Abstract

High blood glucose levels, excessive production of reactive oxygen species (ROS), unbalanced inflammatory responses and impaired angiogenesis render chronic wounds more likely to be colonized by bacteria which can form biofilms, leading to recurrent infections and prolonging disunion. The pH-responsive fibers of poly (vinyl alcohol) (PVA)/poly (acrylic acid) (PAA) -epigallocatechin gallate (EGCG) have been constructed. The fibers were able to swell (pH > 7.4) /shrink (pH < 6.5) reversibly with changes in wound pH, controlling the rate of drug release and thus dynamically modulating the complex inflammatory environment of the wound. At the phase of bacterial infection (pH = 7–9), the polycarboxylic acid groups in the network ionized, and the dynamic hydrogen bond between EGCG and PVA and PAA was broke, triggered an increased release of EGCG (87.4 %). Thereafter, the EGCG cleared excess ROS (greater than80.0 %) from the wound and showed significant antibacterial activity against S. aureus (98 %) and Pseudomonas aeruginosa (96.7 %), inhibited biofilm formation (74 %). At the proliferative phase, the wound switched to acidic (pH ∼ 6.5). Fibers swelled less and tended to shrink. The release of EGCG was slowed down (45.8 %) to promote macrophage polarization and remodel the wound microenvironment.

Full Text
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