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Loading of Polydimethylsiloxane with a Human ApoB-Derived Antimicrobial Peptide to Prevent Bacterial Infections.
De Luca, Maria; Gaglione, Rosa; Della Ventura, Bartolomeo; Cesaro, Angela; Di Girolamo, Rocco; Velotta, Raffaele; Arciello, Angela.
Afiliación
  • De Luca M; Department of Chemical Sciences, University of Naples Federico II, 80126 Naples, Italy.
  • Gaglione R; Department of Chemical Sciences, University of Naples Federico II, 80126 Naples, Italy.
  • Della Ventura B; Istituto Nazionale di Biostrutture e Biosistemi (INBB), 00136 Rome, Italy.
  • Cesaro A; Department of Physics "E. Pancini", University of Naples Federico II, 80126 Naples, Italy.
  • Di Girolamo R; Department of Chemical Sciences, University of Naples Federico II, 80126 Naples, Italy.
  • Velotta R; Machine Biology Group, Departments of Psychiatry and Microbiology, Institute for Biomedical Informatics, Institute for Translational Medicine and Therapeutics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104, USA.
  • Arciello A; Departments of Bioengineering and Chemical and Biomolecular Engineering, School of Engineering and Applied Science, University of Pennsylvania, Philadelphia, PA 19104, USA.
Int J Mol Sci ; 23(9)2022 May 07.
Article en En | MEDLINE | ID: mdl-35563610
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.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Infecciones Bacterianas / Antiinfecciosos Límite: Humans Idioma: En Revista: Int J Mol Sci Año: 2022 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Infecciones Bacterianas / Antiinfecciosos Límite: Humans Idioma: En Revista: Int J Mol Sci Año: 2022 Tipo del documento: Article País de afiliación: Italia