| Literature DB >> 12229260 |
Mariarosa Moneghini1, Dario Voinovich, Beatrice Perissutti, Francesco Princivalle.
Abstract
It is well known that carriers can affect the dissolution of poorly soluble drugs. In this study, our aim was to investigate the dissolution enhancement of carbamazepine solid dispersed or mixed at different loading ratios in crospovidone, polyvinylpyrrolidone, and sodium starch glycolate. The physical state of the drug and the drug-polymer interactions in the solid state were investigated using differential scanning calorimetry (DSC) and x-ray diffraction analysis (XRD). Through the solubilization kinetics and dissolution rates studies, the in vitro drug availability of the systems was evaluated. An improved in vitro dissolution of the drug was obtained in all the binary systems that increased as the polymer content increased.Entities:
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Year: 2002 PMID: 12229260 DOI: 10.1081/pdt-120005725
Source DB: PubMed Journal: Pharm Dev Technol ISSN: 1083-7450 Impact factor: 3.133