579
Views
30
CrossRef citations to date
0
Altmetric
Articles

Bacteria-triggered release of a potent biocide from core-shell polyhydroxyalkanoate (PHA)-based nanofibers for wound dressing applications

, ORCID Icon, ORCID Icon, & ORCID Icon
Pages 394-406 | Received 20 Aug 2019, Accepted 13 Nov 2019, Published online: 28 Nov 2019
 

Abstract

Bacterial infections are a serious issue in wound healing. Extensive use of biocides in wound dressings have raised concerns of biocide resistance and unnecessary harm to normal skin cells. In this paper, we report a new approach to realize bacteria-triggered release of a biocide to the sites of bacterial infections from core-shell polyhydroxyalkanoate (PHA)-based nanofibers prepared by coaxial electrospinning. The hydrophobic PHA-based shell can prevent the biocide from undesirable payload release in physiological environments without pathogens. However, in the presence of pathogens, the PHA-based shell is degraded by the pathogens, and the encapsulated biocide is released. The released biocide subsequently can exert targeted antimicrobial effects on the bacteria. Using Pseudomonas aeruginosa as a model bacterium and dodecyltrimethylammonium chloride as a model biocide, we demonstrated that the core-shell PHA-based nanofibers effectively released encapsulated dodecyltrimethylammonium chloride in the presence of Pseudomonas aeruginosa, resulting in targeted inactivation of Pseudomonas aeruginosa cells.

    Highlights

  • Unique core-shell nanofibers were successfully fabricated from PHAs generated by bacteria.

  • An on-demand release of biocide was achieved from a PHA-based core-shell nanofibours membrane.

  • The membrane’s mechanical properties closely match those of the human skin.

Acknowledgment

This work was financially supported by the Natural Sciences and Engineering Research Council of Canada (NSERC) under Discovery grant No. RGPIN-2019-06094 and NO. RGPIN-2016-05929.

Disclosure statement

No potential conflict of interest was reported by the author(s).

Additional information

Funding

This work was financially supported by the Natural Sciences and Engineering Research Council of Canada (NSERC) under Discovery grant No. RGPIN-2019-06094 and NO. RGPIN-2016-05929.

Log in via your institution

Log in to Taylor & Francis Online

PDF download + Online access

  • 48 hours access to article PDF & online version
  • Article PDF can be downloaded
  • Article PDF can be printed
USD 61.00 Add to cart

Issue Purchase

  • 30 days online access to complete issue
  • Article PDFs can be downloaded
  • Article PDFs can be printed
USD 503.00 Add to cart

* Local tax will be added as applicable

Related Research

People also read lists articles that other readers of this article have read.

Recommended articles lists articles that we recommend and is powered by our AI driven recommendation engine.

Cited by lists all citing articles based on Crossref citations.
Articles with the Crossref icon will open in a new tab.