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Bacteria-Responsive Single and Core-Shell Nanofibrous Membranes Based on Polycaprolactone/Poly(ethylene succinate) for On-Demand Release of Biocides. | LitMetric

Bacteria-Responsive Single and Core-Shell Nanofibrous Membranes Based on Polycaprolactone/Poly(ethylene succinate) for On-Demand Release of Biocides.

ACS Omega

Biomedical Engineering, Faculty of Engineering, Director of Manitoba Firefighters Burn Unit, Professor in the Departments of Surgery and Psychiatry, Rady Faculty of Health Sciences, Department of Biosystems Engineering, and Department of Medical Microbiology, University of Manitoba, Winnipeg R3T 2N2, Canada.

Published: February 2019

AI Article Synopsis

  • * A new bacteria-responsive nanofibrous wound dressing is designed to only release antimicrobial agents when bacteria are present, using polymers that degrade in response to bacterial activity.
  • * The core-shell structure of these nanofibers allows for a controlled release of the antimicrobial agent (BTAC), effectively reducing bacteria and minimizing harm to human cells, suggesting a potential for improved wound care.

Article Abstract

Traditional antibacterial dressings continuously elute biocides, even if there are no bacteria. This unneeded release can cause cytotoxicity, increase costs, and delay healing. We designed a bacteria-responsive nanofibrous wound dressing, which can be degraded in the presence of bacteria to release antimicrobial agents. A model biocide, benzyl dimethyl tetradecyl ammonium chloride (BTAC), was incorporated into bacteria-degradable polymers [polycaprolactone and poly(ethylene succinate)] in two ways: evenly distributed inside the polymers as single nanofibers and encapsulated in a core surrounded by the same polymers as core-shell nanofibers. Because of bacterial activity (both lipase secretion and acidic pH), degradation of the fibers was facilitated and caused the release of incorporated BTAC. BTAC-loaded single and core-shell nanofibers presented >1 log reduction of both and within 2 h. Additionally, the core-shell structure provided a more controlled release of BTAC with prolonged antibacterial properties than single nanofibers. The core-shell nanofibers also exhibited minimal cytotoxicity against human fibroblast cells (>80% viable cells after 24 h contact). These nanofibrous mats have the potential to selectively release antibacterial agents to prevent wound infections without delaying wound healing.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6647954PMC
http://dx.doi.org/10.1021/acsomega.8b03137DOI Listing

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