Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2503385 | International Journal of Pharmaceutics | 2011 | 7 Pages |
Malotilate (MT) is a hepatoprotective drug administered orally. However, MT was found to be a poorly water-soluble drug with low oral bioavailability. In the present investigation, a novel spray-dried emulsion (SDE) loaded with MT was prepared, and its physicochemical properties were characterized by rheological evaluation, particle size measurement, in vitro release, and surface morphology. The pharmacokinetic study of SDE, in comparison to MT suspension with the pure MT powder homogeneously dispersed in 0.5% CMC–Na solution, was also performed in rats after a single oral dose. It was found that SDE exhibited a 2.9-fold higher peak plasma concentration (Cmax) and 2.3-fold higher area under the curve (AUC) than MT suspension.
Graphical abstractSpray-dried malotilate emulsion exhibited a 2.9-fold higher peak plasma concentration (Cmax) and 2.3-fold higher area under the curve (AUC) than MT suspension, a 2.11-fold higher Cmax and 1.83-fold higher AUC than CE.Figure optionsDownload full-size imageDownload as PowerPoint slide