4.8 Article

Interfacial Stacks of Polymeric Nanofilms on Soft Biological Surfaces that Release Multiple Agents

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 8, Issue 40, Pages 26541-26551

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.6b08608

Keywords

stacking of polymeric nanofilms; soft biological interfaces; interfacial constructs; multiple bioactive agents; biomedical surfaces; synergistic effects; biofilms

Funding

  1. NIH from NIAMS [1RC2AR058971-01]
  2. Innovation & Economic Development Research grant from the University of Wisconsin Madison Graduate School
  3. Army Research Office [W911NF-14-1-0140, W911NF-15-1-0568]
  4. NSF (Wisconsin MRSEC) [DMR1121288]

Ask authors/readers for more resources

We report a general and facile method that permits the transfer (stacking) of multiple independently fabricated and nanoscopically thin polymeric films, each containing a distinct bioactive agent, onto soft biomedically relevant surfaces (e.g., collagen-based wound dressings). By using polyelectrolyte multilayer films (PEMs) formed from poly(allyl amine hydrochloride) and poly(acrylic acid) as representative polymeric nanofilms and micrometer-thick water-soluble poly(vinyl alcohol) sacrificial films to stack the PEMs, we demonstrate that it is possible to create stacked polymeric constructs containing multiple bioactive agents (e.g., antimicrobial and antibiofilm agents) on soft and chemically complex surfaces onto which PEMs cannot be routinely transferred by stamping. We illustrate the characteristics and merits of the approach by fabricating stacks of Ga3+ (antibiofilm agent)- and Ag+ (antimicrobial agent)-loaded PEMs as prototypical examples of agent-containing PEMs and demonstrate that the stacked PEMs incorporate precise loadings of the agents and provide flexibility in terms of tuning release rates. Specifically, we show that simultaneous release of Ga3+ and Ag+ from the stacked PEMs on collagen-based wound dressings can lead to synergistic effects on bacteria, killing and dispersing biofilms formed by Pseudomonas aeruginosa (two strains: ATCC 27853 and MPAO1) at sufficiently low loadings of agents such that cytotoxic effects on mammalian cells are avoided. The approach is general (a wide range of bioactive agents other than Ga3+ and Ag+ can be incorporated into PEMs), and the modular nature of the approach potentially allows end-user functionalization of soft biological surfaces for programmed release of multiple bioactive agents.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available