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The effect of superdisintegrants on the properties and dissolution profiles of liquisolid tablets containing rosuvastatin
- Source :
- Pharmaceutical Development and Technology. 22:138-147
- Publication Year :
- 2015
- Publisher :
- Informa UK Limited, 2015.
-
Abstract
- 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.The evaluation of differences among LSS containing varying amounts and types of commercially used superdisintegrants (Kollidon® CL-F, Vivasol® and Explotab®).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.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.Kollidon® CL-F and Vivasol® in concentration ≥2.5% are suitable superdisintegrants for LSS with enhanced release of drug.
- Subjects :
- Drug
Drug Compounding
media_common.quotation_subject
Magnesium Compounds
Pharmaceutical Science
Context (language use)
02 engineering and technology
030226 pharmacology & pharmacy
03 medical and health sciences
0302 clinical medicine
Pharmaceutic Aids
medicine
Rosuvastatin
Rosuvastatin Calcium
Aluminum Compounds
Dissolution
media_common
Chromatography
Chemistry
Anticholesteremic Agents
Silicates
Povidone
Starch
General Medicine
021001 nanoscience & nanotechnology
Bioavailability
Drug Liberation
Solubility
0210 nano-technology
Tablets
medicine.drug
Subjects
Details
- ISSN :
- 10979867 and 10837450
- Volume :
- 22
- Database :
- OpenAIRE
- Journal :
- Pharmaceutical Development and Technology
- Accession number :
- edsair.doi.dedup.....103dca7b228c06b08661ec6422034c6d
- Full Text :
- https://doi.org/10.3109/10837450.2015.1089900