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Cubosomes post-loaded with antimicrobial peptides: Characterization, bactericidal effect and proteolytic stability
RISE - Research Institutes of Sweden, Biovetenskap och material, Kemi och material.ORCID-id: 0000-0003-4742-1702
INSERM U 1066, France ; Université Angers, France.
INSERM U 1066, France ; Université Angers,France.
RISE - Research Institutes of Sweden, Biovetenskap och material, Kemi och material.
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2017 (Engelska)Ingår i: International Journal of Pharmaceutics, ISSN 0378-5173, E-ISSN 1873-3476, Vol. 526, nr 1-2, s. 400-412Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Novel antibiotics, such as antimicrobial peptides (AMPs), have recently attended more and more attraction. In this work, dispersed cubic liquid crystalline gel (cubosomes) was used as drug delivery vehicles for three AMPs (AP114, DPK-060 and LL-37). Association of peptides onto cubosomes was studied at two cubosome/peptide ratios using high performance liquid chromatography, ζ-potential and circular dichroism measurements. AMPs impact on the cubosome structure was investigated using small angle x-ray scattering and cryogenic transmission electron microscopy. The antimicrobial effect of the AMP loaded cubosomes was studied in vitro by minimum inhibitory concentration and time-kill assays. Proteolytic protection was investigated by incubating the formulations with two elastases and the antimicrobial effect after proteolysis was studied using radial diffusion assay. Different association efficacy onto the cubosomes was observed among the AMPs, with LL-37 showing greatest association (>60%). AP114 loaded cubosomes displayed a preserved antimicrobial effect, whereas for LL-37 the broad spectrum bacterial killing was reduced to only comprise Gram-negative bacteria. Interestingly, DPK-060 loaded cubosomes showed a slight enhanced effect against S. aureus and E. coli strains. Moreover, the cubosomes were found to protect LL-37 from proteolytic degradation, resulting in a significantly better bactericidal effect after being subjected to elastase, compared to unformulated peptide.

Ort, förlag, år, upplaga, sidor
Elsevier B.V. , 2017. Vol. 526, nr 1-2, s. 400-412
Nyckelord [en]
Cubosome; Liquid crystalline nanoparticle; Glycerol monooleate; Antimicrobial peptide; Amp; Proteolysis
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URN: urn:nbn:se:ri:diva-30031DOI: 10.1016/j.ijpharm.2017.04.082Scopus ID: 2-s2.0-85019229976OAI: oai:DiVA.org:ri-30031DiVA, id: diva2:1119685
Tillgänglig från: 2017-07-04 Skapad: 2017-07-04 Senast uppdaterad: 2019-07-05Bibliografiskt granskad

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