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Sökning: L773:0939 6411 OR L773:1873 3441 > Cubosomes for topic...

Cubosomes for topical delivery of the antimicrobial peptide LL-37

Boge, Lukas (författare)
RISE,Yta, process och formulering,Chalmers University of Technology, Sweden
Hallstensson, Karin (författare)
RISE,Yta, process och formulering
Ringstad, Lovisa (författare)
RISE,Yta, process och formulering
visa fler...
Johansson, Jenny (författare)
RISE,Kemi och material,Certifiering
Andersson, Therese (författare)
RISE,Kemi och material
Davoudi, Mina (författare)
Lund University, Sweden
Larsson, Per Tomas (författare)
RISE,Kemi och material
Mahlapuu, Margit (författare)
Promore Pharma AB, Sweden; University of Gothenburg, Sweden
Håkansson, Joakim (författare)
RISE,Kemi och material
Andersson, Martin (författare)
Chalmers University of Technology, Sweden
visa färre...
 (creator_code:org_t)
Elsevier BV, 2019
2019
Engelska.
Ingår i: European journal of pharmaceutics and biopharmaceutics. - : Elsevier BV. - 0939-6411 .- 1873-3441. ; 134, s. 60-67
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • In this study, the use of cubosomes for topical delivery of the antimicrobial peptide (AMP) LL-37 was investigated. Topical delivery of AMPs is of great interest for treatment of skin infections caused by bacteria, such as Staphylococcus aureus. AMP containing cubosomes were produced by three different preparation protocols and compared: (i) pre-loading, where LL-37 was incorporated into a liquid crystalline gel, which thereafter was dispersed into nanoparticles, (ii) post-loading, where LL-37 was let to adsorb onto pre-formed cubosomes, and (iii) hydrotrope-loading, where LL-37 was incorporated during the spontaneously formed cubosomes in an ethanol/glycerol monooleate mixture. Particle size and size distribution were analyzed using dynamic light scattering (DLS), liquid crystalline structure by small angle x-ray scattering (SAXS) and release of LL-37 by a fluorescamine assay. Proteolytic protection of LL-37 as well as bactericidal effect after enzyme exposure was investigated. The skin irritation potential of cubosomes was examined by an in vitro epidermis model. Finally, the bacterial killing property of the cubosomes was examined by an ex vivo pig skin wound infection model with Staphylococcus aureus. Data showed that a high loading of LL-37 induced formation of vesicles in case of cubosomes prepared by sonication (pre-loading). No release of LL-37 was observed from the cubosomes, indicating strong association of the peptide to the particles. Proteolysis studies showed that LL-37 was fully protected against enzymatic attacks while associated with the cubosomes, also denoting strong association of the peptide to the particles. As a consequence, bactericidal effect after enzyme exposure remained, compared to pure LL-37 which was subjected to proteolysis. No skin irritation potential of the cubosomes was found, thus enabling for topical administration. The ex vivo wound infection model showed that LL-37 in pre-loaded cubosomes killed bacteria most efficient.

Ämnesord

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

Nyckelord

alcohol
cathelicidin antimicrobial peptide LL 37
cubosome
drug carrier
fluorescamine
glycerol oleate
hydrotrope
nanoparticle
unclassified drug

Publikations- och innehållstyp

ref (ämneskategori)
art (ämneskategori)

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