| Literature DB >> 27188242 |
Omer Mustapha1, Fakhar Ud Din1,2, Dong Wuk Kim1, Jong Hyuck Park1, Kyu Bong Woo3, Soo-Jeong Lim4, Yu Seok Youn5, Kwan Hyung Cho6, Rehmana Rashid1,7, Abid Mehmood Yousaf1,8, Jong Oh Kim2, Chul Soon Yong2, Han-Gon Choi1.
Abstract
To determine if a novel electrospraying technique could be applied to an oral drug delivery system for improving the solubility and oral bioavailability of poorly water-soluble piroxicam; the nanospheres were generated with drug and polyvinylpyrrolidone (PVP) using electrospraying technique; and their physicochemical properties, solubility, release and pharmacokinetics were evaluated in comparison with piroxicam powder. All nanospheres had significantly increased drug solubility and dissolution rates in comparison with the drug powder. In particular, the nanosphere composed of piroxicam and PVP at a weight ratio of 2:8 gave about 600-fold higher solubility, 15-fold higher release rate and 3-fold higher AUC in comparison to piroxicam powder, leading to significantly enhanced oral bioavailability in rats, due to the mingled effect of nanonisation along with transformation to the amorphous state. Thus, this electrospraying technique can be utilised to produce a novel oral nanosphere delivery system with enhanced solubility and oral bioavailability for poorly water-soluble piroxicam.Entities:
Keywords: Piroxicam; electrospraying technique; nanospheres; oral bioavailability; solubility
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Year: 2016 PMID: 27188242 DOI: 10.1080/02652048.2016.1185475
Source DB: PubMed Journal: J Microencapsul ISSN: 0265-2048 Impact factor: 3.142