| Literature DB >> 25761776 |
Attila Balogh1, Balázs Farkas, Kornél Faragó, Attila Farkas, István Wagner, Ivo Van Assche, Geert Verreck, Zsombor K Nagy, György Marosi.
Abstract
Melt blowing (MB) was investigated to prepare a fast dissolving fibrous drug-loaded solid dispersion and compared with solvent-based electrospinning (SES) and melt electrospinning (MES). As a conventional solvent-free technique coupled with melt extrusion and using a high-speed gas stream, MB can provide high-quality micro- and nanofibers at industrial throughput levels. Carvedilol, a weak-base model drug with poor water solubility, was processed using a common composition optimized for the fiber spinning and blowing methods based on a hydrophilic vinylpyrrolidone-vinyl acetate copolymer (PVPVA64) and PEG 3000 plasticizer. Scanning electron microscopy combined with fiber diameter analysis showed diameter distributions characteristic to each prepared fibrous fabrics (the mean value increased toward SES<MB<MES). Differential scanning calorimetry and X-ray diffraction studies revealed that the incorporated drug was in amorphous form regardless the preparation method. The HPLC studies demonstrated that all of the materials produced by the different techniques passed the regulatory purity requirements. The fibers exhibited ultrafast drug release tested under neutral pH conditions; the melt-blown sample dissolved within 2 min owing to its large specific surface area. The presented results confirm the applicability of MB as a novel formulation technique for polymer-based drug delivery systems.Entities:
Keywords: HPLC; continuous pharmaceutical manufacturing; electrospinning; enhanced dissolution rate; extrusion; melt blowing; melt electrospinning; oral drug delivery; solid dispersion; viscosity
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Year: 2015 PMID: 25761776 DOI: 10.1002/jps.24399
Source DB: PubMed Journal: J Pharm Sci ISSN: 0022-3549 Impact factor: 3.534