dc.contributor.author | Hemmingsen, Lisa Myrseth | |
dc.contributor.author | Julin, Kjersti | |
dc.contributor.author | Ahsan, Luqman | |
dc.contributor.author | Basnet, Purusotam | |
dc.contributor.author | Johannessen, Mona | |
dc.contributor.author | Skalko-Basnet, Natasa | |
dc.date.accessioned | 2021-08-05T07:09:07Z | |
dc.date.available | 2021-08-05T07:09:07Z | |
dc.date.issued | 2021-05-12 | |
dc.description.abstract | Burns 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.citation | Hemmingsen 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;19 | en_US |
dc.identifier.cristinID | FRIDAID 1910019 | |
dc.identifier.doi | https://doi.org/10.3390/md19050269 | |
dc.identifier.issn | 1660-3397 | |
dc.identifier.uri | https://hdl.handle.net/10037/21937 | |
dc.language.iso | eng | en_US |
dc.publisher | MDPI | en_US |
dc.relation.ispartof | Hemmingsen, 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.journal | Marine Drugs | |
dc.rights.accessRights | openAccess | en_US |
dc.rights.holder | Copyright 2021 The Author(s) | en_US |
dc.subject | VDP::Medical disciplines: 700::Clinical medical disciplines: 750::Dermatology and venereology: 753 | en_US |
dc.subject | VDP::Medisinske Fag: 700::Klinisk medisinske fag: 750::Dermatologi og venerologi: 753 | en_US |
dc.subject | VDP::Medical disciplines: 700::Basic medical, dental and veterinary science disciplines: 710::Medical microbiology: 715 | en_US |
dc.subject | VDP::Medisinske Fag: 700::Basale medisinske, odontologiske og veterinærmedisinske fag: 710::Medisinsk mikrobiologi: 715 | en_US |
dc.title | Chitosomes-In-Chitosan Hydrogel for Acute Skin Injuries: Prevention and Infection Control | en_US |
dc.type.version | publishedVersion | en_US |
dc.type | Journal article | en_US |
dc.type | Tidsskriftartikkel | en_US |
dc.type | Peer reviewed | en_US |