The effect of superdisintegrants on the properties and dissolution profiles of liquisolid tablets containing rosuvastatin
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články
- Klíčová slova
- Data visualization, disintegration time, dissolution profile, liquisolid systems, superdisintegrant,
- MeSH
- anticholesteremika aplikace a dávkování chemie MeSH
- farmaceutické pomocné látky chemie MeSH
- povidon chemie MeSH
- příprava léků MeSH
- rosuvastatin kalcium aplikace a dávkování chemie MeSH
- rozpustnost MeSH
- silikáty chemie MeSH
- škrob analogy a deriváty chemie MeSH
- sloučeniny hliníku chemie MeSH
- sloučeniny hořčíku chemie MeSH
- tablety chemie MeSH
- uvolňování léčiv MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- aluminum magnesium silicate MeSH Prohlížeč
- anticholesteremika MeSH
- farmaceutické pomocné látky MeSH
- povidon MeSH
- rosuvastatin kalcium MeSH
- silikáty MeSH
- škrob MeSH
- sloučeniny hliníku MeSH
- sloučeniny hořčíku MeSH
- sodium starch glycolate MeSH Prohlížeč
- tablety MeSH
CONTEXT: The preparation of liquisolid systems (LSS) represents a promising method for enhancing a dissolution rate and bioavailability of poorly soluble drugs. The release of the drug from LSS tablets is affected by many factors, including the disintegration time. OBJECTIVE: The evaluation of differences among LSS containing varying amounts and types of commercially used superdisintegrants (Kollidon® CL-F, Vivasol® and Explotab®). MATERIALS AND METHODS: LSS were prepared by spraying rosuvastatin solution onto Neusilin® US2 and further processing into tablets. Varying amounts of superdisintegrants were used and the differences among LSS were evaluated. The multiple scatter plot method was used to visualize the relationships within the obtained data. RESULTS AND DISCUSSION: All disintegrants do not showed negative effect on the flow properties of powder blends. The type and concentration of superdisintegrant had an impact on the disintegration time and dissolution profiles of tablets. Tablets with Explotab® showed the longest disintegration time and the smallest amount of released drug. Fastest disintegration and dissolution rate were observed in tablets containing Kollidon® CL-F (≥2.5% w/w). Also tablets with Vivasol® (2.5-4.0% w/w) showed fast disintegration and complete drug release. CONCLUSION: Kollidon® CL-F and Vivasol® in concentration ≥2.5% are suitable superdisintegrants for LSS with enhanced release of drug.
Citace poskytuje Crossref.org