| Literature DB >> 26530290 |
Jiannan Lu1, Kristina Cuellar2, Nathan I Hammer2, Seongbong Jo1, Andreas Gryczke3, Karl Kolter4, Nigel Langley5, Michael A Repka1,6.
Abstract
The aim of the current study is to develop amorphous solid dispersion (SD) via hot melt extrusion technology to improve the solubility of a water-insoluble compound, felodipine (FEL). The solubility was dramatically increased by preparation of amorphous SDs via hot-melt extrusion with an amphiphilic polymer, Soluplus® (SOL). FEL was found to be miscible with SOL by calculating the solubility parameters. The solubility of FEL within SOL was determined to be in the range of 6.2-9.9% (w/w). Various techniques were applied to characterize the solid-state properties of the amorphous SDs. These included Fourier Transform Infrared Spectrometry spectroscopy and Raman spectroscopy to detect the formation of hydrogen bonding between the drug and the polymer. Scanning electron microscopy was performed to study the morphology of the SDs. Among all the hot-melt extrudates, FEL was found to be molecularly dispersed within the polymer matrix for the extrudates containing 10% drug, while few small crystals were detected in the 30 and 50% extrudates. In conclusion, solubility of FEL was enhanced while a homogeneous SD was achieved for 10% drug loading.Entities:
Keywords: Amorphous solid dispersion; felodipine; hot-melt extrusion; miscibility/solubility; solid-state characterization
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Year: 2015 PMID: 26530290 PMCID: PMC4933522 DOI: 10.3109/03639045.2015.1104347
Source DB: PubMed Journal: Drug Dev Ind Pharm ISSN: 0363-9045 Impact factor: 3.225