Non-leaching, Highly Biocompatible Nanocellulose Surfaces That Efficiently Resist Fouling by Bacteria in an Artificial Dermis Model
| dc.contributor | Aalto-yliopisto | fi |
| dc.contributor | Aalto University | en |
| dc.contributor.author | Hassan, Ghada | en_US |
| dc.contributor.author | Forsman, Nina | en_US |
| dc.contributor.author | Wan, Xing | en_US |
| dc.contributor.author | Keurulainen, Leena | en_US |
| dc.contributor.author | Bimbo, Luis M. | en_US |
| dc.contributor.author | Stehl, Susanne | en_US |
| dc.contributor.author | Van Charante, Frits | en_US |
| dc.contributor.author | Chrubasik, Michael | en_US |
| dc.contributor.author | Prakash, Aruna S. | en_US |
| dc.contributor.author | Johansson, Leena Sisko | en_US |
| dc.contributor.author | Mullen, Declan C. | en_US |
| dc.contributor.author | Johnston, Blair F. | en_US |
| dc.contributor.author | Zimmermann, Ralf | en_US |
| dc.contributor.author | Werner, Carsten | en_US |
| dc.contributor.author | Yli-Kauhaluoma, Jari | en_US |
| dc.contributor.author | Coenye, Tom | en_US |
| dc.contributor.author | Saris, Per E.J. | en_US |
| dc.contributor.author | Österberg, Monika | en_US |
| dc.contributor.author | Moreira, Vânia M. | en_US |
| dc.contributor.department | Department of Bioproducts and Biosystems | en |
| dc.contributor.groupauthor | Bioproduct Chemistry | en |
| dc.contributor.groupauthor | Bio-based Colloids and Materials | en |
| dc.contributor.organization | University of Helsinki | en_US |
| dc.contributor.organization | University of Strathclyde | en_US |
| dc.contributor.organization | Leibniz-Institut für Polymerforschung Dresden | en_US |
| dc.contributor.organization | Ghent University | en_US |
| dc.date.accessioned | 2020-11-30T08:21:04Z | |
| dc.date.available | 2020-11-30T08:21:04Z | |
| dc.date.issued | 2020-07-20 | en_US |
| dc.description.abstract | Bacterial biofilm infections incur massive costs on healthcare systems worldwide. Particularly worrisome are the infections associated with pressure ulcers and prosthetic, plastic, and reconstructive surgeries, where staphylococci are the major biofilm-forming pathogens. Non-leaching antimicrobial surfaces offer great promise for the design of bioactive coatings to be used in medical devices. However, the vast majority are cationic, which brings about undesirable toxicity. To circumvent this issue, we have developed antimicrobial nanocellulose films by direct functionalization of the surface with dehydroabietic acid derivatives. Our conceptually unique design generates non-leaching anionic surfaces that reduce the number of viable staphylococci in suspension, including drug-resistant Staphylococcus aureus, by an impressive 4-5 log units, upon contact. Moreover, the films clearly prevent bacterial colonization of the surface in a model mimicking the physiological environment in chronic wounds. Their activity is not hampered by high protein content, and they nurture fibroblast growth at the surface without causing significant hemolysis. In this work, we have generated nanocellulose films with indisputable antimicrobial activity demonstrated using state-of-the-art models that best depict an "in vivo scenario". Our approach is to use fully renewable polymers and find suitable alternatives to silver and cationic antimicrobials. | en |
| dc.description.version | Peer reviewed | en |
| dc.format.extent | 14 | |
| dc.format.mimetype | application/pdf | en_US |
| dc.identifier.citation | Hassan, G, Forsman, N, Wan, X, Keurulainen, L, Bimbo, L M, Stehl, S, Van Charante, F, Chrubasik, M, Prakash, A S, Johansson, L S, Mullen, D C, Johnston, B F, Zimmermann, R, Werner, C, Yli-Kauhaluoma, J, Coenye, T, Saris, P E J, Österberg, M & Moreira, V M 2020, 'Non-leaching, Highly Biocompatible Nanocellulose Surfaces That Efficiently Resist Fouling by Bacteria in an Artificial Dermis Model', ACS Applied Bio Materials, vol. 3, no. 7, pp. 4095-4108. https://doi.org/10.1021/acsabm.0c00203 | en |
| dc.identifier.doi | 10.1021/acsabm.0c00203 | en_US |
| dc.identifier.issn | 2576-6422 | |
| dc.identifier.other | PURE UUID: f13cbd47-5592-4fa0-b7d9-e38a4a53ed17 | en_US |
| dc.identifier.other | PURE ITEMURL: https://research.aalto.fi/en/publications/f13cbd47-5592-4fa0-b7d9-e38a4a53ed17 | en_US |
| dc.identifier.other | PURE FILEURL: https://research.aalto.fi/files/52777228/acsabm.0c00203.pdf | |
| dc.identifier.uri | https://aaltodoc.aalto.fi/handle/123456789/61833 | |
| dc.identifier.urn | URN:NBN:fi:aalto-2020113020678 | |
| dc.language.iso | en | en |
| dc.publisher | American Chemical Society | |
| dc.relation.fundinginfo | V.M.M. acknowledges Business Finland (former TEKES, project 1297/31/2016), the Huonekalusäätio, Finland (2014, 2015) and Tenovus Scotland, UK (project S18-23) for financial support. G.H. acknowledges the Niemi Foundation, Finland (2018, 2019) for financial support. X.W. thanks The Finnish Cultural Foundation for providing the personal grant. L.M.B. acknowledges the Academy of Finland (decision no. 268616) and the Orion Research Foundation. V.M.M. and D.C.M. thank the Engineering and Physical Sciences Research Council (EPSRC) for funding (Doctoral Training Partnership 2018–19, grant no. EP/R513349/1). F.v.C. and T.C. received funding from the European Union’s Horizon 2020 research and innovation program under the Marie Skłodowska-Curie grant agreement no. 722467 (Print-Aid consortium). The authors thank: Dr. Nina Sipari from the Viikki Metabolomics Unit, University of Helsinki, for her kind assistance with the mass spectrometry analyses; Ritva Kivelä for fluidizing CNF and Prof. M. Skurnik for kindly providing S. aureus strain MRSA 14TK301. Prof. Vincenzo Cerullo and M.Sc. Manlio Fusciello are kindly acknowledged for providing the human fibroblasts and assistance in conducting the haemolysis and fibroblast proliferation assays. Dr. David Watson (University of Strathclyde, UK) is acknowledged for the helpful discussions that he privileged us with over the mass analysis in this work. The authors also acknowledge the Electron Microscopy Unit of the Institute of Biotechnology, University of Helsinki, for facilitating the SEM. The authors would like to acknowledge that part of this work was carried out in the CMAC National Facility, housed within the University of Strathclyde’s Technology and Innovation Centre, and funded with a UKRPIF (UK Research Partnership Institute Fund) capital award, SFC ref H13054, from the Higher Education Funding Council for England (HEFCE). | |
| dc.relation.ispartofseries | ACS Applied Bio Materials | en |
| dc.relation.ispartofseries | Volume 3, issue 7, pp. 4095-4108 | en |
| dc.rights | openAccess | en |
| dc.subject.keyword | antimicrobial | en_US |
| dc.subject.keyword | biofilm | en_US |
| dc.subject.keyword | cellulose nanofibril | en_US |
| dc.subject.keyword | dehydroabietic acid | en_US |
| dc.subject.keyword | surface | en_US |
| dc.title | Non-leaching, Highly Biocompatible Nanocellulose Surfaces That Efficiently Resist Fouling by Bacteria in an Artificial Dermis Model | en |
| dc.type | A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä | fi |
| dc.type.version | publishedVersion |
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