Effect of hydrophobic inclusions on polymer swelling kinetics studied by magnetic resonance imaging
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
26780121
DOI
10.1016/j.ijpharm.2016.01.023
PII: S0378-5173(16)30022-9
Knihovny.cz E-zdroje
- Klíčová slova
- Carnauba wax, Drug dissolution, Gel layer, HPMC, MRI,
- MeSH
- deriváty hypromelózy chemie MeSH
- hydrofobní a hydrofilní interakce MeSH
- kinetika MeSH
- léky s prodlouženým účinkem chemie MeSH
- levetiracetam MeSH
- magnetická rezonanční tomografie MeSH
- piracetam analogy a deriváty chemie MeSH
- rozpustnost MeSH
- tablety MeSH
- teoretické modely MeSH
- uvolňování léčiv MeSH
- vosky chemie MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- carnauba wax MeSH Prohlížeč
- deriváty hypromelózy MeSH
- léky s prodlouženým účinkem MeSH
- levetiracetam MeSH
- piracetam MeSH
- tablety MeSH
- vosky MeSH
The rate of drug release from polymer matrix-based sustained release formulations is often controlled by the thickness of a gel layer that forms upon contact with dissolution medium. The effect of formulation parameters on the kinetics of elementary rate processes that contribute to gel layer formation, such as water ingress, polymer swelling and erosion, is therefore of interest. In the present work, gel layer formation has been investigated by magnetic resonance imaging (MRI), which is a non-destructive method allowing direct visualization of effective water concentration inside the tablet and its surrounding. Using formulations with Levetiracetam as the active ingredient, HPMC as a hydrophilic matrix former and carnauba wax (CW) as a hydrophobic component in the matrix system, the effect of different ratios of these two ingredients on the kinetics of gel formation (MRI) and drug release (USP 4 like dissolution test) has been investigated and interpreted using a mathematical model.
Citace poskytuje Crossref.org
The Combined Use of Imaging Approaches to Assess Drug Release from Multicomponent Solid Dispersions