Loading of Polydimethylsiloxane with a Human ApoB-Derived Antimicrobial Peptide to Prevent Bacterial Infections

Int J Mol Sci. 2022 May 7;23(9):5219. doi: 10.3390/ijms23095219.

Abstract

Background: medical device-induced infections affect millions of lives worldwide and innovative preventive strategies are urgently required. Antimicrobial peptides (AMPs) appear as ideal candidates to efficiently functionalize medical devices surfaces and prevent bacterial infections. In this scenario, here, we produced antimicrobial polydimethylsiloxane (PDMS) by loading this polymer with an antimicrobial peptide identified in human apolipoprotein B, r(P)ApoBLPro.

Methods: once obtained loaded PDMS, its structure, anti-infective properties, ability to release the peptide, stability, and biocompatibility were evaluated by FTIR spectroscopy, water contact angle measurements, broth microdilution method, time-killing kinetic assays, quartz crystal microbalance analyses, MTT assays, and scanning electron microscopy analyses.

Results: PDMS was loaded with r(P)ApoBLPro peptide which was found to be present not only in the bulk matrix of the polymer but also on its surface. ApoB-derived peptide was found to retain its antimicrobial properties once loaded into PDMS and the antimicrobial material was found to be stable upon storage at 4 °C for a prolonged time interval. A gradual and significant release (70% of the total amount) of the peptide from PDMS was also demonstrated upon 400 min incubation and the antimicrobial material was found to be endowed with anti-adhesive properties and with the ability to prevent biofilm attachment. Furthermore, PDMS loaded with r(P)ApoBLPro peptide was found not to affect the viability of eukaryotic cells.

Conclusions: an easy procedure to functionalize PDMS with r(P)ApoBLPro peptide has been here developed and the obtained functionalized material has been found to be stable, antimicrobial, and biocompatible.

Keywords: antimicrobial peptides; antimicrobial resistance; antimicrobial surfaces; bacterial infections; biofilms; host defense peptides; infection prevention; polydimethylsiloxane.

MeSH terms

  • Anti-Bacterial Agents / pharmacology
  • Anti-Infective Agents* / pharmacology
  • Antimicrobial Peptides
  • Apolipoproteins B / chemistry
  • Bacterial Infections*
  • Biofilms
  • Dimethylpolysiloxanes / chemistry
  • Humans
  • Peptides / pharmacology
  • Polymers / pharmacology

Substances

  • Anti-Bacterial Agents
  • Anti-Infective Agents
  • Antimicrobial Peptides
  • Apolipoproteins B
  • Dimethylpolysiloxanes
  • Peptides
  • Polymers

Grants and funding

This research received no external funding.