The anti MRSA biofilm activity of Thymus vulgaris essential oil in nanovesicles.


Journal

Phytomedicine : international journal of phytotherapy and phytopharmacology
ISSN: 1618-095X
Titre abrégé: Phytomedicine
Pays: Germany
ID NLM: 9438794

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 06 11 2018
revised: 15 12 2018
accepted: 20 12 2018
pubmed: 4 3 2019
medline: 25 6 2019
entrez: 4 3 2019
Statut: ppublish

Résumé

Thymus vulgaris essential oil (T) could be an alternative to classical antibiotics against bacterial biofilms, which show increased tolerance to antibiotics and host defence systems and contribute to the persistence of chronic bacterial infections. A nanovesicular formulation of T may chemically protect the structure and relative composition of its multiple components, potentially improving its antibacterial and antibiofilm activity. We prepared and structurally characterized T in two types of nanovesicles: nanoliposomes (L80-T) made of Soybean phosphatidylcholine (SPC) and Polysorbate 80 (P80) [SPC:P80:T 1:0.75:0.3 w:w], and nanoarchaeosomes (A80-T) made of SPC, P80 and total polar archaeolipids (TPA) extracted from archaebacteria Halorubrum tebenquichense [SPC:TPA:P80:T 0.5:0.50.75:0.7 w:w]. We determined the macrophage cytotoxicity and the antibacterial activity against Staphylococcus aureus ATCC 25,923 and four MRSA clinical strains. L80-T (Z potential -4.1 ± 0.6 mV, ∼ 115 nm, ∼ 22 mg/ml T) and A80-T (Z potential -6.6 ± 1.5 mV, ∼ 130 nm, ∼ 42 mg/ml T) were colloidally and chemically stable, maintaining size, PDI, Z potential and T concentration for at least 90 days. While MIC Overall, because of its lower MIC

Sections du résumé

BACKGROUND BACKGROUND
Thymus vulgaris essential oil (T) could be an alternative to classical antibiotics against bacterial biofilms, which show increased tolerance to antibiotics and host defence systems and contribute to the persistence of chronic bacterial infections.
HYPOTHESIS OBJECTIVE
A nanovesicular formulation of T may chemically protect the structure and relative composition of its multiple components, potentially improving its antibacterial and antibiofilm activity.
STUDY DESIGN METHODS
We prepared and structurally characterized T in two types of nanovesicles: nanoliposomes (L80-T) made of Soybean phosphatidylcholine (SPC) and Polysorbate 80 (P80) [SPC:P80:T 1:0.75:0.3 w:w], and nanoarchaeosomes (A80-T) made of SPC, P80 and total polar archaeolipids (TPA) extracted from archaebacteria Halorubrum tebenquichense [SPC:TPA:P80:T 0.5:0.50.75:0.7 w:w]. We determined the macrophage cytotoxicity and the antibacterial activity against Staphylococcus aureus ATCC 25,923 and four MRSA clinical strains.
RESULTS RESULTS
L80-T (Z potential -4.1 ± 0.6 mV, ∼ 115 nm, ∼ 22 mg/ml T) and A80-T (Z potential -6.6 ± 1.5 mV, ∼ 130 nm, ∼ 42 mg/ml T) were colloidally and chemically stable, maintaining size, PDI, Z potential and T concentration for at least 90 days. While MIC
CONCLUSION CONCLUSIONS
Overall, because of its lower MIC

Identifiants

pubmed: 30826631
pii: S0944-7113(18)30619-6
doi: 10.1016/j.phymed.2018.12.025
pii:
doi:

Substances chimiques

Anti-Bacterial Agents 0
Oils, Volatile 0
Phosphatidylcholines 0
Polysorbates 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

339-351

Informations de copyright

Copyright © 2019. Published by Elsevier GmbH.

Auteurs

Ana Paula Perez (AP)

Nanomedicine Research and Development Centre, Science and Technology Department, National University of Quilmes, Bernal, Buenos Aires, Argentina.

Noelia Perez (N)

Nanomedicine Research and Development Centre, Science and Technology Department, National University of Quilmes, Bernal, Buenos Aires, Argentina.

Carlos Mauricio Suligoy Lozano (CMS)

Instituto de Investigaciones en Microbiología y Parasitología Médica (IMPaM-CONICET), Departamento de Microbiología, Parasitología e Inmunología, Facultad de Medicina, Universidad de Buenos Aires, Buenos Aires, Argentina.

Maria Julia Altube (MJ)

Nanomedicine Research and Development Centre, Science and Technology Department, National University of Quilmes, Bernal, Buenos Aires, Argentina.

Marcelo Alexandre de Farias (MA)

Brazilian Nanotechnology National Laboratory, CNPEM, Campinas, São Paulo, Brazil.

Rodrigo Villares Portugal (RV)

Brazilian Nanotechnology National Laboratory, CNPEM, Campinas, São Paulo, Brazil.

Fernanda Buzzola (F)

Instituto de Investigaciones en Microbiología y Parasitología Médica (IMPaM-CONICET), Departamento de Microbiología, Parasitología e Inmunología, Facultad de Medicina, Universidad de Buenos Aires, Buenos Aires, Argentina.

María Jose Morilla (MJ)

Nanomedicine Research and Development Centre, Science and Technology Department, National University of Quilmes, Bernal, Buenos Aires, Argentina.

Eder Lilia Romero (EL)

Nanomedicine Research and Development Centre, Science and Technology Department, National University of Quilmes, Bernal, Buenos Aires, Argentina. Electronic address: elromero@unq.edu.ar.

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Classifications MeSH