableting without external excipients

Cushion-coated pellets for tableting without external excipients

16. February 2024
Cushion-coated pellets for tableting without external excipients

Cushion-coated pellets for tableting without external excipients

Multiple-unit dosage forms prepared by compacting pellets offer important manufacturing and compliance advantages over pellet-filled capsules. However, compaction may negatively affect the release control mechanism of pellets, and subunits may not be readily available after intake. Application of a cushioning layer to the starting units is here proposed as a strategy to obtain tablets with satisfactory mechanical strength, rapid disintegration and maintenance of the expected release profile of individual subunits while avoiding the use of mixtures of pellets and excipients to promote compaction and limit the impact of the forces involved. Cushion-coating with PEG1500, a soft and soluble material, was proved feasible provided that the processing temperature was adequately controlled.

Cushioned gastro-resistant pellets were shown to consolidate under relatively low compaction pressures, which preserved their inherent release performance after tablet disintegration. Adhesion problems associated with the use of PEG1500 were overcome by applying an outer Kollicoat® IR film. Through design of experiment (DoE), robustness of the proposed approach was demonstrated, and the formulation as well as tableting conditions were optimized. The tableted cushion-coated pellet systems manufactured would allow a relatively high load of modified-release units to be conveyed, thus setting out a versatile and scalable approach to oral administration of multiple-unit dosage forms.

Read the article here

Materials

Sugar spheres 20/25 mesh (Surinerts®) were kindly gifted by IPS (International Products & Services, San Donato Milanese, IT); sodium laurylsulfate (Kolliphor®, SLS), polyvinylpirrolidone (Kollidon® 30, PVP), polyvinyl alcohol and poly ethylene glycol co-polymer (Kollicoat® IR, KIR) and methacrylic acid and ethyl acrylate copolymer, in 30% w:w suspension (Kollicoat® MAE 30DP) were kindly gifted by BASF (Ludwigshafen, DE); polyethylene glycol 1500 (Polyglykol® 1500, PEG1500)

Saliha Moutaharrik, Luca Palugan, Matteo Cerea, Ilaria Filippin, Alessandra Maroni, Andrea Gazzaniga, Anastasia Foppoli, Cushion-coated pellets for tableting without external excipients, International Journal of Pharmaceutics, Volume 653, 2024, 123874, ISSN 0378-5173, https://doi.org/10.1016/j.ijpharm.2024.123874.


See more recent articles on MUPS:

  • Multi-particulate formulations: the power of many
  • The Use of Calcium Phosphate-Based Starter Pellets for the Preparation of Sprinkle IR MUPS Formulation of Rosuvastatin Calcium
  • Chrono modulated multiple unit particulate systems (MUPS) via a continuous hot melt double extrusion technique
Tags: excipientsformulation

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