Piroxicam (Px) is a nonsteroidal anti-inflammatory drug
(NSAID)
used for the treatment of osteoarthritis and rheumatoid arthritis.
It is administered orally; however, its poor water solubility causes
low loading to the nonconventional drug delivery systems (DDSs), such
as electrospun fibers. Furthermore, the rapid dissolution of DDS and
fast release of the embedded drugs are crucial for oral delivery of
drugs to patients who are unconscious or suffering from dysphagia.
In this regard, this study reports the development of rapidly dissolving
cyclodextrin (CD)-based inclusion complex (IC) nanofibers by waterborne
electrospinning for fast oral delivery of Px. Scanning electron microscopy
analysis revealed the formation of bead-free fibers with a mean diameter
range of 170–500 nm at various concentrations of Px; increasing
the Px loading decreased the fiber diameter. The formation of IC was
demonstrated by X-ray diffraction (XRD) analysis by the disappearance
of crystalline peaks of Px. Likewise, differential scanning calorimetry
(DSC) analysis showed the disappearance of the melting peak of the
embedded Px due to IC formation. Both Fourier transform infrared (FTIR)
and thermogravimetric analysis (TGA) confirmed the presence of Px
within the fibers.
1
H NMR experiments demonstrated Px preservation
in the fibers after six months. Px-loaded nanofibers were employed
for sublingual drug delivery. To mimic the environment of the mouth,
the nanofibers were treated with artificial saliva, which revealed
the instant dissolution of the nanofibers. Furthermore, dissolution
experiments were performed on the tissues wetted with artificial saliva,
where the dissolution of the fibers could be extended to a few seconds,
demonstrating the suitability of the materials for sublingual oral
drug delivery. Overall, this paper, for the first time, reports the
rapid oral delivery of Px from polymer-free CD fibers produced by
waterborne electrospinning without the requirement of any carrier
polymer and toxic solvent.