| Literature DB >> 30318208 |
Yaoyao Yang1, Wenbing Li2, Deng-Guang Yu3, Guanhua Wang2, Gareth R Williams4, Zhu Zhang5.
Abstract
In this study, novel core-shell nanostructures were fabricated through a modified triaxial electrospinning process. These comprised a drug-protein nanocomposite coated with a thin cellulose acetate (CA) shell. They were generated through the simultaneous treatment of an outer solvent, an unelectrospinnable middle fluid, and an electrospinnable core solution in triaxial electrospinning. SEM and TEM results revealed that the core-shell nanofibers had linear and cylindrical morphologies with a diameter from 0.66 to 0.87 μm, and distinct core-shell structures with a shell thickness from 1.8 to 11.6 nm. The presence of a CA coating eliminated the initial burst release of ibuprofen seen from a monolithic drug-protein composite, and allowed us to precisely manipulate the drug release (for a 90% percentage) over a time period from 23.5 to 43.9 h in a tunable manner. Mathematical relationships between the processing conditions, the nanostructures produced, and their functional performance were elucidated.Entities:
Keywords: 1,1,1,3,3,3-hexafluoro-2-propanol (PubChem CID:13529); Acetic acid (PubChem CID: 176); Acetone (PubChem CID: 180); Basic fuchsin (PubChem CID: 12447); Cellulose acetate (PubChem CID: 3084039); Cellulose acetate nanocoating; Detachable tri-layer spinneret; Gliadin (PubChem CID: 17787981); Ibuprofen (PubChem CID: 3672); Linear drug release; Methylene blue (PubChem CID: 6099); Modified triaxial electrospinning; Process–nanostructure–performance relationship; Structural nanohybrids; Trifluoroacetic acid (PubChem CID: 6422)
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Year: 2018 PMID: 30318208 DOI: 10.1016/j.carbpol.2018.09.061
Source DB: PubMed Journal: Carbohydr Polym ISSN: 0144-8617 Impact factor: 9.381