TY - JOUR
T1 - Multifunctional Antimicrobial Nanofiber Dressings Containing ϵ-Polylysine for the Eradication of Bacterial Bioburden and Promotion of Wound Healing in Critically Colonized Wounds
AU - Mayandi, Venkatesh
AU - Wen Choong, Alvin Chua
AU - Dhand, Chetna
AU - Lim, Fui Ping
AU - Aung, Thet Tun
AU - Sriram, Harini
AU - Dwivedi, Neeraj
AU - Periayah, Mercy Halleluyah
AU - Sridhar, Sreepathy
AU - Fazil, Mobashar Hussain Urf Turabe
AU - Goh, Eunice Tze Leng
AU - Orive, Gorka
AU - W. Beuerman, Roger
AU - Barkham, Timothy Mark Sebastian
AU - Loh, Xian Jun
AU - Liang, Zhao Xun
AU - Barathi, Veluchamy Amutha
AU - Ramakrishna, Seeram
AU - Chong, Si Jack
AU - Verma, Navin Kumar
AU - Lakshminarayanan, Rajamani
N1 - Publisher Copyright:
Copyright © 2020 American Chemical Society.
PY - 2020/4/8
Y1 - 2020/4/8
N2 - Bacterial colonization of acute and chronic wounds is often associated with delayed wound healing and prolonged hospitalization. The rise of multi-drug resistant bacteria and the poor biocompatibility of topical antimicrobials warrant safe and effective antimicrobials. Antimicrobial agents that target microbial membranes without interfering with the mammalian cell proliferation and migration hold great promise in the treatment of traumatic wounds. This article reports the utility of superhydrophilic electrospun gelatin nanofiber dressings (NFDs) containing a broad-spectrum antimicrobial polymer, ϵ-polylysine (ϵPL), crosslinked by polydopamine (pDA) for treating second-degree burns. In a porcine model of partial thickness burns, NFDs promoted wound closure and reduced hypertrophic scarring compared to untreated burns. Analysis of NFDs in contact with the burns indicated that the dressings trap early colonizers and elicit bactericidal activity, thus creating a sterile wound bed for fibroblasts migration and re-epithelialization. In support of these observations, in porcine models of Pseudomonas aeruginosa and Staphylococcus aureus colonized partial thickness burns, NFDs decreased bacterial bioburden and promoted wound closure and re-epithelialization. NFDs displayed superior clinical outcome than standard-of-care silver dressings. The excellent biocompatibility and antimicrobial efficacy of the newly developed dressings in pre-clinical models demonstrate its potential for clinical use to manage infected wounds without compromising tissue regeneration.
AB - Bacterial colonization of acute and chronic wounds is often associated with delayed wound healing and prolonged hospitalization. The rise of multi-drug resistant bacteria and the poor biocompatibility of topical antimicrobials warrant safe and effective antimicrobials. Antimicrobial agents that target microbial membranes without interfering with the mammalian cell proliferation and migration hold great promise in the treatment of traumatic wounds. This article reports the utility of superhydrophilic electrospun gelatin nanofiber dressings (NFDs) containing a broad-spectrum antimicrobial polymer, ϵ-polylysine (ϵPL), crosslinked by polydopamine (pDA) for treating second-degree burns. In a porcine model of partial thickness burns, NFDs promoted wound closure and reduced hypertrophic scarring compared to untreated burns. Analysis of NFDs in contact with the burns indicated that the dressings trap early colonizers and elicit bactericidal activity, thus creating a sterile wound bed for fibroblasts migration and re-epithelialization. In support of these observations, in porcine models of Pseudomonas aeruginosa and Staphylococcus aureus colonized partial thickness burns, NFDs decreased bacterial bioburden and promoted wound closure and re-epithelialization. NFDs displayed superior clinical outcome than standard-of-care silver dressings. The excellent biocompatibility and antimicrobial efficacy of the newly developed dressings in pre-clinical models demonstrate its potential for clinical use to manage infected wounds without compromising tissue regeneration.
KW - bacterial infections
KW - electrospinning
KW - nanofiber dressings
KW - superhydrophilicity
KW - wound healing
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U2 - 10.1021/acsami.9b21683
DO - 10.1021/acsami.9b21683
M3 - Article
C2 - 32172559
AN - SCOPUS:85083080110
SN - 1944-8244
VL - 12
SP - 15989
EP - 16005
JO - ACS Applied Materials and Interfaces
JF - ACS Applied Materials and Interfaces
IS - 14
ER -