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Hydrogel-Nanofiber Composite Systems for Drug Delivery
Ya Liang, Anthony Lowman, and Giuseppe Palmese
Poly(lactide-co-glycolide) (PLGA) is a biodegradable and biocompatible material,
which leads to its promising application for drug delivery. Electrospinning technique
can fabricate micron or submicron sized polymer fibers from PLGA, and the resulting
porous, fibrous mats are favorable for drug delivery. Drugs can be incorporated in fibers
during electrospinning. Embedding the electrospun fibrous mats in a poly(vinyl alcohol)
(PVA) hydrogel can provide mechanical strength for implantation and added diffusion
barriers for drug release.
All samples were incubated at 37oC phosphate buffered saline (PBS) solution (pH = 7.4)
for PLGA degradation and protein release studies. Dry weight loss, morphology and
molecular weight changes of PLGA fibrous mats were used to evaluate the hydrolysis.
Fibrous mats were found to shrink, which reduced porosity, when fibers were swollen at
incubation conditions. Dry weight loss during incubation was an “S”-shaped curve and
fiber morphology had no influence on the hydrolysis rate. However, we noticed that the
presence of PVA hydrogel could prevent PLGA fibrous mats from shrinking during fiber
swelling. We studied protein release from PLGA fibers and hydrogel-nanofiber composites,
respectively. Protein concentrations in PBS solution during incubation were measured to
determine the release rate. Since the release rate is dependent on the hydrolysis rate of
PLGA and protein diffusion, we hope to build the connection among hydrolysis, diffusion
and protein release so that we can predict and control the protein release rate.
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