Mechanistic aspects of drug loading in liquisolid systems with hydrophilic lipid-based mixtures
Jazyk angličtina Země Nizozemsko Médium print-electronic
Typ dokumentu časopisecké články
PubMed
32006624
DOI
10.1016/j.ijpharm.2020.119099
PII: S0378-5173(20)30083-1
Knihovny.cz E-zdroje
- Klíčová slova
- Drug loading, Liquisolid systems, Mesoporous silica, Poor solubility, Semi-volatile mixture, Syloid XDP,
- MeSH
- diferenciální skenovací kalorimetrie metody MeSH
- farmaceutická chemie metody MeSH
- farmaceutická technologie metody MeSH
- hydrofobní a hydrofilní interakce MeSH
- kinetika MeSH
- léčivé přípravky chemie MeSH
- lipidy chemie MeSH
- nosiče léků chemie MeSH
- oxid křemičitý chemie MeSH
- polysorbáty chemie MeSH
- propylenglykol chemie MeSH
- rozpouštědla chemie MeSH
- rozpustnost účinky léků MeSH
- tablety chemie MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- léčivé přípravky MeSH
- lipidy MeSH
- nosiče léků MeSH
- oxid křemičitý MeSH
- polysorbáty MeSH
- propylenglykol MeSH
- rozpouštědla MeSH
- tablety MeSH
Despite the increasing interest in pharmaceutical use of mesoporous silica, there is still only limited knowledge on mechanisms of pore loading and subsequent drug desorption and release. Hence the aim of this work was to address the mechanistic aspects of drug loading into the mesoporous silica pores and to minimise the risk of pore clogging. Hydrophilic solvents (polysorbate 20 and polyethylene glycol 200) with high dissolving capacity for the model drug celecoxib were studied for their surface tension as well as dynamic viscosity by considering hydration. As an innovation in liquisolid systems preparation, a rather simple drug loading method on a mesoporous carrier was introduced by using semi-volatile solvent mixtures. Fast liquid loading into the pores was achieved due to the lowered viscosity and surface tension of the whole solvent system. Drug release kinetics suggested that lipid-based formulations belonging to class IV of Lipid Formulation Classification System may exhibit a lower risk of incomplete desorption from a carrier. The utilisation of volatile solvents during preparation had no negative impact on the liquisolid systems' dissolution behaviour. All prepared formulations showed similar significantly faster dissolution profiles compared to the physical mixture. The novel approach has potential to promote liquisolid applications in pharmaceutics.
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