Micropellet-loaded rods with dose-independent sustained release properties for individual dosing via the Solid Dosage Pen

Int J Pharm. 2016 Feb 29;499(1-2):271-279. doi: 10.1016/j.ijpharm.2016.01.001. Epub 2016 Jan 3.

Abstract

Individual dosing of medicines is relevant for paediatrics, geriatrics and personalised medicine. The Solid Dosage Pen (SDP) allows for individual dosing by cutting monolithic, tablet-like drug carriers of pre-defined heights. The aim of the present study was to develop micropellet-loaded rods (MPLRs) with dose-independent sustained release properties for individual dosing via the Solid Dosage Pen. Therefore, micropellets were successfully layered with carbamazepine and coated with polyvinyl acetate (PVAc) and PVAc/polyvinyl alcohol-polyethylene glycol (PVA-PEG). The tensile strength of the sustained release micropellets (300-450 μm) was more than two times higher (12.6-17.1 MPa) than pressures occurring during ram-extrusion of the MPLRs (below 5.8 MPa). Due to relative crystallinities above 93% for PVAc and PVA-PEG a low solubility of the coating films within the PEG-matrix was observed. The sustained release micropellets were successfully incorporated into MPLRs. Drug release properties of the pellets maintained after embedding into the matrix. Hence, the MPLRs provided dose-independent prolonged drug liberation which was not achieved for drug-loaded rods before. The MPLRs permitted the application of the SDP with a precise drug delivery from individually cut single doses. Storage stability was proven for MPLRs containing PVAc/PVA-PEG coated pellets. In conclusion, the MPLRs combined the advantages of multiparticulate dosage forms with the SDP as a device for individual dosing.

Keywords: Individual dosing; Micropellets; Multiparticulate dosage form; Solid Dosage Pen; Sustained release.

MeSH terms

  • Anticonvulsants / administration & dosage
  • Anticonvulsants / chemistry
  • Carbamazepine / administration & dosage*
  • Carbamazepine / chemistry
  • Chemistry, Pharmaceutical / methods*
  • Crystallization
  • Delayed-Action Preparations
  • Dose-Response Relationship, Drug
  • Drug Carriers / chemistry*
  • Drug Delivery Systems*
  • Drug Liberation
  • Drug Stability
  • Drug Storage
  • Polyethylene Glycols
  • Polyvinyl Alcohol / chemistry
  • Polyvinyls / chemistry
  • Solubility
  • Tensile Strength

Substances

  • Anticonvulsants
  • Delayed-Action Preparations
  • Drug Carriers
  • Polyvinyls
  • polyvinyl acetate
  • Carbamazepine
  • Polyethylene Glycols
  • Polyvinyl Alcohol