MnFe2O4 nanoparticles/cellulose acetate composite nanofiber for controllable release of naproxen.

Nanofibers have been demonstrated to be highly effective for drug delivery applications. Although magnetic nanoparticles (MNPs) have been potentially added to nanofibers for improved drug release stimulation, the effect has been limited. In this study, a magnetic nanofiber membrane composed of cellulose acetate (CA), collagen (COL), and MnFe 2 O 4 MNPs was prepared by electrospinning. Naproxen (NAP) drug was deposited on the nanofibers, and the drug release mechanism and effect of the MNPs on the stimulated NAP release were investigated. The electrical conductivity of the dope solution strongly affected the nanofiber characteristics. Moreover, the MTT cytotoxicity assay proved that CA-COL, CA-COL-NAP, and CA-COL-NAP-MNP nanofibers had low toxicity, as the cell viability was >80%. The NAP release mechanism was determined using zero-order, first-order, Higuchi, and Korsmeyer-Peppas kinetics models. According to the dissolution results, for all nanofibers, the NAP release followed the Korsmeyer-Peppas kinetics model, and the transport mechanism was Fickian diffusion. A high MNP concentration and neutral pH condition were conducive to NAP release. Image 1 • Designing composite nanofiber from cellulose acetate, collagen, MnFe 2 O 4 MNPs along with naproxen as drug loaded. • Higher amount on MNPs give positive impact on make smaller nanofiber. • Explore kinetical release of naproxen from nanofiber that accelerated by magnetic induction. • The release mechanism of naproxen close to Korsmeyer-Peppas kinetics models with Fickian diffusion. [ABSTRACT FROM AUTHOR]