The objective of the present study is to elaborate a new approach for drug loading into electrospun nanofibers
through active loading based on non-solvent evaporation technique. The polymeric nanofibers were achieved by electrospinning
method using PCL, PVA and a blend of sodium alginate & PVA as polymeric constituents. Different methods
such as passive & active (solvent and non-solvent evaporation methods) techniques were used to prepare drug loaded
nanofibers. The resulting nanofibers were characterized for morphology, drug loading, in-vitro release and degree of swelling.
Different kinetic models were applied to the in-vitro release profile of different polymeric nanofibers. The prepared
nanofibers were found to be uniform, non-beaded and non-woven with fiber diameter ranging from 200-450nm. Entrapment
efficiency of metronidazole was increased by 30% when non-solvent evaporation method was used. Moreover the n
value obtained from the Peppas model varied between 0.8-0.9 which was further confirmed that the mechanism of drug
release was anomalous diffusion which refers to combination of both diffusion and erosion mechanism. The impetus for
this development was that the non-solvent evaporation technique can be successfully used for drug loading to polymeric
Keywords: Electrospinning, nanofibers, non-solvent evaporation techniques, swelling index.
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