Evaluation of a 2-aminoimidazole variant as adjuvant treatment for dermal bacterial infections
dc.contributor.author | Draughn, G. Logan | |
dc.contributor.author | Allen, C. Leigh | |
dc.contributor.author | Routh, Patricia A. | |
dc.contributor.author | Stone, Maria R. | |
dc.contributor.author | Kirker, Kelly R. | |
dc.contributor.author | Boegli, Laura | |
dc.contributor.author | Schuchman, Ryan M. | |
dc.contributor.author | Linder, Keith E. | |
dc.contributor.author | Baynes, Ronald E. | |
dc.contributor.author | James, Garth A. | |
dc.contributor.author | Melander, Christian | |
dc.contributor.author | Pollard, Angela | |
dc.contributor.author | Cavanagh, John | |
dc.date.accessioned | 2017-05-12T18:48:32Z | |
dc.date.available | 2017-05-12T18:48:32Z | |
dc.date.issued | 2017-01 | |
dc.description.abstract | 2-Aminoimidazole (2-AI)-based compounds have been shown to efficiently disrupt biofilm formation, disperse existing biofilms, and resensitize numerous multidrug-resistant bacteria to antibiotics. Using Pseudomonas aeruginosa and Staphylococcus aureus, we provide initial pharmacological studies regarding the application of a 2-AI as a topical adjuvant for persistent dermal infections. In vitro assays indicated that the 2-AI H10 is nonbactericidal, resensitizes bacteria to antibiotics, does not harm the integument, and promotes wound healing. Furthermore, in vivo application of H10 on swine skin caused no gross abnormalities or immune reactions. Taken together, these results indicate that H10 represents a promising lead dermal adjuvant compound. | en_US |
dc.description.sponsorship | NIH (RO1 GM55769, R41 AI092952 01A1); V Foundation for Cancer Research | en_US |
dc.identifier.citation | Draughn, G. Logan, C. Leigh Allen, Patricia A. Routh, Maria R. Stone, Kelly R. Kirker, Laura Boegli, Ryan M. Schuchman, Keith E. Linder, Ronald E. Baynes, Garth James, Christian Melander, Angela Pollard, and John Cavanagh. "Evaluation of a 2-aminoimidazole variant as adjuvant treatment for dermal bacterial infections." Drug Design Development and Therapy 11 (January 2017): 153-162. DOI:https://dx.doi.org/10.2147/DDDT.S111865. | en_US |
dc.identifier.issn | 1177-8881 | |
dc.identifier.uri | https://scholarworks.montana.edu/handle/1/12822 | |
dc.language.iso | en_US | en_US |
dc.rights.uri | https://creativecommons.org/licenses/by-nc/3.0/legalcode | en_US |
dc.title | Evaluation of a 2-aminoimidazole variant as adjuvant treatment for dermal bacterial infections | en_US |
dc.type | Article | en_US |
mus.citation.extentfirstpage | 153 | en_US |
mus.citation.extentlastpage | 162 | en_US |
mus.citation.journaltitle | Drug Design Development and Therapy | en_US |
mus.citation.volume | 11 | en_US |
mus.data.thumbpage | 8 | en_US |
mus.identifier.category | Health & Medical Sciences | en_US |
mus.identifier.category | Life Sciences & Earth Sciences | en_US |
mus.identifier.doi | https://dx.doi.org/10.2147/DDDT.S111865 | en_US |
mus.relation.college | College of Engineering | en_US |
mus.relation.department | Chemical & Biological Engineering. | en_US |
mus.relation.researchgroup | Center for Biofilm Engineering. | en_US |
mus.relation.university | Montana State University - Bozeman | en_US |
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