| Literature DB >> 34205186 |
Mohamed F Attia1,2, Ahmed S Montaser3, Md Arifuzzaman1, Megan Pitz4, Khouloud Jlassi5, Angela Alexander-Bryant4, Stephen S Kelly6, Frank Alexis7, Daniel C Whitehead1.
Abstract
In this study we developed electrospun cellulose acetate nanofibers (CANFs) that were loaded with a model non-steroidal anti-inflammatory drug (NSAID) (ibuprofen, Ib) and coated with poly(acrylamide) (poly-AAm) hydrogel polymer using two consecutive steps: an electrospinning process followed by photopolymerization of AAm. Coated and non-coated CANF formulations were characterized by several microscopic and spectroscopic techniques to evaluate their physicochemical properties. An analysis of the kinetic release profile of Ib showed noticeable differences due to the presence or absence of the poly-AAm hydrogel polymer. Poly-AAm coating facilitated a constant release rate of drug as opposed to a more conventional burst release. The non-coated CANFs showed low cumulative drug release concentrations (ca. 35 and 83% at 5 and 10% loading, respectively). Conversely, poly-AAm coated CANFs were found to promote the release of drug (ca. 84 and 99.8% at 5 and 10% loading, respectively). Finally, the CANFs were found to be superbly cytocompatible.Entities:
Keywords: cellulose acetate; drug delivery; electrospinning; kinetic release; nanofibers; poly(acrylamide) hydrogel
Year: 2021 PMID: 34205186 DOI: 10.3390/polym13111863
Source DB: PubMed Journal: Polymers (Basel) ISSN: 2073-4360 Impact factor: 4.329