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dc.contributor.authorHemmingsen, Lisa Myrseth
dc.contributor.authorJulin, Kjersti
dc.contributor.authorAhsan, Luqman
dc.contributor.authorBasnet, Purusotam
dc.contributor.authorJohannessen, Mona
dc.contributor.authorSkalko-Basnet, Natasa
dc.date.accessioned2021-08-05T07:09:07Z
dc.date.available2021-08-05T07:09:07Z
dc.date.issued2021-05-12
dc.description.abstractBurns and other skin injuries are growing concerns as well as challenges in an era of antimicrobial resistance. Novel treatment options to improve the prevention and eradication of infectious skin biofilm-producing pathogens, while enhancing wound healing, are urgently needed for the timely treatment of infection-prone injuries. Treatment of acute skin injuries requires tailoring of formulation to assure both proper skin retention and the appropriate release of incorporated antimicrobials. The challenge remains to formulate antimicrobials with low water solubility, which often requires carriers as the primary vehicle, followed by a secondary skin-friendly vehicle. We focused on widely used chlorhexidine formulated in the chitosan-infused nanocarriers, chitosomes, incorporated into chitosan hydrogel for improved treatment of skin injuries. To prove our hypothesis, lipid nanocarriers and chitosan-comprising nanocarriers (≈250 nm) with membrane-active antimicrobial chlorhexidine were optimized and incorporated into chitosan hydrogel. The biological and antibacterial effects of both vesicles and a vesicles-in-hydrogel system were evaluated. The chitosomes-in-chitosan hydrogel formulation demonstrated promising physical properties and were proven safe. Additionally, the chitosan-based systems, both chitosomes and chitosan hydrogel, showed an improved antimicrobial effect against <i>S. aureus</i> and <i>S. epidermidis</i> compared to the formulations without chitosan. The novel formulation could serve as a foundation for infection prevention and bacterial eradication in acute wounds.en_US
dc.identifier.citationHemmingsen LM, Julin K, Ahsan, Basnet P, Johannessen M, Skalko-Basnet N. Chitosomes-In-Chitosan Hydrogel for Acute Skin Injuries: Prevention and Infection ControL. Marine Drugs. 2021;19en_US
dc.identifier.cristinIDFRIDAID 1910019
dc.identifier.doihttps://doi.org/10.3390/md19050269
dc.identifier.issn1660-3397
dc.identifier.urihttps://hdl.handle.net/10037/21937
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.relation.ispartofHemmingsen, L.M. (2022). Advanced topical delivery systems for membrane-active antimicrobials. Exploring nature to improve antimicrobial wound therapy. (Doctoral thesis). <a href=https://hdl.handle.net/10037/27103>https://hdl.handle.net/10037/27103</a>.
dc.relation.journalMarine Drugs
dc.rights.accessRightsopenAccessen_US
dc.rights.holderCopyright 2021 The Author(s)en_US
dc.subjectVDP::Medical disciplines: 700::Clinical medical disciplines: 750::Dermatology and venereology: 753en_US
dc.subjectVDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Dermatologi og venerologi: 753en_US
dc.subjectVDP::Medical disciplines: 700::Basic medical, dental and veterinary science disciplines: 710::Medical microbiology: 715en_US
dc.subjectVDP::Medisinske Fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Medisinsk mikrobiologi: 715en_US
dc.titleChitosomes-In-Chitosan Hydrogel for Acute Skin Injuries: Prevention and Infection Controlen_US
dc.type.versionpublishedVersionen_US
dc.typeJournal articleen_US
dc.typeTidsskriftartikkelen_US
dc.typePeer revieweden_US


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