Cargando…
Development and Characterization of a Novel Peptide-Loaded Antimicrobial Ocular Insert
Infectious ocular keratitis is the leading cause of blindness worldwide. Bacterial resistance to classical pharmacological treatments raised the interest of researchers towards antimicrobial peptide (AMP)-based therapy. hLF 1-11, a synthetic antimicrobial peptide derived from the N-terminus of human...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277359/ https://www.ncbi.nlm.nih.gov/pubmed/32344824 http://dx.doi.org/10.3390/biom10050664 |
_version_ | 1783543100508995584 |
---|---|
author | Terreni, Eleonora Burgalassi, Susi Chetoni, Patrizia Tampucci, Silvia Zucchetti, Erica Fais, Roberta Ghelardi, Emilia Lupetti, Antonella Monti, Daniela |
author_facet | Terreni, Eleonora Burgalassi, Susi Chetoni, Patrizia Tampucci, Silvia Zucchetti, Erica Fais, Roberta Ghelardi, Emilia Lupetti, Antonella Monti, Daniela |
author_sort | Terreni, Eleonora |
collection | PubMed |
description | Infectious ocular keratitis is the leading cause of blindness worldwide. Bacterial resistance to classical pharmacological treatments raised the interest of researchers towards antimicrobial peptide (AMP)-based therapy. hLF 1-11, a synthetic antimicrobial peptide derived from the N-terminus of human lactoferrin, proved effective against different bacteria and yeast but, like all proteinaceous materials, it is unstable from chemical, physical, and biological points of view. In this study, new freeze-dried solid matrices containing mucoadhesive polymers were prepared and characterized in terms of rheology, hydration time, bioadhesion, drug content, and in vitro release. The formulation HPMC/T2/HA/hLF 1-11(fd) was selected for the delivery of hLF 1-11, since it showed good drug recovery and no chemical degradation up to at least 6 months (long-term stability). Furthermore, the HPMC/T2/HA/hLF 1-11(fd) matrix allowed for the release of the drug in a simulated physiological environment, linked to an optimal hydration time, and the peptide antimicrobial activity was preserved for up to 15 months of storage, a very promising result considering the chemical liability of proteinaceous material. For its properties, the freeze-dried matrix developed in this study could be a good platform for the delivery of antimicrobial peptides in the precorneal area to treat infectious phenomena of the ocular surface. |
format | Online Article Text |
id | pubmed-7277359 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-72773592020-06-15 Development and Characterization of a Novel Peptide-Loaded Antimicrobial Ocular Insert Terreni, Eleonora Burgalassi, Susi Chetoni, Patrizia Tampucci, Silvia Zucchetti, Erica Fais, Roberta Ghelardi, Emilia Lupetti, Antonella Monti, Daniela Biomolecules Article Infectious ocular keratitis is the leading cause of blindness worldwide. Bacterial resistance to classical pharmacological treatments raised the interest of researchers towards antimicrobial peptide (AMP)-based therapy. hLF 1-11, a synthetic antimicrobial peptide derived from the N-terminus of human lactoferrin, proved effective against different bacteria and yeast but, like all proteinaceous materials, it is unstable from chemical, physical, and biological points of view. In this study, new freeze-dried solid matrices containing mucoadhesive polymers were prepared and characterized in terms of rheology, hydration time, bioadhesion, drug content, and in vitro release. The formulation HPMC/T2/HA/hLF 1-11(fd) was selected for the delivery of hLF 1-11, since it showed good drug recovery and no chemical degradation up to at least 6 months (long-term stability). Furthermore, the HPMC/T2/HA/hLF 1-11(fd) matrix allowed for the release of the drug in a simulated physiological environment, linked to an optimal hydration time, and the peptide antimicrobial activity was preserved for up to 15 months of storage, a very promising result considering the chemical liability of proteinaceous material. For its properties, the freeze-dried matrix developed in this study could be a good platform for the delivery of antimicrobial peptides in the precorneal area to treat infectious phenomena of the ocular surface. MDPI 2020-04-25 /pmc/articles/PMC7277359/ /pubmed/32344824 http://dx.doi.org/10.3390/biom10050664 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Terreni, Eleonora Burgalassi, Susi Chetoni, Patrizia Tampucci, Silvia Zucchetti, Erica Fais, Roberta Ghelardi, Emilia Lupetti, Antonella Monti, Daniela Development and Characterization of a Novel Peptide-Loaded Antimicrobial Ocular Insert |
title | Development and Characterization of a Novel Peptide-Loaded Antimicrobial Ocular Insert |
title_full | Development and Characterization of a Novel Peptide-Loaded Antimicrobial Ocular Insert |
title_fullStr | Development and Characterization of a Novel Peptide-Loaded Antimicrobial Ocular Insert |
title_full_unstemmed | Development and Characterization of a Novel Peptide-Loaded Antimicrobial Ocular Insert |
title_short | Development and Characterization of a Novel Peptide-Loaded Antimicrobial Ocular Insert |
title_sort | development and characterization of a novel peptide-loaded antimicrobial ocular insert |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7277359/ https://www.ncbi.nlm.nih.gov/pubmed/32344824 http://dx.doi.org/10.3390/biom10050664 |
work_keys_str_mv | AT terrenieleonora developmentandcharacterizationofanovelpeptideloadedantimicrobialocularinsert AT burgalassisusi developmentandcharacterizationofanovelpeptideloadedantimicrobialocularinsert AT chetonipatrizia developmentandcharacterizationofanovelpeptideloadedantimicrobialocularinsert AT tampuccisilvia developmentandcharacterizationofanovelpeptideloadedantimicrobialocularinsert AT zucchettierica developmentandcharacterizationofanovelpeptideloadedantimicrobialocularinsert AT faisroberta developmentandcharacterizationofanovelpeptideloadedantimicrobialocularinsert AT ghelardiemilia developmentandcharacterizationofanovelpeptideloadedantimicrobialocularinsert AT lupettiantonella developmentandcharacterizationofanovelpeptideloadedantimicrobialocularinsert AT montidaniela developmentandcharacterizationofanovelpeptideloadedantimicrobialocularinsert |