Abstract

Biofilms are prevalent in chronic wounds and once formed are very hard to remove, which is associated with poor outcomes and high mortality rates. Biofilms are comprised of surface-attached bacteria embedded in an extracellular polymeric substance (EPS) matrix, which confers increased antibiotic resistance and host immune evasion. Therefore, disruption of this matrix is essential to tackle the biofilm-embedded bacteria. Here, we propose a novel nanotechnology to do this, based on protease-functionalized nanogel carriers of antibiotics. Such active antibiotic nanocarriers, surface coated with the protease Alcalase 2.4 L FG, "digest" their way through the biofilm EPS matrix, reach the buried bacteria, and deliver a high dose of antibiotic directly on their cell walls, which overwhelms their defenses. We demonstrated their effectiveness against six wound biofilm-forming bacteria, Staphylococcus aureus, Pseudomonas aeruginosa, Staphylococcus epidermidis, Klebsiella pneumoniae, Escherichia coli, and Enterococcus faecalis. We confirmed a 6-fold decrease in the biofilm mass and a substantial reduction in bacterial cell density using fluorescence, atomic force, and scanning electron microscopy. Additionally, we showed that co-treatments of ciprofloxacin and Alcalase-coated Carbopol nanogels led to a 3-log reduction in viable biofilm-forming cells when compared to ciprofloxacin treatments alone. Encapsulating an equivalent concentration of ciprofloxacin into the Alcalase-coated nanogel particles boosted their antibacterial effect much further, reducing the bacterial cell viability to below detectable amounts after 6 h of treatment. The Alcalase-coated nanogel particles were noncytotoxic to human adult keratinocyte cells (HaCaT), inducing a very low apoptotic response in these cells. Overall, we demonstrated that the Alcalase-coated nanogels loaded with a cationic antibiotic elicit very strong biofilm-clearing effects against wound-associated biofilm-forming pathogenic bacteria. This nanotechnology approach has the potential to become a very powerful treatment of chronically infected wounds with biofilm-forming bacteria.

Highlights

  • Biofilms are microbial communities surrounded by a structure referred to as extracellular polymeric substance (EPS), composed of biopolymers such as exopolysaccharides, nucleic acids, lipids, and proteins.[1]

  • We investigated the effect of pH, temperature and time on the free enzyme, and the surface immobilized Alcalase on the Carbopol nanogel particles (Figure S7, electronic supplementary information (ESI))

  • We investigated if Alcalase 2.4 L FG coated Carbopol nanogels were able to disrupt the biofilms formed by the species described above

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Summary

Introduction

Biofilms are microbial communities surrounded by a structure referred to as extracellular polymeric substance (EPS), composed of biopolymers such as exopolysaccharides, nucleic acids, lipids, and proteins.[1]. We investigated the effect of pH, temperature and time on the free enzyme, and the surface immobilized Alcalase on the Carbopol nanogel particles (Figure S7, ESI).

Results
Conclusion
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