However, the possibilities are limited because there are only around 100 polymers

that have good electrospinnability, and often electrospinning can only be achieved for particular molecular weights and within a very narrow concentration window [19]. Only around ten polymers have been used to prepare drug-loaded AZD5363 in vitro nanofibers and often the preparation conditions are extremely strict. Thus, the monolithic nanofibers which result from GSK458 single-fluid electrospinning have limited applicability in the biomedical field. Coaxial electrospinning, employing a concentric spinneret with one needle nested inside another, has however been successfully employed to generate nanofibers from materials which cannot be electrospun in single-fluid processes [20]. Modified coaxial approaches, in which un-electrospinnable liquids are used as shell fluids with a core solution which has good electrospinnability,

are further expanding the range of medicated nanofibers that can be fabricated [14, 15]. Biphasic drug release profiles have drawn considerable attention in pharmaceutics for a number of reasons – one possible application is the ‘burst’ release of a loading dose of drug followed by sustained release over www.selleckchem.com/products/ly-411575.html a prolonged period of time to maintain the systemic drug concentration within the therapeutic window [21–23]. A wide variety of technologies have been exploited to generate drug delivery systems with biphasic release profiles. Electrospinning can achieve this objective through strategies such as preparing multi-layered nanofiber mats or producing nanofibers containing

ifenprodil nanoparticles [21, 24]. Core-shell nanofibers generated using coaxial electrospinning have also been reported to offer biphasic release, with a fast-dissolving shell delivering immediate release followed by sustained release from the core [22]. Generally, both the core and shell fluids used for coaxial spinning have been electrospinnable in such studies [23]. Building on the developments discussed above, this study aimed to deliver three related goals: (i) the implementation of stable and effective coaxial electrospinning to generate high-quality core-shell nanofibers, (ii) employing modified coaxial electrospinning to prepare nanofibers using non-spinnable solutions, and (iii) manipulating structure-activity relationships at the nanoscale to yield accurate and adjustable time-programmed administration of drugs for specific therapeutic needs. A coaxial electrospinning process including a polyvinyl chloride (PVC)-coated concentric spinneret was implemented to prepare core-shell nanofibers of quercetin using an un-spinnable shell fluid containing PVP and quercetin.